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猪PR-39基因的克隆及在大肠杆菌中的串联表达载体的构建
引用本文:扈进冬,吴远征,杨合同.猪PR-39基因的克隆及在大肠杆菌中的串联表达载体的构建[J].中国畜牧兽医,2008,35(12):56-59.
作者姓名:扈进冬  吴远征  杨合同
作者单位:1.山东省科学院中日友好生物技术研究中心,山东省应用微生物重点实验室, 济南 250014;2.山东省科学院生物所, 济南 250014; 3.山东理工大学生命科学院, 淄博 255049
基金项目:国家高技术研究发展计划(863计划) 
摘    要:采用重叠区扩增法人工合成了大肠杆菌偏爱密码子的猪PR 39基因片段,并克隆至pMD18T中,经测序确认正确后,与pET Trx构建了串联表达载体pET-Trx-(PR-39)3,并在大肠杆菌BL21 (DE3)中诱导获得表达。为PR-39的进一步开发与应用打下了基础。

关 键 词:PR-39  串联  载体构建  

Cloning of Gene PR-39 from Pig and Construction of PR-39 as Tandem Repeats Expression Vector in E coli
HU Jin-dong,WU Yuan-zheng,YANG He-tong.Cloning of Gene PR-39 from Pig and Construction of PR-39 as Tandem Repeats Expression Vector in E coli[J].China Animal Husbandry & Veterinary Medicine,2008,35(12):56-59.
Authors:HU Jin-dong  WU Yuan-zheng  YANG He-tong
Institution:1.Biotechnology Center of Shandong Academy of Sciences,Key Laboratory for Applied Microbiology of Shandong Province,Jinan 250014,China; 2.Biology Institute of Shandong Academy of Sciences,Jinan 250014,China;3. School of Life Sciences,Shandong University of Technology,Zibo 255049, China
Abstract:Gene RP-39 from pig with the partiality of E coli was synthesized by the method of gene splicing by overlap extension.The fragment was cloned into pMD18-T and sequenced.Three copies of gene RP-39 were combinated into express vector pET-Trx.Then pET-Trx-(PR-39)3 was transformed into E coli BL21(DE3) and RP-39 was inducted which established good foundation for the future development.
Keywords:gene synthesis  PR-39  tandem repeats  construction of expression vector
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