首页 | 官方网站   微博 | 高级检索  
     

苹果S6PDH基因克隆与原核表达
引用本文:梁东,马锋旺,张敏. 苹果S6PDH基因克隆与原核表达[J]. 西北植物学报, 2008, 28(1): 33-36
作者姓名:梁东  马锋旺  张敏
作者单位:西北农林科技大学,园艺学院,陕西杨陵,712100
基金项目:陕西省重大科技专项计划项目(2006kz05-G4),西北农林科技大学“拔尖人才支持计划”
摘    要:6-磷酸山梨醇脱氢酶(sorbitol-6-phosphate dehydrogenase,S6PDH)是蔷薇科植物中合成山梨醇的重要酶。以苹果叶片为材料,利用RT-PCR法克隆到S6PDHcDNA全长,将其与大肠杆菌表达载体pET-32a( )构建原核表达载体pET-S并转化大肠杆菌BL21,经IPTG诱导表达后,SDS-PAGE检测结果表明该基因表达了1个约54kD的蛋白,为进一步研究目的蛋白的结构和功能提供了试验基础。

关 键 词:苹果  山梨醇  6-磷酸山梨醇脱氢酶  原核表达
文章编号:1000-4025(2008)01-0033-04
收稿时间:2007-07-27
修稿时间:2007-10-22

Cloning and Prokaryotic Expression of Apple S6PDH Gene
LIANG Dong,MA Feng-wang,ZHANG Min. Cloning and Prokaryotic Expression of Apple S6PDH Gene[J]. Acta Botanica Boreali-Occidentalia Sinica, 2008, 28(1): 33-36
Authors:LIANG Dong  MA Feng-wang  ZHANG Min
Abstract:Sorbitol-6-phosphate dehydrogenase(S6PDH) is a key enzyme for the biosynthesis of sorbitol in Rosaceae plants.S6PDH cDNA was amplified by RT-PCR from apple leaf,then was cloned into pET-32a( ) vector to construct recombinant prokaryotic expression vector pET-S.The pET-S was transformed to E.coli BL21.After induced by IPTG,a 54 kD recombinant protein was expressed and separated by SDS-PAGE electrophoresis.The research provides a base for further studying on the protein mechanism and the potential applications of sorbitol-6phosphate dehydrogenase.
Keywords:apple  sorbitol  sorbitol-6-phosphate dehydrogenase  prokaryotic expression
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《西北植物学报》浏览原始摘要信息
点击此处可从《西北植物学报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司    京ICP备09084417号-23

京公网安备 11010802026262号