WorldWideScience

Sample records for actinomycete salinispora tropica

  1. Genome sequencing reveals complex secondary metabolome in themarine actinomycete Salinispora tropica

    Energy Technology Data Exchange (ETDEWEB)

    Udwary, Daniel W.; Zeigler, Lisa; Asolkar, Ratnakar; Singan,Vasanth; Lapidus, Alla; Fenical, William; Jensen, Paul R.; Moore, BradleyS.

    2007-05-01

    Recent fermentation studies have identified actinomycetes ofthe marine-dwelling genus Salinispora as prolific natural productproducers. To further evaluate their biosynthetic potential, we analyzedall identifiable secondary natural product gene clusters from therecently sequenced 5,184,724 bp S. tropica CNB-440 circular genome. Ouranalysis shows that biosynthetic potential meets or exceeds that shown byprevious Streptomyces genome sequences as well as other naturalproduct-producing actinomycetes. The S. tropica genome features ninepolyketide synthase systems of every known formally classified family,non-ribosomal peptide synthetases and several hybrid clusters. While afew clusters appear to encode molecules previously identified inStreptomyces species,the majority of the 15 biosynthetic loci are novel.Specific chemical information about putative and observed natural productmolecules is presented and discussed. In addition, our bioinformaticanalysis was critical for the structure elucidation of the novelpolyenemacrolactam salinilactam A. This study demonstrates the potentialfor genomic analysis to complement and strengthen traditional naturalproduct isolation studies and firmly establishes the genus Salinispora asa rich source of novel drug-like molecules.

  2. Engineering fluorometabolite production: fluorinase expression in Salinispora tropica Yields Fluorosalinosporamide.

    Science.gov (United States)

    Eustáquio, Alessandra S; O'Hagan, David; Moore, Bradley S

    2010-03-26

    Organofluorine compounds play an important role in medicinal chemistry, where they are responsible for up to 15% of the pharmaceutical products on the market. While natural products are valuable sources of new chemical entities, natural fluorinated molecules are extremely rare and the pharmaceutical industry has not benefited from a microbial source of this class of compounds. Streptomyces cattleya is an unusual bacterium in that it elaborates fluoroacetate and the amino acid 4-fluorothreonine. The discovery in 2002 of the fluorination enzyme FlA responsible for C-F bond formation in S. cattleya, and its subsequent characterization, opened up for the first time the prospect of genetically engineering fluorometabolite production from fluoride ion in host organisms. As a proof of principle, we report here the induced production of fluorosalinosporamide by replacing the chlorinase gene salL from Salinispora tropica with the fluorinase gene flA.

  3. Biological activity of sporolides A and B from Salinispora tropica: in silico target prediction using ligand-based pharmacophore mapping and in vitro activity validation on HIV-1 reverse transcriptase.

    Science.gov (United States)

    Dineshkumar, Kesavan; Aparna, Vasudevan; Madhuri, Kantilal Z; Hopper, Waheeta

    2014-03-01

    Sporolides A and B are novel polycyclic macrolides from the obligate marine actinomycetes, Salinispora tropica. The unique and novel structure of sporolides makes them interesting candidates for targeting diverse biological activities. Biological target prediction of sporolides was carried out using ligand-based pharmacophore screening against known inhibitors and drugs. Validation of pharmacophore screening was carried out for the identified hits. New biological targets predicted for sporolides using this method were HIV-1 reverse transcriptase, adenosine A3 receptor, endothelin receptor ET-A, oxytocin receptor, voltage-gated L-type calcium channel α-1C subunit/calcium channel α/Δ subunit 1. Drug-likeness properties were predicted for the selected compounds using QikProp module. Sporolides A and B showed maximum docking score with HIV-1 reverse transcriptase. Structural interaction fingerprints analysis indicated similar binding pattern of the sporolides with the HIV-1 reverse transcriptase. Sporolide B exhibited good inhibitory activity against HIV-1 reverse transcriptase in in vitro fluorescent assay.

  4. Comparative analysis of oligonucleotide primers for high-throughput screening of genes encoding adenylation domains of nonribosomal peptide synthetases in actinomycetes.

    Science.gov (United States)

    Bakal, Tomas; Goo, Kian-Sim; Najmanova, Lucie; Plhackova, Kamila; Kadlcik, Stanislav; Ulanova, Dana

    2015-11-01

    In the biosynthesis of diverse natural bioactive products the adenylation domains (ADs) of nonribosomal peptide synthetases select specific precursors from the cellular pool and activate them for further incorporation into the scaffold of the final compound. Therefore, the drug discovery programs employing PCR-based screening studies of microbial collections or metagenomic libraries often use AD-coding genes as markers of relevant biosynthetic gene clusters. However, due to significant sequence diversity of ADs, the conventional approach using only one primer pair in a single screening experiment could be insufficient for maximal coverage of AD abundance. In this study, the widely used primer pair A3F/A7R was compared with the newly designed aa194F/aa413R one by 454 pyrosequencing of two sets of actinomycete strains from highly dissimilar environments: subseafloor sediments and forest soil. Individually, none of the primer pairs was able to cover the overall diversity of ADs. However, due to slightly shifted specificity of the primer pairs, the total number and diversity of identified ADs were noticeably extended when both primer pairs were used in a single assay. Additionally, the efficiency of AD detection by different primer combinations was confirmed on the model of Salinispora tropica genomic DNA of known sequence.

  5. Production and purification of a bioactive substance against multi-drug resistant human pathogens from the marine-sponge-derived Salinispora sp.

    Institute of Scientific and Technical Information of China (English)

    Satyendra Singh; Pritesh Prasad; Ramesh Subramani; William Aalbersberg

    2014-01-01

    Objective: To isolate, purify, characterize, elucidate structure and evaluate bioactive compounds from the sponge-derived Salinispora sp. FS-0034. Methods: The symbiotic actinomycete strain FS-0034 with an interesting bioactivity profile was isolated from the Fijian marine sponge Theonella sp. Based on colony morphology and obligatory requirement of seawater for growth, and mycelia morphological characteristics the isolate FS-0034 was identified as a Salinispora sp. The bioactive compound was identified by using various spectral analysis of ultraviolet, high resolution electrospray ionization mass spectroscopy, 1H nuclear magnetic resonance, correlated spectroscopy and heteronuclear multiple bond coherence spectral data. A minimum inhibitory concentration assay were performed to evaluate the biological properties of the pure compound against multi-drug resistant pathogens. Results: Bioassay guided fractionation of the ethyl acetate extract of the culture of Salinispora sp. FS-0034 by different chromatographic methods yielded the isolation of an antibacterial compound, which was identified as rifamycin W (compound 1). Rifamycin W was reported for its potent antibacterial activity against methicillin-resistant Staphylococcus aureus, wild typeStaphylococcus aureus and vancomycin-resistant Enterococcus faecium and displayed minimum inhibitory concentrations of 15.62, 7.80 and 250.00 µg/mL, respectively. Conclusions:The present study reported the rifamycin W from sponge-associated Salinispora sp. and it exhibited appreciable antibacterial activity against multi-drug resistant human pathogens which indicated that sponge-associated Actinobacteria are significant sources of bioactive metabolites.

  6. Production and purification of a bioactive substance against multi-drug resistant human pathogens from the marine-sponge-derived Salinispora sp.

    Institute of Scientific and Technical Information of China (English)

    Satyendra; Singh; Pritesh; Prasad; Ramesh; Subramani; William; Aalbersberg

    2014-01-01

    Objective:To isolate,purify,characterize,elucidate structure and evaluate bioactive compounds from the sponge-derived Salinispora sp.FS-0034.Methods:The symbiotic actinomycete strain FS-0034 with an interesting bioactivity profile was isolated from the Fijian marine sponge Theonella sp.Based on colony morphology and obligatory requirement of seawater for growth,and mycelia morphological characteristics the isolate FS-0034 was identified as a Salinispora sp.The bioactive compound was identified by using various spectral analysis of ultraviolet,high resolution electrospray ionization mass spectroscopy,H nuclear magnetic resonance,correlated spectroscopy and heteronuclear multiple bond coherence spectral data.A minimum inhibitory concentration assay were performed to evaluate the biological properties of the pure compound against multi-drug resistant pathogens.Results:Bioassay guided fractionation of the ethyl acetate extract of the culture of Salinispora sp.FS-0034 by different chromatographic methods yielded the isolation of an antibacterial compound,which was identified as rifamycin W(compound 1).Rifamycin W was reported for its potent antibacterial activity against methicillin-resistant Staphylococcus aureus,wild type Staphylococcus aureus and vancomycin-resistant Enterococcus faecium and displayed minimum inhibitory concentrations of 15.62,7.80 and 250.00 μg/mL,respectively.Conclusions:The present study reported the rifamycin W from sponge-associated Salinispora sp.and it exhibited appreciable antibacterial activity against multi-drug resistant human pathogens which indicated that sponge-associated Actinobacteria are significant sources of bioactive metabolites.

  7. The Madeira Archipelago as a significant source of marine-derived actinomycete diversity with anticancer and antimicrobial potential

    Directory of Open Access Journals (Sweden)

    Alejandra Prieto-Davo

    2016-10-01

    Full Text Available Marine-derived actinomycetes have demonstrated an ability to produce novel compounds with medically relevant biological activity. Studying the diversity and biogeographical patterns of marine actinomycetes offers an opportunity to identify genera that are under environmental pressures, which may drive adaptations that yield specific biosynthetic capabilities. The present study describes research efforts to explore regions of the Atlantic Ocean, specifically around the Madeira Archipelago, where knowledge of the indigenous actinomycete diversity is scarce. A total of 400 actinomycetes were isolated, sequenced and screened for antimicrobial and anticancer activities. The three most abundant genera identified were Streptomyces, Actinomadura and Micromonospora. Phylogenetic analyses of the marine OTUs isolated indicated that the Madeira Archipelago is a new source of actinomycetes adapted to life in the ocean. Phylogenetic differences between offshore (>100m from shore and nearshore (<100m from shore populations illustrates the importance of sampling offshore in order to isolate new and diverse bacterial strains. Novel phylotypes from chemically rich marine actinomycete groups like MAR4 and the genus Salinispora were isolated. Anticancer and antimicrobial assays identified Streptomyces, Micromonospora and Salinispora as the most biologically active genera. This study illustrates the importance of bioprospecting efforts at unexplored regions of the ocean to recover bacterial strains with the potential to produce novel and interesting chemistry.

  8. The Madeira Archipelago As a Significant Source of Marine-Derived Actinomycete Diversity with Anticancer and Antimicrobial Potential

    Science.gov (United States)

    Prieto-Davó, Alejandra; Dias, Tiago; Gomes, Sofia E.; Rodrigues, Sara; Parera-Valadez, Yessica; Borralho, Pedro M.; Pereira, Florbela; Rodrigues, Cecilia M. P.; Santos-Sanches, Ilda; Gaudêncio, Susana P.

    2016-01-01

    Marine-derived actinomycetes have demonstrated an ability to produce novel compounds with medically relevant biological activity. Studying the diversity and biogeographical patterns of marine actinomycetes offers an opportunity to identify genera that are under environmental pressures, which may drive adaptations that yield specific biosynthetic capabilities. The present study describes research efforts to explore regions of the Atlantic Ocean, specifically around the Madeira Archipelago, where knowledge of the indigenous actinomycete diversity is scarce. A total of 400 actinomycetes were isolated, sequenced, and screened for antimicrobial and anticancer activities. The three most abundant genera identified were Streptomyces, Actinomadura, and Micromonospora. Phylogenetic analyses of the marine OTUs isolated indicated that the Madeira Archipelago is a new source of actinomycetes adapted to life in the ocean. Phylogenetic differences between offshore (>100 m from shore) and nearshore (< 100 m from shore) populations illustrates the importance of sampling offshore in order to isolate new and diverse bacterial strains. Novel phylotypes from chemically rich marine actinomycete groups like MAR4 and the genus Salinispora were isolated. Anticancer and antimicrobial assays identified Streptomyces, Micromonospora, and Salinispora as the most biologically active genera. This study illustrates the importance of bioprospecting efforts at unexplored regions of the ocean to recover bacterial strains with the potential to produce novel and interesting chemistry. PMID:27774089

  9. Marine actinomycetes from Madeira Archipelago preliminary taxonomic studies

    Directory of Open Access Journals (Sweden)

    Ilda Santos Sanches

    2014-06-01

    Full Text Available The oceans cover 70 % of the Earth´s surface and harbor most of the planet´s biodiversity. However the microbiological component of this diversity remains relatively unexplored. Marine actinomycetes, are a robust resource of chemically prolific novelty. Producing structurally unique biological active secondary metabolites, generating a valuable source for innovative biotechnology and drug discovery[1,2]. As a consequence, the ecological role of actinomycetes and their marine ecosystems may no longer be neglected. It is crucial to move our research efforts into ocean regions for which we know little or nothing about the indigenous microbial diversity. The Portuguese Archipelago, Madeira is located in the Macaronesian Atlantic region, emerging from the African tectonic plate, found in the extreme south of the Tore-Madeira ridge, has a unique biogeography and biodiversity. These distinctive characteristics combined with the fact that Madeira have never been explored, as far as indigenous marine actinomycetes are concerned, makes it from the scientific point of view, the perfect target for our studies. From 662 marine sediment samples collected along Madeira Archipelago (Figure 1 during June of 2012, covering depths from 10-1310 m, a total of 421 actinomycete strains were isolated. In a previous study, an assemblage of 82 strains was selected for taxonomic identification, having into account representative morphological diversity characteristics of the actinomycetes, isolated from Madeira Archipelago. Based on 16S rRNA gene sequencing, it was observed that the genera Streptomyces, Micromonospora and Salinispora were predominant, 81% [3]. Additionally, in a recent study, our team selected 168 strains with Salinispora look-alike morphological features. From these 28 strains were identified as belonging to the seawater-obligate marine actinomycete genus Salinispora. Representing the first report of Salinispora spp. in the Macaronesian Atlantic Ocean

  10. Comparison of Leishmania killicki (syn. L. tropica) and Leishmania tropica Population Structure in Maghreb by Microsatellite Typing.

    OpenAIRE

    Dhekra Chaara; Anne-Laure Bañuls; Najoua Haouas; Loïc Talignani; Patrick Lami; Habib Mezhoud; Zoubir Harrat; Jean-Pierre Dedet; Hamouda Babba; Francine Pratlong

    2015-01-01

    Leishmania (L.) killicki (syn. L. tropica), which causes cutaneous leishmaniasis in Maghreb, was recently described in this region and identified as a subpopulation of L. tropica. The present genetic analysis was conducted to explore the spatio-temporal distribution of L. killicki (syn. L. tropica) and its transmission dynamics. To better understand the evolution of this parasite, its population structure was then compared with that of L. tropica populations from Morocco. In total 198 samples...

  11. Comparison of Leishmania killicki (syn. L. tropica) and Leishmania tropica Population Structure in Maghreb by Microsatellite Typing.

    Science.gov (United States)

    Chaara, Dhekra; Bañuls, Anne-Laure; Haouas, Najoua; Talignani, Loïc; Lami, Patrick; Mezhoud, Habib; Harrat, Zoubir; Dedet, Jean-Pierre; Babba, Hamouda; Pratlong, Francine

    2015-12-01

    Leishmania (L.) killicki (syn. L. tropica), which causes cutaneous leishmaniasis in Maghreb, was recently described in this region and identified as a subpopulation of L. tropica. The present genetic analysis was conducted to explore the spatio-temporal distribution of L. killicki (syn. L. tropica) and its transmission dynamics. To better understand the evolution of this parasite, its population structure was then compared with that of L. tropica populations from Morocco. In total 198 samples including 85 L. killicki (syn. L. tropica) (from Tunisia, Algeria and Libya) and 113 L. tropica specimens (all from Morocco) were tested. Theses samples were composed of 168 Leishmania strains isolated from human skin lesions, 27 DNA samples from human skin lesion biopsies, two DNA samples from Ctenodactylus gundi bone marrow and one DNA sample from a Phlebotomus sergenti female. The sample was analyzed by using MultiLocus Enzyme Electrophoresis (MLEE) and MultiLocus Microsatellite Typing (MLMT) approaches. Analysis of the MLMT data support the hypothesis that L. killicki (syn. L. tropica) belongs to the L. tropica complex, despite its strong genetic differentiation, and that it emerged from this taxon by a founder effect. Moreover, it revealed a strong structuring in L. killicki (syn. L. tropica) between Tunisia and Algeria and within the different Tunisian regions, suggesting low dispersion of L. killicki (syn. L. tropica) in space and time. Comparison of the L. tropica (exclusively from Morocco) and L. killicki (syn. L. tropica) population structures revealed distinct genetic organizations, reflecting different epidemiological cycles.

  12. Comparison of Leishmania killicki (syn. L. tropica and Leishmania tropica Population Structure in Maghreb by Microsatellite Typing.

    Directory of Open Access Journals (Sweden)

    Dhekra Chaara

    2015-12-01

    Full Text Available Leishmania (L. killicki (syn. L. tropica, which causes cutaneous leishmaniasis in Maghreb, was recently described in this region and identified as a subpopulation of L. tropica. The present genetic analysis was conducted to explore the spatio-temporal distribution of L. killicki (syn. L. tropica and its transmission dynamics. To better understand the evolution of this parasite, its population structure was then compared with that of L. tropica populations from Morocco. In total 198 samples including 85 L. killicki (syn. L. tropica (from Tunisia, Algeria and Libya and 113 L. tropica specimens (all from Morocco were tested. Theses samples were composed of 168 Leishmania strains isolated from human skin lesions, 27 DNA samples from human skin lesion biopsies, two DNA samples from Ctenodactylus gundi bone marrow and one DNA sample from a Phlebotomus sergenti female. The sample was analyzed by using MultiLocus Enzyme Electrophoresis (MLEE and MultiLocus Microsatellite Typing (MLMT approaches. Analysis of the MLMT data support the hypothesis that L. killicki (syn. L. tropica belongs to the L. tropica complex, despite its strong genetic differentiation, and that it emerged from this taxon by a founder effect. Moreover, it revealed a strong structuring in L. killicki (syn. L. tropica between Tunisia and Algeria and within the different Tunisian regions, suggesting low dispersion of L. killicki (syn. L. tropica in space and time. Comparison of the L. tropica (exclusively from Morocco and L. killicki (syn. L. tropica population structures revealed distinct genetic organizations, reflecting different epidemiological cycles.

  13. Two peptides, cycloaspeptide A and nazumamide A from a sponge associated marine actinobacterium Salinispora sp.

    Science.gov (United States)

    Bose, Utpal; Hodson, Mark P; Shaw, P Nicholas; Fuerst, John A; Hewavitharana, Amitha K

    2014-04-01

    Marine sponges are a major component of benthic communities and act as a reservoir for microbial species. In terms of biomass, they are the richest source of secondary metabolite production, with the potential to influence both benthic and pelagic systems. In most cases it is the sponge-associated microbes that account for many of the secondary metabolites assigned to the host. Here we report the occurrence of cycloaspeptide A, a fungus-derived cyclic peptide, in a culturable bacterium Salinispora arenicola. We have also identified nazumamide A, a sponge-derived linear tetrapeptide currently used as a thrombin inhibitor, in Salinispora pacifica. Their structures were determined using an integrated approach consisting of: (1) HPLC-UV-Vis-QToF-MS analysis with multimode ionization (ESI and APCI) and fast polarity switching; (2) database searching and matching of monoisotopic masses, retention times, mass spectra of the precursor and product ions of the compounds of interest and the authentic reference standards thereof.

  14. Herbal extract targets in Leishmania tropica.

    Science.gov (United States)

    Mohammad, Bassim I; Al Shammary, Maani N; Abdul Mageed, Roaa H; Yousif, Nasser Ghaly

    2015-12-01

    The present study aims to investigate the effect of some herbal extract such as phenolic compounds on the viability of Leishmania tropica promastigotes in vitro. Four tested chemical agents (caffeic acid (CA), ferulic acid (FA), syringic acid (SA) and 4-hydroxybenzoic acid (4-HBA)) were used in this study. The viability of Leishmania tropica promastigotes was investigated under five different concentrations (10, 15, 20, 25 and 30 mg/ml) of each agent after (72 h). CA was the most active agent on the promastigotes viability after 72 h exposure to 30 mg/ml concentration so that the parasiticidal effect reach (53 × 10(4)) promastigote/ml. FA is the second agent in parasiticidal effect that parasiticidal effect reach to (50 × 10(4) promastigote/ml) at a concentration (30 mg/ml), 4-HBA is the third agent in parasiticidal effect that reach to (48 × 10(4) promastigote/ml) at a concentration (30 mg/ml), SA is the weakest agent in parasiticidal activity that reach to (44 × 10(4) promastigote/ml) at a concentration (30 mg/ml). It can be concluded that (CA, FA, SA and 4-HBA) possess acidal effect on the Leishmania tropica promastigotes in vitro.

  15. "DIFERENTIAION OF LEISHMANIA TROPICA MAJOR FROM LEISHMANIA TROPICA MINOR BY INOCULATION TO LABORATORY ANIMALS "

    Directory of Open Access Journals (Sweden)

    A.Nadim

    1973-08-01

    Full Text Available The subcutaneous inoculation of 16 white mice and 10 golden hamsters with L.tropica major resulted in the development of leishmanial lesions in all, becoming generalized in some.Two of 10 hamsters inoculated intraperitoneally with this parasite developed generalized lesions. On the other hand, the inoculation of L. tropica minor to 128 mice subcutaneously and 170 mice intraperitoneally did not cause any leishmanial lesions , while 22 out of 47 hamsters inoculated with this parasite showed lesions at the site of inoculation.

  16. Characterization of Leishmania (Leishmania) tropica axenic amastigotes.

    Science.gov (United States)

    Nasereddin, Abedelmajeed; Schweynoch, Carola; Schonian, Gabriele; Jaffe, Charles L

    2010-01-01

    Optimum conditions for generating Leishmania (Leishmania) tropica axenic amastigotes (AxA) in culture were determined, pH 5.5/36 degrees C, and the parasites characterized by different techniques, including light microscopy, macrophage infection, stage specific antigen expression and differential display. AxA were morphologically similar to amastigotes and 15.5-fold more infective than stationary phase promastigotes for mouse peritoneal macrophages. Western blotting with promastigote stage specific monoclonal antibodies to either lipophosphoglycan (T2) or a 60 kDa flagella antigen (F3) showed a dramatic decrease in antigen expression when AxA were compared to promastigotes. Similarly F3 gave strong immune fluorescent staining of the promastigote flagellum, but no fluorescence was detected when AxA were examined. Conversely, Western blotting with the amastigote specific monoclonal antibody (T16) showed that this antigen is more highly expressed in AxA than promastigotes. Differential display-PCR was used to identify several parasite genes showing stage specific expression. One gene selectively expressed by AxA was partially sequenced and identified as Leishmania (L.) tropicaamastin. Amastigote specific expression of this gene was further confirmed by reverse transcriptase-PCR (RT-PCR) using AxA and infected macrophages. No amastin expression was observed with promastigotes. Expression of the cysteine protease B (cpb) and protein kinase A catalytic isoform 1 subunit (pkac1) in promastigotes and AxA was also examined by RT-PCR. Pkac1 was strongly expressed by promastigotes, while cpb expression was only seen with AxA or infected macrophages. L. (L.) tropica AxA will prove useful for further studies on parasite differentiation and gene regulation, as well as for drug screening.

  17. Production and purification of a bioactive substance against multi-drug resistant human pathogens from the marine-sponge-derived Salinispora sp.

    Directory of Open Access Journals (Sweden)

    Satyendra Singh

    2014-10-01

    Conclusions: The present study reported the rifamycin W from sponge-associated Salinispora sp. and it exhibited appreciable antibacterial activity against multi-drug resistant human pathogens which indicated that sponge-associated Actinobacteria are significant sources of bioactive metabolites.

  18. Discovering the recondite secondary metabolome spectrum of Salinispora species: a study of inter-species diversity.

    Directory of Open Access Journals (Sweden)

    Utpal Bose

    Full Text Available Patterns of inter-species secondary metabolite production by bacteria can provide valuable information relating to species ecology and evolution. The complex nature of this chemical diversity has previously been probed via directed analyses of a small number of compounds, identified through targeted assays rather than more comprehensive biochemical profiling approaches such as metabolomics. Insights into ecological and evolutionary relationships within bacterial genera can be derived through comparative analysis of broader secondary metabolite patterns, and this can also eventually assist biodiscovery search strategies for new natural products. Here, we investigated the species-level chemical diversity of the two marine actinobacterial species Salinispora arenicola and Salinispora pacifica, isolated from sponges distributed across the Great Barrier Reef (GBR, via their secondary metabolite profiles using LC-MS-based metabolomics. The chemical profiles of these two species were obtained by UHPLC-QToF-MS based metabolic profiling. The resultant data were interrogated using multivariate data analysis methods to compare their (biochemical profiles. We found a high level of inter-species diversity in strains from these two bacterial species. We also found rifamycins and saliniketals were produced exclusively by S. arenicola species, as the main secondary metabolites differentiating the two species. Furthermore, the discovery of 57 candidate compounds greatly increases the small number of secondary metabolites previously known to be produced by these species. In addition, we report the production of rifamycin O and W, a key group of ansamycin compounds, in S. arenicola for the first time. Species of the marine actinobacteria harbour a much wider spectrum of secondary metabolites than suspected, and this knowledge may prove a rich field for biodiscovery as well as a database for understanding relationships between speciation, evolution and chemical

  19. Actinomycete integrative and conjugative elements

    NARCIS (Netherlands)

    Poele, Evelien M. te; Bolhuis, Henk; Dijkhuizen, Lubbert

    2008-01-01

    This paper reviews current knowledge on actinomycete integrative and conjugative elements (AICEs). The best characterised AICEs, pSAM2 of Streptomyces ambofaciens (10.9 kb), SLP1 (17.3 kb) of Streptomyces coelicolor and pMEA300 of Amycolatopsis methanolica (13.3 kb), are present as integrative eleme

  20. Leishmania tropica in Stray Dogs in Southeast Iran

    Directory of Open Access Journals (Sweden)

    Mehdi BAMOROVAT

    2015-10-01

    Full Text Available  Background: Cutaneous leishmaniasis (CL caused by Leishmania tropica is endemic in Kerman, southeastern Iran. While dogs have long been implicated as the main domestic reservoirs of L. infantum, etiological agent of zoonotic visceral leishmaniasis (ZVL, they can also carry L. tropica infection. The objective of the present study was to determine molecular identity and to evaluate histopathological changes due to CL in dogs in a well-known focus of anthroponotic CL (ACL in Kerman, southeastern Iran.Methods: This study was carried out in three prospective series from 1994 to 2013 on dogs. Tissue samples were taken from 471 stray dogs. Pathological specimens including skin, spleen, liver and lymph nodes were prepared for paraffin blocks, sectioning and staining for further histopathological examination. PCR amplification of kDNA was performed to identify the causative agent and sequencing. Overall, two out of 471 stray dogs were infected with L. tropica. Hyperplasia of red pulp by the proliferation of histiocytes, lymphocytes, plasma cells and cytoplasm of histiocytes collection of amastigotes was noted.Results: Based on the results of PCR products and sequencing analysis, the parasites isolated from the lesions of two dogs were characterized as L. tropica, corresponding to a band of 830 bp Conclusion: This finding revealed infection with L. tropica in stray dogs in the city and suburbs of Kerman. This information is essential for public health concerns and planning effective future control programs. The role of dogs as potentional reservoir in the epidemiology of ACL needs further investigation. Keywords: Leishmania tropica, Dog, Histopathology, Molecular, Epidemiology, Iran

  1. Evolutionary history of Leishmania killicki (synonymous Leishmania tropica) and taxonomic implications

    OpenAIRE

    Chaara, Dhekra; Ravel, Christophe; Bañuls, Anne- Laure; Haouas, Najoua; Lami, Patrick; Talignani, Loïc; El Baidouri, Fouad; Jaouadi, Kaouther; Harrat, Zoubir; Dedet, Jean-Pierre; Babba, Hamouda; Pratlong, Francine

    2015-01-01

    Background: The taxonomic status of Leishmania (L.) killicki, a parasite that causes chronic cutaneous leishmaniasis, is not well defined yet. Indeed, some researchers suggested that this taxon could be included in the L. tropica complex, whereas others considered it as a distinct phylogenetic complex. To try to solve this taxonomic issue we carried out a detailed study on the evolutionary history of L. killicki relative to L. tropica. Methods: Thirty-five L. killicki and 25 L. tropica strain...

  2. NOVEL BIOACTIVE COMPOUNDS FROM MANGROVE DERIVED ACTINOMYCETES

    Directory of Open Access Journals (Sweden)

    Kumari Amrita

    2012-09-01

    Full Text Available Mangrove is most productive and unexplored ecosystem that approximately covers one fourth of world coastline with high diversity of thriving organism. Recently the rate of isolation of novel bioactive compounds from microorganism living in mangrove forest has tremendously increased which is reflected in significant hasten for exploration of mangrove actinomycetes. Actinomycetes are group of bacteria which are extremely interesting as active producers of many primary and secondary metabolites. Many survey reports has depicted that the biologically active compounds which have been obtained so far from microbes, 45 percent are produced by actinomycetes, 38 percent by fungi and 17 percent by unicellular bacteria. Actinomycetes from mangrove environment provide diverse and are potential rich source of antibiotics, anticancer, antifungal and antiviral agent, enzyme and enzyme inhibitor. Mangrove actinomycetes are a prolific but underexploited source for the discovery of novel secondary metabolites.

  3. Therapeutically Active Biomolecules from Marine Actinomycetes

    Directory of Open Access Journals (Sweden)

    Mani Jayaprakashvel

    2012-09-01

    Full Text Available For the past few centuries, the biological sources of terrestrial origin have been explored and exploited for bioactive metabolites. This has resulted in the stagnancy of discovering either novel compounds or compounds with novel bioactivities. Thus, researchers across the globe have started exploring our big Oceans, for the search of bioactive metabolites. During the past few decades, the research on bioactive metabolites from marine biological resources has geared up and among the sources marine actinomycetes are proved to be best. Marine actinomycetes, the filamentous bacteria from marine environment have been intensively studied for bioactive metabolites. The biological diversity of marine actinomycetes was found to be enormous, thanks to culture dependent and culture independent biodiversity approaches. This great diversity of marine actinomycetes has offered greater chemical diversity. The diverse chemical compounds of marine actinomycetes have been found to have various biological activities such as antimicrobial, anti-tumor, anti-malarial, anti-algal, antioxidant, anti-inflammatory etc. These various bioactive metabolites of marine actinomycetes are having scope for developing as potent therapeutic agents. The potential of marine actinomycetes is rightly realized though the current biological wealth of these organisms isrelatively unexplored.

  4. Detection and identification of novel actinomycetes.

    Science.gov (United States)

    Williams, S T; Locci, R; Beswick, A; Kurtböke, D I; Kuznetsov, V D; Le Monnier, F J; Long, P F; Maycroft, K A; Palma, R A; Petrolini, B

    1993-10-01

    The actinomycetes are well known as a group of filamentous, Gram-positive bacteria that produce many useful secondary metabolites, including antibiotics and enzymes. Although they have been intensively studied for both theoretical and practical objectives, there is much scope for developing our basic knowledge of the means of detection and isolation of these microbes. This session concentrated on new methods for the detection and identification of novel actinomycetes from a range of environments. Approaches to the detection of actinomycetes ranged from investigations of neglected habitats and extreme environments (e.g. alkaline soils and oil drills) to the analysis of DNA extracted from the environment and use of specific phages. The continuing problems of the identification of actinomycete isolates were also considered. Topics discussed included use of phage typing, DNA probes, and correlation between phenetic and genotypic species of Streptomyces.

  5. Elicitation of secondary metabolism in actinomycetes.

    Science.gov (United States)

    Abdelmohsen, Usama Ramadan; Grkovic, Tanja; Balasubramanian, Srikkanth; Kamel, Mohamed Salah; Quinn, Ronald J; Hentschel, Ute

    2015-11-01

    Genomic sequence data have revealed the presence of a large fraction of putatively silent biosynthetic gene clusters in the genomes of actinomycetes that encode for secondary metabolites, which are not detected under standard fermentation conditions. This review focuses on the effects of biological (co-cultivation), chemical, as well as molecular elicitation on secondary metabolism in actinomycetes. Our review covers the literature until June 2014 and exemplifies the diversity of natural products that have been recovered by such approaches from the phylum Actinobacteria.

  6. [Leishmania tropica in Morocco. IV--Intrafocal enzyme diversity].

    Science.gov (United States)

    Pratlong, F; Rioux, J A; Dereure, J; Mahjour, J; Gallego, M; Guilvard, E; Lanotte, G; Perieres, J; Martini, A; Saddiki, A

    1991-01-01

    Ecoepidemiological analysis of a Moroccan focus of leishmaniasis caused by Leishmania tropica revealed considerable enzymatic diversity. Seven zymodemes belonging to the complex were identified in 149 strains isolated from humans, dogs, and the vector Phlebotomus sergenti. Three distinct subgroups were identifiable, two of which were in turn, composed of three "small variant" zymodemes. The diversity appears to be related to the age of the focus, which may have allowed colonization by zymodemes of different geographic origins. Diversification into "small variants" is apparently the result of recent mutation, possibly associated with genetic exchange.

  7. Protective immunity against Leishmania major induced by Leishmania tropica infection of BALB/c mice.

    Science.gov (United States)

    Mahmoudzadeh-Niknam, Hamid; Kiaei, Simin Sadat; Iravani, Davood

    2011-02-01

    Leishmania (L.) tropica is a causative agent of human cutaneous and viscerotropic leishmaniasis. Immune response to L. tropica in humans and experimental animals are not well understood. We previously established that L. tropica infection induces partial protective immunity against subsequent challenge infection with Leishmania major in BALB/c mice. Aim of the present study was to study immunologic mechanisms of protective immunity induced by L. tropica infection, as a live parasite vaccine, in BALB/c mouse model. Mice were infected by L. tropica, and after establishment of the infection, they were challenged by L. major. Our findings shows that L. tropica infection resulted in protection against L. major challenge in BALB/c mice and this protective immunity is associated with: (1) a DTH response, (2) higher IFN-γ and lower IL-10 response at one week post-challenge, (3) lower percentage of CD4(+) lymphocyte at one month post-challenge, and (4) the source of IFN-γ and IL-10 were mainly CD4(-) lymphocyte up to one month post-challenge suggesting that CD4(-) lymphocytes may be responsible for protection induced by L. tropica infection in the studied intervals.

  8. Miltefosine-induced apoptotic cell death on Leishmania major and L. tropica strains.

    Science.gov (United States)

    Khademvatan, Shahram; Gharavi, Mohammad Javad; Rahim, Fakher; Saki, Jasem

    2011-03-01

    The aim of this study was to assess the cytotoxic effects of various concentrations of miltefosine on Leishmania major (MRHO/IR/75/ER) and L. tropica (MHOM/IR/02/Mash10) promastigotes and to observe the programmed cell death features. The colorimetric MTT assay was used to find L. major and L. tropica viability and the obtained results were expressed as 50% inhibitory concentration (IC50). Also, 50% effective doses (ED50) for L. major and L. tropica amastigotes were also determined. Annexin-V FLUOS staining was performed to study the cell death properties of miltefosine using FACS analysis. Qualitative analysis of the total genomic DNA fragmentation was performed by agarose gel electrophoresis. Furthermore, to observe changes in cell morphology, promastigotes were examined using light microscopy. In both strains of L. major and L. tropica, miltefosine induced dose-dependent death with features of apoptosis, including cell shrinkage, DNA laddering, and externalization of phosphatidylserine. The IC50 was achieved at 22 µM and 11 µM for L. major and L. tropica after 48 hr of incubation, respectively. ED50 of L. major and L. tropica amastigotes were 5.7 µM and 4.2 µM, respectively. Our results indicate that miltefosine induces apoptosis of the causative agent of cutaneous leishmaniasis in a dose-dependent manner. Interestingly, L. major did not display any apoptotic changes when it was exposed to miltefosine in concentrations sufficient to kill L. tropica.

  9. Sequencing and Gene Expression Analysis of Leishmania tropica LACK Gene.

    Directory of Open Access Journals (Sweden)

    Nour Hammoudeh

    2014-12-01

    Full Text Available Leishmania Homologue of receptors for Activated C Kinase (LACK antigen is a 36-kDa protein, which provokes a very early immune response against Leishmania infection. There are several reports on the expression of LACK through different life-cycle stages of genus Leishmania, but only a few of them have focused on L.tropica.The present study provides details of the cloning, DNA sequencing and gene expression of LACK in this parasite species. First, several local isolates of Leishmania parasites were typed in our laboratory using PCR technique to verify of Leishmania parasite species. After that, LACK gene was amplified and cloned into a vector for sequencing. Finally, the expression of this molecule in logarithmic and stationary growth phase promastigotes, as well as in amastigotes, was evaluated by Reverse Transcription-PCR (RT-PCR technique.The typing result confirmed that all our local isolates belong to L.tropica. LACK gene sequence was determined and high similarity was observed with the sequences of other Leishmania species. Furthermore, the expression of LACK gene in both promastigotes and amastigotes forms was confirmed.Overall, the data set the stage for future studies of the properties and immune role of LACK gene products.

  10. Actinomycetes and the IUD: an update.

    Science.gov (United States)

    Gupta, P K; Erozan, Y S; Frost, J K

    1978-01-01

    To date, actinomycetes have been identified in 540 vagino-pancervical (Fast) smears from 520 women. In each case, a foreign body has been present, usually an IUD (517 cases). The Dalkon Shield preponderates, perhaps reflecting physician preference at the center. IUD usage duration has varied from 6 weeks to 13 years. Approximately 25% of symptomatic IUD users requesting treatment have cytologic evidence of actinomycetes. The preoperative diagnosis of pelvic actinomycetes was suggested in most cases based on cytologic evidence alone. Immunofluorescent studies have been performed in 266 cases with species-specific antisera, and Actinomyces israelii identified in 250. Protozoal organisms in the Fast smears have been noted in 8 cases (1.5%) and are commonly intimately associated with Actinomyces. It is agreed that the oropharnyx serves as the possible source of lower genital tract Actinomyces infection. In such cases, IUD removal and antibiotic treatment are recommended.

  11. Leishmania tropica in rock hyraxes (Procavia capensis) in a focus of human cutaneous leishmaniasis.

    Science.gov (United States)

    Talmi-Frank, Dalit; Jaffe, Charles L; Nasereddin, Abedelmajeed; Warburg, Alon; King, Roni; Svobodova, Milena; Peleg, Ofer; Baneth, Gad

    2010-05-01

    Cutaneous leishmaniasis, caused by Leishmania tropica, has recently emerged in urban and rural foci of central and northern Israel, and constitutes a major public health concern. Rock hyraxes (Procavia capensis), the suspected natural reservoir, were trapped in the cutaneous leishmaniasis urban focus of Maale Adumim in central Israel and evaluated for L. tropica infection by real-time kinetoplast DNA (kDNA) polymerase chain reaction (PCR) and serology. Real-time PCR on blood and computerized western blot serology analysis was positive for L. tropica in 58% and 80%, respectively, of the hyraxes tested. Phylogenetic analysis of the ribosomal internal transcribed spacer 1 region indicated that similar genotypes were present in humans and hyraxes from the same habitat. The high rates of infection and exposure to L. tropica among hyraxes supports their involvement in the transmission cycle of this parasite, and their potential role as a reservoir for human disease.

  12. First report of Leishmania tropica from a classical focus of L. major in North-Sinai, Egypt.

    Science.gov (United States)

    Shehata, Magdi G; Samy, Abdallah M; Doha, Said A; Fahmy, Adel R; Kaldas, Rania M; Furman, Barry D; Villinski, Jeffrey T

    2009-08-01

    Cutaneous leishmaniasis (CL) is prevalent in the Egyptian Sinai Peninsula and previous research has consistently documented the etiologic agent to be Leishmania major. We report the first isolation of Leishmania tropica from human cases of CL in a Northern Sinai community bordering Palestine. Parasite culturing, real-time polymerase chain reaction (PCR), gene sequencing, and restriction fragment length polymorphism (RFLP) analyses indicate CL cases in this community were caused by either L. major or L. tropica (three cases each). Two wild-caught rodents (Gerbillus pyramidum floweri) were infected with L. tropica. Phlebotomus papatasi sand flies were found harboring L. major, however only non-infected individuals of Phlebotomus sergenti, a vector for L. tropica, were caught. Patients with L. tropica had not traveled from the region in over a year, suggesting these cases are autochthonous. This scenario is consistent with an incursion of L. tropica from bordering countries and raises concerns about expansion of this parasite further into Egypt.

  13. Stimulation of Leishmania tropica protein kinase CK2 activities by platelet-activating factor (PAF).

    Science.gov (United States)

    Dutra, Patricia M L; Vieira, Danielle P; Meyer-Fernandes, Jose R; Silva-Neto, Mario A C; Lopes, Angela H

    2009-09-01

    Leishmania tropica is one of the causative agents of cutaneous leishmaniasis. Platelet-activating factor (PAF) is a phospholipid mediator in diverse biological and pathophysiological processes. Here we show that PAF promoted a three-fold increase on ecto-protein kinase and a three-fold increase on the secreted kinase activity of L. tropica live promastigotes. When casein was added to the reaction medium, along with PAF, there was a four-fold increase on the ecto-kinase activity. When live L. tropica promastigotes were pre-incubated for 30 min in the presence of PAF-plus casein, a six-fold increase on the secreted kinase activity was observed. Also, a protein released from L. tropica promastigotes reacted with polyclonal antibodies for the mammalian CK2 alpha catalytic subunit. Furthermore, in vitro mouse macrophage infection by L. tropica was doubled when promastigotes were pre-treated for 2 h with PAF. Similar results were obtained when the interaction was performed in the presence of purified CK2 or casein. TBB and DRB, CK2 inhibitors, reversed PAF enhancement of macrophage infection by L. tropica. WEB 2086, a competitive PAF antagonist, reversed all PAF effects here described. This study shows for the first time that PAF promotes the activation of two isoforms of CK2, secreted and membrane-bound, correlating these activities to infection of mouse macrophages.

  14. New Record of Phlebotomus Sergenti, the Vector of Leishmania Tropica, in the Southern Nile Valley of Egypt

    Science.gov (United States)

    2001-01-01

    SCIENTIFIC NOTE NEW RECORD OF PHLEBOTOMUS SERGENTI, THE VECTOR OF LEISHMANIA TROPICA , IN THE SOUTHERN NILE VALLEY OF EGYPT HANAFI A. HANAFI’ GREGORY M...forms of Leishmania tropica , from southern Egypt . Four female and I male P. sergenti were collected from unlit Centers for Disease Control light traps...sergenti (Parrot) is a widely distrib- uted sand fly species that feeds readily on humans and is a known vector of Leishmania tropica (Ash- ford and

  15. Actinomycetes: A Source of Lignocellulolytic Enzymes

    Science.gov (United States)

    Saini, Anita; Aggarwal, Neeraj K.; Sharma, Anuja; Yadav, Anita

    2015-01-01

    Lignocellulose is the most abundant biomass on earth. Agricultural, forest, and agroindustrial activities generate tons of lignocellulosic wastes annually, which present readily procurable, economically affordable, and renewable feedstock for various lignocelluloses based applications. Lignocelluloses are the focus of present decade researchers globally, in an attempt to develop technologies based on natural biomass for reducing dependence on expensive and exhaustible substrates. Lignocellulolytic enzymes, that is, cellulases, hemicellulases, and lignolytic enzymes, play very important role in the processing of lignocelluloses which is prerequisite for their utilization in various processes. These enzymes are obtained from microorganisms distributed in both prokaryotic and eukaryotic domains including bacteria, fungi, and actinomycetes. Actinomycetes are an attractive microbial group for production of lignocellulose degrading enzymes. Various studies have evaluated the lignocellulose degrading ability of actinomycetes, which can be potentially implemented in the production of different value added products. This paper is an overview of the diversity of cellulolytic, hemicellulolytic, and lignolytic actinomycetes along with brief discussion of their hydrolytic enzyme systems involved in biomass modification. PMID:26793393

  16. Natural and experimental evidence of viscerotropic infection caused by Leishmania tropica from North Sinai, Egypt.

    Science.gov (United States)

    Doha, Said A; Shehata, Magdi G; Fahmy, Adel R; Samy, Abdallah M

    2014-08-01

    Cutaneous leishmaniasis (CL) is a neglected clinical form that is quite prevalent in Eastern North parts of the country in Sinai Peninsula. Leishmania tropica was identified by previous reports as the causative agent responsible for viscerotropic infections in-patients and experimental animals. Here, we reported the viscerotropic infections from naturally infected rodent Gerbillus pyramidum floweri collected from North-Sinai. Footpad and tail lesions, spleenomegaly, and malformed dark-colored spleen were the characteristic CL symptoms. The spleen of the rodent found positive to amastigote impression smear. ITS-1 DNA was sequenced and revealed 100% identity of the strain in the current study to the other L. tropica sequences identified from the patients with the suspected CL and inhabited the same study area. The current findings confirmed the susceptibility of gerbil to L. tropica, and raise the concerns for the role of rodents as accidental host suffering the infections. The susceptibility of wild and experimental rodents to the same L. tropica strain was also investigated; BALB/c and G. pyramidum were more susceptible to L. tropica (24.33 ± 4.37 and 25 ± 4.58 days post-infection, respectively). Similar viscerotropic pathologies were reported in experimental infection of only golden hamster (≈ 120 days post-infection), and G. p. floweri (≈ 160 days post-infection).

  17. Heterogeneity of the internal transcribed spacer region in Leishmania tropica isolates from southern Iran.

    Science.gov (United States)

    Ghatee, Mohammad Amin; Sharifi, Iraj; Kuhls, Katrin; Kanannejad, Zahra; Harandi, Majid Fasihi; de Almeida, Marcos E; Hatam, Gholamreza; Mirhendi, Hossein

    2014-09-01

    Most of cutaneous leishmaniasis cases occur in only 7 countries, including Iran. Leishmania tropica is the main cause of anthroponotic cutaneous leishmaniasis in Iran. In order to study the heterogeneity and phylogeny of L. tropica in southern Iran, a total of 61 isolates were obtained from Bam district and the cities Kerman and Shiraz. The internal transcribed spacer (ITS) from the ribosomal DNA locus was amplified and then analysed by sequencing. Analysis of the ITS sequences showed four haplotypes in the isolates, including 3 haplotypes among the 58 isolates from the south eastern region, including Bam district and Kerman city, and 2 haplotypes among the 3 isolates from Shiraz city. The results showed a monophyletic structure for the south eastern population. In comparison to GenBank sequences of L. tropica from different countries, most of the southeast Iranian and Indian isolates are comprised in one cluster, while isolates from other countries and few other Iranian isolates group in a different cluster. Analysis of ITS sequences of south eastern L. tropica showed a homogeneous population which could be the basis for other molecular epidemiology studies using more discriminative markers and tracing possible changes in the population structure of L. tropica.

  18. Isoenzyme and ultrastructural characterization of Leishmania tropica axenic amastigotes and promastigotes.

    Science.gov (United States)

    Hatam, Gholam Reza; Bahrami, Somayeh; Razavi, S Mostafa; Oryan, Ahmad

    2013-02-01

    Leishmania tropica is one of the main etiological agents of cutaneous leishmaniasis in Iran. For ultrastructural and isoenzyme study, axenic amastigotes were cultured in a brain-heart infusion medium containing 20 % fetal calf serum, pH 4.5, and incubated at 37 °C in 5 % CO(2). Different stages of L. tropica revealed the same isoenzyme profiles after comparing four enzyme systems including phosphoglucomutase, 6-phosphogluconate dehydrogenase, malate dehydrogenase, and nucleoside hydrolase II. Different isoenzyme patterns for glucose-phosphate isomerase, glucose-6-phosphate dehydrogenase, nucleoside hydrolase I, and malic enzyme enzymic systems were seen; thus, these isoenzyme systems among the eight systems studied were more efficient in characterizing L. tropica amastigotes. The structure of the axenic amastigotes was essentially similar to that of the promastigotes except for some important characteristics including the flagellum, flagellar pocket, paraxial rod, and the subpellicular microtubules.

  19. Experimental acquisition, development, and transmission of Leishmania tropica by Phlebotomus duboscqi.

    Science.gov (United States)

    Hanafi, Hanafi A; El-Din, El-Shaimaa M Nour; El-Hossary, Shabaan S I; Kaldas, Rania M; Villinski, Jeffrey T; Furman, Barry D; Fryauff, David J

    2013-01-01

    We report experimental infection and transmission of Leishmania tropica (Wright), by the blood-feeding sand fly Phlebotomus duboscqi (Neveu-Lemaire). Groups of laboratory-reared female sand flies that fed "naturally" on L. tropica-infected hamsters, or artificially, via membrane feeding device, on a suspension of L. tropica amastigotes, were dissected at progressive time points post-feeding. Acquisition, retention and development of L. tropica through procyclic, nectomonad, and leptomonad stages to the infective metacyclic promastigote stage, and anterior progression of the parasites from abdominal midgut bloodmeal to the thoracic midgut were demonstrated in both groups. Membrane feeding on the concentrated amastigote suspension led to metacyclic promastigote infections in 60% of sand flies, whereas only 3% of P. duboscqi that fed naturally on an infected hamster developed metacyclics. Sand flies from both groups re-fed on naïve hamsters, but despite infections in 25-50% of membrane-fed and 2-3.5% of naturally fed flies, no skin lesions developed in the hamsters. After four months of observation these animals were euthanized and necropsied. Screening of the organs and tissue by polymerase chain reaction (PCR) that targeted the small subunit RNA gene, amplified generic Leishmania DNA from liver, spleen, bone marrow, and blood, but only from hamsters bitten by membrane-infected P. duboscqi. These results are notable in demonstrating the ability of P. duboscqi, originating from Kenya, to acquire, retain, develop, and transmit a Turkish strain of L. tropica originally isolated from a human case of cutaneous leishmaniasis. This marks the first demonstration of complete development and transmission of L. tropica by a member of the Phlebotomus subgenus of sand flies.

  20. Identification of Leishmania tropica from micro-foci of cutaneous leishmaniasis in the Kenyan Rift Valley.

    Science.gov (United States)

    Odiwuor, Samwel; Muia, Alfred; Magiri, Charles; Maes, Ilse; Kirigi, George; Dujardin, Jean-Claude; Wasunna, Monique; Mbuchi, Margaret; Auwera, Gert Van der

    2012-07-01

    We performed diagnosis and species identification of parasites in lesion samples from suspected cutaneous leishmaniasis patients in four villages, three of which are in a known Leishmania tropica endemic region in Kenya. Samples were analyzed both by microscopy and PCR for Leishmania, and typed by an assay using four ribosomal DNA-based species-identification PCRs. The lesions were demonstrated to be caused by L. tropica, which confirms the re-emergence of cutaneous leishmaniasis from this species after a period of reduced incidence in the endemic zone. Our report highlights the importance of an intervention and sustained Leishmania control program.

  1. Mapping the genes for susceptibility and response to Leishmania tropica in mouse.

    Directory of Open Access Journals (Sweden)

    Yahya Sohrabi

    Full Text Available BACKGROUND: L. tropica can cause both cutaneous and visceral leishmaniasis in humans. Although the L. tropica-induced cutaneous disease has been long known, its potential to visceralize in humans was recognized only recently. As nothing is known about the genetics of host responses to this infection and their clinical impact, we developed an informative animal model. We described previously that the recombinant congenic strain CcS-16 carrying 12.5% genes from the resistant parental strain STS/A and 87.5% genes from the susceptible strain BALB/c is more susceptible to L. tropica than BALB/c. We used these strains to map and functionally characterize the gene-loci regulating the immune responses and pathology. METHODS: We analyzed genetics of response to L. tropica in infected F2 hybrids between BALB/c×CcS-16. CcS-16 strain carries STS-derived segments on nine chromosomes. We genotyped these segments in the F2 hybrid mice and tested their linkage with pathological changes and systemic immune responses. PRINCIPAL FINDINGS: We mapped 8 Ltr (Leishmania tropica response loci. Four loci (Ltr2, Ltr3, Ltr6 and Ltr8 exhibit independent responses to L. tropica, while Ltr1, Ltr4, Ltr5 and Ltr7 were detected only in gene-gene interactions with other Ltr loci. Ltr3 exhibits the recently discovered phenomenon of transgenerational parental effect on parasite numbers in spleen. The most precise mapping (4.07 Mb was achieved for Ltr1 (chr.2, which controls parasite numbers in lymph nodes. Five Ltr loci co-localize with loci controlling susceptibility to L. major, three are likely L. tropica specific. Individual Ltr loci affect different subsets of responses, exhibit organ specific effects and a separate control of parasite load and organ pathology. CONCLUSION: We present the first identification of genetic loci controlling susceptibility to L. tropica. The different combinations of alleles controlling various symptoms of the disease likely co-determine different

  2. Malate dehydrogenases from actinomycetes: structural comparison of Thermoactinomyces enzyme with other actinomycete and Bacillus enzymes.

    OpenAIRE

    1984-01-01

    Malate dehydrogenases from bacteria belonging to the genus Thermoactinomyces are tetrameric, like those from Bacillus spp., and exhibit a high degree of structural homology to Bacillus malate dehydrogenase as judged by immunological cross-reactivity. Malate dehydrogenases from other actinomycetes are dimers and do not cross-react with antibodies to Bacillus malate dehydrogenase.

  3. Multilocus Microsatellite Typing reveals intra-focal genetic diversity among strains of Leishmania tropica in Chichaoua Province, Morocco.

    Science.gov (United States)

    Krayter, Lena; Alam, Mohammad Zahangir; Rhajaoui, Mohamed; Schnur, Lionel F; Schönian, Gabriele

    2014-12-01

    In Morocco, cutaneous leishmaniasis (CL) caused by Leishmania (L.) tropica is a major public health threat. Strains of this species have been shown to display considerable serological, biochemical, molecular biological and genetic heterogeneity; and Multilocus Enzyme Electrophoresis (MLEE), has shown that in many countries including Morocco heterogenic variants of L. tropica can co-exist in single geographical foci. Here, the microsatellite profiles discerned by MLMT of nine Moroccan strains of L. tropica isolated in 2000 from human cases of CL from Chichaoua Province were compared to those of nine Moroccan strains of L. tropica isolated between 1988 and 1990 from human cases of CL from Marrakech Province, and also to those of 147 strains of L. tropica isolated at different times from different worldwide geographical locations within the range of distribution of the species. Several programs, each employing a different algorithm, were used for population genetic analysis. The strains from each of the two Moroccan foci separated into two phylogenetic clusters independent of their geographical origin. Genetic diversity and heterogeneity existed in both foci, which are geographically close to each other. This intra-focal distribution of genetic variants of L. tropica is not considered owing to in situ mutation. Rather, it is proposed to be explained by the importation of pre-existing variants of L. tropica into Morocco.

  4. Leishmania tropica infection, in comparison to Leishmania major, induces lower delayed type hypersensitivity in BALB/c mice.

    Science.gov (United States)

    Mahmoudzadeh-Niknam, Hamid; Kiaei, Simin Sadat; Iravani, Davood

    2007-06-01

    Leishmania tropica and L. major are etiologic agents of human cutaneous leishmaniasis. Delayed type hypersensitivity (DTH) is an immunologic response that has been frequently used as a correlate for protection against or sensitization to leishmania antigen. In BALB/c mice, L. tropica infection results in non-ulcerating disease, whereas L. major infection results in destructive lesions. In order to clarify the immunologic mechanisms of these 2 different outcomes, we compared the ability of these 2 leishmania species in induction of DTH response in this murine model. BALB/c mice were infected with L. major or L. tropica, and disease evolution and DTH responses were determined. The results show that the primary L. major infection can exacerbate the secondary L. major infection and is associated with DTH response. Higher doses of the primary L. major infection result in more disease exacerbation of the secondary L. major infection as well as higher DTH response. L. tropica infection induces lower DTH responses than L. major. We have previously reported that the primary L. tropica infection induces partial protection against the secondary L. major infection in BALB/c mice. Induction of lower DTH response by L. tropica suggests that the protection induced against L. major by prior L. tropica infection may be due to suppression of DTH response.

  5. Investigation of Double-Band Electrophoretic Pattern of ITS-rDNA Region in Iranian Isolates of Leishmania Tropica

    Directory of Open Access Journals (Sweden)

    MA Ghatee

    2013-06-01

    Full Text Available Background: Leishmania tropica is a genetically divergent species. Amplification of entire internal tran­scribed spacer (ITS region of L. tropica isolates obtained from Bam district, one of the well known focus of anthroponotic cutaneous leishmaniasis ACL( in Iran, revealed a double-band pat­tern in agarose gel electrophoresis. This study explains how this pattern occurs.Methods: Twenty seven L. tropica smear preparations were collected from Bam district, south east Iran, and eight L. major and one L. infantum smear preparations were gathered from Shiraz, south west Iran. Furthermore one L. major and one L. infantum cultured standard strains were tested using entire ITS-PCR to survey their electrophoretic pattern. The ITS sequences of L. tropica, L. major, and L. infantum already deposited in GenBank were analyzed. Analysis of GenBank sequences of L. tropica revealed two groups of sequences based on length size, one group having a 100 bp gap. Therefore, a new re­verse primer namely LITS-MG was designed to exclude this gap in PCR products.Results: Whole ITS fragment amplification resulted in a double-band pattern in all L. tropica cases, while a sharp single band was observed for L. infantum and L. major isolates. This result was correspond­ing to the result obtained from in silico analysis of GenBank sequences. Use of LITS-MG primer was expectedly resulted in a single band including ITS1, 5.8s and partial ITS2 product for L. tropica which is appropriate for following molecular studies such as sequencing or restriction analysis.Conclusion: Sequences analysis of GenBank L. tropica sequences and following practical laboratory tests revealed at least two alleles in L. tropica which were confirmed in Bam isolates. This especial double-band pattern is because of a 100 bp fragment difference within ITS-rDNA alleles

  6. In vitro and in vivo activities of Haplophyllum myrtifolium against Leishmania tropica.

    Science.gov (United States)

    Ostan, Ipek; Saglam, Hüsniye; Limoncu, M Emin; Ertabaklar, Hatice; Toz, Seray Ozensoy; Ozbel, Yusuf; Ozbilgin, Ahmet

    2007-10-01

    This study aimed to evaluate the in vitro and in vivo leishmanicidal activity of an endemic Turkish plant and compare its efficacy with a reference drug. In addition to the in vitro activities of the ethanol, acidified and alkaloid extracts and furoquinoline alkaloids skimmianine and gamma-fagarine, in vivo antileishmanial activitiy of the acidified extract of Haplophyllum myrtifolium Boiss. (Rutaceae) were investigated against Leishmania tropica (L. tropica), a causative agent of cutaneous leishmaniasis. All the extracts and pure compounds showed in vitro inhibitory activity against the promastigotes of. L. tropica. The in vitro 50% inhibitory concentrations of y-fagarine, acidified extract, ethanol extract, skimmianine and alkaloid extract against promastigotes were determined as 8.7, 9.4, 10.9, 25.7 and 25.8 microg/ml respectively. In vivo results of Haplophyllum myrtifolium acidified extract showed that this plant has a limited effect on decreasing the lesion size of experimental mice infected with Leishmania tropica. To the best of our knowledge, this is the first time both the in vitro and in vivo antileishmanial activity of Haplophyllum mrytifolium have been reported in the same research.

  7. Cutaneous leishmaniasis (Leishmania tropica) in a German tourist after travel to Greece.

    Science.gov (United States)

    Berens-Riha, Nicole; Fleischmann, Erna; Pratlong, Francine; Bretzel, Gisela; von Sonnenburg, Frank; Löscher, Thomas

    2009-01-01

    We report on a German tourist returning from vacations in Southern Greece with cutaneous leishmaniasis (CL) presenting as multiple erythematosquamous lesions caused by Leishmania tropica (zymodeme MON-57). In spite of its endemicity, only few data are available on the incidence and current distribution of CL in Greece, which may allow for an assessment of the risk for travelers.

  8. Clinical manifestations and genetic variation of Leishmania infantum and Leishmania tropica in Southern Turkey.

    Science.gov (United States)

    Eroglu, Fadime; Koltas, Ismail S; Alabaz, Derya; Uzun, Soner; Karakas, Mehmet

    2015-07-01

    L. infantum was isolated from cutaneous leishmaniasis (CL) skin lesions in patients having no signs and symptoms of visceral leishmaniasis (VL). Similarly, L. tropica had previously been isolated from patients with VL in the absence of cutaneous lesions. It was not certain how visceralization occurred. Smears (207) and bone marrow samples (135) were taken from CL and VL-suspected patients, respectively. Microscopic examination, ITS1-PCR, RFLP and DNA sequencing for all samples were analyzed. The microscopic examination of smears was found to be 61.3% (127/207) in CL-suspected cases and bone marrow samples were found to be positive 8.8% (12/135) in VL-suspected cases. L. tropica 48.6% (72/148), L. infantum 35.8% (53/148), L. major 15.6% (23/148) in CL, and L. infantum 56.3% (18/32), L. donovani 31.2% (10/32), L. tropica 12.5% (4/32) in VL were found with PCR-RFLP. In addition, the DNA sequencing revealed a genetic variation in L. infantum (variants 1-3) and L. tropica (variants 1-5). We assume that the increased disease occurrence may have resulted from geographical expansion of disease, changing patterns of international travel, population migrations, non-immune people into endemic regions of infected people into non-endemic regions. In this study, L. infantum (variant 3) only in CL-patients and L. tropica (variant 2) only in VL-patients were identified. We hypothesize that genetic variation might play a role in the causation of CL and VL in southern Turkey and the genetic variants may differ according to the geographical location among Leishmania strains.

  9. Leishmania tropica infection, in comparison to Leishmania major, induces lower delayed type hypersensitivity in BALB/c mice

    OpenAIRE

    Mahmoudzadeh-Niknam, Hamid; Kiaei, Simin Sadat; Iravani, Davood

    2007-01-01

    Leishmania tropica and L. major are etiologic agents of human cutaneous leishmaniasis. Delayed type hypersensitivity (DTH) is an immunologic response that has been frequently used as a correlate for protection against or sensitization to leishmania antigen. In BALB/c mice, L. tropica infection results in non-ulcerating disease, whereas L. major infection results in destructive lesions. In order to clarify the immunologic mechanisms of these 2 different outcomes, we compared the ability of the...

  10. Draft Genome Sequence of Phosphate-Solubilizing Bacterium Paraburkholderia tropica Strain P-31 Isolated from Pomegranate (Punica granatum) Rhizosphere.

    Science.gov (United States)

    Kaur, Chandandeep; Selvakumar, Govindan; Ganeshamurthy, Arakalgud Nanjundiah

    2016-08-18

    We report the 8.9 Mb draft genome sequence of phosphate-solubilizing bacterium Paraburkholderia tropica strain P-31, isolated from pomegranate (Punica granatum) rhizosphere. The draft genome sequence of Paraburkholderia tropica strain P-31 consists of 8,881,246 bp with a G+C content of 64.7%, 8,039 protein-coding genes, and 49 RNAs.

  11. The route of Leishmania tropica infection determines disease outcome and protection against Leishmania major in BALB/c mice.

    Science.gov (United States)

    Mahmoudzadeh-Niknam, Hamid; Khalili, Ghader; Abrishami, Firoozeh; Najafy, Ali; Khaze, Vahid

    2013-02-01

    Leishmania tropica is one of the causative agents of leishmaniasis in humans. Routes of infection have been reported to be an important variable for some species of Leishmania parasites. The role of this variable is not clear for L. tropica infection. The aim of this study was to explore the effects of route of L. tropica infection on the disease outcome and immunologic parameters in BALB/c mice. Two routes were used; subcutaneous in the footpad and intradermal in the ear. Mice were challenged by Leishmani major, after establishment of the L. tropica infection, to evaluate the level of protective immunity. Immune responses were assayed at week 1 and week 4 after challenge. The subcutaneous route in the footpad in comparison to the intradermal route in the ear induced significantly more protective immunity against L. major challenge, including higher delayed-type hypersensitivity responses, more rapid lesion resolution, lower parasite loads, and lower levels of IL-10. Our data showed that the route of infection in BALB/c model of L. tropica infection is an important variable and should be considered in developing an appropriate experimental model for L. tropica infections.

  12. First report on isolation of Leishmania tropica from sandflies of a classical urban Cutaneous leishmaniasis focus in southern Iran.

    Science.gov (United States)

    Oshaghi, Mohammad A; Rasolian, Mohammad; Shirzadi, Mohammad Reza; Mohtarami, Fatemeh; Doosti, Sogra

    2010-12-01

    Shiraz district in south of Iran is a classical focus of Cutaneous leishmaniasis (CL) and previous research has consistently documented the etiologic agent to be Leishmania tropica and Leishmania major in urban and rural areas, respectively. However, none of the Phlebotomus sergenti, a known vector for L. tropica, of the region has been found infected. We report the first isolation of L. tropica from sandflies in urban community of southern part of Shiraz city. Parasite polymerase chain reaction (PCR) followed by restriction fragment length polymorphism (RFLP) and gene sequencing analyses indicate CL cases in this community were caused by either L. major or L. tropica. Sandflies of P. sergenti were infrequent, however, three out of 10 (30.0%) females captured in urban area were found infected with L. tropica. But, no human cases were found to be infected with L. tropica. Phlebotomus papatasi were found the most dominant and infected species where 41 out of 207 (20%) tested individuals harboring L. major in suburb area of the city. Patients have been lived in the suburb area of the city where people keep normally domestic animals in their houses which provide appropriate environment for completion of sandfly life cycle and expansion of CL disease in the region.

  13. Vectorial competence of Phlebotomus papatasi (Diptera: Psychodidae) to transmit two old world Leishmania species: Leishmania major and L. Tropica.

    Science.gov (United States)

    Darwish, A B; Tewfick, M K; Doha, S A; Abo-Ghalia, A H; Soliman, B A

    2011-12-01

    The vectorial competence of Phlebotomus papatasi for two old world Leishmania species, L. major & L. tropica was investigated. Phlebotomus papatasi originally collected from Suez Governorate, were membrane fed on homogenized hamster's lesion infected with L. major, MHOM/EG/06/RTC-63, and L. tropica, MGER/EG/06/RTC-74 identified from patients with suspected CL in Northern Sinai, Egypt. Fed flies were dissected at different time intervals and examined microscopically to determine the infection rate and parasite intensity. The feeding rate of P. papatasi on L. major (58.69%) was found higher than on L. tropica (45.99%). Infection rate with L. major (60.19%) was significantly higher than that with L. tropica (39.73%). Transmission by bites in case of P. papatasi/L. tropica failed. A characteristic L. major lesion was developed on the foot pads region 120 days post infective bites on healthy hamster. It is therefore concluded that P. papatasi is a much more effective vector for L. major than for L. tropica.

  14. Diversity and bioprospecting of actinomycete endophytes from the medicinal plants.

    Science.gov (United States)

    Nalini, M S; Prakash, H S

    2017-04-01

    The endophytic actinomycetes constitute one of the fascinating group of microorganisms associated with a wide range of plant species. The diversity of actinomycetes in plants and their tissue parts is a matter of debate as no consensus are derived between individual studies. Nevertheless, their diversity correlates with the occurrence in plant species harboured in unique regions of biologically diverse areas called "hot spots." Recent advances in the isolation techniques have facilitated the isolation of rare taxa from these environments. The biosynthetic ability of the endophytic actinomycetes has proven beyond doubt that these organisms have the potential to synthesize an array of compounds with novelty in structure and bioactivity and as a result are preferred in the natural product screening programs. In the years to come, the scientific world may await to discover many more novel actinomycete taxa with metabolic diversity and applications in therapeutics.

  15. Disseminated Leishmaniasis Caused by Leishmania Tropica in a Puppy from Karaj, Central Iran

    Directory of Open Access Journals (Sweden)

    M Mohebali

    2011-06-01

    Full Text Available A 5-month old puppy with muco-cutaneous lesions in the chin, around lips and eyes was exam­ined physically and microscopically for leishmaniasis. Muco-cutaneous lesions containing a large num­ber of amastigotes of Leishmania spp. were observed. Amastigotes were also detected in liver and spleen of the puppy. The animal was positive with Dipstick rK39 kit and high level of anti-Leishmania antibodies was detected by direct agglutination test (DAT. DNA, Using PCR-RFLP technique extracted from cultured Leishmania promastigotes and L. tropica was identified. This is the first report of concurrent mucosal and visceral involvement of L. tropica in a puppy from Iran.

  16. Mixed mucosal leishmaniasis infection caused by Leishmania tropica and Leishmania major.

    Science.gov (United States)

    Shirian, Sadegh; Oryan, Ahmad; Hatam, Gholam Reza; Daneshbod, Yahya

    2012-11-01

    Mixed infections with different Leishmania species could explain differences in the clinical courses of these infections. On identification of Leishmania parasites from Iranian patients with mucosal leishmaniasis (ML), a patient with both oral and nasal lesions was found to be concomitantly infected with Leishmania tropica and L. major. Mixed infection was identified by PCR amplification of Leishmania kinetoplast DNA on scraping of cytological smears and histopathological sections. L. major and L. tropica were isolated from the nasal and oral lesions, respectively. These species were also confirmed by immunohistochemistry. This seems to be the first reported case of concurrent ML infection with two Leishmania species. It indicates that, at least in this patient, previous infection with one of these Leishmania species did not protect against infection with the other. This result has important implications for the development of vaccines against leishmaniases and implies careful attention in the treatment of this infectious disease.

  17. Unresponsiveness to Glucantime treatment in Iranian cutaneous leishmaniasis due to drug-resistant Leishmania tropica parasites.

    Directory of Open Access Journals (Sweden)

    Ramtin Hadighi

    2006-05-01

    Full Text Available BACKGROUND: Recent circumstantial evidence suggests that an increasing number of Iranian patients with cutaneous leishmaniasis are unresponsive to meglumine antimoniate (Glucantime, the first line of treatment in Iran. This study was designed to determine whether the clinical responses (healing, or non-healing were correlated with the susceptibility of Leishmania parasites to Glucantime. METHODS AND FINDINGS: In vitro susceptibility testing was first performed on 185 isolated parasites in the intracellular mouse peritoneal macrophage model. A strong correlation between the clinical outcome and the in vitro effective concentration 50% (EC50 values was observed. Parasites derived from patients with non-healing lesions had EC50 values at least 4-fold higher than parasites derived from lesions of healing patients. A selection of these strains was typed at the molecular level by pulsed-field gels and by sequencing the pteridine reductase 1 (PTR1 gene. These techniques indicated that 28 out of 31 selected strains were Leishmania tropica and that three were Leishmania major. The L. major isolates were part of a distinct pulsed-field group, and the L. tropica isolates could be classified in three related additional pulsed-field groups. For each pulsed-field karyotype, we selected sensitive and resistant parasites in which we transfected the firefly luciferase marker to assess further the in vitro susceptibility of field isolates in the monocyte cell line THP1. These determinations confirmed unequivocally that patients with non-healing lesions were infected with L. tropica parasites resistant to Glucantime. Additional characterization of the resistant isolates showed that resistance is stable and can be reversed by buthionine sulfoximine, an inhibitor of glutathione biosynthesis. CONCLUSIONS: To the authors' knowledge, this is the first report of proven resistant parasites contributing to treatment failure for cutaneous leishmaniasis and shows that

  18. Experimentelle Untersuchung des pathogenen Adhäsionsvorganges der Malaria tropica mit Schwingquarzsensoren

    OpenAIRE

    Kleiner, Stefani

    2011-01-01

    Die Fähigkeit, Plasmodium falciparum-infizierter Erythrozyten über Rezeptor-Ligand-Wechselwirkungen an vaskuläres Endothel zu adhärieren, ist das Schlüsselereignis der Pathogenese der Malaria tropica und der damit verbundenen klinischen Symptomatik. Plasmodium falciparum induziert die Expression von PfEMP 1 an der Oberfläche parasitierter Erythrozyten und ermöglicht dadurch die Anheftung an verschiedenste Rezeptoren der Endothelzellen. Die Zielvorgabe der vorliegenden Arbeit war die experimen...

  19. Cloning, expression, purification and characterization of Leishmania tropica PDI-2 protein

    Directory of Open Access Journals (Sweden)

    Ali Dina

    2016-01-01

    Full Text Available In Leishmania species, protein disulfide isomerase (PDI is an essential enzyme that catalyzes thiol-disulfide interchange. The present work describes the isolation, cloning, sequencing and expression of the pdI-2 gene. Initially, the gene was amplified from L. tropica genomic DNA by PCR using specific primers before cloning into the expression vector pET-15b. The construct pET/pdI-2 was transformed into BL21(DE3 cells and induced for the protein expression. SDS-PAGE and western blot analysis showed that the expressed protein is about 51 kDa. Cloned gene sequence analysis revealed that the deduced amino acid sequence showed significant homology with those of several parasites PDIs. Finally, recombinant protein was purified with a metal-chelating affinity column. The putative protein was confirmed as a thiol - disulfide oxidoreductase by detecting its activity in an oxidoreductase assay. Assay result of assay suggested that the PDI-2 protein is required for both oxidation and reduction of disulfide bonds in vitro. Antibodies reactive with this 51 kDa protein were detected by Western blot analysis in sera from human infected with L. tropica. This work describes for the first time the enzymatic activity of recombinant L. tropica PDI-2 protein and suggests a role for this protein as an antigen for the detection of leishmaniasis infection.

  20. Sequence Analysis of HSP70 Gene of Leishmania major and Leishmania tropica in Chabahar and Mashhad

    Directory of Open Access Journals (Sweden)

    Mansour Dabirzadeh

    2016-04-01

    Full Text Available Background and Objective: Cutaneous leishmaniasis is a parasitic disease and a health problem in different parts of Iran, especially two cities of Mashhad and Chabahar. Due to morphological similarities of most Leishmania species and difference in reservoirs of L. major and L. tropica, it is necessary to determine the parasite specie to combat the disease. Thus, this study used gene sequencing and genotyping of 70-kDa heat shock protein (HSP70 to differentiate the two species of Leishmania. Methods: In this descriptive-analytical study, microscope slides and cultures were prepared from 43 patients suspected of cutaneous leishmaniasis in Chabahar and Mashhad. PCR was performed after genomic DNA extraction and then PCR products were sequenced and analyzed. Results: Of the 43 patients studied, 32 direct smear and culture (74.4% were positive and 11 (25.6% showed negative results, and were therefore excluded from the study. Using HSP70-specific primers, 1962 bp and 1152bp bands were observed for HSP70 of L. major in Chabahar and L. tropica in Mashhad, respectively. Based on the results, there were 18 nucleotide differences between HSP70 of L. major in Chabahar and L. tropica in Mashhad. Conclusion: Due to the morphological similarities between Leishmania species and inability to differentiate species through parasitological methods, the HSP70 gene can be used for identification of the species, and prevention and treatment of the disease.

  1. In Vitro and In Vivo Antileishmanial Effects of Pistacia khinjuk against Leishmania tropica and Leishmania major.

    Science.gov (United States)

    Ezatpour, Behrouz; Saedi Dezaki, Ebrahim; Mahmoudvand, Hossein; Azadpour, Mojgan; Ezzatkhah, Fatemeh

    2015-01-01

    The present study aims to evaluate the in vitro and in vivo antileishmanial activities of Pistacia khinjuk Stocks (Anacardiaceae) alcoholic extract and to compare its efficacy with a reference drug, meglumine antimoniate (MA, Glucantime), against Leishmania tropica and Leishmania major. This extract (0-100 µg/mL) was evaluated in vitro against promastigote and intracellular amastigote forms of L. tropica (MRHO/IR/75/ER) and then tested on cutaneous leishmaniasis (CL) in male BALB/c mice with L. major to reproduce the antileishmanial activity topically. In vitro, P. khinjuk extract significantly (P tropica as a dose-dependent response. In the in vivo assay, after 30 days of treatment, 75% recovery was observed in the infected mice treated with 30% extract. After treatment of the subgroups with the concentration of 20 and 30% of P. khinjuk extract, mean diameter of lesions was significantly (P < 0.05) reduced. To conclude, the present investigation demonstrated that P. vera extract had in vitro and in vivo effectiveness against L. major. Obtained findings also provide the scientific evidences that natural plants could be used in the traditional medicine for the prevention and treatment of CL.

  2. Leishmania tropica experimental infection in the rat using luciferase-transfected parasites.

    Science.gov (United States)

    Talmi-Frank, Dalit; Jaffe, Charles L; Nasereddin, Abedelmajeed; Baneth, Gad

    2012-06-08

    Leishmania tropica is the causative agent of zoonotic cutaneous leishmaniasis in different parts of the Old World. Although it is a common cause of disease in some areas of the world, there is insufficient knowledge on the pathogenicity of this parasite in mammalian hosts and animal models. L. tropica luciferase-transfected metacyclic-stage promastigotes were inoculated into the footpad or ear of Sprague Dawley (SD) rats. Parasite DNA was detected by kDNA real time PCR in the blood at varying levels from 2 days to 5 weeks post infection (PI) in the absence of clinical signs. Parasite DNA was found in the spleen of all rats at the end of the study, and the parasitic load was up to 40 times higher in the spleen when compared with inoculation sites. Parasites were cultured from the spleen, and skin inoculation sites 5 weeks PI. Bioluminescent parasites were observed by in vivo imaging at one day PI, but the technique was not sufficiently sensitive to follow parasite spread after this time. This study provides new evidence for the viscerotropic spread of L. tropica in the rat and demonstrates that the rat can serve as a model for persistent visceralizing infection with this parasite.

  3. Phlebotomus sergenti a common vector of Leishmania tropica and Toscana virus in Morocco

    Directory of Open Access Journals (Sweden)

    Nargys Es-Sette

    2014-04-01

    Full Text Available Background & objectives: An entomological study using CDC miniature light-traps was performed in El Hanchane locality, where cutaneous leishmaniasis (CL was emerging during the summer of 2011. The aim of this study is to identify the vectors of Leishmania and of phleboviruses. Methods: In the field, a total of 643 sandfly specimens were collected, identified by morphological keys and categorized by sex and species. A total of nine distinct species were morphologically identified where seven belonged to the Phlebotomus genus and two species to the Sergentomyia genus. Phlebotomus sergenti was the most abundant species (76%. Phleboviruses were detected by nested RT-PCR using 30 pooled sandflies while P. sergenti females were tested individually for infections of Leishmania species. Results: By using ITS1-PCR-RFLP approach, Leishmania tropica DNA was detected in 10 females, caught in this emerging focus, and provide additional evidence in favour of the role of P. sergenti as vector of L. tropica in Morocco. Real-time PCR screening for phlebovirus RNA, using an assay targeting the polymerase gene, showed positive result in one pool of male P. sergenti. Interpretation & conclusion: In this study, P. sergenti were infected by L. tropica and Toscana virus. To our knowledge, actually this is the first time that Toscana virus has been detected in P. sergenti.

  4. Molecular cloning and expression of the Leishmania tropica KMP-11 gene.

    Science.gov (United States)

    Meriee, Mouayad; Soukkarieh, Chadi; Abbady, Abdul Qader A

    2014-08-01

    Kinetoplastid membrane protein-11 (KMP-11) is a small protein of 11 kDa present in all kinetoplastid protozoa studded so far. This protein which is highly expressed in all stages of the Leishmania life cycle is considered a potential candidate for a leishmaniasis vaccine against many leishmania species. KMP-11 has been recently described in Leishmania tropica. In the present study, the KMP-11 gene was extracted from L. tropica by PCR using two oligonucleotide primers designed to amplify the entire coding region of this gene. Then, the purified PCR products were successfully ligated into a high expression vector the pRSET-GFP. This expression vector provides the opportunity to clone the desired insert as a fusion protein with a GFP and a tag, polyhistidine region. The GFP use as a carrier to improve immune response and the polyhistidine tag facilitates detection of the expressed protein with anti-His antibodies and also purification of the protein using affinity purification. After wards KMP-11 coding region was sequenced and the recombinant protein was induced and purified from Escherichia coli cultures. The results of the present study will increase our knowledge about molecular cloning and expression of the L. tropica KMP-11 gene, and this may be used as an effective target for controlling cutenous leishmaniasis.

  5. Soil actinomycetes in the National Forest Park in northeastern China

    Science.gov (United States)

    Shirokikh, I. G.; Shirokikh, A. A.

    2017-01-01

    The taxonomic and functional structure of actinomycete complexes in the litters and upper horizons of the soils under an artificial coniferous-broad-leaved forest located around the town of Chanchun (Tszilin province, PRC). The complex of actinomycetes included representatives of the Streptomyces, Micromonospora, Streptosporangium, and Streptoverticillium genera and oligosporous forms. In the actinomycete complexes, streptomycetes prevailed in the abundance (61-95%) and frequency of occurrence (100%). In the parcels of Korean pine ( Pinus koraiensis) and Mongolian oak ( Quercus mongolica), streptomycetes of 19 species from 8 series and 4 sections were isolated. The most representative, as in European forest biomes, was the Cinereus Achromogenes series. A distinguishing feature of the streptomycete complex in the biomes studied was the high participation of species from the Imperfectus series. The verification of the functional activity of natural isolates made it possible to reveal strains with high antagonistic and cellulolytic abilities. A high similarity of actinomycete complexes was found in Eurasian forest ecosystems remote from each other, probably due to the similarity of plant polymers decomposable by actinomycetes.

  6. Antimicrobial potential of Actinomycetes species isolated from marine environment

    Institute of Scientific and Technical Information of China (English)

    Valli S; Suvathi Sugasini S; Aysha OS; Nirmala P; Vinoth Kumar P; Reena A

    2012-01-01

    Objective:To evaluate the antimicrobial activity of Actinomycetes species isolated from marine environment. Methods: Twenty one strains of Actinomycetes were isolated from samples of Royapuram, Muttukadu, Mahabalipuram sea shores and Adyar estuary. Preliminary screening was done using cross-streak method against two gram-positive and eight gram-negative bacteria. The most potent strains C11 and C12 were selected from which antibacterial substances were extracted. The antibacterial activities of the extracts were performed using Kirby-Bauer disc diffusion method. Molecular identification of those isolates was done. Results:All those twenty one isolates were active against at least one of the test organisms. Morphological characters were recorded. C11 showed activity against Staphylococcus species (13.0±0.5 mm), Vibrio harveyi (11.0±0.2 mm), Pseudomonas species (12.0±0.3 mm). C12 showed activity against Staphylococcus species (16.0±0.4 mm), Bacillus subtilis (11.0±0.2 mm), Vibrio harveyi (9.0±0.1 mm), Pseudomonas species (10.0±0.2 mm). 16S rRNA pattern strongly suggested that C11 and C12 strains were Streptomyces species. Conclusions: The results of the present investigation reveal that the marine Actinomycetes from coastal environment are the potent source of novel antibiotics. Isolation, characterization and study of Actinomycetes can be useful in discovery of novel species of Actinomycetes.

  7. Antibacterial activity of some actinomycetes from Tamil Nadu, India

    Institute of Scientific and Technical Information of China (English)

    Pachaiyappan Saravana Kumar; John Poonga Preetam Raj; Veeramuthu Duraipandiyan; Savarimuthu Ignacimuthu

    2012-01-01

    Objective:To isolate novel actinomycetes and to evaluate their antibacterial activity. Methods:Three soil samples were collected from Vengodu (village) in Kanchipuram district, Tamil Nadu, India. Actinomycetes were isolated using serial dilution and plating method on actinomycetes isolation agar. Results: Totally 35 isolates were obtained on the basis of colony characteristics on actinomycetes isolation agar. All the isolates were screened for antibacterial activity by cross streak method. Medium and optimization of day were done for the potent strains using Nathan's agar well diffusion method. Isolation of bioactive compounds from significant active isolates was done by using different media. The most active isolate VAS 10 was identified as Actinobacterium Loyola PBT VAS 10 (accession No. JF501398) using 16s rRNA sequence method. The hexane, ethyl acetate, dichloromethane and butanol extracts of VAS 10 were tested against bacteria. The maximum antibacterial activity was observed in dichloromethane and ethyl acetate;maximum zones of inhibition were observed against Enterococcus durans. The rRNA secondary structure and the restriction sites of Actinobacterium Loyola VAS 10 were predicted using Genebee and NEBCutter online tools respectively. Conclusions: The present study showed that among the isolated actinomycetes, Actinobacterium Loyola PBT VAS 10 (accession No. JF501398) showed good antibacterial activity against the tested bacteria.

