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在非生物胁迫条件下通过愈伤组织培养从匙羹藤(Gymnema sylvestre (Retz) R. Br. ex roemer and schultes)中体外生产匙羹藤酸。

In vitro production of gymnemic acid from Gymnema sylvestre (Retz) R. Br. ex roemer and schultes through callus culture under abiotic stress conditions.

作者信息

Ali Ahmed Abdul Bakrudeen, Rao Adhikarla Suryanarayana, Rao Mandali Venkateswara

机构信息

Department of Plant Science, School of Life Sciences, Bharathidasan University, Tiruchirappalli, Tamil Nadu, India.

出版信息

Methods Mol Biol. 2009;547:93-105. doi: 10.1007/978-1-60327-287-2_8.

Abstract

Plant secondary metabolites have enormous potential for research and new drug development. Many secondary metabolites have a complex and unique structure and their production is often enhanced by biotic and abiotic stress conditions. Gymnemic acid (C(43)H(68)O(14)), a pentacyclic triterpenoid isolated from the leaves of Gymnema sylvestre, exhibits potent inhibitory effect on diabetes. The gymnemic acid content is determined by chromatographic methods: Camag HPTLC system equipped with a sample applicator Linomat IV and TLC scanner and integration software CAT 4.0. In HPLC C(18) (ODS) reverse phase column; water 486 UV detector; mobile phase, water/methanol (35:65, HPLC grade) + 0.1% acetic acid are used. Sample (20 microL) is applied with a flow rate of 1 mL/min and read at 230 nm with UV detector. The production of gymnemic acid is significantly higher in callus treated with 2,4-dichloro phenoxy acetic acid (2,4-D) and kinetin (KN). The blue light increases gymnemic acid accumulation upto 4.4-fold as compared with fluorescent light treatment and out of which 2.8 is found in leaves. Gymnemic acid is isolated from callus, grown under stress conditions followed by preparative TLC, simple and reproducible character based on HPTLC and high performance liquid chromatography.

摘要

植物次生代谢产物在研究和新药开发方面具有巨大潜力。许多次生代谢产物具有复杂独特的结构,其产生往往会受到生物和非生物胁迫条件的增强。匙羹藤酸(C(43)H(68)O(14)),一种从匙羹藤叶子中分离出的五环三萜类化合物,对糖尿病具有显著的抑制作用。匙羹藤酸含量通过色谱方法测定:配备自动点样器Linomat IV、薄层色谱扫描仪和积分软件CAT 4.0的Camag高效薄层色谱系统。在高效液相色谱中使用C(18)(ODS)反相柱;水486紫外检测器;流动相为水/甲醇(35:65,高效液相色谱级)+0.1%乙酸。进样量为20微升,流速为1毫升/分钟,用紫外检测器在230纳米处检测。用2,4 - 二氯苯氧乙酸(2,4 - D)和激动素(KN)处理的愈伤组织中匙羹藤酸的产量显著更高。与荧光灯处理相比,蓝光可使匙羹藤酸积累量增加至4.四倍,其中2.8倍的积累量出现在叶片中。匙羹藤酸是从在胁迫条件下生长的愈伤组织中分离得到的,随后通过制备薄层色谱法进行分离,基于高效薄层色谱和高效液相色谱具有简单且可重复的特性。

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