Hakkaart M J, Veltkamp E, Nijkamp H J
Mol Gen Genet. 1981;183(2):326-32. doi: 10.1007/BF00270636.
We studied the expression of gene H, located between 9.3% and 11% on the CLo DF13 genome, as well as the functions of the gene product. We found that treatment of bacterial cells with mitomycin-C results in the induced synthesis of three Clo DF13 specified proteins namely cloacin DF13, immunity protein and protein H. Evidence was obtained that the genes encoding these proteins form one, mitomycin-C induceable, operon; the promoter at 32% in front of the cloacin gene is essential for the induced expression. Furthermore we could demontrate that protein H is involved in the lethal effect of mitomycin-C treatment of bacteriocinogenic cells. The data in this paper show that a high concentration of protein H in cells, due either to an induced expression of gene H (mitomycin-C induction) or to a gene dosage effect (Clo DF13 copl Ts copy control mutant), results in the lysis of bacterial cells. The implication of these data are discussed.
我们研究了位于Clo DF13基因组9.3%至11%之间的基因H的表达情况以及该基因产物的功能。我们发现,用丝裂霉素-C处理细菌细胞会诱导合成三种Clo DF13特定的蛋白质,即杆菌素DF13、免疫蛋白和蛋白质H。有证据表明,编码这些蛋白质的基因形成了一个可被丝裂霉素-C诱导的操纵子;杆菌素基因前32%处的启动子对于诱导表达至关重要。此外,我们能够证明蛋白质H参与了丝裂霉素-C处理产细菌素细胞的致死效应。本文的数据表明,细胞中高浓度的蛋白质H,无论是由于基因H的诱导表达(丝裂霉素-C诱导)还是基因剂量效应(Clo DF13 copl Ts复制控制突变体),都会导致细菌细胞裂解。我们对这些数据的意义进行了讨论。