  8. CRISPR-Cas9 Based Engineering of Actinomycetal Genomes

    DEFF Research Database (Denmark)

    Tong, Yaojun; Charusanti, Pep; Zhang, Lixin

    2015-01-01

    . To facilitate the genetic manipulation of actinomycetes, we developed a highly efficient CRISPR-Cas9 system to delete gene(s) or gene cluster(s), implement precise gene replacements, and reversibly control gene expression in actinomycetes. We demonstrate our system by targeting two genes, actIORF1 (SCO5087......) and actVB (SCO5092), from the actinorhodin biosynthetic gene cluster in Streptomyces coelicolor A3(2). Our CRISPR-Cas9 system successfully inactivated the targeted genes. When no templates for homology-directed repair (HDR) were present, the site-specific DNA double-strand breaks (DSBs) introduced by Cas9....... Moreover, we developed a system to efficiently and reversibly control expression of target genes, deemed CRISPRi, based on a catalytically dead variant of Cas9 (dCas9). The CRISPR-Cas9 based system described here comprises a powerful and broadly applicable set of tools to manipulate actinomycetal genomes....

  9. Alkalithermophilic actinomycetes in a subtropical area of Jujuy, Argentina.

    Science.gov (United States)

    Carrillo, L; Benítez Ahrendts, M R; Maldonado, M J

    2009-01-01

    The objective of this study was to examine the alkalithermophilic actinomycete communities in the subtropical environment of Jujuy, Argentina, characterized by sugarcane crops. Laceyella putida, Laceyella sacchari, Thermoactinomyces intermedius, Thermoactinomyces vulgaris and Thermoflavimicrobium dichotomicum were isolated on the media with novobiocin, from sugar cane plants and renewal rhizospheres, and grass and wood soils. Soil pH was almost neutral or lightly alkaline, except for grass soil acidified by lactic liquor. A smaller number of actinomycetes was found on the living plants and bagasse (recently obtained or stored according to the Ritter method) with respect to decomposed leaves on the soil. Thermophilic species of Laceyella, Thermoactinomyces, Thermoflavimicrobium, Saccharomonospora, Streptomyces and Thermononospora were isolated on the media without novobiocin, from composted sugar cane residues. Air captured near composted bagasse piles, contained alkalithermophilic actinomycete spores.

  10. Synthetic polyester-hydrolyzing enzymes from thermophilic actinomycetes.

    Science.gov (United States)

    Wei, Ren; Oeser, Thorsten; Zimmermann, Wolfgang

    2014-01-01

    Thermophilic actinomycetes produce enzymes capable of hydrolyzing synthetic polyesters such as polyethylene terephthalate (PET). In addition to carboxylesterases, which have hydrolytic activity predominantly against PET oligomers, esterases related to cutinases also hydrolyze synthetic polymers. The production of these enzymes by actinomycetes as well as their recombinant expression in heterologous hosts is described and their catalytic activity against polyester substrates is compared. Assays to analyze the enzymatic hydrolysis of synthetic polyesters are evaluated, and a kinetic model describing the enzymatic heterogeneous hydrolysis process is discussed. Structure-function and structure-stability relationships of actinomycete polyester hydrolases are compared based on molecular dynamics simulations and recently solved protein structures. In addition, recent progress in enhancing their activity and thermal stability by random or site-directed mutagenesis is presented.

  11. Natural infection of North African gundi (Ctenodactylus gundi) by Leishmania tropica in the focus of cutaneous leishmaniasis, Southeast Tunisia.

    Science.gov (United States)

    Bousslimi, Nadia; Ben-Ayed, Soumaya; Ben-Abda, Imène; Aoun, Karim; Bouratbine, Aïda

    2012-06-01

    North African gundis (Ctenodactylus gundi) were trapped in the Leishmania (L.) tropica focus of cutaneous leishmaniasis, situated in southeast Tunisia and evaluated for Leishmania infection by real-time kinetoplast DNA polymerase chain reaction (PCR). Species identification was performed by internal transcribed spacer one (ITS1)-PCR-restriction fragment length polymorphism (RFLP) and high-resolution melting (HRM) analysis of the 7SL RNA gene. Real-time PCR on blood was positive in 6 of 13 (46.2%) tested gundis. Leishmania tropica was identified in five infected gundis and Leishmania major in one specimen. Alignments of the ITS-1 DNA sequences and 7S-HRM curves analysis indicated that similar genotypes were present in humans, a sandfly, and gundis from the same region suggesting a potential role of this rodent as reservoir host of L. tropica in southeast Tunisia.

  12. Biodegradation of the herbicide Diuron in soil by indigenous actinomycetes.

    Science.gov (United States)

    Esposito, E; Paulillo, S M; Manfio, G P

    1998-08-01

    Three actinomycete strains isolated from soil treated with 2,4-D were able to degrade the herbicide Diuron in vitro. Strain CCT 4916 was the most efficient, degrading up to 37% of applied Diuron (100 mg Kg-1 soil) in 7 days, as measured by HPLC and UV/VIS spectroscopy. All strains showed protease and urease activity; intracellular activity of metapyrocatechase and pyrocatechase were not found. Actinomycete strain CCT 4916 produced manganese peroxidase, which could be potentially related to degradation of Diuron.

  13. Antibiotic production by actinomycetes: the Janus faces of regulation.

    Science.gov (United States)

    Cundliffe, Eric

    2006-07-01

    This manuscript reviews some of the common regulatory mechanisms that control antibiotic production in actinomycetes. These ubiquitous bacteria, collectively responsible for the earthy smell of soil, are prolific producers of antibiotics and other secondary metabolites. The content of this review is biased towards the author's current research interests, concerning the action of regulatory gene products that control transcription of antibiotic-biosynthetic genes and the associated involvement of low molecular weight signalling molecules of the gamma-butyrolactone family. As a result, much fertile ground remains unturned particularly in the area of environmental monitoring and responses of actinomycetes to stimuli so perceived. Reviews casting a broader net are cited in the text.

  14. ISOLATION OF ENDOPHYTIC ACTINOMYCETES FROM MEDICINAL PLANTS AND ITS MUTATIONAL EFFECT IN BIOCONTROL ACTIVITY

    Directory of Open Access Journals (Sweden)

    Hema Shenpagam N.*, D. Kanchana Devi ** and Sinduja G.

    2012-11-01

    Full Text Available In the present study, the endophytic actinomycetes were collected from three medicinal plants Azadiracta indica, Ocimum sanctum and Phyllanthus amarus. Endophytic actinomycetes were isolated using different media like Starch casein agar, Starch casein nitrate agar, Actinomycetes isolation agar and Soyabean agar, while it showed more colonies in Starch casein agar. The endophytic actinomycetes were stained and biochemical tests were performed. Antimicrobial compound was purified from the filtrate by ethanol extraction method. Antagonistic activities of endophytic actinomycetes isolates were tested against bacterial pathogens (Staphylococcus aureus, Streptococcus pyogenes, Klebsiella pneumoniae and Pseudomonas aeruginosa and the fungi Rhizopus. For the selected isolates antibiotic resistance was checked using various antibiotic discs like Amoxycillin, Penicillin, Rifampicin and Ampicillin. The strains which showed efficient antibacterial activity were selected to study the effect of mutation by physical and chemical method. In this study, UV mutated endophytic actinomycetes increase antibiotic production than non-mutated endophytic Actinomycetes, whereas in chemical mutation it does not increase the antibiotic production.

  15. Antibiotics production by an actinomycete isolated from the termite gut.

    Science.gov (United States)

    Matsui, Toru; Tanaka, Junichi; Namihira, Tomoyuki; Shinzato, Naoya

    2012-12-01

    As well as the search for new antibiotics, a new resource or strains for the known antibiotics is also important. Microbial symbionts in the gut of termites could be regarded as one of the feasible resource for such purpose. In this study, antibiotic-producing actinomycetes were screened from symbionts of the termite gut. 16SrRNA sequence analysis for the 10 isolates revealed that they belong to actinomycetes such as Streptomyces sp., Kitasatospora sp., and Mycobacterium sp. A culture broth from one of the isolate, namely strain CA1, belonging to the genera Streptomyces exhibited antagonistic activity against actinomycetes (Micrococcus spp.), gram-positive bacteria (Bacillus spp.), and yeast (Candida spp.). The structures of 2 compounds isolated from the culture broth of the strain CA1 were identified as those of actinomycin X2 and its analog, D. This study is the first to report that some symbionts of the termite gut are antibiotic-producing actinomycetes, and suggest that the termite gut is a feasible resource for bioprospecting.

  16. A New Degraded Sesquiterpene from Marine Actinomycete Streptomyces sp. 0616208

    Institute of Scientific and Technical Information of China (English)

    Xiu Chao XIE; Wen Li MEI; You Xing ZHAO; Kui HONG; Hao Fu DAI

    2006-01-01

    A new degraded sesquiterpene was isolated from the marine actinomycete Streptomyces sp. 0616208. Its structure was elucidated as (1α, 4aα, 5α, 7β, 8aβ)-5, 8a-dimethyl-decahydrona-phthalene-1, 4a, 7-triol on the basis of spectroscopic data.

  17. Biodiscovery from rare actinomycetes: an eco-taxonomical perspective.

    Science.gov (United States)

    Kurtböke, D I

    2012-03-01

    Microbial natural products, in particular, the ones produced by the members of the order Actinomycetales, will continue to represent an important route to the discovery of novel classes of bioactive compounds. As a result, the search for and discovery of lesser-known and/or novel actinomycetes is of significant interest to the industry due to a growing need for the development of new and potent therapeutic agents, mainly against drug resistant bacteria. Current advancements in genomics and metagenomics are adding strength to the target-directed search for detection and isolation of bioactive actinomycetes. New discoveries, however, will only stem from a sound understanding and interpretation of knowledge derived from conventional studies conducted since the discovery of streptomycin, on the ecology, taxonomy, physiology and metabolism of actinomycetes, and from a combination of this knowledge with currently available and continuously advancing molecular tools. Such a powerful information platform will then inevitably reveal the whereabouts, taxonomical and chemical identities of previously undetected bioactive actinomycetes including novel species of streptomycetes as potential producers of novel drug candidates.

  18. Environmental and metabolomic study of antibiotic production by actinomycetes

    NARCIS (Netherlands)

    Zhu, Hua

    2014-01-01

    This thesis may be regarded as a concept work, to see how feasible drug discovery approaches still are. For this, a strain collection was built up consisting of actinomycetes from soil in the Qinling and Himalaya mountains, which were subsequently tested for antibiotic production against multi-drug

  19. Genetics of host response to Leishmania tropica in mice - different control of skin pathology, chemokine reaction, and invasion into spleen and liver.

    Directory of Open Access Journals (Sweden)

    Tetyana Kobets

    Full Text Available BACKGROUND: Leishmaniasis is a disease caused by protozoan parasites of genus Leishmania. The frequent involvement of Leishmania tropica in human leishmaniasis has been recognized only recently. Similarly as L. major, L. tropica causes cutaneous leishmaniasis in humans, but can also visceralize and cause systemic illness. The relationship between the host genotype and disease manifestations is poorly understood because there were no suitable animal models. METHODS: We studied susceptibility to L. tropica, using BALB/c-c-STS/A (CcS/Dem recombinant congenic (RC strains, which differ greatly in susceptibility to L. major. Mice were infected with L. tropica and skin lesions, cytokine and chemokine levels in serum, and parasite numbers in organs were measured. PRINCIPAL FINDINGS: Females of BALB/c and several RC strains developed skin lesions. In some strains parasites visceralized and were detected in spleen and liver. Importantly, the strain distribution pattern of symptoms caused by L. tropica was different from that observed after L. major infection. Moreover, sex differently influenced infection with L. tropica and L. major. L. major-infected males exhibited either higher or similar skin pathology as females, whereas L. tropica-infected females were more susceptible than males. The majority of L. tropica-infected strains exhibited increased levels of chemokines CCL2, CCL3 and CCL5. CcS-16 females, which developed the largest lesions, exhibited a unique systemic chemokine reaction, characterized by additional transient early peaks of CCL3 and CCL5, which were not present in CcS-16 males nor in any other strain. CONCLUSION: Comparison of L. tropica and L. major infections indicates that the strain patterns of response are species-specific, with different sex effects and largely different host susceptibility genes.

  20. Phylogenetic structure of Leishmania tropica in the new endemic focus Birjand in East Iran in comparison to other Iranian endemic regions.

    Science.gov (United States)

    Karamian, Mehdi; Kuhls, Katrin; Hemmati, Mina; Ghatee, Mohammad Amin

    2016-06-01

    Iran has been identified being among the countries with the highest number of cutaneous leishmaniasis (CL) cases. South Khorasan province in East Iran is an emerging focus of CL. Species identification of sixty clinical samples by ITS1 PCR-RFLP presented evidence for the dominance of Leishmania tropica (90%) in this region. Analysis of the ITS1 sequence of 19 L. tropica isolates revealed seven closely related sequence types. In addition, ITS1 sequences available in GenBank from other Iranian regions were compiled for comparison with the studied isolates. Iranian L. tropica was distributed in two main clusters. All East Iranian sequence types were grouped with strains from foci from Southeast and Central regions in cluster A, showing highly similar sequences. The highest similarity was observed between most L. tropica from East and all isolates from Southeast regions and from Savojbolagh county in Central Iran. Southwest L. tropica was shown to be paraphyletic as the isolates were distributed in both clusters A and B. All Northeastern L. tropica were part of cluster B, however they showed significant heterogeneity and were distributed in different subclusters. Distribution of L. tropica populations was to some extent congruent with genetic lineages of Phlebotomus sergenti in Iran and may be an evidence for parasite-vector co-evolution. Southeast-East L. tropica was also similar to strains from Herat province in Afghanistan at the East border of Iran. This is the first comprehensive study on population structure of L. tropica in Iran that provides a guideline for appropriate sampling for further molecular based epidemiological studies.

  1. Molecular Evaluation of a Case of Visceral Leishmaniasis Due to Leishmania tropica in southwestern Iran

    Directory of Open Access Journals (Sweden)

    Bahador SARKARI

    2016-03-01

    Full Text Available We describe a case of visceral leishmaniasis (VL due to Leishmania tropica in a 50-year-old Iranian man lived in a VL-endemic area in southwest of Iran. The patient presented with a 3-month history of fever and splenomegaly. Clinical signs and serological findings were suggestive of VL. Spleen biopsy was taken from the patient and intracellular forms of Leishmania amastigotes was seen in Giemsa stained smears. The patient was treated with pentavalent antimonial compound with complete resolution of his systemic signs and symptoms. DNA was extracted from the microscopic slides of the spleen biopsy and the nagt (N-Acetylglucosamine-1-Phosphate Transferase gene of Leishmania was PCR-amplified. Sequence analysis of the PCR product demonstrated that the case has 99% identity with those of available sequences of L. tropica. Intra-species variation within isolate was 0-0.1%; whereas, inter-species differences of the isolate with those of L. major and L. infantum was significantly higher.

  2. Leishmania tropica: the effect of darkness and light on biological activities in vitro.

    Science.gov (United States)

    Allahverdiyev, Adil M; Koc, Rabia Cakir; Ates, Sezen Canim; Bagirova, Malahat; Elcicek, Serhat; Oztel, Olga Nehir

    2011-08-01

    Leishmania parasites can be exposed to effects of light in their vectors and hosts, at various periods. However, there is no information about the effects of light on Leishmania parasites. The aim of this study is to investigate the effects of light on various cell parameters of Leishmania tropica, in vitro. All experiments were conducted on L. tropica promastigotes and amastigote-macrophage cultures, using flow cytometric analysis, MTT and phenol-sulfuric acid assay, DAPI and Giemsa. The results showed that the morphology of parasites has changed; the cell cycle has been affected and this caused parasites to remain at G0/G1 phase. Furthermore the proliferation, infectivity, glucose consumption and mitochondrial dehydrogenase activities of parasites were decreased. Thus, for the first time, in this study, the effects of light on biological activities of Leishmania parasites were shown. These new information about parasites' biology, would be very important to investigate the effects of light on the parasites in infected vectors and hosts.

  3. Epidemiological characteristics of a new focus of cutaneous leishmaniasis caused by Leishmania tropica in Settat, Morocco.

    Science.gov (United States)

    Fatima, Amarir; Faiza, Sebti; Hajiba, Fellah; Francine, Pratlong; Dedet, Jean-Pierre; Bouchra, El Mansouri; Asmae, Hmamouch; Bouchra, Delouane; Khalid, Habbari; Abderrahim, Sadak; Ibrahim, Abassi; Mohamed, Rhajaoui

    2015-10-01

    A new emerging focus of human cutaneous leishmaniasis (HCL) caused by Leishmania tropica was identified within the province of Settat. This study was performed in order to analyze the reasons of the extension of CL in this area, and to describe the clinico-epidemiological characteristic of this emerging focus during 2007-2012. A total of 553 suspected cases of CL were diagnosed in laboratory of Settat, controlled and confirmed in reference national laboratory of leishmaniasis in Rabat. Leishmania parasite is found in 356 cases. Most of them (33.89%) were recorded in localities of Ouled Ghalem (110 cases) and Laamarcha (102 cases) of El Borouj sector. The lesions were typically small, dry and mostly located on the face and extremities. Majority of infection (25%) was recorded among children under 11 years old, and female (72%). Strains of L. tropica were identified by PCR ITS1 from positive slides and zymodeme MON-102 was typed using isoenzyme technique on starch gel electrophoresis.

  4. Evaluation of (131)I-pentamidine for scintigraphy of experimentally Leishmania tropica-infected hamsters.

    Science.gov (United States)

    Inceboz, Tonay; Lambrecht, Fatma Yurt; Eren, Mine Şencan; Girginkardeşler, Nogay; Bekiş, Recep; Yilmaz, Osman; Er, Özge; Özbilgin, Ahmet

    2014-06-01

    We aimed to assess the ability of (131)I-Pentamidine scintigraphy to detect the lesions of Leishmania tropica infection. An experimental model of cutaneous leishmaniasis was developed. The presence of cutaneous leishmaniasis was confirmed. Pentamidine was radioiodinated with (131)I. The radiolabeled pentamidine was validated by the requisite quality control tests to check its radiolabeling efficiency, in vitro stability. (131)I-Pentamidine (activity: 18.5 MBq/100 µl) was injected intracardiacally into infected hamsters. Static whole body images of the hamsters were acquired under the gamma camera at 5 and 30 min, 2, 6 and 24 h following the administration. On the scintigrams, anatomically adjusted regions of interest (ROIs) were drawn over the right feet (target) and left feet (not-target) and various organs. Accumulation of (131)I-Pentamidine at sites of infection is expressed as the target to non-target (T/NT) ratio. The results T/NT ratio decreased with time. In concluding the (131)I-Pentamidine has poor sensitivity in detection of L. tropica infection.

  5. Molecular Evaluation of a Case of Visceral Leishmaniasis Due to Leishmania tropica in Southwestern Iran.

    Science.gov (United States)

    Sarkari, Bahador; Bavarsad Ahmadpour, Niloofar; Moshfe, Abdolali; Hajjaran, Homa

    2016-01-01

    We describe a case of visceral leishmaniasis (VL) due to Leishmania tropica in a 50-year-old Iranian man lived in a VL-endemic area in southwest of Iran. The patient presented with a 3-month history of fever and splenomegaly. Clinical signs and serological findings were suggestive of VL. Spleen biopsy was taken from the patient and intracellular forms of Leishmania amastigotes was seen in Giemsa stained smears. The patient was treated with pentavalent antimonial compound with complete resolution of his systemic signs and symptoms. DNA was extracted from the microscopic slides of the spleen biopsy and the nagt (N-Acetylglucosamine-1-Phosphate Transferase) gene of Leishmania was PCR-amplified. Sequence analysis of the PCR product demonstrated that the case has 99% identity with those of available sequences of L. tropica. Intra-species variation within isolate was 0-0.1%; whereas, inter-species differences of the isolate with those of L. major and L. infantum was significantly higher.

  6. [Leishmania tropica in Morocco. III--The vector of Phlebotomus sergenti. Apropos of 89 isolates].

    Science.gov (United States)

    Guilvard, E; Rioux, J A; Gallego, M; Pratlong, F; Mahjour, J; Martinez-Ortega, E; Dereure, J; Saddiki, A; Martini, A

    1991-01-01

    In a Moroccan focus of cutaneous leishmaniasis caused by Leishmania tropica, 7,907 female sandflies captured with CDC traps were dissected from summer to autumn 1989. Among species of the genus Phlebotomus, only P. sergenti harbored promastigotes. Eighty-nine strains belonging to the complex L. tropica were isolated. The frequency of vector infection was zero in June, rose to 1.3% in August, and reached 9.9% in October, which indicates that the period of high risk is at the end of the hot season. Out of 89 strains isolated, 74 were completely typed and corresponded to the following four zymodemes: MON-102 (one strain), MON-107 (56 strains), MON-122 (two strains), and MON-123 (15 strains). Only the first two were observed in humans. The distribution of zymodemes MON-102 and MON-107 was very different in humans, dogs, and the vector. In one of the sites surveyed, which was strongly dominated by MON-107, the absence of human cases involving this zymodeme suggests the existence of a wild reservoir.

  7. Genetic polymorphisms and drug susceptibility in four isolates of Leishmania tropica obtained from Canadian soldiers returning from Afghanistan.

    Directory of Open Access Journals (Sweden)

    Marie Plourde

    2012-01-01

    Full Text Available BACKGROUND: Cutaneous leishmaniasis (CL is a vector-borne parasitic disease characterized by the presence of one or more lesions on the skin that usually heal spontaneously after a few months. Most cases of CL worldwide occur in Southwest Asia, Africa and South America, and a number of cases have been reported among troops deployed to Afghanistan. No vaccines are available against this disease, and its treatment relies on chemotherapy. The aim of this study was to characterize parasites isolated from Canadian soldiers at the molecular level and to determine their susceptibility profile against a panel of antileishmanials to identify appropriate therapies. METHODOLOGY/PRINCIPAL FINDINGS: Parasites were isolated from skin lesions and characterized as Leishmania tropica based on their pulsed field gel electrophoresis profiles and pteridine reductase 1 (PTR1 sequences. Unusually high allelic polymorphisms were observed at several genetic loci for the L. tropica isolates that were characterized. The drug susceptibility profile of intracellular amastigote parasites was determined using an established macrophage assay. All isolates were sensitive to miltefosine, amphotericin B, sodium stibogluconate (Pentostam and paromomycin, but were not susceptible to fluconazole. Variable levels of susceptibility were observed for the antimalarial agent atovaquone/proguanil (Malarone. Three Canadian soldiers from this study were successfully treated with miltefosine. CONCLUSIONS/SIGNIFICANCE: This study shows high heterogeneity between the two L. tropica allelic versions of a gene but despite this, L. tropica isolated from Afghanistan are susceptible to several of the antileishmanial drugs available.

  8. Molecular identification of Leishmania tropica infections in patients with cutaneous leishmaniasis from an endemic central of Iran.

    Science.gov (United States)

    Eslami, Gilda; Hajimohammadi, Bahador; Jafari, Abbas Ali; Mirzaei, Farzaneh; Gholamrezai, Mostafa; Anvari, Hossein; Khamesipour, Ali

    2014-12-01

    The most common form of the disease is cutaneous leishmaniasis (CL) which is a public health and social problem in many countries especially Iran. In endemic areas where other diseases with similar clinical symptoms occur, definitive diagnosis of CL is very important. The detection and identification of Leishmania in infected patients is crucial for achieving a correct treatment and prognosis. To our knowledge, this is the first comprehensive study in terms of geographical distribution and molecular identification of Leishmania tropica isolates in central of Iran. This study was performed between 2010 and 2011, during which 218 CL suspected patients referred to Shahid Sadoughi University of Medical Sciences in Yazd, Iran for confirmation were examined. After microscopic analysis, DNA extraction was performed for identification. The molecular target region was ITS1 gene. Results showed that out of 218 isolates, 102 (46.8%) samples were positive for Leishman body using molecular assay. After PCR-RFLP, analysis identified 50 (49.01%) samples as L. major and 52 (50.98%) as L. tropica. Two samples showed a different pattern that were reported as unknown. Among L. tropica, six different isolates were identified in this endemic area. Finally, this study showed heterozygosity among L. tropica isolates in this endemic area such as some other studies from the world. This heterozygosity among the strains may suggest a sexual recombination or genetic exchange between strains.

  9. In vitro cultivation of axenic amastigotes and the comparison of antioxidant enzymes at different stages of Leishmania tropica.

    Science.gov (United States)

    Bahrami, S; Hatam, G R; Razavi, M; Nazifi, S

    2011-08-01

    The present study aimed to establish a simple method to yield large amounts of Leishmania tropica amastigote-like forms in axenic cultures and to compare the superoxide dismutase (SOD) and glutathione peroxidase (GPX) enzymes at different stages of L. tropica. Different culture conditions were tested to find the optimum condition of axenic amastigotes generation. Superoxide dismutase (SOD) and glutathione peroxidase (GPX) activities were determined at logarithmic and stationary phases and axenic amastigote stage of the parasite. A high proportion (88%) of amastigote-like forms of L. tropica was observed in BHI medium supplemented with 20% FCS, pH 4.5, and incubated at 37ºC with 5% CO(2). The results showed that SOD activity was at the lowest level in the logarithmic phase of promastigotes and increased towards the stationary phase of promastigotes and amastigote stage. The results showed that the optimum condition for differentiation of L. tropica promastigotes to axenic amastigotes was BHI medium containing 20% FCS at pH 4.5, incubated at 37ºC in the presence of 5% CO(2). It seems that SOD, but not GPX is a major determinant of intracellular survival of the parasite.

  10. Competitive strategies differentiate closely related species of marine actinobacteria.

    Science.gov (United States)

    Patin, Nastassia V; Duncan, Katherine R; Dorrestein, Pieter C; Jensen, Paul R

    2016-02-01

    Although competition, niche partitioning, and spatial isolation have been used to describe the ecology and evolution of macro-organisms, it is less clear to what extent these principles account for the extraordinary levels of bacterial diversity observed in nature. Ecological interactions among bacteria are particularly challenging to address due to methodological limitations and uncertainties over how to recognize fundamental units of diversity and link them to the functional traits and evolutionary processes that led to their divergence. Here we show that two closely related marine actinomycete species can be differentiated based on competitive strategies. Using a direct challenge assay to investigate inhibitory interactions with members of the bacterial community, we observed a temporal difference in the onset of inhibition. The majority of inhibitory activity exhibited by Salinispora arenicola occurred early in its growth cycle and was linked to antibiotic production. In contrast, most inhibition by Salinispora tropica occurred later in the growth cycle and was more commonly linked to nutrient depletion or other sources. Comparative genomics support these differences, with S. arenicola containing nearly twice the number of secondary metabolite biosynthetic gene clusters as S. tropica, indicating a greater potential for secondary metabolite production. In contrast, S. tropica is enriched in gene clusters associated with the acquisition of growth-limiting nutrients such as iron. Coupled with differences in growth rates, the results reveal that S. arenicola uses interference competition at the expense of growth, whereas S. tropica preferentially employs a strategy of exploitation competition. The results support the ecological divergence of two co-occurring and closely related species of marine bacteria by providing evidence they have evolved fundamentally different strategies to compete in marine sediments.

  11. The Development of Leishmania tropica in Sand Flies (Diptera: Psychodidae): A Comparison of Colonies Differing in Geographical Origin and a Gregarine Coinfection.

    Science.gov (United States)

    Jancarova, Magdalena; Hlavacova, Jana; Volf, Petr

    2015-11-01

    Phlebotomus sergenti Parrot, 1917 is the main vector of Leishmania tropica; however, its broad geographical range and molecular heterogeneity suggest possible variability in vector competence. We infected laboratory-reared P. sergenti originating from Turkey and Israel to compare their susceptibility to L. tropica. In both tested groups, heavy late-stage infections with the presence of metacyclic forms and colonization of the stomodeal valve were observed. The similar development of Leishmania in both sand fly colonies indicates that the different geographical origin of P. sergenti is not reflected by a different vector competence to L. tropica. Additionally, we tested the effect of the gregarine Psychodiella sergenti on L. tropica coinfections; no apparent differences were found between P. sergenti infected or not infected by gregarines.

  12. Detection of anti-leishmanial effect of the Lucilia sericata larval secretions in vitro and in vivo on Leishmania tropica: first work.

    Science.gov (United States)

    Polat, Erdal; Cakan, Huseyin; Aslan, Mustafa; Sirekbasan, Serhat; Kutlubay, Zekayi; Ipek, Turgut; Ozbilgin, Ahmet

    2012-10-01

    It is known that some of the enzymes and substances secreted by 2nd and 3rd stages of the Lucilia sericata larvae to have bacteriostatic and bactericidal effects. From this point of view, we investigated the anti-leishmanial effect of larval secretions of the L. sericata on the Leishmania tropica both in vitro and in vivo conditions. In vitro: It was observed that promastigotes of L. tropica had undergone lyzis within 1 min in the larval secretions of L. sericata. However, larval secretion was ineffective on the promastigotes within Novy-MacNeal-Nicolle (NNN) cultures and RPMI 1640 medium. In vivo: Seven groups of male Balb/C mice (6 study groups and 1 control group), each composed of eight weeks old 10 mice were formed. L. tropica promastigotes were injected subcutaneosly to the soles of the SG mice' feet. In study groups, cutaneous lesions were developed Limoncu et al., 1997 in 2 (20%) and 1 (10%) of the SG-1 and SG-2, respectively after 15 days. There were L. tropica in the smears prepared from the lesions and L. tropica was observed in the cultures. Cutaneous lesions were not developed in 8 (80%), 9 (90%) and 10 (100%) of the SG-I, SG-II and SG-III, respectively. There were no cutaneous lesions developed in the soles of the feet. There were no L. tropica in the smears prepared from the infected soles of the feet neither L. tropica was observed in the cultures. Larval secretions were given into the cutaneous lesions to the feet soles of the SG-IV, V and VI mice after 6 months. No healing was observed in the cutaneos lesions of 4 (40%), 5 (50%) and 1 (10%) of SG-IV, SG-V and SG-VI, after 6 months, respectively. There were L. tropica in the smears prepared from the lesions and L. tropica was observed in the cultures. On the other hand, the lesions of 6 (60%), 5 (50%) and 9 (90%) of SG-IV, SG-V and SG-VI were diminished in size and disappeared completely after 6 months. There were L. tropica observed in the smears prepared from the infected soles of the feet and no

  13. Distribution of actinomycetes in oil contaminated ultisols of the Niger Delta (Nigeria)

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The distribution of actinomycetes in oil contaminated sandy loam ultisols of the Niger Delta region of Nigeria was studied to aid in understanding the effect of hydrocarbons on indigenous microbial population in tropical soils. The average total counts of actinomycetes in all the oil samples analysed was 103 cfu/g. Higher counts of actinomycetes were observed during the dry season than during the wet season. The counts of hydrocarbonoclastic actinomycetes correlated positively with the total count of actinomycetes.The actinomycetes were generally restricted to the top soil(0-10 cm soil depth) although a seemingly deeper(down to 40 cm soil depth) distribution was noticed in the dry season. The isolates included oil degrading species of Actinoplanes, Norcadia,Streptomyces and Streptosporangium. Their high oil utilization ability indicates their positive potential and role in the bioremediation of oil-spilled soils.

  14. Genetic diversity of Leishmania tropica strains isolated from clinical forms of cutaneous leishmaniasis in rural districts of Herat province, Western Afghanistan, based on ITS1-rDNA.

    Science.gov (United States)

    Fakhar, Mahdi; Pazoki Ghohe, Hossein; Rasooli, Sayed Abobakar; Karamian, Mehdi; Mohib, Abdul Satar; Ziaei Hezarjaribi, Hajar; Pagheh, Abdol Sattar; Ghatee, Mohammad Amin

    2016-07-01

    Despite the high incidence of cutaneous leishmaniasis (CL) in Afghanistan, there is a little information concerning epidemiological status of the disease and phylogenetic relationship and population structure of causative agents. This study was conducted to determine the prevalence and distribution of CL cases and investigate the Leishmania tropica population structure in rural districts of Heart province in the West of Afghanistan in comparison to neighboring foci. Overall, 4189 clinically suspected CL cases from 177 villages (including 12 districts) in Herat province were enrolled in the referral laboratory of WHO sub-office in Herat city from January 2012 to December 2013. 3861 cases were confirmed as CL by microscopic examination of Giemsa-stained slides. ITS1 PCR-RFLP analysis showed dominance of L. tropica (more than 98%) among 127 randomly chosen samples. Analysis of the ITS1 sequences revealed 4 sequence types among the 21 L. tropica isolates. Comparison of sequence types from Herat rural districts with the representatives of L. tropica from Iran, India, and Herat city showed two main population groups (cluster A and B). All isolates from Herat province, India and Southeast, East, and Central Iran were found exclusively in cluster A. The close proximity of West Afghanistan focus and Birjand county as the capital of Southern Khorasan province in East Iran can explain relatively equal to the genetic composition of L. tropica in these two neighboring regions. In addition, two populations were found among L. tropica isolates from Herat rural districts. Main population showed more similarity to some isolates from Birjand county in East Iran while minor population probably originated from the Southeast and East Iranian L. tropica. Recent study provided valuable information concerning the population structure of L. tropica and epidemiology of ACL in the West of Afghanistan, which could be the basis for molecular epidemiology studies in other regions of Afghanistan.

  15. Unusual multifocal granulomatous disease caused by actinomycetous bacteria in a nestling Derbyan parrot (Psittacula derbiana).

    Science.gov (United States)

    Park, F J; Jaensch, S

    2009-01-01

    A nestling Derbyan parrot (Psittacula derbiana) was presented with unusual subcutaneous swellings of the thigh regions, and poor growth. Histological examination revealed actinomycetous bacteria associated with multifocal systemic granulomas. The clinical and pathological findings of the case are presented, and some relevant aspects of actinomycetous bacterial infections in mammals and birds are discussed. Although granulomatous disease is encountered at times in avian species, the actinomycetous bacteria (Nocardia and Actinomyces spp.) have rarely been reported in association with multifocal granulomatous disease in birds.

  16. 放线菌分类研究进展%Advance on taxonomy of actinomycetes

    Institute of Scientific and Technical Information of China (English)

    刘燕娟; 李婵; 周倩

    2009-01-01

    The status of actinomycetes classification study of the evolution and classification methods were overviewed, as well as domestic actinomycetes classification status,and actinomycetes classification was forecasted.%综述了放线菌分类地位的演变和分类研究方法,以及国内放线菌分类现状,并对放线菌分类研究进行了展望.

  17. Production of Ramoplanin and Ramoplanin Analogs by Actinomycetes

    Science.gov (United States)

    de la Cruz, Mercedes; González, Ignacio; Parish, Craig A.; Onishi, Russell; Tormo, José R.; Martín, Jesús; Peláez, Fernando; Zink, Debbie; El Aouad, Noureddine; Reyes, Fernando; Genilloud, Olga; Vicente, Francisca

    2017-01-01

    Ramoplanin is a glycolipodepsipeptide antibiotic obtained from fermentation of Actinoplanes sp. ATCC 33076 that exhibits activity against clinically important multi-drug-resistant, Gram-positive pathogens including vancomycin-resistant Enterococcus (VRE), methicillin-resistant Staphylococcus aureus (MRSA), and vancomycin-intermediate resistant Clostridium difficile. It disrupts bacterial cell wall through a unique mechanism of action by sequestering the peptidoglycan intermediate Lipid II and therefore does not show cross-resistance with other antibiotics. However, while demonstrating excellent antimicrobial activity in systemic use in animal models of infection, ramoplanin presents low local tolerability when injected intravenously. As a consequence of this limitation, new derivatives are desirable to overcome this issue. During a natural product screening program developed to discover compounds that disrupt bacterial cell wall synthesis by inhibiting peptidoglycan transglycosylation through binding to the intermediate Lipid II, 49 actinomycete strains were identified by HR-LCMS as producers of ramoplanin-related compounds. The producing strains were isolated from environmental samples collected worldwide comprising both tropical and temperate areas. To assess the diversity of this microbial population, the 49 isolates were initially identified to the genus level on the basis of their micromorphology, and 16S sequencing confirmed the initial identification of the strains. These analyses resulted in the identification of members of genus Streptomyces, as well as representatives of the families Micromonosporaceae, Nocardiaceae, Thermomonosporaceae, and Pseudonocardiaceae, suggesting that the production of ramoplanins is relatively widespread among Actinomycetes. In addition, all of these isolates were tested against a panel of Gram-positive and Gram-negative bacteria, filamentous fungi, and yeast in order to further characterize their antimicrobial properties. This

  18. ISOLATION AND ANTIMICROBIAL AND DEGRADATIVE POTENTIAL OF ACTINOMYCETES

    Directory of Open Access Journals (Sweden)

    Padma Singh* and Vani Sharma

    2013-02-01

    Full Text Available Problem Statement: Does the soil Actinomycetes have Antimicrobial and Petrol degradation potential? It is an intriguing question. Actinomycetes are continues to be a subject of study with reference to their Antimicrobial and degradative potential. However studies have been done is limited. Our object was to study its Antimicrobial activity in wide spectrum and to study its degradation potential on Petrol. Approach: In this study we have isolated total 5 Actinomycetes from the Ganga river bed. All the isolates later purified and identified by various Morphological and Biochemical test. Here Nocardia was subjected to antimicrobial test against Streptococcus, Mucor and Aspergillus and it was also subjected to degradation test against Petrol. Result: The 5 isolates are Streptomyces, Micromonospora, Micromono sporangium and 2 different strain of Nocardia (Na1 and Na2. The 2 strains of Nocardia are active against Streptococcus (Na1 29.6mm, Na2 26.6mm, Mucor (Na1 12.5mm, Na2 22.5mm and Aspergillus (Na1 50%, Na2 60%. They also degrade Petrol very effectively, decrease in total organic carbon of the medium was observed during the degradation of petrol. Conclusion: Our observation provides us with evidence that these agents can be used for the production of new antibiotics and as the agent to control the environment pollution.

  19. [Isolation and antimicrobial activities of actinomycetes from vermicompost].

    Science.gov (United States)

    Wang, Xue-jun; Yan, Shuang-lin; Min, Chang-li; Yang, Yan

    2015-02-01

    In this paper, actinomycetes were isolated from vermicompost by tablet coating method. Antimicrobial activities of actinomycetes were measured by the agar block method. Strains with high activity were identified based on morphology and biochemical characteristics, as well as 16S rDNA gene sequence analysis. The results showed that 26 strains of actinomycetes were isolated, 16 of them had antimicrobial activities to the test strains which accounts for 61.54% of all strains. Among the 16 strains, the strain QYF12 and QYF22 had higher antimicrobial activity to Micrococcus luteus, with a formed inhibition zone of 27 mm and 31 mm, respectively. While the strain QYF26 had higher antimicrobial activity to Bacillus subtilis, and the inhibition zone diameter was 21 mm. Based on the identification of strains with high activity, the strain QYF12 was identified as Streptomyces chartreusis, the strain QYF22 was S. ossamyceticus and the strain QYF26 was S. gancidicus. This study provided a theoretical basis for further separate antibacterial product used for biological control.

  20. CRISPR-Cas9 Based Engineering of Actinomycetal Genomes.

    Science.gov (United States)

    Tong, Yaojun; Charusanti, Pep; Zhang, Lixin; Weber, Tilmann; Lee, Sang Yup

    2015-09-18

    Bacteria of the order Actinomycetales are one of the most important sources of pharmacologically active and industrially relevant secondary metabolites. Unfortunately, many of them are still recalcitrant to genetic manipulation, which is a bottleneck for systematic metabolic engineering. To facilitate the genetic manipulation of actinomycetes, we developed a highly efficient CRISPR-Cas9 system to delete gene(s) or gene cluster(s), implement precise gene replacements, and reversibly control gene expression in actinomycetes. We demonstrate our system by targeting two genes, actIORF1 (SCO5087) and actVB (SCO5092), from the actinorhodin biosynthetic gene cluster in Streptomyces coelicolor A3(2). Our CRISPR-Cas9 system successfully inactivated the targeted genes. When no templates for homology-directed repair (HDR) were present, the site-specific DNA double-strand breaks (DSBs) introduced by Cas9 were repaired through the error-prone nonhomologous end joining (NHEJ) pathway, resulting in a library of deletions with variable sizes around the targeted sequence. If templates for HDR were provided at the same time, precise deletions of the targeted gene were observed with near 100% frequency. Moreover, we developed a system to efficiently and reversibly control expression of target genes, deemed CRISPRi, based on a catalytically dead variant of Cas9 (dCas9). The CRISPR-Cas9 based system described here comprises a powerful and broadly applicable set of tools to manipulate actinomycetal genomes.

  1. Functional analysis of the murine T lymphocyte immune response to a protozoan parasite, Leishmania tropica

    Directory of Open Access Journals (Sweden)

    H. D. Engers

    1983-03-01

    Full Text Available The results presented in this review summarize a seirs of experiments designed to characterize the murine T cell imune response to the protozoan parasite Leishmania tropica. Enriched T cell populations and T cell clones specific for L. tropica antigens were derived from lymph nodes of primed mice and maintained in continous culture in vitro. These T lymphocytes were shown (A to express the Lyt 1+ 3- cell surface phenotype, (B to proliferate specifically in vitro in response to parasite antigens, together with a source of irradiated syngeneic macrophages, (C to transfer antigen-specific delayed-type hypersensitivity (DTH responses to normal syngeneic mice, (D to induce specific activation of parasitized macrophages in vitro resulting in the destruction of intracellular parasites, (E to provide specific helper activity for antibody responses in vitro in a hapten-carrier system. Protection studies using these defiened T cell populations should allow the characterization of parasite antigen(s implicated in the induction of cellular immune responses beneficial for the host.Os resultados apresentados nesta revisão, sumariam uma série de experimentos planejados no sentido de caracterizar a resposta imune de linfócitos T de camundongos, para o protozoário parasita Leishmania tropica. Populações enriquecidas de linfócitos T e clones de linfócitos T específicos para antígenos de L. tropica foram derivados de gânglios linfáticos de camundongos primados e a seguir mantidos em cultura contínua in vivo. Ficou demonstrado que estes linfócitos T eram capazes de: A Expressar o fenótipo de superfície celular Lyt 1+ 2-, B Proliferar en vitro especificamente em resposta aos antígenos parasitários quando em presença de macrófagos singênicos irradiados, C Transferir uma resposta tipo hipersensibilidade retardada antiígeno especifico à camundongos normais singênicos, D Induzir ativação específica de macrófagos parasitizados in vitro

  2. Prevalence of Leishmania tropica in school boys of khyber agency, FATA near Pak-Afghan border.

    Science.gov (United States)

    Qureshi, Naveeda Akhtar; Ali, Abid; Rashid, Umer; Tayyab-Ur-Rehman; Ali, Naeem

    2016-12-01

    In Pakistan leishmaniasis occurs periodically throughout the year and various out breaks are reported frequently. In continuation of our research on this neglected disease, the aim of present study is to explore: (1) the prevalence of cutaneous leishmaniasis in school boys; (2) Leishmania species identification in order to epidemiology and dynamics of the disease; (3) Identification of risk factors for Leishmaniasis especially for CL. The data was collected in August 2014 The experimental strategy involved a questionnaire for data collection and along with clinical diagnosis of 134 out of 9368 students for incidence of Leishmania spp. in 7 square kilometres area in the schoolboys at Tehsil Landi Kotal, District Khyber Agency, FATA Pakistan. The parasitological and molecular diagnosis of clinically suspected cutaneous leishmaniasis cases were performed using microscopical examination of Giemsa-stained smears of lesion exudates and minicircle kDNA semi nested PCR, respectively. Microscopy (x=1000) positive cases were 84/134 (62.6%) and 50/134 (37.4%) slides did not showed any presence of amastigotes of Leishmania spp. The samples were amplified using kDNA semi nested PCR and confirmed the presence of L. Tropica (Ac.no KT 985473). PCR positive cases were 97/134 (72.4%) and 37(27.6%) were negative. The prevalence of L. tropica in school boys was 1.4% (134/9368) in the total population studied (n=9368). The parasite prevalence might be greater as only male students were considered in the study due to ethical and social issues and limitations.

  3. Detection of Leishmania major and Leishmania tropica in domestic cats in the Ege Region of Turkey.

    Science.gov (United States)

    Paşa, Serdar; Tetik Vardarlı, Aslı; Erol, Nural; Karakuş, Mehmet; Töz, Seray; Atasoy, Abidin; Balcıoğlu, İ Cüneyt; Emek Tuna, Gülten; Ermiş, Özge V; Ertabaklar, Hatice; Özbel, Yusuf

    2015-09-15

    Leishmaniosis is a group of diseases caused by different species of Leishmania parasites in mammalian species. The aim of the present study was to investigate the presence of Leishmania spp. DNA in cats using real time polymerase chain reaction (RT-PCR) assays targeting internal transcribed spacer (ITS1) and heat-shock protein 70 gene (Hsp70) regions with Leishmania species-specific primers and probes. Blood samples were collected from 147 cats (73 female; 74 male) in the endemic regions for zoonotic visceral leishmaniasis in the western provinces of Turkey and analyzed using two RT-PCR assays. Additionally, Hsp70 RT-PCR products were sequenced. ELISA assays for feline immunodeficiency virus (FIV) and feline leukemia virus (FeLV) were also carried out for 145 of the 147 samples. Overall, 13/147 (8.84%) cats were positive for Leishmania by RT-PCR (4 L. major and 9 L. tropica). FIV and FeLV antibody and/or antigen was detected in 4 and 5 cats among Leishmania DNA positives, respectively. To the best of our knowledge, this study is the first to investigate and report the presence of L. major and L. tropica infections in a large group of domestic cats in Turkey. The results obtained indicate that species identification of Leishmania is essential for epidemiological understanding and that clinical signs alone are not indicative for leishmaniosis in cats, as it is in dogs. This study suggests that extensive research should be carried out in cat populations in order to fully understand the role of cats in the epidemiology of the disease.

  4. Structural characterization of an acidic exoheteropolysaccharide produced by the nitrogen-fixing bacterium Burkholderia tropica.

    Science.gov (United States)

    Serrato, Rodrigo V; Sassaki, Guilherme L; Gorin, Philip A J; Cruz, Leonardo M; Pedrosa, Fábio O; Choudhury, Biswa; Carlson, Russell W; Iacomini, Marcello

    2008-09-05

    An acidic exopolysaccharide (EPS) produced by the diazotrophic bacterium Burkholderia tropica, strain Ppe8, was isolated from the culture supernatant of bacteria grown in a synthetic liquid medium containing mannitol and glutamate. Monosaccharide composition showed Rha, Glc and GlcA in a 2.0:2.0:1.0 molar ratio, respectively. Further structural characterization was performed by a combination of NMR, mass spectrometry and chemical methods. Partial acid hydrolysis of EPS provided a mixture of acidic oligosaccharides that were characterized by ESI-MS, giving rise to ions with m/z 193 (GlcA-H)(-), 339 (GlcA,Rha-H)(-), 501 (GlcA,Rha,Glc-H)(-), 647 (GlcA,Rha2,Glc,-H)(-), 809 (GlcA,Rha2,Glc2,-H)(-) and 851 (GlcA,Rha2,Glc2,OAc-H)(-). Carboxyreduced EPS (EPS-CR) had Glc and Rha in a 3:2 ratio, present as d- and l-enantiomers, respectively. Methylation and NMR analysis of EPS and EPS-CR showed a main chain containing 2,4-di-O-Rhap, 3-O-Rhap and 4-O-Glcp. A GlcA side chain unit was found in the acidic EPS, substituting O-4 of α-l-Rhap units. This was observed as a non-reducing end unit of glucopyranose in the EPS-CR. Acetyl esters occured at O-2 of β-l-Rhap units. From the combined results herein, we determined the structure of the exocellular polysaccharide produced by B. tropica, Ppe8, as being a pentasaccharide repeating unit as shown.

  5. Airway inflammation among compost workers exposed to actinomycetes spores

    Directory of Open Access Journals (Sweden)

    Kari Kulvik Heldal

    2015-05-01

    Full Text Available Objectives. To study the associations between exposure to bioaerosols and work-related symptoms, lung function and biomarkers of airway inflammation in compost workers. Materials and method. Personal full-shift exposure measurements were performed on 47 workers employed at five windrow plants (n=20 and five reactor plants (n=27. Samples were analyzed for endotoxins, bacteria, fungal and actinomycetes spores. Health examinations were performed on workers and 37 controls before and after work on the day exposure was measured. The examinations included symptoms recorded by questionnaire, lung function by spirometry and nasal dimensions by acoustic rhinometry (AR. The pneumoproteins CC16, SP-D and SP-A were measured in a blood sample drawn at the end of the day. Results. The levels of endotoxins (median 3 EU/m[sup]3[/sup] , range 0–730 EU/m[sup]3[/sup] and actinomycetes spores (median 0.2 × 10[sup]6[/sup] spores/m[sup]3[/sup] , range 0–590 × 10[sup]6[/sup] spores/m[sup]3[/sup] were significantly higher in reactor plants compared to windrow plants. However, windrow composting workers reported more symptoms than reactor composting workers, probably due to use of respiratory protection. Exposure-response relationships between actinomycetes spores exposure and respiratory effects, found as cough and nose irritation during a shift, was significantly increased (OR 4.3, 95% CI 1.1–16, OR 6.1, 95% CI 1.5–25, respectively, p<0.05 among workers exposed to 0.02–0.3 × 10[sup]6[/sup] actinomycetes spores/m 3 , and FEV1/FVC% decreased cross shift (b=–3.2, SE=1.5%, p<0.01. Effects were weaker in the highest exposed group, but these workers used respiratory protection, frequently limiting their actual exposure. No relationships were found between exposure and pneumoprotein concentrations. Conclusions. The major agent in the aerosol generated at compost plants was actinomycetes spores which was associated with work related cough symptoms and work

  6. The effect of verapamil on in vitro susceptibility of promastigote and amastigote stages of Leishmania tropica to meglumine antimoniate.

    Science.gov (United States)

    Shokri, Azar; Sharifi, Iraj; Khamesipour, Ali; Nakhaee, Nozar; Fasihi Harandi, Majid; Nosratabadi, Jafar; Hakimi Parizi, Maryam; Barati, Mohammad

    2012-03-01

    Pentavalent antimonials are the standard treatment for cutaneous leishmaniasis (CL) with low efficacy and resistance is emerging. CL is increased significantly in respect to incidence rate and expanding to new foci. In the present study, the effect of verapamil on in vitro susceptibility of promastigote and amastigote stages of Leishmania tropica to meglumine antimoniate (MA, Glucantime) was evaluated using colorimetric assay (MTT) and in a macrophage model, respectively. Verapamil, as a calcium channel blocker, affects drug uptake by preventing of drug efflux from the cells. In promastigote form, several concentrations of MA with or without verapamil showed significant decrease (P tropica to MA. Further works are required to evaluate this synergistic effect on animal model or volunteer human subjects.

  7. Comparative proteomics study on meglumine antimoniate sensitive and resistant Leishmania tropica isolated from Iranian anthroponotic cutaneous leishmaniasis patients.

    Science.gov (United States)

    Hajjaran, H; Azarian, B; Mohebali, M; Hadighi, R; Assareh, A; Vaziri, B

    2012-02-01

    In order to define the protein expressional changes related to the process of meglumine antimoniate resistance in anthroponotic cutaneous leishmaniasis (CL), we performed a comparative proteomics analysis on sensitive and resistant strains of Leishmania tropica isolated from Iranian CL patients. Cell proteins were analysed with 2-dimensional electrophoresis and differentially expressed proteins were identified by matrix-assisted laser desorption/ ionization time-of-flight mass spectrometry. Image analysis of the matched maps identified 7 proteins that were either over- or down-expressed: activated protein kinase c receptor(LACK), alpha tubulin (x2), prostaglandin f2-alpha synthase, protein disulfide isomerase, vesicular transport protein and a hypothetical protein. The study shows the usefulness of proteomics in identifying proteins that may express differences between sensitive and resistant L. tropica isolates.

  8. Evaluation of antileishmanial activity and cytotoxicity of the extracts of Berberis vulgaris and Nigella sativa against Leishmania tropica

    Directory of Open Access Journals (Sweden)

    Hossein Mahmoudvand

    2014-12-01

    Full Text Available Background & objectives: Leishmaniasis is a major public health problem, and the alarming spread of parasite resistance underlines the importance of discovering new therapeutic products. The present study aims to investigate the in vitro antileishmanial activity and cytotoxicity of the ethanolic extract of Berberis vulgaris fruits and chloroform extract of Nigella sativa seeds against Leishmania tropica. Methods: In this study, antileishmanial activity of B. vulgaris and N. sativa extracts on promastigote and amastigote stages of L. tropica in comparison to meglumine antimoniate (MA was evaluated, using MTT assay and macrophage model, respectively. MTT test was also used to assess the cytotoxicity of extracts on murine macrophages. The significance of differences was determined by analysis of variances (ANOVA and student’s t-test using SPSS software. Results: The results showed that ethanolic extract of B. vulgaris (IC50 4.83 μg/ml and chloroform extract of N. sativa (IC50 7.83 μg/ml significantly reduced the viability of promastigotes of L. tropica in comparison to MA (IC50 11.26 μg/ml. Furthermore, extracts of B. vulgaris (IC50 24.03 μg/ml and N. sativa (IC50 30.21 μg/ml significantly decreased the growth rate of amastigotes in each macrophage as compared with positive control (p <0.05. Our findings also revealed that extracts of B. vulgaris and N. sativa had no significant cytotoxicity against murine macrophages. Conclusion: The B. vulgaris and N. sativa extracts exhibited an effective leishmanicidal activity against L. tropica on in vitro model. Further, works are required to evaluate the exact effect of these extracts on Leishmania species using a clinical setting.

  9. Overexpression of ubiquitin and amino acid permease genes in association with antimony resistance in Leishmania tropica field isolates.

    Science.gov (United States)

    Kazemi-Rad, Elham; Mohebali, Mehdi; Khadem-Erfan, Mohammad Bagher; Hajjaran, Homa; Hadighi, Ramtin; Khamesipour, Ali; Rezaie, Sassan; Saffari, Mojtaba; Raoofian, Reza; Heidari, Mansour

    2013-08-01

    The mainstay therapy against leishmaniasis is still pentavalent antimonial drugs; however, the rate of antimony resistance is increasing in endemic regions such as Iran. Understanding the molecular basis of resistance to antimonials could be helpful to improve treatment strategies. This study aimed to recognize genes involved in antimony resistance of Leishmania tropica field isolates. Sensitive and resistant L. tropica parasites were isolated from anthroponotic cutaneous leishmaniasis patients and drug susceptibility of parasites to meglumine antimoniate (Glucantime®) was confirmed using in vitro assay. Then, complementary DNA-amplified fragment length polymorphism (cDNA-AFLP) and real-time reverse transcriptase-PCR (RT-PCR) approaches were utilized on mRNAs from resistant and sensitive L. tropica isolates. We identified 2 known genes, ubiquitin implicated in protein degradation and amino acid permease (AAP3) involved in arginine uptake. Also, we identified 1 gene encoding hypothetical protein. Real-time RT-PCR revealed a significant upregulation of ubiquitin (2.54-fold), and AAP3 (2.86-fold) (P<0.05) in a resistant isolate compared to a sensitive one. Our results suggest that overexpression of ubiquitin and AAP3 could potentially implicated in natural antimony resistance.

  10. Silica nanowire conjugated with loop-shaped oligonucleotides: A new structure to silence cysteine proteinase gene in Leishmania tropica.

    Science.gov (United States)

    Bafghi, Ali Fatahi; Jebali, Ali; Daliri, Karim

    2015-12-01

    The main aim of this study was to evaluate the capability of silica nanowire conjugated with loop-shaped oligonucleotides (SNWCLSOs) to silence cysteine proteinase b (Cpb) gene in Leishmania (L) tropica. On the other hand, its toxicity on amastigotes and mouse peritoneal macrophages was evaluated by 5-diphenyl-tetrazolium bromide (MTT) assay. For control, two loop-shaped oligonucleotides (LSO) were considered. LSO1 and LSO2 were 5'-NH2-cccccaaaaaaaaaaaaaaaaaaaaaaaaaggggg-COOH-3' and LSO2: 5'-NH2-cccccttttttttttttttttttttttttttttttttttttttggggg-COOH-3', respectively. After 72 h incubation at 37 °C, AMSNW, LSO1, and LSO2 had no remarkable toxicity on L. tropica amastigote (2 × 10(5)/mL) and mouse peritoneal macrophages (2 × 10(5)/mL). In case of SNWCLSOs, they had high toxicity on L. tropica amastigote, but they had no effect on mouse peritoneal macrophages. At concentrations of 1, 10, and 25 μg/mL, AMSNW, LSO1 and LSO2 had no effect on the gene expression. But, at concentration of 50 and 100 μg/mL, decrease of gene expression was observed. In case of SNWCLSOs, they could dramatically decrease the gene expression. It could be concluded that since SNWCLSOs could silence Cpb gene with no remarkable toxicity, they are good choice for treat cutaneous leishmaniasis in future. As a new agent, it must be checked in vivo.

  11. Inhibition by Dications of in vitro growth of Leishmania major and Leishmania tropica: causative agents of old world cutaneous leishmaniasis.

    Science.gov (United States)

    Rosypal, Alexa C; Werbovetz, Karl A; Salem, Manar; Stephens, Chad E; Kumar, Arvind; Boykin, David W; Hall, James E; Tidwell, Richard R

    2008-06-01

    Old World cutaneous leishmaniasis is caused by infection with Leishmania major and Leishmania tropica. Pentamidine and related dications exhibit broad spectrum antiprotozoal activity. Based on the previously reported efficacy of these compounds against related organisms, 18 structural analogs of pentamidine were evaluated for in vitro antileishmanial activity, using pentamidine as the standard reference drug for comparison. Furan analogs and reversed amidine compounds were examined for activity against L. major and L. tropica promastigotes. The most active compounds against both Leishmania species were in the reversed amidine series. DB745 and DB746 exhibited the highest activity against L. major and DB745 was the most active compound against L. tropica. Both of these compounds exhibited 50% inhibitory concentrations (IC50) below 1 nM for L. major. Ten reversed amidines were also tested for their ability to inhibit growth in an axenic amastigote model. Nine of 10 reversed amidine analogs were active at concentrations below 1 nM. These results justify further study of dicationic compounds as potential new agents for treating cutaneous leishmaniasis.

  12. Identification of volatile compounds produced by the bacterium Burkholderia tropica that inhibit the growth of fungal pathogens

    Science.gov (United States)

    Tenorio-Salgado, Silvia; Tinoco, Raunel; Vazquez-Duhalt, Rafael; Caballero-Mellado, Jesus; Perez-Rueda, Ernesto

    2013-01-01

    It has been documented that bacteria from the Burkholderia genera produce different kinds of compounds that inhibit plant pathogens, however in Burkholderia tropica, an endophytic diazotrophic and phosphate-solubilizing bacterium isolated from a wide diversity of plants, the capacity to produce antifungal compounds has not been evaluated. In order to expand our knowledge about Burkholderia tropica as a potential biological control agent, we analyzed 15 different strains of this bacterium to evaluate their capacities to inhibit the growth of four phytopathogenic fungi, Colletotrichum gloeosporioides, Fusarium culmorum, Fusarium oxysporum and Sclerotium rolffsi. Diverse analytical techniques, including plant root protection and dish plate growth assays and gas chromatography-mass spectroscopy showed that the fungal growth inhibition was intimately associated with the volatile compounds produced by B. tropica and, in particular, two bacterial strains (MTo293 and TTe203) exhibited the highest radial mycelial growth inhibition. Morphological changes associated with these compounds, such as disruption of fungal hyphae, were identified by using photomicrographic analysis. By using gas chromatography-mass spectroscopy technique, 18 volatile compounds involved in the growth inhibition mechanism were identified, including α-pinene and limonene. In addition, we found a high proportion of bacterial strains that produced siderophores during growth with different carbon sources, such as alanine and glutamic acid; however, their roles in the antagonism mechanism remain unclear. PMID:23680857

  13. Increased prevalence of human cutaneous leishmaniasis in Israel and the Palestinian Authority caused by the recent emergence of a population of genetically similar strains of Leishmania tropica.

    Science.gov (United States)

    Azmi, Kifaya; Krayter, Lena; Nasereddin, Abedelmajeed; Ereqat, Suheir; Schnur, Lionel F; Al-Jawabreh, Amer; Abdeen, Ziad; Schönian, Gabriele

    2016-08-04

    Twelve unlinked microsatellite markers were used to determine the microsatellite profiles of 50 newly and 46 previously typed strains of L. tropica from various Israeli and Palestinian foci. Their microsatellite profiles were compared to those of 99 previously typed strains of L. tropica from 15 countries. Israeli and Palestinian strains of L. tropica fell into three different groups, one of which contained 75 of the 96 Israeli and Palestinian strains. This population separated from all the others at the first hierarchical level by Bayesian statistics and formed a distinct monophyletic group on applying genetic distance and allele frequency analyses. The second cluster contained ten Israeli strains from a specific focus north of the Sea of Galilee, which were previously shown to differ from all other strains of L. tropica in their serological, biochemical and molecular biological parameters. This cluster was closely related to clusters comprising strains of L. tropica from Africa. Four Israeli and five Palestinian strains fell into different genetic entities mostly related to strains from Asian foci of CL. Importation during numerous migrations of humans and, perhaps, infected reservoir animals in the past and, now, through modern travel is the most likely explanation for the existence of so many locally encountered genetic variants of L. tropica in the Israeli-Palestinian region. Geographical and ecological variation may play a role in expanding the genetic heterogeneity once given importations had become established in different foci. Currently, one population is expanding in the area comprising almost all of the Palestinian and Israeli strains of L. tropica isolated since 1996 and investigated in this study, which differ clearly from all other strains of whatsoever origin. This population seems to result from the re-emergence of a previously existing genotype owing to environmental changes and human activities.

  14. [Date palm and fusariosis. VIII.--Parasitism of "Fusarium oxysporum" f. sp. "albedinis" by an actinomycete (author's transl)].

    Science.gov (United States)

    Sabaou, N; Bennaceur, M; Bounaga, D

    1981-01-01

    Fortuitous growth of an actinomycete on Fusarium oxysporum f. sp. albedinis culture has shown a host-parasite process. As a response to the actinomycete, the fungus produces thallospores with various forms which can germinate faster than the non-parasited F. o. albedinis microconidies. However, the strains obtained from thallospores showed as sensible as the mother strain towards actinomycete action.

  15. In Vitro Investigation of Antifungal Activities of Actinomycetes against Microsporum gypseum

    Directory of Open Access Journals (Sweden)

    Naser Keikha

    2013-02-01

    Conclusion: The findings of the present research show that terrigenous actinomycetes have an antifungal effect upon Microsporum gypseum. So, one hopes that-in future-rather than administering antifungal chemicals that have side-effects, dermatophytic infections can be cured by applying these actinomycetes.

  16. Antiviral property of marine actinomycetes against white spot syndrome virus in penaeid shrimps

    Digital Repository Service at National Institute of Oceanography (India)

    Kumar, S.S.; Philip, R.; Achuthankutty, C.T.

    and are continually being screened for new compounds. In this communication, the results of a study made to determine the effectiveness of marine actinomycetes against the white spot disease in penaeid shrimps are presented. Twenty-five isolates of actinomycetes were...

  17. Actinomycete integrative and conjugative pMEA-like elements of Amycolatopsis and Saccharopolyspora decoded

    NARCIS (Netherlands)

    Poele, Evelien M. Te; Samborskyy, Markiyan; Oliynyk, Markiyan; Leadlay, Peter F.; Bolhuis, Henk; Dijkhuizen, Lubbert

    2008-01-01

    Actinomycete integrative and conjugative elements (AICEs) are present in diverse genera of the actinomycetes, the most important bacterial producers of bioactive secondary metabolites. Comparison of pMEA100 of Amycolatopsis mediterranei, pMEA300 of Amycolatopsis methanolica and pSE211 of Saccharopol

  18. New Benzoxazine Secondary Metabolites from an Arctic Actinomycete

    OpenAIRE

    Kyuho Moon; Chan-Hong Ahn; Yoonho Shin; Tae Hyung Won; Keebeom Ko; Sang Kook Lee; Ki-Bong Oh; Jongheon Shin; Seung-Il Nam; Dong-Chan Oh

    2014-01-01

    Two new secondary metabolites, arcticoside (1) and C-1027 chromophore-V (2), were isolated along with C-1027 chromophore-III and fijiolides A and B (3–5) from a culture of an Arctic marine actinomycete Streptomyces strain. The chemical structures of 1 and 2 were elucidated through NMR, mass, UV, and IR spectroscopy. The hexose moieties in 1 were determined to be d-glucose from a combination of acid hydrolysis, derivatization, and gas chromatographic analyses. Arcticoside (1) and C-1027 chromo...

  19. The associations of Leishmania major and Leishmania tropica aspects by focusing their morphological and molecular features on clinical appearances in Khuzestan Province, Iran.

    Science.gov (United States)

    Spotin, Adel; Rouhani, Soheila; Parvizi, Parviz

    2014-01-01

    Cutaneous leishmaniasis has various phenotypic aspects consisting of polymorphic amastigotes with different genetic ranges. Samples were collected from suspected patients of Khuzestan province. Prepared smears were stained, scaled, and measured using ocular micrometer. The Cyt b, ITS-rDNA, and microsatellite genes of Leishmania were amplified and Leishmania species were identified by molecular analyses. Of 150 examined suspected patients, 102 were identified to Leishmania species (90 L. major, nine L. tropica, and three unidentified). The amastigotes of 90 L. major had regular and different irregular shapes within three clinical lesions with no and/or low genetic diversity. Three haplotypes of Cyt b of L. major were found but no variation was observed using ITS-rDNA gene. Interesting findings were that all nine L. tropica had regular amastigote shapes with more genetic variations, also a patient which had coinfection of L. major, L. tropica, and Crithidia. At least two L. major and L. tropica were identified in suspected patients of the regions. Different irregular amastigotes' shapes of L. major can be explained by various reservoir hosts and vectors. In contrast, more molecular variations in L. tropica could be justified by genetic characters. Unidentified Leishmania could be mixed pathogens or nonpathogens with mammals' Leishmania or Crithidia.

  20. Therapeutic Potential of Biologically Reduced Silver Nanoparticles from Actinomycete Cultures

    Directory of Open Access Journals (Sweden)

    M. K. Sukanya

    2013-01-01

    Full Text Available Silver nanoparticles are applied in nanomedicine from time immemorial and are still used as powerful antibiotic and anti-inflammatory agents. Antibiotics produced by actinomycetes are popular in almost all the therapeutic measures, and this study has proven that these microbes are also helpful in the biosynthesis of silver nanoparticles with good surface and size characteristics. Silver can be synthesized by various chemical methodologies, and most of them have turned to be toxic. This study has been successful in isolating the microbes from polluted environment, and subjecting them to the reduction of silver nanoparticles, characterizing the nanoparticles by UV spectrophotometry and transmission electron microscopy. The nanoparticles produced were tested for their antimicrobial property, and the zone of inhibition was greater than those produced by their chemically synthesized counterparts. Actinomycetes, helpful in bioremediating heavy metals, are useful for the production of metallic nanoparticles. The biosynthesized silver nanoparticles loaded with antibiotics prove to be better in killing the pathogens and have opened up new areas for developing nanobiotechnological research based on microbial applications.

  1. Diversity and Antagonistic Activity of Actinomycete Strains From Myristica Swamp Soils Against Human Pathogens

    Directory of Open Access Journals (Sweden)

    Varghese Rlnoy

    2014-05-01

    Full Text Available Under the present investigation Actinomycetes were isolated from the soils of Myristica swamps of southern Western Ghats and the antagonistic activity against different human bacterial pathogens was evaluated. Results of the present study revealed that Actinomycetes population in the soils of Myristica swamp was spatially and seasonally varied. Actinomycetes load was varied from 24×104 to 71×103, from 129×103 to 40×103 and from 31×104 to 84×103 in post monsoon, monsoon and pre monsoon respectively. A total of 23 Actinomycetes strains belonging to six genera were isolated from swamp soils. Identification of the isolates showed that most of the isolates belonged to the genus Streptomyces (11, followed by Nocardia (6, Micromonospora (3, Pseudonocardia (1, Streptosporangium (1, and Nocardiopsis (1. Antagonistic studies revealed that 91.3% of Actinomycete isolates were active against one or more tested pathogens, of that 56.52% exhibited activity against Gram negative and 86.95% showed activity against Gram positive bacteria. 39.13% isolates were active against all the bacterial pathogens selected and its inhibition zone diameter was also high. 69.5% of Actinomycetes were exhibited antibacterial activity against Listeria followed by Bacillus cereus (65.21%, Staphylococcus (60.86%, Vibrio cholera (52.17%, Salmonella (52.17% and E. coli (39.13%. The results indicate that the Myristica swamp soils of Southern Western Ghats might be a remarkable reserve of Actinomycetes with potential antagonistic activity.

  2. Screening of Actinomycete Isolates from Niche Habitats in Manipur for Antibiotic Activity

    Directory of Open Access Journals (Sweden)

    Debananda S. Ningthoujam

    2009-01-01

    Full Text Available Problem statement: The exhaustion of the usual terrestrial sources and the rise of resistant pathogens dictate the search for novel actinomycetes and new antibiotics. In this context, niche habitats such as caves, pristine forests, lakes, rivers, and other wetlands, high salt environments, marine ecosystems and endophytic niches are promising targets for survey of bioactive actinomycetes. Approach: Actinomycetes were isolated from several niche habitats in Manipur, India, on selective media such as SCNA and Chitin agar with or without antibiotics. Selected isolates were subjected to antimicrobial activity screening by Kirby-Bauer method. Results: 172 lake sediment (SCNA, LS1 series, 35 lake sediment (CA, LSCH series, 120 river (NRP, NRB and..series, 39 forest (AML series, 35 cave (KC1 series, 101 salt spring (NH, N3S and .. series, 46 Shirui jungle (SJ series and 66 Shirui hill (SH series actinomycetes isolates were obtained. Of 99 randomly selected isolates screened, 37 had antimicrobial activities against 1 or more indicator strains: 32 against Gram positive bacteria and 8 against Gram negative bacteria; 10 actinomycete strains were antimycotic and 3 had broad-spectrum antibiotic activities. About 18 potent antibacterial, 1 anti pseudomonas, 1 exclusively antifungal and 3 broad-spectrum antimicrobial actinomycetes were chosen for further studies. Conclusion: Niche habitats in Manipur especially wetlands show great promise for discovery of bioactive actinomycetes.

  3. New Dimensions of Research on Actinomycetes: Quest for Next Generation Antibiotics

    Directory of Open Access Journals (Sweden)

    Polpass Arul Jose

    2016-08-01

    Full Text Available Starting with the discovery of streptomycin, the promise of natural products research on actinomycetes has been captivat¬ing researchers and offered an array of life-saving antibiotics. However, most of the actinomycetes have received a little attention of researchers beyond isolation and activity screening. Noticeable gaps in genomic information and associated biosynthetic potential of actinomycetes are mainly the reasons for this situation, which has led to a decline in the discovery rate of novel antibiotics. Recent insights gained from genome mining have revealed a massive existence of previously unrecognized biosynthetic potential in actinomycetes. Successive developments in next-generation sequencing, genome editing, analytical separation and high-resolution spectroscopic methods have reinvigorated interest on such actinomycetes and opened new avenues for the discovery of natural and natural-inspired antibiotics. This article describes the new dimensions that have driven the ongoing resurgence of research on actinomycetes with historical background since the commencement in 1940, for the attention of worldwide researchers. Coupled with increasing advancement in molecular and analytical tools and techniques, the discovery of next-generation antibiotics could be possible by revisiting the untapped potential of actinomycetes from different natural sources.

  4. Anti-leishmanial effect of itraconazole niosome on in vitro susceptibility of Leishmania tropica.

    Science.gov (United States)

    Khazaeli, Payam; Sharifi, Iraj; Talebian, Elham; Heravi, Gioia; Moazeni, Esmaeil; Mostafavi, Mahshid

    2014-07-01

    The novel niosomal system aimed to deliver the active drug entity to the target site. The objective of this study was to prepare and evaluate the effect of itraconazole niosome on the in vitro susceptibility of Leishmania tropica as compared to itraconazole alone or tartar emetic. The overall growth rate of promastigotes treated with various concentrations of itraconazole niosome was significantly lower than that of itraconazole alone (IC₅₀=0.24 μg/ml vs. IC₅₀=0.43 μg/ml, P<0.01). In contrast, the mean multiplication rate of amastigotes inside the macrophages and also the mean number of amastigotes in each macrophage treated with itraconazole niosome (34.9 and 3.0) were significantly lower (P<0.01) than those treated with itraconazole alone (62.0 and 3.8) or tartar emetic (63.9 and 4.2), respectively. These findings indicated that niosomes could be developed as a novel drug delivery for itraconazole in the in vitro model. Further studies are required to evaluate the effect of itraconazole niosome on volunteer human subjects.

  5. Terrestrial actinomycetes from diverse locations of Uttarakhnad, India: Isolation and screening for their antibacterial activity.

    Directory of Open Access Journals (Sweden)

    Vijay Kumar

    2013-09-01

    Full Text Available Uttarakhand region is less explored, but possess a great biodiversity. This diversity can be explored for isolation and characterization of new actinomycetes strains for seeking antimicrobial molecules. It can therefore be predicted that novel bioactive metabolite producing actinomycetes can be discovered to combat multidrug resistant bacterial pathogens.Variations in the viable count of actinomycetes were accessed in different altitudes. Actinomycetes were isolated, indentified and screened for their antibacterial activity.The highest viable counts of actinomycetes were recorded in valleys followed by mid hills and high hills. A total of 512 actinomycetes were isolated which were found to belong the 14 different genera of actinomycetes. Mainly the genus Streptomyces was dominant in all the soil samples. Out of 512 isolates recovered, 23.44% exhibited antibacterial activity against one or more tested bacterial pathogens. Of these 56.67% showed activity against Gram-positive bacteria, 26.67% against Gram-negative bacteria while 16.67% showed broad spectrum activity. Isolate DV1S and GR9a-5 showed highest antibacterial properties against several multi-drug resistant bacterial pathogens and were identified using polyphasic approach. DV1S and GR9a-5 were found to be most closely related with S. massasporeus NBRC 12796(T and Nocardia nova JCM 6044(T respectively.The results of this study strongly support the idea that the viable count of actinomycetes varied greatly with altitude. The actinomycetes species isolated from valleys, mid hills and high hills possess significant capacity to produce compounds which are active against several drug resistant bacterial pathogens.

  6. Phlebotomus sergenti in a cutaneous leishmaniasis focus in Azilal province (High Atlas, Morocco: molecular detection and genotyping of Leishmania tropica, and feeding behavior.

    Directory of Open Access Journals (Sweden)

    Malika Ajaoud

    2015-03-01

    Full Text Available Phlebotomus (Paraphlebotomus sergenti is at least one of the confirmed vectors for the transmission of cutaneous leishmaniasis caused by Leishmania tropica and distributed widely in Morocco. This form of leishmaniasis is considered largely as anthroponotic, although dogs were found infected with Leishmania tropica, suggestive of zoonosis in some rural areas.This survey aimed at (i studying the presence of Leishmania in field caught Phlebotomus sergenti, (ii investigating genetic diversity within Leishmania tropica and (iii identifying the host-blood feeding preferences of Phlebotomus sergenti. A total of 4,407 sand flies were collected in three rural areas of Azilal province, using CDC miniature light traps. Samples collected were found to consist of 13 species: Phlebotomus spp. and 3 Sergentomyia spp. The most abundant species was Phlebotomus sergenti, accounting for 45.75 % of the total. 965 female Phlebotomus sergenti were screened for the presence of Leishmania by ITS1-PCR-RFLP, giving a positive rate of 5.7% (55/965, all being identified as Leishmania tropica. Nucleotide heterogeneity of PCR-amplified ITS1-5.8S rRNA gene-ITS2 was noted. Analyses of 31 sequences obtained segregated them into 16 haplotypes, of which 7 contain superimposed peaks at certain nucleotide positions, suggestive of heterozygosity. Phlebotomus sergenti collected were found to feed on a large variety of vertebrate hosts, as determined by Cytochrome b sequencing of the DNA from the blood meals of 64 engorged females.Our findings supported the notion that Phlebotomus sergenti is the primary vector of Leishmania tropica in this focus, and that the latter is genetically very heterogeneous. Furthermore, our results might be suggestive of a certain level of heterozygosity in Leishmania tropica population. This finding, as well as the feeding of the vectors on different animals are of interest for further investigation.

  7. PCR and Microscopic Identification of Isolated Leishmania tropica from Clinical Samples of Cutaneous Leishmaniasis in Human Population of Kohat Region in Khyber Pakhtunkhwa

    Directory of Open Access Journals (Sweden)

    Nasser M. Abd El-Salam

    2014-01-01

    Full Text Available Leishmania tropica was isolated from the clinical patients of cutaneous leishmaniasis in rural community of Kohat district in Khyber Pakhtunkhwa province and was identified through PCR, microscopy, and culture techniques. A total of 113 samples from the clinical patients were examined through PCR, microscopy, and culture which showed 87.61% (99/113, 53.98% (61/113, and 46.90% (53/113 prevalence. During the study, 186 bp Leishmania tropica was identified through PCR. Thus the sensitivity of PCR is very high as compared to the conventional techniques.

  8. PCR and microscopic identification of isolated Leishmania tropica from clinical samples of cutaneous leishmaniasis in human population of Kohat region in Khyber Pakhtunkhwa.

    Science.gov (United States)

    Abd El-Salam, Nasser M; Ayaz, Sultan; Ullah, Riaz

    2014-01-01

    Leishmania tropica was isolated from the clinical patients of cutaneous leishmaniasis in rural community of Kohat district in Khyber Pakhtunkhwa province and was identified through PCR, microscopy, and culture techniques. A total of 113 samples from the clinical patients were examined through PCR, microscopy, and culture which showed 87.61% (99/113), 53.98% (61/113), and 46.90% (53/113) prevalence. During the study, 186 bp Leishmania tropica was identified through PCR. Thus the sensitivity of PCR is very high as compared to the conventional techniques.

  9. Will the introduction of Leishmania tropica MON-58, in the island of Crete, lead to the settlement and spread of this rare zymodeme?

    Science.gov (United States)

    Ntais, Pantelis; Christodoulou, Vasiliki; Tsirigotakis, Nikolaos; Dokianakis, Emmanouil; Dedet, Jean-Pierre; Pratlong, Francine; Antoniou, Maria

    2014-04-01

    The rare zymodeme, Leishmania tropica MON-58, was isolated from a young Afghan refugee with a facial cutaneous lesion who had come to live in Crete early 2008. The same zymodeme variant was isolated from a local dog that had never travelled outside the island, with symptoms of visceral leishmaniasis, which stayed in the area where the patient worked during the summer months. This is the first record of L. tropica in a host, other than human, in Greece and another example of introduction of a vector borne pathogen in a focus where local vector/s can sustain it, with the risk of initiation of new transmission cycle/s.

  10. Genetic, serological and biochemical characterization of Leishmania tropica from foci in northern Palestine and discovery of zymodeme MON-307

    Directory of Open Access Journals (Sweden)

    Azmi Kifaya

    2012-06-01

    Full Text Available Abstract Background Many cases of cutaneous leishmaniasis (CL have been recorded in the Jenin District based on their clinical appearance. Here, their parasites have been characterized in depth. Methods Leishmanial parasites isolated from 12 human cases of CL from the Jenin District were cultured as promastigotes, whose DNA was extracted. The ITS1 sequence and the 7SL RNA gene were analysed as was the kinetoplast minicircle DNA (kDNA sequence. Excreted factor (EF serotyping and multilocus enzyme electrophoresis (MLEE were also applied. Results This extensive characterization identified the strains as Leishmania tropica of two very distinct sub-types that parallel the two sub-groups discerned by multilocus microsatellite typing (MLMT done previously. A high degree of congruity was displayed among the results generated by the different analytical methods that had examined various cellular components and exposed intra-specific heterogeneity among the 12 strains. Three of the ten strains subjected to MLEE constituted a new zymodeme, zymodeme MON-307, and seven belonged to the known zymodeme MON-137. Ten of the 15 enzymes in the profile of zymodeme MON-307 displayed different electrophoretic mobilities compared with the enzyme profile of the zymodeme MON-137. The closest profile to that of zymodeme MON-307 was that of the zymodeme MON-76 known from Syria. Strains of the zymodeme MON-307 were EF sub-serotype A2 and those of the zymodeme MON-137 were either A9 or A9B4. The sub-serotype B4 component appears, so far, to be unique to some strains of L. tropica of zymodeme MON-137. Strains of the zymodeme MON-137 displayed a distinctive fragment of 417 bp that was absent in those of zymodeme MON-307 when their kDNA was digested with the endonuclease RsaI. kDNA-RFLP after digestion with the endonuclease MboI facilitated a further level of differentiation that partially coincided with the geographical distribution of the human cases from which the strains

  11. New Benzoxazine Secondary Metabolites from an Arctic Actinomycete

    Directory of Open Access Journals (Sweden)

    Kyuho Moon

    2014-04-01

    Full Text Available Two new secondary metabolites, arcticoside (1 and C-1027 chromophore-V (2, were isolated along with C-1027 chromophore-III and fijiolides A and B (3–5 from a culture of an Arctic marine actinomycete Streptomyces strain. The chemical structures of 1 and 2 were elucidated through NMR, mass, UV, and IR spectroscopy. The hexose moieties in 1 were determined to be d-glucose from a combination of acid hydrolysis, derivatization, and gas chromatographic analyses. Arcticoside (1 and C-1027 chromophore-V (2, which have a benzoxazine ring, inhibited Candida albicans isocitrate lyase. Chromophore-V (2 exhibited significant cytotoxicity against breast carcinoma MDA-MB231 cells and colorectal carcinoma cells (line HCT-116, with IC50 values of 0.9 and 2.7 μM, respectively.

  12. New benzoxazine secondary metabolites from an arctic actinomycete.

    Science.gov (United States)

    Moon, Kyuho; Ahn, Chan-Hong; Shin, Yoonho; Won, Tae Hyung; Ko, Keebeom; Lee, Sang Kook; Oh, Ki-Bong; Shin, Jongheon; Nam, Seung-Il; Oh, Dong-Chan

    2014-04-30

    Two new secondary metabolites, arcticoside (1) and C-1027 chromophore-V (2), were isolated along with C-1027 chromophore-III and fijiolides A and B (3-5) from a culture of an Arctic marine actinomycete Streptomyces strain. The chemical structures of 1 and 2 were elucidated through NMR, mass, UV, and IR spectroscopy. The hexose moieties in 1 were determined to be d-glucose from a combination of acid hydrolysis, derivatization, and gas chromatographic analyses. Arcticoside (1) and C-1027 chromophore-V (2), which have a benzoxazine ring, inhibited Candida albicans isocitrate lyase. Chromophore-V (2) exhibited significant cytotoxicity against breast carcinoma MDA-MB231 cells and colorectal carcinoma cells (line HCT-116), with IC₅₀ values of 0.9 and 2.7 μM, respectively.

  13. Actinomycetes inhibit filamentous fungi from the cuticle of Acromyrmex leafcutter ants.

    Science.gov (United States)

    Dângelo, Rômulo Augusto Cotta; de Souza, Danival José; Mendes, Thais Demarchi; Couceiro, Joel da Cruz; Lucia, Terezinha Maria Castro Della

    2016-03-01

    Actinomycetes bacteria associated with leafcutter ants produce secondary metabolites with antimicrobial properties against Escovopsis, a fungus specialized in attacking the gardens of fungus-growing ants, which denies the ants their food source. Because previous studies have used fungi isolated from fungus gardens but not from ant integument, the aims of the present study were to isolate actinomycetes associated with the cuticle of the Acromyrmex spp. and to quantify their inhibition abilities against the filamentous fungal species carried by these ants. The results demonstrated that actinomycetes had varied strain-dependent effects on several filamentous fungal species in addition to antagonistic activity against Escovopsis. The strain isolated from Acromyrmex balzani was identified as a Streptomyces species, whereas the remaining isolates were identified as different strains belonging to the genus Pseudonocardia. These findings corroborate the hypothesis that actinomycetes do not act specifically against Escovopsis mycoparasites and may have the ability to inhibit other species of pathogenic fungi.

