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High frequency in vitro propagation of Holarrhena antidysenterica from nodal buds of mature tree

机译:从成熟树的结芽中高频提取抗鞭毛藻

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摘要

An in vitro method for propagation of Holarrhena antidysenterica Wall. has been developed using nodal explants from mature trees growing in the field. Irrespective of concentrations and combinations of growth regulators used, the axillary and terminal buds sprouted and elongated when inoculated on Murashige and Skoog (MS) medium. The highest numbers of shoots were formed when sprouted shoots were subcultured from MS basal medium onto MS medium containing 2 mg dm?3 N6-benzyladenine (BA) and 0.5 mg dm?3 α-naphthalene acetic acid (NAA). The shoot number further increased upon subculture on MS medium containing 0.5 mg dm?3 BA. By repeated sub-culturing of shoots derived from nodal axillary buds, a high frequency multiplication rate was established. The elongated shoots were excised and rooted in auxin free MS basal medium. Ex vitro rooting of in vitro formed shoots was achieved upon dipping the microshoots for 2 min in 2 mg dm?3 of indole-3-butyric acid solution. Successful field establishment and high (80–90 %) survival of plants was observed.
机译:一种体外培养的整草抗藻壁的方法。已使用田间生长的成熟树木的节点外植体开发了这种植物。不论使用哪种浓度的生长调节剂,只要将其接种在Murashige和Skoog(MS)培养基上,腋芽和末梢芽就会发芽并伸长。将发芽的芽从MS基础培养基传代到含有2 mg dm?3 N6 苄基腺嘌呤(BA)和0.5 mg dm?3 α的MS培养基上时,形成的芽数最多。 -萘乙酸(NAA)。在含有0.5 mg dm?3 BA的MS培养基上继代培养后,芽数进一步增加。通过重复传代结腋芽的芽,确定了高频繁殖率。切下细长的芽,并在无生长素的MS基础培养基中生根。将微芽浸入2 mg dm?3 吲哚-3-丁酸溶液中2分钟,即可获得离体生根芽。观察到成功的田间建立和高(80-90%)植物存活率。

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