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首页> 外文期刊>In Vitro Cellular and Development Biology. Plant: Journal of the Tissue Culture Association >Micropropagation of Uraria picta, a medicinal plant, through axillary bud culture and callus regeneration.
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Micropropagation of Uraria picta, a medicinal plant, through axillary bud culture and callus regeneration.

机译:通过腋芽培养和愈伤组织再生对药用植物Uraria picta进行微繁殖。

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摘要

Micropropagation of U. picta, a leguminous herb, was achieved through axillary bud culture and nodal callus culture. Bud break was best when nodes were cultured on Murashige and Skoog (1962) (MS) medium supplemented with 2.6 鍹 alpha-NAA and 4.4 鍹N6-benzyladenine. Optimum shoot multiplication was observed with adenine sulfate at 2.47 鍹. Competent callus was initiated around the nodal ring of the explant on the basal medium supplemented with cytokinins and auxin (alpha-NAA and benzyladenine), which regenerated into new profusely growing shoots on transferring to 0.13 鍹 benzyladenine. Shoots elongated to 5 nodes with 1.11 鍹 benzyladenine were rooted on half-strength MS basal medium. The rooted plants were successfully established ex vitro with80% survival. About 400 such plants were transferred to the field.
机译:通过腋芽培养和结节愈伤组织培养实现了豆科植物U. picta的微繁。当结节在补充有2.6鍹α-NAA和4.4鍹N6-苄基腺嘌呤的Murashige和Skoog(1962)(MS)培养基上培养时,结节破裂是最好的。用2.47 sulfate的硫酸腺嘌呤观察到最佳的枝条繁殖。感受态愈伤组织是在补充细胞分裂素和生长素(α-NAA和苄基腺嘌呤)的基础培养基上,在外植体的节环周围引发的,在转移至0.13 to苄基腺嘌呤后,这些愈伤组织会再生为新的长出新芽。用1.11鍹苄基腺嘌呤延长至5个节的芽生根于半强度MS基础培养基上。生根的植物在体外成功建立,存活率为80%。大约有400株这样的植物被转移到田间。

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