  14. Mutational analysis of primary alcohol metabolism in the methylotrophic actinomycete Amycolatopsis methanolica

    NARCIS (Netherlands)

    Hektor, Harm J.; Dijkhuizen, Lubbert

    1996-01-01

    Mutants of the methylotrophic actinomycete Amycolatopsis methanolica unable to grow on methanol as carbon source were isolated and characterized. Mutants specifically affected in methanol utilization were deficient in formaldehyde assimilation. Mutants blocked in the first step of primary alcohol ox

  15. Isolation and identification of actinomycetes from a compost-amended soil with potential as biocontrol agents.

    Science.gov (United States)

    Cuesta, Gonzalo; García-de-la-Fuente, Rosana; Abad, Manuel; Fornes, Fernando

    2012-03-01

    The search for new biocontrol strategies to inhibit the growth of phytopathogenic microorganisms has become widely widespread due to environmental concerns. Among actinomycetes, Streptomyces species have been extensively studied since they have been recognized as important sources of antibiotics. Actinomycete strains were isolated from a calcareous soil, 2 two-phase olive mill waste ('alperujo') composts, and the compost-amended soil by using selective media, and they were then co-cultured with 5 phytopathogenic fungi and 1 bacterium to perform an in vitro antagonism assay. Forty-nine actinomycete strains were isolated, 12 of them showing a great antagonistic activity towards the phytopathogenic microorganisms tested. Isolated strains were identified by 16S rDNA sequence analysis and phenotypic procedures. Eleven isolates concerned the genus Streptomyces and 1 actinomycete with chitinolytic activity belonged to the genus Lechevalieria.

  16. Detection of Leishmania donovani and L. tropica in Ethiopian wild rodents.

    Science.gov (United States)

    Kassahun, Aysheshm; Sadlova, Jovana; Dvorak, Vit; Kostalova, Tatiana; Rohousova, Iva; Frynta, Daniel; Aghova, Tatiana; Yasur-Landau, Daniel; Lemma, Wessenseged; Hailu, Asrat; Baneth, Gad; Warburg, Alon; Volf, Petr; Votypka, Jan

    2015-05-01

    Human visceral (VL, also known as Kala-azar) and cutaneous (CL) leishmaniasis are important infectious diseases affecting countries in East Africa that remain endemic in several regions of Ethiopia. The transmission and epidemiology of the disease is complicated due to the complex life cycle of the parasites and the involvement of various Leishmania spp., sand fly vectors, and reservoir animals besides human hosts. Particularly in East Africa, the role of animals as reservoirs for human VL remains unclear. Isolation of Leishmania donovani parasites from naturally infected rodents has been reported in several endemic countries; however, the status of rodents as reservoirs in Ethiopia remains unclear. Here, we demonstrated natural Leishmania infections in rodents. Animals were trapped in 41 localities of endemic and non-endemic areas in eight geographical regions of Ethiopia and DNA was isolated from spleens of 586 rodents belonging to 21 genera and 38 species. Leishmania infection was evaluated by real-time PCR of kinetoplast (k)DNA and confirmed by sequencing of the PCR products. Subsequently, parasite species identification was confirmed by PCR and DNA sequencing of the 18S ribosomal RNA internal transcribed spacer one (ITS1) gene. Out of fifty (8.2%) rodent specimens positive for Leishmania kDNA-PCR and sequencing, 10 were subsequently identified by sequencing of the ITS1 showing that five belonged to the L. donovani complex and five to L. tropica. Forty nine kDNA-positive rodents were found in the endemic localities of southern and eastern Ethiopia while only one was identified from northwestern Ethiopia. Moreover, all the ten ITS1-positive rodents were captured in areas where human leishmaniasis cases have been reported and potential sand fly vectors occur. Our findings suggest the eco-epidemiological importance of rodents in these foci of leishmaniasis and indicate that rodents are likely to play a role in the transmission of leishmaniasis in Ethiopia

  17. Exploring plant growth-promotion actinomycetes from vermicompost and rhizosphere soil for yield enhancement in chickpea

    Directory of Open Access Journals (Sweden)

    M. Sreevidya

    2016-03-01

    Full Text Available Abstract The main objective of the present study was to isolate and characterize actinomycetes for their plant growth-promotion in chickpea. A total of 89 actinomycetes were screened for their antagonism against fungal pathogens of chickpea by dual culture and metabolite production assays. Four most promising actinomycetes were evaluated for their physiological and plant growth-promotion properties under in vitro and in vivo conditions. All the isolates exhibited good growth at temperatures from 20 °C to 40 °C, pH range of 7–11 and NaCl concentrations up to 8%. These were also found highly tolerant to Bavistin, slightly tolerant to Thiram and Captan (except VAI-7 and VAI-40 but susceptible to Benlate and Ridomil at field application levels and were found to produce siderophore, cellulase, lipase, protease, chitinase (except VAI-40, hydrocyanic acid (except VAI-7 and VAI-40, indole acetic acid and β-1,3-glucanase. When the four actinomycetes were evaluated for their plant growth-promotion properties under field conditions on chickpea, all exhibited increase in nodule number, shoot weight and yield. The actinomycetes treated plots enhanced total N, available P and organic C over the un-inoculated control. The scanning electron microscope studies exhibited extensive colonization by actinomycetes on the root surface of chickpea. The expression profiles for indole acetic acid, siderophore and β-1,3-glucanase genes exhibited up-regulation for all three traits and in all four isolates. The actinomycetes were identified as Streptomyces but different species in the 16S rDNA analysis. It was concluded that the selected actinomycetes have good plant growth-promotion and biocontrol potentials on chickpea.

  18. Exploring plant growth-promotion actinomycetes from vermicompost and rhizosphere soil for yield enhancement in chickpea.

    Science.gov (United States)

    Sreevidya, M; Gopalakrishnan, S; Kudapa, H; Varshney, R K

    2016-01-01

    The main objective of the present study was to isolate and characterize actinomycetes for their plant growth-promotion in chickpea. A total of 89 actinomycetes were screened for their antagonism against fungal pathogens of chickpea by dual culture and metabolite production assays. Four most promising actinomycetes were evaluated for their physiological and plant growth-promotion properties under in vitro and in vivo conditions. All the isolates exhibited good growth at temperatures from 20°C to 40°C, pH range of 7-11 and NaCl concentrations up to 8%. These were also found highly tolerant to Bavistin, slightly tolerant to Thiram and Captan (except VAI-7 and VAI-40) but susceptible to Benlate and Ridomil at field application levels and were found to produce siderophore, cellulase, lipase, protease, chitinase (except VAI-40), hydrocyanic acid (except VAI-7 and VAI-40), indole acetic acid and β-1,3-glucanase. When the four actinomycetes were evaluated for their plant growth-promotion properties under field conditions on chickpea, all exhibited increase in nodule number, shoot weight and yield. The actinomycetes treated plots enhanced total N, available P and organic C over the un-inoculated control. The scanning electron microscope studies exhibited extensive colonization by actinomycetes on the root surface of chickpea. The expression profiles for indole acetic acid, siderophore and β-1,3-glucanase genes exhibited up-regulation for all three traits and in all four isolates. The actinomycetes were identified as Streptomyces but different species in the 16S rDNA analysis. It was concluded that the selected actinomycetes have good plant growth-promotion and biocontrol potentials on chickpea.

  19. Actinomycetes from Western Ghats of Tamil Nadu with its antimicrobial properties

    Institute of Scientific and Technical Information of China (English)

    Valan Arasu M; Ignacimuthu S; Agastian P

    2012-01-01

    Objective: To isolate the actinomycetes from Western Ghats of Tamil Nadu with its antimicrobial properties. Methods: Starch casein agar medium supplemented with actidione and nalidixic acid was used to isolate actinomycetes from Western Ghates region of Kanyakumari, Thirunelveli, Dindigul and Nilgiri districts. Modified nutrient medium was used as the base for screening actinomycetes against pathogenic Gram positive, Gram negative and filamentous fungi. Results:Among 367 actinomycetes; 17.71% showed activity against both bacteria and fungi. The highest antibacterial activity was observed against B. subtilis, 140 isolates (38.1%), S. aureus 128 (34.9%);S. epidermidis 123 (33.5%); P. aeruginosa 105 (28.6%); K. pneumoniae 88 (24%); Xanthomonas sp 62 (16.9%). Less number of actinomycetes showed activity against Erwinia, S. typhi, V. fischeri andP. vulgaris. Hundred and three isolates showed activity against B. cinerea and A. niger. Twenty five isolates revealed activity against T. simii. Conclusions: Present investigation concludes that Western Ghats region of Tamil Nadu is the potential place for actinomycetes diversity. Further studying about these medically important strains from this region can be useful in identification of valuable bio-molecules.

  20. Isolation and characterization of medically important aerobic actinomycetes in soil of iran (2006 - 2007).

    Science.gov (United States)

    Aghamirian, Mohammad Reza; Ghiasian, Seyed Amir

    2009-01-01

    The aerobic actinomycetes are a large group of soil-inhabiting bacteria that occur worldwide. Some of them are the main cause of two important diseases, nocardiosis and actinomycetoma. To identify the prevalence and geographic distribution of aerobic actinomycetes in soil of Qazvin province, a study was carried out during 2006-2007. In this study, the incidence and diversity of medically important aerobic actinomycetes was determined in 300 soil samples of different parts of Qazvin. The suspensions of superficial soil samples were prepared by adding of normal saline, streptomycin and chloramphenicol and the supernatants were cultured on brain-heart infusion agar and Sabouraud's dextrose agar contain cycloheximide. The isolated microorganisms were examined by Gram and acid-fast stains and were identified biochemically and morphologically. Of 96 aerobic actinomycetes isolates identified, Actinomadura madurae and Streptomyces somaliensis were the most frequently isolated species each representing 19.8% of isolates, followed by Nocardia asteroides (15.6%), N. otitidiscaviarum (9.4%), N. brasiliensis (7.3%), A. peletieri, S. griseus, and Nocardia spp. (each 5.2%), and N. transvalensis, Nocardiopsis dassonvillei, Actinomadura spp. and Streptomyces spp. (each 3.1%). To the best of our knowledge, this is the first report on epidemiological investigation of medically important aerobic actinomycetes in soil samples from Iran. In recent years, mycetoma and nocardiosis have been increasingly reported in Iran. The results showed that medically important actinomycetes occur in the environment of Iran and soil could be potential source of actinomycotic infections.

  1. Enrichment Method for the Isolation of Bioactive Actinomycetes From Mangrove Sediments of Andaman Islands, India

    Directory of Open Access Journals (Sweden)

    Baskaran, R.

    2011-01-01

    Full Text Available Various pre-treatment methods and three different media were employed for the isolation of bioactive actinomycetes from mangrove sediments of Andaman and Nicobar Islands, India. Sediments from four different sites of mangrove forest were collected and pre-treated by dry heat method, and the media were supplemented with cycloheximide 80 µg/mL and nalidixic acid 75 µg/mL. The mean actinomycetes population density in sediment samples were recorded as 22 CFU-10^-6/gm in KUA medium followed by 12 CFU-10^-6/gm in AIA medium and 8 CFU-10^-6/gm in SCA medium. A total of 42 actinomycetes were isolated, and all the isolates were evaluated for their antibacterial activity against pathogenic bacteria on two different media. Among 42 isolates tested, 22 species were found to be antibacterial metabolite producer against test bacteria namely, Staphylococcus aureus, Bacillus subtilis, Salmonella typhi and Klebsiella pneumoniae. Particularly, the actinomycete strains such as A101, A102, A107, A116, A121, A125, A130, F101, F102, F104, F106, De101 and De102 significantly inhibited the growth of all bacteria which were tested. Of these strains, A107 was identified as Streptomyces spp. This strain had the maximum activity against all used pathogens on both medium. Hence, the isolation, characterization and studies of secondary metabolites of actinomycetes from mangrove sediments in Andaman and Nicobar Island could be a pathway for discovery of antibiotics from marine actinomycetes.

  2. Actinomycetal complex of light sierozem on the Kopet-Dag piedmont plain

    Science.gov (United States)

    Zenova, G. M.; Zvyagintsev, D. G.; Manucharova, N. A.; Stepanova, O. A.; Chernov, I. Yu.

    2016-10-01

    The population density of actinomycetes in the samples of light sierozem from the Kopet Dag piedmont plain (75 km from Ashkhabad, Turkmenistan) reaches hundreds of thousand CFU/g soil. The actinomycetal complex is represented by two genera: Streptomyces and Micromonospora. Representatives of the Streptomyces genus predominate and comprise 73 to 87% of the actinomycetal complex. In one sample, representatives of the Micromonospora genus predominated in the complex (75%). The Streptomyces genus in the studied soil samples is represented by the species from several sections and series: the species of section Helvolo-Flavus series Helvolus represent the dominant component of the streptomycetal complex; their portion is up to 77% of all isolated actinomycetes. The species of other sections and series are much less abundant. Thus, the percentage of the Cinereus Achromogenes section in the actinomycetal complex does not exceed 28%; representatives of the Albus section Albus series, Roseus section Lavendulae-Roseus series, and Imperfectus section belong to rare species; they have been isolated not from all the studied samples of light sierozem, and their portion does not exceed 10% of the actinomycetal complex.

  3. Identification of antimony resistance markers in Leishmania tropica field isolates through a cDNA-AFLP approach.

    Science.gov (United States)

    Kazemi-Rad, Elham; Mohebali, Mehdi; Khadem-Erfan, Mohammad Bagher; Saffari, Mojtaba; Raoofian, Reza; Hajjaran, Homa; Hadighi, Ramtin; Khamesipour, Ali; Rezaie, Sassan; Abedkhojasteh, Hoda; Heidari, Mansour

    2013-10-01

    Pentavalent antimonial compounds have been the first line therapy for leishmaniasis; unfortunately the rate of treatment failure of anthroponotic cutaneous leishmaniasis (ACL) is increasing due to emerging of drug resistance. Elucidation of the molecular mechanisms operating in antimony resistance is critical for development of new strategies for treatment. Here, we used a cDNA-AFLP approach to identify gene(s) which are differentially expressed in resistant and sensitive Leishmania tropica field isolates. We identified five genes, aquaglyceroporin (AQP1) acts in drug uptake, ATP-binding cassette (ABC) transporter (MRPA) involved in sequestration of drug, phosphoglycerate kinase (PGK) implicated in glycolysis metabolism, mitogen activated protein kinase (MAPK) and protein tyrosine phosphatase (PTP) responsible for phosphorylation pathway. The results were confirmed using real time RT-PCR which revealed an upregulation of MRPA, PTP and PGK genes and downregulation of AQP1 and MAPK genes in resistant isolate. To our knowledge, this is the first report of identification of PTP and PGK genes potentially implicated in resistance to antimonials. Our findings support the idea that distinct biomolecules might be involved in antimony resistance in L. tropica field isolates.

  4. IL-10 and TGF-beta control the establishment of persistent and transmissible infections produced by Leishmania tropica in C57BL/6 mice.

    Science.gov (United States)

    Anderson, Charles F; Lira, Rosalia; Kamhawi, Shaden; Belkaid, Yasmine; Wynn, Thomas A; Sacks, David

    2008-03-15

    Leishmania tropica is the causative agent of Old World anthroponotic cutaneous leishmaniasis, which is characterized by lesions that take an extended period of time to heal, often resulting in disfiguring scars, and are more refractory to treatment than leishmaniasis caused by Leishmania major. Immunologic studies involving experimental animal models of L. tropica infection are virtually nonexistent. In the current study, infectious-stage L. tropica were used to establish dermal infections in C57BL/6 and BALB/c mice. In both strains, the lesions were slow to develop and showed minimal pathology. They nonetheless contained a stable number of between 10(4) and 10(5) parasites for over 1 year, which were efficiently picked up by a natural sand fly vector, Phlebotomus sergenti. Control of parasite growth depended on the development of a Th1 response, as C57BL/6 mice genetically deficient in Th1 cytokines and BALB/c mice treated with Abs to IFN-gamma harbored significantly more parasites. By contrast, IL-10-deficient mice harbored significantly fewer parasites throughout the infection. To further study the immunologic mechanisms that may prevent efficient clearance of the parasites, IL-10 and TGF-beta signaling were abrogated during the chronic phase of infection in wild-type C57BL/6 mice. Distinct from chronic L. major infection, IL-10 blockade alone had no effect on L. tropica, but required simultaneous treatment with anti-TGF-beta Abs to promote efficient parasite clearance from the infection site. Thus, chronic infection with L. tropica appears to be established via multiple suppressive factors, which together maintain the host as a long-term reservoir of infection for vector sand flies.

  5. Development of assays using hexokinase and phosphoglucomutase gene sequences that distinguish strains of Leishmania tropica from different zymodemes and microsatellite clusters and their application to Palestinian foci of cutaneous leishmaniasis.

    Directory of Open Access Journals (Sweden)

    Kifaya Azmi

    Full Text Available BACKGROUND/OBJECTIVES: Palestinian strains of L.tropica characterized by multilocus enzyme electrophoresis (MLEE fall into two zymodemes, either MON-137 or MON-307. METHODOLOGY/PRINCIPLE FINDINGS: Assays employing PCR and subsequent RFLP were applied to sequences found in the Hexokinase (HK gene, an enzyme that is not used in MLEE, and the Phosphoglucomutase (PGM gene, an enzyme that is used for MLEE, to see if they would facilitate consigning local strains of L.tropica to either zymodeme MON-137 or zymodeme MON-307. Following amplification and subsequent double digestion with the restriction endonucleases MboI and HaeIII, variation in the restriction patterns of the sequence from the HK gene distinguished strains of L.tropica, L.major and L.infantum and also exposed two genotypes (G among the strains of L.tropica: HK-LtG1, associated with strains of L.tropica of the zymodemes MON-137 and MON-265, and HK-LtG2, associated with strains of L.tropica of the zymodemes MON-307, MON-288, MON-275 and MON-54. Following amplification and subsequent digestion by the restriction endonuclease MboI, variation in the sequence from the PGM gene also exposed two genotypes among the strains of L.tropica: PGM-G1, associated only with strains of L.tropica of the zymodeme MON-137; and PGM-G2, associated with strains of L.tropica of the zymodemes MON-265, MON-307, MON-288, MON-275 and MON-54, and, also, with six strains of L.major, five of L.infantum and one of L.donovani. The use of the HK and PGM gene sequences enabled distinction the L.tropica strains of the zymodeme MON-137 from those of the zymodeme MON-265. This genotyping system 'correctly' identified reference strains of L.tropica of known zymodemal affiliation and also from clinical samples, with a level of sensitivity down to <1 fg in the case of the former and to 1 pg of DNA in the case of the latter. CONCLUSIONS/SIGNIFICANCE: Both assays proved useful for identifying leishmanial parasites in clinical

  6. Screening and characterization of protease producing actinomycetes from marine saltern.

    Science.gov (United States)

    Suthindhiran, Krish; Jayasri, Mangalam Achuthananda; Dipali, Dipa; Prasar, Apurva

    2014-10-01

    In the course of systematic screening program for bioactive actinomycetes, an alkaline protease producing halophilic strain Actinopolyspora sp. VITSDK2 was isolated from marine saltern, Southern India. The strain was identified as Actinopolyspora based on its phenotypic and phylogenetic characters. The protease was partially purified using ammonium sulfate precipitation and subsequently by DEAE cellulose column chromatography. The enzyme was further purified using HPLC and the molecular weight was found to be 22 kDa as determined by SDS-PAGE analysis. The purified protease exhibited pH stability in a wide range of 4-12 with optimum at 10.0. The enzyme was found to be stable between 25 and 80 °C and displayed a maximum activity at 60 °C. The enzyme activity was increased marginally in presence of Mn(2+) , Mg(2+) , and Ca(2+) and decreased in presence of Cu(2+) . PMSF and DFP completely inhibited the activity suggesting it belongs to serine protease. Further, the proteolytic activity was abolished in presence of N-tosyl-L-lysine chloromethyl ketone suggesting this might be chymotrypsin-like serine protease. The protease was 96% active when kept for 10 days at room temperature. The results indicate that the enzyme belong to chymotrypsin-like serine protease exhibiting both pH and thermostability, which can be used for various applications in industries.

  7. Actinomycetes from red sea sponges: Sources for chemical and phylogenetic diversity

    KAUST Repository

    Abdelmohsen, Usama Ramadan

    2014-05-12

    The diversity of actinomycetes associated with marine sponges collected off Fsar Reef (Saudi Arabia) was investigated in the present study. Forty-seven actinomycetes were cultivated and phylogenetically identified based on 16S rRNA gene sequencing and were assigned to 10 different actinomycete genera. Eight putatively novel species belonging to genera Kocuria, Mycobacterium, Nocardia, and Rhodococcus were identified based on sequence similarity values below 98.2% to other 16S rRNA gene sequences available in the NCBI database. PCR-based screening for biosynthetic genes including type I and type II polyketide synthases (PKS-I, PKS-II) as well as nonribosomal peptide synthetases (NRPS) showed that 20 actinomycete isolates encoded each at least one type of biosynthetic gene. The organic extracts of nine isolates displayed bioactivity against at least one of the test pathogens, which were Gram-positive and Gram-negative bacteria, fungi, human parasites, as well as in a West Nile Virus protease enzymatic assay. These results emphasize that marine sponges are a prolific resource for novel bioactive actinomycetes with potential for drug discovery. 2014 by the authors; licensee MDPI.

  8. Diversity and bioprospecting of culturable actinomycetes from marine sediment of the Yellow Sea, China.

    Science.gov (United States)

    Xiong, Zhi-Qiang; Liu, Qiao-Xia; Pan, Zhao-Long; Zhao, Na; Feng, Zhi-Xiang; Wang, Yong

    2015-03-01

    Marine actinomycetes are a potential source of a wide variety of bioactive natural products. In this work, seven pretreatments, three selective isolation media, and five artificial seawater concentrations were used to isolate actinomycetes from the sediments collected from Yellow Sea, China. Statistical analysis showed that only the isolation medium strongly affected the total and bioactive numbers of actinomycete isolates. A total of 613 actinobacterial strains were isolated and screened for antimicrobial activities; 154 isolates showed activity against at least one of nine test drug-resistant microorganisms. Eighty-nine representatives with strong antimicrobial activity were identified phylogenetically based on 16S rRNA gene sequencing, which were assigned to five different actinomycete genera Streptomyces, Kocuria, Saccharomonospora, Micromonospora, and Nocardiopsis. Using PCR-based screening for six biosynthetic genes of secondary metabolites, all 45 isolates with acute activity have at least one biosynthetic gene, 28.8 % of which possess more than three biosynthetic genes. As a case, strain SMA-1 was selected for antimicrobial natural product discovery. Three diketopiperazine dimers including a new compound iso-naseseazine B (1) and two known compounds naseseazine B (2) and aspergilazine A (3) were isolated by bioassay-guided separation. These results suggested that actinomycetes from marine sediments are a potential resource of novel secondary metabolites and drugs.

  9. SCREENING OF ANTIMICROBIAL ACTIVITY AND GENES CODING POLYKETIDE SYNTHETASE AND NONRIBOSOMAL PEPTIDE SYNTHETASE OF ACTINOMYCETE ISOLATES

    Directory of Open Access Journals (Sweden)

    Silvia Kovácsová

    2013-12-01

    Full Text Available The aim of this study was to observe antimicrobial activity using agar plate diffusion method and screening genes coding polyketide synthetase (PKS-I and nonribosomal peptide synthetase (NRPS from actinomycetes. A total of 105 actinomycete strains were isolated from arable soil. Antimicrobial activity was demonstrated at 54 strains against at least 1 of total 12 indicator organisms. Antifungal properties were recorded more often than antibacterial properties. The presence of PKS-I and NRPS genes were founded at 61 of total 105 strains. The number of strains with mentioned biosynthetic enzyme gene fragments matching the anticipated length were 19 (18% and 50 (47% respectively. Overall, five actinomycete strains carried all the biosynthetical genes, yet no antimicrobial activity was found against any of tested pathogens. On the other hand, twenty-one strains showed antimicrobial activity even though we were not able to amplify any of the PKS or NRPS genes from them. Combination of the two methods showed broad-spectrum antimicrobial activity of actinomycetes isolated from arable soil, which indicate that actinomycetes are valuable reservoirs of novel bioactive compounds.

  10. Isolation of actinomycetes from mangrove and estuarine sediments of Cochin and screening for antimicrobial activity

    Institute of Scientific and Technical Information of China (English)

    Emilda Rosmine

    2016-01-01

    Objective:To isolate and screen actinomycetes for antimicrobial activity from mangroves and estuarine soil samples of Cochin. Methods: In the present study, sediment samples collected from mangroves and various stations of Cochin estuary were pretreated and actinomycetes were isolated on different selective media. The isolates were screened for antibiotic activity by following disc diffusion assay (Kirby-Bauer method) against human pathogens, fish pathogens and Gram-positive bacteria. The isolates were identified based on their morphology. Results:Only 2 actinomycete isolates (ER7and ER10) of the 50 isolates screened had antimicrobial activities against one or more pathogens tested. ER7 isolate showed higher antimicrobial activity as compared to that of ER10 isolate. The maximum inhibition zone of crude extract from ER7 was 16.7 mm. The methanol extract of ER7 showed antimicrobial activity against all the pathogens tested with a maximum zone of 21.0 mm. The isolates with antimicrobial activity were found to belong to the genusStreptomyces. Conclusions:There is no significant report on bioactive actinomycetes from the present study areas. Potent antibiotics from the selected isolates could contribute to fight against several human and fish diseases. Further purification, structural elucidation and characterization are recommended to know the quality, novelty and commercial value of these antibiotics. Hence, the mangroves and estuary of Kochi show great promise for the discovery of bioactive actinomycetes.

  11. lsolation and characterization of marine-derived actinomycetes with cytotoxic activity from the Red Sea coast

    Institute of Scientific and Technical Information of China (English)

    Mohamed Saleh Abdelfattah; Usama Wahid Hawas; Lamia Taha Abou El-Kassema; Mennat Allah Gamal Eid

    2016-01-01

    Objective: To isolate and evaluate the cytotoxic activity of different actinomycetes species isolated from the Red Sea coast in Sharm el-Sheikh, Egypt. Methods: Forty actinomycetes strains were isolated from different sediments and seawater samples collected from the Red Sea coast in Egypt. Actinomycetes were recognized by morphological and microscopic examinations. Cell viability and cyto-toxicity induced by the crude extracts on breast cancer cell lines MDA-MB-231 were assessed using methylene blue assay. The strains with promising cytotoxic activity were identified by sequencing and amplifying the 16S rRNA genes. The antibacterial activities of the crude extracts were performed using Kirby-Bauer disc diffusion method. Results: The results indicated that five ethyl acetate extracts exhibited cytotoxicity to-wards breast cancer cell lines MDA-MB-231. The highest cytotoxic activity was found for the ethyl acetate extracts of EGY2 and EGY39. The isolate EGY3 was identified as a new Streptomyces species, while the actinomycete EGY22 was found to be a member of the genus Nocardiopsis sp. The crude extract of the isolate EGY8 showed slightly high antimicrobial activity against different test microorganisms. Conclusions: The results of the present study reveal that marine sediments of the Red Sea are a potent source of novel species of actinomycetes. The isolates may be useful in discovery of novel bioactive compounds and an important step in the development of microbial natural product research.

  12. Isolation and characterization of marine-derived actinomycetes with cytotoxic activity from the Red Sea coast

    Institute of Scientific and Technical Information of China (English)

    Mohamed Saleh Abdelfattah; Mohammed Ismail Youssef Elmallah; Usama Wahid Hawas; Lamia Taha Abou El-Kassema; Mennat Allah Gamal Eid

    2016-01-01

    Objective: To isolate and evaluate the cytotoxic activity of different actinomycetes species isolated from the Red Sea coast in Sharm el-Sheikh, Egypt.Methods: Forty actinomycetes strains were isolated from different sediments and seawater samples collected from the Red Sea coast in Egypt. Actinomycetes were recognized by morphological and microscopic examinations. Cell viability and cytotoxicity induced by the crude extracts on breast cancer cell lines MDA-MB-231 were assessed using methylene blue assay. The strains with promising cytotoxic activity were identified by sequencing and amplifying the 16 S r RNA genes. The antibacterial activities of the crude extracts were performed using Kirby–Bauer disc diffusion method.Results: The results indicated that five ethyl acetate extracts exhibited cytotoxicity towards breast cancer cell lines MDA-MB-231. The highest cytotoxic activity was found for the ethyl acetate extracts of EGY2 and EGY39. The isolate EGY3 was identified as a new Streptomyces species, while the actinomycete EGY22 was found to be a member of the genus Nocardiopsis sp. The crude extract of the isolate EGY8 showed slightly high antimicrobial activity against different test microorganisms.Conclusions: The results of the present study reveal that marine sediments of the Red Sea are a potent source of novel species of actinomycetes. The isolates may be useful in discovery of novel bioactive compounds and an important step in the development of microbial natural product research.

  13. Amylase activity of aquatic actinomycetes isolated from the sediments of mangrove forests in south of Iran

    Directory of Open Access Journals (Sweden)

    Farshid Kafilzadeh

    2015-01-01

    Full Text Available In this study amylase producing actinomycetes were isolated from the sediments of mangrove forests in the south of Iran and the rate of amylase activity was measured. The samples of sediments were collected from one hundred different places in mangrove forests of the south of Iran. Collected samples were diluted then they were purified on the starch (casein agar culture and Woodruff. After that they were examined in terms of amylase production on agar–starch culture. The activity of the produced amylase by the isolated aquatic actinomycetes was measured by dinitrosalicylic acid (DNS method. The results showed that aquatic actinomycetes were isolated from 86 per 100 places in spring (86% and from 61 per 100 places in summer (61%. The highest rates of producing enzyme were related to isolated samples in spring (62.97 U/ml. Biochemical and Bergey’s book tests showed that the most isolated aquatic actinomycetes belonged to Streptomyces genus. As regards this, it is economical and easy to isolate the aquatic actinomycetes which produce amylase that is used in different industries in Iran from the sediments of mangrove forests of the south of Iran. So the isolated strains in this study can be suitable candidates for amylase production after genetic manipulation.

  14. Screening of Actinomycetes From Lipar Area of Oman Sea to Investigate the Antibacterial Compounds

    Directory of Open Access Journals (Sweden)

    Shams

    2015-02-01

    Full Text Available Background Actinomycetes are one of the most important sources for the production of antibacterial compounds. Marine environments, due to their unique characteristics, are considered a good option to search for bacteria with the capability of producing antimicrobial compounds. Objectives The purpose of this study was to isolate the actinomycetes producing antibacterial compounds. Materials and Methods A total of 35 actinomycetes were isolated from Oman Sea (Lipar Area. To investigate antibacterial activity, the isolated actinomycetes were assessed against reference and pathogenic bacteria, including Staphylococcus epidermidis, Staphylococcu intermedius, Staphylococcu chromogenes, Staphylococcu saprophyticus, Bacillus cereus and methicillin-resistance Staphylococcu aureus, Pseudomonas, Listeria, Klebsiella, Salmonella, Acinetobacter, and Escherichia coli O157:H7, using the cross streak method. Results Based on the morphological characterization, 35 isolated cases belonged to actinomycetes and %94 of them had the ability to produce antibacterial compounds. In the cross streak method, most of the isolated bacteria have antibacterial activity against reference S. aureus among Gram-positive bacteria and Acinetobacter among Gram-negative bacteria. Inhibition zone diameters were measured between 2-25 and 1-20 mm for Gram-positive and -negative bacteria, receptivity. Conclusions Preliminary results indicate that the native Iranian Actinobacteria could be considered a suitable option for screening of the new antibacterial compounds. Molecular research and antibacterial compound extraction against the aforementioned pathogenic strains are also being conducted.

  15. Regional genetic differentiation of Phlebotomus sergenti in three Moroccan foci of cutaneous leishmaniasis caused by Leishmania tropica

    Directory of Open Access Journals (Sweden)

    Yahia H.

    2004-06-01

    Full Text Available Phlebotomus sergenti was identified morphologically in samples from three Moroccan foci of leishmaniasis caused by Leishmania tropica in the provinces of Azilal, Essaouira and Taza. Three primary mitochondrial DNA lineages were identified, and they could be markers for regionally distributed cryptic species. Greater mitochondrial diversity in Azilal indicated that this central province could have been the origin of dispersal of P. sergenti or the zone of secondary contact. All except one of the 21 mitochondrial haplotypes showed a marked regional distribution, and this indicates that vector control would not always be followed by rapid, long-distance reinvasion. Only mitochondrial haplotype SER 18 was a putative marker for long-distance dispersal, for which there is no evidence of human assistance.

  16. Harnessing the Potential of Halogenated Natural Product Biosynthesis by Mangrove-Derived Actinomycetes

    Directory of Open Access Journals (Sweden)

    Xiang Xiao

    2013-10-01

    Full Text Available Mangrove-derived actinomycetes are promising sources of bioactive natural products. In this study, using homologous screening of the biosynthetic genes and anti-microorganism/tumor assaying, 163 strains of actinomycetes isolated from mangrove sediments were investigated for their potential to produce halogenated metabolites. The FADH2-dependent halogenase genes, identified in PCR-screening, were clustered in distinct clades in the phylogenetic analysis. The coexistence of either polyketide synthase (PKS or nonribosomal peptide synthetase (NRPS as the backbone synthetases in the strains harboring the halogenase indicated that these strains had the potential to produce structurally diversified antibiotics. As a validation, a new enduracidin producer, Streptomyces atrovirens MGR140, was identified and confirmed by gene disruption and HPLC analysis. Moreover, a putative ansamycin biosynthesis gene cluster was detected in Streptomyces albogriseolus MGR072. Our results highlight that combined genome mining is an efficient technique to tap promising sources of halogenated natural products synthesized by mangrove-derived actinomycetes.

  17. Actinomycetal complexes in drained peat soils of the taiga zone upon pyrogenic succession

    Science.gov (United States)

    Zenova, G. M.; Glushkova, N. A.; Bannikov, M. V.; Shvarov, A. P.; Pozdnyakov, A. I.; Zvyagintsev, D. G.

    2008-04-01

    The number and diversity of actinomycetes in peat soils vary in dependence on the stage of pyrogenic succession. In the cultivated peat soil, the number of actinomycetes after fires decreases by three-four times, mainly at the expense of acidophilic and neutrophilic groups. An increase in the number of mycelial prokaryotes (at the expense of alkaliphilic forms) is seen on the fifth year of functioning of the pyrogenic peat soil. The species diversity of streptomycetes in peat soils also decreases after fires. An increase in the range of streptomycetal species at the expense of neutrophilic and alkaliphilic forms takes place on the fifth year of the pyrogenic succession. Parameters of the actinomycetal complex—the population density, species composition, and ecological features—are the criteria whose changes allow us to judge the state of peat soils in the course of their pyrogenic succession.

  18. A comparative study on selected marine actinomycetes from Pulicat, Muttukadu, and Ennore estuaries

    Institute of Scientific and Technical Information of China (English)

    SChacko Vijai Sharma; Ernest David

    2012-01-01

    Objective: To isolate and make a comparative study of marine sediments actinomycetes from Pulicat estuary, Muttukadu estuary and Ennore estuary, TamilNadu, India. Methods: A unique selective enrichment procedure has resulted in the isolation and identification a total of 304 actinomycetes colonies which were isolated from different stations of marine soil sediments in Pulicat estuary, Muttukadu estuary and Ennore estuary, TamilNadu, India. Results: Among them, 277 isolates were morphologically distinct on the basis of spore mass colour, aerial and substrate mycelium formation and production of diffusible pigment. The majority (60%; 162 isolates) were assigned to the genus Streptomyces. (35%; 104 isolates) were assigned to the genus Actinopolyspora, (5%; 11 isolates) were assigned to the genus Nocardiodes. Conclusions: The present study concluded that the physiological characteristics of actinomycetes Streptomyces, Actinopolyspora and Nocardiodes varied by available nutrients in the medium and the physical conditions.

  19. Exploration of Potential Actinomycetes from CIFOR Forest Origin as Antimicrobial, Antifungus, and Producing Extracellular Xylanase

    Directory of Open Access Journals (Sweden)

    Sipriyadi Sipriyadi

    2016-03-01

    Full Text Available This study aimed to isolate and explore the actinomycetes of CIFOR forest origin as an antimicrobial and antifungal agent, to produce an extracellular xylanase, and to identify isolates based on 16S rRNA gene sequences. Actinomycetes were isolated using Humic-acid Vitamin-B agar (HV media. Actinomycetes colonies that grow on the medium HV was subsequently purified by growing them on yeast malt agar (YMA media, then an antagonistic test of selected bacteria against Bacillus sp., Escherichia coli, Fusarium oxysporum, and Sclerotium sp was performed. Xylanase activity test was detected by observing a clear zone, followed by identification. Total of 35 isolates of actinomycetes isolated based on their colony morphology characteristics and diverse types of spore chains showed Streptomyces spp. of isolates CFR-06, CFR-15, CFR-17, CFR-18, and CFR-19 were able to inhibit the growth of Bacillus sp.. The highest inhibition zone has a diameter of 10.1 mm (isolate CFR-17. Isolates CFR-01 and CFR-15 were able to inhibit the growth of E. coli with the highest inhibition zone diameter of 5.1 mm (isolate CFR-15. Isolates CFR-29 and CFR-12 were able to inhibit the growth of F. oxysporum while isolate CFR-35 were able to inhibit the growth of Sclerotium sp.. Xylanase activity test showed that isolates CFR-12, CFR-20, CFR-22, CFR-24, CFR-25, CFR-30, CFR-33, CFR-34 have an ability to produce extracellular xylanase enzyme. Actinomycetes isolate (Xyl_22 as a potential xylanase enzyme producer was closely related with Streptomyces drozdowicii by the maximum similarity of 99%.How to CiteSipriyadi, S., Lestari, Y., Wahyudi, A., Meryandini, A., & Suhartono, M. T. (2016. Exploration Potential CIFOR Forest actinomycetes origin as Antimicrobial, Anti Fungus and Producing Enzymes Extracellular Xylanase. Biosaintifika: Journal of Biology & Biology Education, 8(1, 94-102.

  20. Antibacterial activity of actinomycetes isolated from different soil samples of Sheopur (A city of central India

    Directory of Open Access Journals (Sweden)

    Hotam S Chaudhary

    2013-01-01

    Full Text Available The main objective of the present study was isolation, purification, and characterization of actinomycetes from soil samples, having antimicrobial activity against 12 selected pathogenic strains. Soils samples were taken from different niche habitats of Sheopur district, Madhya Pradesh, India. These samples were serially diluted and plated on actinomycete isolation agar media. Potential colonies were screened, purified, and stored in glycerol stock. Isolates were morphologically and biochemically characterized. These isolates were subjected to extraction for production of the antibacterial compound. Antibacterial activity and Minimum Inhibitory Concentration (MIC of the purified extract of isolates were evaluated. Totally 31 actinomycete isolates were tested for antagonistic activity against 12 pathogenic microorganisms. Isolates AS14, AS27, and AS28 were highly active, while AS1 showed less activity against the pathogenic microorganisms. Isolate AS7 exhibited the highest antagonistic activity against Bacillus cereus (24 mm and AS16 showed the highest activity against Enterococcus faecalis (21 mm. MIC was also determined for actinomycete isolates against all the tested microorganisms. MIC of actinomycete isolates was found to be 2.5 mg/ml against Shigella dysenteriae, Vancomycin-resistant enterococci, and Klebsiella pneumoniae, and was 1.25 mg/ml for Staphylococcus saprophyticus, Streptococcus pyogenes, Staphylococcus epidermidis, Methicillin-resistant Staphylococcus, Bacillus cereus, Staphylococcus xylosus, Methicillin-resistant Staphylococcus aureus, Enterococcus faecalis, and Staphylococcus aureus. All actinomycetes isolates showed antibacterial activity against S. aureus, while they showed less activity against S. dysenteriae. These isolates had antibacterial activity and could be used in the development of new antibiotics for pharmaceutical or agricultural purposes.

  1. Actinomycetes bioactivos de sedimento marino de la costa central del Perú

    OpenAIRE

    Jorge León; Libia Liza; Isela Soto; D´Lourdes Cuadra; Lilian Patiño; Rito Zerpa

    2013-01-01

    En el presente trabajo evaluamos la actividad antibacteriana y antifúngica de actinomycetes marinos sobre patógenos de origen clínico. Asimismo, fueron evaluadas la capacidad de producir enzimas extracelulares como carbohidrasas, lipasas y proteasas. Los Actinomycetes fueron aislados de sedimentos colectados entre setiembre a diciembre del 2005 de las Bahías de Ancón (Lima) e Independencia (Ica) de 34 y 100 m de profundidad. El aislamiento se realizó en Agar Caseína - Almidón (ACA) y Agar Mar...

  2. Actinomycetes bioactivos de sedimento marino de la costa central del Perú

    Directory of Open Access Journals (Sweden)

    Jorge León

    2013-04-01

    Full Text Available En el presente trabajo evaluamos la actividad antibacteriana y antifúngica de actinomycetes marinos sobre patógenos de origen clínico. Asimismo, fueron evaluadas la capacidad de producir enzimas extracelulares como carbohidrasas, lipasas y proteasas. Los Actinomycetes fueron aislados de sedimentos colectados entre setiembre a diciembre del 2005 de las Bahías de Ancón (Lima e Independencia (Ica de 34 y 100 m de profundidad. El aislamiento se realizó en Agar Caseína - Almidón (ACA y Agar Marino (AM con adición de Cicloheximide (10 μg/mL. Las evaluaciones antimicrobianas fueron realizadas frente a bacterias patógenas antibiótico-multirresistentes y hongos de origen clínico; en tanto, para evaluar su actividad multienzimática se utilizaron sustratos poliméricos diversos. Se aislaron un total de 62 actinomycetes, de los cuales 31 (50% mostraron actividad antibacteriana frente a Staphylococcus aureus, 36 (59% frente a Pseudomonas aeruginosa y 23 (37% a ambos patógenos. Las cepas de actinomycetes I-400A y M10-77 identificadas en cada caso como Streptomyces y Thermoactinomyces fueron las que exhibieron mayor actividad inhibitoria frente a P. aeruginosa y S. aureus respectivamente. Asimismo, 13 actinomycetes (20,97% mostraron actividad antifúngica frente a cultivos de Candida albicans cepa 1511 y 17 (27,42% frente a Candida albicans cepa 1511MIC; sin embargo, ningún actinomycete presentó actividad inhibitoria frente a Aspergillus niger, Aspergillus fumigatus y Trichophyton mentagrophytes. La mayoría de los actinomycetes mostraron tener actividad multienzimática capaz de hidrolizar compuestos poliméricos como el tween-80 (96%, la gelatina (95%, almidón (93%, lecitina (88% y la caseína (74%. Extractos del compuesto activo obtenidos de la cepa M10-77 con etil acetato rindieron notable actividad inhibitoria contra S. aureus. Se concluye que el sedimento marino es fuente de Actinomycetes con gran capacidad de producir sustancias

  3. First report on naturalLeishmania infection ofPhlebotomus sergenti due Leishmania tropica by high resolution melting curve method in South-eastern Iran

    Institute of Scientific and Technical Information of China (English)

    Aghaei Afshar A; Rassi Y; Sharifi I; Vatandoost H; Mollaie HR; Oshaghi MA; Abai MR; Rafizadeh S

    2014-01-01

    Objective:To identify the Leishmaniaspecies in infected sand flies byReal-timePCR coupled withHRM analysis.Methods:Real-timePCR coupled withHRM analysis targeting the first internal transcribed spacer(ITS1) of nuclear ribosomalDNA as the genetic marker was used to identify and distinguish Leishmania species in sand flies specimens.Results:Three out of115 females ofPhlebotomus sergenti(P. sergenti)(2.6%) were positive toLeishmania tropica(L. tropica). Conclusions:This is the first report onP. sergenti as the main and proven vector of anthroponitic cutaneous leishmaniasis inDehbakriCounty usingReal-timePCR coupled withHRM analysis. This method is rapid, sensitive and specific for diagnosing of parasites in infectedSand flies and ideal for large scale genotyping projects.

  4. Effectiveness of meglumine antimoniate against L. tropica in a recently emerged focus of cutaneous leishmaniasis in Birjand, eastern Islamic Republic of Iran.

    Science.gov (United States)

    Karamian, M; Bojd, M S Faroghi; Salehabadi, A; Hemmati, M; Barati, D A

    2015-06-09

    With limited options to treat cutaneous leishmaniasis, constant monitoring of the rate of resistance to pentavalent antimony-based drugs is needed. This study identified the infecting Leishmania species and evaluated the results of meglumine antimoniate (Glucantime®) therapy in a new focus of cutaneous leishmaniasis in Birjand, eastern Islamic Republic of Iran. Smears from 150 patients showed that 141 patients were infected by L. tropica and 9 by L. major. In total, 141 patients with L. tropica infection completed Glucantime® treatment and follow-up; 63.8% were treated intralesionally and 36.2% by intramuscular administration. The overall success rate after one course of therapy with Glucantime® was 96.5% (136/141), and all the failures (5/141) occurred with intramuscular injections. Statistical analysis showed a significant difference between the failure rates of intramuscular and intralesional injections. Children < 10 years old had a significantly higher failure rate than adults.

  5. In Vitro Study of Leishmanicidal Activity of Biogenic Selenium Nanoparticles against Iranian Isolate of Sensitive and Glucantime-Resistant Leishmania tropica.

    Directory of Open Access Journals (Sweden)

    Hossein Mahmoudvand

    2014-12-01

    Full Text Available Sensitive and glucantime (MA resistance Leishmania tropica are referred to those isolates, which are responsive, or non-responsive to one or two full courses of treatment by MA systematically and/or intra-lesionally, respectively. In this study, we evaluated the antileishmanial activity of biogenic selenium nanoparticles (Se NPs alone and in combination with MA against sensitive and glucantime-resistant L. tropica on in vitro model.The Se NPs were synthesized by employing the Bacillus sp. MSh-1. The antileishmanial effects of Se NPs alone and in combination with MA on promastigote and amastigote stages of sensitive and glucantime-resistant L. tropica strains have been investigated using a colorimetric MTT assay and in a macrophage model. In addition hemolytic activity in type O+ human red blood cells and infectivity rate of the promastigotes before and after treatment with the Se NPs was evaluated.In the promastigote stage, various concentrations of Se NPs significantly inhibited (P<0.05 the growth of promastigotes of both strains in a dose-dependent manner. Similarly, Se NPs especially in combination with MA significantly reduced the mean number of amastigotes of both strains in each macrophage. Se NPs showed no hemolytic effect on human RBCs at low concentrations. Moreover, infection rate of macrophages by promastigotes significantly (P<0.05 was reduced when promastigotes pre-treated with Se NPs.The findings of this study suggest a first step in the search of Se NPs as a new antileishmanial agent. Further experiments are needed to investigate antileishmanial effects of biogenic Se NPs on L. tropica using a clinical setting.

  6. Three Leishmania/L. species--L. infantum, L. major, L. tropica--as causative agents of mucosal leishmaniasis in Iran.

    Science.gov (United States)

    Shirian, Sadegh; Oryan, Ahmad; Hatam, Gholam Reza; Daneshbod, Yahya

    2013-07-01

    Cases of human oro-mucosal leishmaniasis are mainly reported in areas where Leishmania (Viannia) braziliensis perpetuates and the damages are mainly located at the cartilaginous nasal septum and frontal portions of the nasal fossa. In Iran, an area free of any L.(V) braziliensis, three Leishmania species are known to perpetuate through distinct (i) blood-feeding sand flies and (ii) rodents or (iii) canidae. Thus while establishing the diagnosis of any human oro-mucosal lesions, three Leishmania species - L. infantum, L. major, and L. tropica - must be considered as potential etiological agents of these damages. With these objectives in mind, features such as localization, extent, severity of oro-mucosal lesions, and duration of symptoms at the time of diagnosis were recorded from 11 patients with respect to the presence or absence of cutaneous lesions in other body parts. The biopsy samples were collected from the oro-mucosal and cutaneous lesions and were processed for further identification of the Leishmania species. The lesions ranged from mucosal nodules without ulceration, nodules with erosion, and shallow to deep ulcerations. Leishmania major was isolated from six (55%) cases showing lesions or scars. The scars were restricted to upper and lower extremities. For the other five patients who did not display any signs of former or active cutaneous leishmaniasis, L. major, L. tropica, and L. infantum were isolated from their lesions. In conclusion L. major, L. infantum, and L. tropica, regardless of common tropism, can be seen in mucosal tissues. However, L. major was the predominant species detected from the lesions in the nasal, gingival, and hard and soft palates, and L. tropica was isolated from the gingival and lower lip lesions. Leishmania infantum was isolated from two severe cases of deep mucosal damage displayed by the epiglottis, cricoarytenoid muscle, and laryngeal mucosa. One important finding was the association of L. major with active or scarred

  7. First detection of Leishmania tropica DNA and Trypanosoma species in Sergentomyia sand flies (Diptera: Psychodidae from an outbreak area of cutaneous leishmaniasis in Ghana.

    Directory of Open Access Journals (Sweden)

    Chukwunonso O Nzelu

    2014-02-01

    Full Text Available BACKGROUND: Leishmania major and an uncharacterized species have been reported from human patients in a cutaneous leishmaniasis (CL outbreak area in Ghana. Reports from the area indicate the presence of anthropophilic Sergentomyia species that were found with Leishmania DNA. METHODOLOGY/PRINCIPAL FINDINGS: In this study, we analyzed the Leishmania DNA positive sand fly pools by PCR-RFLP and ITS1 gene sequencing. The trypanosome was determined using the SSU rRNA gene sequence. We observed DNA of L. major, L. tropica and Trypanosoma species to be associated with the sand fly infections. This study provides the first detection of L. tropica DNA and Trypanosoma species as well as the confirmation of L. major DNA within Sergentomyia sand flies in Ghana and suggests that S. ingrami and S. hamoni are possible vectors of CL in the study area. CONCLUSIONS/SIGNIFICANCE: The detection of L. tropica DNA in this CL focus is a novel finding in Ghana as well as West Africa. In addition, the unexpected infection of Trypanosoma DNA within S. africana africana indicates that more attention is necessary when identifying parasitic organisms by PCR within sand fly vectors in Ghana and other areas where leishmaniasis is endemic.

  8. Habitats of the sandfly vectors of Leishmania tropica and L. major in a mixed focus of cutaneous leishmaniasis in southeast Tunisia.

    Science.gov (United States)

    Tabbabi, Ahmed; Ghrab, Jamila; Aoun, Karim; Ready, Paul Donald; Bouratbine, Aïda

    2011-08-01

    From 2009 to 2010, 3129 sandflies were caught in CDC light traps placed in various habitats in Ghomrassen, Tataouine governorate, southeast Tunisia, a mixed focus of human cutaneous leishmaniasis caused by Leishmania tropica and Leishmania major. Species diversity was quantified in anthropogenic, semi-anthropogenic and semi-natural locations. Sandflies were identified according to morphological characters and also by the comparative sequence analysis of a fragment of the mitochondrial cytochrome b gene to distinguish between two putative local vectors of L. tropica, namely Phlebotomus chabaudi and Phlebotomus riouxi. The lowest sandfly diversities were found in L. major sites, where the incriminated vector P. papatasi predominated in the burrows of the rodent reservoir hosts (Meriones) as well as inside and outside houses of human cases. In L. tropica sites, the incriminated peri-domestic vector Phlebotomus sergenti was the most abundant species inside houses, whereas P. riouxi or P. chabaudi was the dominant species in the semi-natural rocky habitats favoured by the putative rodent reservoir, Ctenodactylus gundi. All specimens of P. chabaudi identified molecularly had the diagnostic cytochrome b characters of P. riouxi, indicating either that the latter represents only a geographical variant of P. chabaudi or that these two species may sometimes hybridize.

  9. High-quality draft genome sequence of Gracilimonas tropica CL-CB462(T) (DSM 19535(T)), isolated from a Synechococcus culture.

    Science.gov (United States)

    Choi, Dong Han; Ahn, Chisang; Jang, Gwang Il; Lapidus, Alla; Han, James; Reddy, T B K; Huntemann, Marcel; Pati, Amrita; Ivanova, Natalia; Markowitz, Victor; Rohde, Manfred; Tindall, Brian; Göker, Markus; Woyke, Tanja; Klenk, Hans-Peter; Kyrpides, Nikos C; Cho, Byung Cheol

    2015-01-01

    Gracilimonas tropica Choi et al. 2009 is a member of order Sphingobacteriales, class Sphingobacteriia. Three species of the genus Gracilimonas have been isolated from marine seawater or a salt mine and showed extremely halotolerant and mesophilic features, although close relatives are extremely halophilic or thermophilic. The type strain of the type species of Gracilimonas, G. tropica DSM19535(T), was isolated from a Synechococcus culture which was established from the tropical sea-surface water of the Pacific Ocean. The genome of the strain DSM19535(T) was sequenced through the Genomic Encyclopedia of Type Strains, Phase I: the one thousand microbial genomes project. Here, we describe the genomic features of the strain. The 3,831,242 bp long draft genome consists of 48 contigs with 3373 protein-coding and 53 RNA genes. The strain seems to adapt to phosphate limitation and requires amino acids from external environment. In addition, genomic analyses and pasteurization experiment suggested that G. tropica DSM19535(T) did not form spore.

  10. Isolation and identification of actinomycetes from a compost-amended soils biocontrol agents

    Energy Technology Data Exchange (ETDEWEB)

    Garcia de la Fuente, R.; Cuesta, G.; Fornes, F.; Abad, M.

    2009-07-01

    Compost capability to suppress soil-borne plant pathogens has become an interesting subject as a strategy for reducing the adverse effects of massive fungicides application in the environmental. In this context, actinomycetes have received considerable attention as biocontrol agents, particularly Streptomyces species. (Author)

  11. Biodiversity, Anti-Trypanosomal Activity Screening, and Metabolomic Profiling of Actinomycetes Isolated from Mediterranean Sponges.

    Directory of Open Access Journals (Sweden)

    Cheng Cheng

    Full Text Available Marine sponge-associated actinomycetes are considered as promising sources for the discovery of novel biologically active compounds. In the present study, a total of 64 actinomycetes were isolated from 12 different marine sponge species that had been collected offshore the islands of Milos and Crete, Greece, eastern Mediterranean. The isolates were affiliated to 23 genera representing 8 different suborders based on nearly full length 16S rRNA gene sequencing. Four putatively novel species belonging to genera Geodermatophilus, Microlunatus, Rhodococcus and Actinomycetospora were identified based on a 16S rRNA gene sequence similarity of < 98.5% to currently described strains. Eight actinomycete isolates showed bioactivities against Trypanosma brucei brucei TC221 with half maximal inhibitory concentration (IC50 values <20 μg/mL. Thirty four isolates from the Milos collection and 12 isolates from the Crete collection were subjected to metabolomic analysis using high resolution LC-MS and NMR for dereplication purposes. Two isolates belonging to the genera Streptomyces (SBT348 and Micromonospora (SBT687 were prioritized based on their distinct chemistry profiles as well as their anti-trypanosomal activities. These findings demonstrated the feasibility and efficacy of utilizing metabolomics tools to prioritize chemically unique strains from microorganism collections and further highlight sponges as rich source for novel and bioactive actinomycetes.

  12. Isolation and characterization of marine-derived actinomycetes with cytotoxic activity from the Red Sea coast

    Directory of Open Access Journals (Sweden)

    Mohamed Saleh Abdelfattah

    2016-08-01

    Conclusions: The results of the present study reveal that marine sediments of the Red Sea are a potent source of novel species of actinomycetes. The isolates may be useful in discovery of novel bioactive compounds and an important step in the development of microbial natural product research.

  13. [Bioactivity of endophytic actinomycetes from medicinal plants and secondary metabolites from strain D62].

    Science.gov (United States)

    Liu, Ning; Zhang, Hui; Zheng, Wen; Huang, Ying; Wang, Hai-Bin

    2007-10-01

    It is believed that genetic recombination of the endophytes with the hosts that occurred in evolutionary time could result in some endophytes producing certain phytochemical originally characteristic of the host. Based on this widely accepted hypothesis, there have been increasing research efforts focused on screening for novel natural products from endophytes. In this study, antimicrobial and antitumor activities of 165 actinomycetes isolated from medicinal plants collected from Xishuangbanna were tested by agar diffusion method and WST-8 assay respectively. The results showed that over 42% of the isolates exhibited antagonism against pathogenic strains, and 54.5% displayed excellent inhibition against mouse melanoma cell line B16 or/and human alveolar epithelial cell line A549. These results are superior to those of soil actinomycetes, indicating tremendous potential of endophytic of actinomycetes for exploration. Six compounds that had both antimicrobial and antitumor activities were separated and purified from isolate Streptomyces sp. D62 by resin adsorption, silica-gel column and sephadex chromatography, etc. On the basis of spectral analyses, they were identified as antimycin A4a (1), antimycin A7a (2), antimycin A2a (3), antimycin A1a (4), 10-hydroxy-10-methyl-dodec-2-en-1,4-olide (5) and 6-(2-(4-aminophenyl)-2-oxoethyl)-3,5-dimethyl-tetrahydropyran-2-one(6), with the last one defined as a novel compound. Based on all these results, it is convinced that endophytic actinomycetes are a promising resource for bioactive natural product discovery.

  14. Genome Sequence of Streptomyces viridosporus Strain T7A ATCC 39115, a Lignin-Degrading Actinomycete

    Energy Technology Data Exchange (ETDEWEB)

    Davis, Jennifer R. [Brown University; Goodwin, Lynne A. [Los Alamos National Laboratory (LANL); Teshima, Hazuki [Los Alamos National Laboratory (LANL); Detter, J. Chris [U.S. Department of Energy, Joint Genome Institute; Tapia, Roxanne [Los Alamos National Laboratory (LANL); Han, Cliff [Los Alamos National Laboratory (LANL); Huntemann, Marcel [U.S. Department of Energy, Joint Genome Institute; Wei, Chia-Lin [Los Alamos National Laboratory (LANL); Han, James [U.S. Department of Energy, Joint Genome Institute; Chen, Amy [U.S. Department of Energy, Joint Genome Institute; Kyrpides, Nikos C [U.S. Department of Energy, Joint Genome Institute; Mavromatis, K [U.S. Department of Energy, Joint Genome Institute; Szeto, Ernest [U.S. Department of Energy, Joint Genome Institute; Markowitz, Victor [U.S. Department of Energy, Joint Genome Institute; Ivanova, N [U.S. Department of Energy, Joint Genome Institute; Mikhailova, Natalia [U.S. Department of Energy, Joint Genome Institute; Ovchinnikova, Galina [U.S. Department of Energy, Joint Genome Institute; Pagani, Ioanna [U.S. Department of Energy, Joint Genome Institute; Pati, Amrita [U.S. Department of Energy, Joint Genome Institute; Woyke, Tanja [U.S. Department of Energy, Joint Genome Institute; Pitluck, Sam [U.S. Department of Energy, Joint Genome Institute; Peters, Lin [U.S. Department of Energy, Joint Genome Institute; Nolan, Matt [U.S. Department of Energy, Joint Genome Institute; Land, Miriam L [ORNL; Sello, Jason K. [Brown University

    2013-01-01

    We announce the availability of the genome sequence of Streptomyces viridosporus strain T7A ATCC 39115, a plant biomass- degrading actinomycete. This bacterium is of special interest because of its capacity to degrade lignin, an underutilized compo- nent of plants in the context of bioenergy. It has a full complement of genes for plant biomass catabolism.

  15. Genome Sequence of Streptomyces viridosporus Strain T7A ATCC 39115, a Lignin-Degrading Actinomycete

    Science.gov (United States)

    Davis, Jennifer R.; Goodwin, Lynne; Teshima, Hazuki; Detter, Chris; Tapia, Roxanne; Han, Cliff; Huntemann, Marcel; Wei, Chia-Lin; Han, James; Chen, Amy; Kyrpides, Nikos; Mavrommatis, Kostas; Szeto, Ernest; Markowitz, Victor; Ivanova, Natalia; Mikhailova, Natalia; Ovchinnikova, Galina; Pagani, Ioanna; Pati, Amrita; Woyke, Tanja; Pitluck, Sam; Peters, Lin; Nolan, Matt; Land, Miriam

    2013-01-01

    We announce the availability of the genome sequence of Streptomyces viridosporus strain T7A ATCC 39115, a plant biomass-degrading actinomycete. This bacterium is of special interest because of its capacity to degrade lignin, an underutilized component of plants in the context of bioenergy. It has a full complement of genes for plant biomass catabolism. PMID:23833133

  16. Comparative genome-scale metabolic modeling of actinomycetes : The topology of essential core metabolism

    NARCIS (Netherlands)

    Alam, Mohammad Tauqeer; Medema, Marnix H.; Takano, Eriko; Breitling, Rainer; Gojobori, Takashi

    2011-01-01

    Actinomycetes are highly important bacteria. On one hand, some of them cause severe human and plant diseases, on the other hand, many species are known for their ability to produce antibiotics. Here we report the results of a comparative analysis of genome-scale metabolic models of 37 species of act

  17. Comparative genome-scale metabolic modeling of actinomycetes: the topology of essential core metabolism.

    NARCIS (Netherlands)

    Alam, M.T.; Medema, M.H.; Takano, E.; Breitling, R.

    2011-01-01

    Actinomycetes are highly important bacteria. On one hand, some of them cause severe human and plant diseases, on the other hand, many species are known for their ability to produce antibiotics. Here we report the results of a comparative analysis of genome-scale metabolic models of 37 species of act

  18. Characterization of cytotoxic compound from marine sediment derived actinomycete Streptomyces avidinii strain SU4

    Directory of Open Access Journals (Sweden)

    S Sudha

    2012-10-01

    Conclusion: This study clearly proves that the marine sediment derived actinomycetes with bioactive metabolites can be expected to provide high quality biological material for high throughout biochemical and anticancer screening programs. These results help us to conclude that the potential of using metabolic engineering and post genomic approaches to isolate more bioactive compounds and make their possible commercial application is not far off.

  19. A mixed community of actinomycetes produce multiple antibiotics for the fungus farming ant Acromyrmex octospinosus

    Directory of Open Access Journals (Sweden)

    Barke Jörg

    2010-08-01

    Full Text Available Abstract Background Attine ants live in an intensely studied tripartite mutualism with the fungus Leucoagaricus gongylophorus, which provides food to the ants, and with antibiotic-producing actinomycete bacteria. One hypothesis suggests that bacteria from the genus Pseudonocardia are the sole, co-evolved mutualists of attine ants and are transmitted vertically by the queens. A recent study identified a Pseudonocardia-produced antifungal, named dentigerumycin, associated with the lower attine Apterostigma dentigerum consistent with the idea that co-evolved Pseudonocardia make novel antibiotics. An alternative possibility is that attine ants sample actinomycete bacteria from the soil, selecting and maintaining those species that make useful antibiotics. Consistent with this idea, a Streptomyces species associated with the higher attine Acromyrmex octospinosus was recently shown to produce the well-known antifungal candicidin. Candicidin production is widespread in environmental isolates of Streptomyces, so this could either be an environmental contaminant or evidence of recruitment of useful actinomycetes from the environment. It should be noted that the two possibilities for actinomycete acquisition are not necessarily mutually exclusive. Results In order to test these possibilities we isolated bacteria from a geographically distinct population of A. octospinosus and identified a candicidin-producing Streptomyces species, which suggests that they are common mutualists of attine ants, most probably recruited from the environment. We also identified a Pseudonocardia species in the same ant colony that produces an unusual polyene antifungal, providing evidence for co-evolution of Pseudonocardia with A. octospinosus. Conclusions Our results show that a combination of co-evolution and environmental sampling results in the diversity of actinomycete symbionts and antibiotics associated with attine ants.

  20. Molecular, chemical and biological screening of soil actinomycete isolates in seeking bioactive peptide metabolites

    Directory of Open Access Journals (Sweden)

    Javad Hamedi

    2015-10-01

    Full Text Available Background and Objective: Due to the evolution of multidrug-resistant strains, screening of natural resources, especially actinomycetes, for new therapeutic agents discovery has become the interests of researchers. In this study, molecular, chemical and biological screening of soil actinomycetes was carried out in order to search for peptide-producing actinomycetes.Materials and Methods: 60 actinomycetes were isolated from soils of Iran. The isolates were subjected to molecular screening for detection NRPS (non-ribosomal peptide synthetases gene. Phylogenic identification of NRPS containing isolates was performed. Chemical screening of the crude extracts was performed using chlorine o-dianisidine as peptide detector reagent and bioactivity of peptide producing strains was determined by antimicrobial bioassay. High pressure liquid chromatography- mass spectrometry (HPLC-MS with UV-visible spectroscopy was performed for detection of the metabolite diversity in selected strain.Results: Amplified NRPS adenylation gene (700 bp was detected among 30 strains. Phylogenic identification of these isolates showed presence of rare actinomycetes genera among the isolates and 10 out of 30 strains were subjected to chemical screening. Nocardia sp. UTMC 751 showed antimicrobial activity against bacterial and fungal test pathogens. HPLC-MSand UV-visible spectroscopy results from the crude extract showed that this strain has probably the ability to produce new metabolites.Conclusion: By application of a combined approach, including molecular, chemical and bioactivity analysis, a promising strain of Nocardia sp. UTMC 751 was obtained. This strain had significant activity against Staphylococcus aureus and Pseudomonas aeruginosa. Strain Nocardia sp. UTMC 751 produce five unknown and most probably new metabolites with molecular weights of 274.2, 390.3, 415.3, 598.4 and 772.5. This strain had showed 99% similarity to Nocardia ignorata DSM 44496 T.

  1. Biodiversity of Actinomycetes associated with Caribbean sponges and their potential for natural product discovery.

    Science.gov (United States)

    Vicente, Jan; Stewart, Allison; Song, Bongkeun; Hill, Russell T; Wright, Jeffrey L

    2013-08-01

    Marine actinomycetes provide a rich source of structurally unique and bioactive secondary metabolites. Numerous genera of marine actinomycetes have been isolated from marine sediments as well as several sponge species. In this study, 16 different species of Caribbean sponges were collected from four different locations in the coastal waters off Puerto Rico in order to examine diversity and bioactive metabolite production of marine actinomycetes in Caribbean sponges. Sediments were also collected from each location, in order to compare actinomycete communities between these two types of samples. A total of 180 actinomycetes were isolated and identified based on 16S rRNA gene analysis. Phylogenetic analysis revealed the presence of at least 14 new phylotypes belonging to the genera Micromonospora, Verruscosispora, Streptomyces, Salinospora, Solwaraspora, Microbacterium and Cellulosimicrobium. Seventy-eight of the isolates (19 from sediments and 59 from sponges) shared 100 % sequence identity with Micromonospora sp. R1. Despite having identical 16S rRNA sequences, the bioactivity of extracts and subsequent fractions generated from the fermentation of both sponge- and sediment-derived isolates identical to Micromonospora sp. R1 varied greatly, with a marked increase in antibiotic metabolite production in those isolates derived from sponges. These results indicate that the chemical profiles of isolates with high 16S rRNA sequence homology to known strains can be diverse and dependent on the source of isolation. In addition, seven previously reported dihydroquinones produced by five different Streptomyces strains have been purified and characterized from one Streptomyces sp. strain isolated in this study from the Caribbean sponge Agelas sceptrum.

  2. Isolation and phylogenetic assignation of actinomycetes in the marine sediments from the Arctic Ocean

    Institute of Scientific and Technical Information of China (English)

    YU Yong; LI Huirong; ZENG Yinxin; CHEN Bo

    2005-01-01

    Actinomycetes in five marine sediments collected from the Arctic Ocean at depths of 43 to 3 050 m were cultivated using a variety of media. A total of 61 actinomycete colonies with substrate mycelia only were observed, and no colonies with aerial mycelia were observed under aerobic conditions at 15 ℃. From these colonies, 28 were selected to represent different morphological types.Denaturing gradient gel electrophoresis (DGGE) was used to check the purity of isolates and select representatives for subsequent sequencing. Phylogentic analyses based on nearly full-length 16S ribosomal RNA gene (rDNA) sequences indicated that the actinomycetes isolated were accommodated within genus Rhodococcus of family Nocardiaceae, genus Dietzia of family Dietziaceae,genera Janibacter and Terrabacter of family Instrasporangiaceae and genera Kocuria and Arthrobacter of family Micrococcaceae. One of the strains (P27-24) from the deep-sea sediment at depth of 3 050 m was found to be identical in 16S rDNA sequence(1474/1474)with the radiation-resistant Kocuria rosea ATCC 187T isolated from air. More than halfofthe isolates showed the similarities ranging from 99.5% to 99.9% in 16S rDNA sequence to dibenzofran-degrading, butyl 2-ethylhexanoate-hydrolysising and nitrile-metabolizing actinomycetes. All the strains isolated were psychrotolerant bacteria and grew better on the media prepared with natural seawater than on the media prepared with deionized water. Three of them (Dietzia sp. P27-10, Rhodococcus sp. S11-3 and Rhodococcus sp.P11-5)had an obligate growth requirement for salt, confirming that these strains are indigenous marine actinomycetes.

  3. Prophylactic immunization against experimental leishmaniasis. III. Protection against fatal Leishmania tropica infection induced by irradiated promastigotes involves Lyt-1/sup +/2/sup -/ T cells that do not mediate cutaneous DTH

    Energy Technology Data Exchange (ETDEWEB)

    Liew, F.Y.; Howard, J.G.; Hale, C.

    1984-01-01

    Protective immunity against fatal L. tropica infection in genetically vulnerable BALB/c mice can be induced by prophylactic immunization with irradiated promastigotes even when heat-killed. Such immunity is adoptively transferable transiently into intact or durably into sub-lethally irradiated (200 or 550 rad) syngeneic recipients by splenic T but not B cells. The effector T cells are of the Lyt-1/sup +/2/sup -/ phenotype, devoid of demonstrable cytotoxic activity. The immune splenic T cell population expresses specific helper activity for antibody synthesis. A causal role for helper T cells in this capacity, however, seems unlikely, because it was shown that antibody does not determine the protective immunity against L. tropica. The immunized donors show no detectable cutaneous DTH or its early memory recall in response to live or killed promastigotes or a soluble L. tropica antigen preparation. Spleen, lymph node, and peritoneal exudate cells from protectively immunized donors similarly fail to transfer DTH locally or systemically. These cells also lack demonstrable suppressive activity against the expression or induction of DTH to L. tropica. Thus, protection against L. tropica induced by prophylactic i.v. immunization with irradiated promastigotes appears to be conferred by Lyt-1/sup +/2/sup -/ T cells that are distinguishable from T cells mediating either both DTH and T help, or cytotoxicity.

  4. Solid lipid nanoparticle loaded with paromomycin: in vivo efficacy against Leishmania tropica infection in BALB/c mice model.

    Science.gov (United States)

    Heidari-Kharaji, Maryam; Taheri, Tahereh; Doroud, Delaram; Habibzadeh, Sima; Rafati, Sima

    2016-08-01

    Leishmaniasis is a parasitic disease transmitted through the bite of an infected phlebotomine sand fly and caused by protozoan parasites of the genus Leishmania. There is no available vaccine for leishmaniasis in human, and the current chemotherapy approaches are hampered by different clinical problems. Most of available drugs are confined to a limited number of toxic chemical compounds, which some parasite strains have evolved drug resistance against. Hence, drug discovery and production of a new anti leishmanial compound is essential. One promising strategy is using the nanoparticle delivery systems with the aim of accelerating the efficacy of the available treatments. In the present study, paromomycin sulfate (PM) was formulated in solid lipid nanoparticles (SLN) and the in vivo efficacy was investigated against Leishmania tropica in BALB/c mice model. To do so, the increase in footpad thickness was measured and real-time PCR was performed to quantify the parasite load after infectious challenge. The level of nitric oxide and cytokines including interleukin-4 (IL-4) and gamma interferon (IFN -γ) were assessed. Altogether, the results show that PM loaded into SLN is significantly more effective than PM alone in inhibiting the parasite propagation and switching towards Th1 response.

  5. Culture conditions for the production of an acidic exopolysaccharide by the nitrogen-fixing bacterium Burkholderia tropica.

    Science.gov (United States)

    Serrato, Rodrigo V; Sassaki, Guilherme L; Cruz, Leonardo M; Pedrosa, Fábio O; Gorin, Philip A J; Iacomini, Marcello

    2006-05-01

    The endophytic diazotrophic bacterium Burkholderia tropica, strain Ppe8, produced copious amounts of exopolysaccharide (EPS) on batch growth in liquid synthetic media containing mannitol and glutamate as carbon and nitrogen sources. The effect of various aeration regimes and carbon source concentrations on EPS production was determined, as well as the effects of temperature and time of growth. The degree of aeration had a great influence on the yield of EPS, in contrast with the C:N ratio of the medium. Growth temperature also affected the EPS yield after the first 24 h of culture but seemed to be irrelevant after that. After isolation and purification, the EPS was analyzed by high-performance size exclusion chromatography and multiangle laser light scattering (HPSEC-MALLS), revealing a molecular mass of 300 kDa. The acid hydrolyzate of EPS was examined by HPLC and found to contain Glc, Rha, GlcA, and an aldobiouronic acid. The latter was found to have a GlcA and a Rha unit. Carboxy-reduced EPS contained Glc and Rha (3:2). The monosaccharide composition of the native acidic EPS was calculated as GlcA, Glc, and Rha in a molar ratio of 1:2:2.

  6. Presence, molecular characteristics and geosmin producing ability of actinomycetes isolated from South Korean terrestrial and aquatic environments.

    Science.gov (United States)

    Lee, Gyu-Cheol; Kim, Yun S; Kim, Min-Jeong; Oh, Sung-Ae; Choi, Ilhwan; Choi, Jaewon; Park, Jong-Geun; Chong, Chom-Kyu; Kim, Yong-Yeon; Lee, Kyeunghee; Lee, Chan Hee

    2011-01-01

    The unpleasant odor of drinking water is one of the major problems in many water utilities in the world. Actinomycetes have long been associated with odorous compounds. Considering the paucity of research on Actinomycetes producing odorous compounds in South Korea, presence of Actinomycetes, their molecular characteristics and ability to produce odorous compounds were investigated in this study. Findings confirmed the presence of Actinomycetes in surface soil, sediment, and water samples from four sites: two artificial lakes [Paldang and Cheongpyeong (CP)], and two streams [Gyeongan (GA) and Yangpyeong]. Surface soil and sediment from CP area had the greatest concentration of Actinomycetes (8.2 x 10(7) and 6.8 x 10(6) colony forming units (CFUs)/gram, dry weight, respectively). When water samples are considered, samples from GA had the highest concentration (1.9 x 10(2) CFU/mL). 16S rRNA sequencing and molecular phylogenetic analysis showed that Streptomyces was the dominant genus (64.1%). In addition, the isolated Actinomycetes synthesized 5.4 ng/L geosmin as demonstrated by thermal desorption unit-gas chromatograph/mass spectrometry analysis.

  7. Glucose metabolism in the antibiotic producing actinomycete Nonomuraea sp ATCC 39727

    DEFF Research Database (Denmark)

    Gunnarsson, Nina; Bruheim, Per; Nielsen, Jens

    2004-01-01

    primary carbon metabolism in further detail, Nonomuraea was cultivated with [1-C-13] glucose as the only carbon source and the C-13-labeling patterns of proteinogenic amino acids were determined by GC-MS analysis. Through this method, the fluxes in the central carbon metabolism during balanced growth were......The actinomycete Nonomuraea sp. ATCC 39727, producer of the glycopeptide A40926 that is used as precursor for the novel antibiotic dalbavancin, has an unusual carbon metabolism. Glucose is primarily metabolized via the Entner-Doudoroff (ED) pathway, although the energetically more favorable Embden...... - Meyerhof - Parnas (EMP) pathway is present in this organism. Moreover, Nonomuraea utilizes a PPi-dependent phosphofructokinase, an enzyme that has been connected with anaerobic metabolism in eukaryotes and higher plants, but recently has been recognized in several actinomycetes. In order to study its...

  8. Quantitative isolation of biocontrol agents Trichoderma spp., Gliocladium spp. and actinomycetes from soil with culture media.

    Science.gov (United States)

    Vargas Gil, S; Pastor, S; March, G J

    2009-01-01

    Soil biodiversity plays a key role in the sustainability of agriculture systems and indicates the level of health of soil, especially when considering the richness of microorganisms that are involved in biological control of soilborne diseases. Cultural practices may produce changes in soil microflora, which can be quantified through the isolation of target microorganisms. Rhizosphere soil samples were taken from an assay with different crop rotations and tillage systems, and populations of Trichoderma spp., Gliocladium spp. and actinomycetes were quantified in order to select the general and selective culture media that better reflect the changes of these microbial populations in soil. The most efficient medium for the isolation of Trichoderma spp. and Gliocladium spp. was potato dextrose agar modified by the addition of chloramphenicol, streptomycin and rose bengal, and for actinomycetes was Küster medium, with cycloheximide and sodium propionate.

  9. Volatile terpenes from actinomycetes: a biosynthetic study correlating chemical analyses to genome data.

    Science.gov (United States)

    Rabe, Patrick; Citron, Christian A; Dickschat, Jeroen S

    2013-11-25

    The volatile terpenes of 24 actinomycetes whose genomes have been sequenced (or are currently being sequenced) were collected by use of a closed-loop stripping apparatus and identified by GC/MS. The analytical data were compared against a phylogenetic analysis of all 192 currently available sequences of bacterial terpene cyclases (excluding geosmin and 2-methylisoborneol synthases). In addition to the several groups of terpenes with known biosynthetic origin, selinadienes were identified as a large group of biosynthetically related sesquiterpenes that are produced by several streptomycetes. The detection of a large number of previously unrecognised side products of known terpene cyclases proved to be particularly important for an in depth understanding of biosynthetic pathways to known terpenes in actinomycetes. Interpretation of the chemical analytical data in the context of the phylogenetic tree of bacterial terpene cyclases pointed to the function of three new enzymes: (E)-β-caryophyllene synthase, selina-3,7(11)-diene synthase and aristolochene synthase.

  10. Isolation and partial characterization of actinomycetes with antimicrobial activity against multidrug resistant bacteria

    Institute of Scientific and Technical Information of China (English)

    Smriti Singh; Pramod Kumar; N Gopalan; Bhuvnesh Shrivastava; RC Kuhad; Hotam Singh Chaudhary

    2012-01-01

    Objective: To isolate strains of Actinomycetes from different locations of Gwalior to evaluate its antimicrobial activity against multidrug resistant pathogenic strains. Method: Soil samples collected from different niche habitats of Gwalior were serially diluted and plated on selective media. Potential colonies were further purified and stored in agar slants and glycerol stocks. Isolates were biochemically characterized and purified isolates were test against pathogenic microorganisms for screening. Isolates with antagonistic properties were inoculated in production media and secondary metabolites or antimicrobial products were extracted. Result: The seven actinomycetes strains showing maximum antibacterial activity were isolated further characterized based on their colony characteristics and biochemical analyses. The isolates were screened for their secondary metabolites activity on three human pathogenic bacteria are Escherichia coli (E. coli), Methicillin-Resistant Staphylococcus aureus (S. aureus) and Vancomycin-Resistant Enterococci (VRE). Discussion: The strain MITS 1005 was found to be more active against the test bacteria.

  11. Inhibition of norsolorinic acid accumulation to Aspergillus parasiticus by marine actinomycetes

    Science.gov (United States)

    Yan, Peisheng; Shi, Cuijuan; Shen, Jihong; Wang, Kai; Gao, Xiujun; Li, Ping

    2014-11-01

    Thirty-six strains of marine actinomycetes were isolated from a sample of marine sediment collected from the Yellow Sea and evaluated in terms of their inhibitory activity on the growth of Aspergillus parasiticus and the production of norsolorinic acid using dual culture plate assay and agar diffusion methods. Among them, three strains showed strong antifungal activity and were subsequently identified as Streptomyces sp. by 16S rRNA gene sequencing analysis. The supernatant from the fermentation of the MA01 strain was extracted sequentially with chloroform and ethyl acetate, and the activities of the extracts were determined by tip culture assay. The assay results show that both extracts inhibited mycelium growth and toxin production, and the inhibitory activities of the extracts increased as their concentrations increased. The results of this study suggest that marine actinomycetes are biologically important for the control of mycotoxins, and that these bacteria could be used as novel biopesticides against mycotoxins.

  12. Evaluation of a Possible Synergistic Effect of Meglumine Antimoniate with Paromomycin, Miltefosine or Allopurinol on in Vitro Susceptibility of Leishmania tropica Resistant Isolate

    Directory of Open Access Journals (Sweden)

    Tahereh Rezaei Riabi

    2013-09-01

    Full Text Available Background: Pentavalent antimonials are still the first choice treatment for leishma­niasis, but with low efficacy and resistance is emerging. In the present study, the effect of meglumine antimoniate (MA, Glucantime combined with paromomy­cin, miltefosine or allopurinol on in vitro susceptibility of Leishmania tropica resistant isolate was evaluated.Method: The drugs were obtained from commercial sources and diluents of each drug in medium were prepared on the day of experiment. J774 A.1 murine macrophage cell lines were attached to the cultured on slide and incubated at 37 0C with 5% CO2 for 24 h. Then the stationary phase promastigotes were added to the cells and after 4 hrs of incubation different concentrations of MA, paromomycin, miltefosine or allopurinol were added and incubated for an additional of 72 h. Then the slides were dried and fixed with methanol, stained by Giemsa and studied under a light microscope. Drug activity was evaluated by assessing the macrophage infection rate and the number of amastigotes per infected macrophage was done by examin­ing 100 macrophages. The experiment was done in triplicates.Result: Various concentrations of MA along with paromomycin, miltefosine or allopurinol significantly inhibited (P<0.01 the proliferation of L. tropica amastigote stage in the macrophage cell line as compared with MA alone or positive control.Conclusion: Combination of Glucantime with paromomycin, miltefosine or allopuri­nol showed a synergistic effect on the clinical isolate of L. tropica in vitro. Use of combination therapy is a new hope and a logical basis for therapy of the pa­tients with cutaneous leishmaniasis. Further investigations are needed to evaluate the therapeutic effects of these drugs on the CL patients.

  13. Protein Profiling on Meglumine Antimoniate (Glucantime® Sensitive and Resistant L. tropica Isolates by 2- Dimentional Gel Electrophoresis: A Preliminary Study

    Directory of Open Access Journals (Sweden)

    R Hadighi

    2009-02-01

    Full Text Available Background: Glucantime® is the first- line drug for the treatment of all forms of leishmaniasis. Unfortunately, the prevalence of parasites becoming resistant to Glucantime® is increasing in several parts of the world including Iran. As protein is the most important target for drugs in response to a variety of signals including drugs so, it seems expression protein patterns in sensitive and resistant Leishmania parasites could greatly help us about the mechanisms of responses to antileishmanial drugs. In this study, we used 2-dimentional gel electrophoresis (2-DE method to determine protein expression profiles between drug (Glucantime® sensitive and resistant Leishmania tropica isolated from Iranian an­throponotic cutaneous leishmaniasis (ACL patients."nMethods: We used from the two confirmed genetically of Glucantime® sensitive (Mash-4 and resistant (Mash-927 field strains of L. tropica, isolated from ACL patients in north eastern Iran. The two Leishmania isolates were cultured, promastigotes were harvested followed by protein extraction using TCA/Aceton to study protein profiling, 2-DE was done and gels stained with silver nitrate."nResults: At least 2236 distinct protein spots were detected. Twelve spots out of them, showed significant changes in expression in resistant compared to sensitive isolates. Of these, 11 protein spots were up- and one was down-regulated."nConclusions: This preliminary study has showed that a number of proteins differentially expressed in drug (Glucan­time® resistance L. tropica and probably the role of these proteins are increasing the parasite resistance against the drug and delay in cell death.

  14. A mixed community of actinomycetes produce multiple antibiotics for the fungus farming ant Acromyrmex octospinosus

    OpenAIRE

    Barke Jörg; Seipke Ryan F; Grüschow Sabine; Heavens Darren; Drou Nizar; Bibb Mervyn J; Goss Rebecca JM; Yu Douglas W; Hutchings Matthew I

    2010-01-01

    This work was supported by a UEA-funded PhD studentship (JB) and an MRC Milstein award, G0801721 (MIH, RJMG and DY). MIH is a Research Councils UK Fellow. DY also received support from the Yunnan provincial government (20080A001) and the Chinese Academy of Sciences (0902281081). Background: Attine ants live in an intensely studied tripartite mutualism with the fungus Leucoagaricus gongylophorus, which provides food to the ants, and with antibiotic-producing actinomycete bacteria. One hypot...

