首页> 美国卫生研究院文献>Iranian Journal of Pharmaceutical Research : IJPR >In-vitro Callus Induction and Rosmarinic Acid Quantification in Callus Culture of Satureja khuzistanica Jamzad (Lamiaceae)
【2h】

In-vitro Callus Induction and Rosmarinic Acid Quantification in Callus Culture of Satureja khuzistanica Jamzad (Lamiaceae)

机译:ature香(Samija khuzistanica Jamzad)(唇形科)的愈伤组织培养物中的体外愈伤组织诱导和迷迭香酸定量

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

In the present study, an efficient protocol has been developed for callus induction and production of RA in callus culture of Satureja khuzistanica for the first time. In-vitro callus induction was achieved from young shoot tip explants cultured on MS and B5 media supplemented with different concentrations of IBA (0.1, 1.0, 2.0 and 5.0 mgL-1) solely or in combination with cytokinins BAP and KIN (1.0, 2.0 and 5.0 mgL-1). B5 medium supplemented with 1.0 mgL-1 IBA plus 5.0 mgL-1 BAP and MS medium fortified with 2.0 mgL-1 IBA and 2.0 mgL-1 BAP were the most favorable media for callus formation with the highest induction rate (96%). Maximum growth index (2.89 and 2.63) and maximum callus biomass (2.34 and 2.33 g fresh weight) were obtained from the callus cultured on B5 medium supplemented with 1.0 mgL-1 IBA plus 5.0 mgL-1 BAP and MS medium fortified with 1.0 mgL-1 IBA plus 1.0 mgL-1 KIN, respectively. Determination and quantification of RA in cultured calli were performed by HPLC UV/MS analysis. Calli induced from the plant and maintained on supplements of IBA and BAP in the absence of light produced RA 7.5% based on dry weight (DW). No differentiation was observed in any callus during the course of this study.
机译:在本研究中,首次开发了一种有效的方案,用于在Satureja khuzistanica的愈伤组织培养物中诱导愈伤组织并产生RA。单独或与细胞分裂素BAP联合在不同浓度的IBA(0.1、1.0、2.0和5.0 mgL -1 )的MS和B5培养基上培养的幼芽尖端外植体可实现离体愈伤组织的诱导和KIN(1.0、2.0和5.0 mgL -1 )。补充了1.0 mgL -1 IBA和5.0 mgL -1 BAP的B5培养基以及MS培养基中添加了2.0 mgL -1 IBA和2.0 mgL < sup> -1 BAP是愈伤组织形成的最有利培养基,诱导率最高(96%)。从在补充有1.0 mgL -1 IBA和5.0 mgL -的B5培养基上培养的愈伤组织获得最大生长指数(2.89和2.63)和最大愈伤组织生物量(2.34和2.33 g鲜重)。 1 BAP和MS培养基分别添加1.0 mgL -1 IBA和1.0 mgL -1 KIN。通过HPLC UV / MS分析进行培养的愈伤组织中RA的测定和定量。从植物中诱导出的愈伤组织,并在没有光照的情况下维持在IBA和BAP的补品中,以干重(DW)计,产生的RA为7.5%。在该研究过程中,在任何愈伤组织中均未观察到分化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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