D. Rathnaprabha, N. Muralikrishna, E. Raghu, Yashodhara, A. Sadanandam
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引用次数: 1

摘要

建立了一种高效、可重复的濒危珍贵药用植物Butea monosperma (Lam.)的快速离体增殖方法。陶布。黄叶变种,通过成熟种子的子叶节。在多种细胞分裂素中,在添加BAP的Murashige和skoog (MS)培养基上诱导直接芽再生的频率较高,在2 mg/L时效果最佳,每个外植体最多可再生8.35±0.32个芽。以2 ~ 3周的时间间隔,在同一再生培养基上重复继代培养,建立芽的增殖。在含1mg /L IBA的MS培养基上培养3周后再生芽生根。将离体培养苗按1:1的比例移栽到含有灭菌土壤和蛭体混合物的花盆中,然后移栽到温室中。成熟植株的成活率为75%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Micropropagation of White Palash tree (Butea monosperma (Lam.) Taub. Var. lutea (Witt.)).
An efficient and reproducible protocol is established for rapid in vitro multiplication of an endangered, valuable medicinal plant, Butea monosperma (Lam.) Taub. Var. lutea , through cotyledonary nodes of mature seeds. Among various cytokinins tested, high frequency of direct shoot regeneration was induced on Murashige and skoog (MS) medium supplemented with BAP, which found to be more effective and showed optimal response at 2 mg/L with a maximum number of 8.35±0.32 multiple shoots per explant. Proliferation of shoots was established by repeated subculturing on to same regeneration medium with 2-3 weeks of time interval. Rooting of regenerated shoots was achieved after 3 weeks of culture on MS medium containing 1 mg/L IBA. In vitro raised plantlets were transferred to pots containing sterilized soil and vermiculate mixture in 1:1 ratio and then shifted to greenhouse. Well established plantlets exhibited 75% survival rate.
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