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dc.contributor.authorFOSTER, TIMOTHY
dc.date.accessioned2020-08-07T13:07:27Z
dc.date.available2020-08-07T13:07:27Z
dc.date.issued1971
dc.date.submitted1971en
dc.identifier.citationFoster, T.J. and Howe, T.G.B., Recombination and complementation between R factors in Escherichia coli K12, Genetical Research Cambridge, 1971, 18, 287 - 297en
dc.identifier.otherY
dc.descriptionPUBLISHEDen
dc.description.abstractRecombination between chloramphenicol-sensitive (Cms) mutants of Rl, and R100, has been demonstrated in Escherichia coli K12 rec+; it occurs at reduced frequency in recB and recC, and is not detectable in reeA, indicating that R factor recombination depends on host functions. Some mutants of R1 also recombine with an R100 mutant in a similar way. recA cells carrying an R1 and an R100 Cms mutant (hetero-R state) have a low level of chloramphenicol-resistance, and form a chloramphenicol acetyl transferase that has lower specific activity than enzyme from hosts carrying wild-type or recombinant factors. These results suggest the occurrence of interallelic complementation between mutant R factors.en
dc.format.extentpp.287en
dc.format.extent297en
dc.language.isoenen
dc.relation.ispartofseriesGenetical Research, Cambridge;
dc.relation.ispartofseries18;
dc.rightsYen
dc.titleRecombination and complementation between R factors in Escherichia coli K12en
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/tfoster
dc.identifier.rssinternalid1905
dc.identifier.doihttp://dx.doi.org/10.1017/S0016672300012696
dc.rights.ecaccessrightsopenAccess
dc.identifier.urihttp://hdl.handle.net/2262/93127


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