Yu Jianxiu, Xu Wei, Zeng Shaoling, Zhang Xinqiang, Liu Jingyu, Xie Ruiyu, Pang Yi
State Key Laboratory for Biocontrol, Zhongshan University, Guangzhou, People's Republic of China 510275.
Curr Microbiol. 2002 Nov;45(5):309-14. doi: 10.1007/s00284-002-3757-y.
Bacillus thuringiensis ( Bt) cyt genes coding hemolytic and cytolytic toxins constitute a gene family, which are divided into two groups: cyt1 and cyt2. A novel cyt2 gene was detected from a soil-isolated Bt strain T301, which was highly homologous to cyt2Ba1 and finally designated cyt2Ba7. Until now, Cyt2Ba has not been expressed alone in Bt or other hosts. In this study, the cyt2Ba7 gene was cloned into the vector pQE30 and expressed as a fusion protein with 6xHistidine residues in Escherichia coli. Unlike cyt1A, cyt2Ba7 was freely expressed and formed cytoplasmic inclusions without the need for a "helper" protein. The 6xHis-tagged Cyt2Ba7 was purified in one step by Ni-NTA affinity chromatography, examined cytolytic activity on Sf9 cells, and developed as an antigen to obtain the antiserum against Cyt2Ba by subcutaneous injection into rabbits. This gene was also cloned into the Bt-E. coli shuttle vector pHT3101 and expressed in Bt strain 4Q7. Immunoblotting analysis revealed that the antiserum was remarkably selective and specific to Cyt2Ba.
编码溶血和细胞溶解毒素的苏云金芽孢杆菌(Bt)cyt基因构成一个基因家族,该家族分为两组:cyt1和cyt2。从土壤分离的Bt菌株T301中检测到一个新的cyt2基因,它与cyt2Ba1高度同源,最终命名为cyt2Ba7。到目前为止,Cyt2Ba尚未在Bt或其他宿主中单独表达。在本研究中,将cyt2Ba7基因克隆到载体pQE30中,并在大肠杆菌中作为带有6x组氨酸残基的融合蛋白表达。与cyt1A不同,cyt2Ba7可以自由表达并形成细胞质内含物,无需“辅助”蛋白。带有6xHis标签的Cyt2Ba7通过Ni-NTA亲和层析一步纯化,检测其对Sf9细胞的细胞溶解活性,并将其作为抗原通过皮下注射到兔子体内获得抗Cyt2Ba的抗血清。该基因也被克隆到Bt-大肠杆菌穿梭载体pHT3101中并在Bt菌株4Q7中表达。免疫印迹分析表明,该抗血清对Cyt2Ba具有显著的选择性和特异性。