Pilsl H, Killmann H, Hantke K, Braun V
Mikrobiologie II, Universität Tübingen, Germany.
J Bacteriol. 1996 Apr;178(8):2431-5. doi: 10.1128/jb.178.8.2431-2435.1996.
The pesticin activity and immunity genes on plasmid pPCP1 of Yersinia pestis were sequenced. They encoded proteins of 40 kDa (pesticin) and 16 kDa (immunity protein); the latter was found in the periplasm. The location of the immunity protein suggests that imported pesticin is inactivated in the periplasm before it hydrolyzes murein. Pesticin contains a TonB box close to the N-terminal end that is identical to the TonB box of colicin B. The DNA sequences flanking the pesticin determinant were highly homologous to those flanking the colicin 10 determinant. It is proposed that through these highly homologous DNA sequences, genes encoding bacteriocins may be exchanged between plasmids by recombination. In the case of pesticin, recombination may have destroyed the lysis gene, of which only a rudimentary fragment exists on pPCP1.
对鼠疫耶尔森菌质粒pPCP1上的杀鼠菌素活性和免疫基因进行了测序。它们编码40 kDa的蛋白质(杀鼠菌素)和16 kDa的蛋白质(免疫蛋白);后者存在于周质中。免疫蛋白的位置表明,导入的杀鼠菌素在水解胞壁质之前就在周质中失活。杀鼠菌素在靠近N端处含有一个与大肠杆菌素B的TonB框相同的TonB框。杀鼠菌素决定簇两侧的DNA序列与大肠杆菌素10决定簇两侧的序列高度同源。有人提出,通过这些高度同源的DNA序列,编码细菌素的基因可能通过重组在质粒之间交换。就杀鼠菌素而言,重组可能破坏了裂解基因,在pPCP1上仅存在一个基本片段。