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Cloning, sequencing and expression of the coat protein gene of Cocksfoot mottle virus
作者姓名:DONG Zhi  GUO Xiaoyu  ZHANG Hailong and ZHANG Feiyun
作者单位:College of Life Science,Capital Normal University,Beijing 100037,China; College of Resources Environment and Tourism,Capital Normal University,Beijing 100037,China; Beijing Key Laboratory for Resources Environment and Geography Information System,Beijing 100037,China
基金项目:Supported by National Natural Science Foundation of China (Grant No. 30571010),Key Program of Scientific and Technological Research of Ministry of Education (No. 204006)
摘    要:The coat protein (CP) gene of Cocksfoot mottle virus (CfMV) was amplified by RT-PCR and inserted into expression vector pGEX-4T-1, and the resulting plasmid was designated as pGEXCfMV-JANCP. The fusion protein GST-CP was expressed in BL21 (DE3) pLysS after IPTG induction. The results of SDS-PAGE and Western blot analysis showed that the CfMV-CP gene was efficiently expressed in E. coli BL21 (DE3) pLysS through IPTG induction and the 56.0 kD protein was obtained.


Cloning, sequencing and expression of the coat protein gene of Cocksfoot mottle virus
DONG Zhi,GUO Xiaoyu,ZHANG Hailong and ZHANG Feiyun.Cloning, sequencing and expression of the coat protein gene of Cocksfoot mottle virus[J].Progress in Natural Science,2007,17(2):222-225.
Authors:DONG Zhi  GUO Xiaoyu  ZHANG Hailong
Abstract:The coat protein (CP) gene of Cocksfoot mottle virus (CfMV) was amplified by RT-PCR and inserted into expression vector pGEX-4T-1, and the resulting plasmid was designated as pGEXCfMV-JANCP. The fusion protein GST-CP was expressed in BL21 (DE3) pLysS after IPTG induction. The results of SDS-PAGE and Western blot analysis showed that the CfMV-CP gene was efficiently expressed in E. coli BL21 (DE3) pLysS through IPTG induction and the 56.0 kD protein was obtained.
Keywords:Cocksfoot mottle virus  sequence analysis  prokaryotic expression  
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