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Tissue culture technology for rapid multiplication of Dendrocalamus giganteus Munro.

机译:组织培养技术,用于快速繁殖巨齿end。

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Micropropagation of Dendrocalamus giganteus through axillary bud culture is described. Multiple shoots were induced from in-vitro culture of nodal shoot segments containing axillary bud. Nodal segments produced axillary shoots in 2-3 weeks on Murashige and Skoog's (MS) medium supplemented with BAP (10-40 micro M). These shoots were excised from mother explants and subcultured on different concentrations of BAP in MS medium. Highest shoot multiplication rate of 5.44 fold was obtained on 20 micro M BAP medium. On MS medium supplemented with Kn only 3-4 fold shoot multiplication was obtained. The addition of BAP (10 micro M) in the kinetin (10 micro M) supplemented medium enhanced the shoot multiplication rate to 6.35 fold. 16-66% roots were formed on excised propagules of 3-5 shoots when transferred to MS medium supplemented with 15-25 micro M IBA. The maximum roots per propagule (8.66) and rooting percentage (90%) was obtained on MS medium supplemented with 25 micro M IBA+0.05 micro M BAP. These tissue culture raised plants were successfully hardened and acclimatized and transferred to field condition..
机译:描述了通过腋芽培养物对巨齿龙的微繁殖。从含有腋芽的节状芽节段的体外培养中诱导出多芽。节点节段在补充BAP(10-40 micro M)的Murashige和Skoog(MS)培养基上2-3周内产生腋芽。这些芽从母外植体上切下,并在MS培养基中以不同浓度的BAP进行亚培养。在20 micro M BAP培养基上获得了最高的芽繁殖率5.44倍。在补充有Kn的MS培养基上,仅获得3-4倍的芽繁殖。在激动素(10 micro M)补充培养基中添加BAP(10 micro M)将枝条繁殖率提高到6.35倍。当转移到补充有15-25 micro M IBA的MS培养基上时,在3-5个嫩芽的切除繁殖体上形成16-66%的根。在补充了25 micro M IBA + 0.05 micro M BAP的MS培养基上获得每个繁殖体的最大根(8.66)和生根百分比(90%)。这些组织培养育成的植物已成功硬化和适应环境,并转移到田间条件下。

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