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dc.contributor.authorClarke, David
dc.contributor.authorFeng, Xuan
dc.contributor.authorDeng, Hai
dc.contributor.authorZhang, Qingzhi
dc.contributor.authorO'Hagan, David
dc.date.accessioned2023-09-26T16:30:20Z
dc.date.available2023-09-26T16:30:20Z
dc.date.issued2023-10-27
dc.identifier293900941
dc.identifierc7becf53-b775-4df7-a028-a8e8bd194e5e
dc.identifier85174955853
dc.identifier.citationClarke , D , Feng , X , Deng , H , Zhang , Q & O'Hagan , D 2023 , ' 3′- O -β-Glucosyl-4′,5′-didehydro-5′-deoxyadenosine is a natural product of the nucleocidin producers  Streptomyces virens  and  Streptomyces calvus ' , Journal of Natural Products , vol. 86 , no. 10 , pp. 2326-2332 . https://doi.org/10.1021/acs.jnatprod.3c00521en
dc.identifier.issn0163-3864
dc.identifier.otherORCID: /0000-0002-0510-5552/work/143335881
dc.identifier.urihttps://hdl.handle.net/10023/28455
dc.descriptionFunding: Leverhulme Trust - RPG-2021-028.en
dc.description.abstract3′-O-β-Glucosyl-4′,5′-didehydro-5′-deoxyadenosine 13 is identified as a natural product of Streptomyces calvus and Streptomyces virens. It is also generated in vitro by direct β-glucosylation of 4′,5′-didehydro-5′-deoxyadenosine 12 with the enzyme NucGT. The intact incorporation of oxygen-18 and deuterium isotopes from (±)[1-18O,1-2H2]-glycerol 14 into C-5′ of nucleocidin 1 and its related metabolites precludes 3′-O-β-glucosyl-4′,5′-didehydro-5′-deoxyadenosine 13 as a biosynthetic precursor to nucleocidin 1.
dc.format.extent7
dc.format.extent2521908
dc.language.isoeng
dc.relation.ispartofJournal of Natural Productsen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subjectMCCen
dc.subject.lccQDen
dc.title3′-O-β-Glucosyl-4′,5′-didehydro-5′-deoxyadenosine is a natural product of the nucleocidin producers Streptomyces virens and Streptomyces calvusen
dc.typeJournal articleen
dc.contributor.sponsorThe Leverhulme Trusten
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. Institute of Behavioural and Neural Sciencesen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doihttps://doi.org/10.1021/acs.jnatprod.3c00521
dc.description.statusPeer revieweden
dc.identifier.grantnumberRPG-2021-028en


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