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植物乳杆菌隐蔽质粒pPB1的完整核苷酸序列及结构组织,该质粒起源于模块交换。

Complete nucleotide sequence and structural organization of pPB1, a small Lactobacillus plantarum cryptic plasmid that originated by modular exchange.

作者信息

de las Rivas B, Marcobal A, Muñoz R

机构信息

Departamento de Microbiología, Instituto de Fermentaciones Industriales, CSIC, Juan de la Cierva 3, 28006 Madrid, Spain.

出版信息

Plasmid. 2004 Nov;52(3):203-11. doi: 10.1016/j.plasmid.2004.09.001.

Abstract

A small cryptic plasmid designated pPB1 was isolated from Lactobacillus plantarum BIFI-38 and its complete 2899 bp nucleotide sequence was determined. Sequence analysis revealed four putative open reading frames. Based on sequence analysis two modules could be identified. First, the replication module consisted of a sequence coding for a replication protein (RepB) and its corresponding target site, and two putative repressor proteins (RepA and RepC). Sequence analysis indicated the possible synthesis of an antisense RNA that might regulate RepB production. A putative lagging-strand initiation site was also found, suggesting that pPB1 replicates via a rolling circle mechanism. The second module of pPB1 consisted of a sequence coding for a putative mobilization protein and its corresponding oriT site. Since the nucleotide sequence of the replication module showed 94.5% identity to the similar region on the Leuconostoc lactis plasmid pCI411, and the nucleotide sequence of the mobilization module had 97.5% identity to L. plantarum plasmid pLB4, it is concluded that pPB1 originated by modular exchange between two such plasmids by homologous recombination. Putative recombination sites where crossover might have taken place were also identified.

摘要

从植物乳杆菌BIFI - 38中分离出一种名为pPB1的小型隐秘质粒,并测定了其完整的2899 bp核苷酸序列。序列分析揭示了四个推定的开放阅读框。基于序列分析可鉴定出两个模块。首先,复制模块由编码复制蛋白(RepB)及其相应靶位点的序列,以及两个推定的阻遏蛋白(RepA和RepC)组成。序列分析表明可能合成一种反义RNA,其可能调节RepB的产生。还发现了一个推定的后随链起始位点,表明pPB1通过滚环机制进行复制。pPB1的第二个模块由编码推定的移动蛋白及其相应oriT位点的序列组成。由于复制模块的核苷酸序列与乳酸明串珠菌质粒pCI411上的相似区域显示出94.5%的同一性,并且移动模块的核苷酸序列与植物乳杆菌质粒pLB4有97.5%的同一性,因此得出结论,pPB1是通过同源重组在两个这样的质粒之间进行模块交换而产生的。还鉴定了可能发生交叉的推定重组位点。

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