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A nonsense mutation in the structural gene for glutamine synthetase leading to loss of nitrogen regulation in Klebsiella aerogenes

dc.contributor.authorBender, Robert A.en_US
dc.contributor.authorEades, Linda J.en_US
dc.date.accessioned2006-09-11T19:06:42Z
dc.date.available2006-09-11T19:06:42Z
dc.date.issued1982-10en_US
dc.identifier.citationBender, Robert A.; Eades, Linda J.; (1982). "A nonsense mutation in the structural gene for glutamine synthetase leading to loss of nitrogen regulation in Klebsiella aerogenes ." MGG Molecular & General Genetics 187(3): 414-418. <http://hdl.handle.net/2027.42/47550>en_US
dc.identifier.issn1617-4623en_US
dc.identifier.issn0026-8925en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47550
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6129565&dopt=citationen_US
dc.description.abstractAn amber mutation ( glnA3711 ), the first nonsense mutation isolated in Klebsiella aerogenes , is described. When amber suppressors were present, the mutant made active glutamine synthetase which was more thermolabile than wild type, showing that glnA3711 lies in the structural gene for glutamine synthetase. Strains carrying the glnA3711 allele were unable to express nitrogen regulation of genes coding for histidase, asparaginase, and glutamate dehydrogenase unless amber suppressors were also present. These results support a model that expression of gene(s) from the glnA promoter is required for nitrogen regulation in K. aerogenes .en_US
dc.format.extent542996 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherLife Sciencesen_US
dc.subject.otherCell Biologyen_US
dc.subject.otherBiochemistry, Generalen_US
dc.subject.otherMicrobial Genetics and Genomicsen_US
dc.titleA nonsense mutation in the structural gene for glutamine synthetase leading to loss of nitrogen regulation in Klebsiella aerogenesen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Cellular and Molecular Biology, Division of Biological Sciences, University of Michigan, 48109, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Cellular and Molecular Biology, Division of Biological Sciences, University of Michigan, 48109, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid6129565en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47550/1/438_2004_Article_BF00332621.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00332621en_US
dc.identifier.sourceMGG Molecular & General Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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