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Position: Home > Articles > Expression ofσC gene of muscovy duck reovirus,MW9710 strain,by using pMAL-p2X system Fujian Journal of Agricultural Sciences 2009,24 (5) 16-19

pMAL-p2X系统表达番鸭呼肠孤病毒MW9710株σC蛋白

作  者:
王劭;陈少莺;林锋强;程晓霞;朱小丽;陈仕龙;欧阳岁东
单  位:
福建省农业科学院畜牧兽医研究所
关键词:
番鸭呼肠孤病毒;σC蛋白;pMAL-p2X;原核表达
摘  要:
根据Genbank中MDRV 89026毒株S4基因序列设计引物,通过RT-PCR获得番鸭呼肠孤病毒MW9710株σC蛋白基因,将此σC蛋白基因插入原核表达载体pMAL-p2X中,得到重组表达质粒(pMAL-p2X-σC)并转化大肠杆菌BL21(DE3)中,经IPTG诱导后能高效表达,SDS-PAGE和Western-blot检测结果发现表达的σC蛋白分子质量约为72 kDa,并以可溶性蛋白和包涵体2种形式同时存在,且具有良好的反应原性。原核表达的可溶性σC蛋白为进一步开展抗原表位和诊断试剂盒研究奠定了基础。
译  名:
Expression ofσC gene of muscovy duck reovirus,MW9710 strain,by using pMAL-p2X system
作  者:
WANG Shao~(1,2),CHEN Shao-ying~(1,2),LIN Feng-qiang~(1,2),CHENG Xiao-xia~(1,2),ZHU Xiao-li~1, CHEN Shi-long~(1,2),OUYANG Sui-dong~1 (1.Institute of Animal Husbandry and Veterinary Medicine,Fujian Academy of Agricultural Sciences, Fuzhou,Fujian 350013,China;2.Fujian Animal Diseases Control Technology Development Center,Fuzhou,Fujian 350013,China)
关键词:
Muscovy duck revoirus;;σC protein;;pMAL-p2X;;prokaryotic expression
摘  要:
To obtain recombinant Muscovy duck reovirus(MDRV) _σC protein by prokaryotic expression for further study on its functions,the encoding sequence of the _σC gene from the MDRV MW9710 strain was amplified with RT-PCR and inserted into pMAL-p2X vector to establish the prokaryotic expression plasmid.After transforming the plasmid,pMAL-p2X-_σC,into E.coil BL21(DE3),the bacteria were induced by IPTG.The protein was expressed efficiently in both soluble and insoluble forms,and was positively recognized by the reference serum.The SDS-PAGE and western-blot analysis showed the recombinant pMAL-p2X-_σC produced had an apparent molecular weight of 72KDa.The soluble _σC protein was purified and obtained using MBP-affinity chromatography.The result provided a foundation for the gene's epitope identification and development of a clinical diagnostic kit in the future.

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