Alpert Carl-Alfred, Crutz-Le Coq Anne-Marie, Malleret Christine, Zagorec Monique
Flore Lactique et Environnement Carné, Institut National de la Recherche Agronomique, 78350 Jouy en Josas, France.
Appl Environ Microbiol. 2003 Sep;69(9):5574-84. doi: 10.1128/AEM.69.9.5574-5584.2003.
The complete nucleotide sequence of the 13-kb plasmid pRV500, isolated from Lactobacillus sakei RV332, was determined. Sequence analysis enabled the identification of genes coding for a putative type I restriction-modification system, two genes coding for putative recombinases of the integrase family, and a region likely involved in replication. The structural features of this region, comprising a putative ori segment containing 11- and 22-bp repeats and a repA gene coding for a putative initiator protein, indicated that pRV500 belongs to the pUCL287 subfamily of theta-type replicons. A 3.7-kb fragment encompassing this region was fused to an Escherichia coli replicon to produce the shuttle vector pRV566 and was observed to be functional in L. sakei for plasmid replication. The L. sakei replicon alone could not support replication in E. coli. Plasmid pRV500 and its derivative pRV566 were determined to be at very low copy numbers in L. sakei. pRV566 was maintained at a reasonable rate over 20 generations in several lactobacilli, such as Lactobacillus curvatus, Lactobacillus casei, and Lactobacillus plantarum, in addition to L. sakei, making it an interesting basis for developing vectors. Sequence relationships with other plasmids are described and discussed.
测定了从清酒乳杆菌RV332中分离出的13 kb质粒pRV500的完整核苷酸序列。序列分析确定了编码推定的I型限制修饰系统的基因、两个编码整合酶家族推定重组酶的基因,以及一个可能参与复制的区域。该区域的结构特征包括一个含有11 bp和22 bp重复序列的推定ori片段以及一个编码推定起始蛋白的repA基因,这表明pRV500属于θ型复制子的pUCL287亚家族。将包含该区域的一个3.7 kb片段与大肠杆菌复制子融合,构建出穿梭载体pRV566,并观察到其在清酒乳杆菌中可用于质粒复制。单独的清酒乳杆菌复制子不能在大肠杆菌中支持复制。已确定质粒pRV500及其衍生物pRV566在清酒乳杆菌中的拷贝数非常低。除清酒乳杆菌外,pRV566在几种乳杆菌中,如弯曲乳杆菌、干酪乳杆菌和植物乳杆菌中,能以合理的速率在20代以上保持稳定,这使其成为开发载体的一个有趣基础。描述并讨论了与其他质粒的序列关系。