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维氏副球菌大质粒pTAV3复制子区域的特征分析及质粒编码性状的探寻

Characterization of the replicator region of megaplasmid pTAV3 of Paracoccus versutus and search for plasmid-encoded traits.

作者信息

Bartosik Dariusz, Baj Jadwiga, Bartosik Aneta A, Wlodarczyk Miroslawa

机构信息

Department of Bacterial Genetics, Institute of Microbiology, Warsaw University, Miecznikowa 1, 02-096 Warsaw, Poland1.

出版信息

Microbiology (Reading). 2002 Mar;148(Pt 3):871-881. doi: 10.1099/00221287-148-3-871.

Abstract

The replicon of the pTAV3 megaplasmid (approx. 400 kb) of Paracoccus versutus has been localized to a 4center dot3 kb EcoRI restriction fragment and its entire nucleotide sequence determined. The G+C content of the entire sequence is 66 mol%, which is within the range (62-66 mol%) previously determined for P. versutus total DNA. ORF1 encodes a replication initiation protein Rep (47.2 kDa), which shares substantial similarity with putative proteins of the Coxiella burnetii plasmids QpH1 and QpDV, and the replication protein of Pseudomonas syringae plasmid pPS10. ORF2, located in the opposite transcriptional orientation to ORF1, encodes a putative protein that shares similarity to a subfamily of ATPases involved in plasmid partitioning. The highest similarity was observed with homologous proteins (RepA) encoded by the repABC family of replicons found in several plasmids of Agrobacterium, Rhizobium and Paracoccus spp. The predicted product of ORF3 was similar to AcoR, Nif and NtrC transcriptional activators. A strong incompatibility determinant (inc) was localized between ORF1 (rep) and ORF2 (parA). The origin of replication of pTAV400 contains a short A+T-rich region and several imperfect palindromic sequences. Curing experiments demonstrated that the megaplasmid bears genes required for growth in minimal media and can therefore be referred to as a mini-chromosome. Megaplasmids pTAV3 of P. versutus UW1 and pKLW2 of Paracoccus pantotrophus DSM 11073 were found to carry closely related, incompatible replicons. It has been shown that plasmid pORI6 (containing oriV of pTAV3 cloned into plasmid pABW1, which does not replicate in Paracoccus spp.) can be trans activated not only by pTAV3, but also by pKLW2. Using pORI6, it was demonstrated that replication systems related to pTAV3 are also present in the replicons of Paracoccus alcaliphilus JCM 7364, Paracoccus thiocyanatus IAM 12816 and Paracoccus methylutens DM 12.

摘要

维氏副球菌的pTAV3巨型质粒(约400 kb)的复制子已定位到一个4.3 kb的EcoRI限制性片段,并测定了其完整的核苷酸序列。整个序列的G+C含量为66 mol%,在先前测定的维氏副球菌总DNA的范围(62 - 66 mol%)内。ORF1编码一个复制起始蛋白Rep(47.2 kDa),它与伯纳特柯克斯体质粒QpH1和QpDV的假定蛋白以及丁香假单胞菌质粒pPS10的复制蛋白有很大的相似性。ORF2位于与ORF1相反的转录方向,编码一个假定蛋白,该蛋白与参与质粒分配的ATP酶亚家族有相似性。与农杆菌、根瘤菌和副球菌属的几个质粒中发现的repABC家族复制子编码的同源蛋白(RepA)有最高的相似性。ORF3的预测产物与AcoR、Nif和NtrC转录激活因子相似。一个强不相容决定簇(inc)定位在ORF1(rep)和ORF2(parA)之间。pTAV400的复制起点包含一个短的富含A+T的区域和几个不完全回文序列。消除实验表明,该巨型质粒携带在基本培养基中生长所需的基因,因此可称为微型染色体。发现维氏副球菌UW1的巨型质粒pTAV3和泛养副球菌DSM 11073的pKLW2携带密切相关的不相容复制子。已表明质粒pORI6(含有克隆到质粒pABW1中的pTAV3的oriV,其在副球菌属中不复制)不仅可以被pTAV3反式激活,也可以被pKLW2激活。使用pORI6证明,与pTAV3相关的复制系统也存在于嗜碱副球菌JCM 7364、硫氰副球菌IAM 12816和甲基营养副球菌DM 12的复制子中。

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