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来自嗜冷明串珠菌的细菌素亮菌素A产生相关基因的分子特征分析。

Molecular characterization of genes involved in the production of the bacteriocin leucocin A from Leuconostoc gelidum.

作者信息

van Belkum M J, Stiles M E

机构信息

Department of Agricultural, Food, and Nutritional Science, University of Alberta, Edmonton, Canada.

出版信息

Appl Environ Microbiol. 1995 Oct;61(10):3573-9. doi: 10.1128/aem.61.10.3573-3579.1995.

Abstract

Leucocin A is a small heat-stable bacteriocin produced by Leuconostoc gelidum UAL187. A 2.9-kb fragment of plasmid DNA that contains the leucocin structural gene and a second open reading frame (ORF) in an operon was previously cloned (J. W. Hastings, M. Sailer, K. Johnson, K. L. Roy, J. C. Vederas, and M. E. Stiles, J. Bacteriol. 173:7491-7500, 1991). When a 1-kb DraI-HpaI fragment containing this operon was introduced into a bacteriocin-negative variant (UAL187-13), immunity but no leucocin production was detected. Leucocin production was observed when an 8-kb SacI-HindIII fragment of the leucocin plasmid was introduced into L. gelidum UAL187-13 and Lactococcus lactis IL1403. Nucleotide sequence analysis of this 8-kb fragment revealed the presence of three ORFs in an operon upstream of and on the strand opposite from the leucocin structural gene. The first ORF (lcaE) encodes a putative protein of 149 amino acids with no apparent function in leucocin A production. The second ORF (lcaC) contains 717 codons that encode a protein homologous to members of the HlyB family of ATP-binding cassette transporters. The third ORF (lcaD) contains 457 codons that encode a protein with marked similarity to LcnD, a protein essential for the expression of the lactococcal bacteriocin lactococcin A. Deletion mutations in lcaC and lcaD resulted in loss of leucocin production, indicating that LcaC and LcaD are involved in production and translocation of leucocin A. The secretion apparatus for lactococcin A did not complement mutations in the lcaCD genes to express leucocin A in L. lactis.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

亮菌素A是由嗜冷明串珠菌UAL187产生的一种小的热稳定细菌素。先前已克隆了一个2.9 kb的质粒DNA片段,该片段在一个操纵子中包含亮菌素结构基因和第二个开放阅读框(ORF)(J. W. 黑斯廷斯、M. 赛勒、K. 约翰逊、K. L. 罗伊、J. C. 韦德拉什和M. E. 斯泰尔斯,《细菌学杂志》173:7491 - 7500,1991年)。当将一个包含该操纵子的1 kb DraI - HpaI片段导入细菌素阴性变体(UAL187 - 13)时,检测到免疫性但未检测到亮菌素产生。当将亮菌素质粒的一个8 kb SacI - HindIII片段导入嗜冷明串珠菌UAL187 - 13和乳酸乳球菌IL1403时,观察到亮菌素产生。对这个8 kb片段的核苷酸序列分析揭示,在亮菌素结构基因上游且位于相反链上的一个操纵子中存在三个ORF。第一个ORF(lcaE)编码一个149个氨基酸的推定蛋白,在亮菌素A产生中无明显功能。第二个ORF(lcaC)包含717个密码子,编码一种与ATP结合盒转运蛋白的HlyB家族成员同源的蛋白。第三个ORF(lcaD)包含457个密码子,编码一种与LcnD有显著相似性的蛋白,LcnD是乳酸乳球菌细菌素乳链菌肽A表达所必需的一种蛋白。lcaC和lcaD中的缺失突变导致亮菌素产生丧失,表明LcaC和LcaD参与亮菌素A的产生和转运。乳链菌肽A的分泌装置不能弥补lcaCD基因中的突变以在乳酸乳球菌中表达亮菌素A。(摘要截短于250字)

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