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dc.contributor.authorFernández-López, Cris-
dc.contributor.authorLorenzo-Díaz, Fabián-
dc.contributor.authorPérez-Luque, Rosa-
dc.contributor.authorRodríguez-González, Lorena-
dc.contributor.authorBoer, Roeland-
dc.contributor.authorLurz, Rudi-
dc.contributor.authorBravo, Alicia-
dc.contributor.authorColl, Miquel-
dc.contributor.authorEspinosa, Manuel-
dc.date.accessioned2013-12-04T12:18:11Z-
dc.date.available2013-12-04T12:18:11Z-
dc.date.issued2013-
dc.identifierdoi: 10.1016/j.plasmid.2013.03.004-
dc.identifierissn: 0147-619X-
dc.identifiere-issn: 1095-9890-
dc.identifier.citationPlasmid 70(1): 120-130 (2013)-
dc.identifier.urihttp://hdl.handle.net/10261/88209-
dc.description.abstractThe MobM relaxase (494 amino acids) encoded by the promiscuous streptococcal plasmid pMV158 recognizes the plasmid origin of transfer, oriTpMV158, and converts supercoiled pMV158 DNA into relaxed molecules by cleavage of the phosphodiester bond of a specific dinucleotide within the sequence 5'-GTGTG/TT-3' (>/> being the nick site). After cleavage, the protein remains stably bound to the 5'-end of the nick site. Band-shift assays with single-stranded oligonucleotides and size-exclusion chromatography allowed us to show that MobM was able to generate specific complexes with one of the inverted repeats of the oriTpMV158, presumably extruded as stem-loop structure. A number of tests have been performed to attain a better characterization of the nicking activity of MobM and its linkage with its target DNA. The optimal pH for DNA relaxation was found to be 6.5. Upon nicking, gel retardation assays showed that MobM formed stable complexes with its target DNA. Moreover, MobM bound to relaxed pMV158 molecules were visualized by electron microscopy. The staphylococcal plasmids pUB110 and pE194, and the streptococcal plasmid pDL287 harbour putative oriTs and may encode Mob proteins homologous to MobM. The oriTpUB110, oriTpDL287, and oriTpE194 sequences share 100%, 70%, and 67% (in a 43-nucleotide stretch and allowing a 3-bp gap) identity to oriTpMV158, respectively. Nicking assays using supercoiled DNAs from pUB110, pDL287, and pE194 showed that MobM was able to relax, to differing degrees, all plasmid DNAs. Our results suggest that cross-recognition of heterologous oriTs by Mob proteins could play an important role in the plasmid spreading between bacteria. © 2013 Elsevier Inc.-
dc.description.sponsorshipResearch financed by the Spanish Ministry of Economy and Competitiveness (grants CSD-2008-00013-INTERMODS and BFU2010-19597 to M.E., BFU2009-11868 to A.B., and BFU2008-02372/BMC, CONSOLIDER CSD 2006-23, and BFU2011-22588 to M.C), the Generalitat de Catalunya (SGR2009-1309 to M.C.), and the European Commission (FP7 Cooperation Project SILVER - GA No. 260644, to M.C.).-
dc.language.isoeng-
dc.publisherElsevier-
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/260644-
dc.rightsopenAccess-
dc.subjectOrigin of transfer-
dc.subjectRolling circle-replicating plasmids-
dc.subjectDNA relaxase-
dc.subjectDNA–protein interactions-
dc.titleNicking activity of the pMV158 MobM relaxase on cognate and heterologous origins of transfer-
dc.typeartículo-
dc.identifier.doi10.1016/j.plasmid.2013.03.004-
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.plasmid.2013.03.004-
dc.date.updated2013-12-04T12:18:11Z-
dc.description.versionPeer Reviewed-
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