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马动脉炎病毒N蛋白基因GST融合表达载体的构建及表达
引用本文:杜建,王志亮,宋厚辉,金宁一,张念祖.马动脉炎病毒N蛋白基因GST融合表达载体的构建及表达[J].动物医学进展,2005,26(9):50-54.
作者姓名:杜建  王志亮  宋厚辉  金宁一  张念祖
作者单位:农业部动物检疫所
基金项目:农业部诊断技术标准;农业部重点实验室基金
摘    要:采用RT-PCR方法扩增出马动脉炎病毒核衣壳蛋白基因0RF7,并将其克隆到pMDl8-T载体,构建成重组质粒pMDl8-N,在上海生物工程公司测序。结果表明,所克隆的核衣壳蛋白基因序列与EAVNC-002532株的同源性为99%。表明0RF7是EAV基因组内的保守序列,将0RF7亚克隆到原核表达载体pGEX-6P-1中,构建成重组质粒pGEX-6P-N,用pGEX-6P-N转化表达菌株BL21(DE3),诱导表达后SDS-PAGE和Westernblotting分析表明,克隆在谷胱苷肽硫转移酶(GST)下游的核衣壳蛋白基因与GST获得了高效融合表达,表达的融合蛋白GST-N分子质量约为40ku,为马动脉炎病毒病血清学诊断方法的建立奠定了基础。

关 键 词:马动脉炎病毒  核衣壳蛋白基因  克隆  原核表达
文章编号:1007-5038(2005)09-0050-05
收稿时间:2005-03-08
修稿时间:2005年3月8日

Construction and Prokaryotic Expression of Equine arteritis virus Fusion N Protein with GST in E.coli
DU Jian,WANG Zhi-liang,SONG Hou-hui,JIN Ning-yi,ZHANG Nian-zu.Construction and Prokaryotic Expression of Equine arteritis virus Fusion N Protein with GST in E.coli[J].Progress In Veterinary Medicine,2005,26(9):50-54.
Authors:DU Jian  WANG Zhi-liang  SONG Hou-hui  JIN Ning-yi  ZHANG Nian-zu
Abstract:The nucleocapsid protein gene(ORF7) of Equine arteritis virus(EAV) was isolated from EAV genome by RT-PCR.The gene was cloned into pMD18-T vector,the recombinant plasmid pMD18-N containing ORF7 was sequenced and compared with other EAV isolates.The result shows that the homologies between the cloned ORF7 and EAV NC-002532 strain reached 99 %,the ORF7 was highly conservative sequence in EAV genome.The ORF7 was subcloned into prokaryotic expressing vector pGEX-6P-1,the recombinant plasmid named pGEX-6P-N was constructed.The pGEX-6P-N was used to transform into E.coli BL21(DE3).The results of SDS-PAGE and Western-blot indicated that the nucleocapsid protein gene cloned in downstream of Glutathione S-transferase(GST) was expressed in a high level and the recombinant fusion protein,which was about 40kDa,had immunologically reactive activity.The study lay on foundation for the development of the diagnosis methods in serology for EAV.
Keywords:Equine arteritis virus  nucleocapsid protein gene  cloning  prokaryotic expression
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