首页> 外文期刊>Acta Physiologiae Plantarum >In vitro propagation and conservation of Indian sarsaparilla, Hemidesmus indicus L. R. Br. through somatic embryogenesis and synthetic seed production
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In vitro propagation and conservation of Indian sarsaparilla, Hemidesmus indicus L. R. Br. through somatic embryogenesis and synthetic seed production

机译:印度sarsaparilla,Hemidesmus indicus L. R. Br。的体外繁殖和保存。通过体细胞胚发生和合成种子生产

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摘要

A protocol has been developed for achieving somatic embryogenesis from callus derived from nodal cuttings and production of synthetic seeds in Hemidesmus indicus L. R. Br. a highly traded ethnomedicinal plant. Proembryogenic, friable, light yellowishcallus was induced from the basal cut end of the nodal cuttings on Murashige and Skoog (MS) medium supplemented with 3 μM indole-3-butyric acid (IBA). The highest rate of somatic embryogenesis (92 %) was observed when the callus was subcultured on halfstrength MS medium supplemented with 2 μM IBA. On induction medium somatic embryos were developed up to the torpedo stage. Further elongation and germination of somatic embryos were obtained in MS medium supplemented with 4 μM 6-benzylaminopurine (BA)in combination with 1.5 μM gibberellic acid (GA3). Somatic embryos were collected and suspended in a matrix of MS medium containing sodium alginate (3 % W/V) dropped into 75 mM calcium chloride (CaCl2·2H2O) solution for the production of synthetic seeds and later transferred to MS medium for germination. The synthetic seeds were successfully germinated on medium even after 120 days of storage at 4 °C. The plantlets were eventually transferred to soil with 92 % success.
机译:已经开发出了一种方案,该方案用于从印度no(Hemidesmus indicus L.R.Br.)的节插和愈伤组织产生的愈伤组织中实现体细胞胚发生。高度交易的民族植物。在补充了3μM吲哚-3-丁酸(IBA)的Murashige和Skoog(MS)培养基上,从节节的基部切割末端诱导出胚原性,易碎,淡黄色的愈伤组织。当愈伤组织在补充2μMIBA的半强度MS培养基上继代培养后,体细胞胚发生率最高(92%)。在诱导培养基上,体细胞胚胎发育至鱼雷阶段。在补充了4μM6-苄基氨基嘌呤(BA)与1.5μM赤霉素(GA3)的MS培养基中获得了体细胞胚的进一步伸长和萌发。收集体细胞胚并将其悬浮在含有海藻酸钠(3%W / V)的MS培养基基质中,滴入75 mM氯化钙(CaCl2·2H2O)溶液中以生产合成种子,然后转移至MS培养基中进行发芽。即使在4°C下储存120天后,合成种子仍能在培养基上成功发芽。最终将小植株转移到土壤中,成功率为92%。

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