  15. Metabolic engineering of antibiotic factories: New tools for antibiotic production in actinomycetes

    DEFF Research Database (Denmark)

    Weber, Tilmann; Charusanti, Pep; Musiol-Kroll, Ewa Maria

    2015-01-01

    Actinomycetes are excellent sources for novel bioactive compounds, which serve as potential drug candidates for antibiotics development. While industrial efforts to find and develop novel antimicrobials have been severely reduced during the past two decades, the increasing threat of multidrug...... them, and to express them in heterologous hosts in much higher throughput than before. These technologies now enable metabolic engineering approaches to optimize production yields and to directly manipulate the pathways to generate modified products....

  16. Three New 2-pyranone Derivatives from Mangrove Endophytic Actinomycete Strain Nocardiopsis sp. A00203

    Directory of Open Access Journals (Sweden)

    Yuemao Shen

    2010-10-01

    Full Text Available Three new 2-pyranone derivatives, namely Norcardiatones A (1, B (2 and C (3, were isolated from the agar cultures of the strain Nocardiopsis sp. A00203, a mangrove endophytic actinomycete. Their structures were elucidated by spectroscopic and mass-spectrometric analyses, including 1D-, 2D-NMR and HR Q-TOF-MS. Compound 1 showed week cytotoxicity against HeLa cells in MTT assay.

  17. Underground Cordon by Microorganisms-Part-III Role of Soil Inhabiting Actinomycetes

    Directory of Open Access Journals (Sweden)

    H. M. Dayal

    1989-04-01

    Full Text Available Certain strains of soil inhabiting actinomycetes were found to substantially corrode aluminium alloy (54-S which has bscn found tobe more resistant to bacterial or fungal corrosion in our earlier studies.These strains did not produce any corrosion on the mild steel and galvanised iron panels which were heavily corroded by bacteria and fungi. The corrosive isolates have been partialiy characterised after their isolation and purification. The extent of corrosion caused by eachstrain has been determined.

  18. Actinomycetes: a repertory of green catalysts with a potential revenue resource.

    Science.gov (United States)

    Prakash, Divya; Nawani, Neelu; Prakash, Mansi; Bodas, Manish; Mandal, Abul; Khetmalas, Madhukar; Kapadnis, Balasaheb

    2013-01-01

    Biocatalysis, one of the oldest technologies, is becoming a favorable alternative to chemical processes and a vital part of green technology. It is an important revenue generating industry due to a global market projected at $7 billion in 2013 with a growth of 6.7% for enzymes alone. Some microbes are important sources of enzymes and are preferred over sources of plant and animal origin. As a result, more than 50% of the industrial enzymes are obtained from bacteria. The constant search for novel enzymes with robust characteristics has led to improvisations in the industrial processes, which is the key for profit growth. Actinomycetes constitute a significant component of the microbial population in most soils and can produce extracellular enzymes which can decompose various materials. Their enzymes are more attractive than enzymes from other sources because of their high stability and unusual substrate specificity. Actinomycetes found in extreme habitats produce novel enzymes with huge commercial potential. This review attempts to highlight the global importance of enzymes and extends to signify actinomycetes as promising harbingers of green technology.

  19. Eco-taxonomic insights into actinomycete symbionts of termites for discovery of novel bioactive compounds.

    Science.gov (United States)

    Kurtböke, D Ipek; French, John R J; Hayes, R Andrew; Quinn, Ronald J

    2015-01-01

    Termites play a major role in foraging and degradation of plant biomass as well as cultivating bioactive microorganisms for their defense. Current advances in "omics" sciences are revealing insights into function-related presence of these symbionts, and their related biosynthetic activities and genes identified in gut symbiotic bacteria might offer a significant potential for biotechnology and biodiscovery. Actinomycetes have been the major producers of bioactive compounds with an extraordinary range of biological activities. These metabolites have been in use as anticancer agents, immune suppressants, and most notably, as antibiotics. Insect-associated actinomycetes have also been reported to produce a range of antibiotics such as dentigerumycin and mycangimycin. Advances in genomics targeting a single species of the unculturable microbial members are currently aiding an improved understanding of the symbiotic interrelationships among the gut microorganisms as well as revealing the taxonomical identity and functions of the complex multilayered symbiotic actinofloral layers. If combined with target-directed approaches, these molecular advances can provide guidance towards the design of highly selective culturing methods to generate further information related to the physiology and growth requirements of these bioactive actinomycetes associated with the termite guts. This chapter provides an overview on the termite gut symbiotic actinoflora in the light of current advances in the "omics" science, with examples of their detection and selective isolation from the guts of the Sunshine Coast regional termite Coptotermes lacteus in Queensland, Australia.

  20. Occupational allergic respiratory diseases in garbage workers: relevance of molds and actinomycetes.

    Science.gov (United States)

    Hagemeyer, O; Bünger, J; van Kampen, V; Raulf-Heimsoth, M; Drath, C; Merget, R; Brüning, Th; Broding, H C

    2013-01-01

    Exposures to molds and bacteria (especially actinomycetes) at workplaces are common in garbage workers, but allergic respiratory diseases due to these microorganisms have been described rarely. The aim of our study was a detailed analysis of mold or bacteria-associated occupational respiratory diseases in garbage workers. From 2002 to 2011 four cases of occupational respiratory diseases related to garbage handling were identified in our institute (IPA). Hypersensitivity pneumonitis (HP) was diagnosed in three subjects (cases 1-3, one smoker, two non-smokers), occupational asthma (OA) was diagnosed in one subject (case 4, smoker), but could not be excluded completely in case 2. Cases 1 and 2 worked in composting sites, while cases 3 and 4 worked in packaging recycling plants. Exposure periods were 2-4 years. Molds and actinomycetes were identified as allergens in all cases. Specific IgE antibodies to Aspergillus fumigatus were detected exclusively in case 4. Diagnoses of HP were essentially based on symptoms and the detection of specific IgG serum antibodies to molds and actinomycetes. OA was confirmed by bronchial provocation test with Aspergillus fumigatus in case 4. In conclusion, occupational HP and OA due to molds occur rarely in garbage workers. Technical prevention measures are insufficient and the diagnosis of HP is often inconclusive. Therefore, it is recommended to implement the full repertoire of diagnostic tools including bronchoalveolar lavage and high resolution computed tomography in the baseline examination.

  1. Mesophilic Actinomycetes in the natural and reconstructed sand dune vegetation zones of Fraser Island, Australia.

    Science.gov (United States)

    Kurtböke, D I; Neller, R J; Bellgard, S E

    2007-08-01

    The natural coastal habitat of Fraser Island located in the State of Queensland, Australia, has been disturbed in the past for mining of the mineral sand ilmenite. Currently, there is no information available on whether these past mining disturbances have affected the distribution, diversity, and survival of beneficial soil microorganisms in the sand dunes of the island. This in turn could deleteriously affect the success of the natural regeneration, plant growth, and establishment on the sand dunes. To support ongoing restoration efforts at sites like these mesophilic actinomycetes were isolated using conventional techniques, with particular emphasis on the taxa previously reported to produce plant-growth-promoting substances and providing support to mycorrhizal fungi, were studied at disturbed sites and compared with natural sites. In the natural sites, foredunes contained higher densities of micromonosporae replaced by increasing numbers of streptomycete species in the successional dune and finally leading to complex actinomycete communities in the mature hind dunes. Whereas in the disturbed zones affected by previous mining activities, which are currently being rehabilitated, no culturable actinomycete communities were detected. These findings suggest that the paucity of beneficial microflora in the rehabilitated sand dunes may be limiting the successful colonization by pioneer plant species. Failure to establish a cover of plant species would result in the mature hind dune plants being exposed to harsh salt and climatic conditions. This could exacerbate the incidence of wind erosion, resulting in the destabilization of well-defined and vegetated successional dunal zones.

  2. Isolation and in vitro selection of actinomycetes strains as potential probiotics for aquaculture

    Science.gov (United States)

    Bernal, Milagro García; Campa-Córdova, Ángel Isidro; Saucedo, Pedro Enrique; González, Marlen Casanova; Marrero, Ricardo Medina; Mazón-Suástegui, José Manuel

    2015-01-01

    Aim: This study was designed to describe a series of in vitro tests that may aid the discovery of probiotic strains from actinomycetes. Materials and Methods: Actinomycetes were isolated from marine sediments using four different isolation media, followed by antimicrobial activity and toxicity assessment by the agar diffusion method and the hemolysis of human blood cells, respectively. Extracellular enzymatic production was monitored by the hydrolysis of proteins, lipids and carbohydrates. Tolerance to different pH values and salt concentrations was also determined, followed by hydrophobicity analysis and genetic identification of the most promising strains. Results: Five out of 31 isolated strains showed antimicrobial activity against three Vibrio species. Three non-hemolytic strains (N7, RL8 and V4) among these active isolates yielded positive results in hydrophobicity tests and exhibited good growth at salt concentrations ranging from 0% to 10%, except strain RL8, which required a salt concentration >0.6%. Although these strains did not grow at pH<3, they showed different enzymatic activities. Phylogenetic analysis revealed that strains N7 and V4 have more than 99% identity with several Streptomyces species, whereas the closest matches to strain RL8 are Streptomyces panacagri and Streptomyces flocculus, with 98% and 98.2% similarity, respectively. Conclusion: Three actinomycetes strains showing probiotic-like properties were discovered using several in vitro tests that can be easily implemented in different institutions around the world. PMID:27047067

  3. Actinomycetes: A Repertory of Green Catalysts with a Potential Revenue Resource

    Directory of Open Access Journals (Sweden)

    Divya Prakash

    2013-01-01

    Full Text Available Biocatalysis, one of the oldest technologies, is becoming a favorable alternative to chemical processes and a vital part of green technology. It is an important revenue generating industry due to a global market projected at $7 billion in 2013 with a growth of 6.7% for enzymes alone. Some microbes are important sources of enzymes and are preferred over sources of plant and animal origin. As a result, more than 50% of the industrial enzymes are obtained from bacteria. The constant search for novel enzymes with robust characteristics has led to improvisations in the industrial processes, which is the key for profit growth. Actinomycetes constitute a significant component of the microbial population in most soils and can produce extracellular enzymes which can decompose various materials. Their enzymes are more attractive than enzymes from other sources because of their high stability and unusual substrate specificity. Actinomycetes found in extreme habitats produce novel enzymes with huge commercial potential. This review attempts to highlight the global importance of enzymes and extends to signify actinomycetes as promising harbingers of green technology.

  4. Actinomycete complexes in soils of industrial and residential zones in the city of Kirov

    Science.gov (United States)

    Shirokikh, I. G.; Solov'eva, E. S.; Ashikhmina, T. Ya.

    2014-02-01

    The number, diversity, and structure of the actinomycetal complexes in the soils of the industrial and residential zones of the city of Kirov are considered. The total content of mobile cadmium, zinc, lead, iron, and nickel in the soils of the industrial biotopes was 1.8 and 6.0 times higher than their concentration in the soils of the residential and background zones, respectively. In the heavy metal (HM)-polluted soils, the share of actinomycetes in the total number of prokaryotes and the relative abundance of the micromono-spores in the actinomycetal complex were much higher and the species diversity of the streptomycetes was lower than these characteristics in the soils of the residential zone. The differences in the composition of the mycelial prokaryote complexes appear to be related to the selective resistance of some of their representatives to heavy metals. The possibility to select the strains resistant to HMs and suitable for use in the bioremediation of polluted soils is considered.

  5. The prevalence of actinomycetes-like organisms found in cervicovaginal smears of 300 IUD wearers.

    Science.gov (United States)

    Jones, M C; Buschmann, B O; Dowling, E A; Pollock, H M

    1979-01-01

    The association of Actinomyces with IUD wearers has been widely documented and the possibility of the recognition of actinomycetes-like organisms in routine Papanicolaou-stained cervicovaginal smears has been reported. We conducted a retrospective study of IUD wearers to determine the prevalence and significance of actinomycetes-like organisms found in such smears. Three hundred smears from current IUD wearers were rescreened for actinomycetes-like organisms. Of this group, 200 patients were from a public health family planning clinic, and 100 were private patients. The incidence for the public health group was 25.5% and for the private patient group, 8%. A case history of actinomycosis is included. Findings such as other infectious agents, abnormal cytology and symptoms are also discussed. Although the presence of Actinomyces probably represents an opportunistic infection, the threat of pelvic actinomycosis with serious complications poses a management problem to the clinician when Actinomyces is reported in a routine Papanicolaou smear. Our findings lead us to question the practicality of the earlier recommendations of IUD removal and antibiotic therapy.

  6. Bioperspective of actinomycetes isolates from coastal soils: A new source of antimicrobial producers

    Directory of Open Access Journals (Sweden)

    Rattanaporn Srivibool

    2006-05-01

    Full Text Available Forty five soil samples were collected from four coastal islands on the east coast of Thailand: Chang, Hwai, Lao-yanai in Trat Province and Pai Islands in Chonburi Province. On 3 isolating media, Actinomycetes Isolation Agar, Starch Casein Agar and Glucose Asparagine Agar, 495 isolates of actinomycetes were found. Preliminary test to search for antimicrobial activity was done with Bacillus subtilis TISTR 008, Staphylococcus aureus TISTR 885, Staphylococus aureus TISTR 517 (ATCC 25923, Micrococcus luteus TISTR 884 and Pseudomonas aeruginosa TISTR 781 and Escherichia coli TISTR 887 (ATCC 25922. Fifty-eight actinomycetes were found to be antimicrobial-producing strains. From the morphological determination, cell wall diaminopimelic acid and sugars in whole-cell hydrolysate studies, among the 58 strains, Streptomyces sp. and Actinomadura sp. were the predominant genera. The other antibiotic active strains were Micromonospora sp., Microbispora sp., Nocardia sp., Pseudonocardia sp., Saccharomonospora sp., Streptoalloteichus sp. and Streptoverticillium sp. Most of them could inhibit gram-positive bacteria, especially M. luteus TISTR 884, and 8 strains (4 strains of Actinomadura, 2 strains of Micromonospora, 1 strain of Microbispora, and 1 strain of Streptomyces could inhibit both gram-positive and gram-negative bacteria.

  7. In-vitro sensitivity of Pakistani Leishmania tropica field isolate against buparvaquone in comparison to standard anti-leishmanial drugs.

    Science.gov (United States)

    Jamal, Qaisar; Khan, Nazma Habib; Wahid, Sobia; Awan, Mahwish Mustafa; Sutherland, Colin; Shah, Akram

    2015-07-01

    In this study, in vitro anti-leishmanial activity of buparvaquone was evaluated against promastigotes and intracellular amastigotes of Pakistani Leishmania tropica isolate KWH23 in relation to the current standard chemotherapy for leishmaniasis (sodium stibogluconate, sodium stibogluconate, amphotericin B and miltefosine). For buparvaquone, mean % inhibition in intracellular amastigotes at four different concentrations (1.35 µM, 0.51 µM, 0.17 µM and 0.057 µM) was 78%, 44%, 20% and 14% respectively, whereas, against promastigotes it was 89%, 77%, 45% and 35% respectively. IC50 values calculated to estimate the anti-leishmanial activity of buparvaquone against intra-cellular amastigotes and promastigotes was 0.53 µM (95% C.I. = 0.32-0.89) and 0.15 µM (95% C.I. = 0.01-1.84) respectively. Amphotericin B was the most potent in-vitro drug tested, with an IC50 of 0.075 µM (95% C.I. = 0.006-0.907) against promastigotes, and 0.065 µM (95% C.I. = 0.048-0.089) against intra-cellular amastigotes. Amphotericin B was more cytotoxic against THP1 cells, with an IC50 of 0.15 µM (95% C.I. = 0.01-0.95) and an apparent in-vitro therapeutic index of 2.0, than was buparvaquone, with an IC50 of 12.03 µM (95% C.I. = 5.36-26.96) against THP1 cells and a therapeutic index of 80.2. The study proposes that buparvaquone may be further investigated as a candidate drug for treatment of cutaneous leishmaniasis.

  8. Anticancer property of sediment actinomycetes against MCF-7 and MDA-MB-231 cell lines

    Institute of Scientific and Technical Information of China (English)

    Ravikumar S; Fredimoses M; Gnanadesigan M

    2012-01-01

    Objective: To investigate the anticancer property of marine sediment actinomycetes against two different breast cancer cell lines. Methods:In vitro anticancer activity was carried out against breast (MCF-7 and MDA-MB-231) cancer cell lines. Partial sequences of the 16s rRNA gene, phylogenetic tree construction, multiple sequence analysis and secondary structure analysis were also carried out with the actinomycetes isolates. Results: Of the selected five actinomycete isolates, ACT01 and ACT02 showed the IC50 value with (10.13±0.92) and (22.34±5.82)μg/mL concentrations, respectively for MCF-7 cell line at 48 h, but ACT01 showed the minimum (18.54±2.49 μg/mL) level of IC50 value with MDA-MB-231 cell line. Further, the 16s rRNA partial sequences of ACT01, ACT02, ACT03, ACT04 and ACT05 isolates were also deposited in NCBI data bank with the accession numbers of GQ478246, GQ478247, GQ478248, GQ478249 and GQ478250, respectively. The phylogenetic tree analysis showed that, the isolates of ACT02 and ACT03 were represented in group I and III, respectively, but ACT01 and ACT02 were represented in group II. The multiple sequence alignment of the actinomycete isolates showed that, the maximum identical conserved regions were identified with the nucleotide regions of 125 to 221st base pairs, 65 to 119th base pairs and 55, 48 and 31st base pairs. Secondary structure prediction of the 16s rRNA showed that, the maximum free energy was consumed with ACT03 isolate (-45.4 kkal/mol) and the minimum free energy was consumed with ACT04 isolate (-57.6 kkal/mol). Conclusions:The actinomycete isolates of ACT01 and ACT02 (GQ478246 and GQ478247) which are isolated from sediment sample can be further used as anticancer agents against breast cancer cell lines.

  9. The biodegradation of layered silicates under the influence of cyanobacterial-actinomycetes associations

    Science.gov (United States)

    Ivanova, Ekaterina

    2013-04-01

    The weathering of sheet silicates is well known to be related to local and global geochemical cycles. Content and composition of clay minerals in soil determine the sorption properties of the soil horizons, water-holding capacity of the soil, stickiness, plasticity, etc. Microorganisms have a diverse range of mechanisms of minerals' structure transformation (acid- and alkali formation, biosorption, complexing, etc). One of the methods is an ability of exopolysaccharide-formation, in particular the formation of mucus, common to many bacteria, including cyanobacteria. Mucous covers cyanobacteria are the specific econiches for other bacteria, including actinomycetes. The objective was to analyze the structural changes of clay minerals under the influence of the cyanobacterial-actinomycetes associative growth. The objects of the study were: 1) the experimental symbiotic association, consisting of free-living heterocyst-formative cyanobacterium Anabaena variabilis Kutz. ATCC 294132 and actinomycete Streptomyces cyaneofuscatus FR837630, 2) rock samples obtained from the Museum of the Soil Science Department of the Lomonosov Moscow State University: kaolinite, consisting of kaolin (96%) Al4 (OH) 8 [Si4O10]; mixed with hydromica, chlorite and quartz; vermiculite, consisting of vermiculite (Ca, Mg, ...)*(Mg, Fe)3(OH)2[(Si, Al)4O10]*4H2O and trioctahedral mica (biotite). The mineralogical compositions of the rocks were determined by the universal X-ray Diffractometer Carl Zeiss Yena. The operationg regime was kept constant (30 kv, 40 mA). The cultivation of the association of actinomycete S. cyanoefuscatus and cyanobacterium A. variabilis caused a reduction in the intensity of kaolinite and hydromica reflexes. However, since both (mica and kaolinite) components have a rigid structure, the significant structural transformation of the minerals was not revealed. Another pattern was observed in the experiment, where the rock sample of vermiculite was used as the mineral

  10. Succession of Actinomycetes During Composting Proccess of Dairy-Farm Waste Investigated by Culture-Dependent and Independent Approaches

    Directory of Open Access Journals (Sweden)

    Mukhlissul Faatih1

    2015-11-01

    Full Text Available Mesophilic, thermophilic, and maturation phases were recognized in composting proccess. Temperaturechanges influence the microbial communities in compost within composting proccess. Actinomycetes account for alarger part of compost microbial population. The aim of this research was to study succession of actinomycetescommunity during composting of dairy-farm waste investigated by culture-dependent and independentapproaches.In culture-independent method, the succession of actinomycetes community was analyzed by nestedpolymerasechain reaction of ribosomal intergenic spacer (nested-PCR RISA using spesific primer F243 and primerR23S followed by a second PCR using primers F968 and R23S. In culture-dependent method actinomycetes fromcompost were isolated on selective media, starch-nitrate medium and humic-acid + vitamins medium. DNA ofactinomycetes was extracted and amplified by repetitive sequence-based PCR (rep-PCR using primer BOXA1R. Thebanding patterns were used to generate dendrograms by UPGMA clustering with NTSYS program. Microcosmcontaining sterile rice-straw and water which is inoculated with each actinomycetes isolates was used for examiningthe ability of each isolate in rice-straw degradation.The experiment results showed that succession of both bacteria and actinomycetes was occured withincomposting proccess of dairy-farm waste. Analysed by culture-independent method revealed that the highestcommunity of compost’s bacteria was on mesophilic, thermophilic, and maturation phases, respectively. WhereasPCR-nested RISA resulted the highest population of actinomycetes was on thermophilic, maturation, and mesophilicphases, respectively. By culture-dependent method was obtained 29 actinomycetes isolates from mesophilic phase,23 isolates from thermophilic phase, and 19 isolates from maturation phase. Genetic diversity analysis of the obtainedisolates showed the presence of phylogenetic grouping on each phase of composting proccess. This result

  11. Monoterpenic aldehydes as potential anti-Leishmania agents: activity of Cymbopogon citratus and citral on L. infantum, L. tropica and L. major.

    Science.gov (United States)

    Machado, M; Pires, P; Dinis, A M; Santos-Rosa, M; Alves, V; Salgueiro, L; Cavaleiro, C; Sousa, M C

    2012-03-01

    In order to contribute for the search of new drugs for leishmaniasis, we study the susceptibility of Leishmania infantum, Leishmania tropica and Leishmania major to Cymbopogon citratus essential oil and major compounds, mrycene and citral. C. citratus and citral were the most active inhibiting L. infantum, L. tropica and L. major growth at IC(50) concentrations ranging from 25 to 52 μg/ml and from 34 to 42 μg/ml, respectively. L. infantum promastigotes exposed to essential oil and citral underwent considerable ultrastructural alterations, namely mitochondrial and kinetoplast swelling, autophagosomal structures, disruption of nuclear membrane and nuclear chromatin condensation. C. citratus essential oil and citral promoted the leishmanicidal effect by triggering a programmed cell death. In fact, the leishmanicidal activity was mediated via apoptosis as evidenced by externalization of phosphatidylserine, loss of mitochondrial membrane potential, and cell-cycle arrest at the G(0)/G(1) phase. Taken together, ours findings lead us to propose that citral was responsible for anti-Leishmania activity of the C. citratus and both may represent a valuable source for therapeutic control of leishmaniasis.

  12. Predicting the risk of an endemic focus of Leishmania tropica becoming established in South-Western Europe through the presence of its main vector, Phlebotomus sergenti Parrot, 1917.

    Science.gov (United States)

    Barón, S D; Morillas-Márquez, F; Morales-Yuste, M; Díaz-Sáez, V; Gállego, M; Molina, R; Martín-Sánchez, J

    2013-09-01

    The aim of the study was the construction of risk maps for exposure to Phlebotomus sergenti, the main vector of Leishmania tropica, with a view to identifying hot spots for the potential establishment of this parasite in the southwest of Europe. Data were collected on the presence/absence of this vector and the ecological and climatic characteristics of 662 sampling sites located in the southeast, centre and northeast of the Iberian Peninsula (south-western Europe). The environmental factors associated with the distribution of P. sergenti were determined. The best predictors for the presence of this dipteran were ‘altitude’, ‘land use’, ‘land surface temperature’, ‘aspect’, ‘adjacent land cover’, ‘absence of vegetation in wall’ and the ‘absence of PVC pipes in the drainage holes of retaining walls’. Risk maps for exposure to the vector were drawn up based on these variables. The validation of the predictive risk model confirmed its usefulness in the detection of areas with a high risk of P. sergenti being present. These locations represent potential hot spots for an autochthonous focus of L. tropica becoming established. The risk maps produced for P. sergenti presence revealed several areas in the centre and south of the Iberian Peninsula to be the most prone to this process, which would make it possible for the disease to enter south-western Europe.

  13. Seroprevalence of Leishmania infection and molecular detection of Leishmania tropica and Leishmania infantum in stray cats of İzmir, Turkey.

    Science.gov (United States)

    Can, Hüseyin; Döşkaya, Mert; Özdemir, H Gökhan; Şahar, Esra Atalay; Karakavuk, Muhammet; Pektaş, Bayram; Karakuş, Mehmet; Töz, Seray; Caner, Ayşe; Döşkaya, Aysu Değirmenci; İz, Sultan Gülce; Özbel, Yusuf; Gürüz, Yüksel

    2016-08-01

    Leishmaniasis caused by more than 20 species of genus Leishmania is transmitted by the bite of infected phlebotomine sand flies. The studies on Leishmania infection in cats is very few in Turkey and therefore we aimed to screen stray cats living in city of İzmir located in western Turkey using nested PCR targeting kinetoplast DNA and serological techniques (ELISA and IFA). Leishmania DNA positive samples were also studied by ITS1 real time PCR. Whole blood and serum samples were obtained from stray cats (n: 1101) living in different counties of İzmir. In serological assays, a serum sample was considered positive in 1:40 dilution in IFA and for ELISA a serum sample was accepted positive when the absorbance value (AV) exceeded the mean AV + Standard Deviation (SD) of the negative control serum samples. According to the results, the seropositivity rates were 10.8% (119/1101) and 15.2% (167/1101) by in house ELISA and IFA, respectively. Among serology coherent samples, the seropositivity rate was 11.1% (116/1047) as detected by both assays after discordant samples (n: 54) were discarded. Of the 1101 stray cats, six (0.54%) were positive by nested PCR while only one of these six samples was positive by ITS1 real time PCR. During PCR, three controls designated as Leishmania infantum, Leishmania tropica, and Leishmania major were used for species identification. According to nested PCR results, L. tropica was identified in two cats (no.76 and 95). In another cat (no. 269), there were two bands in which one of them was well-matched with L. infantum and the other band had ∼850 bp size which does not match with any controls. Remaining three cats (no. 86, 514, and 622) also had the ∼850 bp atypical band size. ITS1 real time PCR detected L. tropica in only one cat (no. 622) which showed an atypical band size in nested PCR. These results indicated that three cats with only one atypical band (no. 86, 514, and 622) and the cat with mixed infection (no. 269) were

  14. SELEKSI DAN PEMANFAATAN ACTINOMYCETES SEBAGAI MIKROBA ANTAGONIS YANG RAMAH LINGKUNGAN TERHADAP Fusarium oxysporum f.sp. cubense SECARA IN VITRO

    Directory of Open Access Journals (Sweden)

    I MADE SUDARMA

    2015-06-01

    Full Text Available A total of 119 different actinomycete isolate were recovered from banana crop habitats with and without Fusarium wilt disease symptom. These were than assessed for their antagonist ability against Fusarium oxysporum £sp. cubense (Foe in vitro. Results indicated that four of all actinomycete isolate active against Foe. The four of actinomycete isolates were Streptomyces sp. l (AAo4, Streptomyces sp.2 (AAo32 , Streptomyces sp.3 (AAo33 and Streptomyces sp. 4 (AAo35. It was can inhibit the Foe mycelium growth, 79,63%, 72,22%, 78,89% and 72,22% respectively. After tested with the 3 times replication, the four Streptomyces spp. isolate effective to control the Foe that attack Bali banana cultivars, such as Susu, Saba, Raja and Ketip.

  15. Screening of actinomycetes from earthworm castings for their antimicrobial activity and industrial enzymes

    Directory of Open Access Journals (Sweden)

    Vijay Kumar

    2012-03-01

    Full Text Available Actinomycetes from earthworm castings were isolated and screened for their antimicrobial activity and industrial enzymes. A total of 48 isolates were obtained from 12 samples of earthworm castings. Highest numbers of isolates were recovered from forest site (58.33 % as compared to grassland (25% and agricultural land (16.66%. The growth patterns, mycelial coloration of abundance actinomycetes were documented. The dominant genera Identified by cultural, morphological and physiological characteristics were Streptomyces (60.41% followed by Streptosporangium (10.41%, Saccharopolyspora (6.25% and Nocardia (6.25%. Besides these, other genera like Micromonospora, Actinomadura, Microbispora, Planobispora and Nocardiopsis were also recovered but in low frequency. Among the 48 isolates, 52.08% were found active against one or more test organisms. Out of 25 active isolates 16% showed activity against bacterial, human fungal as well as phytopathogens. Among 48 isolates 38, 32, 21, 20, 16 and 14 produced enzyme amylase, caseinase, cellulase, gelatinase, xylanase and lipase respectively while 10 isolates produced all the enzymes. More interestingly 2, 3, and 1 isolates produced amylase, xylanase and lipase at 45°C respectively. In the view of its antimicrobial activity as well as enzyme production capability the genus Streptomyces was dominant. The isolate EWC 7(2 was most promising on the basis of its interesting antimicrobial activity and was identified as Streptomyces rochei. The results of these findings have increased the scope of finding industrially important actinomycetes from earthworm castings and these organisms could be promising sources for industrially important molecules or enzymes.

  16. Isolation and characterization of potential antibiotic producing actinomycetes from water and sediments of Lake Tana, Ethiopia

    Institute of Scientific and Technical Information of China (English)

    Gebreselema Gebreyohannes; Feleke Moges; Samuel Sahile; Nagappan Raja

    2013-01-01

    To isolate, evaluate and characterize potential antibiotic producing actinomycetes from water and sediments of Lake Tana, Ethiopia. Methods: A total of 31 strains of actinomycetes were isolated and tested against Gram positive and Gram negative bacterial strains by primary screening. In the primary screening, 11 promising isolates were identified and subjected to solid state and submerged state fermentation methods to produce crude extracts. The fermented biomass was extracted by organic solvent extraction method and tested against bacterial strains by disc and agar well diffusion methods. The isolates were characterized by using morphological, physiological and biochemical methods. Results: The result obtained from agar well diffusion method was better than disc diffusion method. The crude extract showed higher inhibition zone against Gram positive bacteria than Gram negative bacteria. One-way analysis of variance confirmed most of the crude extracts were statistically significant at 95% confidence interval. The minimum inhibitory concentration and minimum bactericidal concentration of crude extracts were 1.65 mg/mL and 3.30 mg/mL against Staphylococcus aureus, and 1.84 mg/mL and 3.80 mg/mL against Escherichia coli respectively. The growth of aerial and substrate mycelium varied in different culture media used. Most of the isolates were able to hydrolysis starch and urea; able to survive at 5% concentration of sodium chloride; optimum temperature for their growth was 30 °C. Conclusions: The results of the present study revealed that freshwater actinomycetes of Lake Tana appear to have immense potential as a source of antibacterial compounds.

  17. Purification and characterization of protease enzyme from actinomycetes and its cytotoxic effect on cancer cell line (A549)

    Institute of Scientific and Technical Information of China (English)

    C Balachandran; V Duraipandiyan; S Ignacimuthu

    2012-01-01

    Objective: To isolate active actinomycetes from soil samples of Northern Himalayas and study their culture characterization, protease production and cytotoxic effects on cancer cell line (A549). Methods: Forty six strains of actinomycetes were isolated from the soil collected from Northern Himalayas, India. Isolation of actinomycetes was performed by serial dilution plate technique. Forty six isolated actinomycetes cultures were grown in ISP 2 medium to study the morphology and biochemical characteristics. Isolated strains were studied for protease enzyme production in skim milk agar medium with solubilising capacity. Seven isolates were studied for melanin pigmentation and different NaCl concentration. Effects of environmental conditions influencing protease enzyme production of seven isolated strains were also studied at different pH, temperature and metal ions (β-mercaptoethanol, dithiothreitol, iodoacetamide, MgSO4, CaCl2 and EDTA). The seven isolates were also studied for lytic enzyme activity using different bacteria and yeast such as Pseudomonas aeruginosa (P. aeruginosa), Enterococcus feacalis (E. feacalis), Escherishia coli (E. coli), Candida albicans (C. albicans), Bacillus subtilis (B. subtilis), Klebsiella pneumonia (K. pneumonia) and Staphylococcus aureus (S. aureus). Results: Isolates ERIA-31 and ERIA-33 produced more protease enzyme activity in modified nutrient agar media compared to other actinomycetes cultures. ERIA-31 and ERIA-33 were tested for cytotoxic effect in human adenocarcinoma cancer cell line (A549). IC50 for ERIA-31 was 57.04 μg/mL and IC50 for ERIA-33 was 55.07 μg/mL. Conclusion: Actinomycete being a protease producing bacteria has the potential for use in industrial purpose, pharmaceuticals, cytotoxic agent and its proteolytic activity. Isolates of ERIA-31 and ERIA-33 produced significant amount of protease enzymes.

  18. EXPLORATION OF ACTINOMYCETES ENDOPHYTICALLY ASSOCIATED WITH PIPER NIGRUM FOR POTENTIAL BIOACTIVITY

    Directory of Open Access Journals (Sweden)

    Jasim B.

    2015-02-01

    Full Text Available Piper nigrum is well known for its metabolite richness. So endophytic microorganisms that reside within such environments can be expected to have promising biosynthetic potential. The current study identified three endophytic actinomycetes with broad bioactivity which can have applications in natural product related pharmacological research. The Verrucosispora sp identified in the study was found to have promising anticancer and antimicrobial activities and Streptomyces sp. was found to have antioxidant activity. The results obtained are supported by many previous reports and this suggests the isolates obtained in the study to have the possible presence of potential known or novel compounds with broad spectrum of activity.

  19. Use of bacteriophage for the selective isolation of thermophilic actinomycetes from composted eucalyptus bark.

    Science.gov (United States)

    Kurtböke, D I; Murphy, N E; Sivasithamparam, K

    1993-01-01

    A method was developed to reduce the numbers of thermophilic bacteria on isolation plates, which in turn facilitated the detection and isolation of thermophilic actinomycetes. The method involves exposing the test material to bacteriophage suspensions prior to inoculation on isolation plates. This method was applied to composted eucalyptus bark samples, which were then inoculated on R8 and 1/2 TSA + 0.2% casein hydrolysate agar plates. The phage susceptibility of thermophilic bacteria provided a selective means of reducing their numbers on isolation plates and hence increased the numbers of Thermomonospora, Saccharopolyspora rectivirgula, and thermophilic Streptomyces spp. on these media in comparison with the numbers recorded from control plates.

  20. Characterization of cytotoxic compound from marine sediment derived actinomycete Streptomyces avidinii strain SU4

    Institute of Scientific and Technical Information of China (English)

    Sudha; S; Masilamani; Selvam; M

    2012-01-01

    Objective:To investigate the cytotoxic activity of actinomycete isolated from marine sediment.Methods:In the present study the DNA was isolated and the ITS region of 16s rRNA was amplified by polymerase chain reaction,using two universal bacterial primers,1492K(5’-GGTTACCTTG’TTAC GACTT-3’)and Eubac27F(5’-AGAGTTTGATCCTGGCTC AG-3’).The amplified products were purified using TIANgel mini purification kit,ligated to MD18-T simple vector(TaKaRa),and transformed into competent cells of Escherichia coli DH5α.16S rRNA gene fragment was sequenced using forward primer M13F(-47)and reverse primer M13R(-48).Blast search sequence similarity was found against the existing non-redundanl nucleotide sequence database thus,identified as Streptomyces sp SU,Streptomyces rubralavandulae strain SU1,Streptomyces cacaoi strain SU2,Streptomyces cavourensis strain SU3,Streptomyces avidinii strain SU4,Streptomyces globisporus strain SU5,Streptomyces variabilis strain SU6,Streptomyces coelicolor strain SU 7.Among the eight identified isolates,one actinomycete Streptomyces avidinii strain SU4 was selected for further study.Results:Crude extract of the actinomycete isolate exhibited IC50in 64.5μg against Hep-2 cell line,250μg in VERO cell line.This value is very close to the criteria of cytotoxicity activity for the crude extracts,as established by the American National Cancer Institute(NCI)is in IC50<30μg/mL.The CC MS analysis showed that the active principle might be 1,2-benzenedicarboxylic acid,bis(2-methylpropyl)ester(12.17%),isooctyl phthalate(15.29%)with the retention time 15.642 and 21.612,respectively.Conclusions:This study clearly proves that the marine sediment derived actinomycetes with bioactive metabolites can be expected to provide high quality biological material for high throughout biochemical and anticancer screening programs.These results help us to conclude that the potential of using metabolic engineering and post genomic

  1. Characterization of cytotoxic compound from marine sediment derived actinomycete Streptomyces avidinii strain SU4

    Institute of Scientific and Technical Information of China (English)

    Sudha S; Masilamani Selvam M

    2012-01-01

    To investigate the cytotoxic activity of actinomycete isolated from marine sediment. Methods: In the present study the DNA was isolated and the ITS region of 16s rRNA was amplified by polymerase chain reaction, using two universal bacterial primers, 1492R (5′-GGTTACCTTGTTAC GACTT-3′) and Eubac27F (5′-AGAGTTTGATCCTGGCTC AG-3′). The amplified products were purified using TIANgel mini purification kit, ligated to MD18-T simple vector (TaKaRa), and transformed into competent cells of Escherichia coli DH5α. 16S rRNA gene fragment was sequenced using forward primer M13F (-47) and reverse primer M13R (-48). Blast search sequence similarity was found against the existing non-redundant nucleotide sequence database thus, identified as Streptomyces sp SU, Streptomyces rubralavandulae strain SU1, Streptomyces cacaoi strain SU2, Streptomyces cavourensis strain SU3, Streptomyces avidinii strain SU4, Streptomyces globisporus strain SU5, Streptomyces variabilis strain SU6, Streptomycescoelicolor strain SU 7. Among the eight identified isolates, one actinomycete Streptomyces avidinii strain SU4 was selected for further study. Results: Crude extract of the actinomycete isolate exhibited IC50 in 64.5 μg against Hep-2 cell line, 250 μg in VERO cell line. This value is very close to the criteria of cytotoxicity activity for the crude extracts, as established by the American National Cancer Institute (NCI) is in IC50 < 30 μg /mL. The GC MS analysis showed that the active principle might be 1,2-benzenedicarboxylic acid, bis(2-methylpropyl) ester (12.17%), isooctyl phthalate (15.29%) with the retention time 15.642 and 21.612, respectively. Conclusions: This study clearly proves that the marine sediment derived actinomycetes with bioactive metabolites can be expected to provide high quality biological material for high throughout biochemical and anticancer screening programs. These results help us to conclude that the potential of using metabolic engineering and post genomic

  2. Investigation of antileishmanial activities of Tio2@Ag nanoparticles on biological properties of L. tropica and L. infantum parasites, in vitro.

    Science.gov (United States)

    Allahverdiyev, Adil M; Abamor, Emrah Sefik; Bagirova, Melahat; Baydar, Serap Yesilkir; Ates, Sezen Canim; Kaya, Figen; Kaya, Cengiz; Rafailovich, Miriam

    2013-09-01

    Leishmaniasis is a public health problem which is caused by protozoon parasites belonging to Leishmania species. The disease threatens approximately 350 million people in 98 countries all over the world. Cutaneous Leishmaniasis (CL) and Visceral Leishmaniasis (VL) are the mostly commonly seen forms of the disease. Treatment of the disease has remained insufficient since current antileishmanial drugs have several disadvantages such as toxicity, costliness and drug-resistance. Therefore, there is an immediate need to search for new antileishmanial compounds. TiO2@Ag nanoparticles (TiAg-Nps) have been demonstrated as promising antimicrobial agents since they provide inhibition of several types of bacteria. The basic antimicrobial mechanism of TiAg-Nps is the generation of reactive oxygen species (ROS). Even though Leishmania parasites are sensitive to ROS, there is no study in literature indicating antileishmanial activities of TiAg-Nps. Herein, in this study, TiAg-Nps are shown to possess antileishmanial effects on Leishmania tropica and Leishmania infantum parasites by inhibiting their biological properties such as viability, metabolic activity, and survival within host cells both in the dark and under visible light. The results indicate that TiAg-Nps decreased viability values of L. tropica, and L. infantum promastigotes 3- and 10-fold, respectively, in the dark, while these rates diminished approximately 20-fold for each species in the presence of visible light, in contrast to control. On the other hand, non-visible light-exposed TiAg-Nps inhibited survival of amastigotes nearly 2- and 2.5-fold; while visible light-exposed TiAg-Nps inhibited 4- and 4.5-fold for L. tropica and L. infantum parasites, respectively. Consequently, it was determined that non-visible light-exposed TiAg-Nps were more effective against L. infantum parasites while visible light-exposed TiAg-Nps exhibited nearly the same antileishmanial effect against both species. Therefore, we think that a

  3. Endophytic Actinomycetes: A Novel Source of Potential Acyl Homoserine Lactone Degrading Enzymes

    Directory of Open Access Journals (Sweden)

    Surang Chankhamhaengdecha

    2013-01-01

    Full Text Available Several Gram-negative pathogenic bacteria employ N-acyl-L-homoserine lactone (HSL quorum sensing (QS system to control their virulence traits. Degradation of acyl-HSL signal molecules by quorum quenching enzyme (QQE results in a loss of pathogenicity in QS-dependent organisms. The QQE activity of actinomycetes in rhizospheric soil and inside plant tissue was explored in order to obtain novel strains with high HSL-degrading activity. Among 344 rhizospheric and 132 endophytic isolates, 127 (36.9% and 68 (51.5% of them, respectively, possessed the QQE activity. The highest HSL-degrading activity was at 151.30±3.1 nmole/h/mL from an endophytic actinomycetes isolate, LPC029. The isolate was identified as Streptomyces based on 16S  rRNA gene sequence similarity. The QQE from LPC029 revealed HSL-acylase activity that was able to cleave an amide bond of acyl-side chain in HSL substrate as determined by HPLC. LPC029 HSL-acylase showed broad substrate specificity from C6- to C12-HSL in which C10HSL is the most favorable substrate for this enzyme. In an in vitro pathogenicity assay, the partially purified HSL-acylase efficiently suppressed soft rot of potato caused by Pectobacterium carotovorum ssp. carotovorum as demonstrated. To our knowledge, this is the first report of HSL-acylase activity derived from an endophytic Streptomyces.

  4. Screening of Marine Actinomycetes from Segara Anakan for Natural Pigment and Hydrolytic Activities

    Science.gov (United States)

    Asnani, A.; Ryandini, D.; Suwandri

    2016-02-01

    Marine actinomycetes have become sources of great interest to natural product chemistry due to their new chemical entities and bioactive metabolites. Since April 2010, we have screened actinobacteria from five sites that represent different ecosystems of Segara Anakan lagoon. In this present study we focus on specific isolates, K-2C which covers 1) actinomycetes identification based on morphology observation and 16S rRNA gene; 2) fermentation and isolation of pigment; 3) structure determination of pigment; and 4) hydrolytic enzymes characterization; Methodologies relevant to the studies were implemented accordingly. The results indicated that K-2C was likely Streptomyces fradiae strain RSU15, and the best fermentation medium should contain starch and casein with 21 days of incubation. The isolate has extracellular as well as intracellular pigments. Isolated pigments gave purple color with λmax of 529.00 nm. The pigment was structurally characterized. Interestingly, Streptomyces K-2C was able to produce potential hydrolytic enzymes such as amylase, cellulase, protease, lipase, urease, and nitrate reductase.

  5. Endophytic actinomycetes: a novel source of potential acyl homoserine lactone degrading enzymes.

    Science.gov (United States)

    Chankhamhaengdecha, Surang; Hongvijit, Suphatra; Srichaisupakit, Akkaraphol; Charnchai, Pattra; Panbangred, Watanalai

    2013-01-01

    Several Gram-negative pathogenic bacteria employ N-acyl-L-homoserine lactone (HSL) quorum sensing (QS) system to control their virulence traits. Degradation of acyl-HSL signal molecules by quorum quenching enzyme (QQE) results in a loss of pathogenicity in QS-dependent organisms. The QQE activity of actinomycetes in rhizospheric soil and inside plant tissue was explored in order to obtain novel strains with high HSL-degrading activity. Among 344 rhizospheric and 132 endophytic isolates, 127 (36.9%) and 68 (51.5%) of them, respectively, possessed the QQE activity. The highest HSL-degrading activity was at 151.30 ± 3.1 nmole/h/mL from an endophytic actinomycetes isolate, LPC029. The isolate was identified as Streptomyces based on 16S  rRNA gene sequence similarity. The QQE from LPC029 revealed HSL-acylase activity that was able to cleave an amide bond of acyl-side chain in HSL substrate as determined by HPLC. LPC029 HSL-acylase showed broad substrate specificity from C6- to C12-HSL in which C10HSL is the most favorable substrate for this enzyme. In an in vitro pathogenicity assay, the partially purified HSL-acylase efficiently suppressed soft rot of potato caused by Pectobacterium carotovorum ssp. carotovorum as demonstrated. To our knowledge, this is the first report of HSL-acylase activity derived from an endophytic Streptomyces.

  6. In vitro actinomycete biofilm development and inhibition by the polyene antibiotic, nystatin, on IUD copper surfaces.

    Science.gov (United States)

    Shanmughapriya, Santhanam; Francis, Arumugam Lency; Kavitha, Senthil; Natarajaseenivasan, Kalimuthusamy

    2012-01-01

    The presence of intrauterine contraceptive devices (IUDs) gives a solid surface for attachment and an ideal niche for biofilm to form and flourish. Pelvic actinomycosis is often associated with the use of IUDs. Treatment of IUD-associated pelvic actinomycosis requires the immediate removal of the IUD. Therefore, this article presents in vitro evidence to support the use of novel antibiotics in the treatment of actinomycete biofilms. Twenty one clinical actinomycetes isolates from endocervical swabs of IUD wearers were assessed for their biofilm forming ability. An in vitro biofilm model with three isolates, Streptomyces strain A4, Nocardia strain C15 and Nocardia strain C17 was subjected to treatment with nystatin. Inhibition of biofilm formation by nystatin was found to be concentration dependent, with MBIC50 values in the range 0.08-0.16 mg ml(-1). Furthermore, at a concentration of 0.16 mg ml(-1), nystatin inhibited the twitching motility of the isolates, providing evidence for a possible mechanism of biofilm inhibition.

  7. Screening Antimicrobial Activity of Actinomycetes Isolated from Raja Ampat, West Papua, Indonesia

    Directory of Open Access Journals (Sweden)

    Wellyzar Sjamsuridzal

    2012-04-01

    Full Text Available In the framework of exploitation of antimicrobial activity of Actinomycetes in Papua, one hundred isolates ofActinomycetes isolated from soil and leaf litter samples from various ecosystems in Batanta and Salawati Island, RajaAmpat, West Papua were screened. We obtained 200 crude extracts from 100 isolates based on two extraction phases.Nonpolar metabolites were extracted by ethyl acetate : methanol (4:1 solvent while the polar metabolites wereconcentrated using a freeze-drying method. Based on the agar dilution method, a total of 43 from 200(21.5% crudeextracts have antimicrobial activity against bacteria and yeasts (Escherichia coli NBRC 14237, Bacillus subtilis NBRC3134, Staphylococcus aureus NBRC 13276, Micrococcus luteus NBRC 1367, Candida albicans NBRC 1594 andSaccharomyces cerevisiae NBRC 10217. Some crude extracts showed anti-Gram negative (1.5%, anti-Gram positive(17% and antifungal (17% activities. Crude metabolites which were extracted using ethyl acetate : methanol weremore effective on antimicrobial activity (35% compared with water extraction (17%. Five most potential isolates (BL-13-5, BL-06-5, BL-14-2, BL-22-3, and Sl-36-1 were identified based on 16S rRNA gene sequence data. Sequencesimilarity search by BLAST program revealed that they show sequence similarities to Streptomyces kanamyceticus(92%, Streptomyces verne (92%, Streptomyces narbonensis (92%, Streptomyces malachitofuscus (98%, andStreptomyces hygroscopicus (96%, respectively.

  8. Streptomyces temperate bacteriophage integration systems for stable genetic engineering of actinomycetes (and other organisms).

    Science.gov (United States)

    Baltz, Richard H

    2012-05-01

    ϕC31, ϕBT1, R4, and TG1 are temperate bacteriophages with broad host specificity for species of the genus Streptomyces. They form lysogens by integrating site-specifically into diverse attB sites located within individual structural genes that map to the conserved core region of streptomycete linear chromosomes. The target genes containing the ϕC31, ϕBT1, R4, and TG1 attB sites encode a pirin-like protein, an integral membrane protein, an acyl-CoA synthetase, and an aminotransferase, respectively. These genes are highly conserved within the genus Streptomyces, and somewhat conserved within other actinomycetes. In each case, integration is mediated by a large serine recombinase that catalyzes unidirectional recombination between the bacteriophage attP and chromosomal attB sites. The unidirectional nature of the integration mechanism has been exploited in genetic engineering to produce stable recombinants of streptomycetes, other actinomycetes, eucaryotes, and archaea. The ϕC31 attachment/integration (Att/Int) system has been the most widely used, and it has been coupled with the ϕBT1 Att/Int system to facilitate combinatorial biosynthesis of novel lipopeptide antibiotics in Streptomyces fradiae.

  9. Antimethicilin resistance agents from marine actinomycetes from soil sediments of Lagos Lagoon

    Directory of Open Access Journals (Sweden)

    Davies Olabisi Flora

    2015-03-01

    Full Text Available Objective: To evaluate the isolation of actinomycetes strains with potential for producing antimicrobials with high methicilin resistance capability. Methods: The soil samples were collected from four different locations of Lagos lagoon. The Actinomycetes were isolated from the samples by serial dilution using spread plate method. Isolates were selected based on their cultural characteristics as well as their Gram reaction and phenotypically and molecularly characterized Streptomyces sp. Isolates were inoculated in starch casein and Kuster’s broth media and secondary metabolites were screened for antimicrobial activity against the following microorganisms: methicillin resistant Staphylococcus aureus, Staphylococcus aureus ATCC 29213, Escherichia coli ATCC 29522, Pseudomonas aeruginosa ATCC 27853, Candida albicans, Enterococcus faecalis ATCC 29212. Coagulase-negative staphylococci isolated from HIV patients were also used (Staphylococcus warneri, Staphylococcus xylosus and Staphylococcus epidermidis. The antimicrobial metabolites of the isolates were identified using gas chromatography-mass spectrometer. Results: Extracts from isolates ULS12 and ULS13 showed antimicrobial activity against methicillin resistant Staphylococcus aureus while ULK3 inhibited Candida albicans only. The gas chromatography-mass spectrometer data analysis showed the antibiotic profile of these isolates. Conclusions: The isolates ULS12 and ULS13 were found to display the highest antimicrobial activity against the test organisms and could be a potential source of new antibiotics.

  10. Isolation, screening and identification of novel isolates of Actinomycetes from India for antimicrobial applications

    Directory of Open Access Journals (Sweden)

    Vineeta Singh

    2016-12-01

    Full Text Available The search for novel bioactive compounds from the natural environment has been rapidly increased with the increase in multi-drug resistant (MDR pathogens. In the present study, the antimicrobial potential of novel actinomycetes has been evaluated by initial screening of six soil samples. Primary and secondary screening was performed against Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Candida albicans, Candida tropicalis, Trichophyton rubrum, and other MDR bacterial and fungal test strains, and at the end thirteen active isolates were selected for further study. Microbial strains were identified on the basis of growth conditions and other biochemical characters. Five most active microbial strains were identified using 16S rRNA sequence homology and designated as Streptomyces xanthophaeus MTCC 11938, Streptomyces variabilis MTCC 12266, Streptomyces xanthochromogenes MTCC 11937, Streptomyces levis EU 124569 and Streptomyces sp. NCIM 5500. Four antibacterial and three antifungal compounds isolated from the above five isolates were purified and partially characterized using UV absorption and IR spectra. Two antibacterial metabolites, belong to chromone and peptide antibiotic, respectively. The antifungal compounds were found to be of non-polyene nature. In conclusion, we study the isolation of novel bacterial strains of actinomycetes for producing novel compounds having antibacterial and antifungal activities from the unexplored agro-ecological niches of India. Also, this study paves the way for further characterization of these isolates of Streptomyces sp. for their optimum utilization for antimicrobial purposes.

  11. Antimethicilin resistance agents from marine actinomycetes from soil sediments of Lagos Lagoon

    Institute of Scientific and Technical Information of China (English)

    Davies Olabisi Flora; Adeleye Isaac Adeyemi; Wang Peng George

    2015-01-01

    Objective:To evaluate theisolation of actinomycetes strains with potential for producing antimicrobials with high methicilin resistance capability. Methods: The soil samples were collected from four different locations of Lagos lagoon. TheActinomycetes were isolated from the samples by serial dilution using spread plate method. Isolates were selected based on their cultural characteristics as well as their Gram reaction and phenotypically and molecularly characterizedStreptomyces sp. Isolates were inoculated in starch casein and Kuster’s broth media and secondary metabolites were screened for antimicrobial activity against the following microorganisms: methicillin resistant Staphylococcus aureus,Staphylococcus aureusATCC29213,Escherichia coliATCC 29522, Pseudomonas aeruginosaATCC27853,Candida albicans,Enterococcus faecalisATCC 29212. Coagulase-negative staphylococci isolated fromHIV patients were also used (Staphylococcus warneri,Staphylococcus xylosus andStaphylococcus epidermidis). The antimicrobial metabolites of the isolates were identified using gas chromatography-mass spectrometer. Results:Extracts from isolatesULS12 andULS13 showed antimicrobial activity against methicillin resistantStaphylococcus aureus whileULK3 inhibitedCandida albicans only. The gas chromatography-mass spectrometerdata analysis showed the antibiotic profile of these isolates. Conclusions: The isolatesULS12 andULS13 were found to display the highest antimicrobial activity against the test organisms and could be a potential source of new antibiotics.

  12. In vitro Antimicrobial Assay of Actinomycetes in Rice AgainstXanthomonas oryzae pv. oryzicola and as Potential Plant Growth Promoter

    Directory of Open Access Journals (Sweden)

    Erneeza Mohd Hata

    2015-12-01

    Full Text Available ABSTRACT The aim of this work was to invitro assay the antimicrobial activity of actinomycetes in rice against Xanthomonas oryzae pv. oryzicola and as potential plant growth promoter. A total of 92 actinomycete strains were isolated from different rice plant components and field locations. Of these, only 21.74% showed antagonistic activity against the Xoc pathogen. Molecular identification via 16s rRNA amplification revealed that 60% of the active antagonistic strains belonged to the genus Streptomyces. Isolates that demonstrated the highest antagonistic activity were also able to produce hydrolytic enzymes and plant growth-promoting hormones. Combination of preliminary screening based on in vitro antagonistic, hydrolytic enzyme and plant growth hormone activity facilitated the best selection of actinomycete candidates as evidenced by strains classification using cluster analysis (Ward's Method. Results from the preliminary screening showed that actinomycetes, especially Streptomycetes, could offer a promising source for both biocontrol and plant growth-promotion agents against BLS disease in rice.

  13. Different Physiological Roles of ATP- and PPi-Dependent Phosphofructokinase Isoenzymes in the Methylotrophic Actinomycete Amycolatopsis methanolica

    NARCIS (Netherlands)

    Alves, A.M.C.R.; Euverink, G.J.W.; Santos, H.; Dijkhuizen, L.

    2001-01-01

    Cells of the actinomycete Amycolatopsis methanolica grown on glucose possess only a single, exclusively PPi-dependent phosphofructokinase (PPi-PFK) (A. M. C. R. Alves, G. J. W. Euverink, H. J. Hektor, J. van der Vlag, W. Vrijbloed, D.H.A. Hondmann, J. Visser, and L. Dijkhuizen, J. Bacteriol. 176:682

  14. Identification of the minimal replicon of plasmid pMEA300 of the methylotrophic actinomycete Amycolatopsis methanolica

    NARCIS (Netherlands)

    Vrijbloed, J.W.; Jelínková, M.; Hessels, G.I.; Dijkhuizen, L.

    1995-01-01

    The actinomycete Amycolatopsis methanolica contains a 13.3 kb plasmid (pMEA300), capable of enhancing the spontaneous mutation frequency of its host. Depending on the growth medium pMEA300 is not only maintained as an integrated element but can additionally be present as a multicopy, autonomously re

  15. Use of the meganuclease I-SceI of Saccharomyces cerevisiae to select for gene deletions in actinomycetes.

    Science.gov (United States)

    Fernández-Martínez, Lorena T; Bibb, Mervyn J

    2014-11-18

    The search for new natural products is leading to the isolation of novel actinomycete species, many of which will ultimately require genetic analysis. Some of these isolates will likely exhibit low intrinsic frequencies of homologous recombination and fail to sporulate under laboratory conditions, exacerbating the construction of targeted gene deletions and replacements in genetically uncharacterised strains. To facilitate the genetic manipulation of such species, we have developed an efficient method to generate gene or gene cluster deletions in actinomycetes by homologous recombination that does not introduce any other changes to the targeted organism's genome. We have synthesised a codon optimised I-SceI gene for expression in actinomycetes that results in the production of the yeast I-SceI homing endonuclease which produces double strand breaks at a unique introduced 18 base pair recognition sequence. Only those genomes that undergo homologous recombination survive, providing a powerful selection for recombinants, approximately half of which possess the desired mutant genotype. To demonstrate the efficacy and efficiency of the system, we deleted part of the gene cluster for the red-pigmented undecylprodiginine complex of compounds in Streptomyces coelicolor M1141. We believe that the system we have developed will be broadly applicable across a wide range of actinomycetes.

  16. Evolution of cyclizing 5-aminolevulinate synthases in the biosynthesis of actinomycete secondary metabolites: outcomes for genetic screening techniques.

    Science.gov (United States)

    Petříčková, Kateřina; Chroňáková, Alica; Zelenka, Tomáš; Chrudimský, Tomáš; Pospíšil, Stanislav; Petříček, Miroslav; Krištůfek, Václav

    2015-01-01

    A combined approach, comprising PCR screening and genome mining, was used to unravel the diversity and phylogeny of genes encoding 5-aminolevulinic acid synthases (ALASs, hemA gene products) in streptomycetes-related strains. In actinomycetes, these genes were believed to be directly connected with the production of secondary metabolites carrying the C5N unit, 2-amino-3-hydroxycyclopent-2-enone, with biological activities making them attractive for future use in medicine and agriculture. Unlike "classical" primary metabolism ALAS, the C5N unit-forming cyclizing ALAS (cALAS) catalyses intramolecular cyclization of nascent 5-aminolevulinate. Specific amino acid sequence changes can be traced by comparison of "classical" ALASs against cALASs. PCR screening revealed 226 hemA gene-carrying strains from 1,500 tested, with 87% putatively encoding cALAS. Phylogenetic analysis of the hemA homologs revealed strain clustering according to putative type of metabolic product, which could be used to select producers of specific C5N compound classes. Supporting information was acquired through analysis of actinomycete genomic sequence data available in GenBank and further genetic or metabolic characterization of selected strains. Comparison of 16S rRNA taxonomic identification and BOX-PCR profiles provided evidence for numerous horizontal gene transfers of biosynthetic genes or gene clusters within actinomycete populations and even from non-actinomycete organisms. Our results underline the importance of environmental and evolutionary data in the design of efficient techniques for identification of novel producers.

  17. Azalomycin F4a 2-ethylpentyl ester, a new macrocyclic lactone, from mangrove actinomycete Streptomyces sp.211726

    Institute of Scientific and Technical Information of China (English)

    Gan Jun Yuan; Kui Hong; Hai Peng Lin; Jia Li

    2010-01-01

    Azalomycin F4a 2-ethylpentyl ester,a new 36-membered macrocyclic lactone antibiotic,was isolated from mangrove actinomycete Streptomyces sp.211726.Its structure was elucidated on the basis of spectroscopic data.The compound showed broad-spectrum antifungal activity and moderate cytotoxicity against human colon tumor cell HCT-116.

  18. Dicty_cDB: Contig-U14269-1 [Dicty_cDB

    Lifescience Database Archive (English)

    Full Text Available .. 81 3e-14 CP000667_2771( CP000667 |pid:none) Salinispora tropica CNB-440, co... 81 3e-14 DQ355149_1( DQ355149 |pid:none) Cercospora...2 2e-08 DQ991505_1( DQ991505 |pid:none) Cercospora nicotianae O-methyltran... 62 2e-08 BT036832_1( BT036832

  19. Biodegradation of anthracene by a novel actinomycete, Microbacterium sp. isolated from tropical hydrocarbon-contaminated soil.

    Science.gov (United States)

    Salam, Lateef B; Obayori, Oluwafemi S; Olatoye, Nojeem O

    2014-01-01

    A novel anthracene-degrading Gram-positive actinomycete, Microbacterium sp. strain SL10 was isolated from a hydrocarbon-contaminated soil at a mechanical engineering workshop in Lagos, Nigeria. The polluted soil had an unusually high total hydrocarbon content of 157 g/kg and presence of various heavy metals. The isolate tolerated salt concentration of more than 4%. It resisted cefotaxime, streptomycin and ciprofloxacin, but susceptible to meropenem, linezolid and vancomycin. The isolate exhibited growth rate and doubling time of 0.82 days(-1) and 0.84 days, respectively on anthracene. It degraded 57.5 and 90.12% of anthracene within 12 and 21 days, respectively while the rate of anthracene utilization by the isolate was 4.79 mg l(-1) d(-1). To the best of our knowledge, this is the first report of isolation and characterization of anthracene-degrading Microbacterium sp.

  20. Nocardia kroppenstedtii sp. nov., an actinomycete isolated from a lung transplant patient with a pulmonary infection.

    LENUS (Irish Health Repository)

    Jones, Amanda L

    2014-03-01

    A novel actinomycete, strain N1286(T), isolated from a lung transplant patient with a pulmonary infection, was provisionally assigned to the genus Nocardia. The strain had chemotaxonomic and morphological properties typical of members of the genus Nocardia and formed a distinct phyletic line in the Nocardia 16S rRNA gene tree. Isolate N1286(T) was most closely related to Nocardia farcinica DSM 43665(T) (99.8% gene sequence similarity) but could be distinguished from the latter by the low level of DNA-DNA relatedness. These strains were also distinguishable on the basis of a broad range of phenotypic properties. It is concluded that strain N1286(T) represents a novel species of the genus Nocardia for which the name Nocardia kroppenstedtii sp. nov. is proposed. The type strain is N1286(T) ( = DSM 45810(T) = NCTC 13617(T)).

  1. Semi-solid-state fermentation: a promising alternative for neomycin production by the actinomycete Streptomyces fradiae.

    Science.gov (United States)

    Machado, Isabel; Teixeira, José A; Rodríguez-Couto, Susana

    2013-06-10

    The production of neomycin by the actinomycete Streptomyces fradiae, under semi-solid-state fermentation conditions was the main subject of this study. Two supports (nylon sponge and orange peelings) were tested in order to determine the most suitable one for the production of neomycin by the above-mentioned microorganism. Nylon sponge led to the highest neomycin production, reaching a maximum value of 13,903 μg/mL on the 10th day of cultivation. As a control, the same experiment was performed under submerged fermentation (SmF) conditions, without solid support. Here the production of neomycin by S. fradiae was about 55-fold lower (i.e. 250 μg/mL) than that obtained for SSF.

  2. Antibiotic Producing Potentials of Three Freshwater Actinomycetes Isolated from the Eastern Cape Province of South Africa

    Directory of Open Access Journals (Sweden)

    Timothy Sibanda

    2010-07-01

    Full Text Available Crude extracts of three actinomycetes species belonging to Saccharopolyspora (TR 046 and TR 039 and Actinosynnema (TR 024 genera were screened for antibacterial activities against a panel of several bacterial strains. The extracts showed antibacterial activities against both gram-negative and gram-positive test bacteria with inhibition zones ranging from 8 to 28 mm (TR 046; 8 to15 mm (TR 039; and 10 to 13 mm (TR 024. The minimum inhibitory concentrations ranged from 0.078 to 10 mg/mL (TR 046; 5 to >10 mg/mL (TR 039; and 1.25 to 5 mg/mL (TR 024. Time-kill studies revealed that crude extract of TR 046 showed strong bactericidal activity against Bacillus pumilus (ATCC14884, reducing the bacterial load by 104 cfu/mL and 102 cfu/mL at 4× MIC and 2× MIC, respectively, after 6 h of exposure. Similarly, against Proteus vulgaris (CSIR 0030, crude extract of TR 046 achieved a 0.9log10 and 0.13log10 cfu/mL reduction at 5 mg/mL (4× MIC and 1.25 mg/mL (2× MIC after 12 h of exposure. The extract was however weakly bactericidal against two environmental bacterial strains (Klebsiella pneumoniae and Staphylococcus epidermidis; and against Pseudomonas aeruginosa (ATCC 19582: the extract showed bacteriostatic activities at all concentrations tested. These freshwater actinomycetes appear to have immense potential as a source of new antibacterial compound(s.

  3. Antibacterial activity of Pseudonocardia sp. JB05, a rare salty soil actinomycete against Staphylococcus aureus.

    Science.gov (United States)

    Jafari, Nesa; Behroozi, Reza; Farajzadeh, Davoud; Farsi, Mohammad; Akbari-Noghabi, Kambiz

    2014-01-01

    Staphylococcus aureus is a Gram-positive bacterium that causes many harmful and life-threatening diseases. Some strains of this bacterium are resistant to available antibiotics. This study was designed to evaluate the ability of indigenous actinomycetes to produce antibacterial compounds against S. aureus and characterize the structure of the resultant antibacterial compounds. Therefore, a slightly modified agar well diffusion method was used to determine the antibacterial activity of actinomycete isolates against the test microorganisms. The bacterial extracts with antibacterial activity were fractionated by silica gel and G-25 sephadex column chromatography. Also, the active fractions were analyzed by thin layer chromatography. Finally, the partial structure of the resultant antibacterial compound was characterized by Fourier transform infrared spectroscopy. One of the isolates, which had a broad spectrum and high antibacterial activity, was designated as Pseudonocardia sp. JB05, based on the results of biochemical and 16S rDNA gene sequence analysis. Minimum inhibitory concentration for this bacterium was 40 AU mL(-1) against S. aureus. The antibacterial activity of this bacterium was stable after autoclaving, 10% SDS, boiling, and proteinase K. Thin layer chromatography, using anthrone reagent, showed the presence of carbohydrates in the purified antibacterial compound. Finally, FT-IR spectrum of the active compound illustrated hydroxyl groups, hydrocarbon skeleton, and double bond of polygenic compounds in its structure. To the best of our knowledge, this is the first report describing the efficient antibacterial activity by a local strain of Pseudonocardia. The results presented in this work, although at the initial stage in bioactive product characterization, will possibly contribute toward the Pseudonocardia scale-up for the production and identification of the antibacterial compounds.

  4. SCREENING, ISOLATION AND PURIFICATION OF ANTIBIOTIC(S FROM MARINE ACTINOMYCETES

    Directory of Open Access Journals (Sweden)

    Attimarad S L

    2012-06-01

    Full Text Available As marine environmental conditions are extremely different from terrestrial ones, it is surmised that marine actinomycetes might produce novel bioactive compounds. Hence marine sediments, collected from the coastal areas of Gokharna and Muradeshwara of Karnataka state, were screened. Seventeen isolates were obtained on starch-casein agar media by soil dilution technique. However, only six isolates namely SUN-A2, SUN-A3, SUN-A4, SUN-A5, SUN-A7 and SUN-A15 showed significant antibacterial activity against both gram-positive and gram-negative bacteria. Further studies were carried out with the most active SUN-A2. Optimization of media, temperature and pH by shake flask fermentation indicated starch-casein, 28o C and pH 7 to be suitable for SUN-A2. The production of antibiotics began after 24 h reached maximum at 72 h and maintained at the same level up to 120 h. Ethyl acetate was used to extract antibacterial compounds from the culture filtrate. TLC was done on silica gel using ethyl acetate: methanol (6:4 and direct bioautography showed the presence of two active substance, one with Rf 0.8 more active than the other with Rf 0.4. Further purification is done by column chromatography using a mixture of dicholoromethane and ethyl acetate. The findings from this investigation reveal that the strain SUN-A2 in order exhibited superior antimicrobial activity to other sediment isolates of actinomycetes.

  5. Himalomycin A and cycloheximide-producing marine actinomycete from Lagos Lagoon soil sediment

    Institute of Scientific and Technical Information of China (English)

    Davies Olabisi Flora; Adeleye IsaacAdeyemi; Wang Peng George

    2015-01-01

    Objective: To isolate and screen Actinomycetes from Lagos Lagoon soil sediments for antibiotic production. Methods: Soil samples were collected from four different locations of Lagos Lagoon and were dried for 2 weeks. Actinomycetes were isolated by serial dilution using spread plate method on starch casein and Kuster’s agar supplemented with 80 μg/mL cycloheximide to prevent fungal growth. The plates were incubated at 28 °C for 1-2 weeks. Isolates were selected based on their cultural characteristics as well as their Gram’s reaction and subcultured on same media for isolation and incubated at 28 °C for 3 days. Pure cultures were maintained on nutrient agar slants at 4 °C. Thereafter, they were inoculated into starch casein and Kuster’s broth media and incubated at 28 °C for 8 days. The resulting crude extracts were screened for antimicrobial activity against the following microorganisms: methicillin resistant Staphylococcus aureus, Staphylococcus aureus ATCC 29213, Escherichia coli ATCC 29522, Pseudomonas aeruginosa ATCC 27853, Candida albicans and Enterococcus faecalis ATCC 29212. Coagulase-negative staphylococci isolated from HIV patients were also used (Staphylococcus warneri, Staphylococcus xylosus and Staphylococcus epidermidis). Extraction of secondary metabolites was carried out and analysed using gas chromatography-mass spectrometer. Results: All the isolates displayed varying antimicrobial activity against at least one of the test organisms. Himalomycin A was identified in the extract from isolate ULS7. The gas chromatography-mass spectrometer data analysis showed the antibiotic profile of these isolates. Conclusions: The isolate ULS7 was found to display the highest antimicrobial activity against the test organisms.

  6. Himalomycin A and cycloheximide-producing marine actinomycete from Lagos Lagoon soil sediment

    Directory of Open Access Journals (Sweden)

    Davies Olabisi Flora

    2015-05-01

    Full Text Available Objective: To isolate and screen Actinomycetes from Lagos Lagoon soil sediments for antibiotic production. Methods: Soil samples were collected from four different locations of Lagos Lagoon and were dried for 2 weeks. Actinomycetes were isolated by serial dilution using spread plate method on starch casein and Kuster’s agar supplemented with 80 μg/mL cycloheximide to prevent fungal growth. The plates were incubated at 28 °C for 1-2 weeks. Isolates were selected based on their cultural characteristics as well as their Gram’s reaction and subcultured on same media for isolation and incubated at 28 °C for 3 days. Pure cultures were maintained on nutrient agar slants at 4 °C. Thereafter, they were inoculated into starch casein and Kuster’s broth media and incubated at 28 °C for 8 days. The resulting crude extracts were screened for antimicrobial activity against the following microorganisms: methicillin resistant Staphylococcus aureus, Staphylococcus aureus ATCC 29213, Escherichia coli ATCC 29522, Pseudomonas aeruginosa ATCC 27853, Candida albicans and Enterococcus faecalis ATCC 29212. Coagulasenegative staphylococci isolated from HIV patients were also used (Staphylococcus warneri, Staphylococcus xylosus and Staphylococcus epidermidis. Extraction of secondary metabolites was carried out and analysed using gas chromatography-mass spectrometer. Results: All the isolates displayed varying antimicrobial activity against at least one of the test organisms. Himalomycin A was identified in the extract from isolate ULS7. The gas chromatography-mass spectrometer data analysis showed the antibiotic profile of these isolates. Conclusions: The isolate ULS7 was found to display the highest antimicrobial activity against the test organisms.

  7. Clear felling and burning effects on soil nitrogen transforming bacteria and actinomycetes population in Chittagong University campus, Bangladesh

    Institute of Scientific and Technical Information of China (English)

    S.M.Sirajul Haque; Rahima Ferdoshi; Sohag Miah; M.Nural Anwar

    2012-01-01

    The effect of forests clear felling and associated burning on the population of soil nitrogen transforming bacteria and actinomycetes are reported at three pair sites of Chittagong University campus,Bangladesh in monsoon tropical climate.Clear felled area or burnt site and 15-21 year mixed plantation of native and exotic species,situated side by side on low hill having Typic Dystrochrepts soil was represented at each pair site.At all the three pair sites,clear felled area or burnt site showed very significantly (p≤0.001) lower population of actinomycetes,Rhizobium,Nitrosomonas,Nitrobacter and ammonifying as well as denitrifying bacteria compared to their adjacent mixed plantation.From environmental consideration,this finding has implication in managing natural ecosystem.

  8. Distribution and generic composition of culturable marine actinomycetes from the sediments of Indian continental slope of Bay of Bengal

    Institute of Scientific and Technical Information of China (English)

    Surajit DAS; P.S.LYLA; S.AJMAL KHAN

    2008-01-01

    Actinomycetes population from continental slope sediment of the Bay of Bengal was studied.Samples were collected during two voyages of FORV Sagar Sampada in 2004 (May-June) and 2005 (July) respectively from 11 transects (each transect had ca.200m,500m,and 1000m depth stations).The physicochemical parameters of overlying water,and sediment samples were also recorded.The actinomycete population ranged from 5.17 to 51.94 CFU/g dry sediment weight and 9.38 to 45.22 CFU/g dry sediment weight during the two cruises respectively.No actinomycete colony was isolated from stations in 1000m depth.Two-way analysis of variance showed significant variation among stations (ANOVA two-way,P0.05),but no significance was found between the two cruises (ANOVA two-way,P0.05).Three actinomycetes genera were identified.Streptomyces was found to be the dominating one in both the cruises,followed by Micromonospora,and Actinomyces.The spore of Streptomyces isolates showed the abundance in spiral spore chain.Spore surface was smooth.Multiple regression analysis revealed that the influencing physico-chemical factors were sediment pH,sediment temperature,TOC,porosity,salinity,and pressure.The media used in the present study was prepared with seawater.Thus,they may represent an autochthonous marine flora and deny the theory of land runoff carriage into the sea for adaptation to the salinity of the seawater and sediments.

  9. Specificity of the mutualistic association between actinomycete bacteria and two sympatric species of Acromyrmex leaf-cutting ants

    DEFF Research Database (Denmark)

    Poulsen, M; Cafaro, M; Boomsma, J J;

    2005-01-01

    Acromyrmex leaf-cutting ants maintain two highly specialized, vertically transmitted mutualistic ectosymbionts: basidiomycete fungi that are cultivated for food in underground gardens and actinomycete Pseudonocardia bacteria that are reared on the cuticle to produce antibiotics that suppress...... the growth of Escovopsis parasites of the fungus garden. Mutualism stability has been hypothesized to benefit from genetic uniformity of symbionts, as multiple coexisting strains are expected to compete and, thus, reduce the benefit of the symbiosis. However, the Pseudonocardia symbionts are likely...

  10. Evolution of cyclizing 5-aminolevulinate synthases in the biosynthesis of actinomycete secondary metabolites: Outcomes for genetic screening techniques

    Directory of Open Access Journals (Sweden)

    Katerina ePetrickova

    2015-08-01

    Full Text Available A combined approach, comprising PCR screening and genome mining, was used to unravel the diversity and phylogeny of genes encoding 5-aminolevulinic acid synthases (ALASs, hemA gene products in streptomycetes-related strains. In actinomycetes, these genes were believed to be directly connected with the production of secondary metabolites carrying the C5N unit, 2-amino-3-hydroxycyclopent-2-enone, with biological activities making them attractive for future use in medicine and agriculture. Unlike classical primary metabolism ALAS, the C5N unit-forming cALAS (cyclizing ALAS catalyses intramolecular cyclization of nascent 5-aminolevulinate. Specific amino acid sequence changes can be traced by comparison of classical ALASs against cALASs. PCR screening revealed 226 hemA gene-carrying strains from 1,500 tested, with 87 % putatively encoding cALAS. Phylogenetic analysis of the hemA homologues revealed strain clustering according to putative type of metabolic product, which could be used to select producers of specific C5N compound classes. Supporting information was acquired through analysis of actinomycete genomic sequence data available in GeneBank and further genetic or metabolic characterization of selected strains. Comparison of 16S rRNA taxonomic identification and BOX-PCR profiles provided evidence for numerous horizontal gene transfers of biosynthetic genes or gene clusters within actinomycete populations and even from non-actinomycete organisms. Our results underline the importance of environmental and evolutionary data in the design of efficient techniques for identification of novel producers.

  11. Degradative crystal–chemical transformations of clay minerals under the influence of cyanobacterium-actinomycetal symbiotic associations

    Directory of Open Access Journals (Sweden)

    Ekaterina Ivanova

    2014-04-01

    Full Text Available Cyanobacteria and actinomycetes are essential components of soil microbial community and play an active role in ash elements leaching from minerals of the parent rock. Content and composition of clay minerals in soil determine the sorption properties of the soil horizons, water-holding capacity of the soil, stickiness, plasticity, etc. The transformative effect of cyanobacterial–actinomycetes associations on the structure of clay minerals – kaolinite, vermiculite, montmorillonite, biotite and muscovite – was observed, with the greatest structural lattice transformation revealed under the influence of association in comparison with monocultures of cyanobacterium and actinomycete. The range of the transformative effect depended both on the type of biota (component composition of association and on the crystal–chemical parameters of the mineral itself (trioctahedral mica – biotite, was more prone to microbial degradation than the dioctahedral – muscovite. The formation of the swelling phase – the product of biotite transformation into the mica–vermicullite mixed-layered formation was revealed as a result of association cultivation. Crystal chemical transformation of vermiculite was accompanied by the removal of potassium (К, magnesium (Mg and aluminum (Al from the crystal lattice. The study of such prokaryotic communities existed even in the early stages of the Earth's history helps to understand the causes and nature of the transformations undergone by the atmosphere, hydrosphere and lithosphere of the planet.contribution of treatments on structure induces and model parameters are discussed in the paper.

  12. Structural and Functional Characterizations of SsgB, a Conserved Activator of Developmental Cell Division in Morphologically Complex Actinomycetes

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Qingping; Traag, Bjørn A.; Willemse, Joost; McMullan, Daniel; Miller, Mitchell D.; Elsliger, Marc-André; Abdubek, Polat; Astakhova, Tamara; Axelrod, Herbert L.; Bakolitsa, Constantina; Carlton, Dennis; Chen, Connie; Chiu, Hsiu-Ju; Chruszcz, Maksymilian; Clayton, Thomas; Das, Debanu; Deller, Marc C.; Duan, Lian; Ellrott, Kyle; Ernst, Dustin; Farr, Carol L.; Feuerhelm, Julie; Grant, Joanna C.; Grzechnik, Anna; Grzechnik, Slawomir K.; Han, Gye Won; Jaroszewski, Lukasz; Jin, Kevin K.; Klock, Heath E.; Knuth, Mark W.; Kozbial, Piotr; Krishna, S. Sri; Kumar, Abhinav; Marciano, David; Minor, Wladek; Mommaas, A. Mieke; Morse, Andrew T.; Nigoghossian, Edward; Nopakun, Amanda; Okach, Linda; Oommachen, Silvya; Paulsen, Jessica; Puckett, Christina; Reyes, Ron; Rife, Christopher L.; Sefcovic, Natasha; Tien, Henry J.; Trame, Christine B.; van den Bedem, Henry; Wang, Shuren; Weekes, Dana; Hodgson, Keith O.; Wooley, John; Deacon, Ashley M.; Godzik, Adam; Lesley, Scott A.; Wilson, Ian A.; van Wezel, Gilles P.; (Leiden-MC); (SLAC); (Scripps); (UV); (UCSD); (Burnham)

    2010-01-20

    SsgA-like proteins (SALPs) are a family of homologous cell division-related proteins that occur exclusively in morphologically complex actinomycetes. We show that SsgB, a subfamily of SALPs, is the archetypal SALP that is functionally conserved in all sporulating actinomycetes. Sporulation-specific cell division of Streptomyces coelicolor ssgB mutants is restored by introduction of distant ssgB orthologues from other actinomycetes. Interestingly, the number of septa (and spores) of the complemented null mutants is dictated by the specific ssgB orthologue that is expressed. The crystal structure of the SsgB from Thermobifida fusca was determined at 2.6 {angstrom} resolution and represents the first structure for this family. The structure revealed similarities to a class of eukaryotic 'whirly' single-stranded DNA/RNA-binding proteins. However, the electro-negative surface of the SALPs suggests that neither SsgB nor any of the other SALPs are likely to interact with nucleotide substrates. Instead, we show that a conserved hydrophobic surface is likely to be important for SALP function and suggest that proteins are the likely binding partners.

  13. Evaluation of antimicrobial activity of the endophytic actinomycete R18(6 against multiresistant Gram-negative bacteria

    Directory of Open Access Journals (Sweden)

    Tiele Carvalho

    2016-03-01

    Full Text Available Endophytic actinomycetes are promising sources of antimicrobial substances. This study evaluates the activity of metabolites produced by the endophytic actinomycete R18(6 against Gram-negative bacteria multiresistant to antimicrobials. R18(6 isolate was grown in submerged cultures under different conditions: carbon source, temperature, pH and incubation time to optimize antimicrobials production. The actinomycete grown in base medium supplemented with 1% glucose, pH 6.5 and incubation at 30 ºC for 96 h with shaking at 100 rpm, exhibited the highest activity against the used Gram-negative bacteria. Minimum inhibitory concentration (MIC of the crude extract produced by the microorganism varied between 1/32 and 1/256. It had bactericide or bacteriostatic activity, depending on the Gram-negative organism. The active extract was stable at high temperatures, and unstable in medium containing proteolytic enzymes. Micromorphology of R18(6 was investigated by optical and scan microscopy, revealing that it was morphologically similar to the genusStreptomyces.

  14. ANALISIS KELAYAKAN TEKNIS DAN FINANSIAL DARI INVESTASI PENGADAAN TRAY DRYER BERBAHAN BAKAR BIOMASSA PADA USAHA ARANG TEMPURUNG KELAPA BERBASIS EKSPOR (Studi Kasus di Tropica Nucifera Industry – Yogyakarta

    Directory of Open Access Journals (Sweden)

    Fanny Widadie

    2013-11-01

    Full Text Available The purpose of the study is to assess the technical and financial feasibility of procurement investment Tray Dryer fueled biomass to operations of coconut shell charcoal briquette in PT. Tropica Nucifera Industry. The result showed that investment-Tray Dryer on cocnut shell charcoal briquette bussiness was highly feasibile both the technical and financial aspects. The technical aspect was seen that the quantity-production capabilities of coconut shell charcoal briquettes using a dryer-Tray Dryer could be increased 15 percent compared the previous consdition-used of solar energy. While the quality of the charcoal briquettes produced from Tray Dryer was a much butter quality, moisture content (6.39%; ash (2.65%; carbon-bound (85.83%, compared to using sunlight, water content (15.89; ash (2.57% and carbon-bound (77.32%.The financial aspects of procurement Tray Dryer investment that its value was more feasible than previous, nothing Tray Dryer. Coconut shell charcoal briquet enterprises without using Tray Dryer was feasible to be done with NPV 1,058,928.12, IRR 63%, Payback Period 1 year and 9 moths, Net B/C 2.25 and analysis of swicthcing value reached 20 percent. And after the business using Tray Drayer, the financial analysis was much more feasible with NPV 2,285,500,498.12, IRR 113%, Payback Period 11 months, Net B/C 3.5 and analysis of switching value reached 50 percent.

