Expression of gene aiiA carrying the promoter of gene cry3Aa in Bacillus thuringiensis.
- Author:
Chen-Guang ZHU
1
;
Ming SUN
;
Zi-Niu YU
Author Information
1. College of Life Science and Technology, Key Laboratory of Agricultural Microbiology of Ministry of Education and Agriculture, Huazhong Agricultural University, Wuhan 430070, China.
- Publication Type:Journal Article
- MeSH:
Acyl-Butyrolactones;
metabolism;
Bacterial Proteins;
genetics;
metabolism;
Daucus carota;
microbiology;
Endotoxins;
genetics;
metabolism;
Hemolysin Proteins;
genetics;
metabolism;
Metalloendopeptidases;
genetics;
metabolism;
Models, Genetic;
Pectobacterium carotovorum;
pathogenicity;
Plant Diseases;
microbiology;
prevention & control;
Promoter Regions, Genetic;
genetics;
Recombinant Proteins;
genetics;
metabolism
- From:Chinese Journal of Biotechnology
2003;19(4):397-401
- CountryChina
- Language:Chinese
-
Abstract:
N-acyl-homoserine lactones (AHLs), are widely conserved signal molecules present in quorum-sensing systems of many Gram-negative bacteria. AHLs molecules mediate the expression of virulence genes of a range of bacterial pathogens. Recently, it has been reported that AiiA protein, which widely exists in Bacillus species, can inactivate the AHLs by hydrolyzing the lactone bond of AHLs, thus attenuate the diseases caused by the expression of virulence genes of bacterial pathogens. Bacillus thuringiensis, a type of Gram-positive bacteria, has been used extensively as a microbial insecticide in the last few decades. However, most of important insecticidal B. thuringiensis strains have not been exploited for bacterial disease control because they usually do not produce antibiotics that are effective against bacteria and fungi. The discovery of AiiA protein in B. thuringiensis shows the application potential of B. thuringiensis on biocontrol against bacterial diseases. In this study, in order to construct the B. thuringiensis recombinant strain that has high expression of AiiA protein, the promoter of insecticidal crystal protein coding gene cry3Aa of B. thuringiensis was selected. The promoter of gene cry3Aa is a non-sporulation promoter, it promotes the transcription earlier and longer than the promoters of other cry genes. The promoter of AiiA protein coding gene aiiA was replaced with the promoter of gene cry3Aa by overlapping PCR, resulting fusion gene pro3A-aiiA. The gene pro3A-aiiA was inserted into shuttle vector pHT304 at site BamH I / Sph I , resulting recombinant plasmid pBMB686. The plasmid pBMB686 was introduced into B. thuringiensis acrystalliferous strain BMB171, the resulting strain BMB686 had a higher and more stable expression level of protein AiiA comparing with the parental strain BMB171. Furthermore, the strain BMB686 exhibited stronger ability of AHLs inactivation and much more effective restraint to the potato's soft rot disease caused by Erwinia carotovora than those of the parental strain BMB171. From these results, it was concluded that the B. thuringiensis strain harvesting the fusion gene pro3A-aiiA may be utilized in the future to control bacterial diseases which are mediated by the AHL quorum-sensing signals.
