Delineation of a lactococcal conjugation system reveals a restriction-modification evasion system

dc.contributor.authorOrtiz Charneco, Guillermoen
dc.contributor.authorKelleher, Philipen
dc.contributor.authorBuivydas, Andriusen
dc.contributor.authorDashko, Sofia,en
dc.contributor.authorde Waal, Paul P.en
dc.contributor.authorvan Peij, Noël N. M. E.en
dc.contributor.authorRoberts, Richard Johnen
dc.contributor.authorMahony, Jenniferen
dc.contributor.authorvan Sinderen, Douween
dc.contributor.funderScience Foundation Ireland
dc.date.accessioned2023-08-16T09:59:34Z
dc.date.available2023-08-16T10:05:09Zen
dc.date.available2023-08-16T09:59:34Z
dc.date.issued2023-06en
dc.date.updated2023-08-16T09:05:13Zen
dc.description.abstractPlasmid pUC11B is a 49.3-kb plasmid harboured by the fermented meat isolate Lactococcus lactis subsp. lactis UC11. Among other features, pUC11B encodes a pMRC01-like conjugation system and tetracycline-resistance. In this study, we demonstrate that this plasmid can be conjugated at high frequencies to recipient strains. Mutational analysis of the 22 genes encompassing the presumed pUC11B conjugation cluster revealed the presence of several genes with essential conjugation functions, as well as a gene, trsR, encoding a putative transcriptional repressor of this conjugation cluster. Furthermore, plasmid pUC11B encodes an anti-restriction protein, TrsAR, which facilitates higher conjugation frequencies when pUC11B is transferred into recipient strains containing Type II or Type III RM systems. These findings demonstrate how RM mechanisms can be circumvented when they act as a biological barrier for conjugation events.en
dc.description.statusPeer revieweden
dc.description.versionPublished Version
dc.format.mimetypeapplication/pdfen
dc.identifier.citationOrtiz Charneco, G., Kelleher, P., Buivydas, A., Dashko, S., De Waal, P. P., Van Peij, N. N. M. E., Roberts, R. J., Mahony, J. and Van Sinderen, D. (2023) ‘Delineation of a lactococcal conjugation system reveals a restriction‐modification evasion system’, Microbial Biotechnology, 16(6), pp. 1250–1263. doi: 10.1111/1751-7915.14221
dc.identifier.doi10.1111/1751-7915.14221en
dc.identifier.endpage1263
dc.identifier.issued6
dc.identifier.journaltitleMicrobial Biotechnology
dc.identifier.startpage1250
dc.identifier.urihttps://hdl.handle.net/10468/14836
dc.identifier.volume16
dc.language.isoenen
dc.publisherJohn Wiley & Sons, Inc.
dc.relation.projectinfo:eu-repo/grantAgreement/SFI/SFI Research Centres/12/RC/2273/IE/Alimentary Pharmabiotic Centre (APC) - Interfacing Food & Medicine/
dc.relation.projectinfo:eu-repo/grantAgreement/SFI/SFI Spokes Programme::Rolling Call/17/SP/4678/IE/BacTrans – Natural DNA Transfer Systems for Bacterial Starter Cultures/
dc.rights© 2023 The Authors. Microbial Biotechnology published by Applied Microbiology International and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectPlasmid pUC11B
dc.subjectMutational analysisp
dc.subjectUC11B conjugation cluster
dc.subjectRM mechanisms
dc.titleDelineation of a lactococcal conjugation system reveals a restriction-modification evasion system
dc.typeArticle (peer-reviewed)
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