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大肠杆菌中质粒RK2的必需基因:trfB区域控制着trfA附近的一个kil基因。

Essential genes of plasmid RK2 in Escherichia coli: trfB region controls a kil gene near trfA.

作者信息

Pohlman R F, Figurski D H

出版信息

J Bacteriol. 1983 Nov;156(2):584-91. doi: 10.1128/jb.156.2.584-591.1983.

Abstract

Plasmid RK2 encodes several kil determinants whose lethal action on Escherichia coli host cells is prevented by RK2 kor genes. Here we show that the mini-RK2 plasmid, pRK248, specifies a kilB component (kilB1) in the region of the replication gene trfA. kilB1 is different from trfA and is completely encoded within the pRK248 HaeII A fragment. Transformation of E. coli cells with hybrid plasmids containing the cloned kilB1 determinant is very inefficient and results in the selection of variant kil- plasmids, many of which show genetic and physical evidence of deletions. If another pRK248 gene (korB1) is present in the cells, kilB1+ plasmids can be established at high efficiency and without any detectable changes. KorB1 is encoded by the trfB region of pRK248 because recombinant plasmids with this region are able to control kilB1 in trans. These results substantiate our earlier explanation for the structure of pRK248 and for the perplexing requirement of the trfB region in this plasmid.

摘要

质粒RK2编码多个杀伤决定簇,其对大肠杆菌宿主细胞的致死作用可被RK2 kor基因阻止。在此我们表明,微型RK2质粒pRK248在复制基因trfA区域指定了一个杀伤B组分(kilB1)。kilB1与trfA不同,完全由pRK248 HaeII A片段编码。用含有克隆的kilB1决定簇的杂交质粒转化大肠杆菌细胞效率非常低,并导致变体杀伤阴性质粒的选择,其中许多显示出缺失的遗传和物理证据。如果细胞中存在另一个pRK248基因(korB1),kilB1+质粒可以高效建立且没有任何可检测到的变化。KorB1由pRK248的trfB区域编码,因为含有该区域的重组质粒能够反式控制kilB1。这些结果证实了我们之前对pRK248结构以及该质粒中trfB区域令人困惑的需求的解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20e9/217871/2e588987aaf1/jbacter00240-0119-a.jpg

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