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A possible role of d -valine and related d -amino acids in repression of enzyme and actinomycin synthesis

dc.contributor.authorBrown, Daleen_US
dc.contributor.authorKatz, Edwarden_US
dc.date.accessioned2006-09-11T18:10:06Z
dc.date.available2006-09-11T18:10:06Z
dc.date.issued1989-01en_US
dc.identifier.citationKatz, Edward; Brown, Dale; (1989). "A possible role of d -valine and related d -amino acids in repression of enzyme and actinomycin synthesis." Applied Microbiology and Biotechnology 30(1): 67-70. <http://hdl.handle.net/2027.42/46758>en_US
dc.identifier.issn0175-7598en_US
dc.identifier.issn1432-0614en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46758
dc.description.abstractThe addition of d -valine and related d -amino acids to the production medium blocks kynurenine formamidase II and actinomycin D synthesis by Streptomyces parvulus . This effect may be due to a direct inhibition of the actinomycin synthetase-catalyzed racemization of l -valine to its peptide bound d -form during antibiotic formation. In addition, the d -amino acid(s) may influence enzyme and actinomycin synthesis through carbon and/or nitrogen catabolite regulation. The relatively slow uptake and metabolism of the d -amino acid would provide a continuous supply of catabolite(s) that repress transcription of actinomycin biosynthetic genes over a long period of time.en_US
dc.format.extent323102 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherChemistryen_US
dc.subject.otherMicrobiologyen_US
dc.subject.otherBiotechnologyen_US
dc.subject.otherMicrobial Genetics and Genomicsen_US
dc.titleA possible role of d -valine and related d -amino acids in repression of enzyme and actinomycin synthesisen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Microbiology, Georgetown University Schools of Medicine and Dentistry, 3900 Reservoir Rd., 20007, Washington, D.C., N.W., USA; Department of Pediatrics, Section of Pediatric Hematology, University of Michigan, 48109-0864, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherDepartment of Microbiology, Georgetown University Schools of Medicine and Dentistry, 3900 Reservoir Rd., 20007, Washington, D.C., N.W., USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46758/1/253_2004_Article_BF00255998.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00255998en_US
dc.identifier.sourceApplied Microbiology and Biotechnologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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