首页> 外文期刊>Journal of Plant Growth Regulation >Optimizing Shoot Formation in Gentiana kurroo Royle for Gentiopicroside Production
【24h】

Optimizing Shoot Formation in Gentiana kurroo Royle for Gentiopicroside Production

机译:优化龙胆秦甙生产的芽型

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

The roots and shoots of Gentiana kurroo Royle are rich sources of gentiopicroside (GPD). The plant is used traditionally for curing many metabolic diseases. The exploitation of G. kurroo in its native habitat has placed the plant on the critically endangered list of plants in India. One of the ways of creating an alternative source of G. kurroo is through in vitro propagation. Although a number of in vitro propagation methods for G. kurroo exist, there are no studies that have optimized methods for rapid in vitro shoot production and the production of GPD. The objective of this study was to develop an effective in vitro shoot multiplication system of G. kurroo. Furthermore, the influence of solid and liquid induction media were investigated. Shoots were regenerated from embryogenic callus and transferred to solid and liquid Murashige and Skoog (MS) and Gamborg (B-5) media fortified with various concentrations of BA containing different auxins. It was observed that the liquid medium produced a higher number of shoots than the solid media. MS supplemented with BA (2 mg/L) and IAA (0.5 mg/L) produced similar to 5.58 shoots per explant on the solid medium, while similar to 16 shoots per explant was obtained in the liquid medium. High-Performance Liquid Chromatography (HPLC) analysis of in vitro shoots grown in the liquid medium produced 9.13 mg/g dry weight (DW) of GPD which is seven-fold higher than that of naturally growing plant shoots. The in vitro protocol for G. kurroo developed in this study may be used for industrial production of GPD.
机译:龙胆的根和芽是龙胆苦苷(GPD)的丰富来源。该植物传统上用于治疗许多代谢疾病。G. kurroo 在其原生栖息地的开发已将该植物列入印度极度濒危植物名单。创造 G. kurroo 替代来源的方法之一是通过体外繁殖。尽管存在许多 G. kurroo 的体外繁殖方法,但尚无研究优化了快速体外芽生产和 GPD 生产的方法。本研究旨在开发一种有效的 G. kurroo 体外新芽增殖系统。此外,还研究了固体和液体感应介质的影响。从胚性愈伤组织再生芽,并转移到固体和液体 Murashige 和 Skoog (MS) 和 Gamborg (B-5) 培养基中,并用含有不同生长素的不同浓度的 BA 强化。据观察,液体培养基产生的枝条数量高于固体培养基。添加BA(2 mg/L)和IAA(0.5 mg/L)的MS在固体培养基上每个外植体产生相似的5.58个枝条,而在液体培养基上每个外植体获得相似的16个枝条。高效液相色谱(HPLC)分析在液体培养基中生长的体外枝条产生了9.13 mg/g干重(DW)的GPD,比自然生长的植物枝条高7倍。G的体外方案。本研究开发的kurroo可用于GPD的工业化生产。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号