Cloning and expression of nucleocapsid protein gene of TGEV HB06 strain
FAN Jinghui1, ZUO Yuzhu1, LI Tanqing1, ZHANG Xiaobo1, ZHAO Yuelan2
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1.College of Animal Science and Veterinary Medicine, Agricultural University of Hebei, Baoding 071001, China; 2.College of Traditional Chinese Veterinary Medicine, Agricultural University of Hebei, Dingzhou 073000, China
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Published
05 Sep 2007
Issue Date
05 Sep 2007
Abstract
The nucleocapsid protein gene of transmissible gastroenteritis virus, 1 149 bp in length, was amplified by RT-PCR from isolated strain HB06 and cloned into pMD18-T. Sequence comparison with other transmissible gastroenteritis virus (TGEV) strains selected from the Gene Bank revealed that the homology of N gene complete sequence shares more than 97% in nucleotide. N gene was cloned into BamHI and EcoRI multiple cloning sites of the prokaryotic expression vector pET 20 b, and named pETN. After being induced by isopropyl-β-D-thiogalactopyranoside (IPTG), the recombinant nucleocapsid protein was expressed. The result of SDS-PAGE and Western-blot showed that the recombinant nucleocapsid protein was 47 kDa and had strong positive reactions with TGEV-specific antibody.
FAN Jinghui, ZUO Yuzhu, LI Tanqing, ZHANG Xiaobo, ZHAO Yuelan.
Cloning and expression of nucleocapsid protein gene of TGEV HB06 strain. Front. Agric. China, 2007, 1(3): 357‒360 https://doi.org/10.1007/s11703-007-0060-5
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