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来自戊糖乳杆菌MD353和植物乳杆菌ATCC 8014的两种隐蔽质粒的结构与功能分析

Structural and functional analysis of two cryptic plasmids from Lactobacillus pentosus MD353 and Lactobacillus plantarum ATCC 8014.

作者信息

Leer R J, van Luijk N, Posno M, Pouwels P H

机构信息

TNO Medical Biological Laboratory, Rijswijk, The Netherlands.

出版信息

Mol Gen Genet. 1992 Aug;234(2):265-74. doi: 10.1007/BF00283847.

Abstract

The DNA sequences of a 2.4 kb plasmid (p353-2) from Lactobacillus pentosus MD353 and a 1.9 kb plasmid (p8014-2) from Lactobacillus plantarum ATCC 8014 show 81.5% overall similarity. Both plasmids carry elements (replication protein gene, plus-origin and minus-origin of replication), which are typical of plasmids that replicate via a rolling-circle mechanism of replication (RCR). Direct evidence for an RCR mechanism was obtained by showing the accumulation of single-stranded plasmid intermediates in the presence of rifampicin. A minus-origin of replication was defined for plasmids p353-2 and p8014-2 based on DNA sequence analysis and on its ability to convert single-stranded into double-stranded plasmid DNA. Plasmids pLPE323, pLPE350 and pLPC37 that are derived from the p353-2 or p8014-2 replicon are structurally and segregationally stable in L. pentosus MD353, L. plantarum ATCC 8014 and in Lactobacillus casei ATCC 393. The presence of Escherichia coli or lambda DNA fragments in vectors derived from p353-2 or p8014-2 does not affect the structural stability but results in segregational instability of the vectors. The instability increases with increasing size of the inserted DNA fragment. Since vectors based on these replicons can be efficiently propagated in a wide variety of Lactobacillus species, they are highly suitable for cloning and expression of foreign DNA in Lactobacillus, provided that selective pressure is applied.

摘要

来自戊糖乳杆菌MD353的一个2.4 kb质粒(p353 - 2)和来自植物乳杆菌ATCC 8014的一个1.9 kb质粒(p8014 - 2)的DNA序列显示出81.5%的总体相似性。这两个质粒都携带一些元件(复制蛋白基因、正复制起始点和负复制起始点),这些元件是通过滚环复制机制(RCR)进行复制的质粒所特有的。通过显示在利福平存在下单链质粒中间体的积累,获得了RCR机制的直接证据。基于DNA序列分析及其将单链转化为双链质粒DNA的能力,为质粒p353 - 2和p8014 - 2定义了一个负复制起始点。源自p353 - 2或p8014 - 2复制子的质粒pLPE323、pLPE350和pLPC37在戊糖乳杆菌MD353、植物乳杆菌ATCC 8014和干酪乳杆菌ATCC 393中在结构上和分离上是稳定的。源自p353 - 2或p8014 - 2的载体中存在大肠杆菌或λDNA片段不会影响结构稳定性,但会导致载体的分离不稳定性。不稳定性随着插入DNA片段大小的增加而增加。由于基于这些复制子的载体可以在多种乳杆菌物种中高效繁殖,因此只要施加选择压力,它们就非常适合在乳杆菌中克隆和表达外源DNA。

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