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类I质粒R62抑制大肠杆菌K12性因子F育性期间的转移基因表达。

Transfer gene expression during fertility inhibition of the Escherichia coli K12 sex factor F by the I-like plasmid R62.

作者信息

Gasson M, Willetts N

出版信息

Mol Gen Genet. 1976 Dec 22;149(3):329-33. doi: 10.1007/BF00268535.

Abstract

Further understanding of how the FinQ fertility inhibition system of the I-like plasmid R62 inhibits transfer of the sex factor F has been gained by the use of a genetic assay for individual transfer gene products. The technique involved construction of a series of Flac plasmids carrying suppressible mutations in individual transfer genes together with a FinQ inhibitor-insensitive traQ mutation. The transfer of the Flac double mutants from a strain carrying wild-type Fhis and R62 then indicated the effect of R62-encoded transfer inhibition on the expression of individual F transfer genes. During such inhibition the products of genes traJ, traA, traE, traB and traC were present in quantities sufficient to permit efficient F transfer, whereas the levels of the traF, traH, traG and traD gene products were so reduced as to limit F transfer. These findings and a failure to obtain recombination between traC and traQ mutations suggest that the R62 fertility inhibition system terminates transcription of the transfer operon between traC and traF.

摘要

通过使用针对单个转移基因产物的遗传检测方法,人们对I类质粒R62的FinQ生育抑制系统如何抑制性因子F的转移有了更深入的了解。该技术涉及构建一系列携带单个转移基因中可抑制突变以及对FinQ抑制剂不敏感的traQ突变的Flac质粒。然后,从携带野生型Fhis和R62的菌株中转移Flac双突变体,这表明R62编码的转移抑制对单个F转移基因表达的影响。在这种抑制过程中,traJ、traA、traE、traB和traC基因的产物数量足以允许高效的F转移,而traF、traH、traG和traD基因产物的水平则降低到限制F转移的程度。这些发现以及未能在traC和traQ突变之间获得重组表明,R62生育抑制系统终止了traC和traF之间转移操纵子的转录。

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