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Sample records for 6-furfurylaminopurine

  1. Effect of exogenous hormones and chilling on dormancy breaking of seed of Asafoetida (Ferula assafoetida L.)

    Otroshy, M.; Zamani, A.; Khodambashi, M.; Ebrahimi, M.; Struik, P.C.

    2009-01-01

    Asafoetida (Ferula assafoetida L.) is a medicinal plant with a problematic seed germination. Seeds of this plant have a long dormancy. The present research was carried out to investigate whether exogenous application of the hormones Gibberellic Acid (GA3), N6-furfurylaminopurine (kinetin) and 6-benz

  2. Effect of cytokinins on shoot regeneration from cotyledon and leaf segment of stem mustard (Brassica juncea var. tsatsai)

    Guo, D.P.; Zhu, Z.J.; Hu, X.X.; Zheng Sijun, S.J.

    2005-01-01

    Cotyledon and leaf segments of stem mustard (Brassica juncea var. tsatsai) were cultured on Murashige and Skoog medium supplemented with various concentrations of different cytokinins [6-benzyladenine (BA), N-(2-chloro-4-pyridyl)-n-phenylurea (CPPU), 6-furfurylaminopurine (KT) and thidiazuron (TDZ)

  3. Obtención de plantas haploides en chile miahuateco (Capsicum annuum L. Obtaining haploid plants from miahuateco chili pepper (Capsicum annuum L.

    Marcelina Vélez Torres

    Full Text Available La regeneración de plantas haploides, es una herramienta importante en los programas de mejoramiento y estudios genéticos, ya que permite obtener líneas puras más rápido que los métodos convencionales a través de la duplicación de plantas haploides. El objetivo de este trabajo fue establecer una metodología que permita la regeneración de plantas haploides de chile tipo miahuateco (Capsicum annuum L.. Las anteras se cultivaron en los medios basales de Murashige y Skoog (1962; Chu et al. (1975, suplementados con 6-furfurilaminopurina (0.1-1 mg L-1, ácido naftalenacético (0.1 mg L-1, ácido indolacético (1 mg L-1 y ácido 2-4 diclorofenoxiacético (1 mg L-1. La embriogénesis se indujo hasta en 2.23% de anteras cuando se cultivaron en una combinación de 6-furfurilaminopurina con 2-4, diclorofenoxiacético (1 mg L-1 de ambos o de ácido indolacético con 6-furfurilaminopurina (0.1 mg L-1 de ambos. El análisis cromosómicos de las plantas regeneradas mostró que eran haploides con número cromósomico 2n= x= 12.Haploid plant regeneration is an important tool in breeding programs and genetics studies, since it helps obtain pure lines faster than conventional methods by the duplication of haploid plants. The aim of this study was to establish a methodology to regenerate haploid Miahuateco chili pepper plants (Capsicum annuum L.. Anthers were grown on Murashige and Skoog (1962; Chu et al. (1975 basal media, supplemented with 6-furfurylaminopurine (0.1-1 mg L-1, naphthaleneacetic acid (0.1 mg L-1, indolacetic acid (1 mg L-1, and 2-4 dichlorophenoxyacetic acid (1 mg L-1. Embryogenesis was induced in 2.23% of anthers grown in a combination of 6-furfurylaminopurine with 2-4 dichlorophenoxyacetic acid (1 mg L-1, of each, or indolacetic acid with 6-furfurylaminopurine (0.1 mg L-1 of each. Chromosome analysis of regenerated plants showed that they were haploids with a chromosome number of 2n= x= 12.

  4. INDUCTION OF CALLUS FORMATION FROM DIFFERENT PARTS OF Citrus grandis (OSBECK FLOWERS

    Zarina Binti Zakaria

    2010-01-01

    Full Text Available The objectives of the present work were to study the capability of pomelo's floral tissues to produce callus and to investigate the influence of plant growth regulators on callus induction and development. Various parts of flower namely petal, sepal, style, ovary, pistil and cup base were cultured onto Murashige and Skoog (MS basal medium supplemented with different levels of 2,4-dichlorophenoxyacetic acid (2,4-D, 6-benzylaminopurine (BAP and 6-Furfurylaminopurine (kinetin. It was found that different parts of flowers favored different levels of hormone for callus induction. The highest formation of callus were obtained from petal and sepal cultured on MS media supplemented with 1.5 mg/l kinetin. A 50 ± 2.3%explants from style and pistil had initiated callus when cultured on MS media supplemented with 0.05 mg/l and 0.10 mg/l BAP, respectively. On the other hand, sucrose agar (SA media alone had managed to induce callus formation from almost every part of the flowers with a success rate between 7.69 ± 0.32 to 50 ± 3.18%. The uncut part of flowers initiated high percentage of callus (14.6 ± 0.35% as shown in the study on petal.

