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Cloning and expression of nucleocapsid protein gene of TGEV HB06 strain

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 homolog...

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Autores principales: Fan, Jinghui, Zuo, Yuzhu, Zhao, Yuelan, Li, Tanqing, Zhang, Xiaobo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Higher Education Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088836/
https://www.ncbi.nlm.nih.gov/pubmed/32214985
http://dx.doi.org/10.1007/s11703-007-0060-5
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author Fan, Jinghui
Zuo, Yuzhu
Zhao, Yuelan
Li, Tanqing
Zhang, Xiaobo
author_facet Fan, Jinghui
Zuo, Yuzhu
Zhao, Yuelan
Li, Tanqing
Zhang, Xiaobo
author_sort Fan, Jinghui
collection PubMed
description 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.
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spelling pubmed-70888362020-03-23 Cloning and expression of nucleocapsid protein gene of TGEV HB06 strain Fan, Jinghui Zuo, Yuzhu Zhao, Yuelan Li, Tanqing Zhang, Xiaobo Front Agric China Research Article 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. Higher Education Press 2007 /pmc/articles/PMC7088836/ /pubmed/32214985 http://dx.doi.org/10.1007/s11703-007-0060-5 Text en © Higher Education Press and Springer-Verlag 2007 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Research Article
Fan, Jinghui
Zuo, Yuzhu
Zhao, Yuelan
Li, Tanqing
Zhang, Xiaobo
Cloning and expression of nucleocapsid protein gene of TGEV HB06 strain
title Cloning and expression of nucleocapsid protein gene of TGEV HB06 strain
title_full Cloning and expression of nucleocapsid protein gene of TGEV HB06 strain
title_fullStr Cloning and expression of nucleocapsid protein gene of TGEV HB06 strain
title_full_unstemmed Cloning and expression of nucleocapsid protein gene of TGEV HB06 strain
title_short Cloning and expression of nucleocapsid protein gene of TGEV HB06 strain
title_sort cloning and expression of nucleocapsid protein gene of tgev hb06 strain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088836/
https://www.ncbi.nlm.nih.gov/pubmed/32214985
http://dx.doi.org/10.1007/s11703-007-0060-5
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