Howard S P, Buckley J T
Mol Gen Genet. 1986 Aug;204(2):289-95. doi: 10.1007/BF00425512.
The structural gene for the hemolytic toxin aerolysin has been cloned into the plasmid vectors pBR322 and pEMBL8+. The gene was localized on the hybrid plasmids by analysis of plasmids generated by transposon mutagenesis. The sequence of the first 683 bases of an insert in pEMBL8+ was determined and shown to encode the amino terminus of the protein as well as a typical signal sequence of 23 amino acids. Aerolysin is produced by E. coli cells containing the cloned aerolysin gene and it is processed normally by removal of the signal sequence, however it is not released from the cell. The protein appears to be translocated across the inner membrane of E. coli as its signal sequence is removed and the processed protein can be released by osmotic shock.
溶血毒素气溶素的结构基因已被克隆到质粒载体pBR322和pEMBL8+中。通过分析转座子诱变产生的质粒,将该基因定位在杂交质粒上。测定了pEMBL8+中一个插入片段的前683个碱基的序列,结果表明它编码该蛋白质的氨基末端以及一个由23个氨基酸组成的典型信号序列。含有克隆的气溶素基因的大肠杆菌细胞能产生气溶素,并且通过去除信号序列能正常加工,然而它不会从细胞中释放出来。由于其信号序列被去除,该蛋白质似乎能穿过大肠杆菌的内膜,并且经过加工的蛋白质可通过渗透压休克释放出来。