首页 | 本学科首页   官方微博 | 高级检索  
     检索      

二色补血草LbGST基因的原核表达载体构建与表达
引用本文:刁桂萍,刘彬令,雷作霖,郭荫久,王玉成.二色补血草LbGST基因的原核表达载体构建与表达[J].东北林业大学学报,2011,39(4):125-126.
作者姓名:刁桂萍  刘彬令  雷作霖  郭荫久  王玉成
作者单位:东北林业大学;
基金项目:中央高校基本科研业务费专项资金项目(DL09AA02); 东北林业大学大学生创新性实验项目
摘    要:从二色补血草(Limonium bicolor)中分离出一个编码谷胱甘肽硫转移酶(LbGST)基因,并将该基因构建到pGEX-4T-2原核表达载体,转入大肠杆菌(Escherichia coli)BL21中,利用0.1 mmol/L的IPTG诱导该基因在大肠杆菌BL21中进行表达.SDS-PAGE检测表明,出现了特异的...

关 键 词:二色补血草  谷胱甘肽硫转移酶  原核表达

Cloning and Prokaryotic Expression of a Glutathione S-Transferase Gene from Limonium bicolor
Diao Guiping,Liu Binling,Lei Zuolin,Guo Yinjiu,Wang Yucheng.Cloning and Prokaryotic Expression of a Glutathione S-Transferase Gene from Limonium bicolor[J].Journal of Northeast Forestry University,2011,39(4):125-126.
Authors:Diao Guiping  Liu Binling  Lei Zuolin  Guo Yinjiu  Wang Yucheng
Institution:Diao Guiping,Liu Binling,Lei Zuolin,Guo Yinjiu,Wang Yucheng(School of Forestry,Northeast Forestry University,Harbin 150040,P.R.China)
Abstract:A glutathione S-transferase(GST) gene was cloned from a cDNA library of Limonium bicolor(Bunge) Kuntze(Plumbaginaceae).The LbGST gene was inserted into the prokaryotic expression vector pGEX-4T-2,and then transformed into E.coli BL21.The expression of GST gene in E.coli BL21 was induced by 0.01 mmol/L IPTG.SDS-PAGE results indicated that a specific band with molecular weight of 50 kDa displayed by transformants was the target peptide,indicating that it was successfully expressed in E.coli.This research will...
Keywords:Limonium bicolor  Glutathione S-transferase  Prokaryotic expression  
本文献已被 CNKI 万方数据 等数据库收录!
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