Ferrari E, Siccardi A G, Galizzi A, Canosi U, Mazza G
J Bacteriol. 1977 Aug;131(2):382-8. doi: 10.1128/jb.131.2.382-388.1977.
Host cell reactivation of ultraviolet-irradiated phage can be used as a probe of the bacterial repair system and to determine phage and cellular contributions to the repair process. Using the Bacillus subtilis phages SPP1, SP01, phie, and phi29, we found that the uvr-1 and polA functions are involved in the host cell reactivation of the four phages. SPP1 was the only phage whose reactivation was also decreased in recA, recD, and recF mutant cells. We studied variations of host cell reactivation for SPP1 during spore outgrowth; at high ultraviolet doses the activity of a spore repair system requiring deoxyribonucleic acid polymerase I became evident. The spore repair system was completely replaced by the vegetative one by 120 min of outgrowth.
紫外线照射噬菌体的宿主细胞再活化可作为细菌修复系统的一种探针,并用于确定噬菌体和细胞对修复过程的贡献。利用枯草芽孢杆菌噬菌体SPP1、SP01、phie和phi29,我们发现uvr-1和polA功能参与了这四种噬菌体的宿主细胞再活化。SPP1是唯一一种在recA、recD和recF突变细胞中再活化也降低的噬菌体。我们研究了芽孢萌发过程中SPP1宿主细胞再活化的变化;在高紫外线剂量下,需要DNA聚合酶I的芽孢修复系统的活性变得明显。到萌发120分钟时,芽孢修复系统完全被营养细胞修复系统取代。