Designer Sinorhizobium meliloti strains and multi-functional vectors enable direct inter-kingdom DNA transfer

dc.contributor.authorBrumwell, Stephanie L.
dc.contributor.authorMacLeod, Michael R.
dc.contributor.authorHuang, Tony
dc.contributor.authorCochrane, Ryan R.
dc.contributor.authorMeaney, Rebecca S.
dc.contributor.authorZamani, Maryam
dc.contributor.authorMatysiakiewicz, Ola
dc.contributor.authorDan, Kaitlyn N.
dc.contributor.authorJanakirama, Preetam
dc.contributor.authorEdgell, David R.
dc.contributor.authorCharles, Trevor C.
dc.contributor.authorFinan, Turlough M.
dc.contributor.authorKaras, Bogumil J.
dc.date.accessioned2026-05-07T19:50:30Z
dc.date.available2026-05-07T19:50:30Z
dc.date.issued2019-06-17
dc.description© 2019 Brumwell et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.description.abstractStorage, manipulation and delivery of DNA fragments is crucial for synthetic biology applications, subsequently allowing organisms of interest to be engineered with genes or pathways to produce desirable phenotypes such as disease or drought resistance in plants, or for synthesis of a specific chemical product. However, DNA with high G+C content can be unstable in many host organisms including Saccharomyces cerevisiae. Here, we report the development of Sinorhizobium meliloti, a nitrogen-fixing plant symbioticα-Proteobacterium, as a novel host that can store DNA, and mobilize DNA to E. coli, S. cerevisiae, and the eukaryotic microalgae Phaeodactylum tricornutum. To achieve this, we deleted the hsdR restriction-system in multiple reduced genome strains of S. meliloti that enable DNA transformation with up to 1.4 x 105 and 2.1 x 103 CFU μg-1 of DNA efficiency using electroporation and a newly developed polyethylene glycol transformation method, respectively. Multi-host and multi-functional shuttle vectors (MHS) were constructed and stably propagated in S. meliloti, E. coli, S. cerevisiae, and P. tricornutum. We also developed protocols and demonstrated direct transfer of these MHS vectors via conjugation from S. meliloti to E. coli, S. cerevisiae, and P. tricornutum. The development of S. meliloti as a new host for inter-kingdom DNA transfer will be invaluable for synthetic biology research and applications, including the installation and study of genes and biosynthetic pathways into organisms of interest in industry and agriculture.
dc.description.sponsorshipGenome Canada Grant, OGI-111 || Natural Sciences and Engineering Research Council of Canada (NSERC), RGPIN-2015-04800 || NSERC, RGPIN-2018-04754 || NSERC, RGPIN-2018-06481 || NSERC, RGPIN-2018-06172.
dc.identifier.urihttps://doi.org/10.1371/journal.pone.0206781
dc.identifier.urihttps://hdl.handle.net/10012/23272
dc.language.isoen
dc.publisherPublic Library of Science
dc.relation.ispartofseriesPLoS ONE; 14(6); e0206781
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectsaccharomyces cerevisiae
dc.subjectDNA isolation
dc.subjectplasmid construction
dc.subjectstreptomycin
dc.subjectgene transfer
dc.subjectantibiotics
dc.subjectDNA cloning
dc.subjectelectroporation
dc.titleDesigner Sinorhizobium meliloti strains and multi-functional vectors enable direct inter-kingdom DNA transfer
dc.typeArticle
dcterms.bibliographicCitationBrumwell SL, MacLeod MR, Huang T, Cochrane RR, Meaney RS, Zamani M, et al. (2019) Designer Sinorhizobium meliloti strains and multi-functional vectors enable direct inter-kingdom DNA transfer. PLoS ONE 14(6): e0206781. https://doi.org/10.1371/journal.pone.0206781
uws.contributor.affiliation1Faculty of Science
uws.contributor.affiliation2Biology
uws.peerReviewStatusReviewed
uws.scholarLevelFaculty
uws.typeOfResourceTexten

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