Chak K F, Ellar D J
Department of Biochemistry, University of Cambridge, UK.
J Gen Microbiol. 1987 Oct;133(10):2921-31. doi: 10.1099/00221287-133-10-2921.
Using a gene probe derived from the cloned var. sotto insecticidal crystal protein (ICP) gene, we have cloned a Bacillus thuringiensis var. aizawai HD-133 ICP gene in Escherichia coli. The gene encodes a polypeptide that is toxic to Lepidoptera in vivo and in vitro. The protein is expressed at a level sufficient to produce phase-bright inclusions in recombinant E. coli strains, and these inclusions can be partially purified using discontinuous sucrose density gradients. Immunoblotting shows that the inclusions contain a 135 kDa polypeptide which reacts strongly with antiserum raised against the B. thuringiensis var. kurstaki HD-1 P1 polypeptide.
利用从克隆的苏云金芽孢杆菌变种 sotto 杀虫晶体蛋白(ICP)基因衍生而来的基因探针,我们在大肠杆菌中克隆了苏云金芽孢杆菌变种 aizawai HD - 133 的 ICP 基因。该基因编码一种在体内和体外对鳞翅目昆虫有毒的多肽。该蛋白在重组大肠杆菌菌株中的表达水平足以产生折光性强的包涵体,并且这些包涵体可以通过不连续蔗糖密度梯度进行部分纯化。免疫印迹显示,这些包涵体含有一种 135 kDa 的多肽,它与针对苏云金芽孢杆菌变种 kurstaki HD - 1 P1 多肽产生的抗血清发生强烈反应。