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Identification of the Tirandamycin Biosynthetic Gene Cluster from Streptomyces sp. 307-9

dc.contributor.authorCarlson, Jacob C.en_US
dc.contributor.authorFortman, J. L.en_US
dc.contributor.authorAnzai, Yojiroen_US
dc.contributor.authorLi, Shengyingen_US
dc.contributor.authorBurr, Douglas A.en_US
dc.contributor.authorSherman, David H.en_US
dc.date.accessioned2010-04-14T20:02:02Z
dc.date.available2011-03-01T16:26:42Zen_US
dc.date.issued2010-03-01en_US
dc.identifier.citationCarlson, Jacob C.; Fortman, J. L.; Anzai, Yojiro; Li, Shengying; Burr, Douglas A.; Sherman, David H. (2010). "Identification of the Tirandamycin Biosynthetic Gene Cluster from Streptomyces sp. 307-9." ChemBioChem 11(4): 564-572. <http://hdl.handle.net/2027.42/69167>en_US
dc.identifier.issn1439-4227en_US
dc.identifier.issn1439-7633en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/69167
dc.description.abstractThe structurally intriguing bicyclic ketal moiety of tirandamycin is common to several acyl-tetramic acid antibiotics, and is a key determinant of biological activity. We have identified the tirandamycin biosynthetic gene cluster from the environmental marine isolate Streptomyces sp. 307–9, thus providing the first genetic insight into the biosynthesis of this natural product scaffold. Sequence analysis revealed a hybrid polyketide synthase–nonribosomal peptide synthetase gene cluster with a colinear domain organization, which is entirely consistent with the core structure of the tirandamycins. We also identified genes within the cluster that encode candidate tailoring enzymes for elaboration and modification of the bicyclic ketal system. Disruption of tamI , which encodes a presumed cytochrome P450, led to a mutant strain deficient in production of late stage tirandamycins that instead accumulated tirandamycin C, an intermediate devoid of any post assembly-line oxidative modifications.en_US
dc.format.extent1739243 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
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dc.publisherWILEY-VCH Verlagen_US
dc.subject.otherChemistryen_US
dc.subject.otherBiochemistry and Biotechnologyen_US
dc.titleIdentification of the Tirandamycin Biosynthetic Gene Cluster from Streptomyces sp. 307-9en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumLife Sciences Institute and Departments of Medicinal Chemistry, Microbiology, Immunology and Chemistry, University of Michigan, 210 Washtenaw Avenue, Ann Arbor, MI (USA), Fax: (+1) 734-615-3641en_US
dc.contributor.affiliationumLife Sciences Institute and Departments of Medicinal Chemistry, Microbiology, Immunology and Chemistry, University of Michigan, 210 Washtenaw Avenue, Ann Arbor, MI (USA), Fax: (+1) 734-615-3641en_US
dc.contributor.affiliationumLife Sciences Institute and Departments of Medicinal Chemistry, Microbiology, Immunology and Chemistry, University of Michigan, 210 Washtenaw Avenue, Ann Arbor, MI (USA), Fax: (+1) 734-615-3641en_US
dc.contributor.affiliationumLife Sciences Institute and Departments of Medicinal Chemistry, Microbiology, Immunology and Chemistry, University of Michigan, 210 Washtenaw Avenue, Ann Arbor, MI (USA), Fax: (+1) 734-615-3641en_US
dc.contributor.affiliationumLife Sciences Institute and Departments of Medicinal Chemistry, Microbiology, Immunology and Chemistry, University of Michigan, 210 Washtenaw Avenue, Ann Arbor, MI (USA), Fax: (+1) 734-615-3641en_US
dc.contributor.affiliationumLife Sciences Institute and Departments of Medicinal Chemistry, Microbiology, Immunology and Chemistry, University of Michigan, 210 Washtenaw Avenue, Ann Arbor, MI (USA), Fax: (+1) 734-615-3641en_US
dc.identifier.pmid20127927en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/69167/1/cbic_200900658_sm_miscellaneous_information.pdf
dc.identifier.doi10.1002/cbic.200900658en_US
dc.identifier.sourceChemBioChemen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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