Bacillus thuringiensis helper protein P20 affects the formation of Cry1Ab.
- Author:
Mu-Jin TANG
1
;
Mei-Jin YUAN
;
Jian-Wu CHEN
;
Yong-Xia SHI
;
Shao-Ling ZENG
;
Jian-Xiu YU
;
Yi PANG
Author Information
1. State Key Laboratory for Biocontrol, Zhongshan University, Guangzhou 510275, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Bacillus thuringiensis;
genetics;
metabolism;
ultrastructure;
Bacterial Proteins;
genetics;
metabolism;
pharmacology;
Biological Assay;
methods;
Blotting, Western;
Electroporation;
Endotoxins;
genetics;
metabolism;
pharmacology;
Hemolysin Proteins;
genetics;
metabolism;
pharmacology;
Microscopy, Electron, Transmission;
Moths;
drug effects;
Promoter Regions, Genetic;
genetics
- From:
Chinese Journal of Biotechnology
2003;19(5):566-571
- CountryChina
- Language:Chinese
-
Abstract:
The Cry1Ab differs most significantly from the other related ICPs by its absence of a carboxyl terminus of 28 amino acids including four cysteines; consequently it is less stable. We report that the helper protein P20 plays a role in the expression and crystallization of Cry1Ab. Three Cry1Ab expression plasmids pT1B, pP1B, and pDP1B, were constructed based on the shuttle vector pHT3101. The vector pT1B does not contain the p20 gene, pP1B carries p20, and pDP1B contains p20 with cry1A(c) promoter. Transformants were obtained by electroporating the plasmids into Bacillus thuringiensis acrystalliferous mutant CryB. Western blot demonstrated that crylAb was expressed as a 130 kD protein in all the transformants, and some of the protein was partially degraded into a 60 kD peptide. Quantitative protein analysis indicated that the amount of the 130 kD protein varied in the transformants and was in the ratio of 1:1.4:1.5 for PT1B, pP1B and pDP1B respectively. For the 60 kD proteins, the ratio was 1:1.1:1.6. Microscopic examination revealed that the size of the typical pyramidal crystals in the three transformants was in the order of T1B < P1B < DP1B. Bioassay showed that T1B, P1B and DP1B were all toxic to the larvae of Helicoverpa armigera with similar LC50. This study suggested that P20 plays a role in the expression and crystallization of Cry1Ab.
