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在不存在接合转移的情况下,质粒R1162 oriT处的位点特异性重组。

Site-specific recombination at oriT of plasmid R1162 in the absence of conjugative transfer.

作者信息

Meyer R

机构信息

Department of Microbiology, University of Texas, Austin 78712.

出版信息

J Bacteriol. 1989 Feb;171(2):799-806. doi: 10.1128/jb.171.2.799-806.1989.

DOI:10.1128/jb.171.2.799-806.1989
PMID:2644236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC209667/
Abstract

R1162 is efficiently comobilized during conjugative transfer of the self-transmissible plasmid R751. Bacteriophage M13 derivatives that contain two directly repeated copies of oriT, the site on R1162 DNA required in cis for mobilization, were constructed. Phage DNA molecules underwent recombination during infection of Escherichia coli, with the product retaining a single functional copy of oriT. Recombination was strand specific and depended on R1162 gene products involved in mobilization, but did not require the self-transmissible plasmid vector. Two genes were identified, one essential for recombination and the other affecting the frequency of recombination. Recombination of bacteriophage DNA could form the basis of a simple model for some of the events occurring during conjugation without the complexity of a true mating system.

摘要

在自我传递质粒R751的接合转移过程中,R1162能高效共转移。构建了含有oriT两个直接重复拷贝的噬菌体M13衍生物,oriT是R1162 DNA上顺式作用的转移所需位点。噬菌体DNA分子在感染大肠杆菌期间发生重组,产物保留oriT的单个功能拷贝。重组是链特异性的,依赖于参与转移的R1162基因产物,但不需要自我传递质粒载体。鉴定出两个基因,一个对重组必不可少,另一个影响重组频率。噬菌体DNA的重组可为接合过程中发生的某些事件提供一个简单模型的基础,而无需真正交配系统的复杂性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9992/209667/135902c1dce9/jbacter00168-0192-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9992/209667/135902c1dce9/jbacter00168-0192-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9992/209667/135902c1dce9/jbacter00168-0192-a.jpg

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