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大肠杆菌K-12中遗传重组RecE途径的遗传分析。

Genetic analysis of the RecE pathway of genetic recombination in Escherichia coli K-12.

作者信息

Gillen J R, Willis D K, Clark A J

出版信息

J Bacteriol. 1981 Jan;145(1):521-32. doi: 10.1128/jb.145.1.521-532.1981.

Abstract

The RecE pathway of genetic recombination in Escherichia coli K-12 was defined to be the pathway that is utilized in deoxyribonucleic acid exonuclease V (ExoV)-defective cells which express constitutively recE+, the structural gene for deoxyribonucleic acid exonuclease VIII. Dependence on ExoVIII was shown by the occurrence in a recB21 sbcA23 strain of recombination deficiency mutations in recE, the structural gene for ExoVIII. Point mutations in recE were found as well as deletion mutations in which the entire Rac prophage, carrying recE, was lost. In addition, strain construction and mutagenesis revealed the dependence of the RecE pathway on recA+ and on recF+. Dependence on a fourth gene was shown by a mutation (rec-77) which does not map near the other genes. The problem of distinguishing the RecE pathway from that previously called RecF is discussed.

摘要

大肠杆菌K-12中遗传重组的RecE途径被定义为在表达组成型recE +(脱氧核糖核酸外切酶VIII的结构基因)的脱氧核糖核酸外切酶V(ExoV)缺陷细胞中所利用的途径。在recB21 sbcA23菌株中recE(ExoVIII的结构基因)发生重组缺陷突变,表明了对ExoVIII的依赖性。发现了recE中的点突变以及缺失突变,在缺失突变中携带recE的整个Rac原噬菌体丢失。此外,菌株构建和诱变揭示了RecE途径对recA +和recF +的依赖性。一个不定位在其他基因附近的突变(rec-77)表明了对第四个基因的依赖性。讨论了区分RecE途径与先前称为RecF途径的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/737b/217302/c5baff651961/jbacter00272-0548-a.jpg

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