Galli D M, LeBlanc D J
Department of Microbiology, University of Texas Health Science Center at San Antonio 78284.
Plasmid. 1994 Mar;31(2):148-57. doi: 10.1006/plas.1994.1016.
The presence of plasmid DNA in Actinobacillus actinomycetemcomitans has been reported. Recently, the construction of an Escherichia coli/A. actinomycetemcomitans shuttle vector, based on the A. actinomycetemcomitans-derived 2.0-kb plasmid pVT736-1, was described (D. J. LeBlanc, A. R. Abu-Al-Jaibat, P. K. Sreenivasan, and P. M. Fives-Taylor, Oral Microbiol. Immunol. (1993) 8, 94-99). The current study was initiated with the determination of the nucleotide sequence of pVT736-1, which revealed the presence of two open reading frames (ORFs) encoding proteins of 293 (ORF1) and 95 (ORF2) amino acids. Evidence that pVT736-1 replicates via a single-stranded (ss) intermediate included: (i) the presence of ssDNA in cells and in cell-free supernatant, (ii) the presence of conserved sequence motifs in the predicted ORF1 protein that are typical of initiator (Rep) proteins associated with replication by a rolling-circle mode, and (iii) 39% amino acid identity between the putative Rep proteins of pVT736-1 and Pf3, a filamentous ssDNA bacteriophage of Pseudomonas aeruginosa. A putative plus origin of replication in pVT736-1 was located upstream of ORF1, in a 200-bp region with potential for secondary hairpin structures. The identification in gram-negative bacteria of extrachromosomal DNA (other than bacteriophage) that replicates by a rolling-circle mode and shows no extensive homology to plasmids from gram-positive organisms is rather unique.
据报道,伴放线放线杆菌中存在质粒DNA。最近,有人描述了基于来源于伴放线放线杆菌的2.0 kb质粒pVT736 - 1构建的大肠杆菌/伴放线放线杆菌穿梭载体(D. J. 勒布朗、A. R. 阿布 - 阿尔 - 贾伊巴特、P. K. 斯里尼瓦桑和P. M. 菲夫斯 - 泰勒,《口腔微生物学与免疫学》(1993年)8卷,94 - 99页)。本研究始于对pVT736 - 1核苷酸序列的测定,结果显示存在两个开放阅读框(ORF),分别编码含293个氨基酸的蛋白质(ORF1)和含95个氨基酸的蛋白质(ORF2)。有证据表明pVT736 - 1通过单链(ss)中间体进行复制,包括:(i)细胞和无细胞上清液中存在ssDNA;(ii)预测的ORF1蛋白中存在保守序列基序,这些基序是与滚环模式复制相关的起始蛋白(Rep)所特有的;(iii)pVT736 - 1的推定Rep蛋白与铜绿假单胞菌的丝状ssDNA噬菌体Pf3之间有39%的氨基酸同一性。pVT736 - 1中一个推定的正链复制起点位于ORF1上游,在一个具有潜在二级发夹结构的200 bp区域内。在革兰氏阴性细菌中鉴定出通过滚环模式复制且与革兰氏阳性生物的质粒无广泛同源性的染色体外DNA(噬菌体除外)是相当独特的。