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弓形虫RH株微线体蛋白MIC3基因的克隆与表达
引用本文:李军建,张仁利,傅玉才,耿艺介,黄达娜,胡忠. 弓形虫RH株微线体蛋白MIC3基因的克隆与表达[J]. 热带医学杂志, 2010, 10(10)
作者姓名:李军建  张仁利  傅玉才  耿艺介  黄达娜  胡忠
作者单位:汕头大学医学院寄生虫教研室;深圳市疾病预防控制中心;
摘    要:目的 克隆和表达弓形虫微线体蛋白MIC3基因。方法 从弓形虫RH株分离总的RNA,反转成cDNA.根据MIC3基因序列,设计合成一对引物,用聚合酶链式反应(PCR)方法从弓形虫cDNA中扩增MIC3基因片段,插入pGEM-T载体,并转化大肠杆菌Top10,经PCR、双酶切、测序验证后,将MIC3基因片段定向亚克隆到载体pET-28a中构建原核表达重组质粒pET-28a-MIC3,重组子在E.coli BL21中经IPTG诱导表达,并对表达产物进行SDS-PAGE和Western-blot分析。结果 从弓形虫RH株cDNA中扩增出792bp大小的MIC3基因片段并诱导表达27 300 Mr的重组MIC3蛋白。结论 成功构建和表达了弓形虫pET-28a-MIC3重组质粒,为弓形虫病诊断抗原和疫苗的研究莫定了基础。

关 键 词:弓形虫  MIC3  PCR  基因克隆  原核表达

Cloning and Expression of MIC3 Gene of Toxoplasma gondii RH Strain
LI Jun-jian,ZHANG Ren-li,FU Yu-cai,GENG Yi-jie,HUANG Da-na,HU Zhong. Cloning and Expression of MIC3 Gene of Toxoplasma gondii RH Strain[J]. Journal Of Tropical Medicine, 2010, 10(10)
Authors:LI Jun-jian  ZHANG Ren-li  FU Yu-cai  GENG Yi-jie  HUANG Da-na  HU Zhong
Affiliation:LI Jun-jian1,2,ZHANG Ren-li2*,FU Yu-cai1,GENG Yi-jie2,HUANG Da-na2,HU Zhong1(1.Shantou University,Shantou 515063,2.Shenzhen Center for Disease Control and Prevention,Shenzhen 518020,China)
Abstract:Objective To clone and express the gene encoding micronemal protein MIC3 of Toxoplasma gondii RH.Methods Total RNA,isolated from T.gondii was reverse-transcribed into cDNAs.According to the sequence of MIC 3 gene,a pair of primers were designed and synthesized.A specific cDNA fragment of MIC3 gene was obtained by amplification of the cDNAs of T.gondii.After purification,the fragments of PCR products was cloned into pGEM-T vector,and then transferred into E.coli Top10.Positive clones was isolated and verifie...
Keywords:Toxoplasma gondii  MIC3  PCR  gene cloning  protein expression  
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