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Expression of vip2A(c) gene from Bacillus thuringiensis in insect cells

Published online by Cambridge University Press:  20 March 2007

Shi Yong-Xia
Affiliation:
State Key Laboratory for Biocontrol, Zhongshan (Sun Yat-sen) University, Guangzhou 510275, China Guangdong Inspection and Quarantine Technology Center, Guangzhou 510623, China
Lv Lei
Affiliation:
State Key Laboratory for Biocontrol, Zhongshan (Sun Yat-sen) University, Guangzhou 510275, China
Xu Wei
Affiliation:
State Key Laboratory for Biocontrol, Zhongshan (Sun Yat-sen) University, Guangzhou 510275, China
Yuan Mei-Jin
Affiliation:
State Key Laboratory for Biocontrol, Zhongshan (Sun Yat-sen) University, Guangzhou 510275, China
Pang Yi*
Affiliation:
State Key Laboratory for Biocontrol, Zhongshan (Sun Yat-sen) University, Guangzhou 510275, China
*
*Corresponding author. E-mail: ls12@zsu.edu.cn

Abstract

Recombinant Bac-GV2 DNA was obtained by inserting a fused gfp gene with the Bacillus thuringiensis vip2A(c) gene encoding a possible enzymatic component under the control of the polyhedrin gene promoter of the baculovirus Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV). The Trichoplusia ni cell line TnHi5 was transfected with Bac-GFP and Bac-GV2 DNAs respectively. Fluorescent cells expressing the fusion protein GV2 were much fewer than those expressing green fluorescent protein (GFP) alone, and did not obviously increase in number from 2 to 5 days after transfection. This result showed that the Vip2A fusion protein might have an ADP-ribosylating activity on cell skeleton actin, exerting an influence on the production and diffusion of the budded virus from insect cells.

Type
Research Article
Copyright
China Agricultural University and Cambridge University Press 2006

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