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Resistance of bacteriophage PBS2 infection to rifampicin, an inhibitor of RNA synthesis

dc.contributor.authorPrice, Alan R.en_US
dc.contributor.authorFrabotta, Maryen_US
dc.date.accessioned2006-04-17T16:46:29Z
dc.date.available2006-04-17T16:46:29Z
dc.date.issued1972-09-26en_US
dc.identifier.citationPrice, Alan R., Frabotta, Mary (1972/09/26)."Resistance of bacteriophage PBS2 infection to rifampicin, an inhibitor of RNA synthesis." Biochemical and Biophysical Research Communications 48(6): 1578-1585. <http://hdl.handle.net/2027.42/34038>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WBK-4DPC601-9X/2/fd35d8c1b961ec44ef0426b0deadb829en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34038
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=4404678&dopt=citationen_US
dc.description.abstractThe induction of viral enzymes, the synthesis of DNA, and the production of progeny phage during infection of by bacteriophage PBS2 are all unaffected by the presence of rifampicin. Rifampicin, rifamycin SV, streptovaricin, and streptolydigin (all of which inhibit . RNA synthesis by binding to DNA-dependent RNA polymerase) have no effect on PBS2 infection. However, actinomycin D and Lucanthone (which inhibit DNA-dependent RNA synthesis by binding to DNA) both prevent PBS2 replication. Therefore, PBS2 phage may utilize a rifampicin-resistant RNA polymerase to transcribe its uracil-containing DNA during phage infection.en_US
dc.format.extent452096 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleResistance of bacteriophage PBS2 infection to rifampicin, an inhibitor of RNA synthesisen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Biological Chemistry, University of Michigan, Ann Arbor, Michigan 48104, USAen_US
dc.contributor.affiliationumDepartment of Biological Chemistry, University of Michigan, Ann Arbor, Michigan 48104, USAen_US
dc.identifier.pmid4404678en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34038/1/0000315.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0006-291X(72)90894-7en_US
dc.identifier.sourceBiochemical and Biophysical Research Communicationsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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