首页 | 本学科首页   官方微博 | 高级检索  
     

结核分支杆菌早期分泌性蛋白ESAT-6基因真核表达重组质粒的构建及鉴定
引用本文:蒋玉凤,张建军,钟森,史小玲,邓存良,王明勇. 结核分支杆菌早期分泌性蛋白ESAT-6基因真核表达重组质粒的构建及鉴定[J]. 泸州医学院学报, 2003, 26(6): 498-500
作者姓名:蒋玉凤  张建军  钟森  史小玲  邓存良  王明勇
作者单位:泸州医学院附属医院感染病科,四川泸州,646000
摘    要:
目的 :构建结核分支杆菌早期分泌性蛋白ESAT - 6真核表达重组质粒。方法 :以结核杆菌H37Rv株基因组DNA为模板 ,用PCR法对ESAT - 6基因进行扩增 ,PCR反应产物经酶切后 ,克隆于真核表达载体pcDNA3.1( )上。结果 :构建了结核杆菌基因ESAT - 6真核表达重组质粒pcDNA3.1( ) -ESAT - 6 ,测序报告ESAT - 6基因已正向克隆到真核表达质粒pcDNA3.1( )上。结论 :结核杆菌早期分泌性蛋白ESAT - 6真核表达重组质粒的成功构建为结核病的诊断、重组疫苗应用和免疫效应检测打下了基础。

关 键 词:结核分枝杆菌  早期分泌性蛋白  克隆  真核表达
文章编号:1000-2669(2003)6-0498-03
修稿时间:2003-07-20

CONSTRUCTION AND IDENTIFICATION OF EUKARYOTIC EXPRESSION RECOMBINANT PLASMID OF ESAT-6 FROM MYCOBACTERIUM TUBERCULOSIS
Jiang Yufeng,et al. CONSTRUCTION AND IDENTIFICATION OF EUKARYOTIC EXPRESSION RECOMBINANT PLASMID OF ESAT-6 FROM MYCOBACTERIUM TUBERCULOSIS[J]. Journal of Luzhou Medical College, 2003, 26(6): 498-500
Authors:Jiang Yufeng  et al
Affiliation:Jiang Yufeng,et al Department of Infectious disease,Luzhou Medical hospital
Abstract:
Objective: To Construct eukaryotic expression recombinant plasmid of ESAT-6. Methods: The gene encoding for protein ESAT-6 was amplified from M.tuberculosis H37Rv genomic DNA by using PCR technique and ESAT-6 gene was ligated to eukaryotic expression vector pcDNA3.1( ).Result: ESAT-6 gene was successfully inserted into the eukaryotic expression vector pcDNA3.1( ).Conclusion: The recombinant eukaryotic expression plasmid pcDNA3.1( )-ESAT-6 has been constructed. It may lay foudations for the diagnosis, the application of new vaccine of tuberculosis and the detecting of immunity effectiveness.
Keywords:Mycobacterium tuberculosis  ESAT-6  Eukaryotic expression
本文献已被 CNKI 维普 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