Godessart N, Muñoa F J, Regue M, Juárez A
Departamento de Microbiología, Facultad de Biología, Barcelona, Spain.
J Gen Microbiol. 1988 Oct;134(10):2779-87. doi: 10.1099/00221287-134-10-2779.
Transposon mutagenesis was used to isolate two Escherichia coli mutants which express very large amounts of haemolysin when carrying the multicopy plasmid pANN202-312. E. coli strain Hha-2 was isolated by Mud1 mutagenesis, and strain Hha-3 by Tn5 mutagenesis. The transposon insertion was chromosomal in both mutants and could be demonstrated to be unrelated to the haemolytic region of the plasmid. The substantial increase in both extracellular and intracellular haemolysin production was dependent upon plasmid copy number and was drastically reduced when either mutant carried the low-copy-number haemolytic plasmid pHly152. In both mutants, the marked increase in extracellular production was dependent upon the specific haemolysin transport genes, hlyB and hlyD. The lack of either gene function resulted in no external haemolysin production. SDS-PAGE analysis showed no change in the pattern of outer-membrane proteins of the mutants, although changes (differing between the two mutants) were seen in their periplasmic proteins. The mutations of both strains (termed hha-2 and hha-3) were mapped at minute 10.5 of the E. coli chromosome. No relation to any known gene affecting gene regulation in E. coli could be found.
转座子诱变被用于分离两个大肠杆菌突变体,当它们携带多拷贝质粒pANN202 - 312时会表达大量溶血素。通过Mud1诱变分离出大肠杆菌菌株Hha - 2,通过Tn5诱变分离出菌株Hha - 3。在这两个突变体中转座子插入均在染色体上,并且可以证明与质粒的溶血区域无关。细胞外和细胞内溶血素产量的显著增加取决于质粒拷贝数,当任一突变体携带低拷贝数溶血性质粒pHly152时,产量会大幅降低。在这两个突变体中,细胞外产量的显著增加取决于特定的溶血素转运基因hlyB和hlyD。缺乏任何一个基因功能都会导致细胞外无溶血素产生。SDS - PAGE分析表明,突变体的外膜蛋白模式没有变化,尽管它们的周质蛋白有变化(两个突变体之间不同)。这两个菌株(称为hha - 2和hha - 3)的突变定位在大肠杆菌染色体的10.5分钟处。未发现与大肠杆菌中任何已知影响基因调控的基因有相关性。