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首页> 外文期刊>Dynamic Chiropractic >Evaluation of genetic fidelity of in vitro propagated shampoo ginger (Zingiber zerumbet (L.) Smith) using DNA based markers
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Evaluation of genetic fidelity of in vitro propagated shampoo ginger (Zingiber zerumbet (L.) Smith) using DNA based markers

机译:使用基于DNA的标记评估体外繁殖的洗发姜(Zingiber zerumbet(L.)Smith)的遗传保真度

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Drug yielding potential of shampoo ginger (Zingiber zerumbet(L.) Smith) is due to the presence of important phytoconstituent such as Zerumbone, which is currently being explored for its effects on cancer and HIV. Slow multiplication rate, high susceptibility to rhizome rot and leaf spot disease restricted the availability of the wild gingers. Thus, a protocol has been developed forin vitropropagation of Z.zerumbetusing sprouted bud explants from rhizome. The explants in MS media with 4 mg/L benzyl adenine, 1 mg/L indole-3-acetic acid showed highest percentage of response, that is, 93.8%. The aseptic shoots ofZ.zerumbetwere formed with 5 multiple shoots on MS media with 3 mg/Lbenzyl adenine and 1 mg/Lindole-3-acetic acid and 100 mg/Ladenine sulfate.In vitrogrown plantlets ofZ. zerumbetcould be conserved in MS media containing 0.5 mg dm-3of benzyladenine and 60 mg/Lof sucrose subcultured at an interval of eight months. Survival ofin vitroconserved plants on multiplication media was 85%. Genetic stability of micropropagated clones were periodically evaluated at an interval of 6 months up to 30 months in culture using random amplified polymorphic DNA (RAPD) and inter simple sequence repeat (ISSR) analysis and genetic uniformity in all regenerants was confirmed.
机译:香波姜(Zingiber zerumbet(L.)Smith)的潜在产药潜力是由于存在重要的植物成分,例如Zerumbone,目前正在研究其对癌症和HIV的作用。繁殖速度慢,对根茎腐烂和叶斑病的敏感性高,限制了野生生姜的供应。因此,已经开发了用于使用来自根茎的发芽的芽外植体体外繁殖Z.zerum的方案。 MS培养基中含有4 mg / L苄基腺嘌呤,1 mg / L吲哚-3-乙酸的外植体显示出最高的响应百分比,即93.8%。在含3 mg / L苄基腺嘌呤和1 mg / Lindole-3-乙酸和100 mg / Ladenine硫酸盐的MS培养基上,用5个多重芽形成Z.zerumbet的无菌芽。 SERUMBET可以在含有0.5 mg dm-3苄基腺嘌呤和60 mg / L蔗糖的MS培养基中保存,间隔8个月。在复制培养基上体外保存的植物的存活率为85%。使用随机扩增多态性DNA(RAPD)和简单序列重复(ISSR)分析,在培养中的6个月至30个月的间隔中定期评估微繁殖克隆的遗传稳定性,并确认所有再生子的遗传均一性。

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