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酒酒球菌DNA的序列分析:隐蔽质粒pLo13的结构

Sequence analysis of Leuconostoc oenos DNA: organization of pLo13, a cryptic plasmid.

作者信息

Fremaux C, Aigle M, Lonvaud-Funel A

机构信息

Laboratorie de microbiologie, Université de Bordeaux II, Talence, France.

出版信息

Plasmid. 1993 Nov;30(3):212-23. doi: 10.1006/plas.1993.1053.

Abstract

A Leuconostoc oenos plasmid, pLo13, was studied to analyze its genetic organization and to define its functions. The nucleotide sequence (3948 bp) revealed three major open reading frames. Features commonly found in plasmids that replicate via a rolling-circle mechanism were identified within pLo13: first, a sequence coding for a protein with an amino acid sequence homologous to the plasmid recombination enzymes (Pre), but for which a specific target site similar to those previously described was not found; second, a sequence probably encoding a replication protein (Rep). The putative pLo13 Rep protein amino acid sequence is divergent from the pC194-pUB110 family Rep proteins. However, the consensus sequence of the Rep protein active site was found, as well as the Rep protein consensus target site. No sequence similar to the previously described minus-origins (SSOs) are present in pLo13; nevertheless, a 200-bp sequence rich in imperfect palindromes may be involved in the minus-strand replication. These overall differences are in agreement with the previously reported important phylogenetic distance existing between Ln. oenos and other lactic acid bacteria.

摘要

对酒酒球菌质粒pLo13进行了研究,以分析其基因组织并确定其功能。核苷酸序列(3948 bp)显示出三个主要的开放阅读框。在pLo13中鉴定出了通过滚环机制复制的质粒中常见的特征:第一,一个编码蛋白质的序列,其氨基酸序列与质粒重组酶(Pre)同源,但未发现与先前描述的类似的特定靶位点;第二,一个可能编码复制蛋白(Rep)的序列。推测的pLo13 Rep蛋白氨基酸序列与pC194-pUB110家族的Rep蛋白不同。然而,发现了Rep蛋白活性位点的共有序列以及Rep蛋白共有靶位点。pLo13中不存在与先前描述的负链起始位点(SSOs)相似的序列;尽管如此,一个富含不完全回文的200 bp序列可能参与负链复制。这些总体差异与先前报道的酒酒球菌与其他乳酸菌之间存在的重要系统发育距离一致。

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