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dc.contributor.authorvan der Donk, Wilfred A.
dc.contributor.authorCubillos, Andres Fernando
dc.contributor.authorBecker, Jamie William
dc.contributor.authorThompson, Jessica Weidemier
dc.contributor.authorChisholm, Sallie (Penny)
dc.date.accessioned2018-04-24T13:42:28Z
dc.date.available2018-04-24T13:42:28Z
dc.date.issued2017-06
dc.date.submitted2017-01
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/114915
dc.description.abstractLanthipeptides are ribosomally derived peptide secondary metabolites that undergo extensive posttranslational modification. Prochlorosins are a group of lanthipeptides produced by certain strains of the ubiquitous marine picocyanobacteria Prochlorococcus and Synechococcus. Unlike other lanthipeptide-producing bacteria, picocyanobacteria use an unprecedented mechanism of substrate promiscuity for the production of numerous and diverse lanthipeptides using a single lanthionine synthetase. Through a cross-scale analysis of prochlorosin biosynthesis genes-from genomes to oceanic populations-we show that marine picocyanobacteria have the collective capacity to encode thousands of different cyclic peptides, few of which would display similar ring topologies. To understand how this extensive structural diversity arises, we used deep sequencing of wild populations to reveal genetic variation patterns in prochlorosin genes. We present evidence that structural variability among prochlorosins is the result of a diversifying selection process that favors large, rather than small, sequence changes in the precursor peptide genes. This mode of molecular evolution disregards any conservation of the ancestral structure and enables the emergence of extensively different cyclic peptides through short mutational paths based on indels. Contrary to its fast-evolving peptide substrates, the prochlorosin lanthionine synthetase evolves under a strong purifying selection, indicating that the diversification of prochlorosins is not constrained by commensurate changes in the biosynthetic enzyme. This evolutionary interplay between the prochlorosin peptide substrates and the lanthionine synthetase suggests that structure diversification, rather than structure refinement, is the driving force behind the creation of new prochlorosin structures and represents an intriguing mechanism by which natural product diversity arises. Keywords: lanthipeptides; prochlorosin; RiPPs; Prochlorococcus; Synechococcusen_US
dc.description.sponsorshipGordon and Betty Moore Foundation (Grant GBMF495)en_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/PNAS.1700990114en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceNational Academy of Sciencesen_US
dc.titleEvolutionary radiation of lanthipeptides in marine cyanobacteriaen_US
dc.typeArticleen_US
dc.identifier.citationCubillos-Ruiz, Andres et al. “Evolutionary Radiation of Lanthipeptides in Marine Cyanobacteria.” Proceedings of the National Academy of Sciences 114, 27 (June 2017): E5424–E5433 © 2017 The Authorsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Civil and Environmental Engineeringen_US
dc.contributor.mitauthorCubillos, Andres Fernando
dc.contributor.mitauthorBerta-Thompson, Jessica Weidemier
dc.contributor.mitauthorBecker, Jamie William
dc.contributor.mitauthorChisholm, Sallie W
dc.relation.journalProceedings of the National Academy of Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/ConferencePaperen_US
eprint.statushttp://purl.org/eprint/status/NonPeerRevieweden_US
dc.date.updated2018-04-20T13:19:08Z
dspace.orderedauthorsCubillos-Ruiz, Andres; Berta-Thompson, Jessie W.; Becker, Jamie W.; van der Donk, Wilfred A.; Chisholm, Sallie W.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8566-5567
dc.identifier.orcidhttps://orcid.org/0000-0003-2795-2418
dc.identifier.orcidhttps://orcid.org/0000-0003-4564-3192
dc.identifier.orcidhttps://orcid.org/0000-0003-1480-2445
mit.licensePUBLISHER_POLICYen_US


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