  5. Effect of growth retardants, cytokinins and auxins on the multiplication and rooting in vitro of Alstroemeria x hybrida "Juanita"

    Małgorzata Podwyszyńska

    2013-12-01

    Full Text Available Rhizome cultures of "Jiianita" Polish cultivar of Alstroemeria x hybrida were used to enhance an effectiveness of micropropagation method of new cultivars and selections. The effect of cytokinins (BAP. kinetin and 2iP, auxins (IAA, IBAand NAA, growth retardants (paclobutrazol and flurprimidol alone or in combination were studied in relation to rhizome branching. aerial shoot production and rooting of rhizome. The greatest number of aerial shoots as well as the shortest shoots were observed at the highest BAP concentration (6 mg l-1. However, the rhizonies had the poorest rooting ability. BAP at low concentrations combined with kinetin or 2iP also strongly stimulated aerial shoot formation and rhizome branching. Unfortunately. those shoots were of poor qualily. Application of BAP at low concentration with paclobutrazol (0,1-0,5 mg l-1 or flurprimidol (0,01- 1 mg l-1 in presence of 1 mg l-1 NAA resulted in high number of aerial shoots (5-6, reduction of their length and higher rooting ability of the rhizomes. Gr(wth retardants applied with NAA strongly stimulated formation of the roots but suppressed their elongation. Abbreviations: BAP - 6=benzylaminopurine; kinetin - 6-furfurylaminopurine; 2iP - 6-‌γ,γ-dime-thylallylamino]purine; IAA-indole-3-acetic acid; IBA-indole-3-butyric acid; NAA- naphthaleneacetic acid; paclobutrazol (ICI PP-333 - (2-RS,3-RS-1-(4-chlorophenyl-4-4-dimethyl-2(1,2,3-triazol-1-yl-pentan-3-ol flurprimidol (Dowelanco - α-(1-niethylethy 1-α-[4-trifluro-niethoxyphenyl]-5-pyridinemethanol.

  6. OPTIMIZATION OF HORMONE COMPOSITION OF NUTRIENT MEDIUM FOR IN VITRO EFFICIENT REGENERATION OF BREAD WHEAT

    E. D. Nikitina

    2016-08-01

    Full Text Available Optimal values of phytohormones in the differential nutrient medium providing the efficient realization of morphogenetic potencies of four spring bread wheat varieties (Skala, Spectr, Zarnitsa and Zhnitsa from immature embryo cultures have been determined. For callus induction explants 1.5 – 1.7 mmin size were used, which were subsequently passed to the medium by Linsmaier&Skoog possessing 0.8 % of agar, 3 % of sucrose and 2.0 mg l-1 dichlorophenoxyacetic acid (2,4-D. Cell cultures were incubated in darkness at the temperature 26±1 °С. 30 – 35 days after in accordance with the scheme of complete factorial experiment of 32 type calli were passed to differential medium supplemented with 2,4-D at levels 0.5; 2.5; 4.0 mg l-1 and with kinetin (6-furfurylaminopurine at levels 0.5; 2.25 and 4.0 mg l-1. Number of replications for each of 9 variants was four. As a result, 20 mathematic models (4 varieties × 5 stages of regeneration designed as polynomial quadric equation were obtained. On the ground of the analysis of models it was established that optimal values for factors are not equal both for cultures of genotypes analyzed and for different regeneration stages. For callus tissues of Skala and Spectr an optimal value of kinetin for all regeneration stages was 0.5 mg l-1 except for the frequency of morphogenesis. Optimal values of 2,4-D for the same varieties were within 2.3 – 3.2 mg l-1. For cell cultures of Zarnitsa and Zhnitsa recommended concentration intervals made up 1.3 – 2.2 mg l-1 on kinetin except for the frequency of rhizogenesis, and 1.9 – 2.7 on 2,4-D. The level of exogenous phytohormones necessary for stem differentiation was lower than the one for root formation. The dependence of morphogenesis results on the hormonal status of the explant has been discussed.

  7. Multiplicação in vitro de gemas axilares de acácia-negra (Acacia mearnsii De Wild. In vitro multiplication of black watlle (Acacia mearnsii De Wild. axillary buds

    Norton Borges Júnior

    2004-08-01

    Full Text Available A acácia-negra (Acacia mearnsii De Wild. é uma espécie de difícil micropropagação devido à pequena capacidade de multiplicação e desenvolvimento de gemas. O presente estudo visou determinar a influência de diferentes citocininas na proliferação de gemas axilares em segmentos nodais de A. mearnsii. Plântulas germinadas in vitro forneceram explantes que foram inoculadas em meio básico B5 (GAMBORG et al., 1968. Testaram-se as citocininas: BAP (6-benzilaminopurina, BA (6-benziladenosina, 2iP (gama,gama-isopenteniladenina e cinetina (6-furfuralamino-purina. Diferentes concentrações desses reguladores de crescimento foram empregadas: 1 mgL-1, 2 mgL-1 e 3 mgL-1. Utilizou-se o delineamento de blocos casualizados, em arranjo fatorial, com seis repetições e cinco plantas por parcela. As avaliações foram feitas aos 30 dias, através da contagem de gemas alongadas e da presença de calos. A utilização de BAP a 2 mgL-1 promoveu a maior taxa de multiplicação de gemas (3,5 brotos/explante.Black wattle (Acacia mearnsii de Wild. is difficult to micropropagate due to the low ability of multiplication and development of shoots. Thus, the present study aimed at determining the influence of various cytokinins on axillary bud proliferation in nodal segments of A. mearnsii. Explants from in vitro germinated seedlings were inoculated on B5 (Gamborg et al., 1968 basal medium. BAP (6-benzylaminopurine, BA (6-benzyladenine, 2iP (gamma,gamma-dimethylallylamino-purine and Kinetin (6-furfurylaminopurine were tested at the concentrations 1 mgL-1, 2 mgL-1, and 3 mgL-1. A randomized block design, in factorial arrangement with 6 replications, and 5 plants per plot was used. The assessments were made after 30 days, by counting the elongated shoots and the presence of callus. The use of BAP at 2 mgL-1 promoted the highest rate of bud multiplication (3,5 shoots/explant.

