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热诱导后噬菌体λ溶原菌中核糖体RNA的降解

Degradation of ribosomal RNA in bacteriophage lambda lysogens after thermal induction.

作者信息

Ono T, Ohnishi Y

出版信息

Microbiol Immunol. 1981;25(5):433-44. doi: 10.1111/j.1348-0421.1981.tb00046.x.

DOI:10.1111/j.1348-0421.1981.tb00046.x
PMID:6168891
Abstract

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.

摘要

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。

相似文献

1
Degradation of ribosomal RNA in bacteriophage lambda lysogens after thermal induction.热诱导后噬菌体λ溶原菌中核糖体RNA的降解
Microbiol Immunol. 1981;25(5):433-44. doi: 10.1111/j.1348-0421.1981.tb00046.x.
2
Evidence of cell fragility caused by gene kil following lambda induction.λ诱导后基因敲除导致细胞脆弱性的证据。
Virology. 1983 Jul 15;128(1):166-75. doi: 10.1016/0042-6822(83)90327-6.
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The fate of ribosomes in Escherichia coli cells starved for a carbon source.缺乏碳源的大肠杆菌细胞中核糖体的命运
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The Escherichia coli CRISPR system protects from λ lysogenization, lysogens, and prophage induction.大肠杆菌 CRISPR 系统可抵御 λ 溶原菌、溶原菌和噬菌体诱导。
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Inhibition of streptomycin-dependent mutation in Escherichia coli on the lytic growth of bacteriophage lambda.链霉素依赖性突变在大肠杆菌中对噬菌体λ裂解生长的抑制作用。
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Differential stability of E. coli ribosomal particles and free RNA towards thermal degradation studied by microcalorimetry.通过微量量热法研究大肠杆菌核糖体颗粒和游离RNA对热降解的差异稳定性。
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[Transposition of the kanamycin resistance determinant (Tn601) from plasmid 5T to the genome of bacteriophage lambda and the expression of this gene after prophage induction].[卡那霉素抗性决定子(Tn601)从质粒5T转位至噬菌体λ基因组以及原噬菌体诱导后该基因的表达]
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引用本文的文献

1
S gene expression and the timing of lysis by bacteriophage lambda.噬菌体λ的S基因表达与裂解时间
J Bacteriol. 1995 Jun;177(11):3283-94. doi: 10.1128/jb.177.11.3283-3294.1995.
2
Nucleolytic processing of ribonucleic acid transcripts in procaryotes.原核生物中核糖核酸转录本的核酸裂解加工
Microbiol Rev. 1986 Dec;50(4):428-51. doi: 10.1128/mr.50.4.428-451.1986.
3
Bacteriophage lysis: mechanism and regulation.噬菌体裂解:机制与调控。
Microbiol Rev. 1992 Sep;56(3):430-81. doi: 10.1128/mr.56.3.430-481.1992.