  15. 红树林海洋淤泥中放线菌的分离与鉴定%Identification and Analysis of Actinomycetes in Marine Mud of Mangrove

    Institute of Scientific and Technical Information of China (English)

    陈森洲; 刘菁; 陈建宏; 骆耐香; 钟毓娟; 蒋莲秀

    2011-01-01

    To explore actinomycetes resources in marine mud of mangrove in Beihai city of Guangxi province,actinomycete samples in marine mud of mangrove were separated by using seawater prepared Gause culture medium, total DNA of 10 typical strains of actinomycetes was screened, separated and extracted, 16Sr DNA was amplified by PCR with universal primers. The results from DNA sequencing and comparison identification of amplified product show that 10 typical strains of actinomycetes belong to 2 genera, 8 of which are common actinomycetes and belong to Streptomyces (80%), the other 2 are rare actinomycetes and belong to Nocardia (20%). All above indicate that there are abundant species of actinomycetes in marine mud of mangrove in Beihai city of Guangxi province.%为了解广西北海红树林海洋淤泥中的放线菌资源,采用海水配制高氏培养基分离红树林海洋淤泥中的放线菌样品,从中筛选、分离、提取lO株典型放线菌菌株总DNA,用放线菌通用引物对16Sr DNA进行PCR扩增,对获得的扩增结果进行DNA序列测定和对比鉴定.结果表明,10株典型放线菌菌株为2种菌属,其中有8株为链霉菌属(80%),为常见放线菌;有2株为拟诺卡氏菌属(20%),为稀有放线菌.表明,广西北海红树林海洋淤泥蕴含着种类丰富的放线菌.

  16. Genome Sequence and Analysis of the Soil Cellulolytic ActinomyceteThermobifida fusca

    Energy Technology Data Exchange (ETDEWEB)

    Lykidis, Athanasios; Mavromatis, Konstantinos; Ivanova, Natalia; Anderson, Iain; Land, Miriam; DiBartolo, Genevieve; Martinez, Michele; Lapidus, Alla; Lucas, Susan; Copeland, Alex; Richardson, Paul; Wilson,David B.; Kyrpides, Nikos

    2007-02-01

    Thermobifida fusca is a moderately thermophilic soilbacterium that belongs to Actinobacteria. 3 It is a major degrader ofplant cell walls and has been used as a model organism for the study of 4secreted, thermostable cellulases. The complete genome sequence showedthat T. fusca has a 5 single circular chromosome of 3642249 bp predictedto encode 3117 proteins and 65 RNA6 species with a coding densityof 85percent. Genome analysis revealed the existence of 29 putative 7glycoside hydrolases in addition to the previously identified cellulasesand xylanases. The 8 glycosyl hydrolases include enzymes predicted toexhibit mainly dextran/starch and xylan 9 degrading functions. T. fuscapossesses two protein secretion systems: the sec general secretion 10system and the twin-arginine translocation system. Several of thesecreted cellulases have 11 sequence signatures indicating theirsecretion may be mediated by the twin-arginine12 translocation system. T.fusca has extensive transport systems for import of carbohydrates 13coupled to transcriptional regulators controlling the expression of thetransporters and14 glycosylhydrolases. In addition to providing anoverview of the physiology of a soil 15 actinomycete, this study presentsinsights on the transcriptional regulation and secretion of16 cellulaseswhich may facilitate the industrial exploitation of thesesystems.

  17. Amycolatopsis thailandensis sp. nov., a poly(L-lactic acid)-degrading actinomycete, isolated from soil.

    Science.gov (United States)

    Chomchoei, Atchareeya; Pathom-Aree, Wasu; Yokota, Akira; Kanongnuch, Chartchai; Lumyong, Saisamorn

    2011-04-01

    A novel actinomycete that was capable of degrading poly(l-lactic acid), strain CMU-PLA07(T), was isolated from soil in northern Thailand. Strain CMU-PLA07(T) had biochemical, chemotaxonomic, morphological and physiological properties that were consistent with its classification in the genus Amycolatopsis. 16S rRNA gene sequence analysis showed that the isolate formed a phyletic line within the genus Amycolatopsis. Strain CMU-PLA07(T) was most similar to Amycolatopsis coloradensis IMSNU 22096(T) (99.5 % 16S rRNA gene sequence similarity) and Amycolatopsis alba DSM 44262(T) (99.4 %). However, strain CMU-PLA07(T) was distinguishable from the type strains of species of the genus Amycolatopsis on the basis of DNA-DNA relatedness and phenotypic data. Therefore, strain CMU-PLA07(T) is considered to represent a novel species of the genus Amycolatopsis, for which the name Amycolatopsis thailandensis sp. nov. is proposed. The type strain is CMU-PLA07(T) ( = JCM 16380(T) = BCC 38279(T)).

  18. Nocardiopsis arabia sp. nov., a halotolerant actinomycete isolated from a sand-dune soil.

    Science.gov (United States)

    Hozzein, Wael N; Goodfellow, Michael

    2008-11-01

    The taxonomic status of an unknown actinomycete isolated from a sand-dune soil was established using a polyphasic approach. Isolate S186(T) had chemotaxonomic and morphological properties consistent with its classification in the genus Nocardiopsis, grew on agar plates at NaCl concentrations of up to 15 % (w/v) and formed a distinct phyletic line in the Nocardiopsis 16S rRNA gene sequence tree. Its closest phylogenetic neighbours were Nocardiopsis chromatogenes, Nocardiopsis composta, Nocardiopsis gilva and Nocardiopsis trehalosi, with sequence similarity to the various type strains of 96.9 %, but it was readily distinguished from the type strains of these and related species using a range of phenotypic properties. It is apparent from the genotypic and phenotypic data that strain S186(T) belongs to a novel species of the genus Nocardiopsis, for which the name Nocardiopsis arabia sp. nov. is proposed. The type strain is S186(T) (=CGMCC 4.2057(T) =DSM 45083(T)).

  19. Antibiotic-producing ability by representatives of a newly discovered lineage of actinomycetes.

    Science.gov (United States)

    Busti, Elena; Monciardini, Paolo; Cavaletti, Linda; Bamonte, Ruggiero; Lazzarini, Ameriga; Sosio, Margherita; Donadio, Stefano

    2006-03-01

    The discovery of new antibiotics and other bioactive microbial metabolites continues to be an important objective in new drug research. Since extensive screening has led to the discovery of thousands of bioactive microbial molecules, new approaches must be taken in order to reduce the probability of rediscovering known compounds. The authors have recently isolated slow-growing acidophiles belonging to the novel genera Catenulispora and Actinospica within the order Actinomycetales. These strains, which likely belong to a new suborder, grow as filamentous mycelia, have a genome size around 8 Mb, and produce antimicrobial activities. In addition, a single strain harbours simultaneously genes encoding type I and type II polyeketide synthases, as well as non-ribosomal peptide synthetases. The metabolite produced by one strain was identified as a previously reported dimeric isochromanequinone. In addition, at least the Catenulispora strains appear globally distributed, since a PCR-specific signal could be detected in a significant fraction of acidic soils from different continents, and similar strains have been independently isolated from an Australian soil (Jospeh et al., Appl Environ Microbiol 69, 7210-7215, 2003). Thus, these previously uncultured actinomycetes share several features with Streptomyces and related antibiotic-producing genera, and represent a promising source of novel antibiotics.

  20. Cloning and characterization of the first actinomycete β-propeller phytase from Streptomyces sp. US42.

    Science.gov (United States)

    Boukhris, Ines; Farhat-Khemakhem, Ameny; Bouchaala, Kameleddine; Virolle, Marie-Joëlle; Chouayekh, Hichem

    2016-10-01

    A gene encoding an extracellular phytase was cloned for the first time from an Actinomycete, Streptomyces sp. US42 and sequenced. The sequence of this gene revealed an encoded polypeptide (PHY US42) exhibiting one and six residues difference with the putative phytases of Streptomyces lividans TK24 and Streptomyces coelicolor A3(2), respectively. The molecular modeling of PHY US42 indicated that this phytase belongs to the group of β-propeller phytases that are usually calcium-dependent. PHY US42 was purified and characterized. Its activity was calcium-dependent and maximal at pH 7 and 65 °C. The enzyme was perfectly stable at pH ranging from 5 to 10 and its thermostability was greatly enhanced in the presence of calcium. Indeed, PHY US42 maintained 80% of activity after 10 min of incubation at 75 °C in the presence of 5 mM CaCl2 . PHY US42 was also found to exhibit high stability after incubation at 37 °C for 1 h in the presence of bovine bile and digestive proteases like of pepsin, trypsin, and chymotrypsin. Considering its biochemical properties, PHY US42 could be used as feed additive in combination with an acid phytase for monogastric animals.

  1. Biofilm formation and partial biodegradation of polystyrene by the actinomycete Rhodococcus ruber: biodegradation of polystyrene.

    Science.gov (United States)

    Mor, Roi; Sivan, Alex

    2008-11-01

    Polystyrene, which is one of the most utilized thermoplastics, is highly durable and is considered to be non-biodegradable. Hence, polystyrene waste accumulates in the environment posing an increasing ecological threat. In a previous study we have isolated a biofilm-producing strain (C208) of the actinomycete Rhodococcus ruber that degraded polyethylene films. Formation of biofilm, by C208, improved the biodegradation of polyethylene. Consequently, the present study aimed at monitoring the kinetics of biofilm formation by C208 on polystyrene, determining the physiological activity of the biofilm and analyzing its capacity to degrade polystyrene. Quantification of the biofilm biomass was performed using a modified crystal violet (CV) staining or by monitoring the protein content in the biofilm. When cultured on polystyrene flakes, most of the bacterial cells adhered to the polystyrene surface within few hours, forming a biofilm. The growth of the on polystyrene showed a pattern similar to that of a planktonic culture. Furthermore, the respiration rate, of the biofilm, exhibited a pattern similar to that of the biofilm growth. In contrast, the respiration activity of the planktonic population showed a constant decline with time. Addition of mineral oil (0.005% w/v), but not non-ionic surfactants, increased the biofilm biomass. Extended incubation of the biofilm for up to 8 weeks resulted in a small reduction in the polystyrene weight (0.8% of gravimetric weight loss). This study demonstrates the high affinity of C208 to polystyrene which lead to biofilm formation and, presumably, induced partial biodegradation.

  2. Streptomyces alkalithermotolerans sp. nov., a novel alkaliphilic and thermotolerant actinomycete isolated from a soda lake.

    Science.gov (United States)

    Sultanpuram, Vishnuvardhan Reddy; Mothe, Thirumala; Mohammed, Farooq

    2015-02-01

    An alkaliphilic actinomycete, strain AC3(T), was isolated from Lonar soda lake, in India. Based on 16S rRNA gene sequence analysis it was identified that the strain belongs to the class Actinobacteria and was most closely related to Streptomyces sodiiphilus JCM 13581(T) (96.4 % sequence similarity), Streptomyces leeuwenhoekii DSM 42122(T) (96.1 %), Streptomyces albus NRRL B-2365(T) (96.1 %), Streptomyces panacagri Gsoil 519(T) (96.0 %), Streptomyces fimbriatus NBRC 15411(T) (95.9 %) and other members of the genus Streptomyces (cream substrate and white aerial mycelia on most tested media. The optimum pH for growth was determined to be 9.5-10.0 with no growth at pH 7.0. The DNA G+C content of strain AC3(T) was determined to be 71.2 mol %. The results of the polyphasic analysis allowed a clear differentiation of strain AC3(T) from all other members of the genus Streptomyces. Strain AC3(T) is thus considered to represent a novel member of the genus Streptomyces, for which the name Streptomyces alkalithermotolerans sp. nov. is proposed. The type strain is AC3(T) (=KCTC 29497(T) = JCM 30167(T)).

  3. Biotechnological potential of endophytic actinomycetes associated with Asteraceae plants: isolation, biodiversity and bioactivities.

    Science.gov (United States)

    Tanvir, Rabia; Sajid, Imran; Hasnain, Shahida

    2014-04-01

    Endophytic actinomycetes from five Asteraceae plants were isolated and evaluated for their bioactivities. From Parthenium hysterophorus, Ageratum conyzoides, Sonchus oleraceus, Sonchus asper and Hieracium canadense, 42, 45, 90, 3, and 2 isolates, respectively, were obtained. Of the isolates, 86 (47.2 %) showed antimicrobial activity. Majority of the isolates were recovered from the roots (n = 127, 69.7 %). The dominant genus was Streptomyces (n = 96, 52.7 %), while Amycolatopsis, Pseudonocardia, Nocardia and Micromonospora were also recovered. Overall, 36 of the 86 isolates were significantly bioactivity while 18 (20.9 %) showed strong bioactivity. In total, 52.1 and 66.6 % showed potent cytotoxicity and antioxidant activities. The LC50 for 15 strains was <20 μg/ml. Compared to the ascorbate standard (EC50 0.34 μg/ml), all isolates gave impressive results with notable EC50 values of 0.65, 0.67, 0.74 and 0.79 μg/ml.

  4. Streptomyces gamaensis sp. nov., a novel actinomycete with antifungal activity isolated from soil in Gama, Chad.

    Science.gov (United States)

    Zhao, Shanshan; Ye, Lan; Liu, Chongxi; Abagana, Adam Yacoub; Zheng, Weiwei; Sun, Pengyu; Li, Jiansong; Xiang, Wensheng; Wang, Xiangjing

    2016-12-22

    During an investigation exploring potential sources of novel species and natural products, a novel actinomycete with antifungal activity, designated strain NEAU-Gz11(T), was isolated from a soil sample, which was collected from Gama, Chad. The isolate was found to have morphological and chemotaxonomic characteristics typical of members of the genus Streptomyces. 16S rRNA gene sequence similarity studies showed that strain NEAU-Gz11(T) belongs to the genus Streptomyces with high sequence similarity to Streptomyces hiroshimensis JCM 4098(T) (98.0 %). Similarities to other type strains of the genus Streptomyces were lower than 98.0 %. However, the physiological and biochemical characteristics and low levels of DNA-DNA relatedness could differentiate the isolate genotypically and phenotypically from S. hiroshimensis JCM 4098(T). Therefore, the strain is concluded to represent a novel species of the genus Streptomyces, for which the name Streptomyces gamaensis sp. nov. is proposed. The type strain is NEAU-Gz11(T) (=CGMCC 4.7304(T)=DSM 101531(T)).

  5. Actinomadura gamaensis sp. nov., a novel actinomycete isolated from soil in Gama, Chad.

    Science.gov (United States)

    Abagana, Adam Yacoub; Sun, Pengyu; Liu, Chongxi; Cao, Tingting; Zheng, Weiwei; Zhao, Shanshan; Xiang, Wensheng; Wang, Xiangjing

    2016-06-01

    A novel single spore-producing actinomycete, designated strain NEAU-Gz5(T), was isolated from a soil sample from Gama, Chad. A polyphasic taxonomic study was carried out to establish the status of this strain. The diamino acid present in the cell wall is meso-diaminopimelic acid. Glucose, mannose and madurose occur in whole cell hydrolysates. The polar lipids were found to consist of diphosphatidylglycerol, phosphatidylethanolamine, phosphatidylinositol mannoside and an unidentified glycolipid. The predominant menaquinones were identified as MK-9(H8) and MK-9(H6). The predominant cellular fatty acids were found to be C16:0, iso-C15:0, iso-C16:0 and C18:0 10-methyl. Phylogenetic analysis based on the 16S rRNA gene showed that strain NEAU-Gz5(T) belongs to the genus Actinomadura and is closely related to Actinomadura oligospora JCM 10648(T) (ATCC 43269(T); 98.3 % similarity). However, the low level of DNA-DNA relatedness and some different phenotypic characteristics allowed the strain to be distinguished from its close relatives. Therefore, it is concluded that strain NEAU-Gz5(T) represents a novel species of the genus of Actinomadura, for which the name Actinomadura gamaensis sp. nov. is proposed. The type strain is NEAU-Gz5(T) (= CGMCC 4.7301(T) = DSM 100815(T)).

  6. Generic and functional diversity in endophytic actinomycetes from wild Compositae plant species at South Sinai - Egypt.

    Science.gov (United States)

    El-Shatoury, Sahar A; El-Kraly, Omnia A; Trujillo, Martha E; El-Kazzaz, Waleed M; El-Din, El-Sayeda Gamal; Dewedar, Ahmed

    2013-09-01

    The diversity of culturable endophytic actinomycetes associated with wild Compositae plants is scantily explored. In this study, one hundred and thirty one endophytic actinobacteria were isolated from ten Compositae plant species collected from South Sinai in Egypt. Microscopic and chemotaxonomic investigation of the isolates indicated fourteen genera. Rare genera, such as Microtetraspora, and Intrasporangium, which have never been previously reported to be endophytic, were identified. Each plant species accommodated between three to eight genera of actinobacteria and unidentified strains were recovered from seven plant species. The generic diversity analysis of endophytic assemblages grouped the plant species into three main clusters, representing high, moderate and low endophytic diversity. The endophytes showed high functional diversity, based on forty four catabolic and plant growth promotion traits; providing some evidence that such traits could represent key criteria for successful residence of endophytes in the endosphere. Stress-tolerance traits were more predictive measure of functional diversity differences between the endophyte assemblages (Shannon's index, p = 0.01). The results indicate a potential prominent role of endophytes for their hosts and emphasize the potency of plant endosphere as a habitat for actinobacteria with promising future applications.

  7. Diversity and Bioactivity of Actinomycetes from Marine Sediments of the Yellow Sea

    Institute of Scientific and Technical Information of China (English)

    ZHANG Shumin; YE Liang; TANG Xuexi

    2012-01-01

    Among the 116 actinomycetes collected from marine sediments of the Yellow Sea,56 grew slowly and appeared after 2-3 weeks of incubation.Among the 56 strains,only 3 required seawater (SW) for growth,and 21 grew well in the medium prepared with SW rather than distilled water (DW),while the remaining 32 grew well either with SW or with DW.Six representatives with different morphological characteristics,including 1 SW-requiring strain and 5 well-growing with SW strains,were selected for phylogenetic analysis based on 16S rRNA gene.Two strains belong to Micrococcaceae and Nocardiopsaceae respectively.The other 4strains belong to the family of Streptomycetaceae.In the analyzed 6 strains,one was related to Nocardiopsis spp.and the other three were related to Streptomyces spp.,representing new taxa.Bioactivity testing of fermentation products from 3 SW-requiring strains and 21 well-growing with SW strains revealed that 17 strains possessed remarkable activities against gram-positive pathogen or/and tumor cells,suggesting that they were prolific resources for natural drug discovery.

  8. Hydrophobic nature and effects of culture conditions on biofilm formation by the cellulolytic actinomycete Thermobifida fusca

    Directory of Open Access Journals (Sweden)

    Almaris N. Alonso

    2015-09-01

    Full Text Available Thermobifida fusca produces a firmly attached biofilm on nutritive and non-nutritive surfaces, such as cellulose, glass, plastic, metal and Teflon®. The ability to bind to surfaces has been suggested as a competitive advantage for microbes in soil environments. Results of previous investigations indicated that a Gram-positive cellulolytic soil bacteria, Cellulomonas uda, a facultative aerobe, specifically adhered to nutritive surfaces forming biofilms, but cells did not colonize non-nutritive surfaces. Cell surface hydrophobicity has been implicated in the interactions between bacteria and the adhesion to surfaces. It was recently described that the cellulolytic actinomycete T. fusca cells hydrophobicity was measured and compared to the cellulolytic soil bacteria C. uda. Also, T. fusca biofilm formation on non-nutritive surface, such as polyvinyl chloride, was examined by testing various culture ingredients to determine a possible trigger mechanism for biofilm formation. Experimental results showed that partitioning of bacterial cells to various hydrocarbons was higher in T. fusca cells than in C. uda. The results of this study suggest that the attachment to multiple surfaces by T. fusca could depend on nutrient availability, pH, salt concentrations, and the higher hydrophobic nature of bacterial cells. Possibly, these characteristics may confer T. fusca a selective advantage to compete and survive among the many environments it thrives.

  9. Diversity and bioactivity of actinomycetes from marine sediments of the Yellow Sea

    Science.gov (United States)

    Zhang, Shumin; Ye, Liang; Tang, Xuexi

    2012-03-01

    Among the 116 actinomycetes collected from marine sediments of the Yellow Sea, 56 grew slowly and appeared after 2-3 weeks of incubation. Among the 56 strains, only 3 required seawater (SW) for growth, and 21 grew well in the medium prepared with SW rather than distilled water (DW), while the remaining 32 grew well either with SW or with DW. Six representatives with different morphological characteristics, including 1 SW-requiring strain and 5 well-growing with SW strains, were selected for phylogenetic analysis based on 16S rRNA gene. Two strains belong to Micrococcaceae and Nocardiopsaceae respectively. The other 4 strains belong to the family of Streptomycetaceae. In the analyzed 6 strains, one was related to Nocardiopsis spp. and the other three were related to Streptomyces spp., representing new taxa. Bioactivity testing of fermentation products from 3 SW-requiring strains and 21 well-growing with SW strains revealed that 17 strains possessed remarkable activities against gram-positive pathogen or/and tumor cells, suggesting that they were prolific resources for natural drug discovery.

  10. Trehalose lipid biosurfactants produced by the actinomycetes Tsukamurella spumae and T. pseudospumae.

    Science.gov (United States)

    Kügler, Johannes H; Muhle-Goll, Claudia; Kühl, Boris; Kraft, Axel; Heinzler, Raphael; Kirschhöfer, Frank; Henkel, Marius; Wray, Victor; Luy, Burkhard; Brenner-Weiss, Gerald; Lang, Siegmund; Syldatk, Christoph; Hausmann, Rudolf

    2014-11-01

    Actinomycetales are known to produce various secondary metabolites including products with surface-active and emulsifying properties known as biosurfactants. In this study, the nonpathogenic actinomycetes Tsukamurella spumae and Tsukamurella pseudospumae are described as producers of extracellular trehalose lipid biosurfactants when grown on sunflower oil or its main component glyceryltrioleate. Crude extracts of the trehalose lipids were purified using silica gel chromatography. The structure of the two trehalose lipid components (TL A and TL B) was elucidated using a combination of matrix-assisted laser desorption/ionization time-of-flight/time-of-flight/tandem mass spectroscopy (MALDI-ToF-ToF/MS/MS) and multidimensional NMR experiments. The biosurfactants were identified as 1-α-glucopyranosyl-1-α-glucopyranosid carrying two acyl chains varying of C4 to C6 and C16 to C18 at the 2' and 3' carbon atom of one sugar unit. The trehalose lipids produced demonstrate surface-active behavior and emulsifying capacity. Classified as risk group 1 organisms, T. spumae and T. pseudospumae hold potential for the production of environmentally friendly surfactants.

  11. Antibiotic pigment from desert soil actinomycetes; biological activity, purification and chemical screening

    Directory of Open Access Journals (Sweden)

    Selvameenal L

    2009-01-01

    Full Text Available An actinomycete strain, Streptomyces hygroscopicus subsp. ossamyceticus (strain D10 was isolated from Thar Desert soil, Rajasthan during the year 2006 and found to produce a yellow color pigment with antibiotic activity. Crude pigment was produced from strain D10 by solid state fermentation using wheat bran medium followed by extraction with ethyl acetate. The antimicrobial activity of the crude pigment was evaluated against drug resistant pathogens such as methicillin-resistant Staphylococcus aureus, vancomycin-resistant Staphylococcus aureus, extended spectrum b-lactamase producing cultures of Escherichia coli, Pseudomonas aeruginosa and Klebsiella sp. About 420 mg of crude pigment was produced per 10 g of wheat bran medium. In the disc diffusion method the crude ethyl acetate extract showed a minimum of 10 mm inhibition against Klebsiella sp. and maximum of 19 mm of inhibition against Escherichia coli. The crude pigment was partially purified using thin layer chromatography with the solvent system chloroform:methanol (30:70 and the Rf value was calculated as 0.768. Antimicrobial activity of the partially purified compound from thin layer chromatography was determined using the bioautography method. The purified pigment showed minimum of 15 mm inhibition against Klebsiella sp. and a maximum of 23 mm of inhibition against vancomycin-resistant Staphylococcus aureus in the disc diffusion method. Based on the results of chemical screening, the pigment was tentatively identified as group of sugar containing molecules.

  12. 16S rRNA-based PCR-DGGE analysis of actinomycete communities in fields with continuous cotton cropping in Xinjiang, China.

    Science.gov (United States)

    Zhang, Wei; Long, XuanQi; Huo, XiangDong; Chen, YiFeng; Lou, Kai

    2013-08-01

    The purpose of this study was to examine the variations in the microbial community structure of soil actinomycetes in fields with continuous cropping of cotton in Xinjiang Autonomous Region, China. Soil samples were collected from four depths in fields with 7-year continuous cotton cropping. The community structure of soil actinomycetes was examined using the 16S rRNA-based polymerase chain reaction-density gradient gel electrophoresis (PCR-DGGE) techniques. The microbial diversity indices of the soil samples from different depths generally decreased along with the period of continuous cotton cropping. When the period of continuous cropping of cotton reached 5 years, the diversity indices rose again and gradually stabilized at a level slightly lower than that of soils with original ecology (i.e., 0-year cotton cropping). Cluster analysis showed that at the 1-20-cm depth, the actinomycete community structure of the soil subjected to 1-year cotton cropping was similar to that of soil subjected to 0-year cotton cropping, whereas that of soils after 3-year continuous cotton cropping showed high similarity. At the 21-40-cm depth, the actinomycete community structure showed various changes but generally recovered to its original pattern after repeated fluctuations. Principal component analysis showed that at the 1-30-cm depth, the actinomycete community structure varied similarly regardless of the period of continuous cotton cropping. In contrast, there were no clear actinomycete community structure variation trends at the 31-40-cm soil depth. Homology comparison of sequences recovered from the DGGE bands showed that the obtained sequences shared similarities >88 %. Alignment with the known homologous sequences indicated a lack of microorganisms related to soil-borne cotton diseases. Continuous cotton cropping exerted significant influences on the community structure of soil actinomycetes in Xinjiang Autonomous Region, which were largely determined by the soil depth and

  13. 植物内生放线菌多样性研究进展%Research Progress in Diversity of Endophytic Actinomycetes

    Institute of Scientific and Technical Information of China (English)

    冯天祥; 陆可茵; 陆兰依塔; 陈海敏; 盛清

    2015-01-01

    植物内生放线菌作为植物内生菌资源的一大类,具有丰富的多样性,其次级代谢产物也十分丰富,而且还具有各种生物学活性。通过了解植物内生放线菌资源的多样性,可以对其产生的生物活性物质进行筛选和分析,从而筛选出具有良好药理活性的物质应用于临床。从植物内生放线菌宿主植物、组织分布、种类和数量以及活性基因4个方面综述了植物内生放线菌的多样性资源,介绍植物内生放线菌新的微生物物种,总结了植物内生放线菌目前研究中存在的问题及展望。%Endophytic actinomycetes display abundant diversity and have a capacity to produce a huge number of sec-ondary metabolites exhibiting a broad variety of biological activities as a kind of endophyte resources.Biological activi-ties produced by endophytic actinomycetes are screened and analyzed via understanding the biodiversity of endophytic actinomycetes resources so that favorable pharmacological active substances were screened for clinical diseases.Re-cently, with the development of researches about endophytic actinomycetes, many novel microorganism species were reported.This review focuses on diversity resources of endophytic actinomycetes from four aspects:host plants of en-dophytic actinomycetes, distribution in host plants tissue, species and number diversity and active gene and introduces the researches of novel endophytic actinomycetes species.Finally, this article summarizes the problems of endophytic actinomycetes at present researches and gives the possible further research direction.Endophytic actinomycetes which are emerging microbial resources have an important effect on science researches and progress of mankind.

  14. Investigation on Actinomycetes Population in Yuxi Normal University%玉溪师范学院校园内土壤放线菌资源调查

    Institute of Scientific and Technical Information of China (English)

    陈艳; 李淑英; 刘家忠; 李红梅; 陈丽君; 刘菊安

    2012-01-01

    [Objective] Actinomycetes population in Yuxi normal university was investigated to provide information on the development and the utilization of actinomycetes resource. [Method] Ten soil samples from plant rhizosphere in Yuxi normal university were collected. Actinomycetes were isolated by spreading the samples on Gao 1 agar medium. Isolaets were identified at genus level.[Result] The number of actinomycetes was different in different plant rhizosphere. Streptomyces dominated. [Conclusion] Actinomycetes populations were rich in the soil of Yuxi normal university. Streptomyces dominated, mainly for the inerogriseus and the griseofuscus.%[目的]调查玉溪师范学院校园内土壤的放线菌资源,为云南放线菌资源开发利用提供资料.[方法]从玉溪师范学院校园内采集10种植物根际土壤,采用涂布平板法分离,用高氏一号培养基培养,采用国内通用的方法进行鉴定.[结果]不同植物根际分离到的放线菌数量不同;链霉菌占绝对优势.[结论]玉溪师院校园内土壤中放线菌资源丰富,链霉菌占绝对优势,主要为烬灰类群、灰褐类群.

  15. Comparison of the Proteome Profiling of Iranian isolates of Leish¬mania tropica, L. major and L. infantum by Two- Dimen¬sional Electrophoresis (2-DE and Mass-spectrometry

    Directory of Open Access Journals (Sweden)

    Homa HAJJARAN

    2015-12-01

    Full Text Available Background: The mechanisms of virulence and species differences of Leishmania parasites are under the influence of gene expression regulations at posttranscriptional stages. In Iran, L. major and L. tropica are known as principal agents of cutaneous leishmaniasis, while L. infantum causes visceral leishmaniasis.Methods: As a preliminary study, we compared the proteome mapping of the above three Iranian isolates of Leishmania species through the 2-dimension electrophoresis (2-DE, and identified the prominent proteins by Liquid Chromatography (LC mass spectrometry.Results: We reproducibly detected about 700 protein spots in each species by using the Melanie software. Totally, 264 proteins exhibited significant changes among 3 species. Forty nine protein spots identified in both L. tropica and L. major were similar in position in the gel, whereas only 35 of L. major proteins and 10 of L. tropica proteins were matched with those of L. infantum. Having identified 24 proteins in the three species, we sought to pro­vide possible explanations for their differential expression patterns and discuss their rele­vance to cell biology.Conclusion: The comparison of proteome profiling pattern of the 3 species identified limit up and limit down regulated or absent /present proteins. In addition, the LC-MS data analy­sis showed that most of the protein spots with differential abundance in the 3 species are involved in cell motility and cytoskeleton, cell signaling and vesicular trafficking, intracellu­lar survival / proteolysis, oxidative stress defense, protein synthesis, protein ubiquitina­tion / proteolysis, and stress related proteins. Differentially proteins distributed among the species maybe implicated in host pathogenecity interactions and parasite tropism to cutaneous or visceral tissue macrophages

  16. Antifungal Production of a Strain of Actinomycetes spp Isolated from the Rhizosphere of Cajuput Plant: Selection and Detection of Exhibiting Activity Against Tested Fungi

    Directory of Open Access Journals (Sweden)

    Alimuddin A

    2015-11-01

    Full Text Available Actinomycetes are bacteria known to constitute a large part of the rhizosphere microbiota. Their isolation is an important step for screening of new bioactive compounds. Culturable actinomycetes populations from cajuput plant rhizosphere soils in Wanagama I Forest UGM Yogyakarta were collected to study about their antifungal activity. Among 17 of a total 43 isolates that showed activity were screened for producing antifungi substances. Screening for antifungal activity of isolates were performed with dual culture bioassay in vitro. One isolate that was designated as Streptomyces sp.GMR-22 was the strongest against all tested fungi and appeared promising for a sources of antifungal. Culture’s supernatant and mycelia were extracted with chloroform, ethyl acetate and methanol, respectively. Antifungal activity of crude extracts was tested by diffusion method against tested fungi. The result indicates that isolates of actinomycetes from cajuput plant rhizosphere could be an interesting sources of antifungal bioactive substances.

  17. Nonomuraea flavida sp. nov., a novel species of soil actinomycete isolated from Aconitum napellus rhizosphere.

    Science.gov (United States)

    Chen, Shaofeng; Shi, Jindi; Li, Dan; Wu, Yingying; Huang, Yaojian

    2015-11-01

    A novel actinomycete strain, YN-5-1T, isolated from the rhizosphere soil of a medicinal plant, Aconitum napellus, was characterized by a polyphasic approach to determine its taxonomic position. The strain showed highest 16S rRNA gene sequence similarities of 97.3, 97.2 and 97.1 % to Nonomuraea turkmeniaca DSM 43926T, Nonomuraea ferruginea DSM 43553T and Nonomuraea candida DSM 45086T, respectively. A wide range of genotypic and phenotypic characteristics, as well as levels of DNA-DNA relatedness between strain YN-5-1T and N. turkmeniaca DSM 43926T (57.46 %), N. ferruginea DSM 43553T (53.50 %) and N. candida DSM 45086T (48.80 %), distinguished the novel isolate from its closest phylogenetic neighbours. The morphological characteristics of strain YN-5-1T were typical of the genus Nonomuraea. Chemotaxonomic characteristics, such as diagnostic diamino acid of the peptidoglycan, whole-cell sugars, phospholipid type, major menaquinone and major fatty acids, further supported the assignment of strain YN-5-1T to the genus Nonomuraea. The G+C content of the genomic DNA was 72.1 mol%. Based on the above data, strain YN-5-1T is considered to represent a novel species of the genus Nonomuraea, for which the name Nonomuraea flavida sp. nov. is proposed. The type strain is YN-5-1T ( = CCTCC AB 2012909T = KCTC 29143T).

  18. Sphaerisporangium dianthi sp. nov., an endophytic actinomycete isolated from a root of Dianthus chinensis L.

    Science.gov (United States)

    Xing, Jia; Liu, Chongxi; Zhang, Yuejing; He, Hairong; Zhou, Ying; Li, Lianjie; Zhao, Junwei; Liu, Shuanghe; Wang, Xiangjing; Xiang, Wensheng

    2015-01-01

    A novel actinomycete, designated strain NEAU-CY18(T), was isolated from the root of a Chinese medicinal plant Dianthus chinensis L and subjected to a polyphasic taxonomic study. The novel strain was found to develop spherical sporangia with non-motile spores on aerial mycelium. The cell-wall peptidoglycan was found to contain meso-diaminopimelic acid. The whole-cell sugars were identified as madurose, mannose, ribose, galactose and glucose. The phospholipid profile was found to contain diphosphatidylglycerol, phosphatidylmethylethanolamine, phosphatidylethanolamine, hydroxy-phosphatidylmethylethanolamine, phosphatidylglycerol, phosphatidylinositol, phosphatidylinositol mannosides and an unidentified phospholipid. The predominant menaquinones were identified as MK-9(H4), MK-9(H2) and MK-9(H6). The major fatty acids were identified as C17:0 10-methyl, iso-C16:0 and C16:0. EzTaxon-e analysis of the 16S rRNA gene sequence indicated that the strain belongs to the genus Sphaerisporangium and was most closely related to Sphaerisporangium cinnabarinum JCM 3291(T) (98.9 %) and Sphaerisporangium melleum JCM 13064(T) (98.3 %). Phylogenetic analysis based on the 16S rRNA gene sequence indicated that strain NEAU-CY18(T) forms a monophyletic clade with S. cinnabarinum JCM 3291(T), an association that was supported by a bootstrap value of 97 % in the neighbour-joining tree and also recovered with the maximum-likelihood algorithm. Comparisons of some phenotypic properties and low DNA-DNA relatedness values enabled the strain to be differentiated from S. cinnabarinum JCM 3291(T) and S. melleum JCM 13064(T). Therefore, it is concluded that strain NEAU-CY18(T) represents a novel Sphaerisporangium species, for which the name Sphaerisporangium dianthi sp. nov. is proposed. The type strain is NEAU-CY18(T) ( = CGMCC 4.7132(T) = DSM 46736(T)).

  19. Identification and Antibiosis of a Novel Actinomycete Strain RAF-11 Isolated From Iraqi Soil.

    Directory of Open Access Journals (Sweden)

    Rabah Forar Laidi

    2013-04-01

    Full Text Available A total of 35 actinomycetes strains were isolated from and around Baghdad, Iraq, at a depth of 5-10 m, by serial dilution agar plating method. Nineteen out of them showed noticeable antimicrobial activities against at least, to one of the target pathogens. Five among the nineteen were active against both Gram positive and Gram negative bacteria, yeasts and moulds. The most active isolate, strain RAF-11, based on its largest zone of inhibition and strong antifungal activity, especially against Candida albicans and Aspergillus niger, the causative of candidiasis and aspergillosis respectively, was selected for identification. Morphological and chemical studies indicated that this isolate belongs to the genus Streptomyces. Analysis of the 16S rDNA sequence showed a high similarity, 98 %, with the most closely related species, Streptomyces labedae NBRC 15864T/AB184704, S. erythrogriseus LMG 19406T/AJ781328, S. griseoincarnatus LMG 19316T/AJ781321 and S. variabilis NBRC 12825T/AB184884, having the closest match. From the taxonomic features, strain RAF-11 matched with S. labedae, in the morphological, physiological and biochemical characters, however it showed significant differences in morphological characteristics with this nearest species, S. labedae, which encourage us to consider our starin as a novel isolate and was given the suggested name, Streptomyces labedae strain RAF-11. ISP-4 broth medium supplemented with glucose and soybean powder at concentrations of 1g % and 0.1g % as carbon and nitrogen sources respectively, for 120h incubation at 28 °C, increased the active compounds production, where we recorded a strong activity against yeasts, 42mm inhibition zone against Candida albicans, 41mm against C. pseudotropicalis, 40mm against C. tropicalis, followed by 38mm against Rhodotorula minota and Aspergillus niger then, 35mm against both Aspergillus flavus and Bacillus subtilis. N-butanol was best solvent for antibiotic extraction compared to

  20. Diketopiperazine Derivatives from the Marine-Derived Actinomycete Streptomyces sp. FXJ7.328

    Directory of Open Access Journals (Sweden)

    Weiming Zhu

    2013-03-01

    Full Text Available Five new diketopiperazine derivatives, (3Z,6E-1-N-methyl-3-benzy lidene-6-(2S-methyl-3-hydroxypropylidenepiperazine-2,5-dione (1, (3Z,6E-1-N-methyl-3-benzylidene-6-(2R-methyl-3-hydroxypropylidenepiperazine-2,5-dione (2, (3Z,6Z-3- (4-hydroxybenzylidene-6-isobutylidenepiperazine-2,5-dione (3, (3Z,6Z-3-((1H-imidazol-5-yl-methylene-6-isobutylidenepiperazine-2,5-dione (4, and (3Z,6S-3-benzylidene-6-(2S-but-2-ylpiperazine-2,5-dione (5, were isolated from the marine-derived actinomycete Streptomyces sp. FXJ7.328. The structures of 1–5 were determined by spectroscopic analysis, CD exciton chirality, the modified Mosher’s, Marfey’s and the C3 Marfey’s methods. Compound 3 showed modest antivirus activity against influenza A (H1N1 virus with an IC50 value of 41.5 ± 4.5 μM. In addition, compound 6 and 7 displayed potent anti-H1N1 activity with IC50 value of 28.9 ± 2.2 and 6.8 ± 1.5 μM, respectively. Due to the lack of corresponding data in the literature, the 13C NMR data of (3Z,6S-3-benzylidene-6-isobutylpiperazine-2,5-dione (6 were also reported here for the first time.

  1. Thermodynamics of a Ca(2+)-dependent highly thermostable alkaline protease from a haloalkliphilic actinomycete.

    Science.gov (United States)

    Gohel, S D; Singh, S P

    2015-01-01

    An alkaline protease from salt-tolerant alkaliphilic actinomycetes, Nocardiopsis alba OK-5 was purified by a single-step hydrophobic interaction chromatography and characterized. The purified protease with an estimated molecular mass of 20 kDa was optimally active at 70 °C in 0-3 M NaCl and 0-100 mM Ca(2+) displaying significant stability at 50-80 °C. The enzyme was stable at 80 °C in 100 mM Ca(2+) with Kd of 17 × 10(-3) and t1/2 of 32 min. The activation energy (Ea), enthalpy (ΔH*), and entropy (ΔS*) for the protease deactivation calculated in the presence of 200 mM Ca(2+) were 38.15 kJ/mol, 35.49 kJ/mol and 183.48 J/mol, respectively. The change in free energy (ΔG*) for protease deactivation at 60 °C in 200 mM Ca(2+) was 95.88 kJ/mol. Decrease in ΔH* reflected reduced cooperativity of deactivation and unfolding. The enzyme was intrinsically stable that counteracted heat denaturation by a weak cooperativity during the unfolding. Further, the enzyme was highly stable in the presence of various cations, surfactants, H2O2, β-mercaptoethanol, and commercial detergents. The compatibility of the enzyme with various cations, surfactants, and detergent matrices suggests its suitability as an additive in the detergents and peptide synthesis.

  2. Rare actinomycetes Nocardia caishijiensis and Pseudonocardia carboxydivorans as endophytes, their bioactivity and metabolites evaluation.

    Science.gov (United States)

    Tanvir, Rabia; Sajid, Imran; Hasnain, Shahida; Kulik, Andreas; Grond, Stephanie

    2016-04-01

    Two strains identified as Nocardia caishijiensis (SORS 64b) and Pseudonocardia carboxydivorans (AGLS 2) were isolated as endophytes from Sonchus oleraceus and Ageratum conyzoides respectively. The analysis of their extracts revealed them to be strongly bioactive. The N. caishijiensis extract gave an LC50 of 570 μg/ml(-1) in the brine shrimp cytotoxicity assay and an EC50 of 0.552 μg/ml(-1) in the DPPH antioxidant assay. Antimicrobial activity was observed against Methicillin resistant Staphlococcus aureus (MRSA) and Escherichia coli ATCC 25922 (14 mm), Klebsiella pneumoniae ATCC 706003 (13 mm), S. aureus ATCC 25923 (11 mm) and Candida tropicalis (20 mm). For the extract of P. carboxydivorans the EC50 was 0.670 μg/ml(-1) and it was observed to be more bioactive against Bacillus subtilis DSM 10 ATCC 6051 (21 mm), C. tropicalis (20 mm), S. aureus ATCC 25923 (17 mm), MRSA (17 mm), E. coli K12 (W1130) (16 mm) and Chlorella vulgaris (10 mm). The genotoxicity testing revealed a 20 mm zone of inhibition against the polA mutant strain E. coli K-12 AB 3027 suggesting damage to the DNA and polA genes. The TLC and bioautography screening revealed a diversity of active bands of medium polar and nonpolar compounds. Metabolite analysis by HPLC-DAD via UV/vis spectral screening suggested the possibility of stenothricin and bagremycin A in the mycelium extract of N. caishijiensis respectively. In the broth and mycelium extract of P. carboxydivorans borrelidin was suggested along with α-pyrone. The HPLC-MS revealed bioactive long chained amide derivatives such as 7-Octadecenamide, 9, 12 octadecandienamide. This study reports the rare actinomycetes N. caishijiensis and P. carboxydivorans as endophytes and evaluates their bioactive metabolites.

  3. Actinopolyspora biskrensis sp. nov., a novel halophilic actinomycete isolated from Northern Sahara.

    Science.gov (United States)

    Saker, Rafika; Bouras, Noureddine; Meklat, Atika; Zitouni, Abdelghani; Schumann, Peter; Spröer, Cathrin; Klenk, Hans-Peter; Sabaou, Nasserdine

    2015-03-01

    A novel halophilic, filamentous actinomycete, designated H254(T), was isolated from a Saharan soil sample collected from Biskra (Northern Sahara), and subjected to a polyphasic taxonomic characterization. The strain is Gram-positive, aerobic, and halophilic, and the optimum NaCl concentration for growth is 15-20 % (w/v). The cell-wall hydrolysate contained meso-diaminopimelic acid, and the diagnostic whole-cell sugars were arabinose and galactose. The diagnostic phospholipid detected was phosphatidylcholine, and MK-9(H4) was the predominant menaquinone. The major fatty acid profiles were anteiso-C17:0 (32.8 %), C15:0 (28 %), and iso-C17:0 (12.3 %). Comparative analysis of the 16S rRNA gene sequences revealed that the strain H254(T) formed a well-separated sub-branch within the radiation of the genus Actinopolyspora, and the microorganism was most closely related to Actinopolyspora saharensis DSM 45459(T) (99.2 %), Actinopolyspora halophila DSM 43834(T) (99.1 %), and Actinopolyspora algeriensis DSM 45476(T) (99.0 %). Nevertheless, the strain had relatively lower mean values for DNA-DNA relatedness with the above strains (57.2, 68.4, and 45.6 %, respectively). Based on phenotypic features and phylogenetic position, we propose that strain H254(T) represents a novel species of the genus Actinopolyspora, for which the name Actinopolyspora biskrensis sp. nov. is proposed. The type strain of A. biskrensis is strain H254(T) (=DSM 46684(T) =CECT 8576(T)).

  4. Discovery of phosphonic acid natural products by mining the genomes of 10,000 actinomycetes.

    Science.gov (United States)

    Ju, Kou-San; Gao, Jiangtao; Doroghazi, James R; Wang, Kwo-Kwang A; Thibodeaux, Christopher J; Li, Steven; Metzger, Emily; Fudala, John; Su, Joleen; Zhang, Jun Kai; Lee, Jaeheon; Cioni, Joel P; Evans, Bradley S; Hirota, Ryuichi; Labeda, David P; van der Donk, Wilfred A; Metcalf, William W

    2015-09-29

    Although natural products have been a particularly rich source of human medicines, activity-based screening results in a very high rate of rediscovery of known molecules. Based on the large number of natural product biosynthetic genes in microbial genomes, many have proposed "genome mining" as an alternative approach for discovery efforts; however, this idea has yet to be performed experimentally on a large scale. Here, we demonstrate the feasibility of large-scale, high-throughput genome mining by screening a collection of over 10,000 actinomycetes for the genetic potential to make phosphonic acids, a class of natural products with diverse and useful bioactivities. Genome sequencing identified a diverse collection of phosphonate biosynthetic gene clusters within 278 strains. These clusters were classified into 64 distinct groups, of which 55 are likely to direct the synthesis of unknown compounds. Characterization of strains within five of these groups resulted in the discovery of a new archetypical pathway for phosphonate biosynthesis, the first (to our knowledge) dedicated pathway for H-phosphinates, and 11 previously undescribed phosphonic acid natural products. Among these compounds are argolaphos, a broad-spectrum antibacterial phosphonopeptide composed of aminomethylphosphonate in peptide linkage to a rare amino acid N(5)-hydroxyarginine; valinophos, an N-acetyl l-Val ester of 2,3-dihydroxypropylphosphonate; and phosphonocystoximate, an unusual thiohydroximate-containing molecule representing a new chemotype of sulfur-containing phosphonate natural products. Analysis of the genome sequences from the remaining strains suggests that the majority of the phosphonate biosynthetic repertoire of Actinobacteria has been captured at the gene level. This dereplicated strain collection now provides a reservoir of numerous, as yet undiscovered, phosphonate natural products.

  5. Saccharopolyspora griseoalba sp. nov., a novel actinomycete isolated from the Dead Sea.

    Science.gov (United States)

    Jiang, Yingying; Wei, Xiaomin; Chen, Xiu; Jiang, Yi; Xue, Quanhong; Lai, Hangxian; Jiang, Chenglin

    2016-12-01

    A novel halotolerant actinomycete, designated strain AFM 10238(T), was isolated from a sediment sample collected from the Dead Sea of Israel. The isolate grew at 15-45 °C, pH 6-12 and with 0-15 % (w/v) NaCl. Strain AFM 10238(T) contains meso-diaminopimelic acid as cell wall diamino acid, and galactose and arabinose as the whole cell sugars. The major polar lipids are phosphatidylcholine, phosphatidylglycerol, and diphosphatidylglycerol. Major fatty acids are iso-C16:0, iso-C17:0, iso-C15:0, anteiso-C17:0 and C17:1 ω8c. MK-9(H4) is the predominant menaquinone and the DNA G + C content is 72.7 mol%. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain AFM10238(T) belongs to the genus Saccharopolyspora. The 16S rRNA gene sequence similarity between strain AFM 10238(T) and its close neighbours, Saccharopolyspora halophila YIM 90500(T) , Saccharopolyspora spinosa DSM 44228(T), Saccharopolyspora dendranthemae KLBMP 1305(T) and Saccharopolyspora cebuensis DSM 45019(T) were 98.2, 97.2, 97.1 and 97.0 %, respectively. Sequence similarities to other type strains of this genus were below 97 %. DNA-DNA relatedness data, together with phenotypic and chemotaxonomic differences, clearly distinguished the isolate from its close neighbours. On the basis of the data from this polyphasic analysis, a novel species Saccharopolyspora griseoalba sp. nov. is proposed. The type strain is AFM 10238(T) (= DSM 46,663 = CGMCC 4.7124).

  6. Amycolatopsis flava sp. nov., a halophilic actinomycete isolated from Dead Sea.

    Science.gov (United States)

    Wei, Xiaomin; Jiang, Yingying; Chen, Xiu; Jiang, Yi; Lai, Hangxian

    2015-10-01

    A novel halophilic, filamentous actinomycete, designated strain AFM 10111(T), was isolated from a sediment sample collected from the Dead Sea of Israel and its taxonomic position was established by using a polyphasic taxonomic approach. The isolate grew at 20-35 °C, pH 5-12 and with 1-30 % NaCl. The substrate mycelium is white or yellow, well developed, branched and fragments into squarish, rod-like elements. The isolate contained meso-diaminopimelic acid as cell-wall diamino acid, and arabinose and galactose as whole-cell sugars. The major menaquinone was MK-9(H4). The polar lipids were diphosphatidylglycerol, phosphatidylglycerol, phosphatidylinositol, phosphatidylethanolamine phosphatidylmethylethanolamine and one unidentified phospholipid. Major fatty acids were iso-C16:0, iso-C16:1 H, C17:1 ω6c. The DNA G + C content was 67.7 mol %. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain AFM 10111(T) belongs to the genus Amycolatopsis, and formed a distinct clade with Amycolatopsis marina CGMCC 4.3568(T) and Amycolatopsis palatopharyngis CGMCC 4.1729(T), with the sequence similarity 98.4 and 98.6 %. The level of DNA-DNA relatedness between the strain AFM 10111(T) and A. marina CGMCC 4.3568(T) and A. palatopharyngis CGMCC 4.1729(T) were 46.9 ± 3.08 and 49.4 ± 1.25 %. The combined genotypic and phenotypic data indicate that strain AFM 10111(T) represents a novel species of the genus Amycolatopsis, for which the name Amycolatopsis flava sp. nov. is proposed. The type strain is AFM 10111(T) (= DSM 46658(T) = CGMCC 4.7123(T)).

  7. Tartrolon D, a cytotoxic macrodiolide from the marine-derived actinomycete Streptomyces sp. MDG-04-17-069.

    Science.gov (United States)

    Pérez, Marta; Crespo, Cristina; Schleissner, Carmen; Rodríguez, Pilar; Zúñiga, Paz; Reyes, Fernando

    2009-12-01

    Exploration of marine-derived actinomycetes as a source of antitumor compounds has led to the isolation of a new member of the tartrolon series, tartrolon D (4). This new compound was obtained from Streptomyces sp. MDG-04-17-069 fermentation broths and displayed strong cytotoxic activity against three human tumor cell lines. Additionally, the known compound ikarugamycin (5) was also found in the culture broths of the same microorganism. The structure of this new tartrolon was established by a combination of spectroscopic techniques (1D and 2D NMR, HRMS, and UV) as well as by comparison with published data for similar compounds.

  8. In Vitro and In Vivo Plant Growth Promoting Activities and DNA Fingerprinting of Antagonistic Endophytic Actinomycetes Associates with Medicinal Plants.

    Science.gov (United States)

    Passari, Ajit Kumar; Mishra, Vineet Kumar; Gupta, Vijai Kumar; Yadav, Mukesh Kumar; Saikia, Ratul; Singh, Bhim Pratap

    2015-01-01

    Endophytic actinomycetes have shown unique plant growth promoting as well as antagonistic activity against fungal phytopathogens. In the present study forty-two endophytic actinomycetes recovered from medicinal plants were evaluated for their antagonistic potential and plant growth-promoting abilities. Twenty-two isolates which showed the inhibitory activity against at least one pathogen were subsequently tested for their plant-growth promoting activities and were compared genotypically using DNA based fingerprinting, including enterobacterial repetitive intergenic consensus (ERIC) and BOX repetitive elements. Genetic relatedness based on both ERIC and BOX-PCR generates specific patterns corresponding to particular genotypes. Exponentially grown antagonistic isolates were used to evaluate phosphate solubilization, siderophores, HCN, ammonia, chitinase, indole-3-acetic acid production, as well as antifungal activities. Out of 22 isolates, the amount of indole-3-acetic acid (IAA) ranging between 10-32 μg/ml was produced by 20 isolates and all isolates were positive for ammonia production ranging between 5.2 to 54 mg/ml. Among 22 isolates tested, the amount of hydroxamate-type siderophores were produced by 16 isolates ranging between 5.2 to 36.4 μg/ml, while catechols-type siderophores produced by 5 isolates ranging from 3.2 to 5.4 μg/ml. Fourteen isolates showed the solubilisation of inorganic phosphorous ranging from 3.2 to 32.6 mg/100ml. Chitinase and HCN production was shown by 19 and 15 different isolates, respectively. In addition, genes of indole acetic acid (iaaM) and chitinase (chiC) were successively amplified from 20 and 19 isolates respectively. The two potential strains Streptomyces sp. (BPSAC34) and Leifsonia xyli (BPSAC24) were tested in vivo and improved a range of growth parameters in chilli (Capsicum annuum L.) under greenhouse conditions. This study is the first published report that actinomycetes can be isolated as endophytes from within these

  9. In Vitro and In Vivo Plant Growth Promoting Activities and DNA Fingerprinting of Antagonistic Endophytic Actinomycetes Associates with Medicinal Plants.

    Directory of Open Access Journals (Sweden)

    Ajit Kumar Passari

    Full Text Available Endophytic actinomycetes have shown unique plant growth promoting as well as antagonistic activity against fungal phytopathogens. In the present study forty-two endophytic actinomycetes recovered from medicinal plants were evaluated for their antagonistic potential and plant growth-promoting abilities. Twenty-two isolates which showed the inhibitory activity against at least one pathogen were subsequently tested for their plant-growth promoting activities and were compared genotypically using DNA based fingerprinting, including enterobacterial repetitive intergenic consensus (ERIC and BOX repetitive elements. Genetic relatedness based on both ERIC and BOX-PCR generates specific patterns corresponding to particular genotypes. Exponentially grown antagonistic isolates were used to evaluate phosphate solubilization, siderophores, HCN, ammonia, chitinase, indole-3-acetic acid production, as well as antifungal activities. Out of 22 isolates, the amount of indole-3-acetic acid (IAA ranging between 10-32 μg/ml was produced by 20 isolates and all isolates were positive for ammonia production ranging between 5.2 to 54 mg/ml. Among 22 isolates tested, the amount of hydroxamate-type siderophores were produced by 16 isolates ranging between 5.2 to 36.4 μg/ml, while catechols-type siderophores produced by 5 isolates ranging from 3.2 to 5.4 μg/ml. Fourteen isolates showed the solubilisation of inorganic phosphorous ranging from 3.2 to 32.6 mg/100ml. Chitinase and HCN production was shown by 19 and 15 different isolates, respectively. In addition, genes of indole acetic acid (iaaM and chitinase (chiC were successively amplified from 20 and 19 isolates respectively. The two potential strains Streptomyces sp. (BPSAC34 and Leifsonia xyli (BPSAC24 were tested in vivo and improved a range of growth parameters in chilli (Capsicum annuum L. under greenhouse conditions. This study is the first published report that actinomycetes can be isolated as endophytes from

  10. Cephamycins, a New Family of β-Lactam Antibiotics I. Production by Actinomycetes, Including Streptomyces lactamdurans sp. n1

    Science.gov (United States)

    Stapley, E. O.; Jackson, M.; Hernandez, S.; Zimmerman, S. B.; Currie, S. A.; Mochales, S.; Mata, J. M.; Woodruff, H. B.; Hendlin, D.

    1972-01-01

    A number of actinomycetes isolated from soil were found to produce one or more members of a new family of antibiotics, the cephamycins, which are structurally related to cephalosporin C. The cephamycins were produced in submerged fermentation in a wide variety of media by one or more of eight different species of Streptomyces, including a newly described species, S. lactamdurans. These antibiotics exhibit antibacterial activity against a broad spectrum of bacteria which includes many that are resistant to the cephalosporins and penicillins. PMID:4790552

  11. Research Progress of Active Metabolite of Marine Actinomycetes%海洋放线菌活性代谢产物的研究进展

    Institute of Scientific and Technical Information of China (English)

    宗志友; 魏刚; 斯聪聪; 王莹

    2011-01-01

    The research background of marine actinomycetes are briefly introduced in this paper. The research progresses of the active metabolite of marine actinomycetes in recent years are summarized and these metabolites are discussed individually according to their structures.%简要介绍了海洋放线菌的研究背景,重点对近年来发现的由海洋放线菌产生的活性代谢产物的研究进展作一概述,并对这些代谢产物依据其结构进行分类概述.

  12. Cytotoxicity of actinomycetes associated with the ascidian Eudistoma vannamei (Millar, 1977, endemic of northeastern coast of Brazil

    Directory of Open Access Journals (Sweden)

    Paula C Jimenez

    2013-04-01

    Full Text Available Previous studies demonstrated that the crude extract of the ascidian Eudistoma vannamei, endemic from northeasttern Brazil, strongly hinders growth of tumor cells in vitro by inducing apoptosis due to tryptophan derivatives, which are commonly found in bacteria. This study presents a bioactivity-guided screening among actinomycetes, associated with E. vannamei, aiming at recognizing active principles with biological relevance. Twenty strains of actinomycetes, designated as EVA 0101 through 0120, were isolated from colonies of E. vannamei among which 11 were selected for cytotoxicity evaluation. The extracts from EVA 0102, 0103, 0106, 0109 and 0113 were the most active, and were further studied for IC50 determination and chemical analysis by ¹H NMR. IC50 values obtained ranged from 3.62 µg mL-1 (for EVA 0109 in leukemia cells to 84.65 µg/mL (for EVA 0106 in melanoma cells. All active extracts exhibited the same TLC and spectroscopic profiles, suggesting the presence of quinones and other related secondary metabolites. Furthermore, these strains were identified and compared based on their respective 16S rRNA sequences. The results herein identified the five strains as Micromonospora spp. while phylogenetic analysis suggests that they are possibly two different Micromonospora species producing the cytotoxic compounds.

  13. Effect of crude extracts of selected actinomycetes on biofilm formation of A. schindleri, M. aci, and B. cereus.

    Science.gov (United States)

    Saleem, Hafiz Ghulam Murtaza; Aftab, Usman; Sajid, Imran; Abbas, Zaigham; Sabri, Anjum Nasim

    2015-05-01

    Actinomycetes are well known group of gram positive bacteria for their potential to produce antibiotics. This study sought to assess the ability of the selected actinomycetes to control biofilm forming bacteria isolated from different dental plaque samples. On the basis of morphological differences three out of ten different dental plaque bacterial isolates were selected for further study. These isolates were biochemically and genetically characterized and were identified as Acinetobacter schinndleri, Moraxella aci, and Bacillus cereus. Antibiotic resistant profile was measured through disc diffusion method and found that all three isolates were moderately sensitive to ofloxacin and erythromycin and resistant to trimethoprim. Antibacterial activity of ten different Streptomyces strains was assessed through an agar plug and well diffusion method against three dental biofilm forming bacteria. Two Streptomyces strains named as S. erythrogriseus and S. labedae showed good antibacterial activity against Moraxella and Acinetobacter strains. Ability of the four active antibiotic producing strains to inhibit biofilm formation was assessed using microtiter biofilm detection assay. It was found that biofilm forming ability of Acinetobacter and Moraxella was inhibited by S. labedae an antibiotic producing strain, while S. macrosporeus can only inhibit biofilm formation by B. cereus.

  14. Screening of Actinomycetes from mangrove ecosystem for L-asparaginase activity and optimization by response surface methodology.

    Science.gov (United States)

    Usha, Rajamanickam; Mala, Krishnaswami Kanjana; Venil, Chidambaram Kulandaisamy; Palaniswamy, Muthusamy

    2011-01-01

    Marine actinomycetes were isolated from sediment samples collected from Pitchavaram mangrove ecosystem situated along the southeast coast of India. Maximum actinomycete population was noted in rhizosphere region. About 38% of the isolates produced L-asparaginase. One potential strain KUA106 produced higher level of enzyme using tryptone glucose yeast extract medium. Based on the studied phenotypic characteristics, strain KUA106 was identified as Streptomyces parvulus KUA106. The optimization method that combines the Plackett-Burman design, a factorial design and the response surface method, which were used to optimize the medium for the production of L-asparaginase by Streptomycetes parvulus. Four medium factors were screened from eleven medium factors by Plackett-Burman design experiments and subsequent optimization process to find out the optimum values of the selected parameters using central composite design was performed. Asparagine, tryptone, d) extrose and NaCl components were found to be the best medium for the L-asparaginase production. The combined optimization method described here is the effective method for screening medium factors as well as determining their optimum level for the production of L-asparaginase by Streptomycetes parvulus KUAP106.

  15. Isolation and evaluation of proteolytic actinomycete isolates as novel inducers of pearl millet downy mildew disease protection

    Science.gov (United States)

    Jogaiah, Sudisha; Kurjogi, Mahantesh; Govind, Sharathchandra Ramasandra; Huntrike, Shekar Shetty; Basappa, Vedamurthy Ankala; Tran, Lam-Son Phan

    2016-01-01

    Native endophytic actinomycetes isolated from pearl millet roots were examined for their efficacy to protect pearl millet against downy mildew. Nineteen of 39 isolates were found to be proteolytic, of which 7 strains could directly suppress the sporangium formation of Sclerospora graminicola, the pearl millet downy mildew pathogen. Thus, mycelial suspensions containing either spores or cell-free extract of these 7 isolates were used for seed-coating and -soaking treatments to test for their induction of downy mildew resistance. Results indicated that seed-coating overall provided better protection to downy mildew than seed-soaking. In both treatments, the tested isolates demonstrated differential abilities in downy mildew disease protection, with Streptomyces griseus SJ_UOM-07-09 and Streptosporangium roseum SJ_UOM-18-09 showing the highest protection rates. Additionally, the levels of disease protection conferred by the actinomycetes were just slightly lower than that of the systemic fungicide Apron, suggesting their effectiveness. Further studies revealed that the more rapid root colonization by SJ_UOM-18-09 resulted in faster and higher induced resistance in comparison with SJ_UOM-07-09 under greenhouse conditions, indicating that SJ_UOM-18-09 was superior than SJ_UOM-07-09 in inducing resistance. Results from this study provide comprehensive information on biocontrol functions of SJ_UOM- 18-09 with great potential to control downy mildew disease in pearl millet. PMID:27499196

  16. Broad spectrum antimicrobial activity of forest-derived soil actinomycete, Nocardia sp. PB-52

    Directory of Open Access Journals (Sweden)

    Priyanka eSharma

    2016-03-01

    Full Text Available A mesophilic actinomycete strain designated as PB-52 was isolated from soil samples of Pobitora Wildlife Sanctuary of Assam, India. Based on phenotypic and molecular characteristics, the strain was identified as Nocardia sp. which shares 99.7% sequence similarity with Nocardia niigatensis IFM 0330 (NR_112195. The strain is a Gram-positive filamentous bacterium with rugose spore surface which exhibited a wide range of antimicrobial activity against Gram-positive bacteria including methicillin resistant Staphylococcus aureus (MRSA, Gram-negative bacteria and yeasts. Optimization for the growth and antimicrobial metabolite production of the strain PB-52 was carried out in batch culture under shaking condition. The optimum growth and the antimicrobial metabolite production by the strain PB-52 was recorded in GLM medium at 28ºC, initial pH 7.4 of the medium and incubation period of eight days. Based on polyketide synthases (PKS and nonribosomal peptide synthetases (NRPS gene-targeted PCR amplification, the occurrence of both of these biosynthetic pathways was detected which might be involved in the production of antimicrobial metabolite in PB-52. Extract of the fermented broth culture of PB-52 was prepared with organic solvent extraction method using ethyl acetate. The ethyl acetate extract of PB-52 (EA-PB-52 showed lowest minimum inhibitory concentration (MIC against Staphylococcus aureus MTCC 96 (0.975 μg/ml whereas highest was recorded against Klebsiella pneumoniae ATCC 13883 (62.5 μg/ml. Scanning electron microscopy (SEM revealed that treatment of the test microorganisms with EA-PB-52 destroyed the targeted cells with prominent loss of cell shape and integrity. In order to determine the constituents responsible for its antimicrobial activity, EA-PB-52 was subjected to chemical analysis using gas chromatography-mass spectrometry (GC-MS. GC-MS analysis showed the presence of twelve different chemical constituents in the extract, some of which

  17. Complete Genome Sequence of Micromonospora Strain L5, a Potential Plant-Growth-Regulating Actinomycete, Originally Isolated from Casuarina equisetifolia Root Nodules

    Energy Technology Data Exchange (ETDEWEB)

    Hirsch, A. M.; Alvarado, J.; Bruce, D.; Chertkov, O.; De Hoff, P. L.; Detter, J. C.; Fujishige, N. A.; Goodwin, L. A.; Han, J.; Han, S.; Ivanova, N.; Land, M. L.; Lum, M. R.; Milani-Nejad, N.; Nolan, M.; Pati, A.; Pitluck, S.; Tran, S. S.; Woyke, T.; Valdes, M.

    2013-08-29

    Micromonospora species live in diverse environments and exhibit a broad range of functions including antibiotic production, biocontrol, and ability to degrade complex polysaccharides. To learn more about these versatile actinomycetes, we sequenced the genome of strain L5, originally isolated from root nodules of an actinorhizal plant growing in Mexico.

  18. Pharmaceutical composition to protect an animal against a disorder arising from an infection with a bacterium that belongs to the group of nocardioform actinomycetes

    NARCIS (Netherlands)

    Arnoldus, Christiaan Jacobs; van der Geize, Robert; Dijkhuizen, Lubbert

    2011-01-01

    The invention pertains to a pharmaceutical composition to protect an animal against a disorder arising from an infection with a bacterium that belongs to the group of nocardioform actinomycetes having the ability to survive within macrophages of the animal, comprising live bacteria of a nocardioform

  19. XML In Vitro Comparison of MIC Crude Extracts of Active Actinomycetes Isolated with Terbinafine, Griseofulvin Ketoconazole and Fluconazole against Microsporum Canis, Microsporum Gypseum and Trichophyton Mentagrophytes

    Directory of Open Access Journals (Sweden)

    Keikha, N. (MSc

    2015-05-01

    Full Text Available Background and Objective: Dermatophytes are the fungi that have the ability to attack the keratinized tissues such as the skin, hair and nails. Infections caused by these organisms are named dermatophytosis. We aimed to compare Minimum inhibitory concentration (MIC of Crude extracts of Active Actinomycete Isolates with Terbinafine, Griseofulvin, Ketoconazole and Fluconazole Drugs against Microsporum Canis, Microsporum gypseum and Trichophyton mentagrophytes. Material and Methods: In this experimental study, in order to find MIC by actionmycete, 100 isolates were studied and then crude extracts of the active actinomycete isolates were prepared in sterile conditions. Finally, the crude extracts obtained at different concentrations were used to obtain the MIC of Microsporum Canis, Microsporum gypseum and Trichophyton mentagrophytes. Moreover, various concentrations of the drugs such as terbinafine, griseofulvin, ketoconazole and fluconazole in solvent Dimethyl sulfoxide (DMSO were prepared and their growth inhibitory effect was evaluated and then compared with the results obtained from the crude extract of active actinomycete isolates. Results: the crude extracts obtained from active Actioiomycetes isolates and the drugs such as terbinafine, griseofulvin, ketoconazole and fluconazole, in a dose-dependent manner, could inhibit the growth of Microsporum Canis, Microsporum gypseum and Trichophyton Mentagrophytes. Conclusion: compared to MIC of Crude extract of active actinomycete isolates, Terbinafine has a significant effect on the growth inhibition in all of the fungal Dermatophytes and then griseofulvin, ketoconazole and fluconazole are in the next rank, respectively.

  20. Antibiotics Resistance Profiling and In-Vitro Inhibition of Clinical Klebsiella Strains by Actinomycetes Isolated From Different Ecological Niches in Pakistan

    Directory of Open Access Journals (Sweden)

    Noureen

    2016-02-01

    Full Text Available Background Multidrug resistance among different pathogens is increasing immensely day by day. To control these problems, we need new potent antimicrobial agents in repository of antibiotics. Objectives This study aimed at investigation of antibiotics resistance pattern of pathogenic Klebsiella strains isolated from clinical samples in Lahore region Pakistan and study inhibition of resistant strains by natural extracts obtained from actinomycetes isolated from different ecological niches in Pakistan. Materials and Methods The isolated Klebsiella strains were identified by morphological, biochemical and physiological characterization along with 16S rRNA gene sequencing. Antibiotics susceptibility was determined by standard Kirby Bauer disc diffusion assay. The biological and chemical screening was performed for detection of active secondary metabolites produced by actinomycetes against resistant Klebsiella strains. Biological screenings include antimicrobial activity by agar diffusion assay and brine shrimp microwell cytotoxicity assay. In chemical screening, the crude extracts of actinomycetes strains were analysed by TLC and HPLC-UV techniques. Results The isolated Klebsiella strains showed resistance against most of the antibiotics as follows; ceftriaxone > cephalexin > cefpirome > cefoxitin = cefepime > levofloxacin > ciprofloxacin = ceftrazidime = fusidum > cefoperazone > ampicillin sulbactam. The actinomycetes strain A19, A20, A2, A10, A6 and A8 exhibited remarkable activity against resistant Klebsiella strains. The strains A19 and 20 showed excellent inhibitory effects on all isolated multidrug resistant Klebsiella strains. Conclusions The clinical Klebsiella strains isolated from Lahore region, Pakistan exhibited resistance to most commonly used antibiotics, which can be a serious threat to public health. The study reported some potential actinomycetes strains, which exhibit promising activity against multidrug resistant Klebsiella strains.

  1. Metagenomic of Actinomycetes Based on 16S rRNA and nifH Genes in Soil and Roots of Four Indonesian Rice Cultivars Using PCR-DGGE

    Directory of Open Access Journals (Sweden)

    Mahyarudin

    2015-07-01

    Full Text Available The research was conducted to study the metagenomic of actinomycetes based on 16S ribosomal RNA (rRNA and bacterial nifH genes in soil and roots of four rice cultivars. The denaturing gradient gel electrophoresis profile based on 16S rRNA gene showed that the diversity of actinomycetes in roots was higher than soil samples. The profile also showed that the diversity of actinomycetes was similar in four varieties of rice plant and three types of agroecosystem. The profile was partially sequenced and compared to GenBank database indicating their identity with closely related microbes. The blast results showed that 17 bands were closely related ranging from 93% to 100% of maximum identity with five genera of actinomycetes, which is Geodermatophilus, Actinokineospora, Actinoplanes, Streptomyces and Kocuria. Our study found that Streptomyces species in soil and roots of rice plants were more varied than other genera, with a dominance of Streptomyces alboniger and Streptomyces acidiscabies in almost all the samples. Bacterial community analyses based on nifH gene denaturing gradient gel electrophoresis showed that diversity of bacteria in soils which have nifH gene was higher than that in rice plant roots. The profile also showed that the diversity of those bacteria was similar in four varieties of rice plant and three types of agroecosystem. Five bands were closely related with nifH gene from uncultured bacterium clone J50, uncultured bacterium clone clod-38, and uncultured bacterium clone BG2.37 with maximum identity 99%, 98%, and 92%, respectively. The diversity analysis based on 16S rRNA gene differed from nifH gene and may not correlate with each other. The findings indicated the diversity of actinomycetes and several bacterial genomes analyzed here have an ability to fix nitrogen in soil and roots of rice plant.

  2. Cultivable actinomycetes from rhizosphere of birch (Betula pendula) growing on a coal mine dump in Silets, Ukraine.

    Science.gov (United States)

    Ostash, Bohdan; Gren, Tetiana; Hrubskyy, Yaroslav; Tistechok, Stepan; Beshley, Stepan; Baranov, Volodymyr; Fedorenko, Victor

    2014-08-01

    Five actinomycete strains were isolated from the rhizosphere of birch, one of a few native tree forms capable of thriving on the upper level of a coal mine dump near the village of Silets (Lvivska region, Ukraine). No such strains were isolated from surrounding gangue, or from nearby grass Calamagrostis epigeios. Using 16S rDNA sequencing and analysis of cell wall aminoacids, four of these strains were shown to belong to genus Streptomyces and one to be Amycolatopsis. The isolates were able to produce siderophores and antibacterial compounds. In comparison to the reference strain Streptomyces coelicolor M145, certain rhizospheric isolates displayed somewhat increased survival in the presence of copper, iron(III), or chromium(VI) salts. The Amycolatopsis isolate was also shown to accumulate significant quantities of heavy metals from waste extracts. Possible roles of the described strains in coal mine dump ecology are discussed.

  3. Production and characterization of lipopeptide biosurfactant by a sponge-associated marine actinomycetes Nocardiopsis alba MSA10.

    Science.gov (United States)

    Gandhimathi, R; Seghal Kiran, G; Hema, T A; Selvin, Joseph; Rajeetha Raviji, T; Shanmughapriya, S

    2009-10-01

    A sponge-associated marine actinomycetes Nocardiopsis alba MSA10 was screened and evaluated for the production of biosurfactant. Biosurfactant production was confirmed by conventional screening methods including hemolytic activity, drop collapsing test, oil displacement method, lipase production and emulsification index. The active compound was extracted with three solvents including ethyl acetate, diethyl ether and dichloromethane. The diethyl ether extract was fractionated by TLC and semi-preparative HPLC to isolate the pure compound. In TLC, a single discrete spot was obtained with the R (f) 0.60 and it was extrapolated as valine. Based on the chemical characterization, the active compound was partially confirmed as lipopeptide. The optimum production was attained at pH 7, temperature 30 degrees C, and 1% salinity with glucose and peptone supplementation as carbon and nitrogen sources, respectively. Considering the biosurfactant production potential of N. alba, the strain could be developed for large-scale production of lipopeptide biosurfactant.

  4. Characterization and phylogenetic analysis of novel polyene type antimicrobial metabolite producing actinomycetes from marine sediments:Bay of Bengal India

    Institute of Scientific and Technical Information of China (English)

    Valan Arasu M; Asha KRT; Duraipandiyan V; Ignacimuthu S; Agastian P

    2012-01-01

    To isolate and indentify the promising antimicrobial metabolite producingStreptomyces strains from marine sediment samples from Andrapradesh coast of India. Methods:Antagonistic actinomycetes were isolated by starch casein agar medium and modified nutrient agar medium with 1% glucose used as a base for primary screening. Significant antimicrobial metabolite producing strains were selected and identified by using biochemical and 16S rDNA level. Minimum inhibitory concentrations of the organic extracts were done by using broth micro dilution method. Results: Among the 210 actinomycetes, 64.3% exhibited activity against Gram positive bacteria, 48.5 % showed activity towards Gram negative bacteria, 38.8% exhibited both Gram positive and negative bacteria and 80.85 % isolates revealed significant antifungal activity. However, five isolates AP-5, AP-18, AP-41 and AP-70 showed significant antimicrobial activity. The analysis of cell wall hydrolysates showed the presence of LL-diaminopimelic acid and glycine in all the isolates. Sequencing analysis indicated that the isolates shared 98.5%-99.8%sequence identity to the 16S rDNA gene sequences of the Streptomyces taxons. The antimicrobial substances were extracted using hexane and ethyl acetate from spent medium in which strains were cultivated at 30℃for five days. The antimicrobial activity was assessed using broth micro dilution technique. Each of the culture extracts from these five strains showed a typical polyene-like property. The lowest minimum inhibitory concentrations of ethyl acetate extracts against Escherichia coli and Curvularia lunata were 67.5 and 125.0 μg/mL, respectively. Conclusions: It can be concluded that hexane and ethyl acetate soluble extracellular products of novel isolates are effective against pathogenic bacteria and fungi.

  5. Screening and Identifying of Antagonistic Actinomycetes against Ralstonia Solancearum%烟草青枯菌拮抗放线菌的筛选及鉴定

    Institute of Scientific and Technical Information of China (English)

    陆铮铮; 彭丽娟; 丁海霞; 左希; 彭杰; 蒋选利

    2013-01-01

    In order to select effective antagonistic actinomycetes against Ralstonia solanacearum, we isolated 56 strains of actinomycetes from healthy tobacco rhizosphere soils. By pairing culture on plate method to screen antagonistic actinomycetes, we attained 3 strains of antagonistic actinomycetes, whose average inhibition diameters were more than 20 mm. We identified 3 strains of actinomycetes according to culture characteristics on differential culture mediums, spore and spore chain morphology, physiological and biochemical, molecular biology methods. The results showed that the 3 strains of actinomycetes were Streptomyces roseofulvus, Streptomyces olivaceoviridis and Streptomyces corchorusii. Among them, the best was S. roseofulvus, and average inhibition diameter was 54.66 mm. Average inhibition diameter of S.olivaceoviridis was 43.20 mm, and average inhibition diameter of S. corchorusii was 20.34 mm.%  为筛选出烟草青枯菌的有效拮抗菌,本研究从烟草根围土壤中分离了97株放线菌,通过平板对峙培养法筛选出抑菌圈直径均达20 mm以上的拮抗放线菌3株。根据其在鉴别培养基上的培养特征、孢子和孢子链的形态特征,生理生化特性以及16SrDNA序列分析对这3株拮抗放线菌进行鉴定。结果表明,3株拮抗放线菌都属于链霉菌属(Streptomyces),分别为粉红孢类群中的玫瑰暗黄链霉菌(S. roseofulvus Preobrazhenskaya)、绿色类群中的橄榄绿链霉菌(S. olivaceoviridis Preobrazhenskaya)和灰褐类群中的黄麻链霉菌(S. corchorusii Ahmed)。其中,玫瑰暗黄链霉菌菌株对青枯劳尔氏菌的拮抗效果最好,其平均抑菌圈直径可达54.66 mm;橄榄绿链霉菌菌株的拮抗效果次之,其平均抑菌圈直径为43.20 mm;黄麻链霉菌平均抑菌圈直径为20.34 mm。

  6. Diversity of actinomycetes in Taiwan strait marine sediments%台湾海峡海洋沉积物放线菌的多样性

    Institute of Scientific and Technical Information of China (English)

    梁效伟; 陈名洪; 林如; 王海龙; 谢阳; 连云阳; 江红

    2012-01-01

    目的 探究台湾海峡海洋沉积物中放线菌的多样性及发现合成药物先导化合物的新菌源.方法 采用6种选择性培养基分离15份来自台湾海峡沉积物样品中含有的放线菌.挑选不同培养特征的放线菌进行初步分类鉴别、16S rRNA基因序列系统进化分析及基于PCR的烯二炔抗生素基因筛选.结果 共分离到497株放线菌,挑选的95株放线菌分别属于放线菌7个科,11个属.16S rRNA基因序列分析结果提示分离到的小单孢菌科菌种存在数个潜在新种,95株菌中有27%的菌株含有烯二炔抗生素核弹头的生物合成基因片段.结论 海洋环境蕴含丰富的放线菌资源,具有产生烯二炔类抗生素的潜能.%Objective To investigate the diversity of actinomycetes isolated from Taiwan strait marine sediments and isolate new actinomycetes for discovering compounds of pharmaceutical importance. Methods Six selective media were used to isolate actinomycetes from 15 sediment samples. Actinobacterial diversity in these sediments was investigated by phylogenetic analysis based on 16S rRNA gene sequences. To detect potential producer strains of enediyne antibiotics, PCR based screening strategy was used. Results A total of 497 strains of actinomycetes were isolated and 95 representative isolates were selected on the basis of their morphologies on different media. 16S rRNA gene sequences phylogenetic analysis showed that these strains belonged to seven families including eleven genera. Phylogenetic analyses also grouped many of the strains into clades distinct from alt known genera within Micromonosporaceae, indicating that they may be new genera. 27% of the above 95 strains were detected and found containing enediyne polyketide synthase (PK.S) gene. Conclusion The results confirm that marine sediments are rich source of rare actinomycetes and the actinomycetes from marine environment have the potential of producing enediyne family antibiotics.

  7. Pesquisas sobre a imunidade da Framboesia tropica no homem: observações feitas em 33 superinoculações e 7 reinoculações

    Directory of Open Access Journals (Sweden)

    F. Nery Guimarães

    1946-03-01

    em germes. 5 Existe na framboesia trópica uma verdadeira imunidade além de uma simples resistência á superinoculação devido a presença da infecção ativa ou latente. Com efeito, pacientes tratados em determinado período da molestia e curados clinica e sorologicamente, mostraram resistência parcial á reinoculação, reagindo de modo semelhante a outros do mesmo período de molestia e não tratados. 6 A imunidade na framboesia tropica se manifesta seja como uma resistência á superinoculação ou reinoculação seja como uma modificação da lesão boubatica inicial, seja, finalmente, como uma resistência á generalização da doença. 7 Os resultados das esperiências sugerem que as diferentes manifestações cutaneas da molestia são condicionadas até certo ponto pelo estado imunitario do organismo infectado. 8 Os diferentes gráus de imunidade, encontrados na framboesia trópica, estão até certo ponto relacionados com o tempo de doença. Porém, são atingidos mais ou menos ràpidamente, segundo o organismo infectado e, talvez segundo a virulência do treponema, do mesmo modo como os chamados "secundarismo" e 'terciarismo" da doença.The following conclusions are drawn from the results of the 40 experiments described above: 1 From the 2nd to the 8th month there is a great resistance to super-infection. a Such resistance seems to be independent of the presence of cutaneous lesions and occurred even in cases with only the initial lesion. b Within this period, resistance disappears with treatment: patients treated and reinoculated acquire yaws in the normal time. This fact suggests that this resistance is conditioned by the presence of an active or latent infection, being not a true immunity (an immunity in its classical conception. c When homovirus is used, resistance lasted about one year of the disease. 2 From the 10th month to the 4th year of the disease, there is a partial resistance, which manifests itself by two modes, according to the nature of

  8. 盐碱土壤放线菌的研究概况%Research Advances of Actinomycetes in Saline-alkali Soil

    Institute of Scientific and Technical Information of China (English)

    胡磊; 景彩虹; 薄乐涛; 达文燕; 杨建文; 姚健; 牛世全

    2012-01-01

    盐碱土壤放线菌是极端微生物的重要组成部分,也是一类极具应用前景的微生物资源.讨论了盐碱土壤放线菌的分离问题,并对其分类的发展与现状进行了概述,同时还就筛选抗生素高产菌株作了介绍.%Actinomycetes existing in saline—alkali soil are important members of extreme environmental microorganisms with wide application prospect. The screening methods for isolating actinmycetes from saline-alkali soil was discussed; and the development and current situation of their identification were briefly summarized. Furthermore, the screening of high antibiotics producing actinomycetes was also introduced.

  9. The Bio - control and Application of Actinomycetes against Plant Diseases%放线菌对植物病害的防治作用及应用

    Institute of Scientific and Technical Information of China (English)

    贾雨; 贾丽苑; 黄建新

    2012-01-01

    Actinomycetes are one of the most important bio - control micro - organisms which produce antibiotics and enzymes and are advantageous in the bio - control of plant diseases. This study addresses the bio - control of actinomycetes against plant diseases in terms of actinomycetes' action on phytopathogen and on the plants' disease resistance under the soil environ- ment. The paper also gives a brief introduction to the applications of actinomycetes in the bio - control of plant diseases, research hotspot and development trend.%放线菌是产生抗生素和酶的重要微生物资源之一,在防治植物病害中有很多优势.主要从放线菌与植物病原菌的作用和土壤环境中的放线菌对植物的抗病作用两方面,介绍了放线菌对植物病害的防治作用;简述目前放线菌在植病生防中的应用状况;以及研究热点和发展趋势.

  10. Structure of an MmyB-like regulator from C. aurantiacus, member of a new transcription factor family linked to antibiotic metabolism in actinomycetes.

