Stephens S K, Floriano B, Cathcart D P, Bayley S A, Witt V F, Jiménez-Díaz R, Warner P J, Ruiz-Barba J L
Cranfield Biotechnology Centre, Cranfield University, Bedford, United Kingdom.
Appl Environ Microbiol. 1998 May;64(5):1871-7. doi: 10.1128/AEM.64.5.1871-1877.1998.
A 4.5-kb region of chromosomal DNA carrying the locus responsible for the production of plantaricin S, a two-peptide bacteriocin produced by Lactobacillus plantarum LPCO10 (R. Jiménez-Díaz, J. L. Ruiz-Barba, D. P. Cathcart, H. Holo, I. F. Nes, K. H. Sletten, and P. J. Warner, Appl. Environ. Microbiol. 61:4459-4463, 1995), has been cloned, and the nucleotide sequence has been elucidated. Two genes, designated plsA and plsB and encoding peptides alpha and beta, respectively, of plantaricin S, plus an open reading frame (ORF), ORF2, were found to be organized in an operon. Northern blot analysis showed that these genes are cotranscribed, giving a ca. 0.7-kb mRNA, whose transcription start point was determined by primer extension. Nucleotide sequences of plsA and plsB revealed that both genes are translated as bacteriocin precursors which include N-terminal leader sequences of the double-glycine type. The role of ORF2 is unknown at the moment, although it might be expected to encode an immunity protein of the type described for other bacteriocin operons. In addition, several other potential ORFs have been found, including some which may be responsible for the regulation of bacteriocin production. Two of them, ORF8 and ORF14, show strong homology with histidine protein kinase and response regulator genes, respectively, which have been found to be involved in the regulation of the production of other bacteriocins from lactic acid bacteria. A third ORF, ORF5, shows homology with gene agrB from Staphylococcus aureus, which is involved in the mechanism of regulation of the virulence phenotype in this species. Thus, an agr-like regulatory system for the production of plantaricin S is postulated.
携带负责植物乳杆菌LPCO10产生的双肽细菌素——植物乳杆菌素S(R. Jiménez-Díaz、J. L. Ruiz-Barba、D. P. Cathcart、H. Holo、I. F. Nes、K. H. Sletten和P. J. Warner,《应用与环境微生物学》61:4459 - 4463,1995年)的4.5 kb染色体DNA区域已被克隆,其核苷酸序列也已阐明。发现两个分别命名为plsA和plsB的基因,它们分别编码植物乳杆菌素S的α和β肽,加上一个开放阅读框(ORF)即ORF2,这些基因组成一个操纵子。Northern印迹分析表明这些基因是共转录的,产生一条约0.7 kb的mRNA,其转录起始点通过引物延伸确定。plsA和plsB的核苷酸序列显示这两个基因都作为细菌素前体进行翻译,其中包括双甘氨酸类型的N端前导序列。目前ORF2 的作用尚不清楚,不过预计它可能编码一种与其他细菌素操纵子中描述的类型相同的免疫蛋白。此外,还发现了其他几个潜在的开放阅读框,包括一些可能负责细菌素产生调控的开放阅读框。其中两个,ORF8和ORF14,分别与组氨酸蛋白激酶和应答调节基因有很强的同源性,已发现它们参与调控乳酸菌产生其他细菌素。第三个开放阅读框ORF5与金黄色葡萄球菌的agrB基因有同源性,该基因参与该物种毒力表型的调控机制。因此,推测存在一个类似agr的调控系统用于植物乳杆菌素S的产生。