首页> 外文期刊>Physiology and Molecular Biology of Plants >Multiple shoot regeneration and alkaloid cerpegin accumulation in callus culture of Ceropegia juncea Roxb.
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Multiple shoot regeneration and alkaloid cerpegin accumulation in callus culture of Ceropegia juncea Roxb.

机译:Ceropegia juncea Roxb愈伤组织培养中的多次芽再生和生物碱cerpegin积累。

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This is the first report of in vitro propagation and alkaloid accumulation in callus cultures of Ceropegia juncea Roxb. a source of “Soma” drug in Ayurvedic medicine. Multiple shoots and callus induction was optimized by studying the influence of auxins [IAA (Indole-3-acetic acid), NAA (2-Naphthalene acetic acid) and 2,4-D (2,4-Dichlorophenoxyacetic acid.)] and cytokinins [BA (6-benzyladenine) and Kin (Kinetin)] alone and in combinations. The best response for multiple shoot induction was obtained in nodal explants on MS medium supplemented with 7.5 μM Kin (8.5 ± 3 shoots per explants). The shoots were rooted on half strength MS (Murashige and Skoog’s) medium fortified with either IAA or NAA (0.5–2.0 μM). The plantlets were transferred directly to the field with 100 % success rate. Supplementation of MS medium with auxins and cytokinins enhanced the growth of callus but inhibited the shoot regeneration in nodal explants. Best callus induction and proliferation observed on MS + 1 μM 2,4-D+5 μM BA. However the maximum cerpegin content (470 μg/g dry weight) was recorded in dried callus derived on MS+10 μM IAA+5 μM BA. Quantitative TLC (Thin layer chromatography) studies of the callus revealed a phytochemical profile similar to that of naturally grown plants. The calli were maintained by subculturing at 4 weeks interval on fresh parent medium over a period of 34 months. The optimized in vitro propagation and callus culture protocol offers the possibilities of using organ/callus culture technique for vegetative propagation and production of cerpegin alkaloid.
机译:这是Ceropegia juncea Roxb愈伤组织培养物中体外繁殖和生物碱积累的首次报道。阿育吠陀医学中“索玛”药物的来源。通过研究生长素[IAA(吲哚-3-乙酸),NAA(2-萘乙酸)和2,4-D(2,4-二氯苯氧基乙酸)]和细胞分裂素的影响,优化了多芽和愈伤组织的诱导。单独或组合使用[BA(6-苄基腺嘌呤)和Kin(激动素)]。在节点外植体上,在补充了7.5μMKin的MS培养基(每个外植体8.5±3个芽)上,获得了最佳的多芽诱导响应。枝条扎根于半强度MS(Murashige和Skoog's)培养基上,该培养基使用IAA或NAA(0.5–2.0μM)强化。将小苗直接转移到田间,成功率为100%。补充生长素和​​细胞分裂素的MS培养基可促进愈伤组织的生长,但抑制结节外植体的芽再生。在MS + 1μM2,4-D + 5μMBA上观察到最佳的愈伤组织诱导和增殖。但是,在源自MS + 10μMIAA + 5μMBA的干燥愈伤组织中记录了最大的cerpegin含量(470μg/ g干重)。愈伤组织的定量TLC(薄层色谱)研究显示,植物化学特征与自然生长的植物相似。通过在新鲜的母体培养基上每隔4周传代培养34个月来维持愈伤组织。优化的体外繁殖和愈伤组织培养方案提供了使用器官/愈伤组织培养技术进行无性繁殖和生产cerpegin生物碱的可能性。

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