首页> 外文期刊>International Journal of Agriculture, Environment and Biotechnology >An Efficient Micropropagation Protocol for Rauvolfia hookeri Srinivas and Chithra and Assessment of Clonal Fidelity by RAPD Analysis
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An Efficient Micropropagation Protocol for Rauvolfia hookeri Srinivas and Chithra and Assessment of Clonal Fidelity by RAPD Analysis

机译:一种有效的钩藤轮虫和Chithra微繁殖方案,并通过RAPD分析评估克隆保真度

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An efficient in vitro propagation protocol via shoot multiplication was developed for Rauvolfia hookeri, a rare medicinal species endemic to the southern Western Ghats of India. Shoot tip explants cultured on half strength Murashige and Skoog medium supplemented with various cytokinins (6-benzylaminopurine, 6-furfurylaminopurine and Thidiazuron) either alone or in combinations produced multiple shoots. When either cytokinin was used alone, 6-benzylaminopurine was found nearly twice more successful than 6-furfurylaminopurine. The highest shoot proliferation was obtained when 6-benzylaminopurine and 6-furfurylaminopurine was used at 22.2 muM and 4.64 muM respectively. Thidiazuron gave the lowest response for shoot proliferation. The effect of indole-3-butyric acid and naphthalene acetic acid was evaluated for in vitro root induction. Rhizogenesis of excised shoots was of the shoots was readily achieved on half strength Murashige and Skoog medium containing various concentrations of indole-3-butyricacid and naphthale ne acetic acid. Indole-3-butyric acid was found to be more effective than naphthalene acetic acid and resulted in the highest frequency of shoots that rooted (86.5%) and mean number of roots per shoot (3.66) when used at 7.38 muM concentration. The micropropagated plants were hardened and transferred to green house condition wherein 70% plants established and were morphologically similar to mother plant. Genetic stability of regenerated plants has been checked by Random Amplified Polymorphic DNA using ten selected decamer primers.
机译:针对印度洋西高止山脉特有的稀有药用物种Rauvolfia hookeri,开发了一种通过芽繁殖的有效体外繁殖方案。在单独或组合使用多种细胞分裂素(6-苄基氨基嘌呤,6-糠基氨基嘌呤和噻二唑酮)补充的半强度Murashige和Skoog培养基上培养的茎尖外植体产生了多个芽。当单独使用两种细胞分裂素时,发现6-苄基氨基嘌呤的成功率是6-糠基氨基嘌呤的近两倍。当6-苄基氨基嘌呤和6-糠基氨基嘌呤分别以22.2μM和4.64μM使用时,获得最高的芽增殖。噻二唑对芽增殖的响应最低。评价了吲哚-3-丁酸和萘乙酸的体外根诱导作用。在含有不同浓度的吲哚-3-丁酸和萘乙酸的半强度Murashige和Skoog培养基上,容易获得切下的芽的发根。发现吲哚-3-丁酸比萘乙酸更有效,当以7.38μM的浓度使用时,可导致最高的发芽频率(86.5%)和平均每发芽数(3.66)。微繁殖的植物被硬化并转移到温室条件下,其中70%的植物建立并且在形态上与母植物相似。已使用十种选定的decamer引物通过随机扩增多态性DNA检查了再生植物的遗传稳定性。

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