Stoddard G W, Petzel J P, van Belkum M J, Kok J, McKay L L
Department of Food Science and Nutrition, University of Minnesota, St. Paul 55108.
Appl Environ Microbiol. 1992 Jun;58(6):1952-61. doi: 10.1128/aem.58.6.1952-1961.1992.
The genes responsible for bacteriocin production and immunity in Lactococcus lactis subsp. lactis biovar diacetylactis WM4 were localized and characterized by DNA restriction fragment deletion, subcloning, and nucleotide sequence analysis. The nucleotide sequence of a 5.6-kb AvaII restriction fragment revealed a cluster with five complete open reading frames (ORFs) in the same orientation. DNA and protein homology analyses, combined with deletion and Tn5 insertion mutagenesis, implicated four of the ORFs in the production of and immunity to lactococcin A. The last two ORFs in the cluster were the lactococcin A structural and immunity genes, lcnA and lciA. The two ORFs immediately upstream of lcnA and lciA were designated lcnC and lcnD, and the proteins that they encoded showed similarities to proteins of signal sequence-independent secretion systems. lcnC encodes a protein of 716 amino acids that could belong to the HlyB family of ATP-dependent membrane translocators. LcnC contains an ATP binding domain in a conserved C-terminal stretch of approximately 200 amino acids and three putative hydrophobic segments in the N terminus. The lcnD product, LcnD, of 474 amino acids, is essential for lactococcin A expression and shows structural similarities to HlyD and its homologs. On the basis of these results, a secretion apparatus that is essential for the full expression of active lactococcin A is postulated.
负责乳酸乳球菌乳亚种双乙酰乳酸亚种WM4中细菌素产生和免疫的基因,通过DNA限制性片段缺失、亚克隆和核苷酸序列分析进行了定位和表征。一个5.6kb的AvaII限制性片段的核苷酸序列显示出一个具有五个同向完整开放阅读框(ORF)的簇。DNA和蛋白质同源性分析,结合缺失和Tn5插入诱变,表明其中四个ORF与乳球菌素A的产生和免疫有关。该簇中的最后两个ORF是乳球菌素A的结构基因和免疫基因,即lcnA和lciA。紧接在lcnA和lciA上游的两个ORF被命名为lcnC和lcnD,它们编码的蛋白质与不依赖信号序列的分泌系统的蛋白质相似。lcnC编码一种716个氨基酸的蛋白质,可能属于ATP依赖的膜转运体的HlyB家族。LcnC在大约200个氨基酸的保守C末端区域含有一个ATP结合结构域,在N末端有三个推定的疏水片段。lcnD产物LcnD为474个氨基酸,对乳球菌素A的表达至关重要,并且在结构上与HlyD及其同源物相似。基于这些结果,推测了一种对活性乳球菌素A的充分表达至关重要的分泌装置。