Suppr超能文献

广泛宿主范围的IncP质粒R18的两个进入排斥基因的鉴定与表征

Identification and characterization of two entry exclusion genes of the promiscuous IncP plasmid R18.

作者信息

Lessl M, Krishnapillai V, Schilf W

机构信息

Lehrstuhl für Genetik, Universität Bayreuth, FRG.

出版信息

Mol Gen Genet. 1991 May;227(1):120-6. doi: 10.1007/BF00260716.

Abstract

Two entry exclusion genes (designated eexA and eexB) from the promiscuous IncP alpha plasmid R18 have been isolated by molecular cloning. They are located between coordinates 26.6-27.4 kb and 27.4-27.6 kb, respectively and are transcribed clockwise on the conventional R18 map. The product of the eexA gene has an apparent molecular mass of 28 kDa and its N-terminus contains a putative signal sequence for protein export. A recombinant plasmid containing R18 eex genes exerted Eex activity towards another promiscuous IncP alpha plasmid, R702, about 50 times more strongly than plasmid R18 itself. Analysis of the DNA sequence revealed no similarity to the eex genes of the F plasmid of Escherichia coli. R18 eexA includes a potential korB binding site and is followed by a potential transcription terminator. A Tn7 insertion at coordinate 20.0 kb of R18 resulted in a host range mutant pM01185, which leads to loss of Eex activity and of conjugative transfer of the plasmid into some bacterial species.

摘要

通过分子克隆从具有广泛宿主范围的IncPα质粒R18中分离出两个进入排斥基因(命名为eexA和eexB)。它们分别位于坐标26.6 - 27.4 kb和27.4 - 27.6 kb之间,并且在传统的R18图谱上顺时针转录。eexA基因的产物表观分子量为28 kDa,其N端含有一个假定的蛋白质输出信号序列。含有R18 eex基因的重组质粒对另一个具有广泛宿主范围的IncPα质粒R702发挥Eex活性,其强度比质粒R18本身强约50倍。DNA序列分析表明,它与大肠杆菌F质粒的eex基因没有相似性。R18 eexA包含一个潜在的korB结合位点,后面跟着一个潜在的转录终止子。在R18的坐标20.0 kb处插入Tn7导致宿主范围突变体pM01185,这导致Eex活性丧失以及质粒向某些细菌物种的接合转移丧失。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验