Manning P A, Brown M H, Heuzenroeder M W
Gene. 1984 Nov;31(1-3):225-31. doi: 10.1016/0378-1119(84)90213-0.
We have cloned the DNA encoding the haemolysin of Vibrio cholerae El Tor strain 017 into the plasmid vector pBR322. The resultant plasmid, pPM431, has a 6.2-kb PstI DNA insert which leads to the production of the haemolysin in Escherichia coli K-12. Deletion analysis and transposon mutagenesis have allowed us to localize several regions affecting haemolysin production. A number of these mutants have been analysed in E. coli K-12 minicells. Three proteins have been identified: A, 80 kDal; B, 71 kDal; and C, 22 kDal. A is the haemolysin which appears to be cell-associated in E. coli K-12, and B and C are required for its efficient production. We suggest that the genes for proteins A, B and C be designated hlyA, hlyB and hlyC, respectively.
我们已将编码霍乱弧菌埃尔托生物型017溶血素的DNA克隆到质粒载体pBR322中。所得质粒pPM431有一个6.2kb的PstI DNA插入片段,可导致大肠杆菌K-12产生溶血素。缺失分析和转座子诱变使我们能够定位几个影响溶血素产生的区域。已在大肠杆菌K-12微小细胞中分析了许多这些突变体。已鉴定出三种蛋白质:A,80kDal;B,71kDal;C,22kDal。A是溶血素,在大肠杆菌K-12中似乎与细胞相关,B和C是其有效产生所必需的。我们建议将蛋白质A、B和C的基因分别命名为hlyA、hlyB和hlyC。