dc.contributor.author | FOSTER, TIMOTHY | |
dc.date.accessioned | 2020-08-07T13:07:27Z | |
dc.date.available | 2020-08-07T13:07:27Z | |
dc.date.issued | 1971 | |
dc.date.submitted | 1971 | en |
dc.identifier.citation | Foster, T.J. and Howe, T.G.B., Recombination and complementation between R factors in Escherichia coli K12, Genetical Research Cambridge, 1971, 18, 287 - 297 | en |
dc.identifier.other | Y | |
dc.description | PUBLISHED | en |
dc.description.abstract | Recombination 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.extent | pp.287 | en |
dc.format.extent | 297 | en |
dc.language.iso | en | en |
dc.relation.ispartofseries | Genetical Research, Cambridge; | |
dc.relation.ispartofseries | 18; | |
dc.rights | Y | en |
dc.title | Recombination and complementation between R factors in Escherichia coli K12 | en |
dc.type | Journal Article | en |
dc.type.supercollection | scholarly_publications | en |
dc.type.supercollection | refereed_publications | en |
dc.identifier.peoplefinderurl | http://people.tcd.ie/tfoster | |
dc.identifier.rssinternalid | 1905 | |
dc.identifier.doi | http://dx.doi.org/10.1017/S0016672300012696 | |
dc.rights.ecaccessrights | openAccess | |
dc.identifier.uri | http://hdl.handle.net/2262/93127 | |