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由Tn10切除导致的pDU202 tra::Tn10质粒转移基因中突变的遗传分析。

Genetic analysis of mutations in the transfer genes of pDU202 tra::Tn10 plasmids, caused by the excision of Tn10.

作者信息

Kehoe M A, Foster T J

出版信息

Mol Gen Genet. 1977 Nov 29;157(1):109-18. doi: 10.1007/BF00268693.

Abstract

Transfer-deficient derivatives of pDU202 (a Tcs deletion mutant of R100-1) caused by the insertion of Tn10 into the R factor's transfer genes have been described previously. Tetracyline-sensitive mutants of four of these were selected. In the majority of cases the Tcs mutation was caused by a deletion of the Tcr genes which was often accompanied either by a deletion of some of the flanking transfer genes or by a secondary mutation which was probably an inversion. A number of preferred end points for the deletions and inversions occur in the transfer operon of pDU202. Analysis of the mutants by complementation tests with Flac tra elements confirmed that the order of genes in the promoter distal part of the tra region of pDU202 is traKBCFHGSD and traI.

摘要

先前已描述过因Tn10插入R因子转移基因而导致的pDU202(R100 - 1的Tcs缺失突变体)转移缺陷衍生物。从中挑选出了四个对四环素敏感的突变体。在大多数情况下,Tcs突变是由Tcr基因缺失引起的,这种缺失通常伴随着一些侧翼转移基因的缺失,或者由可能是倒位的二次突变引起。在pDU202的转移操纵子中出现了许多缺失和倒位的优选终点。通过用Flac tra元件进行互补试验对突变体进行分析,证实了pDU202的tra区域启动子远端部分基因的顺序是traKBCFHGSD和traI。

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