Pugsley A P
Mol Gen Genet. 1983;190(3):379-83. doi: 10.1007/BF00331062.
Escherichia coli K-12 cells carrying the high copy number plasmid ColE2-P9 and a sfiA-lacZ gene fusion exhibit abnormally high levels of SOS-regulated phi sfiA-lacZ expression. Increased sfiA-lacZ expression is caused by the action of colicin E2, which is a DNase, rather than by the presence of multiple copies of a binding site for LexA protein, the repressor for the sfiA and colicin E2 genes. Expression of sfiA-lacZ was reduced to normal levels if the ColE2+ strain lacked the outer membrane colicin E2 receptor protein (BtuB) or if they carried an increased number of colicin E2 immunity genes. The results suggest that cultures of ColE2+ strains contain a small number of cells which produce colicin which can then enter other, non-producing cells in the culture and cause sufficient damage to the DNA to induce the SOS system. The levels of colicin E2 immunity in the producing cells is presumably sufficient to prevent extensive lethal effects of the colicin, but insufficient to prevent limited endonuclease activity. An important consequence of this phenomenon is that the DNase action of colicin E2 can stimulate its own production.
携带高拷贝数质粒ColE2 - P9和sfiA - lacZ基因融合体的大肠杆菌K - 12细胞表现出异常高水平的SOS调节的φsfiA - lacZ表达。sfiA - lacZ表达增加是由核酸酶大肠杆菌素E2的作用引起的,而不是由LexA蛋白(sfiA和大肠杆菌素E2基因的阻遏物)结合位点的多个拷贝的存在引起的。如果ColE2 +菌株缺乏外膜大肠杆菌素E2受体蛋白(BtuB),或者如果它们携带数量增加的大肠杆菌素E2免疫基因,则sfiA - lacZ的表达会降至正常水平。结果表明,ColE2 +菌株的培养物中含有少量产生大肠杆菌素的细胞,这些大肠杆菌素随后可以进入培养物中的其他非产生细胞,并对DNA造成足够的损伤以诱导SOS系统。产生细胞中的大肠杆菌素E2免疫水平大概足以防止大肠杆菌素产生广泛的致死效应,但不足以防止有限的核酸内切酶活性。这种现象的一个重要后果是大肠杆菌素E2的DNase作用可以刺激其自身的产生。