    Directory of Open Access Journals (Sweden)

    Qingping Xu

    Full Text Available Actinomycetes are important bacterial sources of antibiotics and other secondary metabolites. Many antibiotic gene clusters are controlled by pathway-specific activators that act in response to growth conditions. Here we present the crystal structure of an MmyB-like transcription regulator MltR (PDB code 3pxp (Caur_2278 from Chloroflexus aurantiacus, in complex with a fatty acid (myristic acid. MltR is a distant homolog of the methylenomycin activator MmyB and consists of an Xre-type N-terminal DNA-binding domain and a C-terminal ligand-binding module that is related to the Per-Arnt-Sim (PAS domain. This structure has enabled identification of a new family of bacterial transcription factors that are distributed predominantly in actinomycetes. Bioinformatics analysis of MltR and other characterized family members suggest that they are likely associated with antibiotic and fatty acid metabolism in actinomycetes. Streptomyces coelicolor SCO4944 is a candidate as an ancestral member of the family. Its ortholog in S. griseus, SGR_6891, is induced by A-factor, a γ-butyrolactone that controls antibiotic production and development, and is adjacent to the A-factor synthase gen, afsA. The location of mltR/mmyB homologs, in particular those adjacent to less well-studied antibiotic-related genes, makes them interesting genetic markers for identifying new antibiotic genes. A model for signal-triggered DNA-binding by MltR is proposed.

  11. Recent advances in the bioactive metabolites of marine actinomycetes%海洋放线菌活性代谢产物研究最新进展

    Institute of Scientific and Technical Information of China (English)

    朱峰; 刘晓红; 林永成

    2007-01-01

    近年来海洋放线菌代谢产物的研究取得了很大进展,从海洋放线菌中分离到许多结构新奇、有特殊生理活性和有潜在实用价值的新化合物.研究表明海洋放线菌有可能成为抗生紊等药物工业的又一重要微生物资源.本文分类介绍了2001年到2005年间海洋放线菌代谢产物的研究进展,重点在于从海洋放线菌发现的新化合物及其生物活性.%Studis on the metabolites of marine actinomycetes have been rapidly developed recently.A number of unique structural compounds with special bioactivities and potential values were isolated from marine actinomycetes,which were expected to be another important microorganism resources for pharmaceutical industries.The recent advances in the bioactive metabolites of marine actinomycetes were reviewed in this paper with the literature published during 2001~2005.The emphasis is on the novel compounds and the relative bioactivities based on the structural classification.

  12. Genome sequence of a new Streptomyces coelicolor generalized transducing bacteriophage, ΦCAM.

    Science.gov (United States)

    Monson, Rita; Salmond, George P C

    2012-12-01

    Streptomyces coelicolor is a model system for the study of Streptomyces, a genus of bacteria responsible for the production of many clinically important antibiotics. Here we report the genome sequence of ΦCAM, a new S. coelicolor generalized transducing bacteriophage, isolated from a soil sample originating from Lincolnshire, United Kingdom. Many open reading frames within ΦCAM shared high levels of similarity to a prophage from Salinispora tropica and a putative prophage in Streptomyces sp. strain C.

  13. Screening of Mangrove Forest Actinomycetes and Its Antitumor Activity Detection%红树林放线菌筛选及其抗肿瘤活性测定

    Institute of Scientific and Technical Information of China (English)

    周中流; 徐立军

    2012-01-01

    Objective To isolate and purify the microbial strains from sea mud samples collected in Zhanjiang mangrove wetland for screening and detecting the antitumor activity. Methods The morphological method was adopted to identify actinomycetes strains. The MTT assay was applied to measure two tumor cells lines ( A549 and K562 ) cytotoxicity of 72 strains of actinomycete fermentation broth. Results By identification of isolated 72 strains of actinomycete, 18 percents of actinomycete fermentation broth showed the cytotoxicity in varying degrees. Especially,the fermentation broth of N2010-37 and N2010-68 revealed obvious antitumor activity on the above - mentioned two tumor cells lines. Conclusion The research results establish the foundation for seeking the antitumor components from mangrove forest actinomycete in Zhanjiang.%目的 从我国湛江红树林采集的海泥样品中分离纯化微生物菌株并进行筛选及抗肿瘤活性测定.方法 采用形态学方法鉴定放线菌菌株;采用四氮唑盐(MTT)法测定筛选出的72株放线菌发酵液对肺癌细胞A549与人类慢性髓性白血病细胞K562两种肿瘤细胞的细胞毒活性.结果 经鉴定分离得到了72株放线菌,其中18%的放线菌发酵液具有不同程度的细胞毒活性.N2010-37和N2010-68两株放线菌发酵液对上述两种肿瘤细胞株作用较显著.结论 该研究结果为从湛江红树林放线菌中寻找抗肿瘤活性成分奠定了基础.

  14. Comparative study of different methods for isolation of marine actinomycetes%海洋放线菌不同分离方法的比较研究

    Institute of Scientific and Technical Information of China (English)

    常显波; 刘文正; 尹琦; 张晓华

    2012-01-01

    The isolation techniques for marine actinomycetes from the inter-tidal sediment at Qingdao were studied by using the series dilution and plate spreading methods. The impacts of different pretreatments, diluents, seawater concentrations and media on the isolation of actinomycetes were investigated. The results showed that the growth of bacteria were obviously restrained in the samples when pretreated with 55℃ for 6 minutes, which enhanced the isolation of actinomycetes from the inter-tidal sediment; dilution of the samples with 1/4 Ringer's solution and spreading them on the media prepared with pure seawater could improve the isolation of actinomycetes. The 9 media exhibited significant differences on the number of actinomycetes recovered, with media Ml, M6, M7 and M8 being more effective than others.%采用平板涂布法,以青岛海区潮间带沉积物为对象进行海洋放线菌的分离方法研究.具体分析了不同样品预处理方式、稀释液、海水浓度和培养基种类等对分离效果的影响.结果表明,55℃预处理样品6 min能有效减少细菌数量,利于潮间带沉积物中放线菌的分离;以1/4林格氏溶液稀释样品、纯海水配置培养基,可以分离得到较多的放线菌;不同培养基对沉积物中放线菌的分离效果差别很大,本实验设置的M1 ~ M9培养基中,M1、M6、M7和M8培养基的分离效果优于其他5种.

  15. Nematicidal activity of fervenulin isolated from a nematicidal actinomycete, Streptomyces sp. CMU-MH021, on Meloidogyne incognita.

    Science.gov (United States)

    Ruanpanun, Pornthip; Laatsch, Hartmut; Tangchitsomkid, Nuchanart; Lumyong, Saisamorn

    2011-06-01

    An isolate of the actinomycete, Streptomyces sp. CMU-MH021 produced secondary metabolites that inhibited egg hatch and increased juvenile mortality of the root-knot nematode Meloidogyne incognita in vitro. 16S rDNA gene sequencing showed that the isolate sequence was 99% identical to Streptomyces roseoverticillatus. The culture filtrates form different culture media were tested for nematocidal activity. The maximal activity against M. incognita was obtained by using modified basal (MB) medium. The nematicidal assay-directed fractionation of the culture broth delivered fervenulin (1) and isocoumarin (2). Fervenulin, a low molecular weight compound, shows a broad range of biological activities. However, nematicidal activity of fervenulin was not previously reported. The nematicidal activity of fervenulin (1) was assessed using the broth microdilution technique. The lowest minimum inhibitory concentrations (MICs) of the compound against egg hatch of M. incognita was 30 μg/ml and juvenile mortality of M. incognita increasing was observed at 120 μg/ml. Moreover, at the concentration of 250 μg/ml fervenulin (1) showed killing effect on second-stage nematode juveniles of M. incognita up to 100% after incubation for 96 h. Isocoumarin (2), another bioactive compound produced by Streptomyces sp. CMU-MH021, showed weak nematicidal activity with M. incognita.

  16. Bioaugmenting anaerobic digestion of biosolids with selected strains of Bacillus, Pseudomonas, and Actinomycetes species for increased methanogenesis and odor control.

    Science.gov (United States)

    Duran, Metin; Tepe, Nalan; Yurtsever, Deniz; Punzi, Vito L; Bruno, Charles; Mehta, Raj J

    2006-12-01

    The objective of this study was to evaluate the effects of bioaugmenting anaerobic biosolids digestion with a commercial product containing selected strains of bacteria from genera Bacillus, Pseudomonas, and Actinomycetes, along with ancillary organic compounds containing various micronutrients. Specifically, the effects of the bioaugment in terms of volatile solids destruction and generation and fate of odor-causing compounds during anaerobic digestion and during storage of the digested biosolids were studied. Two bench-scale anaerobic digesters receiving primary and secondary clarifier biosolids from various full-scale biological wastewater treatment plants were operated. One of the digesters received the bioaugment developed by Organica Biotech, while the other was operated as control. The bioaugmented digester generated 29% more net CH(4) during the 8 weeks of operation. In addition, the average residual propionic acid concentration in the bioaugmented digester was 54% of that in the control. The monitoring of two organic sulfide compounds, methyl mercaptan (CH(3)SH) and dimethyl sulfide (CH(3)SCH(3)), clearly demonstrated the beneficial effects of the bioaugmentation in terms of odor control. The biosolids digested in the bioaugmented digester generated a negligible amount of CH(3)SH during 10 days of post-digestion storage, while CH(3)SH concentration in the control reached nearly 300 ppm(v) during the same period. Similarly, peak CH(3)SCH(3) generated by stored biosolids from the bioaugmented digester was only 37% of that from the control.

  17. A novel alkaloid from marine-derived actinomycete Streptomyces xinghaiensis with broad-spectrum antibacterial and cytotoxic activities.

    Directory of Open Access Journals (Sweden)

    Wence Jiao

    Full Text Available Due to the increasing emergence of drug-resistant bacteria and tumor cell lines, novel antibiotics with antibacterial and cytotoxic activities are urgently needed. Marine actinobacteria are rich sources of novel antibiotics, and here we report the discovery of a novel alkaloid, xinghaiamine A, from a marine-derived actinomycete Streptomyces xinghaiensis NRRL B24674(T. Xinghaiamine A was purified from the fermentation broth, and its structure was elucidated based on extensive spectroscopic analysis, including 1D and 2D NMR spectrum as well as mass spectrometry. Xinghaiamine A was identified to be a novel alkaloid with highly symmetric structure on the basis of sulfoxide functional group, and sulfoxide containing compound has so far never been reported in microorganisms. Biological assays revealed that xinghaiamine A exhibited broad-spectrum antibacterial activities to both Gram-negative persistent hospital pathogens (e.g. Acinetobacter baumannii, Pseudomonas aeruginosa and Escherichia coli and Gram-positive ones, which include Staphylococcus aureus and Bacillus subtilis. In addition, xinghaiamine A also exhibited potent cytotoxic activity to human cancer cell lines of MCF-7 and U-937 with the IC50 of 0.6 and 0.5 µM, respectively.

  18. Chapter 5. Applying the genetics of secondary metabolism in model actinomycetes to the discovery of new antibiotics.

    Science.gov (United States)

    van Wezel, Gilles P; McKenzie, Nancy L; Nodwell, Justin R

    2009-01-01

    The actinomycetes, including in particular members of the filamentous genus Streptomyces, are the industrial source of a large number of bioactive small molecules employed as antibiotics and other drugs. They produce these molecules as part of their "secondary" or nonessential metabolism. The number and diversity of secondary metabolic pathways is enormous, with some estimates suggesting that this one genus can produce more than 100,000 distinct molecules. However, the discovery of new antimicrobials is hampered by the fact that many wild isolates fail to express all or sometimes any of their secondary metabolites under laboratory conditions. Furthermore, the use of previously successful screening strategies frequently results in the rediscovery of known molecules: the all-important novel structures have proven to be elusive. Mounting evidence suggests that streptomycetes possess many regulatory pathways that control the biosynthetic gene clusters for these secondary metabolic pathways and that cell metabolism plays a significant role in limiting or potentiating expression as well. In this article we explore the idea that manipulating metabolic conditions and regulatory pathways can "awaken" silent gene clusters and lead to the discovery of novel antimicrobial activities.

  19. Degradation of carbonyl sulfide by Actinomycetes and detection of clade D of β-class carbonic anhydrase.

    Science.gov (United States)

    Ogawa, Takahiro; Kato, Hiromi; Higashide, Mitsuru; Nishimiya, Mami; Katayama, Yoko

    2016-09-25

    Carbonyl sulfide (COS) is an atmospheric trace gas and one of the sources of stratospheric aerosol contributing to climate change. Although one of the major sinks of COS is soil, the distribution of COS degradation ability among bacteria remains unclear. Seventeen out of 20 named bacteria belonging to Actinomycetales had COS degradation activity at mole fractions of 30 parts per million by volume (ppmv) COS. Dietzia maris NBRC 15801(T) and Mycobacterium sp. THI405 had the activity comparable to a chemolithoautotroph Thiobacillus thioparus THI115 that degrade COS by COS hydrolase for energy production. Among 12 bacteria manifesting rapid degradation at 30 ppmv COS, Dietzia maris NBRC 15801(T) and Streptomyces ambofaciens NBRC 12836(T) degraded ambient COS (∼500 parts per trillion by volume). Geodermatophilus obscurus NBRC 13315(T) and Amycolatopsis orientalis NBRC 12806(T) increased COS concentrations. Moreover, six of eight COS degrading bacteria isolated from soils had partial nucleotide sequences similar to that of the gene encoding clade D of β-class carbonic anhydrase, which included COS hydrolase. These results indicate the potential importance of Actinomycetes in the role of soils as sinks of atmospheric COS.

  20. Genetic transformation of marine Actinomycete sp. Isolate M048 and expression of a recombinant plasmid carrying the apc gene

    Institute of Scientific and Technical Information of China (English)

    HOU Yanhua; LI Fuchao; QIN Song; WANG Quanfu

    2006-01-01

    Optimal conditions for protoplasts formation of marine Actinomycete sp. isolate M048 were described, dense and disperse mycelia were cultured in SGGP medium, 0.5% glycine, lysozyme exposure (2 mg/cm3, 37 ℃, 40 min), and the concentration of sucrose in protoplast buffer was 0.4 mol/dm3 for keeping the balance of osmotic pressure. Using PEG-mediated protoplasts transformation, the transformation frequency was 89 transformants per microgramme of pIJ702. Meanwhile, an effective transformation procedure was established based on intergeneric conjugation from E. coli ET12567 (pUZ8002) using shuttle vectors pPM801, pPM803 and a(ψ)C31-derived integration vector pIJ8600 containing oriT and attP fragments. Transformation frequencies were 5.30×10-4±0.26×10-4, 8.92×10-4±0.19×10-4 and 6.38×10-5±0.41×10-5, respectively. Further, the heterologous expression of the allophycocyanin gene (apc) in the strain M048 was used to demonstrate this transformation system. SDS-PAGE and Western blot analysis confirmed the expression of recombinant APC (rAPC).

  1. 促己酸菌产己酸的优良放线菌的筛选%Screening of Fine Actinomycetes that Promoting Caproic Acid Bacteria Producing Caproic Acid

    Institute of Scientific and Technical Information of China (English)

    郭威; 黄宇; 谢逾群; 方尚玲; 陈茂彬

    2016-01-01

    Research on actinomycetes related to liquor-making was not deep enough.More research were spent on molds, yeasts and bacteria.The paper screened an excellent actinomycetes named GW01 which can promoting caproic acid bacteria producing caproic acid. Moreover, GW01 can better adapt to the environment of pits.The development of actinomycetes GW01 may contribute to a better understanding of liquor brewing actinomycetes,and open up liquor brewing actinomycetes strain resources.%目前酿酒微生物的研究主要集中在霉菌、酵母菌和细菌。白酒酿造相关放线菌的研究存在进展缓慢、严重滞后、菌种资源匮乏等问题。以放线菌对己酸菌产己酸的影响为基础,筛选到一株优良放线菌GW01。该放线菌对己酸菌产己酸有较好促进作用,还对窖池环境有良好的适应性。放线菌GW01的开发有助于更好认识白酒酿造中的放线菌,拓展了白酒酿造放线菌资源。

  2. Study on method of actinomycetes isolation from Dead Sea%死海嗜盐耐盐放线菌分离方法研究

    Institute of Scientific and Technical Information of China (English)

    任海柯; 来航线; 王晨霞; 韦小敏

    2012-01-01

    【Objective】 The study was to explore an optimal method of actinomycetes isolation from Dead Sea,so as to improve the isolation of actinomycetes from soil with high salt concentration.【Method】 Actinomycete counts and numbers of actinomycete species were analyzed from three aspects:sample pre-treatments,cultural media and salt concentrations of media.Nine pre-treatments,including chemical,physical and accumulation culture methods,three types of cultural media,ISP5,HV and CMKA,and three salt concentrations of each medium(150,225,300 g/L) were tested.【Result】 ① For sample pre-treatments,numbers of actinomycete species isolated from the chemical+physical pre-treated sample were apparently higher than that from others,whereas species numbers isolated from the accumulation cultured sample were the least on three media.② With all of the three salt concentrations,numbers of actinomycete species and actinomycete counts isolated from soil samples both led a trend:CMKA〉HV〉ISP5.③ On three media,numbers of actinomycete species isolated from samples showed:300 g/L〉225 g/L〉150 g/L,while actinomycete counts showed:150 g/L〉225 g/L〉300 g/L.【Conclusion】 Pretreating soil samples with chemical+physical method and using 225 g/L salt concentration CMKA medium is the best way to isolate actinomycetes from Dead Sea.%【目的】探讨死海高盐地区分离嗜盐耐盐放线菌的最佳方法,为高盐地区放线菌的分离提供理论依据。【方法】采用物理方法(微波)、化学方法(加入孢子活化剂)、富集培养法及3种方法的组合共计9种方法,对死海地区土样进行预处理,然后在3种复合盐含量(150,225,300g/L)及不同培养基(ISP5、CMKA、HV)条件下,研究复合盐含量及培养基对分离放线菌种类和数量的影响,并筛选嗜盐耐盐放线菌的最佳分离方法。【结果】①在3种培养基上,对土样采用9种方法进行预处理,其中物理+化学

  3. Isolation of Actinomycetes from Mangrove in Guangxi and Extraction of Its Genomic DNA%广西红树林放线菌的分离和DNA的提取

    Institute of Scientific and Technical Information of China (English)

    徐雅娟; 陈森洲; 骆耐香; 孔杰; 黄大林

    2009-01-01

    The actinomycetes in sea mud samples that from mangrove in Guangxi was isolated and its genomic DNA was extracted for 16S rDNA PCR amplification, and the isolated actinomycetes was identified. The results showed that the genomic DNA of actinomycetes from mangrove soil could successfully amplified 16S rDNA.%从广西红树林海泥样本中分离放线菌,提取其基因组DNA并进行16S rDNA PCR扩增,对所得放线菌进行鉴定.结果表明,从红树林土壤中提取的放线菌基因组DNA可成功扩增出16S rDNA.

  4. 内生放线菌对鬼臼毒素的微生物转化%Microbial Transformation of Podophyllotoxin by Endophytic Actinomycetes

    Institute of Scientific and Technical Information of China (English)

    曹松; 曾志刚

    2012-01-01

    The microbial transformation of podophyllotoxin by endophytic actinomycetes isolated from the rhizoma of Taoerqi ( Sinopodophyllum hexandrum) was investigated to obtain some structural analogues or derivatives of podophyllotoxin. Endophytic actinomycetes were isolated from the rhizoma of S. Hexandrum by surface-sterilization method, and screening test for the microbial transformation of podophyllotoxin was carried out using thin layer chromatography and high performance liquid chromatography ( HPLC ). Bio-transformed products of podophyllotoxin were isolated and purified by silica column chromatography and preparative HPLC, and chemical structures of transformed products were elucidated on the basis of chemical spectral data. The endophytic actinomycetes was identified by morphological characteristics, physiological and biochemical characteristics, and the analysis of fragment of 16S rRNA gene. The results showed that among totally isolated 20 endophytic actinomycetes, one was found to be able transform podophyllotoxin into 4'-demethylepipodophyllotoxin, which was identified preliminarily as Streptomyces sp. Endophytic actinomycetes Streptomyces sp. Was able to modify the chemical structure of podophyllotoxin by demethylation and isomerization reaction, it was deduced that this actinomycetes possessed 0-demethylation and isomerization enzyme.%调查桃儿七根茎内生放线菌对鬼臼毒素的微生物转化,以期获得一些鬼臼毒素的结构类似物或衍生物.利用表面消毒法分离内生放线菌;采用薄层层析和高效液相色谱(HPLC)方法筛选转化鬼臼毒素的内生放线菌;利用硅胶柱层析和制备HPLC分离纯化生物转化产物;应用波谱技术解析转化产物的化学结构;通过形态学、生理生化特征和16S rRNA基因序列分析对内生放线菌进行初步鉴定.从桃儿七根茎中分离出20株内生放线菌,经筛选发现其中1株放线菌能转化鬼臼毒素,其产物为4′-去甲基表

  5. Micromonospora taraxaci sp. nov., a novel endophytic actinomycete isolated from dandelion root (Taraxacum mongolicum Hand.-Mazz.).

    Science.gov (United States)

    Zhao, Junwei; Guo, Lifeng; He, Hairong; Liu, Chongxi; Zhang, Yuejing; Li, Chuang; Wang, Xiangjing; Xiang, Wensheng

    2014-10-01

    A novel actinomycete, designated strain NEAU-P5(T), was isolated from dandelion root (Taraxacum mongolicum Hand.-Mazz.). Strain NEAU-P5(T) showed closest 16S rRNA gene sequence similarity to Micromonospora chokoriensis 2-19/6(T) (99.5%), and phylogenetically clustered with Micromonospora violae NEAU-zh8(T) (99.3%), M. saelicesensis Lupac 09(T) (99.0%), M. lupini Lupac 14N(T) (98.8%), M. zeae NEAU-gq9(T) (98.4%), M. jinlongensis NEAU-GRX11(T) (98.3%) and M. zamorensis CR38(T) (97.9%). Phylogenetic analysis based on the gyrB gene sequence also indicated that the isolate clustered with the above type strains except M. violae NEAU-zh8(T). The cell-wall peptidoglycan consisted of meso-diaminopimelic acid and glycine. The major menaquinones were MK-9(H8), MK-9(H6) and MK-10(H2). The phospholipid profile contained diphosphatidylglycerol, phosphatidylethanolamine and phosphatidylinositol. The major fatty acids were C(16:0), iso-C(15:0) and C(17:0). Furthermore, some physiological and biochemical properties and low DNA-DNA relatedness values enabled the strain to be differentiated from members of closely related species. Therefore, it is proposed that strain NEAU-P5(T) represents a novel species of the genus Micromonospora, for which the name Micromonospora taraxaci sp. nov. is proposed. The type strain is NEAU-P5(T) (=CGMCC 4.7098(T) = DSM 45885(T)).

  6. Optimizing water treatment practices for the removal of actinomycetes and earthy odor in water of Bovilla reservoir

    Directory of Open Access Journals (Sweden)

    ADELA KULLAJ

    2014-06-01

    Full Text Available Bovilla reservoir, which is situated 15 km North-East of Tirana the capital city of Albania is one of the major hidrotechnical works of this country. This reservoir is a warm monomictic water body and stratifies higher in the summer season. The predominant trophic state of Bovilla reservoir is oligotrophy. From autumn 2001 this reservoir repeatedly manifests an unpleasant taste and odor which is defined as musty- earthy. Taste and odor control has become an important issue for drinking water suppliers worldwide. Consumers react very sensitively to changes in the organoleptic quality of their drinking water. The reason is that odor compounds present a very low threshold of perception (10–20 ng/L. Bovilla water treatment plant treats 1800 L/s raw water taken from Bovilla reservoir, using oxidation, coagulation and flocculation, sedimentation, filtration and disinfection process. In cases of bad odor powdered activated carbon (PAC is added at the rapid mix section. Throughout the monitoring period were done: quality and sensory analysis of raw water on a weekly frequency, analysis of treated water after coagulation, laboratory scale experiments using different doses of chemicals, applying optimized doses in full scale and PAC adsorption experiments. The aims of this study were: to predict the PAC doses required to treat water of Bovilla reservoir containing bad taste and odor, to establish the removal efficiency of taste and odor by three types of activated carbons with different iodine number and to assess the impact of NaOCl and other chemical in the treatment process of the plant in removing actinomycetes and bad odor. Results have shown that traditional treatment processes are usually inadequate in removing taste and odor and optimization of plant practices is required. Powdered activated carbon (PAC can effectively remove taste and odor when the correct dose is applied.

  7. Utilization of Agro-industrial Wastes for the Simultaneous Production of Amylase and Xylanase by Thermophilic Actinomycetes

    Directory of Open Access Journals (Sweden)

    Renu Singh

    2012-12-01

    Full Text Available Agro-industrial wastes such as sugarcane bagasse, wheat bran, rice bran, corn cob and wheat straw are cheapest and abundantly available natural carbon sources. The present study was aimed to production of amylase and xylanase simultaneously using agro-industrial waste as the sole carbon source. Seven thermophilic strains of actinomycete were isolated from the mushroom compost. Among of these, strain designated MSC702 having high potential to utilize agro-industrial wastes for the production of amylase and xylanase. Strain MSC702 was identified as novel species of Streptomyces through morphological characterization and 16S rRNA gene sequence. Enzyme production was determined using 1% (w/v of various agro-industrial waste in production medium containing (g/100mL: K2HPO4(0.1, (NH42SO4(0.1, NaCl (0.1, MgSO4(0.1 at pH 7.0 after incubation of 48 h at 50°C. The amylase activity (373.89 IU/mL and xylanase activity (30.15 IU/mL was maximum in rice bran. The decreasing order of amylase and xylanase activity in different type of agro-industrial wastes were found rice bran (RB > corn cob (CC > wheat bran (WB > wheat straw (WS > sugarcane bagasse (SB and rice bran (RB > wheat bran (WB > wheat straw (WS > sugarcane bagasse (SB > corn cob (CC, respectively. Mixed effect of different agro-industrial wastes was examined in different ratios. Enzyme yield of amylase and xylanase was ~1.3 and ~2.0 fold higher with RB: WB in 1:2 ratio.

  8. Endophytic actinomycetes from spontaneous plants of Algerian Sahara: indole-3-acetic acid production and tomato plants growth promoting activity.

    Science.gov (United States)

    Goudjal, Yacine; Toumatia, Omrane; Sabaou, Nasserdine; Barakate, Mustapha; Mathieu, Florence; Zitouni, Abdelghani

    2013-10-01

    Twenty-seven endophytic actinomycete strains were isolated from five spontaneous plants well adapted to the poor sandy soil and arid climatic conditions of the Algerian Sahara. Morphological and chemotaxonomical analysis indicated that twenty-two isolates belonged to the Streptomyces genus and the remaining five were non-Streptomyces. All endophytic strains were screened for their ability to produce indole-3-acetic acid (IAA) in vitro on a chemically defined medium. Eighteen strains were able to produce IAA and the maximum production occurred with the Streptomyces sp. PT2 strain. The IAA produced was further extracted, partially purified and confirmed by thin layer chromatography (TLC) analysis. The 16S rDNA sequence analysis and phylogenetic studies indicated that strain PT2 was closely related to Streptomyces enissocaecilis NRRL B 16365(T), Streptomyces rochei NBRC 12908(T) and Streptomyces plicatus NBRC 13071(T), with 99.52 % similarity. The production of IAA was affected by cultural conditions such as temperature, pH, incubation period and L-tryptophan concentration. The highest level of IAA production (127 μg/ml) was obtained by cultivating the Streptomyces sp. PT2 strain in yeast extract-tryptone broth supplemented with 5 mg L-tryptophan/ml at pH 7 and incubated on a rotary shaker (200 rpm) at 30 °C for 5 days. Twenty-four-hour treatment of tomato cv. Marmande seeds with the supernatant culture of Streptomyces sp. PT2 that contained the crude IAA showed the maximum effect in promoting seed germination and root elongation.

  9. Bioactive 2(1H-Pyrazinones and Diketopiperazine Alkaloids from a Tunicate-Derived Actinomycete Streptomyces sp.

    Directory of Open Access Journals (Sweden)

    Lamiaa A. Shaala

    2016-08-01

    Full Text Available As a part of our ongoing effort to allocate marine microbial bioactive leads, a tunicate-derived actinomycete, Streptomyces sp. Did-27, was investigated. Three new 2(1H-pyrazinones derivatives, (S-6-(sec-butyl-3-isopropylpyrazin-2(1H-one (1, (S-3-(sec-butyl-6-isopropylpyrazin-2(1H-one (2 and (S-6-(sec-butyl-3-isobutylpyrazin-2(1H-one (3, together with the known (1H-pyrazinones analogues deoxymutaaspergillic acid (4, 3,6-diisobutyl-2(1H-pyrazinone (5 and 3,6-di-sec-butyl-2(1H-pyrazinone (6, and the diketopiperazine alkaloids cyclo(6-OH-d-Pro-l-Phe (7, bacillusamide B (8, cyclo(l-Pro-l-Leu and cyclo(l-Pro-l-Ile (10 were isolated from this strain. The structures of the compounds were determined by study of their one- and two-dimensional NMR spectra as well as high-resolution mass spectral determinations. Compound 4 was reported previously as a synthetic product, while compound 6 was reported as 2-hydroxy-3,6-di-sec-butylpyrazine. Herein, we report the complete NMR data for compounds 4 and 6. The compounds were evaluated for their cytotoxic activities against three cell lines. Compound 5 showed potent and selective activity against HCT-116 cell line with IC50 of 1.5 μg/mL, while 1–10 showed variable cytotoxic activities against these cancer cell lines. These results provide further understanding about the chemistry and bioactivities of the alkylated 2(1H-pyrazinone derivatives.

  10. Degradation of Textile Dye Reactive Navy – Blue Rx (Reactive blue–59 by an Isolated Actinomycete Streptomyces krainskii SUK – 5

    Directory of Open Access Journals (Sweden)

    Mane, U. V.

    2008-01-01

    Full Text Available The isolated Actinomycete, Streptomyces krainskii, SUK -5 was found to decolorize and degrade textile dye Reactive blue–59.This azo dye was decolorized and degraded completely by Streptomyces krainskii SUK–5 at 24 h in shaking condition in the nutrient medium at pH 8. Induction in the activity of Lignin Peroxidase,and NADH-DCIP Reductase and MR reductase represents their role in degradation .The biodegradation was monitored by TLC, UV vis spectroscopy, FTIR. and GCMS analysis. Microbial and phytotoxicity studies of the product were carried out.

  11. Diversity of foam producing nocardioform actinomycetes isolated from biological foam from activated sludge plants in Comunidad Valenciana; Diversidad de actinomicetos nocardioformes productores de espumas biologicas aislados de plantas depuradoras de aguas residuales de la Comunidad Valenciana

    Energy Technology Data Exchange (ETDEWEB)

    Soler, A.; Alonso, J.L.; Cuesta, G.

    2009-07-01

    The formation of biological foams in activated sludge systems is one of the most important problems of solid separation in wastewater treatment plants. Nocardioform actinomycetes are the most important filamentous bacteria responsible of foam formation. This group of microorganisms has hydrophobic cellular surfaces due to the mycolic acids. These foams interfere in wastewater treatment process because retain many suspended solids, block conductions and produce overflowing in the digesters and corridors. To identify correctly the nocardioform actinomycetes we have to do poli phasic taxonomy that includes 16S rDNA sequences analysis, determinate several chemo taxonomic markers and some phenotypic tests. (Author) 18 refs.

  12. Determination of the Residual Anthracene Concentration in Cultures of Haloalkalitolerant Actinomycetes by Excitation Fluorescence, Emission Fluorescence, and Synchronous Fluorescence: Comparative Study

    Directory of Open Access Journals (Sweden)

    Reyna del Carmen Lara-Severino

    2016-01-01

    Full Text Available Polycyclic aromatic hydrocarbons (PAHs are compounds that can be quantified by fluorescence due to their high quantum yield. Haloalkalitolerant bacteria tolerate wide concentration ranges of NaCl and pH. They are potentially useful in the PAHs bioremediation of saline environments. However, it is known that salinity of the sample affects fluorescence signal regardless of the method. The objective of this work was to carry out a comparative study based on the sensitivity, linearity, and detection limits of the excitation, emission, and synchronous fluorescence methods, during the quantification of the residual anthracene concentration from the following haloalkalitolerant actinomycetes cultures Kocuria rosea, Kocuria palustris, Microbacterium testaceum, and 4 strains of Nocardia farcinica, in order to establish the proper fluorescence method to study the PAHs biodegrading capacity of haloalkalitolerant actinobacteria. The study demonstrated statistical differences among the strains and among the fluorescence methods regarding the anthracene residual concentration. The results showed that excitation and emission fluorescence methods performed very similarly but sensitivity in excitation fluorescence is slightly higher. Synchronous fluorescence using Δλ=150 nm is not the most convenient method. Therefore we propose the excitation fluorescence as the fluorescence method to be used in the study of the PAHs biodegrading capacity of haloalkalitolerant actinomycetes.

  13. Production of Induced Secondary Metabolites by a Co-Culture of Sponge-Associated Actinomycetes, Actinokineospora sp. EG49 and Nocardiopsis sp. RV163

    Directory of Open Access Journals (Sweden)

    Yousef Dashti

    2014-05-01

    Full Text Available Two sponge-derived actinomycetes, Actinokineospora sp. EG49 and Nocardiopsis sp. RV163, were grown in co-culture and the presence of induced metabolites monitored by 1H NMR. Ten known compounds, including angucycline, diketopiperazine and β-carboline derivatives 1–10, were isolated from the EtOAc extracts of Actinokineospora sp. EG49 and Nocardiopsis sp. RV163. Co-cultivation of Actinokineospora sp. EG49 and Nocardiopsis sp. RV163 induced the biosynthesis of three natural products that were not detected in the single culture of either microorganism, namely N-(2-hydroxyphenyl-acetamide (11, 1,6-dihydroxyphenazine (12 and 5a,6,11a,12-tetrahydro-5a,11a-dimethyl[1,4]benzoxazino[3,2-b][1,4]benzoxazine (13a. When tested for biological activity against a range of bacteria and parasites, only the phenazine 12 was active against Bacillus sp. P25, Trypanosoma brucei and interestingly, against Actinokineospora sp. EG49. These findings highlight the co-cultivation approach as an effective strategy to access the bioactive secondary metabolites hidden in the genomes of marine actinomycetes.

  14. 嗜盐嗜碱放线菌的研究进展与展望%Research on Progress of Halophilic Basophilic Actinomycetes

    Institute of Scientific and Technical Information of China (English)

    加苏尔·阿不都克里木; 旭格拉; 塔衣尔; 阿不都克里木·热依木; 木尼热木·阿力木江; 迪丽拜尔·托合提

    2015-01-01

    Haloalkaliphilic extremophiles were survied in saline alkali soil. Halophilic basophilic Actinomycetes with the genetic characteristics and the special supersedes way, produced a variety of secondary me⁃tabolites, was one of microbial resources with great application prospect. This paper mainly reviewed Halophilic ba⁃sophilic Actinomycetes Resources, standard classification, distribution, system science, development and utilization prospects.%嗜盐嗜碱极端微生物主要分布于地球上的盐碱土壤中,嗜盐嗜碱放线菌适应并长期生存这一特殊极端环境,已具备独特的遗传特性和新陈代谢途径,能够产生具有开发利用价值的多种次生代谢产物,是一类极具应用前景的微生物资源。文章主要综述了嗜盐嗜碱放线菌的资源、分类标准、分布、系统学及其发展趋势、开发利用前景。

  15. Research advances on endophytic actinomycetes and their bioactive metabolites%植物内生放线菌及其生理活性物质研究进展

    Institute of Scientific and Technical Information of China (English)

    黄小龙; 周双清; 陈吉良

    2011-01-01

    Endophytic actinomycetes are a new microbiological resources for development of potentials. Till now, many kinds of endophytic actinomycetes were isolated from many living internal plant tissues. Endophytic actinomycetes can produce a lot of important physiological bioactive metabolites such as antibiotics , plant growth promoters , plant growth inhibitors and new characteristic enzymes.This paper summarized the recent advances on the studies of endophytic actinomycetes of plants and their bioactive metabolites.%植物内生放线菌是一类具有巨大开发潜力的新微生物资源.目前从许多活体植物组织内已分离到种类众多的植物内生放线菌,已有的研究表明植物内生放线菌能产生许多重要的生理活性物质,如抗生素类物质、植物生长促进剂、植物生长抑制剂以及具有新特性的酶类.植物内生放线菌在农业生产、医药新药的筛选上显示出广阔的应用前景.

  16. Selection and evaluation of reference genes for RT-qPCR expression studies on Burkholderia tropica strain Ppe8, a sugarcane-associated diazotrophic bacterium grown with different carbon sources or sugarcane juice.

    Science.gov (United States)

    da Silva, Paula Renata Alves; Vidal, Marcia Soares; de Paula Soares, Cleiton; Polese, Valéria; Simões-Araújo, Jean Luís; Baldani, José Ivo

    2016-11-01

    Among the members of the genus Burkholderia, Burkholderia tropica has the ability to fix nitrogen and promote sugarcane plant growth as well as act as a biological control agent. There is little information about how this bacterium metabolizes carbohydrates as well as those carbon sources found in the sugarcane juice that accumulates in stems during plant growth. Reverse transcription quantitative PCR (RT-qPCR) can be used to evaluate changes in gene expression during bacterial growth on different carbon sources. Here we tested the expression of six reference genes, lpxC, gyrB, recA, rpoA, rpoB, and rpoD, when cells were grown with glucose, fructose, sucrose, mannitol, aconitic acid, and sugarcane juice as carbon sources. The lpxC, gyrB, and recA were selected as the most stable reference genes based on geNorm and NormFinder software analyses. Validation of these three reference genes during strain Ppe8 growth on the same carbon sources showed that genes involved in glycogen biosynthesis (glgA, glgB, glgC) and trehalose biosynthesis (treY and treZ) were highly expressed when Ppe8 was grown in aconitic acid relative to other carbon sources, while otsA expression (trehalose biosynthesis) was reduced with all carbon sources. In addition, the expression level of the ORF_6066 (gluconolactonase) gene was reduced on sugarcane juice. The results confirmed the stability of the three selected reference genes (lpxC, gyrB, and recA) during the RT-qPCR and also their robustness by evaluating the relative expression of genes involved in glycogen and trehalose biosynthesis when strain Ppe8 was grown on different carbon sources and sugarcane juice.

  17. 微波处理对嗜碱和嗜盐海洋放线菌分离效果的影响%Effects of microwave irradiation on isolation of basophilic and halophilic marine actinomycetes

    Institute of Scientific and Technical Information of China (English)

    丁彦博; 蔡超靖; 穆云龙; 单越琦; 路新华; 蒋沁

    2012-01-01

    [Objective] Study the effects of microwave irradiation on isolation of basophilic and halophilic marine actinomycetes. [Methods] Seven marinemud samples were radiated by microwave and then gradient diluted for isolation of basophilic and halophilic marine actinomycetes in three media. [Results] Microwave irradiation could highly significantly increase the total quantity of basophilic and halophilic marine actinomycetes respectively in four and three marinemud samples. The total quantity of basophilic and halophilic marine rare actinomycetes of Micromonospora, Actinoplanes and Nocardia were significantly increased after microwave irradiation. The species of other marine rare actinomycetes such as Catellatospora, Microbispora, Streptosporangium were increased to one to four in different samples. [Conclusion] Microwave irradiation could significantly increase the total quantity of basophilic and halophilic marine actinomycetes and the species of marine rare actinomycetes.%[目的]研究微波处理对于分离嗜碱和嗜盐海洋放线菌的效果.[方法]用微波处理7份海泥样品,梯度稀释后涂布于3种分离培养基,分离具有嗜碱和嗜盐特性的海洋放线菌.[结果]微波处理后的7份样品中,4份样品中嗜碱海洋稀有放线菌和3份样品的嗜盐海洋稀有放线菌数量极显著提高;7份样品中的嗜碱、嗜盐海洋小单孢菌属、游动放线菌属、诺卡氏菌属等稀有放线菌数量均有显著增加,不同样品中新分离到链孢菌属、小双孢菌属、链孢囊菌属及其他未鉴定的海洋稀有放线菌,分离到属的数量提高了1-4个.[结论]微波处理不仅显著提高嗜碱和嗜盐海洋放线菌的分离数量,而且明显增加了海洋稀有放线菌的分离种类.

  18. Screening of Ferulic acid degrading actinomycetes and their degradation and inhibiting effect%阿魏酸降解放线菌的筛选及其降解与拮抗效果研究

    Institute of Scientific and Technical Information of China (English)

    王晓辉; 薛泉宏

    2011-01-01

    【目的】筛选用于降解西瓜根泌自毒物质阿魏酸的放线菌,研究其降解与拮抗效果。【方法】以127株放线菌为供筛菌株,采用液体发酵培养法筛选阿魏酸降解放线菌,并研究放线菌对阿魏酸的降解率及对西甜瓜枯萎病菌等病原菌的拮抗性。【结果】①从127株供试放线菌中筛选出了编号为25,28及Z30的3株放线菌,在纯培养条件下,以阿魏酸为惟一碳源时,25、28、Z30 3株放线菌对阿魏酸均有较好的降解效果,降解率分别为94.3%,92.6%和90.1%。②在以阿魏酸、淀粉为混合碳源时,3株放线菌对阿魏酸均有较强的降解作用,降解率最高达100%。③纯细胞培养时,3株放线菌对阿魏酸仅有微弱的降解效果。④3株放线菌对西甜瓜枯萎病菌有较强的拮抗作用。【结论】筛选的3株放线菌具有降解西瓜自毒物质阿魏酸及拮抗西甜瓜枯萎病菌的双重功能。%【Objective】 The experiment was to screen degradaeng actinomycetes of ferulic acid and to study the degradation and inhibitory effect of the actinomycetes.【Method】 Liquid fermentation experiment was carried out to screen degradating actinomycetes of ferulic acid from 127 actinomyces strains and to study the degradation rate of ferulic acid by the actinomyces and their inhibiting effect on melon and cucumber fusarium wilt pathogen.【Result】 ①The actinomycetes 25,28 and Z30 were screened from 127 tested actinomycetes strains.Under pure culture conditions,the ferulic acid was the sole carbon source.The degradation rates of ferulic acid completed by the actinomycetes 25,28 and Z30 were 94.3%,92.6% and 90.1%,respectively.②In a mixture of ferulic acid and starch as carbon sources,the degradation rate of ferulic acid completed by the three actinomycetes was 100%.③The degradation rate of ferulic acid by three actinomycetes as pure cell was low.④The three strains of actinomycets have good inhibiting effect on the melon and

  19. Volatile metabolites from actinomycetes

    DEFF Research Database (Denmark)

    Scholler, C.E.G.; Gurtler, H.; Pedersen, R.;

    2002-01-01

    and identified or characterized by gas chromatography-mass spectrometry. A total of 120 VOCs were characterized by retention index and mass spectra. Fifty-three compounds were characterized as terpenoid compounds, among which 18 could be identified. Among the VOCs were alkanes, alkenes, alcohols, esters, ketones...

  20. [THE ROLE OF (p)ppGpp MOLECULES IN FORMATION OF "STRICT RESPONSE" IN BACTERIA AND BIOSYNTHESIS OF ANTIBIOTICS AND MORPHOLOGICAL DIFFERENTIATION IN ACTINOMYCETES].

    Science.gov (United States)

    Klymyshin, D; Stephanyshyn, O; Fedorenko, V

    2016-01-01

    Strict response is a pleiotropic physiological response of cells caused by lack of aminoacetylated tRNAs. Experimentally, this response occurs due to the lack of amino acids in the environment and the limitation of tRNA aminoacylation even in the presence of the corresponding amino acids in the cell. Many features of this response indicate its dependence on the accumulation of ppGpp molecules. There is a correlation between the growth rate of actinomycetes and biosynthesis of their secondary metabolites. Introduction of additional relA gene copies of ppGpp synthetase can affect the production of antibiotics in streptomycetes. The article presents the authors' own experimental data, dedicated to the influence of heterologous relA gene expression in Streptomyces nogalater cells.

  1. Isolation of Actinomycetes from Xisha Islands and Their Antimicrobial Activities%西沙群岛海域海洋放线菌的分离及其抗菌活性

    Institute of Scientific and Technical Information of China (English)

    房耀维; 王淑军; 刘姝; 吕明生; 焦豫良; 陈国强; 潘建梅

    2014-01-01

    Antimicrobial activities of actinomycete isolated from samples collected in Xisha Islands,Hainan Province, China were studied. The isolation of the samples adopted exsiccation,radiation,freezing,heating and others eleven sample pretreatment processes. Among them the typical strains were characterized and investigated for their growth and dependence on seawater. Staphylococcus aureus,E. coli,Saccharomyces cerevisiae,and Penicillium expansum were taken as indicators to test their antimicrobial activities. 383 actinomycete strains were isolated from samples collected in Xisha Islands. 23 of them were marine obligate actinomycetes. 93 typical strains were characterized and belonged to 9 families and 11 genera. The media used to isolated actinomycete strains had significantly affected the number and kinds of the strains. Six actinomycetes strains had antimicrobial activities against four tested indicators strains,among them four were marine obligate actinomycetes indicating that marine environment has abundant resources of actinomy-cetes. These actinomycetes,especially the marine obligate actinomycetes are hopeful to be a source to discover and develop novel antibiotic substances provide source for strain seeds.%分离西沙群岛海域放线菌并研究其抗菌活性。采用干燥、辐射、冷冻及加热处理等11种样品预处理方式和10种培养基对海洋放线菌进行分离,对代表性菌株进行鉴定,并考察分离放线菌生长的海水依赖性。进一步以金黄色葡萄球菌、大肠埃希菌、啤酒酵母和扩展青霉为指示菌考察分离放线菌的抗菌活性。从西沙群岛海域样品中分离获得放线菌383株,其中专性海洋放线菌23株。选定93株代表菌株进行鉴定,93株菌隶属于9个科,11个属。不同培养基对分离放线菌菌株的数量及种类影响显著。6株放线菌对4种指示菌均有抑菌活性,其中4株为专性海洋放线菌,表明海洋环境具有丰富的放线

  2. Genome-wide analysis of the role of GlnR in Streptomyces venezuelae provides new insights into global nitrogen regulation in actinomycetes

    Directory of Open Access Journals (Sweden)

    Bibb Mervyn J

    2011-04-01

    Full Text Available Abstract Background GlnR is an atypical response regulator found in actinomycetes that modulates the transcription of genes in response to changes in nitrogen availability. We applied a global in vivo approach to identify the GlnR regulon of Streptomyces venezuelae, which, unlike many actinomycetes, grows in a diffuse manner that is suitable for physiological studies. Conditions were defined that facilitated analysis of GlnR-dependent induction of gene expression in response to rapid nitrogen starvation. Microarray analysis identified global transcriptional differences between glnR+ and glnR mutant strains under varying nitrogen conditions. To differentiate between direct and indirect regulatory effects of GlnR, chromatin immuno-precipitation (ChIP using antibodies specific to a FLAG-tagged GlnR protein, coupled with microarray analysis (ChIP-chip, was used to identify GlnR binding sites throughout the S. venezuelae genome. Results GlnR bound to its target sites in both transcriptionally active and apparently inactive forms. Thirty-six GlnR binding sites were identified by ChIP-chip analysis allowing derivation of a consensus GlnR-binding site for S. venezuelae. GlnR-binding regions were associated with genes involved in primary nitrogen metabolism, secondary metabolism, the synthesis of catabolic enzymes and a number of transport-related functions. Conclusions The GlnR regulon of S. venezuelae is extensive and impacts on many facets of the organism's biology. GlnR can apparently bind to its target sites in both transcriptionally active and inactive forms.

  3. Identification and preliminary characterization of non-polyene antibiotics secreted by new strain of actinomycete isolated from sebkha of Kenadsa, Algeria

    Institute of Scientific and Technical Information of China (English)

    Omar; Messaoudi; Mourad; Bendahou; Ibrahim; Benamar; Djamal-Elddine; Abdelwouhid

    2015-01-01

    Objective: To study the antimicrobial activity of actinomycetes isolated from sabkha of Kenadsa and identification of the isolate interesting. Methods: Eighteen strains were isolated, using four culture media from sebkha of Kenadsa(Bechar, Southwestern Algeria). Screening of antimicrobial activity consisted of two steps: in primary screening, antibacterial activity was determined by using the agar plug method against test strains; in secondary screening, better isolate which showed a good activity in the first screening was selected to extract antimicrobial substances. The antimicrobial activities of extracts were evaluated by using Kirby-Bauer disc diffusion method. Partial characterization of antimicrobial products was performed on the basis of chemical revelations, UV-vis spectrometry and infrared spectroscopy. The identification of isolate interesting was performed through morphological, chemical, biochemical and physiological characteristics. Results: All isolates showed antimicrobial activity against at least one microorganism test. One isolate, LAM143 cG 3, was selected for its broad spectrum and high antimicrobial activity. The isolate LAM143 c G3 was identified as Spirillospora sp. The comparison between the species of this genus(Spirillospora rubra and Spirillospora albida) and our isolate indicated the existence of several physiological and biochemical differences which led us to suppose that this was a new member of this genus. Primary characterization of antimicrobial substances produced by the isolate LAM143 c G3 indicated the presence of amines and phenols. The UV–vis spectrum suggested a non-polyenic nature of substances secreted by our isolate, while infrared confirmed the presence of amine groups.Conclusions: The result of the present study revealed that sebkha of Kenadsa was rich in rare actinomycetes, that secreted interesting antimicrobial substance.

  4. 垃圾堆肥放线菌发酵过滤液对高羊茅初期生长的影响%Effects of actinomycetes fermented filtrates from MSW compost on seedling growth of tall fescue

    Institute of Scientific and Technical Information of China (English)

    程田; 赵树兰; 多立安

    2012-01-01

    通过向草坪基质中加入不同浓度生活垃圾堆肥放线菌发酵滤液,研究了堆肥放线菌发酵液对草坪草高羊茅萌发及初期生长的影响。结果表明:各浓度放线菌发酵滤液对高羊茅的生长指标和叶绿素含量均有显著的促进作用,其中,以稀释4倍的放线菌发酵滤液的促进效果最为明显。在稀释4倍的放线菌发酵滤液的处理下,高羊茅的发芽率、株高、地上干重、地下干重和叶绿素含量分别比对照提高了17.3%、17.9%、20.0%、66.7%和60.3%。虽然,不同浓度的放线菌发酵滤液对高羊茅的萌发和初期生长均具有一定的促进作用,但以稀释4倍的放线菌发酵滤液效果为最佳。%The effect of different concentrations of actinomycetes fermented filtrate from municipal solid waste(MSW) compost on germination and seedling growth of tall fescue was studied.The results showed that different treatments of actinomycetes filtrates promoted the seed germination and growth.Among the three treatments,4 times diluted actinomycetes filtrate had the most obvious effect.Compared with the control,4 times diluted actinomycetes filtrate increased the germination rate,seedling height,aboveground dry weight,underground dry weight and total chlorophyll content by 17.3%,17.9%,20%,66.7% and 60.3% respectively.It could be concluded that actinomycetes filtrates at different concentrations could promote seed germination and seedling growth,and 4 times diluted actinomycetes filtrate was the most effective.

  5. 浅议达托霉素在环境放线菌中的抗性机制%Extraction of Supporting Drug Resistance Mechanism of Actinomycetes in the Environment

    Institute of Scientific and Technical Information of China (English)

    倪慧慧

    2013-01-01

    本文通过对所有环境放线菌耐受达托霉素的程度上,进行了药性、药理的研究,并且为出现临床耐药机制提供了预警,从而说明了达托霉素在环境放线菌中具有很高的抗性频率,其中它的主要抗性机制之一是灭活达托霉素。%This article through to al environmental actinomycetes tolerance of the extent of toxin, the medicinal properties, pharmacological research, and provides a warning in clinical drug resistance mechanism, which shows up to Joe drug resistance of actinomycetes in the environment of has the very high frequency, which is one of the main resistance mechanism of inactivated a toxin.

  6. 放线菌A4产淀粉酶发酵条件的优化%Optimization of the Fermentation Conditions for Amylase-Producing Actinomycetes A4

    Institute of Scientific and Technical Information of China (English)

    李堆淑

    2013-01-01

    In order to provide a certain theoretical reference for industrial production of amylase-producing actinomycetes, according to the nutritional requirement and growth characteristics of amylase-producing actinomycetes A, . the author analyzed the effects of different factors on fermentation of amylase-producing actinomycetes A,. The results showed that the optimal fermentation conditions included cornmeal 3.00%, liquid volume 80. 17 ml, pH 7. 75. beef extract 0. 5% and peptone 0. 49%. Under the optimum conditions, the average enzyme activity of amylase-producing actinomycetes A4 reached 1.939 U/mL.%为给工业化生产放线菌产淀粉酶提供一定的理论依据,根据产淀粉酶放线菌菌株A4的营养需要和生长特性,分析了不同因素对放线菌A4产淀粉酶发酵的影响.结果表明:放线菌A4产淀粉酶的最佳发酵条件为玉米粉3.00%、装液量80.17 mL、pH 7.75、牛肉膏0.5%和蛋白胨0.49%,在此条件下,产淀粉酶放线菌菌株A4的平均酶活力达1.939 U/mL.

  7. 一株产生物活性物质放线菌的分离鉴定%Isolation and Identification of a Strain of Actinomycetes Producing Bioactive Substance

    Institute of Scientific and Technical Information of China (English)

    詹建立; 陈芸; 陈涛

    2014-01-01

    基于16S rRNA 序列分析,本文对塔什库尔干县土壤中的放线菌进行了初步分离和鉴定。通过平板培养法,对分离鉴定的放线菌菌株进行活性物质的分析和研究,从塔县土壤中分离得到8株放线菌,其中 CT -1产生的活性物质能够抑制 Bacillus subtilis。从8株放线菌选出3株16S rRNA 的序列分析,推断放线菌 CT -1、CT -3和 CT -7菌株同属于内芽孢杆菌属(Paenibacillus)。实验表明这3株放线菌虽然来源相同却有不同的生理生化特性。%Based on the analysis of 16S rRNA sequence, this study isolated and identified actinomycetes isolated from the soil of Taxkorgan County. Then, by the method of culturing on the plates, we analyzed and studied the active substance of the isolated actinomycetes. It is shown that the three separated actinomycetes possibly belonged to the genus of Paenibacillus, and their physio-logical and biochemical charateristics are different. Meanwhile, the strains of actinomycetes CT-1 had the antibacterial effects on Bacillus subtilis.

  8. The Effects of Actinomycetes in Pit Mud of Nongxiang Baijiu(Liquor) on Liquor Quality%浓香型白酒窖泥中放线菌对酒质的影响

    Institute of Scientific and Technical Information of China (English)

    李东; 黄明

    2015-01-01

    放线菌是原核生物的一个类群。其在土壤、空气和水中,尤其是含水量低、有机物丰富、呈中性或微碱性的土壤中数量较多。而泥土中散发出来的土腥味就主要是由放线菌中链霉菌产生的土腥素造成的。通过对放线菌生长的土壤浸取液对浓香型白酒酒质的影响,初步探索了放线菌对浓香型白酒生产的影响。%Actinomycetes is a group of prokaryotes. It is distributed in the soil, air and water, and it is rich especially in soil with low moisture content or rich organic substances, and in neutral or slightly alkaline soil. The smell of the soil mainly comes from geosmin produced by Strep-tomyces in Actinomycetes. In this paper, the effects of soil leaching solution (soil with the growth of Actinomycetes) on the quality of Nongx-iang Baijiu(liquor) were investigated.

  9. 海洋放线菌代谢产物蒽环类化合物研究进展%Research Progress in Anthracycline Compounds Produced by Marine Actinomycetes

    Institute of Scientific and Technical Information of China (English)

    马毅敏; 陆园园; 邢莹莹; 奚涛

    2011-01-01

    The marine actinomycetes are likely to be important sources of new natural products. In recent years,plenty of novel structures have been isolated from marine actinomycetes. Among them,there are many novel anthracycline metabolites with good antibacterial and antitumor activities. Anthracycline compounds isolated from marine actinomycetes and their activities were summarized in this paper,and a perspective in regard to the future development of the marine natural products was also discussed.%海洋放线菌代谢产物是抗肿瘤活性物质的重要来源.近年来,从海洋放线菌中分离到很多新化合物,其中许多结构新颖的蒽环类代谢产物具有良好的抗菌抗肿瘤活性.文章对近年来从海洋放线菌中分离得到的蒽环类代谢产物进行了归纳,并展望今后海洋天然产物的发展方向.

  10. Isolation of an Antagonistic Actinomycete Strain against Dioscorea opposita Thunb Anthracnose and Its Primary Identification%一株淮山炭疽病拮抗放线菌的分离及初步鉴定

    Institute of Scientific and Technical Information of China (English)

    黄小龙; 曹树威; 周双清; 黄东益; 汤维

    2011-01-01

    [目的]从海南药用植物根际分离得到对淮山炭疽病具有拮抗活性的放线菌菌株,并时其分类地位进行鉴定.[方法]采用HV培养基从盾叶鸡蛋花根际土壤分离放线菌菌株;通过平板对峙培养和发酵代谢产物抑菌试验筛选活性放线菌;根据形态特征,结合16SrRNA基因序列分析鉴定活性放线菌的分类地位.[结果]从盾叶鸡蛋花的根际土壤分离到12株放线菌,筛选到1株对淮山炭疽病菌具有良好拮抗活性的菌株51173,菌株51173鉴定为链霉菌属Streptomyces violaceasniger 16S rRNA gene Glade中的成员.[结论]放线菌菌株51173在淮山炭疽病菌的生物防治中将具有很好的开发应用前景.%[Objective]The paper was to isolate actinomycete strains with antagonistic activity against Dioscorea opposita Thunb anthracnose from the rhizosphere soil of medicinal plants in Hainan Province, and identify its taxonomic status. [ Method ] Using HV medium, actinomycete strains were isolated from the rhizosphere soil of frangipani (Plumeria rubra L. ). The active antagonistic actinomycetes were selected by using confrontation culture method and inhibition test of fermentation products. According to morphology,combined with 16S rRNA gene analysis,the taxonomic status of active actinomycetes was identified. [ Result]Twelve strains of actinomycetes were isolated from the rhizosphere soil of medicinal plant frangipani(P. rubra L. ). Strain 51173 showed significant antifungal activity against Colletotrichum gloeosporioides, which was identified to be a member of Streptomyces violaceusniger 16S rRNA gene clade. [ Conclusion] Strain 51173 showed a good application potential for biological control against D. opposita Thunb anthracnose.

  11. 芦笋老茎堆肥中嗜热放线菌的分离和鉴定%Isolation and Identification of Thermophilic Actinomycetes in Asparagus Old Stem Compost

    Institute of Scientific and Technical Information of China (English)

    陈婷婷; 王丽芳; 王琪; 韩建荣

    2013-01-01

    采用稀释涂布法对芦笋老茎堆肥不同发酵阶段6个样品中的嗜热可培养放线菌进行分离,经纯化得到菌落形态有明显区别的23个菌株;根据16S rDNA序列分析结果,其中,4株的序列与白浅灰链霉菌Streptomyces albogriseolus的同源性最高,5株的序列与热普通链霉菌Streptomyces thermovulgaris的同源性最高,2株的序列与假浅灰链霉菌Streptomyces pseudogriseolus的同源性最高,1株的序列与刺棘链霉菌Streptomyces espinosus的同源性最高,有11株在GenBank数据库中未找到与其相似的已知链霉菌种的序列,分类地位待定.结果说明,芦笋老茎堆肥中优势的嗜热可培养放线菌主要是白浅灰链霉菌和热普通链霉菌.%The culturable thermophilic actinomycetes in the asparagus old stem compost samples at different fermentation stages were investigated. By dilution-plate method, twenty-three strains of actinomycetes were isolated from the samples. According to 16S rDNA sequence analysis, preliminary identification of these actinomycetes strains was done. Among these 23 stains of actinomycetes, four strains showed the highest similarity to Streptomyces albogriseolus, five strains to Streptomyces thermovulgaris, two strains to Streptomyces pseudogriseolus, and one strain to Streptomyces espinosus. Eleven strains could not be identified because there were no matched gene sequences of Streptomyces spp. To be found in the GenBank. The results indicated that Streptomyces albogriseolus and Streptomyces thermovulgaris were the most frequently isolated thermophilic actinomycetes from the asparagus old stem compost.

  12. Impact of Travel Disturbance on Soil Actinomycetes Communities Structure of Yaoquan Mountain in Wudalianchi%人类干扰对五大连池药泉山放线菌群落结构影响

    Institute of Scientific and Technical Information of China (English)

    关健飞; 王继华; 张雪萍; 龚雪; 王淼; 周小倩

    2016-01-01

    To understand the effect of travel disturbance on soil ecological system, the paper taking Yaoquan mountain of Wudalianchi as a research case, the impact of travel disturbance on actinomycetes communities structure was studied, and response relationship between soil chemical properties and actinomycetes communities' structure was analyzed. The results indicated that the soil actinomycetes number was between 0. 48 × 107 cfu/g and 5. 13 × 107 cfu/g of Yaoquan mountain. And 118 actinomycetes were isolated and purified, which belonged to 11 genera. The similar rate was 65. 38℅ of the whole mountain actinomycetes community structure. Micromonospora frequency separation is more consistent in the active area, Micropolyspora and Streptomyces frequency separation are larger in the buffer and background zone. 5 chemical factors and 5 kinds of enzyme activity have different degree of response relationship with actinomycetes population distribution. Sucrase has larger impact on actinomycetes community structure followed by organic matter, urease, and available phosphorus. Actinomyces andStreptomyces are distributed widely, mainly in the central positions, and they are common genus for each sample point Actinomyces. Streptoverticillium is positively correlated to sucrase, Micromonospora is positively correlated to phosphatase, and Frankia is positively correlated to urease, while Actinomadura is positively correlated to available phosphorus.%为了解人类干扰对土壤生态系统的影响,以五大连池药泉山为研究对象,研究人类干扰对土壤放线菌群落结构的影响以及放线菌群落结构与土壤化学性质、酶活性变化之间的响应关系. 研究结果表明:药泉山土壤中可培养放线菌数量为0. 48 × 107 ~5. 13 × 107 cfu/g,共分离放线菌118株,分属于11个属. 药泉山土壤中放线菌相似度为65. 38℅. 小单孢菌属(Micromonospora)在活动区分离频率较为一致;小

  13. 繁茂膜海绵中可培养稀有放线菌的多样性%Phylogenetic diversity of the culturable rare actinomycetes in marine sponge Hymeniacidon perlevis by improved isolation media

    Institute of Scientific and Technical Information of China (English)

    信艳娟; 吴佩春; 邓麦村; 张卫

    2009-01-01

    [Objective] Based on the molecular diversity information, seven actinomycete-selective culture media and isolation conditions were modified to isolate and cultivate diverse rare actinomycetes from Hymeniacidon perlevis. [Methods] Modified, selective cultivation and enrichment media were used, with the addition of an elemental solution of simulating the elemental composition of marine sponge H. perlevis. Restriction Fragment Length Polymorphism (RFLP) analysis of 16S rDNA sequence was used to reveal the diversity of culturable rare actinomycetes. [Results] A total of 59 actinomycete strains were isolated from the marine sponge H. perlevis . A total of 27 representative actinomycetes were selected according to their morphological feature, color and pigments. They gave 15 different RFLP patterns after digesting their PCR products of 16s rDNA with Hha I . The results showed that these isolates belonged to 10 genera: Streptomyces, Nocardiopsis, Micromonospora, Cellulosimicrobium, Gordonia, Nocardia, Prauseria, Pseudonocardia, Saccharomonospora and Microbacterium. [ Conclusion] The modified isolation media and selective cultivation procedures are highly effective in the recovery of culturable actinomycetes from the marine sponge H. perlevis , resulting in the highest diversity of culturable rare actinomycetes from any sponges.%[目的]本文旨在尝试改进分离培养方法从大连海域繁茂膜海绵中筛选稀有放线菌,并对其多样性进行研究.[方法]根据繁茂膜海绵元素组成配制微量元素溶液,加入到放线菌分离培养基中,同时将部分培养基稀释成寡营养培养基,结合富集培养法,对繁茂膜海绵中放线菌进行分离培养.采用16S rDNA的限制性片断长度多态性(.Restriction Fragment Length Polymorphism,RFLP)分析和序列分析,揭示其多样性.[结果]共获得可培养放线菌59株,通过形态、颜色观察,将其归为27个类群.RFLP分析表现为15种不同的图谱类型.16S rDNA序列分

  14. An actinomycete isolate from solitary wasp mud nest having strong antibacterial activity and kills the Candida cells due the shrinkage and the cytosolic loss

    Directory of Open Access Journals (Sweden)

    Vijay eKumar

    2014-08-01

    Full Text Available An actinomycetes strain designated as MN 2(6 was isolated from the solitary wasp mud nest. The isolate was identified using polyphasic taxonomy. It produced the extensive branched brown substrate and white aerial hyphae that changed into grayish black. The aerial mycelia produced the spiral spore chains with rugose spore surface. The growth was observed between temperature range of 27-37°C, pH 8-10 and below salt concentration of 6% (w/v. The comparative analysis of 16S rRNA gene sequence and phylogenetic relationship showed that strain MN 2(6 lies in clade with Streptomyces hygroscopicus subsp. hygroscopicus NRRL 2387T, Streptomyces sporocinereus NBRC 100766T and Streptomyces demainii NRRL B-1478T with which it shares a 16S rRNA gene sequence similarity of 99.3%. The strain MN 2(6 can be differentiated from type strains based on phenotypic characteristics. The strain MN 2(6 showed most promising activity against Gram-positive, Gram-negative bacteria, acid-fast bacilli and Candida species suggesting broad-spectrum characteristics of the active metabolite. Evaluation of anti-candidal activity of the metabolite of strain MN 2(6 by scanning electron microscopy (SEM revealed changed external morphology of yeast. It kills the Candida cells due to the shrinkage and the cytosolic loss. However, further studies are required to elucidate the structure of the active metabolite produced by the isolate MN 2(6

  15. Switching antibiotics production on and off in actinomycetes by an IclR family transcriptional regulator from Streptomyces peucetius ATCC 27952.

    Science.gov (United States)

    Chaudhary, Amit Kumar; Singh, Bijay; Maharjan, Sushila; Jha, Amit Kumar; Kim, Byung-Gee; Sohng, Jae Kyung

    2014-08-01

    Doxorubicin, produced by Streptomyces peucetius ATCC 27952, is tightly regulated by dnrO, dnrN, and dnrI regulators. Genome mining of S. peucetius revealed the presence of the IclR (doxR) type family of transcription regulator mediating the signal-dependent expression of operons at the nonribosomal peptide synthetase gene cluster. Overexpression of doxR in native strain strongly repressed the drug production. Furthermore, it also had a negative effect on the regulatory system of doxorubicin, wherein the transcript of dnrI was reduced to the maximum level in comparision with the other two. Interestingly, the overexpression of the same gene also had strong inhibitory effects on the production of actinorhodin (blue pigment) and undecylprodigiosin (red pigment) in Streptomyces coelicolor M145, herboxidiene production in Streptomyces chromofuscus ATCC 49982, and spinosyn production in Saccharopolyspora spinosa NRRL 18395, respectively. Moreover, DoxR exhibited pleiotropic effects on the production of blue and red pigments in S. coelicolor when grown in different agar media, wherein the production of blue pigment was inhibited in R2YE medium and the red pigment was inhibited in YEME medium. However, the production of both blue and red pigments from S. coelicolor harboring doxR was halted in ISP2 medium, whereas S. coelicolor produced both pigmented antibiotics in the same plate. These consequences demonstrate that the on and off production of these antibiotics was not due to salt stress or media compositions, but was selectively controlled in actinomycetes.

  16. Microbispora sp. LGMB259 endophytic actinomycete isolated from Vochysia divergens (Pantanal, Brazil) producing β-carbolines and indoles with biological activity.

    Science.gov (United States)

    Savi, Daiani C; Shaaban, Khaled A; Vargas, Nathalia; Ponomareva, Larissa V; Possiede, Yvelise M; Thorson, Jon S; Glienke, Chirlei; Rohr, Jürgen

    2015-03-01

    Endophytic actinomycetes encompass bacterial groups that are well known for the production of a diverse range of secondary metabolites. Vochysia divergens is a medicinal plant, common in the "Pantanal" region (Brazil) and was focus of many investigations, but never regarding its community of endophytic symbionts. During a screening program, an endophytic strain isolated from the V. divergens, was investigated for its potential to show biological activity. The strain was characterized as Microbispora sp. LGMB259 by spore morphology and molecular analyze using nucleotide sequence of the 16S rRNA gene. Strain LGMB259 was cultivated in R5A medium producing metabolites with significant antibacterial activity. The strain produced 4 chemically related β-carbolines, and 3 Indoles. Compound 1-vinyl-β-carboline-3-carboxylic acid displayed potent activity against the Gram-positive bacterial strains Micrococcus luteus NRRL B-2618 and Kocuria rosea B-1106, and was highly active against two human cancer cell lines, namely the prostate cancer cell line PC3 and the non-small-cell lung carcinoma cell line A549, with IC50 values of 9.45 and 24.67 µM, respectively. 1-Vinyl-β-carboline-3-carboxylic acid also showed moderate activity against the yeast Saccharomyces cerevisiae ATCC204508, as well as the phytopathogenic fungi Phyllosticta citricarpa LGMB06 and Colletotrichum gloeosporioides FDC83.

  17. Biocontrol of Rhizoctonia solani damping-off and promotion of tomato plant growth by endophytic actinomycetes isolated from native plants of Algerian Sahara.

    Science.gov (United States)

    Goudjal, Yacine; Toumatia, Omrane; Yekkour, Amine; Sabaou, Nasserdine; Mathieu, Florence; Zitouni, Abdelghani

    2014-01-20

    Thirty-four endophytic actinomycetes were isolated from the roots of native plants of the Algerian Sahara. Morphological and chemical studies showed that twenty-nine isolates belonged to the Streptomyces genus and five were non-Streptomyces. All isolates were screened for their in vitro antifungal activity against Rhizoctonia solani. The six that had the greatest pathogen inhibitory capacities were subsequently tested for their in vivo biocontrol potential on R. solani damping-off in sterilized and non-sterilized soils, and for their plant-growth promoting activities on tomato seedlings. In both soils, coating tomato seeds with antagonistic isolates significantly reduced (P<0.05) the severity of damping-off of tomato seedlings. Among the isolates tested, the strains CA-2 and AA-2 exhibited the same disease incidence reduction as thioperoxydicarbonic diamide, tetramethylthiram (TMTD) and no significant differences (P<0.05) were observed. Furthermore, they resulted in a significant increase in the seedling fresh weight, the seedling length and the root length of the seed-treated seedlings compared to the control. The taxonomic position based on 16S rDNA sequence analysis and phylogenetic studies indicated that the strains CA-2 and AA-2 were related to Streptomyces mutabilis NBRC 12800(T) (100% of similarity) and Streptomyces cyaneofuscatus JCM 4364(T) (100% of similarity), respectively.

  18. Isolation and Molecular Identification of Actinomycetes That Highly Inhibited the Activity of S. aureus%高抑制金黄色葡萄球菌活性放线菌的分离及分子鉴定

    Institute of Scientific and Technical Information of China (English)

    窦会娟; 李林珂; 刘新胜; 孔连海

    2011-01-01

    Metabolin was screened and isolated from hospital soil, which was the actinomycete with highly inhibition for S. aureus activity,and molecular identification was carried out for actinomycete. Photocopy dish was used, and Staphylococcus aureus was viewed as indicator bacteria for the isolation of actinomycetes, then carrying out identification based on 16S rDNA sequence analysis. The results indicate that A01 bacterial strain fermentation broth have better inhibition effect on S. aureus, and have good relationship with Streptomyces sp. VTTE-042674 and even reach to 99.86%, thus, it belongs to Streptomyces avermitilis. 16S rDNA sequence of the bacterial strain have already included by GenBank, moreover, the sequence registration number are HQ660584.%从医院土壤中筛选分离代谢物具有较高抑制金黄色葡萄球菌活性的放线菌,并对其进行分子鉴定.结果得出,采用影印平皿法,以金黄色葡萄球菌为指示菌进行放线菌的分离,通过16S rDNA序列分析进行鉴定.结果得出,A01菌株发酵液对金黄色葡萄球菌抑制效果较好,与Streptomyces sp.VTTE-042674亲缘关系最近,达到99.86%,应属于链霉菌属.该菌株的16S rDNA序列已被GenBank收录,序列登录号为 HQ660584.

  19. Effect Study on Isolation and Screening of Antagonistic Actinomycetes in Soil%土壤拮抗放线菌的分离与筛选效果研究

    Institute of Scientific and Technical Information of China (English)

    刘炳源; 周晶

    2013-01-01

    针对青海地区不同类型的土壤进行放线菌的分离、筛选。结果表明,10-3倍土壤稀释浓度为分离放线菌的最佳土壤稀释浓度;重铬酸钾是一种高效、方便、廉价的杂菌抑制剂,共筛得102株形态各异的放线菌,有32株菌分别对9种指示菌有较强的拮抗性,26株对不同细菌有较强抑菌活性,6株对真菌有抑菌活性,其中第24号放线菌对不同的指示菌的拮抗性最好。%Actinomycetes in different types of soil from Qinghai Area were isolated and screened. The results showed that the best soil diluted concentration for separating Actinomyces was 10-3 times. Heavy chromic acid potassium was a kind of high efficient,convenient,inexpensive,mixed bacteria inhibitors,and 102 strains Actinomycetes with different morphology were screened,in which 32 strains had stronger mineralocorticoid resistance on 9 indication bacteria respectively ,26 strains had a inhibitor on different bacteria ,6 strains had antibacterial activity on fungus ,the mineralocorticoid resistance of 24th Actinomycetes was the best for different instructions.

  20. 红树林底泥放线菌( N2010-37)发酵液的化学成分%Chemical Compounds of Actinomycete strain ( N2010-37 ) of Bottom Mud in Mangrove

    Institute of Scientific and Technical Information of China (English)

    周中流

    2011-01-01

    Objective: To study the chemical components of the cultured filaments of an actinomycete strain ( N2010-37 ) . Method: Compounds were isolated and purified by chromatographic techniques and recrystallization, and the structures were identified by spectral methods together with physiochemical analysis. Result: Seven compounds were identified. There were 6, 7-dimethoxy-5, 8-dihydroxylflavone ( Ⅰ ) , 5, 6, 7, 8-tetramethoxyflavone ( Ⅱ ) , P-hydroxybenzonic acid ( Ⅲ ) , P-hydroxybenzaldehyde ( Ⅳ ) , uracil ( Ⅴ ) , adenosine (Ⅵ), daucosterol ( Ⅶ ) . Conclusion: Compounds Ⅰ and Ⅱ were isolated from marine actinomycete for the first time. Compounds Ⅲ-Ⅶ have been isolated from this actinomycete for the first time.%目的:研究红树林底泥放线菌(N2010-37)中化学成分.方法:放线菌(N2010-37)发酵菌丝体经95%乙醇提取,溶剂分级萃取,应用多种柱色谱分离和谱学分析方法对乙酸乙酯萃取部位化学成分进行研究.结果:从乙酸乙酯部位分离得到7个化合物,分别为6,7-二甲氧基-5,8-二羟基黄酮(Ⅰ),5,6,7,8-四甲氧基黄酮(Ⅱ),对羟基苯甲酸(Ⅲ),对羟基苯甲醛(Ⅳ),尿嘧啶(V),腺嘌呤核苷(Ⅵ),胡萝卜苷(Ⅶ).结论:化合物Ⅰ和化合物Ⅱ首次从海洋放线菌次级代谢产物中分离得到,化合物Ⅲ~Ⅶ为首次从该放线菌中分离得到.

  1. Study on Antifungal Activity of Secondary Metabolites of A Marine Actinomycete%一株海洋放线菌次级代谢产物抗真菌活性的研究

    Institute of Scientific and Technical Information of China (English)

    李扬; 杨依顺; 窦洁; 王慧; 杨岱琳; 周长林

    2013-01-01

    随着真菌感染的发病率及抗药性的逐年上升,筛选新的抗真菌活性物质已成为临床治疗系统性真菌感染的迫切需要.以双层琼脂扩散法测定抗真菌活性,研究10株海洋放线菌的发酵液及其菌体甲醇提取液对白色念珠菌的抑制作用.结果筛选到一株胞内含有抗真菌活性物质的海洋放线菌Actinomycete A9,经10 L发酵罐发酵,将菌体甲醇提取物及发酵液乙酸乙酯萃取液浓缩合并,利用硅胶柱层析、葡聚糖凝胶柱层析Sephadex LH-20等分离纯化手段,最终获得1 mg浅黄色针状晶体的单一化合物,纯度为99.9%.同时,以ConA、LPS诱导的小鼠脾淋巴细胞增殖为模型,发现Actinomycete A9经硅胶柱层析分离后的抗真菌组分(10 μg/mL)能够抑制ConA、LPS诱导的小鼠脾淋巴细胞增殖,表明海洋放线菌Actinomycete A9的胞内活性物质具有抗真菌及免疫抑制活性,为后续研究奠定了基础.

  2. 生防放线菌的酶学特性及其代谢产物%Enzymatic Characteristics and Metabol ites of Biocontrol Actinomycetes

    Institute of Scientific and Technical Information of China (English)

    李堆淑

    2015-01-01

    为获得更多特异性各异的生防放线菌,采用皿内琼脂块法和试管斜面划线法,对从陕西省商洛市土壤分离的11株生防放线菌菌株(MX1,MX2,MX3,MX4,MX5,MX6,MX7,MX8,MX9,SY1,SY2)和供试细黄链霉菌进行生理生化试验。结果表明:有8株菌株产脂肪酶,SY1、MX1和细黄链霉菌的浑浊圈很明显,直径大于15 mm 的菌株共计4株;有10株菌株产生卵磷脂酶,直径大于15 mm 的菌株共计5株;有11株菌株对淀粉的水力较强,直径大于15 mm 的共计6株;仅4株菌株可水解酪蛋白。12株供试菌株革兰氏染色均呈阳性;V-P 试验,MX1、MX2和 SY1呈阳性,MX6呈弱阳性;甲基红试验,MX2、MX3和细黄链霉菌呈阳性,MX9呈弱阳性;共有9株菌株可使明胶液化,占供试菌株的75%;仅 SY2产纤维素酶,有3株菌株产过氧化氢酶;有2株菌株能使牛奶培养基凝固,4株菌株能使其胨化。%The biophysical and biochemical test of 11 actinomycetes strains(MX1,MX2,MX3,MX4, MX5,MX6,MX7,MX8,MX9,SY1 and SY2)isolated from soil of Shangluo City in Shaanxi and tested Streptomyces microflavus was conducted by the agar block and test-tube slant streak plate methods to obtain more biocontrol actinomycetes with different specificities.Results:The diameter of hydrolyzation circle of 4 strains from 8 strains with producing lipase is more than 15 mm, and SY1, MX1 and Streptomyces microflavus strains have obvious hydrolyzation circles.The diameter of hydrolyzation circle of 5 strains from 10 strains with producing lecithinase is more than 15 mm.The diameter of hydrolyzation circle of 6 strains from 11 strains with strong starch hydrolysis capacity is more than 15 mm.4 strains can hydrolyze casein.12 tested strains present positive in gram stain test.MX1,MX2 and SY1 strains present positive and MX6 strain presents weakly positive in V-P test.MX2,MX3 and Streptomyces microflavus strains present positive and

  3. Discovery of a vast amount of unknown actinomycetes from extreme environments in Xinjiang and Qinghai Province, China%新疆青海极端环境发现大量未知放线菌

    Institute of Scientific and Technical Information of China (English)

    徐丽华; 李文均; 崔晓龙; 李铭刚; 张利平; 徐平; 毛培宏; 文孟良; 李一青; 姜成林

    2003-01-01

    Soil and sediment samples were collected from saline and alkaline soil and lakes in Xinjiang and QinghaiProvince, P. R. China. Halophilic, alkalophilic and psychrophilic actinornycetes and actinohacteria in these samples wereisolated. The strains were identified by using cultural, physiological, biochemical, molecular biological procedures. Onenew family(Yaniaceae), two new genera( Yania and Streptomonospora) and eight new species of halophilic actino-mycetes and actinobacteria, four new species of alkalophilic and one new species of psychrophilic actinomycetes werefound. Basing on the research results that there is a very high density of new or unknown actinomycetes resources inthe extreme environments in Xinjiang and Qinghai, China. It is inexorable that new species contains new genes, newmetabolites, new activities, and must have new use. Actinomycetes under high salt and alkaline environments may bean important source for discovery of new drugs.%从新疆、青海的重盐碱地区、盐湖采集样品,分离其中的嗜盐、嗜碱及低温放线菌.研究了它们在几种盐的不同浓度,不同pH条件下的生长情况.利用多相分类程序进行鉴定,发现嗜盐放线菌、放线细菌的新科1个(Yaniaceae),新属2个(Yania and Streptomonospora),新种8个,嗜碱放线菌新种4个,低温放线菌新种1个.对其中部分新种、新属做了描述.认为新疆、青海的重盐碱地区蕴藏着大量的未知放线菌资源;新菌种必然有新基因,新产物,新活性和新用途,是药物开发的重要来源.

  4. Optimization of Fermentation Conditions for Actinomycetes G5%拮抗农业致病菌放线菌G5发酵条件的优化

    Institute of Scientific and Technical Information of China (English)

    刘杨; 王勇; 康静芹; 张良

    2014-01-01

    微生物的发酵过程十分复杂,培养基配方的组成以及培养条件的变化都会对菌体的代谢造成很大的影响。为了使抗生素的产量达到最大化,试验运用了Plackett-Burman试验设计、最陡爬坡试验、Box-Behnken试验设计对放线菌(Actinomycetes)G5进行了发酵条件优化。利用Plackett-Burman试验设计对影响放线菌G5发酵的诸多相关因素进行评估并筛选出3个主要因素,即碳源含量、培养温度和培养时间;之后根据3个主要因素的作用大小和方向进行了最陡爬坡试验;最后运用Box-Behnken试验设计确定最优值,得出其最优培养条件为淀粉含量21.66 g/L、培养温度27.70℃、培养时间7.75 d。在此条件下,抗生素对苹果轮纹病菌的抑菌圈直径为23.00 mm,与模型预测值基本一致。%Microbial fermentation process were very complex due to effects of culture medium composition and culture condi-tions on cell metabolism. Fermentation conditions for actinomycetes G5 were optimized with Plackett-Burman experimental de-sign, steepest ascent experiments, and Box-Behnken design. Three main factors affecting the fermentation of actinomycetes G5 screened by Plackeet-Burman design were carbon content, temperature and culture days. Then the steepest ascent experiments were conducted based on the action degree and direction of the three main factors. The optimal conditions were finally deter-mined by Box-Behnken design. The results showed that the optimal fermentation condition for actinomycetes G5 were starch content of 21.66 g/L, culture temperature of 27.70℃ and culture days of 7.75 d. Under these conditions, the bacterial inhibi-tion diameter of the acquired antibiotics against physalospora piricola was 23.00 mm, equal to the model prediction.

