Servicio de Microbiología, Hospital Universitario Marqués de Valdecilla e Instituto de Formación e Investigación Marqués de Valdecilla, Santander 39008, Spain.
Proc Natl Acad Sci U S A. 2013 Aug 13;110(33):13606-11. doi: 10.1073/pnas.1310037110. Epub 2013 Jul 31.
Plasmid pAD1 is a 60-kb conjugative element commonly found in clinical isolates of Enterococcus faecalis. The relaxase TraX and the primary origin of transfer oriT2 are located close to each other and have been shown to be essential for conjugation. The oriT2 site contains a large inverted repeat (where the nic site is located) adjacent to a series of short direct repeats. TraX does not show any of the typical relaxase sequence motifs but is the prototype of a unique family of relaxases (MOBC). The present study focuses on the genetic, biochemical, and structural analysis of TraX, whose 3D structure could be predicted by protein threading. The structure consists of two domains: (i) an N-terminal domain sharing the topology of the DNA binding domain of the MarR family of transcriptional regulators and (ii) a C-terminal catalytic domain related to the PD-(D/E)XK family of restriction endonucleases. Alignment of MOBC relaxase amino acid sequences pointed to several conserved polar amino acid residues (E28, D152, E170, E172, K176, R180, Y181, and Y203) that were mutated to alanine. Functional analysis of these mutants (in vivo DNA transfer and cleavage assays) revealed the importance of these residues for relaxase activity and suggests Y181 as a potential catalytic residue similarly to His-hydrophobe-His relaxases. We also show that TraX binds specifically to dsDNA containing the oriT2 direct repeat sequences, confirming their role in transfer specificity. The results provide insights into the catalytic mechanism of MOBC relaxases, which differs radically from that of His-hydrophobe-His relaxases.
质粒 pAD1 是一种常见于临床分离的粪肠球菌的 60kb 可接合元件。松弛酶 TraX 和主要转移原点 oriT2 彼此靠近,已被证明对接合至关重要。oriT2 位点包含一个大的反向重复(nic 位点位于此处),紧邻一系列短的直接重复。TraX 没有显示任何典型的松弛酶序列基序,但它是独特的松弛酶家族(MOBC)的原型。本研究集中于 TraX 的遗传、生化和结构分析,其 3D 结构可通过蛋白质穿线预测。该结构由两个结构域组成:(i)一个 N 端结构域,其拓扑结构与 MarR 家族转录调节剂的 DNA 结合结构域相似;(ii)一个 C 端催化结构域,与 PD-(D/E)XK 家族的限制内切酶有关。MOBC 松弛酶氨基酸序列的比对指出了几个保守的极性氨基酸残基(E28、D152、E170、E172、K176、R180、Y181 和 Y203),这些残基突变为丙氨酸。这些突变体的功能分析(体内 DNA 转移和切割试验)表明这些残基对松弛酶活性很重要,并表明 Y181 是一个潜在的催化残基,类似于 His-hydrophobe-His 松弛酶。我们还表明,TraX 特异性结合含有 oriT2 直接重复序列的 dsDNA,证实了它们在转移特异性中的作用。这些结果为 MOBC 松弛酶的催化机制提供了深入的了解,该机制与 His-hydrophobe-His 松弛酶有很大的不同。