Steen M T, Chung Y J, Hansen J N
Department of Chemistry and Biochemistry, University of Maryland, College Park 20742.
Appl Environ Microbiol. 1991 Apr;57(4):1181-8. doi: 10.1128/aem.57.4.1181-1188.1991.
The location and organization of the nisin locus in Lactococcus lactis ATCC 11454 were studied. Primer extension of in vivo mRNA transcripts of the gene that encodes the nisin prepropeptide sequence indicated the presence of a promoter at least 4 kb upstream from the nisin gene and that the mRNA has several processing sites. Restriction fragment patterns using rare-cutting enzymes, orthogonal pulsed-field clamped homogeneous electric field (CHEF) agarose gel electrophoresis, and hybridization with nisin gene probes showed that the nisin prepropeptide gene was located on a megabase-size restriction fragment, which was taken as proof of a chromosomal location. This is contrary to earlier reports, which had indicated that genes for nisin production were located on plasmids. There was no evidence of more than one chromosomal location or more than one copy of the nisin gene. The restriction patterns indicated that the size of the L. lactis genome is about 2,500 kb. The previously observed (G. W. Buchman, S. Banerjee, and J. N. Hansen, J. Biol. Chem. 263: 16260-16266, 1988) downstream open reading frame (ORF) was fully sequenced to reveal an 851-amino-acid coding region, an upstream putative mRNA processing site, and a putative rho-independent terminator. The ORF was analyzed for secondary structural features, and the sequence data bases were searched for homologies. The ORF contained many amphipathic helices, a C-terminal transmembrane helix, and homologies to some membrane-associated proteins. It lacked an N-terminal membrane insertion sequence and accordingly appears to be associated with, and anchored to, the cytoplasmic side of the membrane. An additional ORF that possessed a ribosome-binding sequence and tandem promoters, indicating the beginning of a new operon, was identified still farther downstream. The results were consistent with the nisin gene being part of a polycistronic operon with a size greater than 8.5 kb.
对乳酸乳球菌ATCC 11454中乳链菌肽基因座的位置和组织进行了研究。对编码乳链菌肽前原肽序列的基因的体内mRNA转录本进行引物延伸,结果表明在乳链菌肽基因上游至少4 kb处存在一个启动子,且该mRNA有多个加工位点。使用稀有切割酶的限制性片段图谱、正交脉冲场钳制均匀电场(CHEF)琼脂糖凝胶电泳以及与乳链菌肽基因探针杂交表明,乳链菌肽前原肽基因位于一个兆碱基大小的限制性片段上,这被视为染色体定位的证据。这与早期报道相反,早期报道表明乳链菌肽产生基因位于质粒上。没有证据表明存在多个染色体定位或多个乳链菌肽基因拷贝。限制性图谱表明乳酸乳球菌基因组大小约为2500 kb。对先前观察到的(G. W. Buchman、S. Banerjee和J. N. Hansen,《生物化学杂志》263: 16260 - 16266,1988)下游开放阅读框(ORF)进行了全序列测定,以揭示一个851个氨基酸的编码区、一个上游假定的mRNA加工位点和一个假定的不依赖ρ因子的终止子。对该ORF进行了二级结构特征分析,并在序列数据库中搜索同源性。该ORF包含许多两亲性螺旋、一个C端跨膜螺旋,并且与一些膜相关蛋白具有同源性。它缺乏N端膜插入序列,因此似乎与膜的细胞质侧相关并锚定在其上。在更下游还鉴定出了另一个具有核糖体结合序列和串联启动子的ORF,这表明一个新操纵子的开始。结果与乳链菌肽基因是一个大小大于8.5 kb的多顺反子操纵子的一部分相一致。