Department of Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Groningen, The Netherlands.
PLoS One. 2012;7(4):e35285. doi: 10.1371/journal.pone.0035285. Epub 2012 Apr 19.
Most strains of Neisseria gonorrhoeae carry a Gonococcal Genetic Island which encodes a type IV secretion system involved in the secretion of ssDNA. We characterize the GGI-encoded ssDNA binding protein, SsbB. Close homologs of SsbB are located within a conserved genetic cluster found in genetic islands of different proteobacteria. This cluster encodes DNA-processing enzymes such as the ParA and ParB partitioning proteins, the TopB topoisomerase, and four conserved hypothetical proteins. The SsbB homologs found in these clusters form a family separated from other ssDNA binding proteins.
METHODOLOGY/PRINCIPAL FINDINGS: In contrast to most other SSBs, SsbB did not complement the Escherichia coli ssb deletion mutant. Purified SsbB forms a stable tetramer. Electrophoretic mobility shift assays and fluorescence titration assays, as well as atomic force microscopy demonstrate that SsbB binds ssDNA specifically with high affinity. SsbB binds single-stranded DNA with minimal binding frames for one or two SsbB tetramers of 15 and 70 nucleotides. The binding mode was independent of increasing Mg(2+) or NaCl concentrations. No role of SsbB in ssDNA secretion or DNA uptake could be identified, but SsbB strongly stimulated Topoisomerase I activity.
CONCLUSIONS/SIGNIFICANCE: We propose that these novel SsbBs play an unknown role in the maintenance of genetic islands.
大多数淋病奈瑟菌菌株携带淋球菌遗传岛,该岛编码一种参与 ssDNA 分泌的 IV 型分泌系统。我们对 GGI 编码的 ssDNA 结合蛋白 SsbB 进行了特征描述。SsbB 的密切同源物位于不同变形菌遗传岛中保守的遗传簇内。该簇编码 DNA 处理酶,如 ParA 和 ParB 分区蛋白、TopB 拓扑异构酶和四个保守的假设蛋白。这些簇中发现的 SsbB 同源物形成了一个与其他 ssDNA 结合蛋白分离的家族。
方法/主要发现:与大多数其他 SSB 不同,SsbB 不能补充大肠杆菌 ssb 缺失突变体。纯化的 SsbB 形成稳定的四聚体。电泳迁移率变动分析和荧光滴定分析以及原子力显微镜表明,SsbB 特异性地以高亲和力结合 ssDNA。SsbB 以最小的结合框架结合单链 DNA,对于 15 和 70 个核苷酸的一个或两个 SsbB 四聚体,结合框架分别为 15 和 70 个核苷酸。结合模式不依赖于增加的 Mg(2+)或 NaCl 浓度。未发现 SsbB 在 ssDNA 分泌或 DNA 摄取中的作用,但 SsbB 可强烈刺激拓扑异构酶 I 活性。
结论/意义:我们提出这些新型 SsbB 在遗传岛的维持中发挥未知作用。