Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/130442
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dc.creatorReis, J.P.A
dc.creatorFigueiredo, S.A.C
dc.creatorSousa, M.L
dc.creatorLeão, P.N.
dc.date.accessioned2020-12-04T15:17:04Z-
dc.date.available2020-12-04T15:17:04Z-
dc.date.issued2020
dc.identifier.issnISSN 2041-1723
dc.identifier.urihttps://hdl.handle.net/10216/130442-
dc.description.abstractEsterification reactions are central to many aspects of industrial and biological chemistry. The formation of carboxyesters typically occurs through nucleophilic attack of an alcohol onto the carboxylate carbon. Under certain conditions employed in organic synthesis, the carboxylate nucleophile can be alkylated to generate esters from alkyl halides, but this reaction has only been observed transiently in enzymatic chemistry. Here, we report a carboxylate alkylating enzyme – BrtB – that catalyzes O-C bond formation between free fatty acids of varying chain length and the secondary alkyl halide moieties found in the bartolosides. Guided by this reactivity, we uncovered a variety of natural fatty acid-bartoloside esters, previously unrecognized products of the bartoloside biosynthetic gene cluster. © 2020, The Author(s).
dc.description.sponsorshipWe acknowledge funding by the European Research Council, through a Starting Grant (Grant Agreement 759840) to P.N.L., and by Fundação para a Ciência e Tecnologia (FCT) through project PTDC/BIA-BQM/29710/2017 and grant IF/01358/2014 to P.N.L. The work was also partially supported by Strategic Funding UIDB/04423/2020 and UIDP/04423/2020 by FCT and the European Regional Development Fund, as part of the program PT2020. We thank Emily Balskus (Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA) for helpful discussions and Ralph Urbatzka (CIIMAR, University of Porto, Porto, Portugal) for help with cytotoxicity assays.
dc.language.isoeng
dc.publisherNature Communications
dc.relation.ispartofNature Communications volume 11, Article number: 1458 (2020)
dc.rightsopenAccess
dc.subjectalcohol
dc.subjectcarbon
dc.subjectcarboxylic acid
dc.subjectenzyme
dc.subjectfatty acid bartoloside ester
dc.subjectfatty acid ester
dc.subjecthalide
dc.subjectnucleophile
dc.subjectoxygen
dc.subjectprotein brtb
dc.subjectunclassified drug
dc.subjectalkylating agent
dc.subjectbacterial protein
dc.subjectester
dc.subjectfatty acid
dc.subjectpolycyclic aromatic hydrocarbon
dc.subjecttransferase
dc.subjectcatalysis
dc.subjectcatalyst
dc.subjectchemical bonding
dc.subjectchemical compound
dc.subjectchemical reaction
dc.subjectenzyme
dc.subjectenzyme activity
dc.subjectArticle
dc.subjectcatalysis
dc.subjectchemical binding
dc.subjectchemical bond
dc.subjectcontrolled study
dc.subjectesterification
dc.subjectgene cluster
dc.subjectnonhuman
dc.subjectnucleophilicity
dc.subjectsynthesis
dc.subjectalkylation
dc.subjectenzymology
dc.subjectgenetics
dc.subjectmetabolism
dc.subjectmultigene family
dc.subjectprocedures
dc.subjectSynechocystis
dc.subjectAlkylating Agents
dc.subjectAlkylation
dc.subjectBacterial Proteins
dc.subjectChemistry Techniques, Synthetic
dc.subjectEsterification
dc.subjectEsters
dc.subjectFatty Acids
dc.subjectMultigene Family
dc.subjectPolycyclic Aromatic Hydrocarbons
dc.subjectSynechocystis
dc.subjectTransferases
dc.titleBrtB is an O-alkylating enzyme that generates fatty acid-bartoloside esters
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoCentro Interdisciplinar de Investigação Marinha e Ambiental
dc.identifier.doihttps://doi.org/10.1038/s41467-020-15302-z
dc.relation.publisherversionhttps://www.nature.com/articles/s41467-020-15302-z
Appears in Collections:CIIMAR - Artigo em Revista Científica Internacional

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