  8. Application of plant growth regulators, a simple technique for improving the establishment success of plant cuttings in coastal dune restoration

    Balestri, Elena; Vallerini, Flavia; Castelli, Alberto; Lardicci, Claudio

    2012-03-01

    Exogenous application of plant growth regulators (PGRs) may be an effective technique for increasing the rooting ability and the growth of vegetative fragments (cuttings) of plants used in dune restoration programs. Various concentrations (0, 50 and 100 mg l-1) of two auxins, alpha-naphtaleneacetic acid (NAA) and indole-3-butyric acid (IBA), and two cytokinins, 6-furfurylaminopurine (Kinetin) and 6-benzylaminopurine (BAP), were applied separately to cuttings of two widely used species for restoration, Ammophila arenaria and Sporobuls virginicus. Root development and production of new buds in cuttings were examined under laboratory conditions one month after application. Cuttings were also examined one year after transplanting into a sandy substratum under natural conditions, to test for possible long term effects of PGRs on plant establishment success and growth. The response of the two study species to PGRs differed substantially. In A. arenaria the auxin NAA at 100 mg l-1 reduced the time for root initiation and increased the rooting capacity of cuttings, while the cytokinin Kinetin at 50 mg l-1 facilitated root growth. No auxin had effect on rooting or growth of S. virginicus cuttings, but treatment with 100 mg l-1 Kinetin resulted in higher rooting success than the control. One year after planting, the cuttings of A. arenaria treated with 100 mg l-1 NAA showed a higher establishment success (90% vs. 55%) and produced more culms and longer roots than the control; those treated with cytokinins did not differ in the establishment success from the control, but had longer roots, more culms and rhizomes. On the other hand, the cuttings of S. virginicus treated with 100 mg l-1 Kinetin showed a higher establishment success (75% vs. 35%) and had more culms than the control. Therefore, in restoration activities that involved A. arenaria, a pre-treatment of cuttings with NAA would be beneficial, as it allows the production of a higher number of well-developed plants with

  9. In vitro multiplication of Tabernaemontana fuchsiaefolia L. (Apocynaceae Multiplicação in vitro de Tabernaemontana fuchsiaefolia L. (Apocynaceae

    Arildo José Braz de Oliveira

    2003-08-01

    Full Text Available This study describes a simple and promising for in vitro multiplication of Tabernaemontana fuchsiaefolia, a species abundantly found in southern Brazil utilized for medicinal purposes and as a source of compounds that may be used to develop new synthetic drugs. Apical and hypocotyl explants were cultured in MS medium containing different concentrations of the cytokinins benzylaminopurine (BA and 6-furfurylaminopurine (kinetin, supplemented with phloroglucinol (1, 3, 5-hydroxybenzene to stimulate growth and shoot proliferation. Cytokinin added to the culture media positively influenced the micropropagation of T. fuchsiaefolia.and kinetin induced more shoots per explant than BA cytokinin. A favorable effect of phloroglucinol on apical and lateral buds from hypocotyls was also achieved in medium containing no kinetin or in all kinetin concentrations tested. Short pulses of auxin 3-indolebutyric acid (IBA 5.0 mg/l resulted in satisfactory rooting in apical microcuttings. The addition of phloroglucinol to MS medium induced rhizogenesis in 29% of the nodal segments transferred to MS medium in the absence of IBA and in 50% of the nodal segments transferred to MS medium containing 0.5 mg/l IBA and in nodal segments previously submitted to short pulses of IBA.O presente estudo relata um método simples e promissor para multiplicação in vitro de Tabernaemontana fuchsiaefolia, uma espécie abundantemente encontrada no sul do Brasil, utilizada com propósitos medicinais e como fonte de compostos que podem ser usados para desenvolver novas drogas sintéticas. Para estimular o crescimento e a proliferação de caules, os explantes apicais e os hipocótilos foram cultivados em meio MS contendo diferentes concentrações das citocininas 6-benzil-amino-purina (BA e cinetina (KIN e suplementado com fluoroglucinol (1, 3, 5-hidroxibenzeno. A micropropagação de T. fuchsiaefolia foi positivamente influenciada por citocininas e a cinetina induziu à formação de