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dc.contributor.authorParajuli, Anirudra
dc.contributor.authorKwak, Daniel H.
dc.contributor.authorDalponte, Luca
dc.contributor.authorLeikoski, Niina
dc.contributor.authorGalica, Tomas
dc.contributor.authorUmeobika, Ugochukwu
dc.contributor.authorTrembleau, Laurent
dc.contributor.authorBent, Andrew
dc.contributor.authorSivonen, Kaarina
dc.contributor.authorWahlsten, Matti
dc.contributor.authorWang, Hao
dc.contributor.authorRizzi, Ermanno
dc.contributor.authorDe Bellis, Gianluca
dc.contributor.authorNaismith, Jim
dc.contributor.authorJaspars, Marcel
dc.contributor.authorLiu, Xinyu
dc.contributor.authorHoussen, Wael
dc.contributor.authorFewer, David Peter
dc.date.accessioned2017-02-06T00:32:52Z
dc.date.available2017-02-06T00:32:52Z
dc.date.issued2016-03-07
dc.identifier243429965
dc.identifier885e827e-43a6-4297-929a-f79f643f33a7
dc.identifier84961147896
dc.identifier000371521000007
dc.identifier.citationParajuli , A , Kwak , D H , Dalponte , L , Leikoski , N , Galica , T , Umeobika , U , Trembleau , L , Bent , A , Sivonen , K , Wahlsten , M , Wang , H , Rizzi , E , De Bellis , G , Naismith , J , Jaspars , M , Liu , X , Houssen , W & Fewer , D P 2016 , ' A unique Tryptophan C-prenyltransferase from the kawaguchipeptin biosynthetic pathway ' , Angewandte Chemie International Edition , vol. 55 , no. 11 , pp. 3596-3599 . https://doi.org/10.1002/anie.201509920en
dc.identifier.issn1521-3773
dc.identifier.otherBibtex: urn:d1fa2be2eb20c6a8ff8e80f33011081d
dc.identifier.urihttps://hdl.handle.net/10023/10234
dc.descriptionThis work was supported by funding of the Academy of Finland (259505), Helsinki University Research grant (490085) and ESCMID grant (4720572) to D.P.F., University of Pittsburgh Central Research Development Fund to X.L., Technology Strategy Board grant (131181) to W.H., M.J. and J.H.N. National Programme of Sustainability I of the Ministry of Education of the Czech Republic I grant (LO1416) to T.G.en
dc.description.abstractCyanobactins are a rapidly growing family of linear and cyclic peptides produced by cyanobacteria. Kawaguchipeptins A and B, two macrocyclic undecapeptides reported earlier from Microcystis aeruginosa NIES-88, are shown to be products of the cyanobactin biosynthetic pathway. The 9 kb kawaguchipeptin (kgp) gene cluster was identified in a 5.26 Mb draft genome of Microcystis aeruginosa NIES-88. We verified that this gene cluster is responsible for the production of the kawaguchipeptins through heterologous expression of the kgp gene cluster in Escherichia coli. The KgpF prenyltransferase was overexpressed and was shown to prenylate C-3 of Trp residues in both linear and cyclic peptides in vitro. Our findings serve to further enhance the structural diversity of cyanobactins to include tryptophan-prenylated cyclic peptides.
dc.format.extent4
dc.format.extent1016373
dc.language.isoeng
dc.relation.ispartofAngewandte Chemie International Editionen
dc.subjectBiosynthesisen
dc.subjectCyanobactinsen
dc.subjectPeptidesen
dc.subjectPrenylationen
dc.subjectPrenyltransferasesen
dc.subjectQD Chemistryen
dc.subjectQR Microbiologyen
dc.subjectNDASen
dc.subject.lccQDen
dc.subject.lccQRen
dc.titleA unique Tryptophan C-prenyltransferase from the kawaguchipeptin biosynthetic pathwayen
dc.typeJournal articleen
dc.contributor.sponsorBBSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doi10.1002/anie.201509920
dc.description.statusPeer revieweden
dc.date.embargoedUntil2017-02-05
dc.identifier.urlhttp://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.201509920/suppinfoen
dc.identifier.grantnumberBB/K015508/1en


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