Polyhedrosis Virus in Bacillus thuringiensis

作     者：YE Xiang-li XIA Li-qiu 

作者机构：Key Laboratory of Microbial Biology of Hunan Province/College of Life Science Hunan Normal University Changsha 410081 P.R China College of Medicine Hunan Normal University Changsha 410013 P.R.China 

出 版 物：《Agricultural Sciences in China》 (中国农业科学（英文版）)

年 卷 期：2011年第10卷第1期

页      面：92-100页

核心收录：

学科分类：0710[理学-生物学] 1007[医学-药学(可授医学、理学学位)] 100705[医学-微生物与生化药学] 07[理学] 09[农学] 0904[农学-植物保护] 071005[理学-微生物学] 10[医学] 

基　　金：supported by the National Natural Science Foundation of China (30570050, 30670052) the National High Technology R&D Program of China (863Program, 2006AA02Z187) the National Ph D Programs Foundation of China (200-60542006) the Natural Science Foundation of Hunan Province, China(06JJ50062, 06JJ2009) 

主　　题：Bacillus thuringiensis Autographa californica multicapsid nucleopolyhedrovirus crylAc gene p74 gene fusion gene 

摘      要：This study was conducted to build a recombinant strain with highly insecticidal activity and a wide host range by using the crylAc and p74 gene. Firstly, the p74 gene was amplified from the genosome ofAutographa californica multicapsid nucleopolyhedrovirus. The crylAc gene and the terminator gene of crylAc, named crylAct, were amplified from the plasmid of Bt 4.0718 strain. Three T vectors, named pTp74, pT1Ac, and pT1Act which held the aimed gene p74, cry1Ac, and crylAct, respectively, and two middle vectors, named pTp74Act and pTIAcp74 which held the aimed fusion gene p74-crylAct and cry lAc-p74, respectively, were built by using pMDI 8-T. Then pTiAcp74 and the shuttle plasmid were digested and linked and an expressing-vector pH1Acp74 was built. Finally, pH1Acp74 was transformed into the acrystalliferous strain XBU001 and the aimed recombinant strain XBU-H1Acp74 was obtained. The expression of Bt transformant XBU-H1Acp74 was analyzed by SDS-PAGE which showed XBU-H1Acp74 could produce 130 kDa CrylAc protein and 50 kDa P74 protein. The insecticidal activity of transformant against Spodoptera exigua was evaluated compared with the contrast strains HTX-42 （only crylAc gene was transformed into XBU001） after autolysis. The LCs0 of HTX-42 was higher than that of the XBU-H IAcp74＇s, which implied that P74 could increase the efficacy and range of Bt Cry toxins in insect control. The fusion gene of crylAc and p74 were constructed successfully which will be served as the foundation lbr constructing the fusion genes of Bt cry gene and other foreign genes.