Ono T, Ohnishi Y
Microbiol Immunol. 1981;25(5):433-44. doi: 10.1111/j.1348-0421.1981.tb00046.x.
Stable RNA of Escherichia coli was extensively degraded about 40 min after thermal induction of lysogenized lambda cI857 phages at 42 degrees C. When several nuclease-deficient host cells were tested, RNase I activity in the host cells was inferred to be involved in the RNA degradation. Ribosomal structure was detectably altered before the degradation of ribosomal RNA was observed. 30S and 50S subunits began to sediment at 25-28S and 45-58S, respectively, still containing intact RNA. Nonpermissive host cells lysogenized with lambda cI857 susR produced progeny phages in normal burst size after thermal induction and then degraded stable RNA, though they were not lysed. In contrast cells lysogenized with lambda cI857 susS produced ten times more progeny phages under the same condition, but did not degrade stable RNA. These results indicate that the lambda S gene product, which acts as a positive effector of lysis, induced the degradation of stable RNA, presumably by a still uncharacterized effect on the cytoplasmic membrane.
在42℃对溶源化的λcI857噬菌体进行热诱导后约40分钟,大肠杆菌的稳定RNA被大量降解。当测试几种核酸酶缺陷型宿主细胞时,推测宿主细胞中的核糖核酸酶I活性与RNA降解有关。在观察到核糖体RNA降解之前,核糖体结构就已发生可检测到的改变。30S和50S亚基分别开始在25 - 28S和45 - 58S处沉降,此时仍含有完整的RNA。用λcI857 susR溶源化的非允许宿主细胞在热诱导后产生正常爆发量的子代噬菌体,然后降解稳定RNA,尽管它们没有裂解。相比之下,用λcI857 susS溶源化的细胞在相同条件下产生的子代噬菌体数量多十倍,但不降解稳定RNA。这些结果表明,作为裂解正效应物的λS基因产物诱导了稳定RNA的降解,推测是通过对细胞质膜产生一种尚未明确的作用来实现的。