Petranović M, Salaj-Smic E, Petranović D, Trogovcević Z
J Bacteriol. 1979 Dec;140(3):848-51. doi: 10.1128/jb.140.3.848-851.1979.
The fate of the prophage part of the lysogenic chromosome was followed in the course of post-ultraviolet incubation. For this purpose, lambda cI857 ind prophage, which can be induced by heat but not by ultraviolet light, was used. The prophage, intially more resistant than its repair-proficient host cell, was rapidly inactivated. This inactivation was not caused by the impaired capacity of irradiated cells to support growth of the phage. Over the entire dose range tested, little, if any, sensitivity difference between the host and the prophage was found at the end of cell division delay. Rapid inactivation of the prophage was also observed in uvr cells after small doses of ultraviolet light. The same small doses did not cause inactivation in lysogens carrying a mutation in the gene recA. This suggests that the functional gene recA is required for inactivation of the prophage part of the lysogenic chromosome.
在紫外线照射后的培养过程中,对溶原性染色体上原噬菌体部分的命运进行了追踪。为此,使用了λcI857 ind原噬菌体,它可被热诱导但不能被紫外线诱导。原噬菌体最初比其具有修复能力的宿主细胞更具抗性,但很快就被灭活了。这种灭活不是由受照射细胞支持噬菌体生长的能力受损引起的。在整个测试剂量范围内,在细胞分裂延迟结束时,宿主和原噬菌体之间几乎没有发现敏感性差异。在uvr细胞中,小剂量紫外线照射后也观察到原噬菌体的快速灭活。相同的小剂量不会导致携带recA基因突变的溶原菌发生灭活。这表明功能性recA基因是溶原性染色体上原噬菌体部分灭活所必需的。