Department of Food Science and Technology, Agricultural University of Athens, Greece.
Int J Food Microbiol. 2010 Jul 15;141(3):222-8. doi: 10.1016/j.ijfoodmicro.2010.05.018. Epub 2010 May 25.
The pLAC1 plasmid of Lactobacillus acidipiscis ACA-DC 1533, a strain isolated from traditional Kopanisti cheese, was characterised. Nucleotide sequence analysis revealed a circular molecule of 3478bp with a G+C content of 37.2%. Ab initio annotation indicated four putative open reading frames (orfs). orf1 and orf4 were found to encode a replication initiation protein (Rep) and a mobilization protein (Mob), respectively. The deduced products of orf2 and orf3 revealed no significant homology to other known proteins. However, in silico examination of the plasmid sequence supported the existence of a novel operon that includes rep, orf2 and orf3 in pLAC1 and that this operon is highly conserved also in plasmids pLB925A02, pSMA23, pLC88 and pC7. RT-PCR experiments allowed us to verify that these three genes are co-transcribed as a single polycistronic mRNA species. Furthermore, phylogenetic analysis of pLAC1 Rep and Mob proteins demonstrated that they may have derived from different plasmid origins, suggesting that pLAC1 is a product of a modular evolution process. Comparative analysis of full length nucleotide sequences of pLAC1 and related Lactobacillus plasmids showed that pLAC1 shares a very similar replication backbone with pLB925A02, pSMA23 and pLC88. In contrast, mob of pLAC1 was almost identical with the respective gene of plasmids pLAB1000, pLB4 and pPB1. These findings lead to the conclusion that pLAC1 acquired mob probably via an ancestral recombination event. Our overall work highlights the importance of characterizing plasmids deriving from non-starter 'wild' isolates in order to better appreciate plasmid divergence and evolution of lactic acid bacteria.
从传统 Kopanisti 奶酪中分离出的嗜酸乳杆菌 ACA-DC 1533 的 pLAC1 质粒的特性。核苷酸序列分析显示,该质粒为一个 3478bp 的环形分子,G+C 含量为 37.2%。从头预测表明存在四个可能的开放阅读框(orf)。orf1 和 orf4 分别编码复制起始蛋白(Rep)和移动蛋白(Mob)。orf2 和 orf3 的推导产物与其他已知蛋白无明显同源性。然而,对质粒序列的计算机分析支持了 pLAC1 中存在一个新的操纵子的存在,该操纵子包括 rep、orf2 和 orf3,并且该操纵子在质粒 pLB925A02、pSMA23、pLC88 和 pC7 中也高度保守。RT-PCR 实验使我们能够验证这三个基因作为单个多顺反子 mRNA 被共同转录。此外,pLAC1 Rep 和 Mob 蛋白的系统发育分析表明,它们可能来自不同的质粒起源,表明 pLAC1 是模块化进化过程的产物。pLAC1 和相关乳杆菌质粒全长核苷酸序列的比较分析表明,pLAC1 与 pLB925A02、pSMA23 和 pLC88 具有非常相似的复制骨架。相比之下,pLAC1 的 mob 与质粒 pLAB1000、pLB4 和 pPB1 的相应基因几乎相同。这些发现表明,pLAC1 通过祖先重组事件获得了 mob。我们的整体工作强调了表征来自非启动野生分离物的质粒的重要性,以便更好地了解质粒的变异和乳酸菌的进化。