  5. 抑制茶饼病菌放线菌及细菌的筛选与鉴定%Screening and Identification of Actinomycete and Bacteria Strains with I nhibition Function Against Exobasidium vexans

    Institute of Scientific and Technical Information of China (English)

    韦思梅; 彭丽娟

    2015-01-01

    The antagonism actinomycete and bacteria strains against E.vexans were screened from tea rhizoaphere soil by plate dilution and spraying methods and then identified by ITS sequence analysis based on the morphological characteristics to solve pesticides residues in control of tea blister blight.The results showed that antagonism actinomycete C6 strain with 27.00 mm of average inhibition zone and bacterium B-9 strain with 32.00 mm of average inhibition zone is screened from 59 actinomycete strains and 19 bacterium strains isolated from tea rhizoaphere soil respectively.The antagonism actinomycete C6 strain and bacterium B-9 strain is identified as Streptomyces acidiscabies and Bacillus subtilis respectively.%为筛选出用于生产上防治茶饼病的生防菌,克服化学农药防治造成的农药残留问题,采用平板稀释和喷雾法,从茶树根际土壤中筛选抑制茶饼病菌的拮抗放线菌和细菌,结合形态学特征与 ITS 序列测定的方法对拮抗菌进行鉴定。结果表明:从采集土样中共分离到59株放线菌和19株细菌,从中各筛选出1株对茶饼病菌具有拮抗作用的放线菌(C6)和细菌(B-9),平均抑菌圈直径分别为27.00 mm 和32.00 mm;经鉴定,C6为酸疮痂链霉菌(Streptomyces acidiscabies ),B-9为枯草芽孢杆菌(Bacillus subtilis )。

  6. 秦岭太白山北坡土壤拮抗性放线菌分布及特性%Distribution and characteristics of soil antagonistic actinomycetes on northern slope of Taibai Mountain, Qinling

    Institute of Scientific and Technical Information of China (English)

    朱文杰; 薛泉宏; 曹艳茹; 薛磊; 申光辉; 来航线

    2011-01-01

    Twelve representative soil samples were collected from different altitudes on the northern slope of Taibai Mountain to study the distribution and characteristics of soil antagonistic actinomyces by using agar block method. There existed a great deal of soil antagonistic actinomyces in the study area. Among the 141 actinomycete strains isolated, 116 strains (82. 3% ) showed antagonism toward 12 target bacteria or fungi. The antagonistic strains at altitudes 800-1845, 3488, 3655, and 3670 m occupied 73.7% -86.8% , 81.3% , 78.9% and 82.3% of the total, respectively. 42. 1% of the strains at altitudes 1200-2300 m and >3400 m showed strong and broad spectrum antagonistic activity, suggesting that there was a great potential for the isolation of actinomycete strains with strong anti-biotic capability at these altitudes. 24. 1 % of the antagonistic actinomycetes showed antagonism against Staphyloccocus aureu, and 2.4% , 6.9% and 11. 2% of them showed activity toward Verticillium dahliae in cotton, Phytophthora sp. In strawberry and Neonectria radkiccla in ginseng, respectively. This study showed that the soil actinomycete antagonistic potentiality (SAAP) could be used as a quantitative indicator to evaluate the potential of antagonistic actinomycete resources in soil.%以太白山北坡12个不同海拔高度的代表性土样为研究对象,采用皿内琼脂块法筛选拮抗性放线茵.结果表明:在太白山北坡不同海拔高度土壤中生存着大量拮抗性放线菌,在分离出的141株放线菌中,有82.3%的放线菌对21种靶标菌有拮抗作用.其中,海拔800~1845、3488、3655和3670 m土壤中的拮抗性放线菌分别占其总数73.7%~86.8%、81.3%、78.9%及82.3%,在海拔1200~2300及3400 m以上土壤中分离到的广谱强拮抗性放线菌占其总数的42.1%.在拮抗性放线菌中,对金黄色葡萄球菌有强拮抗性的放线菌占拮抗菌总数的24.1%,对棉花黄萎病、草莓疫霉及人参

  7. 稀有放线菌的选择性分离、鉴定及生物活性研究%Selective Iolation and Identification of Rare Actinomycetes from Marine Habitats and Its bioactivity

    Institute of Scientific and Technical Information of China (English)

    刘最; 李玉中; 林慧敏; 宋瑞洪

    2016-01-01

    聚乳酸(PLA)和丝蛋白粉分别作为选择性碳、氮源可以有效提高稀有放线菌的分离效率,同时海洋环境中蕴藏着丰富的活性稀有放线菌,是发现新药的有效途径。为了筛选并鉴定海洋环境中产生活性物质的稀有放线菌,以聚乳酸和丝蛋白粉分别作为选择性碳、氮源,配制6种分离培养基,用平板稀释法分离放线菌;并用滤纸片法和MTT法对供测菌株发酵产物进行活性筛选。结果表明:共分离出96株稀有放线菌,分属于11个属;其中,80株菌对7种靶标菌显示出一定的抗菌活性;78株菌对肿瘤细胞具有不同程度的细胞毒活性。另外,比较了6种培养基对稀有放线菌的分离效果。从分离结果来看,最理想的是聚乳酸培养基。%Poly-L-lactic acid and silk protein powder as selective carbon, nitrogen for isolation of rare actinomycetes is worth further researches. Marine habitats are rich in rare actinomycetes with bioactivity and may be an effective method of ifnding new medicine. This study was aimed to isolate and identify rare actinomycetes with bioactivity isolated from marine habitats. Rare actinomycetes were isolated using poly-L-lactic acid and silk protein as a selective carbon, nitrogen from six samples by agar plate dilution method. To test the biological active effects, we used paper-disk method with seven indicator organisms to detect the antimicrobial activity by its fermentation extracts, MTT assay with 2 human tumor cell lines to monitor anti-tumor activitiy. Among of them, by eliminating the same strains from one genus and then 120 strains were identiifed by 16SrRNA gene sequence analysis, 96 strains were classiifed into 11 genera besides Streptomyces. 80 strains displayed anti-microbial activities. Meanwhile, 78 strains displayed anti-tumor activities. Six types of culture medium for isolating rare actinomycetes had been compared, and results revealed that poly

  8. The Screening of Antibacterial Antagonistic Actinomycetes and the Optimization of Fermentation Process%抗菌拮抗放线菌的筛选以及发酵工艺的优化

    Institute of Scientific and Technical Information of China (English)

    张辉; 杨俊青; 周天惠; 赵宝华

    2013-01-01

    从石家庄郊区常年种植且土壤板结的棉花地、重金属污染区、实验化学药品污染区、工业污水区等土壤中筛选出对致病真菌(以白色念珠菌为主)的拮抗性放线菌,利用静止悬浮微培养技术筛选到2株拮抗性放线菌.研究了摇床发酵的时间、温度、转速,发酵培养基的pH、碳源及氮源等理化因子对拮抗放线菌抑菌效果的影响;初步探讨了拮抗放线菌抑菌效果最适的摇床发酵条件.结果表明,拮抗放线菌的发酵产物对白色念珠菌、金黄色葡萄球菌等抑制作用明显,拮抗放线菌的最适发酵理化因子为时间96 h、温度29℃、转速220 r/min、发酵培养基pH7.1、最佳碳源为淀粉、最佳氮源为玉米浆.%Actinomycetes that are antagonistic to pathogenic fungi (especially Candida albicans) were screened from the soil in land that had been planted cotton perennially and had become hardened in Shijiazhuang suburb,and from soil in heavy metal-contaminated areas,laboratory chemicals-contaminated areas,and industrial sewage districts.High-throughput screening was performed through still suspension micro-culture technology.The impact of time,temperature,and rotational speed of fermentation in incubator shaker,and the pH,carbon source,nitrogen source,and other physical and chemical factors of fermentation media on the inhibitory effect of antagonistic actinomycetes were investigated.The optimum condition of antagonistic actinomycetes fermentation in incubator was also explored.The results indicated that the fermentation products of antagonistic actinomycetes had inhibitory effect on C.albicans,Staphylococcus aureus and other microbes;the optimum condition of antagonistic actinomycetes fermentation was determined to be fermentated at 29 ℃ and 220 r/min for 96 h,with the pH of the fermentation medium adjusted to 7.1,and with starch and corn syrup as the best carbon source and nitrogen source,respectively.

  9. Metabolomics of the Bio-Degradation Process of Aflatoxin B1 by Actinomycetes at an Initial pH of 6.0

    Directory of Open Access Journals (Sweden)

    Manal Eshelli

    2015-02-01

    Full Text Available Contamination of food and feed by Aflatoxin B1 (AFB1 is a cause of serious economic and health problems. Different processes have been used to degrade AFB1. In this study, biological degradation of AFB1 was carried out using three Actinomycete species, Rhodococcus erythropolis ATCC 4277, Streptomyces lividans TK 24, and S. aureofaciens ATCC 10762, in liquid cultures. Biodegradation of AFB1 was optimised under a range of temperatures from 25 to 40 °C and pH values of 4.0 to 8.0. An initial concentration of 20 µg/mL of AFB1 was used in this study. The amount of AFB1 remaining was measured against time by thin layer chromatography (TLC and high-performance liquid chromatography (HPLC, coupled with UV and mass spectrometry (LC-MS. All species were able to degrade the AFB1, and no significant difference was found between them. AFB1 remained in the liquid culture for R. erythropolis, S. lividans and S. aureofaciens were 0.81 µg/mL, 2.41 µg/mL and 2.78 µg/mL respectively, at the end of the first 24 h. Degradation occurred at all incubation temperatures and the pH with the optimal conditions for R. erythropolis was achieved at 30 °C and pH 6, whereas for S. lividans and S. aureofaciens the optimum conditions for degradation were 30 °C and pH 5. Analysis of the degradative route indicated that each microorganism has a different way of degrading AFB1. The metabolites produced by R. erythropolis were significantly different from the other two microorganisms. Products of degradation were identified through metabolomic studies by utilizing high-resolution mass spectral data. Mass spectrometric analysis indicated that the degradation of AFB1 was associated with the appearance of a range of lower molecular weight compounds. The pathway of degradation or chemical alteration of AFB1 was followed by means of high resolution Fourier transform mass spectrometry (HR-FTMS analysis as well as through the MS2 fragmentation to unravel the degradative pathway for

  10. Characterization of the iron-regulated desA promoter of Streptomyces pilosus as a system for controlled gene expression in actinomycetes

    Directory of Open Access Journals (Sweden)

    Martín Juan F

    2003-05-01

    Full Text Available Abstract Background The bioavailability of iron is quite low since it is usually present as insoluble complexes. To solve the bioavailability problem microorganisms have developed highly efficient iron-scavenging systems based on the synthesis of siderophores that have high iron affinity. The systems of iron assimilation in microorganisms are strictly regulated to control the intracellular iron levels since at high concentrations iron is toxic for cells. Streptomyces pilosus synthesizes the siderofore desferrioxamine B. The first step in desferrioxamine biosynthesis is decarboxylation of L-lysine to form cadaverine, a desferrioxamine B precursor. This reaction is catalyzed by the lysine decarboxylase, an enzyme encoded by the desA gene that is repressed by iron. Results The binding of the DmdR (acronym for divalent metal dependent repressor to the desA promoter in presence of Fe2+ or other divalent ions has been characterized. A 51 bp DNA fragment of the desA promoter containing the 9 bp inverted repeat was sufficient for binding of the DmdR repressor, as observed by the electrophoretic mobility shift assay. The desA mobility shift was prevented by neutralizing DmdR with anti-DmdR antibodies or by chelating the divalent metal in the binding reaction with 2,2'-dipyridyl. Binding to the desA promoter was observed with purified DmdR repressors of Streptomyces coelicolor or Rhodococcus fascians suggesting that there is a common mechanism of iron-regulation in actinomycetes. The complete desA promoter region was coupled using transcriptional fusions to the amy reporter gene (encoding α-amylase in low copy or multicopy Streptomyces vectors. The iron-regulated desA promoter was induced by addition of the iron chelating agent 2,2'-dipyridyl resulting in a strong expression of the reporter gene. Conclusions The iron-regulated desA promoter can be used for inducible expression of genes in Streptomyces species, as shown by de-repression of the promoter

  11. Screening of rhizospheric actinomycetes for various in-vitro and in-vivo plant growth promoting (PGP traits and for agroactive compounds

    Directory of Open Access Journals (Sweden)

    Sumaira Anwar

    2016-08-01

    Full Text Available In this study 98 rhizospheric actinomycetes were isolated from different wheat and tomato fields, Punjab, Pakistan. The isolates were characterized morphologically, biochemically and genetically and were subjected to a comprehensive in vitro screening for various plant growth promoting (PGP traits. About 30% of the isolates screened were found to be the promising plant growth promoting rhizobacteria (PGPRs, which exhibited maximum genetic similarity (up to 98-99% with different species of the genus Streptomyces by using16S rRNA gene sequencing. The most active indole acetic acid (IAA producer Streptomyces nobilis WA-3, Streptomyces Kunmingenesis WC-3 and Streptomyces enissocaesilis TA-3 produce 79.5, 79.23 and 69.26 µg/ml IAA respectively at 500µg/ml L-tryptophan. The highest concentration of soluble phosphate was produced by Streptomyces sp. WA-1 (72.13 mg/100ml and S. djakartensis TB-4 (70.36 mg/100ml. All rhizobacterial isolates were positive for siderophore, ammonia and hydrogen cyanide production. Strain S. mutabilis WD-3 showed highest concentration of ACC-deaminase (1.9 mmol /l. For in-vivo screening, seed germination and plant growth experiment were conducted by inoculating wheat (Triticum aestivum seeds with the six selected isolates. Significant increases in shoot length was observed with S. nobilis WA-3 (65 %, increased root length was recorded in case of S. nobilis WA-3 (81 % as compared to water treated control plants. Maximum increases in plant fresh weight were recorded with S. nobilis WA-3 (84 %, increased plant dry weight was recorded in case of S. nobilis WA-3 (85 % as compared to water treated control plants. In case of number of leaves, significant increase was recorded with S. nobilis WA-3 (27 % and significant increase in case of number of roots were recorded in case of strain S. nobilis WA-3 (30 % as compared to control plants. Over all the study revealed that these rhizospheric plant growth promoting (PGP Streptomyces

  12. Diversity Analysis of Endophytic Actinomycetes Isolated from Sophora alopecuroides L.of Lingwu Baijitan National Nature Reserve in Ningxia%宁夏灵武白芨滩国家级自然保护区苦豆子内生放线菌区系分析

    Institute of Scientific and Technical Information of China (English)

    顾沛雯; 郝丽; 徐润; 马海龙; 胡美娟

    2011-01-01

    从宁夏灵武白芨滩国家级自然保护区不同土壤类型、不同优势植被的6个样区,采集苦豆子种子及健康植株60份,分离出内生放线菌288株.鉴定表明,同一植株不同组织中,内生放线菌数量以根部最多,其次为种子,叶部最少;淡灰钙土中苦豆子内生放线菌数量比风沙土中多;旱中生杂类草沙生植被草原苦豆子内生放线菌数量最多.各样区苦豆子共分离出11个属的内生放线菌,以链霉菌属和诺卡氏菌属为优势属,其中链霉菌属以白孢类群和灰褐类群为主.%The 288 endophytic actinomycetes were separated and cultivated from 60 samples of healthy seeds and plant of Sophora alopecuroid.es L. In six sample areas, where were sampled from different vegetations and the soil types in Lingwu Baijitan National Nature Reserve of Ningxia. Endophytic actinomycetes were classified according to their morphological characteristics. The results showed that the quantities of endophytic actinomycetes from different parts of S. Alopecuroid.es L. Were varied and there were more endophytic actinomycetes in the roots than that in the seeds and leafs for the same plant. The quantities of endophytic actinomycetes from S. Alopecuroides L. Were significantly more in sierozem than that in aeolian and the salinized sandy soil. There were the most endophytic actinomycetes from S. Alopecuroides L. In the desert steppe with xerophytic mesophytic sandy weeds than that in the other five desert steppe types. These endophytic actinomycetes from S. Alopecuroides L. In the desert steppe of Lingwu Baijitan National Nature Reserve were attributed to 11 genus. Stretomyces and Norcardia were dominant. Albacores and Greyosporus were dominant in Stretomyces.

  13. Study of Combined Application of Actinomycetes Biocontrol Agents and Potassium Humate on Disease Resistance and Growth-promoting Effect of Amorphophallus Konjac%放线菌剂与腐植酸钾对魔芋抗病促生效果研究

    Institute of Scientific and Technical Information of China (English)

    张忠良; 刘列平; 何斐

    2014-01-01

    With no actinomycetes and potassium humate treatments as control(CK), the effect of actinomycetes and potassium humate on disease resistance and growth-promoting of Amorphophallus konjac in the plot trials were evalu-ated. Results showed that:(1) Combined application of potassium humate and actinomycetes No.3 had strong disease resistance and growth-promoting effect. Under 30, 60, 90 gram per plant of potassium humate combined with actinomy-cetes No.3 treatment, biocontrol effect increased by 9.8%~41.6%, yield increased by 17.1%~76.3%and growth factor increased by 20.1%~64.2% compared with the group without potassium humate. Among which, the combined ap-plication of 60 gram per plant of potassium humate and actinomycetes No.3 had the most obvious effect. (2) Combined application of actinomycetes and potassium humate had signiifcant anti-disease and growth-promoting effect. Three kind of actinomycetes combined with 60 gram per plant of potassium humate treatment, biocontrol effect increased by 11.7%~89.7%, yield increased by 33.3%~150.9% and growth factor increased by 38.5%~175.0% compared with the group without actinomycetes. In particular, No. 2 and No. 3 actinomycetes had obvious effect. These results sug-gested that the combined application of actinomycetes and potassium humate not only promoted A. konjac growth and yield, but also reduced the incidence of disease.%分别以不施菌剂、不施腐植酸钾为对照,采用小区试验,探讨生防放线菌剂与腐植酸钾配施条件下二者对魔芋的防病促生作用。试验结果表明:(1)​当腐植酸钾与3号放线菌配施时,具有较强的防病促生作用。30克/株、60克/株、90克/株腐植酸钾分别配施3号菌剂时,与不施腐植酸钾对照相比,魔芋病害相对防效、增产率及增长系数分别提高了9.8%~41.6%、17.1%~76.3%和20.1%~64.2%。其中,60克/株腐植酸钾配施3号菌剂时效果最明显。(2)​当放线菌剂与腐植酸钾配施

  14. Structural observations of Cycas revolute coralloid root and disassociation of endophytic actinomycetes%苏铁珊瑚根结构观察及其内生放线菌分离

    Institute of Scientific and Technical Information of China (English)

    曹妍; 伍建榕

    2012-01-01

    Cycad is the most primitive extant gymnosperms, which is considered to be living fossil. In order to explore the structure and the endophytes actinomycetes of cycad coralloid root, the paraffin section was used to do the observation on microstructure; TWYECM1), Gao one (M2) and Glycerin - asparagine mediums were used to seprate the endophytic actinomycetes in the coralloid roots and through 16S rRNA sequence analysis, the Actinomycetes were identified. The results indicate that the periderm, outer cortex, cyanobacterial zone, internal cortex and vascular cylinder consisted of the cycad coralloid root; the cells of the external and internal cortex presented to be a circular form on the cross section, and pelotons that were stained to be red existed in some cells of them. 13 strains of actionmycetes were separated from the cycad coralloid root through the above three mediums, and they belong to streptomyces and nocardiopsis.%苏铁类是现存最原始的裸子植物类群,被认为是活化石.为了探究清苏铁珊瑚根的结构和内生放线菌的多样性,本研究采用石蜡切片法对苏铁珊瑚根进行显微结构观察,用改良的TWYE (M1)、高氏1号(M2)和甘油—天冬酰胺(M3)培养基对珊瑚根的内生放线菌进行分离,并通过16S rRNA系列分析鉴定其种属.结果表明:苏铁珊瑚根由周皮、外部皮层、藻胞层、内部皮层和维管柱组成;外部皮层和内部皮层细胞在横切面上呈圆形,而且在有的细胞中能看到被染成暗红色的菌丝团的存在;利用以上三种培养基从苏铁珊瑚根中共分离到了13株放线菌,隶属于链霉菌属和拟诺卡氏菌属.

  15. Cloning of the Germicidin Biosyntheic Gene from Endophytic Actinomycete A00122%内生放线菌A00122中germicidin生物合成基因的克隆

    Institute of Scientific and Technical Information of China (English)

    吴莹莹; 李瑶瑶; 郑忠辉; 白林泉; 黄耀坚

    2011-01-01

    在植物和细菌中,Ⅲ型聚酮合酶能够产生种类多样的次生代谢产物.在药用植物内生放线菌A00122的发酵产物中,分离到了一个已知的Ⅲ型聚酮类化合物germicidin.对A00122菌株建立了基因组文库,根据已知的同源基因Sco 7221设计引物作为探针对文库进行PCR筛选,并通过Southern杂交的方法从阳性克隆5-3-10中定位了包含germicidin基因的片段,经测序得到长度为1 185 bp的完整合成基因.该基因的获得为深入研究Ⅲ型聚酮合酶的底物选择性,通过定向改造的方法获得非天然Ⅲ型聚酮类化合物提供了重要基础.%The type Ⅲ polyketide synthases (PKSs) generate backbones of a variety of plant and bacterial secondary metabolites. In previous work,many endophytic actinomycetes were isolated from different pharmaceutical plants,whereas the secondary metabolic products of theses strains were studied. A known type Ⅲ PKSs compound,germicidin, was isolated from one of the endophytic actinomycete A00122. Primers for A00122 genomic library screening were designed based on the homologous gene Sco 7221 and the PCR product was used as the probe for Southern blotting. Finally,a 1 185 bp gene was cloned and sequenced from one of the positive cosmid 5-3-10 , which was identified to be involved in the biosynthesis of germicidin from A00122. Since it is the first germicicin biosynthetic gene from endophytic actinomycetes,this study provides an important foundation for accepting chemically and structurally divergent unnatural novel type Ⅲ PKSs compounds by directed mutation of proteins.

  16. Antibióticos antifúngicos produzidos por actinomicetos do Brasil e sua determinação preliminar nos meios experimentais Antifungal antibiotics produced by Brazilian actinomycetes and its preliminary determination in experimental media

    Directory of Open Access Journals (Sweden)

    Keidi Ujikawa

    2003-06-01

    Full Text Available Várias amostras de solo do Brasil foram semeadas em placas de ágar e diversas cepas de actinomicetos produtoras de antibióticos antifúngicos foram isoladas. Foram desenvolvidos meios para eliciação da biossíntese dos antibióticos e métodos para determinação rápida do seu rendimento. Ao todo, foram isoladas 41 cepas de actinomicetos aeróbios produtoras de metabólitos antifúngicos. Destes, 11 (26,8% eram macrolídeos tetraênicos, 13 (31,7% macrolídeos pentaênicos, 1 (2,4%, macrolídeo oxopentaênico, 1 (2,4% macrolídeo hexaênico e 6 (14,6% macrolídeos heptaênicos. Os antibióticos antifúngicos produzidos pelas restantes 9 cepas ativas (21,9% não eram poliênicos. Os poliênicos mais utilizados atualmente na clínica são do tipo tetraênico (nistatina e heptaênico (anfotericina B. Um meio à base de leite de soja favoreceu extraordinariamente a eliciação da biossíntese de polienos por algumas cepas, enquanto que para outras não houve favorecimento e para outras foi prejudicial. Os rendimentos obtidos atingiram cerca de 6000 U de antibióticos poliênicos por mL.Various Brazilian soil samples were seeded in agar plates and several strains of antifungal antibiotic producing actinomycetes were isolated. Antibiotic biosynthesis elicitation media were developed and methods for determination of yields were studied. A total of 41 antifungal antibiotic producing strains of aerobic actinomycetes resulted. Among the antibiotics produced, 11 (26.8% were grouped as macrolide tetraenes, 13 (31.7% as pentaenes, 1 (2.4% as oxo pentaene, 1 (2.4% as hexaene and 6 (14.6% as heptaenes. Several of these strains also produced antibacterial antibiotics, like polyether antibiotics. The remaining 9 active strains (21.9% produced non polyene type of antifungals. A medium based on soybean milk favored extraordinarily the elicitation of polyenes biosynthesis by some native strains, while with other strains, this was not favored, while with

  17. Efecto rizosférico de Parmelia sp y Solanum lixioides sobre actinomicetos y ensayos de antibiosis in vitro Rhizozpheric effect of Parmelia sp and Solanum lixioides on actinomycetes and their in vitro antimicrobial activity

    Directory of Open Access Journals (Sweden)

    Zárate Lyda

    1999-11-01

    Full Text Available

    La presencia de actinomicetos en muestras de suelo alrededor de raíces y rizoides de Parmelia sp y de Solanum lixioides fue investigado. 5e evaluó el efecto rizosférico del liquen Parmelia sp sobre poblaciones de actinomicetos con un R/5 ~ 2.5, mientras el radio R/5 resultante en S.lixioides fue <1. En los ensayos de antibiosis los mejores resultados se obtuvieron al modificar el medio de cultivo, o medio mínimo de Hopwood (1967, con relación a medio estándar. Se determinó el espectro de actividad antibiótica de 9 aislamientos, sobre organismos Gram positivos: Staphylococcus aureus, Bacillus subtilis y Gram negativos: Escherichia coli, Klebsiella pneumoniae y Pseudomonas aeruginosa. Los aislamientos A-2, A-4, A-5 YA-6 presentaron un amplio espectro de actividad antimicrobiana sobre E. coli, B. subtilis y K. pneumoniae. A-11, presentó una antibiosis selectiva y en grado alto sobre P. aeruginosa.

    The occurrence of actinomycetes from rhizospheric soils of Parmelia sp and Solanum lixioides was investigated. The rhizospheric effect from Parmelia sp (Lichen upon actinomycetes isolates was evaluated and was (R/5 ~ 2.5, while by the solanaceae the resultant ratio R/5 was <1. For the antibiosis assays the better results were obtained by moditying the culture médium (Hopwood minimun medium, 1967. The antimicrobial activity from nine isolates against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Klebsiella pneumoniae; Pseudomonas aeruginosa was determined. A-2, A-4, A-S and A-6 isolates showed a broad spectrum of antimicrobial activity, while A-'Il showed a selective antimicrobial activity against P. aeruginosa.

  18. Isolation of marine actinomycetes and studies on the secondary metabolites of strain Streptomyces sp.AH17-3%海洋放线菌分离及菌株Streptomyces sp.AH17-3的次级代谢产物研究

    Institute of Scientific and Technical Information of China (English)

    崔萌纳; 袭蕊; 李德海; 顾谦群; 朱天骄

    2012-01-01

    Objective To isolate actinomycetes strains from marine samples and study on the secondary metabolites of one marine-derived actinomycete. Methods The extract of the actinomycetes was purified by solvent extraction, column chromatography and preparative HPLC. The structures were established by physicochemical properties and spectral analysis, and comparison with the data of literatures. The proliferation inhibition activities were evaluated by SRB method. Results The 174 actinomycetes were i-solated from the marine samples, four polyketide compounds were identified as germicidin A(1), ger-micidin B (2), daidzein (3), genistein (4). And the compound 1 showed weak cytotoxic activities, its IC50 was 3. 5 × 10-7M. Conclusion The marine-derived actinomycetes were important microbial resources of medicine, and compounds 1 and 2 were isolated from marine-derived actinomycetes for the first time.%目的 对海洋放线菌进行分离及抗肿瘤活性筛选,并对一株具有抗肿瘤活性的海洋放线菌AH17-3的次级代谢产物进行研究.方法 采用溶剂萃取、柱色谱层析及制备HPLC等方法对菌株AH17-3的发酵产物进行化学分离,通过理化性质及波谱学方法并参阅文献进行化合物结构鉴定,以SRB法评价化舍物的抗肿瘤活性.结果 从海洋样品中分离放线菌174株,从菌株AH17-3中分离得到了4个聚酮类化合物,经鉴定其结构分别为germicidin A(1)、germicidin B(2)、daidzein(3)、genistein(4).其中化合物1具有弱的细胞毒活性,其IC50为3.5×10-7M.结论 海洋放线菌是重要的药用微生物资源,化合物1,2均为首次从海洋放线菌中分离得到.

  19. Preliminary Identification of Six Antagonistic Actinomycetes in Soil Determination of Its Fungicidal Activities%6株土壤拮抗放线菌的初步鉴定及其抗菌活性测定

    Institute of Scientific and Technical Information of China (English)

    龙建友; 夏建荣

    2011-01-01

    [目的]初步鉴定6株放线菌种类,并测定其发酵产物的抗菌活性.[方法]采用形态学方法鉴定6株放线菌菌株种类,以抑制菌丝生长速率法、孢子萌发法、盆栽和大田试验系统测定6株放线菌菌株发酵产物的杀菌活性.[结果]形态学初步鉴定结果表明,6株菌株属于链霉菌属.生物测定结果表明,500 μg/ml的6株放线菌发酵产物,对棉花枯萎病菌的菌丝生长抑制率均在90%以上;对番茄灰霉病菌、烟草赤星病菌、南瓜枯萎病菌的菌丝生长抑制率也在80%以上.其中,GZ-204和GZ-331菌株发酵产物对小麦根腐病菌和玉米弯孢叶斑病菌的孢子萌发抑制率分别为97.8%、98.2%和99.5%、94.6%.盆栽试验结果表明,GZ-204和GZ-331菌株发酵产物对小麦白粉病的保护效果分别为78.8%和87.1%,治疗效果为62.4%和68.5%.田间试验结果表明,GZ-204和GZ-331菌株发酵200倍稀释液对小麦白粉病的防治效果分别达50.5%,69.2%.[结论]研究结果为新型土壤放线菌源农药的研制奠定了基础.%[ Objective ] The paper was to preliminarily identify the species of six strains of actinomycetes, and to determine the fungicidul activities of their fermentation products. [ Method] The species of six strains of actinomycetes were identified by morphological method, and the fungicidal activities of the fermentation products of six strains of actinomycetes were systematically determined by series of methods including mycelial growth rate inhibition method, spore germination method, pottirg and field test. [ Result] Morphological identification results showed that six strains belonged to streptomyces. Biological determination results indicated that the inhibition rates of the fermentation products of six strains of actinomycetes with the concentration of 500 μg/ml against the mycelial growth of Fusarium oxysporum f. sp. Vasinfectum were all greater than 90%; the inhibition rates against the mycelial growth of Botrytis

  20. 樱桃园土壤优势放线菌的分离及其促长功能研究%Isolation of Dominant Actinomycetes from Cherry Orchard Soil and Their Functions in Bio-Control and Plant Promotion

    Institute of Scientific and Technical Information of China (English)

    刘灵芝; 秦嗣军; 吕德国; 王冰营

    2013-01-01

    [目的]分离、筛选樱桃园土壤优势放线菌菌株,研究其在生物防治与植物促长中的应用潜力.[方法]采用皿内拮抗与发酵液促生试验分析优势放线菌菌株抗生与促进生长功能.对具有良好抑菌与促进生长作用的菌株F4-5,通过16S rDNA序列分析研究其分类地位.[结果]从樱桃[(Cerasus avium Moench (L.)/C.sachalinensis (L.) Kom.)园土壤中共分离获得32株优势放线菌菌株.与5月和11月相比,8月土壤中放线菌数量最多.各时期分离优势放线菌的抑菌作用与促进生长能力随生育期而各异,总体上,2010年8月分离菌株抑菌与促进生长效果较为明显.放线菌菌株F4-5对金黄色葡萄球菌(Staphylococcus aureus)、大肠杆菌(Escherichia coli)、枯草芽孢杆菌(Bacillus subtilis)和蜡质芽孢杆菌(Bacillus cereus) 4株供试细菌,以及木霉(Trichoderma viride)、根霉(Rhizopus stolonifer)和黑曲霉(Aspergillus niger) 3株供试真菌均表现出明显抑制效果,具有广谱抗生性.同时,菌株F4-5亦可显著促进山荆子(Malus baccata (L.) Brokh.)种子萌发与胚根生长,较对照分别提高了201.1%和43.5%,表现出抗生与促进生长双重效应.根据形态、培养特征及16S rDNA序列分析,初步鉴定菌株F4-5为灰黄链霉菌(Streptomyces flavogriseus).[结论]不同时期樱桃园土壤放线菌数量、分布、抗生及促进种子萌发特性变化较大,灰黄链霉菌F4-5菌株具有良好的广谱抗生性与促进种子萌发、胚根生长的作用.%[Objective] The dominant actinomycetes in cherry orchard soil were isolated and collected at different growth phases to study their application potential in biocontrol and plant growth promotion.[Method] All isolates were assayed for antagonistic activity,fermentation activity in vitro experiments to analyze their antagonistic and growth promoting function.Strain F4-5 with good microorganism inhibiting effect and plant growth promoting functions was

  1. Diversity and anti-microbial activity of endophytic actinomycetes isolated from Stell-era chamaejasme sampled in Aba,Sichuan%阿坝地区狼毒内生放线菌多样性及抗菌活性

    Institute of Scientific and Technical Information of China (English)

    廖敏; 张波; 范中菡; 陈熊春蕊; 张小平

    2016-01-01

    通过可培养方法以四川省阿坝地区药用植物狼毒为研究对象,探究其内生放线菌多样性及抗菌活性,为开发新型生物活性物质提供依据。结果如下,1)多种因素决定了狼毒内生放线菌分离数量,其中土壤有机质与其相关系数为0.86,在0.05水平相关性显著。2)高氏一号培养基分离52株内生放线菌,占总数30.4%;植株不同部位分离内生放线菌结果为根部>茎部>叶部>花部。3)16S rDNA-RFLP 将供试菌株分成11个遗传群,代表菌株系统发育分析表明,供试菌株以链霉菌属为主,其余菌株包括诺卡氏菌属、北里孢菌属、克里布所菌属。4)对代表菌株NRPS 、PKS 基因分析共获得4个 PKS 基因和2个 NRPS 基因;大部分代表菌株对3种病原真菌有抗菌活性,菌株 SCAUEⅢD11-1效果最好。综上,狼毒内生放线菌分离结果受多因素影响,具有较丰富的多样性;功能基因筛选及抗菌活性结果揭示出阿坝地区狼毒内生放线菌具有潜在的运用价值。%In order to develop new biologically active substances in medicinal plants,an isolation and culture method was employed to investigate the taxonomic diversity and anti-microbial activities of endophytic actino-mycetes isolated from Stellera chamaejasme sampled in Aba,Sichuan.It was found that the number of iso-lates was affected by many factors,especially organic matter content which was significantly positively correla-ted with the isolate number (P <0.05,r=0.86).Fifty two isolates were obtained on Gauze No.1 growth me-dium,accounting for 30.4% of total isolations.The numbers of isolates decreased in the following order:root, stem,leaf and flower.Analysis using 16S rDNA-RFLP divided these isolated strains into 11 clusters and fur-ther phylogenic analysis classified representative strains as genera Streptomyces ,Nocardia,Kitasatospora and Kribbella,respectively,with Streptomyces being

  2. The Study on Antifungal Activity and Screening of Actinomycete X1 Strain from Soil%土壤放线菌X1的筛选及其抑菌活性初探

    Institute of Scientific and Technical Information of China (English)

    徐路明; 郝明亮; 王金果; 王桂芳; 罗兰

    2011-01-01

    Screening antifungal actinomycetes are foundation of agricultural antibiotics exploitation. The antifungal activity of 6 strains actinomycetes from soil were studied by mycelium growth rate, spore germination test. The antifungal activities of different extracts of actinomycete X1 strain were studied. The results of mycelium growth rate showed that the Xl strain displayed a broad spectrum inhibitory activity to all the tested 12 plant pathogenic fungi, of which the inhibition rate against 3 pathogens were 100%, such as Valsa mali, Physalospora piricola and Coniella diplodiella. The results of spore germination test demonstrated that the X1 strain also had an inhibition rate of 100% against germination of spores of Fusarium oxysporum. The inhibition rate to 3 plant pathogens was over 90% with ethyl acetate of Xl strain at the concentration of 1 mg/mL. The X1 strain displayed a broad spectrum inhibitory activity, which had great potential for controlling plant pathogens.%筛选具有抑菌活性的放线茵是开发农用活性抗生素的基础.笔者采用生长速率法和孢子萌发法,测定了从土壤中分离出的6株拮抗放线茵的抑菌活性,并对抑茵活性较好的放线茵X1菌株进行初步研究.生长速率法试验表明,放线茵X1菌株发酵液对供试12种植物病原茵茵丝生长均有不同程度的抑制作用,发酵液对苹果腐烂病菌、苹果轮纹病菌和葡萄白腐病茵茵丝的抑制率均为100%.孢子萌发试验表明,放线茵X1菌株发酵液对黄瓜枯萎病菌孢子萌发的抑制率为100%.在浓度为1 mg/mL时,放线茵X1菌株发酵液乙酸乙酯萃取物对苹果腐烂病菌、苹果轮纹病菌和葡萄白腐病菌茵丝的抑菌率均大于90%.放线茵X1菌株抑茵谱较广,对植物病茵的防治有很大的研究开发潜力.

  3. Replica Plating and Gene Screening Combined to Separate AHBA Synthase Gene Positive Actinomycetes%平板影印与AHBA合成酶基因筛选用于安莎类抗生素产生菌的分离

    Institute of Scientific and Technical Information of China (English)

    徐祯; 徐庆妍; 胡志钰; 郑忠辉; 黄耀坚

    2012-01-01

    基因筛选是筛选具有抗生素产生潜力微生物的新方法.针对筛选中单菌落分离纯化不仅工作量大,而且耗费时间,采用一种将平板影印技术与PCR扩增技术相结合从土壤中快速获得具有安莎类抗生素产生潜力的放线菌的方法.根据安莎类抗生素合成途径中的3-氨基-5-羟基苯甲酸合成酶(AH BAs)基因的保守性,通过放线菌的培养、影印、AH-BAs基因的PCR扩增,已从33份土样中获得8株AHBAs阳性菌株.结果表明:该方法是一种非常有效的能够快速获得AHBAs基因阳性菌株的方法,并且该方法可扩展用于从土壤中分离其他有价值的抗生素产生菌.%Gene mining is a new strategy to discover microbial natural products. However,it is laborious to inoculate and purify tested strains before gene amplification,so gene mining can not be applied to large amounts of samples. Herein,a high throughput method for the gene mining of soil actinomycetes, combining the replica plating technique and PCR amplification was recommended. In the present work,3-amino-5-hydroxybenxoic acid synthase (AHBAs) were used as amplicated gene. Through soil actinomyctes culture, colony replica planting,PCR amplification of AHBAs genes,isolation of positive strains and characterization of fermentation extracts, eight AHBAs positive strains were selected from 33 plants rhizosphere soil samples. The results showed that the replica plating-gene screening combined technique was useful for the rapid selection of ansamycin-producing actinomycetes, and it could be applied to search for producers of other antibiotics in natural soils.

  4. 1株抑制植物种子萌发放线菌的筛选和鉴定%Screening and identification of an actinomycetes strain with inhibition activity on seed germination of plant

    Institute of Scientific and Technical Information of China (English)

    朱宏建; 雷湘华; 周倩; 娄敏; 刘双清; 高必达

    2012-01-01

    为了探寻抑制杂交水稻“穗芽”的新型活性物质,从陕西华山自然保护区土样中分离获得54株放线菌,分别利用其发酵液对杂交水稻种子进行发芽试验验,发现菌株HND02发酵液稀释5倍后,对杂交水稻种子萌发有较强的抑制作用,发芽率仅为45.5%,根系不能生长.该菌株发酵液5倍稀释液处理空心菜、儿菜、萝卜、甘蓝、白菜、花椰菜种子,发芽率分别为26.7%、20.0%、62.5%、25.0%、50.0%、65.0%.经形态观察、培养特征和生理生化鉴定,结合16S rRNA基因序列分析,将HND02菌株鉴定为华丽黄链霉菌(Streptomyces flaveus).%"Pre-harvest sprouting"in rice seriously affected the yield and quality of hybrid rice. To find new active substances for inhibiting "Pre-harvest sprouting", fifty-four actinomycetes were isolated from the cultivated soil samples of Huashan nature reserve, Shanxi Province and tested on seed germination of hybrid rice. Among these actinomycetes, strain HND02 exhibited strong inhibition on seed germination. After treated with 5-fold diluted fermentation broth of this strain, rice seed germination rate was 45.5% and rice roots could not grow. The same fermentation broth diluted 5-fold was tested on the spinach, infant food, radish, cabbage, Chinese cabbage, cauliflower, the seed germination rates of which were 26.7%, 20.0%, 62.5%, 25.0%, 50.0% and 65.0% respectively. The strain HND02 was identified as Streptomyces flaveus by morphology, culture characteristics, physiological and biochemical tests and 16S rRNA analysis.

  5. 土壤放线菌K2的筛选、鉴定及其抑菌活性初探%The Study on Antifungal Activity, Screening and Identification of Actinomycete K2 Strain from Soil

    Institute of Scientific and Technical Information of China (English)

    赵丽坤; 田永强; 高磊; 孙盈

    2013-01-01

      筛选具有抑制植物病原菌活性的放线菌是农用抗生素开发的基础。通过平板对峙法筛选出8株拮抗放线菌菌株,采用生长速率法测定获得一株对植物病原菌有较好抑菌作用的菌株K2,并采用抑制菌丝生长速率法对其抑菌谱进行研究,以及进行菌种鉴定。生长速率法试验表明,放线菌菌株K2发酵液对10种供试植物病原菌菌丝生长均有不同程度的抑制作用,其中以对尖孢镰刀菌(Fusarium oxysporum)抑制效果最好,抑菌率可达57.38%。根据形态学特征、生理生化特征和基于16S rDNA序列比对,鉴定菌株 K2属于链霉菌属(Streptomyces)的一个菌株。放线菌 K2的代谢产物具有较广的抑菌谱,对植物病原菌的防治有很大的研究开发潜力。%Screening antifungal actinomycetes were the foundation of agricultural antibiotics exploitation. The antifungal activity of 8 strains actinomycetes were studied by flat confrontation, one strain named K2 was got by mycelim growth rate, its antimicrobial spectrum was studied and strains identification with mycelim growth rate. The result of mycelium growth rate showed that K2 had a broad spectrum inhibitory activity to all the tested 10 plant pathogenic fungi. Among these, activity against Fusarium oxysporum was the highest with inhibition rate of 57.38%. The results based on morphological characteristics, physiological and biochemical characterization and 16S rDNA sequence analysis of strain K2 showed that it was possibly Streptomyces. The K2 strain displayed a broad spectrum inhibitory activity, which had great potential for controlling plant pathogens.

  6. The Effects of Antagonistic Actinomycetes G19 on Microbial Diversity in Replanted Peach Rhizosphere%拮抗放线菌G19对模拟再植毛桃根际微生物多样性的影响

    Institute of Scientific and Technical Information of China (English)

    邸宁; 刘志民; 马焕普

    2011-01-01

    为了了解不同处理对微生物多样性变化的影响,试验采用Biolog技术对施用拮抗放线菌发酵液后的毛桃根际微生物的多样性进行了分析,结果表明:施放线菌G-19后,其根际细菌和放线菌数量增加,真菌数量明显减少,与正常土的变化趋势相似;再植土则相反,真菌数量大幅上升,细菌数量下降.微生物代谢活性及微生物群落多样性指数显示施用了放线菌G-19的根际微生物也是最丰富和稳定的,毛桃幼苗的生长也以施放线菌G-19发酵液的效果最好,这说明拮抗放线菌G-19有改善桃再植土壤微生态的作用.%The aim was to compare the difference in microbial diversity of different treatments. In this study, microbial diversity of peach rhizosphere which fermented antagonistic actinomycetes was measured by Biolog Eco plate facilities. The results showed that the number of bacteria and actinomycetes in peach rhizosphere increased significantly and the number of fungi decreased. That was similar to the normal soil. By contrast, the number of fungi increased significantly and the number of bacteria and actinomycetes decreased in replant soil. Microbial metabolic activity and microbial community diversity index application of actinomycetes G19 in rhizosphere microorganisms was the most abundant and stable. Seedling growth of peach was the best after strains G19 fermentation broth treatment. It indicated that antagonistic actinomycetes G19 could improve the ecological environment of the soil in replant peach rhizosphere.

  7. 放线菌Z802031次级代谢产物放线菌素X2的研究%Actinomycin X2 as a Secondary Metabolite Produced by Actinomycete Z802031

    Institute of Scientific and Technical Information of China (English)

    孙肇暘; 张明明; 秦德华; 杨秀萍

    2011-01-01

    从西藏卡拉山地区土样分离到的一株放线菌Z802031能够产生具有抗菌、抑制肿瘤细胞生长的次级代谢产物.对其产生的抗肿瘤活性物质进行发酵、提取、分离,得到五个组分,经MTT法检测有两个组分具有显著的抗肿瘤活性,并对其中之一进行分离纯化,并获得单体,对该单体进行质谱、核磁共振、红外、紫外等波谱分析、鉴别,结果表明,Z802031菌株发酵液中起到抗菌抗肿瘤作用的主成分之一是放线菌素X2.%Actinomycete Z802031 which isolated from Kala mount in Tibet could produce metabolites of antibacterial and antitumor activity. By fermenting,extracting and severing, five components were separated from the fermentation of Z802031 and two of them have remarkable tumor cell growth inhibiting effect detected by MTT assay. The major one was further isolated and purified as monomer and identified as Actinomycin X2 on the basis of spectroscopic analysis, mainly including MS, NMR, IR and UV.

  8. Screening of antagonistic actinomycetic strains and their inhibitions against Phytophthora in festans%致病疫霉拮抗放线菌的筛选及抑菌作用初步研究

    Institute of Scientific and Technical Information of China (English)

    刘月; 蒋继志; 郭俊亭; 郭文; 李丽艳

    2012-01-01

    为获得对致病疫霉具有显著且稳定拮抗作用的放线菌,利用对峙培养法和滤纸片法测定了从土壤中分离纯化出的放线菌活体及其发酵液对致病疫霉生长的抑制作用,并对其中抑菌效果显著的Sy11菌株的抑菌方式、对致病疫霉的感应性、传代稳定性以及对致病疫霉菌体形态的影响进行了初步研究.结果表明,分离纯化出的74株放线菌中有17株对致病疫霉具有拮抗作用,但其发酵液对致病疫霉均无抑制作用;Sy11菌株只有感应到致病疫霉存在时才分泌对致病疫霉的抑菌物质;连续传代25次后,Sy11菌株的抑制率仍然保持在81%以上;Sy11菌株可导致致病疫霉菌丝体严重变形,但只是抑制其生长,并未杀死致病疫霉.这些结果表明,Sy11菌株在防治马铃薯晚疫病方面具有较大的应用潜力.%In order to obtain highly effective and stably antagonistic actinomycetes strains a-gainst Phytophthora infestans, the inhibitory effects of living and fermentation filtrates of actinomycetic strains isolated from vegetable-grown soil on mycelial growth of P. infestans were detected with dual-culture and filter paper methods, and inhibitory manner, response to P. infestans, stability of inhibition effect after continuous passage culture, and influence on P. infestans mycelial morphological character were investigated in this experiment. The results showed that 17 of 74 strains were evidently antagonistic to P. infestans, but all of fermentation liquors of 17 strains were not antagonistic to P. infestans. Syll strain had response to P. infestans, and could produce and secrete some substances inhibiting P. infestans. After continuous passage culture for 25 times, the inhibitory rate of Syll strain on P. infestans still maintained over 81%. Syll strain could cause to lose original sketch and structure seriously. However, Syll strain just inhibited P. infestans but did not kill it. These results indicated

  9. Antibacterial Actinomycetes Community from Sediment of Coral Reefs in the Offshore Areas of Beibu Gulf%北部湾近海珊瑚礁区系沉积物抗菌活性放线菌类群

    Institute of Scientific and Technical Information of China (English)

    龚斌; 黄蕾; 张艳秋; 彭春艳; 熊拯; 方怀义; 庞庭才; 黄鹄

    2013-01-01

    Using antibacterial activity against E. coli and Bacillus subtilis as initial screening, 51 Actinomycetes strains possessing different antibacterial activities were isolated from 5 sediment samples of coral reefs in the offshore areas of Beibu Gulf, among them 9 strains showed comparatively strong antibacterial abilities. It could be determined that they belonged to the genus of Streptomyces based on their colonies and spores morphology. RAPD-PCR analysis indicated that the 9 strains also belonged to 6 types, 16S rDNA sequence and phylogenetic tree analysis indicated that the 9 strains could be divided into 6 different types of 4 major groups. And the results showed that RAPD-PCR cluster analysis had fairly large compatibility with 16S rDNA sequence cluster analysis. Physiological and biochemical identi-fication results showed that the isolates existed differences from Actinomyces model strain in physiological and biochem-ical features. This indicated that the isolates may likely be novel species of Actinomyces. These 6 Actinomyces strains had broad spectrum of antibacterial activity, and existed a certain differences in antibacterial activities, suggested that they may excrete secondary metabolites of multiple different structures and functions. The study results showed that sediment of coral reefs in the offshore areas of Beibu Gulf stores abundant source of Actinomycetes for medicine devel-opment.%通过对大肠埃希菌和枯草芽胞杆菌抗菌活性初步筛选,从北部湾近海珊瑚礁区5个沉积物样品中成功分离得到51株具有不同抗菌活性的放线菌,其中9株具有较强抗菌能力。根据这9株放线菌的菌落和孢子形态,可确定它们都属于链霉菌属。 RAPD-PCR分析表明这9株放线菌为6种不同类型,16S rDNA序列和系统发生树分析表明,9株放线菌可划分到4个大的类群6种不同类型,且结果显示RAPD-PCR聚类分析与16S rDNA序列聚类分析的结果具有较大的一致性。生理生

  10. Screening, identification and optimization of fermentation conditions of an antagonistic actinomycetes strain to Setosphaeria turcica%玉米大斑病生防放线菌的筛选鉴定及发酵条件优化

    Institute of Scientific and Technical Information of China (English)

    赵淑莉; 任飞娥; 刘金亮; 秦建春; 潘洪玉

    2012-01-01

    [Objective ] To isolate and screen antagonistic actinomyces strains with inhibitory activity on Setosphaeria turcica from soil. [ Method] Actinomycetes were isolated by Pour Plate method. Antagonistic actinomycetes were screened by confrontation culture, cylinder plate, suppression of mycelial growth and spore germination method in vitro. Strain BZ45 were identified by morphological, cultural, physiological and biochemical characteristics and 16S rDNA sequence analysis. The fermentation condition was optimized by single factor and orthogonal experiment. [Result] Strain BZ45 showed antagonistic to 8 plant pathogens. Its filtrate inhibited the mycelial growth and spore germination of Setosphaeria turcica CC9. Strain BZ45 belonged to Streptomyces spectabilis. The optimum culture conditions of strain BZ45 were with a medium of 1. 5% fructose, 3.0% peptone, 0.1% KH2PO4, 0.04% NaCl, 0.1% CaCO3 at initial pH of 7. 2, liquid volume 50 mL in 250 mL flask, 200 rpm at 28^ , inoculation size of 10% for 4 d. [Conclusion] Strain BZ45 was identified as Streptomyces spectabilis and antagonistic against Setosphaeria turcica CC9.%[目的]从土壤中筛选对玉米大斑病菌具有较强拮抗作用的放线菌菌株.[方法]采用稀释涂布法分离;采用平板对峙法、牛津杯法、抑制菌丝生长速率法、抑制孢子萌发法进行拮抗菌的筛选;根据菌株BZ45的形态与培养特征、生理生化特性、16SrDNA序列分析对其进行鉴定.通过单因素试验和正交设计试验优化培养基组分及发酵条件.[结果]通过分离筛选得到一株具有强抑制作用的放线菌菌株BZ45,它对常见的8种病原真菌均有拮抗作用,菌株BZ45的发酵滤液对玉米大斑病菌(Setosphaeria turcica)CC9的菌丝生长和孢子萌发均有较强的抑制作用.菌株BZ45与链霉菌中的壮观链霉菌(Streptomyces spectabilis)的亲缘关系较近,且形态与培养特征、生理生化特性与壮观链霉菌的基本相符.研究表

  11. Growth Promotion and Disease Control Effect Determination of Endophytic Actinomycetes from Medicago sativa%首蓿内生拮抗放线菌的促生防病作用研究

    Institute of Scientific and Technical Information of China (English)

    王燕; 张绒仙

    2011-01-01

    [ Objective ] The research aimed to screen antagonistic endophytic actinomycetes from Medicago sativa. [ Method ] Growth promotion and disease control effect determination has been done by using Mx1, Mx3 and Mx5, which wcre isolated from the healthy Medicago sativa[ Result ] The result that the comparative control of Mx3 extracts could be 56.56%, 44.67% to Botrytis cinerea and Gaeumannomyces graminis var.tritici, respectively; the control effect of Mx3 extract was higher than it' s suspension. Mx3 extract had good effect on plant height and leaf quantity of tomato growing in the greenhouse; its growth-promoting abihty on wheat and cucumber was higher than water control. [ Conclusion ] Mx3 could promote growth of root, bud on both tomato and wheat, but it could restrain the growth of cucumber root.%[目的]从首蓿内生放线菌中筛选拮抗菌株.[方法]采用已从健康首蓿组织中分离得到的内生放线菌Mx1、Mx3、Mx5进行温室促生防病测定.[结果]菌株Mx3的发酵液对番茄灰霉病的防效可达56.56%,对小麦全蚀病的防效为44.67%;发酵液对2种病害的防效都明显高于菌悬液.对温室番茄株高、叶片数生长影响最明显;对小麦、黄瓜的促生均高于对照.[结论]菌株Mx3促生效果最好,其发酵液的防病效果明显优于菌悬液.

  12. Isolation & Identification of an Actinomycetes Strain and Analysis of Its Metabolites%一株放线菌的分离鉴定及其代谢产物研究

    Institute of Scientific and Technical Information of China (English)

    杨帆; 陈良强; 林琳; 王和玉; 王莉

    2014-01-01

    利用高氏平板从酱香型白酒生产环境土壤中筛选分离得到1株放线菌NS01,利用形态学、16S rRNA序列同源性鉴定目的菌株为链霉菌属(Streptomyces sp.)。分别采用液态与固态培养基培养目的菌种,通过顶空固相微萃取技术进行萃取,再利用气相色谱质谱联用仪分析代谢产物,结果发现该菌代谢大量的萜烯类物质。代谢产物中的倍半萜烯类物质:2-甲基异莰醇、土臭素具有土臭味和霉味,该类物质可能与酱香型白酒酿造过程中出现霉味有关。%An actinomycetes strain NS01 was isolated from the soil in the production environment of Maotai by use of Gause's culture plate. And it was identified as Streptomyces sp. by 16S rRNA gene sequence analysis and morphological analysis. After the culture of strain NS01 by liquid culture medium and by solid culture medium respectively, its metabolites were extracted by HS-SPME and then analyzed by GC-MS. It was found that its metabolites contained a large number of terpenes. 2-methylisoborneol and geosmin in the sesquiterpenes in the metabolites might be relat ed to the musty-odor of base liquor.

  13. Aminophthalocyanine-Mediated Photodynamic Inactivation of Leishmania tropica.

    Science.gov (United States)

    Al-Qahtani, Ahmed; Alkahtani, Saad; Kolli, Bala; Tripathi, Pankaj; Dutta, Sujoy; Al-Kahtane, Abdullah A; Jiang, Xiong-Jie; Ng, Dennis K P; Chang, Kwang Poo

    2016-04-01

    Photodynamic inactivation ofLeishmaniaspp. requires the cellular uptake of photosensitizers, e.g., endocytosis of silicon(IV)-phthalocyanines (PC) axially substituted with bulky ligands. We report here that when substituted with amino-containing ligands, the PCs (PC1 and PC2) were endocytosed and displayed improved potency againstLeishmania tropicapromastigotes and axenic amastigotesin vitro The uptake of these PCs by bothLeishmaniastages followed saturation kinetics, as expected. Sensitive assays were developed for assessing the photodynamic inactivation ofLeishmaniaspp. by rendering them fluorescent in two ways: transfecting promastigotes to express green fluorescent protein (GFP) and loading them with carboxyfluorescein succinimidyl ester (CFSE). PC-sensitizedLeishmania tropicastrains were seen microscopically to lose their motility, structural integrity, and GFP/CFSE fluorescence after exposure to red light (wavelength, ∼650 nm) at a fluence of 1 to 2 J cm(-2) Quantitative fluorescence assays based on the loss of GFP/CFSE from liveLeishmania tropicashowed that PC1 and PC2 dose dependently sensitized both stages for photoinactivation, consistent with the results of a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) cell viability assay.Leishmania tropicastrains are >100 times more sensitive than their host cells or macrophages to PC1- and PC2-mediated photoinactivation, judging from the estimated 50% effective concentrations (EC50s) of these cells. Axial substitution of the PC with amino groups instead of other ligands appears to increase its leishmanial photolytic activity by up to 40-fold. PC1 and PC2 are thus potentially useful for photodynamic therapy of leishmaniasis and for oxidative photoinactivation ofLeishmaniaspp. for use as vaccines or vaccine carriers.

  14. Dicty_cDB: Contig-U13374-1 [Dicty_cDB

    Lifescience Database Archive (English)

    Full Text Available 667_3335( CP000667 |pid:none) Salinispora tropica CNB-440, co... 37 0.65 EF610853_1( EF610853 |pid:none) Anoche...tus sp. Mad-01 cytochrome ox... 37 0.66 EF610856_1( EF610856 |pid:none) Anochetus sp. Mad-01 cytochrome o...x... 37 0.66 EF610849_1( EF610849 |pid:none) Anochetus sp. Mad-01 cytochrome ox... 37 0.66 EF610846_1( EF610846 |pid:none) Anoche...tus sp. Mad-01 cytochrome ox... 37 0.66 EF610861_1( EF610861 |pid:none) Anoche..._5228( CP000473 |pid:none) Solibacter usitatus Ellin6076, ... 36 1.5 EF610886_1( EF610886 |pid:none) Anochet

  15. The fluorinase, the chlorinase and the duf-62 enzymes.

    Science.gov (United States)

    Deng, Hai; O'Hagan, David

    2008-10-01

    The fluorinase from Streptomyces cattleya and chlorinase from Salinispora tropica have a commonality in that they mediate nucleophilic reactions of their respective halide ions to the C-5' carbon of S-adenosyl-L-methionine (SAM). These enzyme reactions fall into the relatively small group of S(N)2 substitution reactions found in enzymology. These enzymes have some homology to a larger class of proteins expressed by the duf-62 gene, of which around 200 representatives have been sequenced and deposited in databases. The duf-62 genes express a protein which mediates a hydrolytic cleavage of SAM to generate adenosine and L-methionine. Superficially this enzyme operates very similarly to the halogenases in that water/hydroxide replaces the halide ion. However structural examination of the duf-62 gene product reveals a very different organisation of the active site suggesting a novel mechanism for water activation.

  16. Response of Microbe Quantity and Actinomycetes Community of Heavy Metal Contaminated Soils in Leadzinc Mine%铅锌矿区重金属污染对微生物数量及放线菌群落结构的影响

    Institute of Scientific and Technical Information of China (English)

    李小林; 颜森; 张小平; 韦成健

    2011-01-01

    采集四川省汉源县富泉乡万顺铅锌矿区5个不同重金属浓度的土壤样品,进行了微生物数量及放线菌多样性的研究.经分离、纯化得到43株不同的放线菌,然后对其进行BOXAIR-PCR和16S rDNA PCR-RFLP分析.结果表明,铅锌矿区重金属复合污染对土壤微生物数量有较大的影响,随着铅锌矿区重金属污染程度的加剧,土壤微牛物的总数下降.相关性分析表明,重金属含量与细菌数量呈极显著负相关(P<0.01),与放线菌数量、真菌数量呈显著负相关(P<0.05).供试菌株的16S rDNA用Hae Ⅲ、Hinf Ⅰ和Taq Ⅰ酶切后具有32种遗传图谱类型.BOXAIR-PCR的聚类结果表明在86%的水平上,所有菌株分为10个遗传类型,结果基本与16S rDNA PCR-RFLP聚类差异不大.来源于高重金属的含量样品的菌株基本聚在一起,可能是重金属含量影响了放线菌的分布.同时,16S rDNA序列聚类分析结合系统发育树分析表明链霉菌属是汉源铅锌矿区主要的放线菌属并且具有遗传多样性.%To understand the influence of the heavy metal pollution on actinomycetes, the microbe quantity of soils, diversity and dominant microbial groups of actinomycetes were tested.Forty-three strains of actinomycetes in the lead-zinc mine soils were isolated from Fuquan town, Hanyuan country, Sichuan Province.The genetic diversity was evaluated by BOXAIR and 16S rDNA PCR-RFLP.The results indicated that heavy metals pollution had a significant impact on the number of soil microbes in lead-zinc district.With the intensification of heavy metal pollution levels, the total number of soil microorganisms declined.There was a very significant negative correlation between the number of bacteria and heavy metal content(P<0.01 ), whereas significant negative correlation for the numher of fungi and actinomycetes(P<0.05 ).The strains used in numerical taxonomy were analyzed by 16S rDNA PCR-RFLP with three kinds of restriction eadonucleases

  17. Inductive effects of fungal pathogens of American Ginseng and Ginseng on chitinase and cellulase of antigonistic actinomycetes%西洋参和人参病原真菌菌体对放线菌2种水解酶的诱导

    Institute of Scientific and Technical Information of China (English)

    于妍华; 薛泉宏; 唐明

    2011-01-01

    【目的】研究特定拮抗放线菌对西洋参人参土传病害病原真菌的接触抗菌机理。【方法】以5株西洋参、人参土传病害病原真菌菌体为惟一碳源,用液体培养及3,5二硝基水杨酸(DNS)法研究5株供试病原真菌对9株拮抗放线菌几丁质酶和纤维素酶合成的诱导作用;采用搭片法,观察9株拮抗放线菌与5株供试病原真菌菌丝间的相互作用。【结果】①以5株病原真菌菌体为惟一碳源时,可诱导9株拮抗放线菌合成几丁质酶和纤维素酶;9株放线菌的几丁质酶和纤维素酶活性分别为7.17~11.58和6.14~21.20 U,其中西洋参恶疫霉菌体对9株放线%【Objective】 Inhibitory mechanism of antigonistic actimomycetes fighting against fungal pathogens of soil-borne disease in American Ginseng and Ginseng was studied.【Method】 The inductiveness was assessed by the activity of chitinase and cellulase,which were induced from 9 strains of antigonistic actinomycete by using 5 dried strains of fungal pathogens of American Ginseng and Ginseng as C-source in liquid culture medium and DNS measurement,and the mutual effects were observed between antigonistic actinomycetes and fungal pathogens of American Ginseng and Ginseng through the method of building pieces on plate.【Result】 ①The activity of chitinase and cellulase,which was mainly distributed among 7.17-11.58 and 6.14-21.20 U,respectively,differed from 9 strains of antigonistic antinomycete induced from 5 strains of fungal pathogen of American Ginseng and Ginseng.The powder of Phytophthora cactorum could induce antigonistic actinomycetes to produce much more chitinase and cellulase.②The mutural effects between mycelia of Act11,Act13,Act24 and Cylindrocarpon destructans,Cylindrocarpon sp.,such as winding and decomposition,were observed distinctively.【Conclusion】 The mycelia of 5 strains of fungal pathogen of American Ginseng and Ginseng could induce 9 strains of antigonistic actinomycete

  18. 放线菌制剂对人参生长及根域土壤微生物区系的影响%Effects of actinomycetes agent on ginseng growth and rhizosphere soil microflora

    Institute of Scientific and Technical Information of China (English)

    张鸿雁; 薛泉宏; 申光辉; 王东胜

    2013-01-01

    Taking the ginseng in Xiao Xing' an Mountains of Northeast China as test object,this paper studied the effects of applying Streptomyces pactum (Act12) on ginseng growth and on the soil microflora in root zone and root surface.After treated with Act12,the yield and quality of ginseng' s medicinal part improved,the induced enzyme activities in leaves and the root activity increased,and the numbers and proportions of soil bacteria and actinomycetes increased significantly while those of soil fungi decreased.Compared with the control,the soil microflora in treatment Act12 changed.The numbers of the dominant bacteria Pseudomonas fluorescens,Pseudomonas koreensis,and Microbacterium oxydans were much higher in root zone soil and root surface soil,and the pathogen Plectosphaerella cucumerina decreased in root zone soil and disappeared in root surface soil.These results suggested that the addition of Act12 could improve the soil microflora,enhance the resistance and root activity of ginseng plant,and increase the ginseng yield and its quality.%以小兴安岭地区人参为研究对象,探索放线菌制剂对人参的促生效应及对人参根区、根表土壤微生物区系的影响.结果表明:经放线菌制剂Streptomyces pactum(Act12)处理后,人参药用部分产量增加,品质改善;叶片诱导酶活性提高,根系活力增强;土壤中细菌、放线菌的数量和比例显著增加,真菌的数量和比例减少.与对照相比,土壤微生物区系结构改变:优势菌荧光假单胞菌、韩国假单胞菌和氧化微杆菌在根区、根表土壤中的数量大幅提高;病原真菌烟色织孢霉在根区土壤中减少,在根表土壤中消失.表明施用放线菌制剂Act12能够改善土壤微生物区系,提高人参植株的抗性和根系活力,增加产量并改善品质.

  19. Study of Agro-Active Metabolites of Marine Actinomycete Y-0117%海洋放线菌Y-0117农用活性代谢产物的研究

    Institute of Scientific and Technical Information of China (English)

    杨巍民; 斯聪聪; 杨星; 徐文平; 陶黎明

    2013-01-01

    在农用抗生素筛选中发现代号为Y-0117的海洋放线菌菌株所产生的代谢产物对植物病原真菌具有良好的抑制作用.对Y-0117发酵液进行萃取、硅胶柱层析、制备薄层色谱、制备HPLC,分离纯化得到两个活性组分0117A和0117B.通过紫外光谱、质谱、核磁共振等手段,确定0117A的分子式为C35H56O8,分子量为604,结构与已知化合物Bafilomycin D相同;0117B的分子式为C42H60O12,分子量为756,结构与近期发现具有抗癌活性的已知化合物Hygrobafilomycin相同.研究发现0117B对多种植物病原真菌具有良好的抑制活性,对稻瘟病菌的最小抑制浓度为15.63 μg·mL-1.%The secondary metabolites generated by marine Actinomycete Y-0117 had good bioactivity against many plant pathogenic fungi. Through fermentation, solvent extraction, silica gel chromatography, thin layer chromatography and high performance liquid chromatography,two antifungal macrolide compounds 0117A and 0117B were isolated from the culture extract of strain Y-0117 by bioassay-guided fractionation. The spectra data of UV,ESI-MS,NMR were used to identify these compounds. The molecular formula of compound 0117A was confirmed as C35 H56O8 with molecular weight of 604 and the structure as the same as the known compound ba-filomycin D. The molecular formula of the compound 0117B was confirmed as C42 H60O12 with the molecular weight of 756 and the structure as the same as hygrobafilomycin which was found with anti-cancer activity. The compound 0117B had good bioactivity against several plant pathogenic fungi, the MIC of compound 0117B a-gainst Pyricularia oryzae was only 15. 63 μg·mL-1, This paper firstly reported the compound 0117B activity in anti-plant pathogenic fungi.

  20. Preliminary Study on Antibiotic Activity of the Extract From Antarctic Actinomycete NJ-F2%南极放线菌NJ-F2萃取物的抗菌活性初步研究

    Institute of Scientific and Technical Information of China (English)

    李江; 林学政; 沈继红; 王能飞; 李光友

    2009-01-01

    Actinomycete NJ-F2 is isolated from the sea-mud sampled during the 24th Antarctic Scientific Expedition of China . The bacteriostatic activity of the extract with acetic ether from the fermented NJ-F2 is detected in the in-vitro experiment and the 16S rDNA method is employed to analyze the NJ-F2 phylogenesis. As it is shown from the experimental results,the minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) against both Staphylococcus aureus and Bacillus subtilis are 0. 25 mg/mL and 5. 0 mg/mL respectively,and MIC and MBC against both Eschericidal coil and Aerobac-tor aerogenes are 0. 5 mg/mL and 5. 0 mg/mL respectively. No antibacterial activity can be found against fungi. It is learnt from the 16S rDNA analysis that NJ-F2 is of Streptomyces sp.%从南极第24次科学考察采集的海泥样品中分离获得放线菌NJ-F2,对NJ-F2发酵液的乙酸乙酯萃取物进行体外抗菌实验,并采用16S rDNA方法对NJ-F2进行系统发育分析.结果表明萃取物对金黄色葡萄球菌和枯草芽孢杆菌的最低抑菌浓度(MIC)、最低杀菌浓度(MBC)分别为0.25 mg/mL,5.0 mg/mL;而对大肠杆菌和产气杆菌的MIC、MBC分别为0.5 mg/mL,5.0 mg/mL,但对真菌没有抗菌作用;16SrDNA分析结果表明NJ-F2为链霉菌属(Streptomyces sp.).

  1. Identification of an Actinomycete Antagonistic Against Cylindrocarpon destructans and Its Optimized Fermentation Conditions%人参锈腐病拮抗放线茵的鉴定及发酵条件

    Institute of Scientific and Technical Information of China (English)

    姜云; 陈长卿; 王琳; 马贵龙

    2011-01-01

    An actinomycete strain 1a-3 antagonistic against Cylindrocarpon destructans was isolated from the soil in ginseng fields. It was identified as Streptomyces griseochromogenes according to the morphological characteristics, cultural characteristics, physiological and biochemical properties, cell wall components and 16S rDNA sequences analysis. Single factor experiment and multiple factor experiment showed that the culture medium which contained 1 g/L glucose, 3 g/L com flour, 2 g/L soybean flour, 0.3 g/L yeast flour, 0. 1 g/L KH,PO4, 0. 3 g/L CaCO, and 0. 1 g/L NaCl was the best for fermentation. The optimal fermentation condition was obtained as initial pH 7.0, fermentation temperature 28 degrees C, and fermentation time 60 h.%从人参田土壤中筛选到1株对人参锈腐病菌(Cylindrocarpon destructans)有较强拮抗作用的菌株1a-3,通过形态特征、培养特性、生理生化特性、细胞壁组分分析和16S rDNA同源性序列分析,确定该菌株为链霉菌属灰产色链霉菌(Streptomyces griseochromogenes).经单因子和各因子正交试验,确定的最适发酵培养基配方为,葡萄糖1 g/L、玉米粉3g/L、大豆粉2g/L、酵母粉0.3 g/L、KH2PO40.1 g/L、CaCO30.3g/L、NaCl 0.1 g/L;最适培养条件为起始pH值7.0、28℃摇瓶培养60h.

  2. Optimization of Fermentation Conditions of an Endophytic Actinomycetes from Tobacco Plant%一株烟草内生拮抗放线菌发酵条件优化

    Institute of Scientific and Technical Information of China (English)

    孙会强; 周赛男; 谭周进; 伍兵; 谢丙炎; 申可佳

    2011-01-01

    为提高烟草内生放线菌Y12发酵时产生抑菌物质的产量,通过摇瓶正交优化试验,确定了Y12的三角瓶发酵条件.发酵培养基组成为:黄豆粉1.5%,蛋白胨1.5%,葡萄糖1.5%,可溶性淀粉1.5%,MgSO4·7H20 0.05%,(NH4)S040.25%,NaCl 0.4%,KH2PO40.1%,CaCO30.5%;培养基初始pH 7.5,培养温度30℃,发酵时间72 h.经过优化发酵液的抑菌圈直径增加了44.9%.%In order to increase the yield of the antibacterial substance produced by an endophytic actinomycetes, Y12, from tobacco plant in the process of fermentation, a series of orthogonal experiments on Y12 were carried out in the shaking flasks to obtain optimal components of the fermentation media as well as the fermentation conditions. It was concluded that the optimal proportion of the fermentation medium was: 1.5% soybean flour, 1.5% peptone, 1.5% glucose, 1.5% soluble starch, 0.05% MgSO4-7H2O,0.25% (NH4)SO4,0.4% NaCl, 0.1% KH2PO4 and 0.5% CaCO3. The optimal fermentation conditions were: Medium' s initial Ph value 7.5, fermentation temperature 30 °C, and fermentation time 72 hours. It was observed from the experiments that the inhibition diameters of the zymotic fluid increased by 44.9% under the optimized conditions. Fig 2, Tab 2, Ref 17

  3. 番茄溃疡病菌拮抗菌株Z-L-22的鉴定及其活性物质%Identification and analysis of an actinomycete strain suppressing Clavibacter michiganensis subsp. Michiganensis

    Institute of Scientific and Technical Information of China (English)

    张艳; 张维宏; 王松红; 李亚宁; 赵志泉; 刘大群; 杨文香

    2009-01-01

    [目的]鉴定一株对番茄溃疡病病原菌一密执安棒形杆菌密执安亚种(Clavibacter michiganensis subsp.michiganensis,Cmm)具有强拮抗作用的放线菌菌株Z-L-22,并分析其代谢产物,为开发新的生物活性物质奠定基础.[方法]根据菌株Z-L-22的形态特征、培养特征、生理生化特征、细胞壁组分和16s rDNA序列对菌株Z-L-22的进行了鉴定.通过薄层层析、纸层析和特征性鉴别试验对活性物质进行分离、回收和鉴定.并利用抗生素合成基因保守区域设计的引物用对基因组DNA进行PCR扩增.[结果]菌株Z-L-22属于链霉菌属,各特征与西唐链霉菌(Streptomyces setonii)相似.获得了2个主要活性成分,均为放线菌素类抗生素.利用放线菌素类抗生素合成酶保守引物在该菌基因组中扩增到770 bp的相关基因片段.[结论]活性菌株Z-L-22鉴定为西唐链霉菌,命名为西唐链霉菌Z-L-22.该菌产生的抗生活性物质为放线菌素类抗生素,本研究为开发该菌株奠定基础.%[Objective] To identify and analyze bioactive compounds of an actinomycete strain Z-L-22 suppressing Clavibacter michiganensis subsp. michiganensis, the causal agent of bacterial canker of tomato. [Methods] Morphological, biological and biochemical characterization,chemotaxonomy analysis and 16S rDNA sequences homology analysis were performed to identify the strain Z-L-22. Bioactive compounds were separated and retrieved by thin layer chromatography. Paper chromatography and confirmation tests were used to identify the antibiotic. PCR was carried out using the primers targeted to synthetase of the antibiotic. [Results] Strain Z-L-22 belonged to Streptomyces sp. and was similar to Streptomyces setonii. Two main bioactive components were isolated by thin layer chromatography, which were all identified as actinomycin. New actinomycin synthetase gene was cloned using the primers designed from actinomycin synthetase conserve domain. [Conclusion

  4. Efecto Antagónico in vitro de Actinomicetos Aislados de Purines de Chipaca (Bidens pilosa L. Frente a Phytophthora infestans (Mont de Bary In vitro Antagonistic Effect of Actinomycetes Isolated from Chipaca (Bidens pilosa L. Purins Against Phytophthora infestans (Mont de Bary

    Directory of Open Access Journals (Sweden)

    Yudy Astrid Fonseca Ardila

    2011-12-01

    Full Text Available Se estudió el efecto inhibidor de los actinomicetos presentes en purines o extractos fermentados de plantas de chipaca (Bidens pilosa L., sobre el crecimiento de Phytophthora infestans (Mont de Bary, causante del tizón tardío de la papa. Se elaboraron cuatro purines de flores, raíces, hojas-tallos y su mezcla. De estos purines se obtuvieron 25 aislamientos de actinomicetos, cada uno de los cuales se enfrentó con P. infestans en placas de medio de cultivo, utilizando la técnica de anillos de Gauze y estableciendo las concentraciones iniciales de esporas mediante conteos microscópicos en cámara de Neubauer. Los actinomicetos no crecieron en el purin de flores debido, posiblemente, a que en él no se utiliza suelo rizosférico o porque su pH (9 es mayor que el rango normal de crecimiento de estos microorganismos ( pH 6 -; 8. Se evidenció inhibición del crecimiento del oomycete por parte de 8 aislamientos de actinomicetos con porcentajes de inhibición entre 33,3 - 77,8%, provenientes de los purines de raíces, tallos-hojas y mezcla de partes de la planta. La mayor inhibición se obtuvo en los aislamientos AC001, AC010, AC011 y AC025 con conteos de 0,4, 6,0, 3,0, y 3,6 x10(5 esporas mL-1.Purins or liquid fermented extracts of chipaca (Bidens pilosa L. were prepared to establish the inhibitory effect of the actinomycetes found in such biopharmaceutical preparations on the growth of Phytophthora infestans (Mont de Bary, the causative of potato late blight disease. Four purins made from flowers, roots, leaf-steams and a mixture of them were prepared; 25 actinomycete isolates were obtained from these purins and their ability to resist challenge by P. infestans was ascertained in medium plates using the ring Gauze technique and establishing initial concentrations of spores by microscopic counting in Neubauer chamber. Actinomycetes did not grow in flower purin as rhizosphere soil was not used in its preparation or because this particular pH (9

  5. Produção de biomassa de erva-cidreira [Lippia alba (Mill. N.E.Br.] sob adubação com composto de capim elefante inoculado e sem inoculação de actinomicetos Biomass production of Lippia alba (Mill. N.E.Br. under fertilization with compost inoculated elephant grass and without inoculation of actinomycetes

    Directory of Open Access Journals (Sweden)

    E.V.G. Gama

    2012-01-01

    and inoculated with the actinomycete Streptomyces genus, AC16, AC26, AC92 and AC103. The compounds were placed in polyethylene bags containing 10.0 kg of soil added in a proportion equivalent to 20 t ha-1 and re-apply after the first harvest. The harvests of the shoots were taken at 75 and 165 days after transplantation. The roots were harvested after the second harvest. Dealing with organic fertilization promoted the average increase in biomass production of lemon grass 184, 83, 125, 115 and 122% for the dry stem biomass (MSPA in the first harvest, second harvest of MSPA, total shoot biomass (MSTPA, dry biomass of the root (MSR and the total crop biomass (MST, respectively, compared with the control, but no effect of inoculation of actinomycetes in compost. Under the conditions of this study was conducted, it was concluded that the organic compound fertilizer with elephant grass positively influenced the production of dry biomass of L. alba, but the injection of the compounds of the actinomycetes, without influence.

  6. Isolation,activity and biodiversity of actinomycetes from marine sediments of Yellow Sea and Lushan soil samples%黄海海域沉积物和庐山土壤样品中放线菌的分离、活性及生物多样性研究

    Institute of Scientific and Technical Information of China (English)

    王燕萍; 熊智强; 杨靖亚; 王勇

    2015-01-01

    Using uniform design method,the optimal pretreatment conditions were the heat treatment at 50 ℃ for 20 min, no ultrasonic treatment and phenol addition. Under the optimal conditions,86 strains and 11 strains of actinomycetes were isolated from marine sediments of the Yellow Sea and Lushan soil samples,respectively. Based on molecular identifica-tion,86 actinomycetes of marine sediments belonged to 3 different genera and 11 strains of Lushan soil samples belonged to 4 different genera. Antimicrobial activities of the 97 isolated strains showed that 18. 5% of strains had inhibition zone to Escherichia coli,and 7. 2% of strains had anti-Bacillus subtilis activity,but all strains could not inhibit against Saccharo-myces cerevisiae.%本研究采用均匀实验设计优化预处理条件来分离黄海海泥和庐山土壤样品中的放线菌。通过均匀实验得到最优的预处理条件为湿热50℃处理20 min,不进行超声处理以及添加苯酚。经过形态排重后,从海泥和庐山样品中分离得到86株和11株不同表型的放线菌。通过进一步的分子生物学鉴定,海泥中的86株放线菌分别属于3个不同的属,而庐山样品的11株分别属于4个不同的属。对这97株放线菌进行抗菌实验发现,18.5%的菌株对大肠杆菌有抑菌活性,7.2%的菌株对枯草芽孢杆菌有抑菌活性,但对酿酒酵母都无抑菌活性。

  7. 秦巴山区三尖杉根际土壤放线菌的分离、筛选及活性菌株的鉴定%Isolation, screening and identification of active actinomycete from Cephalotaxus fortunei rhizosphere soil in Qinba Mountains

    Institute of Scientific and Technical Information of China (English)

    晏丽; 阮昌应; 解修超; 彭浩; 陈文强; 邓百万

    2016-01-01

    采用选择性分离方法从秦巴山区三尖杉植物根际土样中分离得到放线菌35株,以白色念珠菌( Candida albicans)、大肠杆菌( Escherichia coli)、枯草芽孢杆菌( Bacillus subtilis)、金黄色葡萄球菌(Staphylococcus aureus)、沙门氏杆菌(Salmonella typhl)为靶标菌,采用滤纸片扩散法研究三尖杉根际土壤放线菌发酵液的抑菌活性。结果表明,16株放线菌表现出至少对一种靶标菌有抗性,占总分离菌株的45.7%,其中,菌株CF003对所有靶标菌均具有活性;经形态学和16S rRNA基因序列鉴定,这16株放线菌分属于链霉菌属( Streptomyces)和小单孢菌属( Micromonospora)。%35 strains of actinomycetes isolated from Cephalotaxus fortunei rhizosphere soil in Qinba Mountains,China,were studied in this paper.Phylogenetic analysis based on 16S rRNA gene sequences indica-ted that the 16 strains belong to small group of actinobacterial genera including Streptomyces and Micromonospo-ra.Candida albicans,Escherichia coli,Bacillus subtilis,Staphylococcus aureus,Salmonella typhl were selected as indicator bacteria when the antimicrobial activities of these actinomycetes were tested through antimicrobial ex-periments in the exterior body.The result showed that 16 strains (45.7%) exhibited activity against at least one target strain,and the CF003 strain has strong inhibition to all target strains.

