Barry E M, Weiss A A, Ehrmann I E, Gray M C, Hewlett E L, Goodwin M S
Department of Microbiology and Immunology, Medical College of Virginia, Richmond 23298.
J Bacteriol. 1991 Jan;173(2):720-6. doi: 10.1128/jb.173.2.720-726.1991.
In these studies, the Bordetella pertussis adenylate cyclase toxin-hemolysin homology to the Escherichia coli hemolysin is extended with the finding of cyaC, a homolog to the E. coli hlyC gene, which is required for the production of a functional hemolysin molecule in E. coli. Mutations produced in the chromosome of B. pertussis upstream from the structural gene for the adenylate cyclase toxin revealed a region which was necessary for toxin and hemolytic activities of the molecule. These mutants produced the 216-kDa adenylate cyclase toxin as determined by Western blot (immunoblot) analysis. The adenylate cyclase enzymatic activities of these mutants were equivalent to that of wild type, but toxin activities were less than 1% of that of wild type, and the mutants were nonhemolytic on blood agar plates and in in vitro assays. The upstream region restored hemolytic activity when returned in trans to the mutant strains. This genetic complementation defined a gene which acts in trans to activate the adenylate cyclase toxin posttranslationally. Sequence analysis of the upstream region defined an open reading frame with homology to the E. coli hlyC gene. In contrast to E. coli, this open reading frame is oriented oppositely from the adenylate cyclase toxin structural gene.
在这些研究中,百日咳博德特氏菌腺苷酸环化酶毒素 - 溶血素与大肠杆菌溶血素的同源性得到扩展,发现了cyaC,它是大肠杆菌hlyC基因的同源物,大肠杆菌中功能性溶血素分子的产生需要该基因。在百日咳博德特氏菌染色体上腺苷酸环化酶毒素结构基因上游产生的突变揭示了一个对该分子的毒素和溶血活性必不可少的区域。通过蛋白质印迹(免疫印迹)分析确定,这些突变体产生了216 kDa的腺苷酸环化酶毒素。这些突变体的腺苷酸环化酶酶活性与野生型相当,但毒素活性不到野生型的1%,并且这些突变体在血琼脂平板上和体外试验中无溶血活性。当以反式导入突变菌株时,上游区域恢复了溶血活性。这种遗传互补确定了一个基因,该基因通过反式作用在翻译后激活腺苷酸环化酶毒素。上游区域的序列分析确定了一个与大肠杆菌hlyC基因具有同源性的开放阅读框。与大肠杆菌不同,这个开放阅读框的方向与腺苷酸环化酶毒素结构基因相反。