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与乳酸链球菌ML3中的细胞聚集和高频接合转移相关的重组质粒的遗传和物理特性分析

Genetic and physical characterization of recombinant plasmids associated with cell aggregation and high-frequency conjugal transfer in Streptococcus lactis ML3.

作者信息

Anderson D G, McKay L L

出版信息

J Bacteriol. 1984 Jun;158(3):954-62. doi: 10.1128/jb.158.3.954-962.1984.

Abstract

Restriction mapping was employed to characterize the 104-kilobase (kb) cointegrate lactose plasmids from 15 independent transconjugants derived from Streptococcus lactis ML3 as well as the 55-kb lactose plasmid ( pSK08 ) and a previously uncharacterized 48.4-kb plasmid ( pRS01 ) from S. lactis ML3. The data revealed that the 104-kb plasmids were cointegrates of pSK08 and pRS01 and were structurally distinct. The replicon fusion event occurred within adjacent 13.8- or 7.3-kb PvuII fragments of pSK08 and interrupted apparently random regions of pRS01 . Correlation of the transconjugants' clumping and conjugal transfer capabilities with the interrupted region of pRS01 identified pRS01 regions coding for these properties. In the 104-kb plasmids, the pRS01 region was present in both orientations with respect to the pSK08 region. The replicon fusion occurred in recombination-deficient (Rec-) strains and appeared to introduce a 0.8 to 1.0-kb segment of DNA within the junction fragments. The degeneration of the cointegrate plasmids was monitored by examining the lactose plasmids from nonclumping derivatives of clumping transconjugants. These plasmids displayed either precise or imprecise excision of pRS01 sequences or had dramatically reduced copy numbers. Both alterations occurred by rec-independent mechanisms. Alterations of a transconjugant 's clumping phenotype also occurred by rec-independent inversion of a 4.3-kb KpnI-PvuII fragment within the pRS01 sequences of the cointegrate plasmid.

摘要

采用限制酶切图谱分析来表征来自乳酸链球菌ML3的15个独立转接合子的104千碱基(kb)共整合乳糖质粒,以及来自乳酸链球菌ML3的55 kb乳糖质粒(pSK08)和一个先前未表征的48.4 kb质粒(pRS01)。数据显示,104 kb质粒是pSK08和pRS01的共整合体,且结构不同。复制子融合事件发生在pSK08相邻的13.8 kb或7.3 kb PvuII片段内,并打断了pRS01中明显随机的区域。转接合子的聚集和接合转移能力与pRS01的中断区域的相关性确定了编码这些特性的pRS01区域。在104 kb质粒中,pRS01区域相对于pSK08区域以两种方向存在。复制子融合发生在重组缺陷(Rec-)菌株中,并且似乎在连接片段内引入了一段0.8至1.0 kb的DNA片段。通过检查聚集转接合子的非聚集衍生物中的乳糖质粒来监测共整合质粒的退化。这些质粒显示出pRS01序列的精确或不精确切除,或者拷贝数大幅减少。这两种改变都是通过不依赖rec的机制发生的。转接合子聚集表型的改变也通过共整合质粒pRS01序列内4.3 kb KpnI - PvuII片段的不依赖rec的倒位发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/147a/215534/bc9db986c3d8/jbacter00235-0198-a.jpg

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