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Ketopremithramycins and ketomithramycins; four new aureolic acid-type compounds obtained upon inactivation of two genes involved in the biosynthesis of the deoxysugar moieties of the antitumor drug mithramycin by Streptomyces Argillaceus; reveal novel insights into post-PKS tailoring steps of the mithramycin biosynthetic pathway

dc.contributor.authorRemsing, Lily
dc.contributor.authorGarcía-Bernardo Junquera, José
dc.contributor.authorGonzález, A.
dc.contributor.authorKünzel, Eva
dc.contributor.authorRix, Uwe
dc.contributor.authorFernández Braña, Alfredo Javier 
dc.contributor.authorBearden, D. W.
dc.contributor.authorMéndez Fernández, María del Carmen 
dc.contributor.authorSalas Fernández, José Antonio 
dc.contributor.authorRohr, Jürgen
dc.date.accessioned2017-04-24T11:44:59Z
dc.date.available2017-04-24T11:44:59Z
dc.date.issued2002
dc.identifier.citationJournal of the American Chemical Society, 124(8), p. 1606-1614 (2002); doi:10.1021/ja0105156
dc.identifier.issn0002-7863
dc.identifier.issn1520-5126
dc.identifier.urihttp://hdl.handle.net/10651/42083
dc.description.sponsorshipThis work was supported by grants of the South Carolina Commission of Higher Education (2000−2001), the U.S. Department of Defense, and the National Institutes of Health (R01CA91901) to J.R., and by the Spanish Ministry of Education and Science to J.A.S. through the “Plan Nacional en Biotecnologia” (R01CA91901). Drs. William Cotham and Michael Walla, Department of Chemistry and Biochemistry, University of South Carolina, are acknowledged for recording the FAB mass spectra.
dc.format.extentp. 1606-1614
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.relation.ispartofJournal of the American Chemical Society
dc.rights©
dc.sourceScopus
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0037181040&doi=10.1021%2fja0105156&partnerID=40&md5=2a20ebd7b42d5957b1840f10df877297
dc.titleKetopremithramycins and ketomithramycins; four new aureolic acid-type compounds obtained upon inactivation of two genes involved in the biosynthesis of the deoxysugar moieties of the antitumor drug mithramycin by Streptomyces Argillaceus; reveal novel insights into post-PKS tailoring steps of the mithramycin biosynthetic pathway
dc.typejournal article
dc.identifier.doi10.1021/ja0105156
dc.relation.projectIDR01CA91901
dc.relation.projectIDBIO97-0771
dc.relation.publisherversionhttp://dx.doi.org/10.1021/ja0105156


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