Kennedy C K
J Bacteriol. 1971 Oct;108(1):10-9. doi: 10.1128/jb.108.1.10-19.1971.
Escherichia coli K-12 colicinogenic for ColE1 yielded mutants that appeared to produce colicin at 43 C but not at 30 or 37. These mutants proved to have the mutation recA(-) Further study revealed that both recA(-) and recA(+) bacteria, when carrying ColE1 or ColE2, produce more colicin during growth at higher temperatures or after brief exposure to temperatures beyond the growth range. Counts of lacunae demonstrated that the increase of colicin production is due to an increase in the number of cells that yield colicin. Heat treatment causes lacunae to increase by the same factor in recA(+) and recA(-) cells, although recA(-) bacteria produce 500 times fewer lacunae than recA(+). Inhibition of protein synthesis, notably by chloramphenicol, also induces colicin production in as much as 90% of the cells after removal of inhibition (to permit colicin synthesis). Induction of colicin production by chloramphenicol requires that ribonucleic acid synthesis continue during the period of inhibition. These results are discussed in relation to the regulation of colicin production.
对ColE1具有产大肠杆菌素能力的大肠杆菌K - 12产生了一些突变体,这些突变体在43℃时似乎能产生大肠杆菌素,但在30℃或37℃时则不能。这些突变体被证明具有recA(-)突变。进一步的研究表明,携带ColE1或ColE2的recA(-)和recA(+)细菌在较高温度下生长期间或短暂暴露于超出生长范围的温度后,都会产生更多的大肠杆菌素。对噬菌斑的计数表明,大肠杆菌素产量的增加是由于产生大肠杆菌素的细胞数量增加所致。热处理使recA(+)和recA(-)细胞中的噬菌斑以相同的倍数增加,尽管recA(-)细菌产生的噬菌斑比recA(+)细菌少500倍。蛋白质合成的抑制,尤其是氯霉素引起的抑制,在解除抑制(以允许大肠杆菌素合成)后还能诱导多达90%的细胞产生大肠杆菌素。氯霉素诱导大肠杆菌素产生需要在抑制期间核糖核酸合成继续进行。结合大肠杆菌素产生的调控对这些结果进行了讨论。