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IncJ质粒R391向重组缺陷型大肠杆菌K12的转移:R391作为接合转座子的证据。

Transfer of the IncJ plasmid R391 to recombination deficient Escherichia coli K12: evidence that R391 behaves as a conjugal transposon.

作者信息

Murphy D B, Pembroke J T

机构信息

Department of Chemical and Environment Science, University of Limerick, Ireland.

出版信息

FEMS Microbiol Lett. 1995 Dec 15;134(2-3):153-8. doi: 10.1111/j.1574-6968.1995.tb07930.x.

Abstract

A study of the IncJ plasmid R391 confirmed a low frequency of transfer between recombination proficient (recA+) Escherichia coli (10(-5) donor -1). Reanalysis of its transfer to recombination deficient (recA) E. coli revealed an equivalent transfer frequency to and from all mutants tested. Extrachromosomal DNA could not be detected in either recA+ or recA transconjugants, while R391 proved refractory to curing in both backgrounds implying a high degree of stability. The integration of R391 into a specific region of the chromosome was demonstrated by its transfer as part of the exogenote mobilised from the transfer origins of Hfr strains BW6165 and JC158. Transfer of R391 coupled to recA independent chromosomal integration has significant implications as to the nature and classification of the element. We propose that R391 behaves like a conjugal transposon.

摘要

一项关于IncJ质粒R391的研究证实,在重组能力强(recA+)的大肠杆菌之间转移频率较低(10(-5)供体-1)。重新分析其向重组缺陷(recA)大肠杆菌的转移发现,与所有测试突变体之间的转移频率相当。在recA+或recA转接合子中均未检测到染色体外DNA,而R391在两种背景下均难以消除,这意味着其具有高度稳定性。R391作为从Hfr菌株BW6165和JC158的转移起点动员的外基因子的一部分进行转移,证明了其整合到染色体的特定区域。R391与recA独立染色体整合相关的转移对该元件的性质和分类具有重要意义。我们认为R391的行为类似于接合转座子。

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