Polyhedrosis Virus in Bacillus thuringiensis

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...

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Published inAgricultural sciences in China Vol. 10; no. 1; pp. 92 - 100
Main Authors YE, Xiang-li, XIA, Li-qiu
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.01.2011
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ISSN1671-2927
DOI10.1016/S1671-2927(11)60311-8

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Abstract 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.
AbstractList This study was conducted to build a recombinant strain with highly insecticidal activity and a wide host range by using the cry 1 Ac and p74 gene. Firstly, the p74 gene was amplified from the genosome of Autographa californica multicapsid nucleopolyhedrovirus. The cry1Ac gene and the terminator gene of cry1Ac, named cry1Act, 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 cry1Act, respectively, and two middle vectors, named pTp74Act and pT1Acp74 which held the aimed fusion gene p74-cry1Act and cry1Ac-p74, respectively, were built by using pMD18-T. Then pT1Acp74 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 Cry1Ac protein and 50 kDa P74 protein. The insecticidal activity of transformant against Spodoptera exigua was evaluated compared with the contrast strains HTX-42 (only cry1Ac gene was transformed into XBU001) after auto lysis. The LC₅† of HTX-42 was higher than that of the XBU-H1Acp74's, which implied that P74 could increase the efficacy and range of Bt Cry toxins in insect control. The fusion gene of cry1Ac and p74 were constructed successfully which will be served as the foundation for constructing the fusion genes of Bt cry gene and other foreign genes.
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.
This study was conducted to build a recombinant strain with highly insecticidal activity and a wide host range by using the cry 1 Ac and p74 gene. Firstly, the p74 gene was amplified from the genosome of Autographa californica multicapsid nucleopolyhedrovirus. The cry1Ac gene and the terminator gene of cry1Ac, named cry1Act, 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 cry1Act, respectively, and two middle vectors, named pTp74Act and pT1Acp74 which held the aimed fusion gene p74-cry1Act and cry1Ac-p74, respectively, were built by using pMD18-T. Then pT1Acp74 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 Cry1Ac protein and 50 kDa P74 protein. The insecticidal activity of transformant against Spodoptera exigua was evaluated compared with the contrast strains HTX-42 (only cry1Ac gene was transformed into XBU001) after auto lysis. The LC 50 of HTX-42 was higher than that of the XBU-H1Acp74's, which implied that P74 could increase the efficacy and range of Bt Cry toxins in insect control. The fusion gene of cry1Ac and p74 were constructed successfully which will be served as the foundation for constructing the fusion genes of Bt cry gene and other foreign genes.
Author YE Xiang-li XIA Li-qiu
AuthorAffiliation 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
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Cites_doi 10.1099/vir.0.81592-0
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Issue 1
Keywords Autographa californica multicapsid nucleopolyhedrovirus
p74 gene
cry1Ac gene
fusion gene
Bacillus thuringiensis
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Snippet 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...
This study was conducted to build a recombinant strain with highly insecticidal activity and a wide host range by using the cry 1 Ac and p74 gene. Firstly, the...
This study was conducted to build a recombinant strain with highly insecticidal activity and a wide host range by using the cry 1 Ac and p74 gene. Firstly, the...
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SubjectTerms Autographa californica multicapsid nucleopolyhedrovirus
Autographa californica multiple nucleopolyhedrovirus
Bacillus thuringiensis
Bt毒素
cry1Ac gene
cry1Ac基因
fusion gene
gene fusion
genes
host range
insect control
insecticidal properties
lethal concentration 50
p74 gene
p74基因
plasmids
polyacrylamide gel electrophoresis
Spodoptera exigua
toxins
viruses
基因转化
核多角体病毒
重组菌株
Title Polyhedrosis Virus in Bacillus thuringiensis
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Volume 10
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