  8. Isolation and biocontrol potential of bacteria and actinomycetes from soils suppressive to Rhizoctonia bare-patch disease in South Australia%南澳大利亚丝核菌抑病土中细菌与放线菌的分离及其对病害的生物防治作用

    Institute of Scientific and Technical Information of China (English)

    杨合同; Maarten RYDER; 唐文华

    2005-01-01

    Bacteria and actinomycetes were quantitatively isolated from a soil collected from Avon, South Australia, which is suppressive to wheat bare-patch disease caused by Rhizoctonia solani anastomosis group 8. The percentage of isolates antagonistic to R. solani AG-8 isolate 21 was measured from the total population of bacteria and actinomycetes. Heat treatment (60℃, 10min.), a process previously shown to remove the suppressive qualities of this soil, significantly reduced the counts of total bacteria and actinomycetes on agar plates, but did not reduce the percentage of antagonists. Nine isolates were chosen from 2700 isolates, based on their strong inhibition of R. solani AG-8 isolate 21, Gaeumannomyces graminis var. tritici (Ggt) isolate 8, Fusarium graminearum isolate Fg, Verticillium dahliae isolate Vd5, Bipolaris sorokiniana isolate Bs, Pythium irregulare isolate BH40, and Rhizoctonia solani AG-4 isolate 1664 causing damping-off of cotton. Seven of the nine antagonistic isolates were either chitinase-or endoglucanase-positive, with strong chitinase production appearing to be associated with strong biocontrol activity.The nine antagonistic isolates were identified as Bacillus megaterium (isolate Ap25), B. subtilis (isolate Ap113), Streptomyces spp. (isolate Ap117), Bacillus coagulans (isolate Ap123), Streptoverticillium reticulum (isolate Ap89), Cellulomonas flavigena (isolate Ap75) or were actinomycetes (isolates Ap116, Ap111 and Ap139).B. megaterium Ap25 and B. subtilis Ap113 were the most effective in disease reduction and seedling growth promotion.These two isolates were inhibitory in vitro to a beneficial Trichoderma pseudokoningii isolate A5MH, which was isolated from the same soil sample, but did not significantly reduce the efficacy of A5MH in disease control and seedling growth promotion.%从南澳大利亚埃文采集的土壤样品中计数分离了细菌和放线菌,该土壤对Rhizoctonia solani 融合群8引起的小麦根腐病具有抑制作

  9. 根结线虫拮抗放线菌的筛选及菌株HAL0002的鉴定与活性物质分析%Screening of actinomycetes against root-knot nematodes and the active compounds produced by strain HA10002

    Institute of Scientific and Technical Information of China (English)

    曾庆飞; 黄惠琴; 朱军; 鲍时翔

    2011-01-01

    为了筛选获得对根结线虫具有拮抗能力的强活性放线菌菌株,并从菌株中发现新的杀线虫活性化合物,从海南东寨港红树林采集海泥样品9份,从五指山原始森林等地采集土壤样品51份,用平板稀释法对海泥和土壤样品进行分离;以南方根结线虫2龄幼虫为靶标线虫,采用24孔细胞培养板液体线虫法进行初筛和复筛;根据形态特征、培养特征、生理生化特征和16S rDNA序列对复筛出的活性菌株进行鉴定;菌株发酵液经溶媒萃取、硅胶柱层析、Sephadex LH-20凝胶过滤和制备薄层板层析,采用活性跟踪法从中分离纯化杀线虫活性化合物;化合物经光谱及波谱分析和文献对照,进行结构鉴定.从60份样品中分离得到356株菌落形态有差异的放线菌.初筛得到16株对根结线虫校正死亡率在80%以上的菌株,复筛获得3株线虫校正死亡率在95%以上的菌株,其中分离自海泥样品中的菌株HA10002抗线虫活性最强,发酵原液的校正死亡率达100%.HA10002经鉴定为白浅灰链霉菌,从其发酵液中分离获得2个活性化合物,其中A26-3为Nocardamine,A22-1的结构正在进一步鉴定中.上述结果表明,筛选出的放线菌HA10002能合成2种以上杀根结线虫的活性代谢产物,是一株遗传稳定且具有开发潜力的活性菌株.%In order to isolate new actinomycete strains with high nematicidal activity, and to discover new compounds against root-knot nematodes, nine mangrove sediments collected from Dongzhaigang mangrove and 51 soil samples from Five-finger Mountain) in Hainan Province were isolated using dilution-plate method. Strains were selected by using Meloidogyne incognita as target nematodes. The selected antagonistic strains were identified through morphological observation and 16S Rdna sequencing and analyses. Fermentation broth of the strain was separated and purified by means of solvent extraction, column chromatography

  10. Genomic islands predict functional adaptation in marine actinobacteria

    Energy Technology Data Exchange (ETDEWEB)

    Penn, Kevin; Jenkins, Caroline; Nett, Markus; Udwary, Daniel; Gontang, Erin; McGlinchey, Ryan; Foster, Brian; Lapidus, Alla; Podell, Sheila; Allen, Eric; Moore, Bradley; Jensen, Paul

    2009-04-01

    Linking functional traits to bacterial phylogeny remains a fundamental but elusive goal of microbial ecology 1. Without this information, it becomes impossible to resolve meaningful units of diversity and the mechanisms by which bacteria interact with each other and adapt to environmental change. Ecological adaptations among bacterial populations have been linked to genomic islands, strain-specific regions of DNA that house functionally adaptive traits 2. In the case of environmental bacteria, these traits are largely inferred from bioinformatic or gene expression analyses 2, thus leaving few examples in which the functions of island genes have been experimentally characterized. Here we report the complete genome sequences of Salinispora tropica and S. arenicola, the first cultured, obligate marine Actinobacteria 3. These two species inhabit benthic marine environments and dedicate 8-10percent of their genomes to the biosynthesis of secondary metabolites. Despite a close phylogenetic relationship, 25 of 37 secondary metabolic pathways are species-specific and located within 21 genomic islands, thus providing new evidence linking secondary metabolism to ecological adaptation. Species-specific differences are also observed in CRISPR sequences, suggesting that variations in phage immunity provide fitness advantages that contribute to the cosmopolitan distribution of S. arenicola 4. The two Salinispora genomes have evolved by complex processes that include the duplication and acquisition of secondary metabolite genes, the products of which provide immediate opportunities for molecular diversification and ecological adaptation. Evidence that secondary metabolic pathways are exchanged by Horizontal Gene Transfer (HGT) yet are fixed among globally distributed populations 5 supports a functional role for their products and suggests that pathway acquisition represents a previously unrecognized force driving bacterial diversification

  11. Bergey's Manual of Systematic Bacteriology (second edition) Volume 5 and the study of Actinomycetes systematic in China%“伯杰氏系统细菌学手册(第二版)”第5卷与我国的放线菌系统学研究

    Institute of Scientific and Technical Information of China (English)

    阮继生

    2013-01-01

    “伯杰氏系统细菌学手册”(下文简称“伯杰氏手册”),是世界各国分类学家普遍接受的学术观点的汇总,集科学性、统一性和实用性于一身.2012年5月,随着“伯杰氏手册”第二版第5卷(放线菌专刊)分A、B两册出版,这部经典巨著在Michael Goodfellow等的领导下精心组织并顺利完成.“伯杰氏手册”第5卷对放线菌分类系统做出了重大调整,正式建立了放线菌门,包括6个纲、23个目(含一个未确定目)、53个科、222个属、近3000个种,其分类阶元为细菌域、放线菌门,在门下为纲、目、科、属和种.“伯杰氏手册”收录了我国放线菌分类学研究的大量成果,这是我国四代放线菌分类学家们共同努力的结果.但需要指出的是,由于“伯杰氏手册”过于严谨、保守的著书宗旨与漫长的出版周期,对DNA基因多位点序列分析(MLSA)技术、基因芯片技术和基因组技术等在分类学领域中所做出的新研究成果采纳不足,而这部分内容或许在不久的将来会使原核生物分类学发生深刻的改变.%Bergey's Manual of Systematic Bacteriology (hereinafter referred to as "Bergey's Manual") is the collection of academic views accepted by taxonomists in many countries.It has scientificity,unitarity and practicality." Bergey's Manual" (special issue of Actinomycetes) divided into two parts (part A and part B) was published in May,2012.Under the guidance and the organization of Michael Goodfellow et al.,the great work has been completed successfully in May 2012." Bergey's Manual" made a great modification on the systematic of Actinomycetes and formally set up the phylum of Actinobacteria,which encompasses 6 classes,23 orders (include one order incertae sides),53 families,222 genera and about 3000 species.The taxonomic catalogue is Bacteria,phylum of Actinobacteria,under the phylum there are class,order,family,genera and species." Bergey's Manual" collected a great deal

  12. Isolating of antifungal activity substance from endophytic actinomycete Lj20 and the role in disease control%放线菌Lj20抗真菌物质的分离及其在病害防治中的作用

    Institute of Scientific and Technical Information of China (English)

    陈红兵; 马林; 韩巨才; 曹挥

    2011-01-01

    Endophytic actinomycete Lj20 with antifungal activity was isolated from healthy capsicum plants. In order to determine its potential application in biological control, the antifungal activity substance was separated and purified from metabolites of Lj20 by the means of macroporous absorbing resin,centrifugal thin layer chromatography and column chromatography. The inhibitory efficacy of Lj20 metabolites on Botrytis cinerea Pers was also studied by means of the inhibition rate of mycelium growth in vitro and the control efficacy in the greenhouse. The results showed that the structure of a compound isolated from the Lj20 metabolites was identified as 3, 5-di-tert-butyl-4-hydroxybenzyl methyl ether by analysis of IR (infrared spectroscopy) and 1H-NMR (proton nuclear magnetic resonance spectroscopy) spectroscopic data. This compound indicated the inhibition efficacy on B. cinerea in vitro with the EC50 was 174.94 mg/L. In addition, the control efficacy of crude extracts from Lj20 fermentation on B. cinerea reached 62.5% at the concentration of 500 mg/L in the greenhouse experiments, indicating that this endophytic actinomycete Lj20 had a potential value for further exploitation and utilization.%菌株Lj20是从健康辣椒植株分离得到的一株有杭真菌活性的植物内生放线菌,为了进一步明确其生物防治潜力,利用大孔吸附树脂、离心薄层层析以及柱层析等技术对Lj20代谢产物中的抗真菌活性物质进行了分离和提纯,并采用生长速率法测定了其代谢产物对黄瓜灰霉病菌的抑制作用,同时在温室中对Lj20发酵液粗提物的防病效果进行了试验.从Lj20代谢产物中分离得到一个抗真菌活性物质,该化合物时黄瓜灰霉病菌具有较强抑制作用,EC50值为174.94 mg/L;500mg/LLj20发酵液粗提物对黄瓜灰霉病的防治效果达62.5%;经鉴定其化合物结构为3,5-二叔丁基-4-羟基-卞基甲醚.结果表明,放线菌Lj20有进一步开发和利用的价值.

  13. 极端耐盐放线菌白色普氏菌YIM90005T四氢嘧啶及5-羟基四氢嘧啶合成相关基因的克隆%Cloning and characterization of gene cluster for biosynthesis of ectoine and 5 -hydroxyectoine from extreme halotolerant actinomycete strain Prauserella alba YIM 90005T

    Institute of Scientific and Technical Information of China (English)

    李岩; 董雷; 王磊; 方福瑾; 何敏; 曹中莹; 梁媛; 唐蜀昆; 李文均

    2011-01-01

    [Objective]To study adaptive mechanism in hypersaline environments of extreme halotolerant filamentous actinomycetes.[Methods]Using HPLC we analyzed compatible solutes from extreme halotolerant filamentous actinomycete strain Prauserella alba YIM 90005 that was cultivated at different NaCl concentrations.[Results]Ectoine and 5-hydroxyectoine were two major compatible solutes for strain Prauserella alba YIM 90005.Ectoine accumulated to the maximum content of 18.77 μg/mg dry cell weight after being inoculated in 10% NaCl ( w/v).And 5-hydroxyectoine reached 22.98 μg/mg dry cell weight after being inoculated in 24% NaCl (w/v).The ectA ( acyltransferase) , ectB (aminotransferase) , ectC (ectoine synthase) and ectD ( ectoine hydroxylase) genes cluster encoding genes on ectoine and hydroxyectoine synthesis were further cloned by designing the degenerate primer and genome walking methods.The sequence analysis indicated that ectABCD was an operon.Furthermore, the expression of ectB and ectD inoculated at different salt concentrations was quantified by real-time PCR, and the results indicated that the expression of the gene cluster would be increasing as the salt concentration increased.[Conclusion]5-hydroxyectoine was the major compatible solute for osmotic regulation of strain Prauserella alba YIM 90005 to adapt high salt concentration.%[目的]为了研究耐盐放线菌对高盐环境的适应机理.[方法]用HPLC定量检测了极端耐盐、丝状产孢放线菌--白色普氏菌(Prauserella alba)YIM 90005T在不同盐浓度下胞内相容性溶质的种类和含量.[结果]结果发现,四氢嘧啶和5-羟基四氢嘧啶是其主要的相容性溶质.在培养基NaCI浓度为10%时,四氢嘧啶在胞内累积浓度最大,为18.77μg/mg干菌体重.之后随NaCl浓度的升高,胞内的四氢嘧啶含量逐渐减少,而5-羟基四氢嘧啶的含量逐渐增加,在该菌耐受的最高NaCl浓度下(24% w/v),胞内5-羟基四氢嘧啶含量达到最大值,为22

  14. The Optimum Culture Condition of Actinomycete K13 and Its Inhibition on the Pathogen of Strawberry Gray Mold%放线菌K13最适培养条件及其对草莓灰霉病菌的抑制作用

    Institute of Scientific and Technical Information of China (English)

    徐斌; 陈银凤; 张云; 魏利辉; 张青; 陈夕军

    2015-01-01

    为实现对草莓灰霉病的生态防控,利用对峙培养法,从土壤中分离得到1株对草莓灰霉病菌具有强拮抗活性的放线菌K13,该菌对多种植物病原菌生长具有抑制作用。 K13菌株产生抗菌物质的最佳条件为:在初始pH 值8.0的高氏一号培养液中,28℃下持续振荡培养6 d。 K13能显著抑制草莓灰霉病菌菌丝的生长,采用菌落直径法测定抑制率为55.93%;其还能够抑制草莓灰霉病菌产孢、孢子萌发和芽管伸长,培养滤液2倍稀释时抑制率分别可达72.53%、65.43%和59.83%。显微观察显示,该拮抗放线菌可引起草莓灰霉病菌菌丝扭曲、畸形、断裂,甚至解离。以上结果表明,放线菌K13对草莓灰霉病菌的生长发育具有较强的抑制作用,可用于生防菌剂的研发。%To realize the ecological control of strawberry gray mold,strain K13,one antagonistic actinomy-cete strain against the pathogen Botrytis cinerea,was isolated from the soil by confrontation culture,which could significantly inhibit the growth of many plant pathogenic fungi. The optimal condition of producing antifungal substance by K13 was inoculating the strain into Gause’ s medium with the initial pH value of 8. 0 at 28 ℃ with continuous shaking culture for 6 d. Results showed that K13 could inhibit the hypha growth of B. cinerea,with the inhibition rate of 55. 93% using colony diameter method. It could also inhi-bit the spore bearing,spore germination and germ-tube elongation of B. cinerea,and the inhibition rates were 72. 53%,65. 43% and 59. 83% respectively when the culture filtrate was diluted by two folds. Mi-croscopic observation indicated that the actinomycete filtrates could make the fungus hypha distortion,de-formation,fracture and even disintegration. All these mean that K13 can inhibit the growth and develop-ment of B. cinerea strongly and has the potential of being developed into bio-control agents.

  15. 放线菌FIM06-0063产生的安莎类化合物的分离、纯化及其结构鉴定%Isolation,purification, and structure identification of ansamycin compounds from Actinomycetes FIM06-0063

    Institute of Scientific and Technical Information of China (English)

    毛思雨; 陈宏; 陈丽; 王传喜; 陈晓明; 贾纬; 谢颖; 郑卫

    2013-01-01

    目的 分离、纯化、鉴定来自放线菌FIM06-0063发酵液中的安莎类化合物.方法 采用大孔吸附柱层析、硅胶柱层析等方法对FIM06-0063菌株的次级代谢产物进行分离纯化,以紫外、质谱、核磁等方法对获得的组分进行结构鉴定.结果 从FIM06-0063菌株发酵液中共分离到4个安莎类化合物,经波谱方法鉴定,分别为:9-甲氧基-安丝菌素P-3(9-methoxy-ansamitocin P-3,1),安丝菌素P-2(ansamitocin P-2,2),安丝菌素P-3(ansamitocin P-3,3)和安丝菌素P-4(ansamitocin P-4,4).结论 首次从微生物发酵液中分离得到化合物1,为一个新的天然产物.活性研究表明该化合物对HL60肿瘤细胞具有增殖抑制活性,其IC50值为72.68nmol/L.%Objective To isolate, purify and identify the structure of ansamycin compounds from the fermentation broth of Actinomycetes FIM06-0063. Methods The secondary metabolites were isolated and purified by macroporous resin column chromatography, silica gel chromatography and other ways. The chemical structures were identified by UV, MS and NMR spectra. Results Four compounds isolated from the fermentation broth of FIM06-0063 were identified as 9-methoxy-ansamitocin P-3 (1), ansamitocin P-2 (2), ansamitocin P-3 (3) and ansamitocin P-4 (4) on the basis of spectral data. Conclusion Compound 1 is a new natural product isolated from the broth of strain FIM06-0063 and showes growth inhibitory activity against the tumor cell lines HL60 with IC50 values of 72.68nmol/L.

  16. 五味子叶枯病病原菌的生物学特性及其拮抗放线菌的初筛∗%Biological Characteristics of the Pathogen of Schisandra chinensis Leaf Blight and Screening of Antagonistic Actinomycete Strain against the Pathogen

    Institute of Scientific and Technical Information of China (English)

    王壮; 张爱华; 雷锋杰; 匙坤; 张连学

    2015-01-01

    采用室内平皿培养法研究五味子叶枯病菌的生物学特性,平板对峙法筛选拮抗放线菌。结果表明:叶枯病病原菌在PDA及PDBA培养基上最有利于菌丝生长及产孢;温度对菌丝生长和产孢量影响较大,25℃为其最适温度,同样温度下,黑暗条件显著有利于产生孢子,光照更利于菌丝生长;pH 6~7为菌株生长最适pH;最佳碳、氮源分别为果糖及蛋白胨;孢子致死温度测定为54℃。筛选到2株对五味子叶枯病病原菌拮抗效果较好的放线菌A-25-8和A38,其拮抗率分别为66�26%和66�10%。%Petri dish culture method was used to study biological characteristics of Schisandra chinensis leaf blight pathogen, and plate confrontation method was used to screen antagonistic actino⁃mycetes. The results showed that mycelia grew faster and spore generated more in medium PDA and PDBA. Temperature affected mycelia growth and spore generation at 25 ℃. At the same tempera⁃ture, dark condition was significantly beneficial for spore generation and light condition was benefi⁃cial for mycelial growth. pH 6~7 was most suitable for the pathogen. Fructose and peptone were the best carbon source and nitrogen source for the pathogen. Deadly temperature for the spore was 54 ℃. Two strains ( A-25-8 and A38 ) of the 28 actinomycetes had potential antagonistic effects against leaf blight pathogen and inhibition rate was 66�26% and 66�10%, respectively.

  17. 新疆高盐极端环境可培养放线菌的的种群及其生物活性初步研究%Preliminary studies on population and bioactivity of educable actinomycetes from hyperhaline extreme environment in xinjiang

    Institute of Scientific and Technical Information of China (English)

    阿尔新; 旭格拉; 张金辉

    2013-01-01

    Objective To study the population and bioactivity of actinomycetes from soil in hyperhaline region of Xingjang ,China and accumulate microbial resources .Methods Using two isolation methods ,four different kinds of cultural media ,123 isolates were purified from twenty e soil samples in salt field of Fuhai county of Altay and Lopnor area .100 among 123 strains were cultured and both of their cultural broths and its organic extracts were assayed by antibacterial andnematicide model .Based on the morphological characteristics and biological activity ,61 strains were selected to carry out the 16S rRNA sequences test .Results 100 isolates were purified ,43strains exhibi-ted positive Results in one or two screening model ,the total positive rate was 43% .the 16S rRNA sequences test showed that the 61 strains belongs to 7 different genera ,including Streptomyces ,Nocardiopsis ,Pseudonocardia ,Prauserella ,Saccharopolyspora Halophilic , Actinomyces and Thermomonospora .The sequence similarity of strain L-068 may be a potential new species .Conclusion The studies dem-onstrated there are untapped actinomycetal resources e in hyperhaline region of Xingjang ,China and its bioactive secondary metabolites de-served further exploration for microbial drugs .%目的:积累微生物资源,研究从土壤中选择性分离放线菌的种群及其次生代谢产物的生物活性评价。方法采用两种分离方法,4种高盐培养基对来自新疆高盐环境-阿勒泰福海县盐场和罗布泊地区等采集的土壤样品中的放线菌进行了选择性分离纯化;以3种致病真菌灰葡萄孢菌(Botrytis cinerea)、番茄早疫病菌(Alternaria solani)、稻瘟病菌(Magnaporth grisea)和4种致病细菌大肠埃希氏(Escherichia coli)、金黄色葡萄球菌(Staphy lococcus aureus)、枯草芽孢杆菌(Bacillus subtilis),草分枝杆菌(Mycobacterium phlei)为指示菌,对其中分离的100株放线菌发酵液及其乙酸乙酯

  18. Coexistence of Leishmania tropica and Leishmania infantum in Sefrou province, Morocco.

    Science.gov (United States)

    Asmae, Hmamouch; Fatima, Amarir; Hajiba, Fellah; Mbarek, Karzaz; Khadija, Bekhti; Mohamed, Rhajaoui; Faiza, Sebti

    2014-02-01

    Cutaneous leishmaniasis (CL) has been recently emerged in new foci, posing a public health problem. Increasing cases of CL have been reported during recent years in Sefrou province, a previously non-endemic area. The present study was designed for epidemiological and parasitological characterization of the disease for the first time in this area. The results of a retrospective analysis of CL cases reports, between 2000 and 2011 showed that the incidence was estimated to 463/100,000 inhabitants/year, with a total of 1242 cases were notified from 1997 to 2011. Most patients were infected in the sector El Menzel (22.81%) and Sefrou (20.51%). Other cases have been reported in the 15 other sectors, reflecting the geographical spread of the disease. The highest rate lesions were found in the age group of 9 years or less with significant differences (p-valuetropica and L. infantum by species-specific ITS1-PCR-RFLP assay. CL remains an emergent disease in Sefrou with an incidence and a continuously geographical spread. Recent environmental changes, auspicious to vectors had probably contributed to that situation.

  19. Experimental Acquisition, Development, and Transmission of Leishmania tropica by Phlebotomus duboscqi

    Science.gov (United States)

    2013-01-01

    major across the Sahel region of Africa (Dedet et al., 1982; Beach et al., 1984; Killick-Kendrick, 1990). The role of P. duboscqi in trans- mitting L...ml of sterile phosphate-buffered saline (PBS). 2.4. Sand fly infection by membrane feeding device The homogenate of tissue amastigotes in PBS was

  20. The gastric caeca of pentatomids as a house for actinomycetes

    Directory of Open Access Journals (Sweden)

    Zucchi Tiago D

    2012-06-01

    Full Text Available Abstract Background Microbes are extensively associated with insects, playing key roles in insect defense, nutrition and reproduction. Most of the associations reported involve Proteobacteria. Despite the fact that Actinobacteria associated with insects were shown to produce antibiotic barriers against pathogens to the hosts or to their food and nutrients, there are few studies focusing on their association with insects. Thus, we surveyed the Actinobacteria diversity on a specific region of the midgut of seven species of stinkbugs (Hemiptera: Pentatomidae known to carry a diversity of symbiotically-associated Proteobacteria. Results A total of 34 phylotypes were placed in 11 different Actinobacteria families. Dichelops melacanthus held the highest diversity with six actinobacteria families represented by nine phylotypes. Thyanta perditor (n = 7, Edessa meditabunda (n = 5, Loxa deducta (n = 4 and Pellaea stictica (n = 3 were all associated with three families. Piezodorus guildini (n = 3 and Nezara viridula (n = 3 had the lowest diversity, being associated with two (Propionibacteriaceae and Mycobacteriaceae and one (Streptomyceataceae families, respectively. Corynebacteriaceae and Mycobacteriaceae were the most common families with phylotypes from three different insect species each one. Conclusions Many phylotypes shared a low 16S rRNA gene similarity with their closest type strains and formed new phyletic lines on the periphery of several genera. This is a strong indicative that stinkbug caeca can harbor new species of actinobacteria, which might be derived from specific associations with the species of stinkbugs studied. Although the well-known role of actinobacteria as a source of biomolecules, the ecological features of these symbionts on the stinkbugs biology remain unknown.

  1. Hyoscyamine-producing marine Actinomycetes from Lagos Lagoon sediment

    Institute of Scientific and Technical Information of China (English)

    Davies; Olabisi; Flora; Adeleye; Isaac; Adeyemi; Wang; Peng; George

    2015-01-01

    Objective:To isolate and screen Actinoniycetes from Lagos Lagoon soil sediments for production of bioactive metabolites.Methods:Sediment samples were collected from four different locations of Lagos Lagoon and were dried for 2 weeks after which the Actinoniycetes were isolated by serial dilution using the spread plate method on starch casein and Kuster’s agar supplemented with 80 ug/mL cycloheximide to prevent fungal growth.The plates were incubated at 28 C for 1-2 weeks.Isolates were selected based on their colonial characteristics as well as their Gram’s reaction and subciiltured using the same media for isolation until pure cultures were obtained and incubated at 28 C for 3 d.Thereafter,they were inoculated into starch casein and Kuster’s broth media and incubated for 8 d.The secondary metabolites were screened for antimicrobial activity against the following microorganisms:methicillin resistant Staphylococcus aureus.Staphylococcus aureus ATCC 29213.Escherichia coli ATCC 29522.Pseudomonas aeruginosa ATCC 27853.Candida albicans and Enterocolitis faecal is ATCC 29212.Coagulasenegative staphylococci isolated from HIV patients were also used(Staphylococcus warneri.Staphylococcus xylosus and Staphylococcus epidennidis).The antimicrobial metabolites of the Actinoniycetes isolates were identified using gas chromatography(GC).Results:Crude extracts of isolates showed antimicrobial activity against some of the test organisms.The GC data analysis showed the antibiotic profile of these isolates.Conclusions:Analysis of the crude extracts of the isolates using GC method,revealed the presence of antibiotics including an anticholinergic hyoscyamine among other conclusions.

  2. Influence of Xenobiotic Substances on Actinomycete Comunities in Soil

    OpenAIRE

    2012-01-01

    Sulfonylurea herbicides are frequently used in agricultural crops even if they determine quantitative and qualitativechanges in soil microbial communities. In this study it was used increasing doses of two sulfonylurea herbicides,tribenuron-methyl and nicosulfuron, in order to establish their effect on actinomyces communities from soil underlaboratory conditions. Using nutritive gelose with soil extract and Gause medium the main species of actinomyceswere identified: Streptomyces albus, Strep...

  3. Gas vesicles in actinomycetes : old buoys in novel habitats?

    NARCIS (Netherlands)

    Keulen, Geertje van; Hopwood, David A.; Dijkhuizen, Lubbert; Sawers, R. Gary

    2005-01-01

    Gas vesicles are gas-filled prokaryotic organelles that function as flotation devices. This enables planktonic cyanobacteria and halophilic archaea to position themselves within the water column to make optimal use of light and nutrients. Few terrestrial microbes are known to contain gas vesicles. G

  4. Caerulomycin A- An antifungal compound isolated from marine actinomycetes.

    Digital Repository Service at National Institute of Oceanography (India)

    Ambavane, V.; Tokdar, P.; Parab, R.; Sreekumar, E.S.; Mahajan, G.B.; Mishra, P.D.; DeSouza, L.; Ranadive, P.

    krusei GO3FlucR 0.78 - 1.56 0.313 - 0.625 64 NT: Not Tested. 4. Discussion The global antifungal market was estimated at $9.4 billion in 2010 and is expected to grow at a rate of 1.9% during 2010-2017. The major class of antifungal compound includes... Genetics Analysis Using Maximum Likelihood, Evolutionary Distance and Maximum Parsimony Methods. Molecular Biology and Evolution, 28, 2731-2739. http://dx.doi.org/10.1093/molbev/msr121 [24] Antifungals Market to 2017—Generic Erosion of Major Polyenes...

  5. [Enzyme activity of an actinomycete producer of carotenes and macrotetrolides].

    Science.gov (United States)

    Nefelova, M V; Sverdlova, A N

    1982-01-01

    The activity of pyruvate dehydrogenase and dehydrogenases of the tricarboxylic acid cycle was assayed in the mycelium of Streptomyces chrysomallus var. Carotenoides growing under different conditions of the medium. The activity of the enzymes increased when acetic, citric and succinic acids were added at different periods of the growth. Moreover, addition of the acids increased the time of intensive functioning of the dehydrogenases whose activity abruptly decreased after 60 h of the growth under the control conditions.

  6. The rare fluorinated natural products and biotechnological prospects for fluorine enzymology.

    Science.gov (United States)

    Chan, K K Jason; O'Hagan, David

    2012-01-01

    Nature has hardly evolved a biochemistry of fluorine although there is a low-level occurrence of fluoroacetate found in selected tropical and subtropical plants. This compound, which is generally produced in low concentrations, has been identified in the plants due to its high toxicity, although to date the biosynthesis of fluoroacetate in plants remains unknown. After that, fluorinated entities in nature are extremely rare, and despite increasingly sophisticated screening and analytical methods applied to natural product extraction, it has been 25 years since the last bona fide fluorinated natural product was identified from an organism. This was the reported isolation of the antibiotic 4-fluorothreonine and the toxin fluoroacetate in 1986 from Streptomyces cattleya. This bacterium has proven amenable to biochemical investigation, the fluorination enzyme (fluorinase) has been isolated and characterized, and the biosynthetic pathway to these bacterial metabolites has been elucidated. Also the fluorinase gene has been cloned into a host bacterium (Salinispora tropica), and this has enabled the de novo production of a bioactive fluorinated metabolite from fluoride ion, by genetic engineering. Biotechnological manipulation of the fluorinase offers the prospects for the assembly of novel fluorinated metabolites by fermentation technology. This is particularly attractive, given the backdrop that about 15-20% of pharmaceuticals licensed each year (new chemical entities) contain a fluorine atom.

  7. Discovery and characterization of a marine bacterial SAM-dependent chlorinase.

    Science.gov (United States)

    Eustáquio, Alessandra S; Pojer, Florence; Noel, Joseph P; Moore, Bradley S

    2008-01-01

    Halogen atom incorporation into a scaffold of bioactive compounds often amplifies biological activity, as is the case for the anticancer agent salinosporamide A (1), a chlorinated natural product from the marine bacterium Salinispora tropica. Significant effort in understanding enzymatic chlorination shows that oxidative routes predominate to form reactive electrophilic or radical chlorine species. Here we report the genetic, biochemical and structural characterization of the chlorinase SalL, which halogenates S-adenosyl-L-methionine (2) with chloride to generate 5'-chloro-5'-deoxyadenosine (3) and L-methionine (4) in a rarely observed nucleophilic substitution strategy analogous to that of Streptomyces cattleya fluorinase. Further metabolic tailoring produces a halogenated polyketide synthase substrate specific for salinosporamide A biosynthesis. SalL also accepts bromide and iodide as substrates, but not fluoride. High-resolution crystal structures of SalL and active site mutants complexed with substrates and products support the S(N)2 nucleophilic substitution mechanism and further illuminate halide specificity in this newly discovered halogenase family.

  8. 海洋放线菌Y12-26代谢产物中bafilomycins分离纯化及结构鉴定%Isolation, purification and structure identification of secondary metabolites produced by marine actinomycete Y12-26

    Institute of Scientific and Technical Information of China (English)

    魏刚; 苏超; 张道敬; 宗志友; 斯聪聪; 陶黎明

    2011-01-01

    Objective To know the active components in the secondary metabolites produced by marine actinomycete Y 12-26 exhibited antagonistic activity against Pyricularia oryzae.Methods By bioassay-guided isolation and purification, the active antifungal compounds were isolated and purified from the culture extract of strain Y12-26 with solvent extract, silica gel chromatography, thin layer chromatography, and high performance liquid chromatography and other ways, and their structure were elucidation with the help of spectra data analysis of UV, ESIMS, NMR and others.Results Three antifungal macrolide compounds Y12-26-A2a, A3a and A3b were isolated from the culture extract of strain Y12-26.the molecular formula of the compound Y12-26-A2a was confirmed as C35H56O8,as the same as the known compound bafilomycin D.The molecular formula of the compound Y12-26-A3a was confirmed as C35H58O9, the structure is the same as bafilomycin Al.The molecular formula of the compound Y 12-26-A3b was confirmed as C35H58O8, which was identificated as a new compound named bafilomycin K.Conclusion The MIC of the three compoundsY 12-26-A2a, A3a and A3b against P oryzae were 125, 16 and 31 μg/mL.%目的 了解海洋放线菌Y12-26的次级代谢产物中对稻瘟病菌(Pyricularia oryzae)等植物病原真菌具有较好的拮抗活性的具体化合物.方法 以P.oryzae指示菌进行活性跟踪,对其代谢物进行分离提取,通过有机溶剂萃取、硅胶柱层析、TLC和HPLC制备等方法分离得到活性化合物,并通过UV、MS、NMR等方法进行结构鉴定.结果 从海洋放线菌Y12-26发酵物中分离得到了3个大环内酯类活性化合物Y12-26-A2a、A3a和A3b,确定Y12-26-A2a分子式为CHO,与bafilomycin D结构相同;Y12-26-A3a分子式为CHO,与bafilomycin A1结构相同;Y12-26-A3b为新结构化合物,分子式为CHO,命名为bafilomycin K.结论 化合物Y12-26-A2a、A3a和A3b对P.oryzae的MIC分别为125、16和31μg/mL.

  9. 一株拮抗放线菌的鉴定及其对黄瓜枯萎病的生防效应研究%IDENTIFICATION AND BIOCONTROL EFFECT OF A STRAIN OF ACTINOMYCETE ANTAGONISTIC TO WILT DISEASE OF CUCUMBER

    Institute of Scientific and Technical Information of China (English)

    梁银; 张谷月; 王辰; 王世梅; 沈其荣

    2013-01-01

    Morphological,cultural and physio-biochemical traits and 16S rRNA sequence was analyzed of a strain of actinomycete,separated from the soil of the Zijin Mountain in Nanjing,China and coded as CT205,for identification and orientation in the classification system.The PDA agar plate method was used to determine antifungal activity of Strain CT205 and a pot experiment using pathogenic soil from a field that had been cultivated with cucumber consecutively for year was conducted to investigate the effect of Stain CT205 controlling cucumber Fusarium wilt.Based on the 16S rRNA sequence analysis,Strain CT205 was tentatively identified as Streptomyces albospinus (99% identity).And the pot experiment showed that the strain inhibited quite effectively Fusarium oxysporum f.sp.cucumerinum,Fusarium oxysporum f.sp.niveum,and Phytophthora nicotianae,and to a varying extent,Bacillus subtillus,Saccharomyces cerevisiae,Rhizoctonia cerealis,Ralstonia solanacearum.Besides its cucumber Fusarium wilt controlling efficiency being 51.85%,the strain promoted somewhat the growth of cucumber.When the strain was prepared with organic manure into complex biomanure,the disease controlling efficiency may reach as high as 81.85%.The findings demonstrate that the strain has certain potential application value.%鉴定从土壤中分离的一株拮抗放线菌(编号CT205),探索其防治植物病害的潜能.通过形态特征、生理生化特征和16S rRNA基因序列分析研究菌株CT205的分类地位,采用平板对峙法测定其抗菌活性,利用连作致病土盆栽试验评价其对黄瓜枯萎病的防治作用.初步鉴定菌株CT205为白刺链霉菌(Streptomyces albospinus),菌株CT205对供试的枯草杆菌、啤酒酵母、小麦纹枯、土豆青枯等植物病原菌均有不同程度的抑制作用,其中对黄瓜枯萎病、西瓜枯萎病、烟草疫霉3种供试病原真菌的抑制作用较强.盆栽试验表明,施用放线菌CT205对黄瓜生长有一定的促生作

  10. Drug Targeting to Macrophages With Solid Lipid Nanoparticles Harboring Paromomycin: an In Vitro Evaluation Against L. major and L. tropica.

    Science.gov (United States)

    Kharaji, Maryam Heidari; Doroud, Delaram; Taheri, Tahereh; Rafati, Sima

    2016-10-01

    Leishmaniasis is a worldwide disease that leads to high mortality and morbidity in human populations. Today, leishmaniasis is managed via drug therapy. The drugs that are already in clinical use are limited to a number of toxic chemical compounds and their parasite drug resistance is increasing. It is therefore essential, in order to circumvent the current difficulties, to design a new anti-leishmanial drug treatment strategy. Besides producing new, active anti-leishmanial entities, another promising strategy could be developing novel delivery systems and formulations of the existing pharmaceutical ingredients to improve drug efficacy. In the present study, paromomycin sulfate (PM), as one of the promising anti-leishmanial drugs, was formulated in solid lipid nanoparticles (SLN), and its in vitro efficacy was investigated against different strains of Leishmania using a MTT test, Parasite-Rescue-Transformation-Assay, SYTO Green staining, and fluorescent microscope imaging. The results show that PM-loaded SLN is significantly more effective than PM in inhibiting parasite propagation (P SLN formulations is size dependent. According to our results, delivery of the drugs to the macrophages via nanoparticle utilization seems to be an accessible and practical approach.

  11. NCBI nr-aa BLAST: CBRC-CREM-01-1327 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-CREM-01-1327 ref|ZP_01648217.1| putative ABC transporter permease protein [Salinispora arenicola... CNS205] gb|ABV98616.1| conserved hypothetical protein [Salinispora arenicola CNS-205] ZP_01648217.1 1e-38 37% ...

  12. NCBI nr-aa BLAST: CBRC-TGUT-10-0002 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-TGUT-10-0002 ref|ZP_01649534.1| hypothetical protein SareDRAFT_0855 [Salinispora arenicola... CNS205] gb|ABV96792.1| conserved hypothetical protein [Salinispora arenicola CNS-205] ZP_01649534.1 0.005 27% ...

  13. NCBI nr-aa BLAST: CBRC-GGAL-14-0008 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-GGAL-14-0008 ref|ZP_01650692.1| protein of unknown function DUF81 [Salinispora arenicola... CNS205] gb|ABV98083.1| protein of unknown function DUF81 [Salinispora arenicola CNS-205] ZP_01650692.1 0.001 27% ...

  14. NCBI nr-aa BLAST: CBRC-MMUS-04-0045 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-MMUS-04-0045 ref|ZP_01649449.1| hypothetical protein SareDRAFT_1509 [Salinispora arenicola... CNS205] gb|ABV97463.1| hypothetical protein Sare_1567 [Salinispora arenicola CNS-205] ZP_01649449.1 1.2 38% ...

  15. NCBI nr-aa BLAST: CBRC-HSAP-07-0048 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available protein [Salinispora arenicola CNS205] gb|ABV98555.1| conserved hypothetical protein [Salinispora arenicola CNS-205] ZP_01648159.1 0.015 28% ... ...CBRC-HSAP-07-0048 ref|ZP_01648159.1| putative ABC-2 type transport system permease

  16. NCBI nr-aa BLAST: CBRC-ETEL-01-0539 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-ETEL-01-0539 ref|ZP_01649941.1| glycosyl transferase, family 51 [Salinispora arenicola... CNS205] gb|ABV99811.1| glycosyl transferase family 51 [Salinispora arenicola CNS-205] ZP_01649941.1 9.9 28% ...

  17. NCBI nr-aa BLAST: CBRC-DNOV-01-2845 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-DNOV-01-2845 ref|ZP_01649121.1| conserved hypothetical protein [Salinispora arenicola... CNS205] gb|ABV99981.1| conserved hypothetical protein [Salinispora arenicola CNS-205] ZP_01649121.1 3.1 37% ...

  18. NCBI nr-aa BLAST: CBRC-AGAM-01-0097 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-AGAM-01-0097 ref|ZP_01647447.1| oxidoreductase-like [Salinispora arenicola CNS...205] gb|ABV97571.1| oxidoreductase domain protein [Salinispora arenicola CNS-205] ZP_01647447.1 0.71 29% ...

  19. NCBI nr-aa BLAST: CBRC-CREM-01-1327 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available protein [Salinispora arenicola CNS205] gb|ABV98555.1| conserved hypothetical protein [Salinispora arenicola CNS-205] ZP_01648159.1 9e-42 38% ... ...CBRC-CREM-01-1327 ref|ZP_01648159.1| putative ABC-2 type transport system permease

  20. NCBI nr-aa BLAST: CBRC-DNOV-01-1927 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-DNOV-01-1927 ref|ZP_01650371.1| glycosyl transferase, family 39 [Salinispora arenicola... CNS205] gb|ABV98138.1| glycosyl transferase family 39 [Salinispora arenicola CNS-205] ZP_01650371.1 1.6 35% ...

  1. NCBI nr-aa BLAST: CBRC-OPRI-01-0076 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-OPRI-01-0076 ref|YP_001535031.1| hypothetical protein Sare_0105 [Salinispora arenicola... CNS-205] gb|ABV96040.1| conserved hypothetical protein [Salinispora arenicola CNS-205] YP_001535031.1 0.089 30% ...

  2. NCBI nr-aa BLAST: CBRC-PHAM-01-0721 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-PHAM-01-0721 ref|YP_001537951.1| Beta-ketoacyl synthase [Salinispora arenicola... CNS-205] gb|ABV98960.1| Beta-ketoacyl synthase [Salinispora arenicola CNS-205] YP_001537951.1 0.52 40% ...

  3. NCBI nr-aa BLAST: CBRC-HSAP-07-0051 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available protein [Salinispora arenicola CNS205] gb|ABV98555.1| conserved hypothetical protein [Salinispora arenicola CNS-205] ZP_01648159.1 0.003 27% ... ...CBRC-HSAP-07-0051 ref|ZP_01648159.1| putative ABC-2 type transport system permease

  4. NCBI nr-aa BLAST: CBRC-PABE-08-0010 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available protein [Salinispora arenicola CNS205] gb|ABV98555.1| conserved hypothetical protein [Salinispora arenicola CNS-205] ZP_01648159.1 4e-04 27% ... ...CBRC-PABE-08-0010 ref|ZP_01648159.1| putative ABC-2 type transport system permease

  5. NCBI nr-aa BLAST: CBRC-CREM-01-1275 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-CREM-01-1275 ref|ZP_01646394.1| heavy metal translocating P-type ATPase [Salinispora arenicola... CNS205] gb|ABV96465.1| heavy metal translocating P-type ATPase [Salinispora arenicola CNS-205] ZP_01646394.1 1e-123 72% ...

  6. NCBI nr-aa BLAST: CBRC-FCAT-01-0500 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-FCAT-01-0500 ref|ZP_01650268.1| major facilitator superfamily MFS_1 [Salinispora arenicola... CNS205] gb|ABV98438.1| major facilitator superfamily MFS_1 [Salinispora arenicola CNS-205] ZP_01650268.1 0.75 34% ...

  7. NCBI nr-aa BLAST: CBRC-CREM-01-1365 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-CREM-01-1365 ref|ZP_01647653.1| hypothetical protein SareDRAFT_3349 [Salinispora arenicola... CNS205] gb|ABV99270.1| conserved hypothetical protein [Salinispora arenicola CNS-205] ZP_01647653.1 7e-28 43% ...

  8. NCBI nr-aa BLAST: CBRC-OSAT-11-0006 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-OSAT-11-0006 ref|ZP_01647180.1| putative membrane protein [Salinispora arenicola... CNS205] gb|ABW00506.1| protein of unknown function DUF571 [Salinispora arenicola CNS-205] ZP_01647180.1 0.006 28% ...

  9. NCBI nr-aa BLAST: CBRC-CREM-01-1355 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-CREM-01-1355 ref|ZP_01647712.1| anthranilate phosphoribosyltransferase [Salinispora arenicola... CNS205] gb|ABV99332.1| anthranilate phosphoribosyltransferase [Salinispora arenicola CNS-205] ZP_01647712.1 2e-82 53% ...

  10. NCBI nr-aa BLAST: CBRC-CREM-01-1370 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-CREM-01-1370 ref|ZP_01646325.1| major facilitator superfamily MFS_1 [Salinispora arenicola... CNS205] gb|ABV96388.1| major facilitator superfamily MFS_1 [Salinispora arenicola CNS-205] ZP_01646325.1 3e-35 39% ...

  11. NCBI nr-aa BLAST: CBRC-GGOR-01-1354 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-GGOR-01-1354 ref|YP_001537546.1| hypothetical protein Sare_2718 [Salinispora arenicola... CNS-205] gb|ABV98555.1| conserved hypothetical protein [Salinispora arenicola CNS-205] YP_001537546.1 0.002 27% ...

  12. NCBI nr-aa BLAST: CBRC-CPOR-01-0137 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-CPOR-01-0137 ref|ZP_01650035.1| DNA internalization-related competence protein... ComEC/Rec2 [Salinispora arenicola CNS205] gb|ABV99640.1| DNA internalization-related competence protein ComEC/Rec2 [Salinispora arenicola CNS-205] ZP_01650035.1 0.19 28% ...

  13. NCBI nr-aa BLAST: CBRC-CPOR-01-0386 [SEVENS

    Lifescience Database Archive (English)

    Full Text Available CBRC-CPOR-01-0386 ref|ZP_01650035.1| DNA internalization-related competence protein... ComEC/Rec2 [Salinispora arenicola CNS205] gb|ABV99640.1| DNA internalization-related competence protein ComEC/Rec2 [Salinispora arenicola CNS-205] ZP_01650035.1 0.52 27% ...

  14. Genome Sequence of the Ethene- and Vinyl Chloride-Oxidizing Actinomycete Nocardioides sp Strain JS614

    Energy Technology Data Exchange (ETDEWEB)

    Coleman, Nicholas V [University of Sydney, Australia; Wilson, Neil L [University of Sydney, Australia; Barry, Kerrie [U.S. Department of Energy, Joint Genome Institute; Bruce, David [Los Alamos National Laboratory (LANL); Copeland, A [U.S. Department of Energy, Joint Genome Institute; Dalin, Eileen [U.S. Department of Energy, Joint Genome Institute; Detter, J. Chris [U.S. Department of Energy, Joint Genome Institute; Glavina Del Rio, Tijana [U.S. Department of Energy, Joint Genome Institute; Goodwin, Lynne A. [Los Alamos National Laboratory (LANL); Hammon, Nancy [U.S. Department of Energy, Joint Genome Institute; Han, Shunsheng [Los Alamos National Laboratory (LANL); Hauser, Loren John [ORNL; Israni, Sanjay [U.S. Department of Energy, Joint Genome Institute; Kim, Edwin [U.S. Department of Energy, Joint Genome Institute; Kyrpides, Nikos C [U.S. Department of Energy, Joint Genome Institute; Land, Miriam L [ORNL; Lapidus, Alla L. [U.S. Department of Energy, Joint Genome Institute; Larimer, Frank W [ORNL; Lucas, Susan [U.S. Department of Energy, Joint Genome Institute; Pitluck, Sam [U.S. Department of Energy, Joint Genome Institute; Richardson, Paul [U.S. Department of Energy, Joint Genome Institute; Schmutz, Jeremy [Stanford University; Tapia, Roxanne [Los Alamos National Laboratory (LANL); Thompson, Sue [Los Alamos National Laboratory (LANL); Tice, Hope [U.S. Department of Energy, Joint Genome Institute; Spain, Jim C [Georgia Institute of Technology; Gossett, James G [Cornell University; Mattes, Timothy E [University of Iowa

    2011-01-01

    Nocardioides sp. strain JS614 grows on ethene and vinyl chloride (VC) as sole carbon and energy sources and is of interest for bioremediation and biocatalysis. Sequencing of the complete genome of JS614 provides insight into the genetic basis of alkene oxidation, supports ongoing research into the physiology and biochemistry of growth on ethene and VC, and provides biomarkers to facilitate detection of VC/ethene oxidizers in the environment. This is the first genome sequence from the genus Nocardioides and the first genome of a VC/ethene-oxidizing bacterium.

  15. Partial Purification and Characterization of a Thermostable Actinomycete beta-Amylase.

    Science.gov (United States)

    Obi, S K; Odibo, F J

    1984-03-01

    A thermostable amylase, possibly a beta-amylase from Thermoactinomyces sp. no. 2 isolated from soil, is reported. The enzyme was purified 36-fold by acetone precipitation, ion-exchange chromatography, and Sephadex G-200 gel filtration, and the molecular weight was estimated at 31,600. The enzyme was characterized by demonstration of optimum activity at 60 degrees C and pH 7 and by retention of 70% activity at 70 degrees C (30 min). It was stimulated by Mn and Fe but strongly inhibited by Hg. Maltose was the only detectable product of hydrolysis of starches and was quantitatively highest in plantain starch hydrolysate.

  16. γ-Resorcylate Catabolic-Pathway Genes in the Soil Actinomycete Rhodococcus jostii RHA1

    Science.gov (United States)

    Kasai, Daisuke; Araki, Naoto; Motoi, Kota; Yoshikawa, Shota; Iino, Toju; Imai, Shunsuke; Masai, Eiji

    2015-01-01

    The Rhodococcus jostii RHA1 gene cluster required for γ-resorcylate (GRA) catabolism was characterized. The cluster includes tsdA, tsdB, tsdC, tsdD, tsdR, tsdT, and tsdX, which encode GRA decarboxylase, resorcinol 4-hydroxylase, hydroxyquinol 1,2-dioxygenase, maleylacetate reductase, an IclR-type regulator, a major facilitator superfamily transporter, and a putative hydrolase, respectively. The tsdA gene conferred GRA decarboxylase activity on Escherichia coli. Purified TsdB oxidized NADH in the presence of resorcinol, suggesting that tsdB encodes a unique NADH-specific single-component resorcinol 4-hydroxylase. Mutations in either tsdA or tsdB resulted in growth deficiency on GRA. The tsdC and tsdD genes conferred hydroxyquinol 1,2-dioxygenase and maleylacetate reductase activities, respectively, on E. coli. Inactivation of tsdT significantly retarded the growth of RHA1 on GRA. The growth retardation was partially suppressed under acidic conditions, suggesting the involvement of tsdT in GRA uptake. Reverse transcription-PCR analysis revealed that the tsd genes constitute three transcriptional units, the tsdBADC and tsdTX operons and tsdR. Transcription of the tsdBADC and tsdTX operons was induced during growth on GRA. Inactivation of tsdR derepressed transcription of the tsdBADC and tsdTX operons in the absence of GRA, suggesting that tsd gene transcription is negatively regulated by the tsdR-encoded regulator. Binding of TsdR to the tsdR-tsdB and tsdT-tsdR intergenic regions was inhibited by the addition of GRA, indicating that GRA interacts with TsdR as an effector molecule. PMID:26319878

  17. Phenotypic mutants of the intracellular actinomycete Rhodococcus equi created by in vivo Himar1 transposon mutagenesis.

    Science.gov (United States)

    Ashour, Joseph; Hondalus, Mary K

    2003-04-01

    Rhodococcus equi is a facultative intracellular opportunistic pathogen of immunocompromised people and a major cause of pneumonia in young horses. An effective live attenuated vaccine would be extremely useful in the prevention of R. equi disease in horses. Toward that end, we have developed an efficient transposon mutagenesis system that makes use of a Himar1 minitransposon delivered by a conditionally replicating plasmid for construction of R. equi mutants. We show that Himar1 transposition in R. equi is random and needs no apparent consensus sequence beyond the required TA dinucleotide. The diversity of the transposon library was demonstrated by the ease with which we were able to screen for auxotrophs and mutants with pigmentation and capsular phenotypes. One of the pigmentation mutants contained an insertion in a gene encoding phytoene desaturase, an enzyme of carotenoid biosynthesis, the pathway necessary for production of the characteristic salmon color of R. equi. We identified an auxotrophic mutant with a transposon insertion in the gene encoding a putative dual-functioning GTP cyclohydrolase II-3,4-dihydroxy-2-butanone-4-phosphate synthase, an enzyme essential for riboflavin biosynthesis. This mutant cannot grow in minimal medium in the absence of riboflavin supplementation. Experimental murine infection studies showed that, in contrast to wild-type R. equi, the riboflavin-requiring mutant is attenuated because it is unable to replicate in vivo. The mutagenesis methodology we have developed will allow the characterization of R. equi virulence mechanisms and the creation of other attenuated strains with vaccine potential.

  18. Four new antibacterial xanthones from the marine-derived actinomycetes Streptomyces caelestis

    KAUST Repository

    Liu, Ling-Li

    2012-11-20

    Four new polycyclic antibiotics, citreamicin ? A (1), citreamicin ? B (2), citreaglycon A (3), and dehydrocitreaglycon A (4), were isolated from marine-derived Streptomyces caelestis. The structures of these compounds were elucidated by 1D and 2D NMR spectra. All four compounds displayed antibacterial activity against Staphylococcus haemolyticus, Staphylococcus aureus, and Bacillus subtillis. Citreamicin ? A (1), citreamicin ? B (2) and citreaglycon A (3) also exhibited low MIC values of 0.25, 0.25, and 8.0 ?g/mL, respectively, against methicillin-resistant Staphylococcus aureus (MRSA) ATCC 43300. 2012 by the authors; licensee MDPI.

  19. Effect of proteases on biofilm formation of the plastic-degrading actinomycete Rhodococcus ruber C208.

    Science.gov (United States)

    Gilan, Irit; Sivan, Alex

    2013-05-01

    In most habitats, the vast majority of microbial populations form biofilms on solid surfaces, whether natural or artificial. These biofilms provide either increased physical support and/or a source of nutrients. Further modifications and development of biofilms are regulated by signal molecules secreted by the cells. Because synthetic polymers are not soluble in aqueous solutions, biofilm-producing bacteria may biodegrade such materials more efficiently than planktonic strains. Bacterial biofilms comprise bacterial cells embedded in self-secreted extracellular polymeric substances (EPS). Revealing the roles of each component of the EPS will enable further insight into biofilm development and the EPS structure-function relationship. A strain of Rhodococcus ruber (C208) displayed high hydrophobicity and formed a dense biofilm on the surface of polyethylene films while utilizing the polyolefin as carbon and energy sources. This study investigated the effects of several proteases on C208 biofilm formation and stability. The proteolysis of C208 biofilm gave conflicting results. Trypsin significantly reduced biofilm formation, and the resultant biofilm appeared monolayered. In contrast, proteinase K enhanced biofilm formation, which was robust and multilayered. Presumably, proteinase K degraded self-secreted proteases or quorum-sensing peptides, which may be involved in biofilm detachment processes, leading to a multilayered, nondispersed biofilm.

  20. Degradation and induction specificity in actinomycetes that degrade p-nitrophenol.

    OpenAIRE

    1993-01-01

    We have isolated two soil bacteria (identified as Arthrobacter aurescens TW17 and Nocardia sp. strain TW2) capable of degrading p-nitrophenol (PNP) and numerous other phenolic compounds. A. aurescens TW17 contains a large plasmid which correlated with the PNP degradation phenotype. Degradation of PNP by A. aurescens TW17 was induced by preexposure to PNP, 4-nitrocatechol, 3-methyl-4-nitrophenol, or m-nitrophenol, whereas PNP degradation by Nocardia sp. strain TW2 was induced by PNP, 4-nitroca...

  1. Degradation and induction specificity in actinomycetes that degrade p-nitrophenol

    Energy Technology Data Exchange (ETDEWEB)

    Hanne, L.F.; Kirk, L.L.; Appel, S.M.; Narayan, A.D.; Bains, K.K. (California State Univ., Chico, CA (United States))

    1993-10-01

    We have isolated two soil bacteria (identified as Arthrobacter aurescens TW17 and Nocardia sp. strain TW2) capable of degrading p-nitrophenol (PNP) and numerous other phenolic compounds. A. aurescens TW17 contains a large plasmid which correlated with the PNP degradation phenotype. Degradation of PNP by A. aurescens TW 17 was induced by preexposure to PNP, 4-nitrocatechol, 3-methyl-4-nitrophenol, or m-nitrophenol, whereas PNP degradation by Nocardia sp. strain TW2 was induced by PNP, 4-nitrocatechol, phenol, p-cresol, or m-nitrophenol. A. aurescens TW17 initially degraded PNP to hydroquinone and nitrite. Nocardia sp. strain TW2 initially converted PNP to hydroquinone or 4-nitrocatechol, depending upon the inducing compound.

  2. Identification of the Entner-Doudoroff pathway in an antibiotic-producing actinomycete species

    DEFF Research Database (Denmark)

    Gunnarsson, Nina; Mortensen, Uffe Hasbro; Sosio, M.;

    2004-01-01

    The metabolic network of the central carbon metabolism represents the backbone of cellular metabolism and provides the precursors and cofactors required for synthesis of secondary metabolites. It is therefore pivotal to map the operating metabolic network in the central carbon metabolism in order...

  3. Cure from the cave: volcanic cave actinomycetes and their potential in drug discovery

    Directory of Open Access Journals (Sweden)

    Cheeptham N.

    2013-01-01

    Full Text Available Volcanic caves have been little studied for their potential as sources of novel microbial species and bioactive compounds with new scaffolds. We present the f irst study of volcanic cave microbiology from Canada and suggest that this habitat has great potential for the isolation of novel bioactive substances. Sample locat ions were plot ted on a contour map that was compiled in ArcView 3.2. Over 400 bacterial isolates were obtained from the Helmcken Falls cave in Wells Gray Provincial Park, British Columbia. From our preliminary screen, of 400 isolates tested, 1% showed activity against extended spectrum ß-lactamase E. coli, 1.75% against Escherichia coli, 2.25% against Acinetobacter baumannii, and 26.50% against Klebsiella pneumoniae. In addition, 10.25% showed activity against Micrococcus luteus, 2% against methicillin resistant Staphylococcus aureus, 9.25% against Mycobacterium smegmatis, 6.25% Pseudomonas aeruginosa and 7.5% against Candida albicans. Chemical and physical characteristics of three rock wall samples were studied using scanning electron microscopy and f lame atomic absorption spectrometry. Calcium (Ca, iron (Fe, and aluminum (Al were the most abundant components while magnesium (Mg, sodium (Na, arsenic (As, lead (Pb, chromium (Cr, and barium (Ba were second most abundant with cadmium (Cd and potassium (K were the least abundant in our samples. Scanning electron microscopy (SEM showed the presence of microscopic life forms in all three rock wall samples. 16S rRNA gene sequencing of 82 isolates revealed that 65 (79.3% of the strains belong to the Streptomyces genus and 5 (6.1% were members of Bacillus, Pseudomonas, Nocardia and Erwinia genera. Interestingly, twelve (14.6% of the 16S rRNA sequences showed similarity to unidentif ied ribosomal RNA sequences in the library databases, the sequences of these isolates need to be further investigated using the EzTaxon-e database (http://eztaxon-e. ezbiocloud.net/ to determine whether or not these are novel species. Nevertheless, this suggests the possibility that they could be unstudied or rare bacteria. The Helmcken Falls cave microbiome possesses a great diversity of microbes with the potential for studies of novel microbial interactions and the isolation of new types of antimicrobial agents.

  4. Structural biological study of self-resistance determinants in antibiotic-producing actinomycetes.

    Science.gov (United States)

    Sugiyama, Masanori

    2015-09-01

    As antibiotics act to inhibit the growth of bacteria, the drugs are useful for treating bacterial infectious diseases. However, microorganisms that produce antibiotics must be protected from the lethal effect of their own antibiotic product. In this review, the fruit of our group's current research on self-protection mechanisms of Streptomyces producing antibiotics that inhibit DNA, protein and bacterial cell wall syntheses will be described.

  5. Selection of a Thermophilic Alkalitolerant Actinomycete and Conditions for CMCase Production

    Institute of Scientific and Technical Information of China (English)

    QI Yun; ZHAO Lin; LIAO Yinzhang; TAN Xin

    2005-01-01

    Five thermophilic strains that can degrade cellulose were isolated from the compost of a waste management in Guangzhou, China. Since one of them degraded cellulose effectively, it was chosen as the study strain. Based on its morphology, spores′ susceptibility to heat, cell wall composition and other characteristics, the organism was classified as Thermomonospora fusca. Conditions for production of carboxy methyl cellulase (CMCase) were examined. The optimal temperature and pH value for enzyme production were 50 ℃ and 10.5, respectively. Cellulosic materials and easily metabolisable carbohydrates served as carbon sources for the growth of the strain. Only cotton, avicel,carboxy methyl cellulose (CMC) acted as potent inducers for the production of cellulases by this strain. Despite excellent growth on easily metabolisable carbohydrates, only constitutive levels of cellulases were produced. The optimal carbon and nitrogen sources for CMCase production were cotton and soybean respectively. The high thermostability, wide pH stability, and cheap nitrogen source show well potential use for composting treatment and commercial detergents.

  6. Geodermatophilus poikilotrophi sp. nov.: A Multitolerant Actinomycete Isolated from Dolomitic Marble

    Directory of Open Access Journals (Sweden)

    Maria del Carmen Montero-Calasanz

    2014-01-01

    Full Text Available A novel Gram-reaction-positive, aerobic actinobacterium, tolerant to mitomycin C, heavy metals, metalloids, hydrogen peroxide, desiccation, and ionizing- and UV-radiation, designated G18T, was isolated from dolomitic marble collected from outcrops in Samara (Namibia. The growth range was 15–35°C, at pH 5.5–9.5 and in presence of 1% NaCl, forming greenish-black coloured colonies on GYM Streptomyces agar. Chemotaxonomic and molecular characteristics of the isolate matched those described for other representatives of the genus Geodermatophilus. The peptidoglycan contained meso-diaminopimelic acid as diagnostic diaminoacid. The main phospholipids were phosphatidylethanolamine, phosphatidylcholine, phosphatidylinositol, and small amount of diphosphatidylglycerol. MK-9(H4 was the dominant menaquinone and galactose was detected as diagnostic sugar. The major cellular fatty acids were branched-chain saturated acids iso-C16:0 and iso-C15:0 and the unsaturated C17:1ω8c and C16:1ω7c. The 16S rRNA gene showed 97.4–99.1% sequence identity with the other representatives of genus Geodermatophilus. Based on phenotypic results and 16S rRNA gene sequence analysis, strain G18T is proposed to represent a novel species, Geodermatophilus poikilotrophi. Type strain is G18T (= DSM 44209T = CCUG 63018T. The INSDC accession number is HF970583. The novel R software package lethal was used to compute the lethal doses with confidence intervals resulting from tolerance experiments.

  7. Crystal structure of the caseinolytic protease gene regulator, a transcriptional activator in actinomycetes.

    Science.gov (United States)

    Russo, Santina; Schweitzer, Jens-Eric; Polen, Tino; Bott, Michael; Pohl, Ehmke

    2009-02-20

    Human pathogens of the genera Corynebacterium and Mycobacterium possess the transcriptional activator ClgR (clp gene regulator) which in Corynebacterium glutamicum has been shown to regulate the expression of the ClpCP protease genes. ClgR specifically binds to pseudo-palindromic operator regions upstream of clpC and clpP1P2. Here, we present the first crystal structure of a ClgR protein from C. glutamicum. The structure was determined from two different crystal forms to resolutions of 1.75 and 2.05 A, respectively. ClgR folds into a five-helix bundle with a helix-turn-helix motif typical for DNA-binding proteins. Upon dimerization the two DNA-recognition helices are arranged opposite to each other at the protein surface in a distance of approximately 30 A, which suggests that they bind into two adjacent major grooves of B-DNA in an anti-parallel manner. A binding pocket is situated at a strategic position in the dimer interface and could possess a regulatory role altering the positions of the DNA-binding helices.

  8. Optimization of the Fermentation Process of Actinomycete Strain Hhs.015T

    Directory of Open Access Journals (Sweden)

    Xinxuan Wang

    2010-01-01

    inoculation volume of 15.8%. The antimicrobial activity was increased by 20% by optimizing the environmental parameters. The results obtained allow an efficient production of components with antimicrobial activity by strain Hhs.015T on a large scale at low costs.

  9. Streptomyces manipurensis sp. nov., a novel actinomycete isolated from a limestone deposit site in Manipur, India.

    Science.gov (United States)

    Nimaichand, Salam; Zhu, Wen-Yong; Yang, Ling-Ling; Ming, Hong; Nie, Guo-Xing; Tang, Shu-Kun; Ningthoujam, Debananda S; Li, Wen-Jun

    2012-06-01

    A novel actinobacterium, designated MBRL 201(T), was isolated from a sample collected from a limestone quarry at Hundung, Manipur, India. The strain was characterized using polyphasic taxonomy. Comparison of the 16S rRNA gene sequence of strain MBRL 201(T) and other Streptomyces species showed sequence similarities ranging from 93.0 to 99.6 % and strain MBRL 201(T) showed closest similarities to Streptomyces virginiae NBRC 12827(T) (99.6 %) and Streptomyces cinnamonensis NBRC 15873(T) (99.6 %). The DNA relatedness between MBRL 201(T) and the type strains of S. virginiae NBRC 12827(T) and S. cinnamonensis NBRC 15873(T) were 44.5 and 35.6 % respectively. Strain MBRL 201(T) contained LL: -diaminopimelic acid (A(2)pm) as the diagnostic diamino acid, with glucose as the main sugar, while small amounts of galactose, glucose, mannose, rhamnose, ribose and xylose were also present in cell-wall hydrolysates. The major fatty acids identified were anteiso-C(15:0) (38.9 %), iso-C(15:0) (19.9 %) and anteiso-C(17:1) (14.7 %). The predominant menaquinones detected were MK-9(H(6)) and MK-9(H(8)), while the polar lipids were diphosphatidylglycerol, phosphatidylmethylethanolamine, phosphatidylglycerol, phosphatidylethanolamine, phosphatidylinositol and phosphatidylinositolmannosides, with other unknown phospholipids and lipids. The G+C content of the genomic DNA was 72.9 %. The phenotypic and genotypic data showed that strain MBRL 201(T) merits recognition as a representative of a novel species of the genus Streptomyces. It is proposed that the isolate should be classified in the genus Streptomyces as a novel species, Streptomyces manipurensis sp. nov. The type strain is MBRL 201(T) (=DSM 42029(T) = JCM 17351(T)).

  10. Identification and antifungal activity of an actinomycete strain against Alternaria spp.

    Directory of Open Access Journals (Sweden)

    Fen Gao

    2014-10-01

    Full Text Available Alternaria alternata (Fries Keissler is a phytopathogenic fungus responsible for tobacco brown spot disease. This study aims to evaluate the antifungal activity of strain 163 against A. alternata and clarify its taxonomic status. The evaluation of the antifungal activity of strain 163 and its bacteria-free filtrate of fermentation broth was done through measuring the diameters of inhibition zones, and testing the antimicrobial spectrum and the inhibition effect on mycelial growth in vitro. The biocontrol activity of the bacteria-free filtrate in vivo was evaluated by using detached tobacco leaves method and assaying the inhibition rate to disease incidence in growth chamber. A polyphasic approach was taken in the identification of strain 163. The bacterial strain 163 showed inhibitory effect in vitro against A. alternata. The bacteria-free filtrate of the strain 163 fermentation broth showed a 56.7% inhibition rate in a detached leaf assay. In growth chamber conditions, it showed greater biocontrol activity when applied before plants being inoculated with A. alternata than after, the inhibition rate being 46.05%. Investigations into the morphological, cultural, physiological and biochemical properties of strain 163 found it to be most similar to Streptomyces microflavus. Its classification into cell wall type I and sugar type C further confirmed its Streptomyces characteristics. Construction of a phylogenetic tree based on 16S rDNA verified that strain 163 was most closely related to Streptomyces microflavus. From polyphasic taxonomical analysis, strain 163 was found to be identical to S. microflavus.

  11. Isolation and molecular identification of actinomycetes from mycetoma patients in Sudan

    Directory of Open Access Journals (Sweden)

    Mogahid M Elhassan

    2013-01-01

    Full Text Available Introduction: In order to minimize chance of amputation due to actinomycetoma, it is important to correctly identify the causative agents. Microscopic examination of grains is not definite and further confirmatory diagnostic tests are needed. This study aims to investigate the prevalence of actinomycetoma and to explore the usefulness of strb1 gene in the diagnosis of the disease. Materials & Methods: The present study is a prospective cross-section laboratory-based study in which clinical samples (n = 100 from patients with mycetoma lesions were collected. The samples were cultured on Lowenstein Jensen and glucose yeast extract agar media. Grown colonies were initially identified using Gram′s stain, Ziehl Neelsen stain, and selected biochemical reactions. Confirmation was done by the analysis of polymerase chain reaction amplified strb1 gene. Results: Actinomycetoma was represented by a high ratio (12% among the study population. Nine out of the 12 isolates (75% were found to belong to the genus Streptomyces; whereas three isolates (25% were identified as Nocardia spp. on the basis of phenotypic and mycolic acid contents. Conclusion: It could be concluded that actinomycetoma exists with significant prevalence (12% among patients investigated in the present study. Streptomyces is the most important etiological agent of actinomycetoma compared to Nocardia.

  12. Arthrobacter cupressi sp. nov., an actinomycete isolated from the rhizosphere soil of Cupressus sempervirens.

    Science.gov (United States)

    Zhang, Jian; Ma, Yuchao; Yu, Huimin

    2012-11-01

    An actinobacterial strain, designated D48(T), was isolated from the rhizosphere soil of a cypress tree collected from Mianyang in Sichuan province, China. The strain was Gram-stain-positive, catalase-positive, oxidase-negative and non-motile, with lysine as the peptidoglycan diagnostic diamino acid and acetyl as the peptidoglycan acyl type. The predominant menaquinone was MK-9(H(2)); small amounts of MK-7(H(2)), MK-10(H(2)) and MK-6 were also present. The major fatty acids were anteiso-C(15:0), anteiso-C(17:0) and iso-C(16:0). The isolate underwent a rod-coccus morphological cycle, had a high DNA G+C content, was aerobic and grew between 12 and 37 °C (optimum, 28 °C). On the basis of the phenotypic and chemotaxonomic analyses, 16S rRNA gene sequence comparisons and DNA-DNA hybridization data, the isolate represents a novel species of the genus Arthrobacter, for which the name Arthrobacter cupressi sp. nov. is proposed. The type strain is D48(T) (=DSM 24664(T)=CGMCC 1.10783(T)).

  13. Disease Vector Ecology Profile: Yugoslav Republics. 2nd Edition

    Science.gov (United States)

    1993-10-27

    Leishmaniasis (CL), Oriental Sore. INFECTIOUS AGENTS: Protozoan, Leishmania infantum (previously reported as L. donovani infantum) for VL and L. tropica ...caecutiens lurida flavipes micans italicus montana melicharii muehlfeldi parallelogrammus pilosa rufipes tropica sepulcralis

  14. Survivability and Infectivity of Viscerotropic Leishmania Tropica from Operation Desert Storm Participants in Human Blood Products Maintained Under Blood Bank Conditions

    Science.gov (United States)

    1993-01-01

    AD-A272 136 PN PAGE OfN Mao_.•. few- ol :i. :1datn ’ o 1. A REPORT TYPE ANdO OATE COVERED 4-TITEuANOSUSTTTU Survivability and Infectivity of Viscero...the kinetics and frequency of peripheral appropriate are ones to prevent transfusion-re- blood parasitemia in humans (donors), the type lated...leucocytes. -Itn J (C1n Pathol 75: 435- hepaticas concomitantes estudiadas en biopsia 438. eon aguja de Vim-Silverman. .Aca .%fed Cos- 15. Nuwavri-Salti

  15. Development and Production of a Leishmania Skin Test

    Science.gov (United States)

    2009-03-01

    manufacturing process of Leishmania tropica Skin Test Antigen (LtSTA) was made during this contract period to increase the yield and robustness of the...interest group. 15. SUBJECT TERMS LtSTA = Leishmania tropica Skin Test Antigen 16. SECURITY CLASSIFICATION OF: 17. LIMITATION OF ABSTRACT... tropica Skin Test Antigen (LtSTA), is a sterile injectable microfluidized lysate of Leishmania tropica (WR#1063:C1A) promastigotes. The product is heat

  16. Field Evaluation of a Fluorogenic Probe-Based PCR Assay for Identification of a Visceral Leishmaniasis Gene Target

    Science.gov (United States)

    2004-06-01

    family loci and aligning homologous regions within Leishmania donovani complex species that excluded species from L. tropica , L. major, L. aethiopica...Genebank. Leishmania tropica , L. major, L. aethiopica, and L. mexicana complex species genomic sequences were aligned and visually evaluated to validate...Species LVL Leishmania donovani + Leishmania tropica - Leishmania major - Leishmania mexicana - Leishmania braziliensis - Leishmania guyanensis

  17. An analysis of the sponge Acanthostrongylophora igens’ microbiome yields an actinomycete that produces the natural product manzamine A

    Directory of Open Access Journals (Sweden)

    Amanda Leigh Waters

    2014-10-01

    Full Text Available Sponges have generated significant interest as a source of bioactive and elaborate secondary metabolites that hold promise for the development of novel therapeutics for the control of an array of human diseases. However, research and development of marine natural products can often be hampered by the difficulty associated with obtaining a stable and sustainable production source. Herein we report the first successful characterization and utilization of the microbiome of a marine invertebrate to identify a sustainable production source for an important natural product scaffold. Through molecular-microbial community analysis, optimization of fermentation conditions and MALDI-MS imaging, we provide the first report of a sponge-associated bacterium (Micromonospora sp. that produces the manzamine class of antimalarials from the Indo-Pacific sponge Acanthostrongylophora ingens (Thiele, 1899 (Class Demospongiae, Order Haplosclerida, Family Petrosiidae. These findings suggest that a general strategy of analysis of the macroorganism’s microbiome could significantly transform the field of natural products drug discovery by gaining access to not only novel drug leads, but the potential for sustainable production sources and biosynthetic genes at the same time.

  18. Optimizing water treatment practices for the removal of actinomycetes and earthy odor in water of Bovilla reservoir

    OpenAIRE

    ADELA KULLAJ; MARGARITA HYSKO

    2014-01-01

    Bovilla reservoir, which is situated 15 km North-East of Tirana the capital city of Albania is one of the major hidrotechnical works of this country. This reservoir is a warm monomictic water body and stratifies higher in the summer season. The predominant trophic state of Bovilla reservoir is oligotrophy. From autumn 2001 this reservoir repeatedly manifests an unpleasant taste and odor which is defined as musty- earthy. Taste and odor control has become an important issue for drinking water ...

  19. Stereoselective reduction of carbonyl compounds with Actinomycete: purification and characterization of three alpha-keto ester reductases from Streptomyces avermitilis.

    Science.gov (United States)

    Ishihara, Kohji; Kato, Chiaki; Yamaguchi, Hitomi; Iwai, Rieko; Yoshida, Momoko; Ikeda, Natsumi; Hamada, Hiroki; Masuoka, Noriyoshi; Nakajima, Nobuyoshi

    2008-12-01

    We achieved the purification of three alpha-keto ester reductases (Streptomyces avermitilis keto ester reductase, SAKERs-I, -II, and -III) from Streptomyces avermitilis NBRC14893 whole cells. The molecular masses of the native SAKERs-I, -II, and -III were estimated to be 72, 38, and 36 kDa, respectively, by gel filtration chromatography. The subunit molecular masses of SAKERs-I, -II, and -III were also estimated to be 32, 32, and 34 kDa, respectively, by SDS-polyacrylamide gel electrophoresis. The purified SAKERs-II and -III showed a reducing activity for alpha-keto esters (in particular, for ethyl pyruvate). SAKER-I showed a high reducing activity not only toward the alpha- and beta-keto esters, but also toward alpha-keto acid. The N-terminal region amino acid sequences of SAKERs-I, -II, and -III were identical to that of a putative oxidoreductase, SAV2750, a putative oxidoreductase, SAV1849, and a putative oxidoreductase, SAV4117, respectively, hypothetical proteins coded on the S. avermitilis genome.

  20. Draft Genome Sequence of Marine Actinomycete Streptomyces sp. Strain NTK 937, Producer of the Benzoxazole Antibiotic Caboxamycin.

    Science.gov (United States)

    Olano, Carlos; Cano-Prieto, Carolina; Losada, Armando A; Bull, Alan T; Goodfellow, Michael; Fiedler, Hans-Peter; Méndez, Carmen; Salas, José A

    2014-07-03

    Streptomyces sp. strain NTK 937 is the producer of the benzoxazole antibiotic caboxamycin, which has been shown to exert inhibitory activity against Gram-positive bacteria, cytotoxic activity against several human tumor cell lines, and inhibition of the enzyme phosphodiesterase. In this genome announcement, we present a draft genome sequence of Streptomyces sp. NTK 937 in which we identified at least 35 putative secondary metabolite biosynthetic gene clusters.

  1. Characterization and phylogenetic analysis of novel polyene type antimicrobial metabolite producing actinomycetes from marine sediments:Bay of Bengal India

    Institute of Scientific and Technical Information of China (English)

    Valan; Arasu; M; Asha; KRT; Duraipandiyan; V; Ignacimuthu; S; Agastian; P

    2012-01-01

    Objective:To isolate and indentify the promising antimicrobial metabolite producing Streptomyces strains from marine sediment samples from Andraprudesh coast of India.Methods:Antagonistic aetinomycetes were isolated by starch casein agar medium and modified nutrient agar medium with 1%glucose used as a base for primary screening.Significant antimicrobial metabolite producing strains were selected and identified by using biochemical and 16S rDNA level.Minimum inhibitory concentrations of the organic extracts were done by using broth micro dilution method.Results:Among the 210 actinomyeetes,64.3%exhibited activity against Gram positive bacteria,48.5%showed activity towards Cram negative bacteria,38.8%exhibited both Cram positive and negative bacteria and 80.85%isolates revealed significant antifungal activity.However,five isolates AP-5,AP-18,AP-41 and AP-70 showed significant antimicrobial activity.The analysis of cell wall hydrolysates showed the presence of LL-diaminopimelic acid and glycine in all the isolates.Sequencing analysis indicated that the isolates shared 98.5%-99.8%sequence identity to the 16S rDNA gene sequences of the Streptomyces taxons.The antimicrobial substances were extracted using hexane and ethyl acetate from spent medium in which strains were cultivated at 30X for five days.The antimicrobial activity was assessed using broth micro dilution technique.Each of the culture extracts from these five strains showed a typical polyenelike property.The lowest minimum inhibitory concentrations of ethyl acetate extracts against Escherichia coli and Cumularia lunula were 67.5 and 125.0μg/mL,respectively.Conclusions:It can be concluded that hexane and ethyl acetate soluble extracellular products of novel isolates are effective against pathogenic bacteria and fungi.

  2. Complete genome sequence of Streptomyces sp. strain CFMR 7, a natural rubber degrading actinomycete isolated from Penang, Malaysia.

    Science.gov (United States)

    Nanthini, Jayaram; Chia, Kim-Hou; Thottathil, Gincy P; Taylor, Todd D; Kondo, Shinji; Najimudin, Nazalan; Baybayan, Primo; Singh, Siddharth; Sudesh, Kumar

    2015-11-20

    Streptomyces sp. strain CFMR 7, which naturally degrades rubber, was isolated from a rubber plantation. Whole genome sequencing and assembly resulted in 2 contigs with total genome size of 8.248 Mb. Two latex clearing protein (lcp) genes which are responsible for rubber degrading activities were identified.

  3. PREPHENATE DEHYDRATASE OF THE ACTINOMYCETE AMYCOLATOPSIS-METHANOLICA - PURIFICATION AND CHARACTERIZATION OF WILD-TYPE AND DEREGULATED MUTANT PROTEINS

    NARCIS (Netherlands)

    EUVERINK, GJW; WOLTERS, DJ; DIJKHUIZEN, L

    1995-01-01

    Prephenate dehydratase (PDT) is a key regulatory enzyme in L-phenylalanine biosynthesis in the Gram-positive bacterium Amycolatopsis methanolica. The PDT protein was purified to homogeneity (1957-fold) from wild-type cells with a final yield of 6.5%. It was characterized as a 150 kDa homotetrameric

  4. Advanced Development of Leishmania Topical Skin Test Antigen

    Science.gov (United States)

    2012-09-28

    tropica promastigotes is a complex mixture of substances, including proteins in the range of 8 kDa to 70 kDa. In Leishmania naïve adult humans, the lysate...humans. 15. SUBJECT TERMS LtSTA = Leishmania tropica Skin test Antigen 16. SECURITY CLASSIFICATION OF: 17. LIMITATION OF ABSTRACT 18. NUMBER OF... tropica (LtSTA) developed by Allermed was intended to be used to screen military and civilian personnel for infection with Leishmania during and

  5. Susceptibility of Inbred Mice to Leishmania major Infection: Genetic Analysis of Macrophage Activation and Innate Resistance to Disease in Individual Progeny of P/J (Susceptible) and C3H/HeN (Resistant) Mice

    Science.gov (United States)

    1990-12-01

    mediated immu- ease and defective macrophage activation in Bx mice that nity in mice highly susceptible to Leishmania tropica . J. Exp. could not be...inbred mice to Leishmania tropica infec- tion: correlation of susceptibility with in vitro defective macro- LITERATURE CITED phage microbicidal...probability and phage activation to kill Leishmania tropica : characterization of statistics. Chemical Rubber Co., Cleveland. P/J mouse macrophage defects for

  6. Impact of Phlebotomine Sand Flies on U.S. Military Operations at Tallil Air Base, Iraq: 2. Temporal and Geographic Distribution of Sand Flies

    Science.gov (United States)

    2007-01-01

    be important vectors of Leish- mania in Iraq. P. sergenti and P. papatasi are almost certainly the primary vectors of Leishmania tropica (Wright...acterization of two of the Leishmania isolates indi- cated that they were unlike L. infantum, L. donovani, L. tropica , L. majo, or L. aethiopica. In 1985, Sukkar...Lane. 1988. Phlebotomus sergenti, a vec- tor of Leishmania tropica in Saudi Arabia. Trans. R. Soc. Trop. Med. Hyg. 82: 416. Azizi, K., Y. Rassi, E

  7. Advanced Developement of Leishmania Tropical Skin Test Antigen

    Science.gov (United States)

    2011-09-01

    Approved for Public Release; Distribution Unlimited 13. SUPPLEMENTARY NOTES 14. ABSTRACT Leishmania tropica Skin Test Antigen ( LtSTA) is lysate...31, 2011 on a Leishmania Skin test (LtSTA) made from the promastigotes of Leishmania tropica . During the last reporting period between June 18, 2009...sequences of other Leishmania species, closely related parasites and humans. In as much as the L. tropica genome has not been completely assembled, the

  8. Molecular Identification of Leishmania Species Causing Cutaneous Leishmaniasis In Mashhad area, Iran

    Directory of Open Access Journals (Sweden)

    Mohammad Karimian Shirazi

    2014-08-01

    Results: In first step of PCR, all of sampled were positive for Leishmania spp and in second step Leishmania tropica and L.major were detected in 94% and 6% in positive –PCR amplicon , respectively. Conclusion: Based on the results, Leishmania tropica is more prevalent than L.major in Mashhad area

  9. Effect of Lures and Trap Placement on Sand Fly and Mosquito Traps

    Science.gov (United States)

    2008-01-01

    Phlebotomus guggisbergi, a vector of Leishmania tropica in Kenya. Med. Vet. Entomol. 7:216-218. Killick-Kendrick, R. 1999. The biology and control...Acta Tropica 101:106-114. Hoel, D.E, Butler, J.F., Fawaz, E.Y., Watany, N., El-Hossary, S.S., and Villinski, J. 2007. Response of phlebotomine sand

  10. A Randomized Controlled Trial of Local Heat Therapy Versus Intravenous Sodium Stibogluconate for the Treatment of Cutaneous Leishmania Major Infection

    Science.gov (United States)

    2010-01-01

    Dermatotrophic Leishmania species such as L. major, L. tropica , and L. mexicana are thermosensitive with higher temperatures limiting amastigote replication...Wahid M, Bismullah M, Quinnell RJ, et al. (2005) Efficacy of thermotherapy to treat cutaneous leishmaniasis caused by Leishmania tropica in Kabul...A Randomized Controlled Trial of Local Heat Therapy Versus Intravenous Sodium Stibogluconate for the Treatment of Cutaneous Leishmania major

  11. 1株湿地稀有放线菌的多相分类鉴定%Polyphasic Taxonomy of a Rare Marine Actinomycetes

    Institute of Scientific and Technical Information of China (English)

    唐树戈; 张柳; 于基成; 刘秋; 齐小辉

    2014-01-01

    Strain S402003 was isolated from marine sediment collected from Yalu River in Dandong, Liaoning Province. Based on the polyphasic studies, including the morphology, physiological and biochemical characteristics, chemotaxonomy and 16S rRNA gene sequence analysis, the results showed that strain S402003 had lipase activity and was capable to reduce nitrate, belongs to the mild salt-tolerant and basophilic bacteria. It was primarily identified as Brevibacterium linens with the similarity 98.834%.%从鸭绿江滨海湿地样品中分离得到1株稀有海洋放线菌S402003,通过形态观察、培养特征、生理生化特征、化学组分鉴定以及16S rRNA基因序列分析对其进行多相分类鉴定。结果表明:该菌株具有脂酶活性,能还原硝酸盐,属于轻度耐盐、嗜碱菌。该菌株属于Brevibacterium linens,相似性为98.834%。

  12. Identification of ATP-Dependent Phosphofructokinase as a Regulatory Step in the Glycolytic Pathway of the Actinomycete Streptomyces coelicolor A3(2)

    NARCIS (Netherlands)

    Alves, A.M.C.R.; Euverink, G.J.W.; Bibb, M.J.; Dijkhuizen, L.

    1997-01-01

    The ATP-dependent phosphofructokinase (ATP-PFK) of Streptomyces coelicolor A3(2) was purified to homogeneity (1,600-fold) and characterized (110 kDa, with a single type of subunit of 40 kDa); it is allosterically inhibited by phosphoenolpyruvate. Cloning of the pfk gene of S. coelicolor A3(2) and an

  13. Advances on actinomycetic terpenoid biosynthesis%放线菌萜类化合物生物合成研究进展

    Institute of Scientific and Technical Information of China (English)

    李文利; 湛桂花; 郑华

    2011-01-01

    萜类化合物(Terpenoids)是自然界中化学结构最为丰富的一类化合物.近年来,从放线菌中分离到了一系列结构新颖的萜类化合物.通过直接克隆或基因组采掘(Genome mining)的方法,它们的生物合成基因簇被相继分离和鉴定,从而推动了放线菌中萜类化合物生物合成途径及关键酶的分子作用机理的研究.文章主要综述了近5年放线菌萜类化合物生物合成研究进展.%Terpenoids are the most diverse class of natural products. Recently, a series of terpenoids with novel structures have been isolated from actinomyces. Their biosynthetic gene clusters have been identified and characterized either by direct cloning or genomic mining, which promoted investigations of their biosynthetic pathways, as well as the key enzymatic mechanisms. This paper provides a brief overview of the major research published in the last five years.

  14. Bacterial Type I Glutamine Synthetase of the Rifamycin SV Producing Actinomycete, Amycolatopsis mediterranei U32, is the Only Enzyme Responsible for Glutamine Synthesis under Physiological Conditions

    Institute of Scientific and Technical Information of China (English)

    Wen-Tao PENG; Jin WANG; Ting WU; Jian-Qiang HUANG; Jui-Shen CHIAO; Guo-Ping ZHAO

    2006-01-01

    The structural gene for glutamine synthetase, glnA, from Amycolatopsis mediterranei U32 was cloned via screening a genomic library using the analog gene from Streptomyces coelicolor. The clone was functionally verified by complementing for glutamine requirement of an Escherichia coli glnA null mutant under the control of a lac promoter. Sequence analysis showed an open reading frame encoding a protein of466 amino acid residues. The deduced amino acid sequence bears significant homologies to other bacterial type I glutamine synthetases, specifically, 71% and 72% identical to the enzymes of S. coelicolor and Mycobacterium tuberculosis, respectively. Disruption of this glnA gene in A. mediterranei U32 led to glutamine auxotrophy with no detectable glutamine synthetase activity in vivo. In contrast, the cloned glnA+ gene can complement for both phenotypes in trans. It thus suggested that in A. mediterranei U32, the glnA gene encoding glutamine synthetase is uniquely responsible for in vivo glutamine synthesis under our laboratory defined physiological conditions.

  15. Separating, Antagonistic Activity and Identifying of Actinomycetes(BOS-009)%放线菌BOS-009的分离、拮抗活性及鉴定