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首页|期刊导航|中国现代中药|22个白木香倍半萜合酶(AsTPS)基因的健康与伤害诱导表达特性研究

22个白木香倍半萜合酶(AsTPS)基因的健康与伤害诱导表达特性研究

吕菲菲 孙佩文 刘培卫 李俊 徐艳红 魏建和

中国现代中药2017,Vol.19Issue(8):1076-1082,7.
中国现代中药2017,Vol.19Issue(8):1076-1082,7.DOI:10.13313/j.issn.1673-4890.2017.8.005

22个白木香倍半萜合酶(AsTPS)基因的健康与伤害诱导表达特性研究

Study on Background and Wound Induced Expression of 22 Sesquiterpene Synthase Genes of Aquilaria sinensis

吕菲菲 1孙佩文 2刘培卫 1李俊 3徐艳红 2魏建和2

作者信息

  • 1. 中国医学科学院北京协和医学院药用植物研究所海南分所(海南省南药资源保护与开发重点实验室,国家中医药管理局沉香可持续利用重点研究室),海南 海口570311
  • 2. 中国医学科学院北京协和医学院药用植物研究所(中草药物质基础与资源利用教育部重点实验室,濒危药材繁育国家工程实验室),北京 100193
  • 3. 海南省食品药品检验所五指山分所,海南 五指山572200
  • 折叠

摘要

Abstract

Objective:TO confirm the expression mode of 22 sesquiterpene synthase in healthy and wound Aquilaria sinensis,and selected the key enzymes for catalyzing agarwood sesquiterpene synthesis.Methods:The branch of A.sinensis were treated by all broken method,the gene expression was tested by PCR and qRT-PCR.Results:1 gene expressed neither in the healthy nor wound trees.3 genes were silenced in healthey trees,but were obviously response to the external stimuli.Other 18 genes expressed in healthy samples among which 7 genes expression increased rapidly and the relative expression level was thousands of times and 11 genes also were induced to express but the relative expression level was dozens to hundreds times in short time after trees were wounded.Conclusion:21 sesquiterpene synthase genes are induced-genes and catalyze synthesis of agarwood sesquiterpenes.Among of them,3 enzymes are the pivotal enzymes for catalyzing sesquiterpene synthesis and 7 enzymes are the key enzymes for sesquiterpene synthesis in early period of agarwood formation in wound A.sinensis.

关键词

沉香/白木香/倍半萜合酶/伤害诱导/基因表达

Key words

Agarwood/Aquilaria sinensis/sesquiterpene synthase/wound-induce/gene expression

引用本文复制引用

吕菲菲,孙佩文,刘培卫,李俊,徐艳红,魏建和..22个白木香倍半萜合酶(AsTPS)基因的健康与伤害诱导表达特性研究[J].中国现代中药,2017,19(8):1076-1082,7.

基金项目

国家自然科学基因项目(NO.:81673549),海南省重大科技计划项目(ZDKJ2016004) (NO.:81673549)

海南省自然科学基金(NO.20163150) (NO.20163150)

中国现代中药

OACSTPCD

1673-4890

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