Haggoud A, Trinh S, Moumni M, Reysset G
Unité des Anaérobies, Institut Pasteur, Paris, France.
Plasmid. 1995 Sep;34(2):132-43. doi: 10.1006/plas.1995.9994.
The nucleotide sequence of the DNA replication origin region of a Bacteroides vulgatus plasmid, pIP417, encoding 5-nitroimidazole resistance has been determined. This region of 1934 bp presents some characteristics similar to those of other replication protein-dependent origins. It contains a large open reading frame which could encode a basic Rep protein (RepA) of 36.8 kDa. Upstream of this ORF exist an AT-rich region, three direct repeats (iterons) of 21 bp, multiple DnaA binding sites, and sites, and sites for the integration host factor (IHF). Moreover, the amino acid sequence of the pIP417 RepA protein shows similarities with those of other Rep proteins encoded by plasmids of gram-negative bacteria: pRO1600 from Pseudomonas aeruginosa; pPS10 from Pseudomonas syringae; pFA3 from Neisseria gonorrhoeae; and two cryptic plasmids from Campylobacter hyointestinalis and Butyrivibrio fibrisolvens. Although RepA can be expressed in an Escherichia coli in vitro transcription-translation assay, vectors containing the pIP417 replication origin did not replicate in E. coli. The homology of the pIP417 replication region with the corresponding regions of other Bacteroides spp, plasmids was also studied by Southern blot hybridization. The results indicated that the repA gene of plasmid pIP417 is homologous to that of plasmid pIP421, but not of plasmid pIP419. The replication region of plasmid pIP421 was sequenced and showed about 80% identity at the nucleotide level with that of pIP417. A small (3634-bp) cloning vector (pFK12) of entirely defined nucleotide sequence was constructed for Bacteroides spp.
已确定编码5-硝基咪唑抗性的脆弱拟杆菌质粒pIP417的DNA复制起始区域的核苷酸序列。这个1934 bp的区域呈现出一些与其他依赖复制蛋白的起始区域相似的特征。它包含一个大的开放阅读框,可编码一个36.8 kDa的碱性复制蛋白(RepA)。在这个开放阅读框的上游存在一个富含AT的区域、三个21 bp的直接重复序列(迭代子)、多个DnaA结合位点以及整合宿主因子(IHF)的位点。此外,pIP417 RepA蛋白的氨基酸序列与革兰氏阴性菌质粒编码的其他Rep蛋白的氨基酸序列相似:铜绿假单胞菌的pRO1600;丁香假单胞菌的pPS10;淋病奈瑟菌的pFA3;以及猪肠弯曲杆菌和溶纤维丁酸弧菌的两个隐蔽质粒。尽管RepA可以在大肠杆菌的体外转录-翻译试验中表达,但含有pIP417复制起始区域的载体在大肠杆菌中不复制。还通过Southern印迹杂交研究了pIP417复制区域与其他拟杆菌属质粒相应区域的同源性。结果表明,质粒pIP417的repA基因与质粒pIP421的repA基因同源,但与质粒pIP419的repA基因不同源。对质粒pIP421的复制区域进行了测序,结果显示其在核苷酸水平上与pIP417的复制区域有大约80%的同一性。构建了一个核苷酸序列完全确定的小(3634 bp)克隆载体(pFK12)用于拟杆菌属。