Lee Ju-Hoon, Halgerson Jamie S, Kim Jeong-Hwan, O'Sullivan Daniel J
Department of Food Science and Nutrition and Center for Microbial and Plant Genomics, University of Minnesota, Cargill Building for Microbial and Plant Genomics, St. Paul, MN 55108, USA.
Appl Environ Microbiol. 2007 Jul;73(14):4417-24. doi: 10.1128/AEM.00099-07. Epub 2007 May 25.
While plasmids are very commonly associated with the majority of the lactic acid bacteria, they are only very rarely associated with Lactobacillus delbrueckii, with only four characterized to date. In this study, the complete sequence of a native plasmid, pDOJ1, from a strain of Lactobacillus delbrueckii subsp. bulgaricus was determined. It consisted of a circular DNA molecule of 6,220 bp with a G+C content of 44.6% and a characteristic ori and encoded six open reading frames (ORFs), of which functions could be predicted for three-a mobilization (Mob) protein, a transposase, and a fused primase-helicase replication protein. Comparative analysis of pDOJ1 and the other available L. delbrueckii plasmids (pLBB1, pJBL2, pN42, and pLL1212) revealed a very similar organization and amino acid identities between 85 and 98% for the putative proteins of all six predicted ORFs from pDOJ1, reflecting a common origin for L. delbrueckii plasmids. Analysis of the fused primase-helicase replication gene found a similar fused organization only in the theta replicating group B plasmids from Streptococcus thermophilus. This observation and the ability of the replicon to function in S. thermophilus support the idea that the origin of plasmids in L. delbrueckii was likely from S. thermophilus. This may reflect the close association of these two species in dairy fermentations, particularly yogurt production. As no vector based on plasmid replicons from L. delbrueckii has previously been constructed, an Escherichia coli-L. delbrueckii shuttle cloning vector, pDOJ4, was constructed from pDOJ1, the p15A ori, the chloramphenicol resistance gene of pCI372, and the lacZ polylinker from pUC18. This cloning vector was successfully introduced into E. coli, L. delbrueckii subsp. bulgaricus, S. thermophilus, and Lactococcus lactis. This shuttle cloning vector provides a new tool for molecular analysis of Lactobacillus delbrueckii and other lactic acid bacteria.
虽然质粒与大多数乳酸菌密切相关,但它们与德氏乳杆菌的关联却非常罕见,迄今为止仅鉴定出4种。在本研究中,测定了一株德氏乳杆菌保加利亚亚种天然质粒pDOJ1的完整序列。它由一个6220 bp的环状DNA分子组成,G+C含量为44.6%,具有一个特征性ori,并编码6个开放阅读框(ORF),其中3个的功能可以预测——一个转移(Mob)蛋白、一个转座酶和一个融合的引发酶-解旋酶复制蛋白。对pDOJ1和其他可用的德氏乳杆菌质粒(pLBB1、pJBL2、pN42和pLL1212)的比较分析显示,其组织非常相似,pDOJ1所有6个预测ORF的假定蛋白之间的氨基酸同一性在85%至98%之间,这反映了德氏乳杆菌质粒的共同起源。对融合的引发酶-解旋酶复制基因的分析发现,只有在嗜热链球菌的θ复制B组质粒中存在类似的融合结构。这一观察结果以及该复制子在嗜热链球菌中发挥功能的能力支持了德氏乳杆菌质粒起源可能来自嗜热链球菌的观点。这可能反映了这两个物种在乳制品发酵,特别是酸奶生产中的密切关联。由于此前尚未构建基于德氏乳杆菌质粒复制子的载体,因此从pDOJ1、p15A ori、pCI372的氯霉素抗性基因和pUC18的lacZ多克隆位点构建了一种大肠杆菌-德氏乳杆菌穿梭克隆载体pDOJ4。该克隆载体已成功导入大肠杆菌、德氏乳杆菌保加利亚亚种、嗜热链球菌和乳酸乳球菌。这种穿梭克隆载体为德氏乳杆菌和其他乳酸菌的分子分析提供了一种新工具。