Delver E P, Belogurova N G, Tupikova E E, Varfolomeyev S D, Belogurov A A
Department of Genetic Engineering, Cardiology Research Center, Moscow, Russia.
Mol Gen Genet. 1996 Nov 27;253(1-2):166-72. doi: 10.1007/s004380050309.
The 1882-bp nucleotide sequence of the cryptic plasmid pNB2 isolated from the thermophilic bacterium Clostridium thermosaccharolyticum was determined. pNB2 DNA has very low GC content (27%) and may serve as a model for studying the modes of maintenance and replication of AT-rich DNA under conditions of thermophilic growth. The plasmid sequence revealed three open reading frames (ORFs) which would encode polypeptides of 289, 68 and 59 amino acids, respectively, and these proteins were synthesized in E. coli extracts primed with the plasmid. We found that the product of ORF289 may be initiated at the non-ATG start codon, TTG, and has similarities with the conserved motifs of Rep proteins encoded by rolling circle (RC) plasmids of the pC194/pUB110 family. Southern hybridization analysis of lysates of C. thermosaccharolyticum cells harboring pNB2 revealed single-stranded intermediates, suggesting that this plasmid is able to replicate in clostridial cells via the RC mechanism. The most significant similarities are found between pNB2 Rep protein and the Rep proteins of three RC plasmids of the pC194 family (pTB913, pBC1 and pST1) isolated from thermophilic bacteria. Comparative analysis of these Rep proteins showed that despite the significant level of divergence, these Rep proteins share a high degree of similarity in the regions of five well-known conserved domains of RC Rep proteins and fall into two groups in accordance with the similarities found in their active sites.
测定了从嗜热细菌嗜热解糖梭菌中分离出的隐蔽质粒pNB2的1882bp核苷酸序列。pNB2 DNA的GC含量非常低(27%),可作为研究嗜热生长条件下富含AT的DNA的维持和复制模式的模型。该质粒序列揭示了三个开放阅读框(ORF),分别编码289、68和59个氨基酸的多肽,这些蛋白质在以该质粒为引物的大肠杆菌提取物中合成。我们发现ORF289的产物可能起始于非ATG起始密码子TTG,并且与pC194/pUB110家族滚环(RC)质粒编码的Rep蛋白的保守基序相似。对携带pNB2的嗜热解糖梭菌细胞裂解物的Southern杂交分析揭示了单链中间体,表明该质粒能够通过RC机制在梭菌细胞中复制。在pNB2 Rep蛋白与从嗜热细菌中分离出的pC194家族的三个RC质粒(pTB913、pBC1和pST1)的Rep蛋白之间发现了最显著的相似性。对这些Rep蛋白的比较分析表明,尽管存在显著的差异水平,但这些Rep蛋白在RC Rep蛋白五个著名保守结构域的区域中具有高度相似性,并根据其活性位点的相似性分为两组。