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SBR基因原核表达质粒的构建
引用本文:张苗,陈洪雷,姜广水,杨丕山,卞继峰.SBR基因原核表达质粒的构建[J].泰山医学院学报,2008,29(2):90-92.
作者姓名:张苗  陈洪雷  姜广水  杨丕山  卞继峰
作者单位:1. 解放军第88医院,山东,泰安,271000
2. 山东大学口腔医学院,山东,济南,250012
3. 山东大学西校区分子生物学教研室,山东,济南,250012
摘    要:目的构建可用于大肠杆菌表达系统的含变形链球菌唾液结合区段(SBR)基因的表达载体pcMVT7-SBR。方法用定向克隆方法将SBR基因插入表达载体pcMVT7,构建重组原核表达质粒pcMVT7-SBR。结果经酶切鉴定及DNA序列测定,重组质粒pcMVT7-SBR序列及阅读框架正确。结论SBR表达载体构建成功,为防龋疫苗的动物实验研究奠定基础。

关 键 词:唾液结合区段  构建  防龋疫苗
文章编号:1004-7115(2008)02-0090-03
修稿时间:2007年10月8日

Construction of prokaryotic expression vector of SBR gene
ZHANG Miao,CHEN Hong-lei,JIANG Guang-shui,YANG Pi-shan,BIAN Ji-feng.Construction of prokaryotic expression vector of SBR gene[J].Journal of Taishan Medical College,2008,29(2):90-92.
Authors:ZHANG Miao  CHEN Hong-lei  JIANG Guang-shui  YANG Pi-shan  BIAN Ji-feng
Institution:ZHANG Miao; CHEN Hong-lei; JIANG Guang-shui; YANG Pi-shan; BIAN Ji-feng(The 88th Hospital of PLA; Taian 271000; China);
Abstract:Objective: To obtain the prokaryotic expression vector containing the saliva binding region(SBR) gene of Streptococcus mutans.Methods: By directional cloning method,SBR gene fragment was cloned into the expression vector pcMVT7 and recombinant prokaryotic expression plasmid pcMVT7-SBR with right reading frame was successfully constructed.Results: Restriction endonuclease and DNA sequencing techniques were used to identify the recombinant plasmid DNA.The results were in correspondence with the initial design...
Keywords:SBR  construction  anti-caries vaccine
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