Publication:
New developments in RiPP discovery, enzymology and engineering.

dc.contributor.authorMontalbán-López, Manuel
dc.contributor.authorScott, Thomas A
dc.contributor.authorRamesh, Sangeetha
dc.contributor.authorRahman, Imran R
dc.contributor.authorvan Heel, Auke J
dc.contributor.authorViel, Jakob H
dc.contributor.authorBandarian, Vahe
dc.contributor.authorDittmann, Elke
dc.contributor.authorGenilloud, Olga
dc.contributor.authorGoto, Yuki
dc.contributor.authorGrande Burgos, María José
dc.contributor.authorHill, Colin
dc.contributor.authorKim, Seokhee
dc.contributor.authorKoehnke, Jesko
dc.contributor.authorLatham, John A
dc.contributor.authorLink, A James
dc.contributor.authorMartínez, Beatriz
dc.contributor.authorNair, Satish K
dc.contributor.authorNicolet, Yvain
dc.contributor.authorRebuffat, Sylvie
dc.contributor.authorSahl, Hans-Georg
dc.contributor.authorSareen, Dipti
dc.contributor.authorSchmidt, Eric W
dc.contributor.authorSchmitt, Lutz
dc.contributor.authorSeverinov, Konstantin
dc.contributor.authorSüssmuth, Roderich D
dc.contributor.authorTruman, Andrew W
dc.contributor.authorWang, Huan
dc.contributor.authorWeng, Jing-Ke
dc.contributor.authorvan Wezel, Gilles P
dc.contributor.authorZhang, Qi
dc.contributor.authorZhong, Jin
dc.contributor.authorPiel, Jörn
dc.contributor.authorMitchell, Douglas A
dc.contributor.authorKuipers, Oscar P
dc.contributor.authorvan der Donk, Wilfred A
dc.date.accessioned2023-02-09T09:40:47Z
dc.date.available2023-02-09T09:40:47Z
dc.date.issued2020-09-16
dc.description.abstractCovering: up to June 2020Ribosomally-synthesized and post-translationally modified peptides (RiPPs) are a large group of natural products. A community-driven review in 2013 described the emerging commonalities in the biosynthesis of RiPPs and the opportunities they offered for bioengineering and genome mining. Since then, the field has seen tremendous advances in understanding of the mechanisms by which nature assembles these compounds, in engineering their biosynthetic machinery for a wide range of applications, and in the discovery of entirely new RiPP families using bioinformatic tools developed specifically for this compound class. The First International Conference on RiPPs was held in 2019, and the meeting participants assembled the current review describing new developments since 2013. The review discusses the new classes of RiPPs that have been discovered, the advances in our understanding of the installation of both primary and secondary post-translational modifications, and the mechanisms by which the enzymes recognize the leader peptides in their substrates. In addition, genome mining tools used for RiPP discovery are discussed as well as various strategies for RiPP engineering. An outlook section presents directions for future research.
dc.identifier.doi10.1039/d0np00027b
dc.identifier.essn1460-4752
dc.identifier.pmcPMC7864896
dc.identifier.pmid32935693
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864896/pdf
dc.identifier.unpaywallURLhttps://pure.rug.nl/ws/files/159031004/d0np00027b.pdf
dc.identifier.urihttp://hdl.handle.net/10668/16260
dc.issue.number1
dc.journal.titleNatural product reports
dc.journal.titleabbreviationNat Prod Rep
dc.language.isoen
dc.organizationFundación MEDINA (Centro de Excelencia en Investigación de Medicamentos Innovadores en Andalucía)
dc.organizationFundación MEDINA
dc.page.number130-239
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, N.I.H., Extramural
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.pubmedtypeReview
dc.rights.accessRightsopen access
dc.subject.meshBiological Products
dc.subject.meshComputational Biology
dc.subject.meshEnzymes
dc.subject.meshHydroxylation
dc.subject.meshMethylation
dc.subject.meshPeptides
dc.subject.meshPhosphorylation
dc.subject.meshProtein Engineering
dc.subject.meshProtein Processing, Post-Translational
dc.subject.meshProtein Sorting Signals
dc.subject.meshRibosomes
dc.titleNew developments in RiPP discovery, enzymology and engineering.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number38
dspace.entity.typePublication

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