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Involvement of kil and kor genes in the phenotype of a host-range mutant of RP4
Authors:Peter T Barth  Kim Ellis  David H Bechhofer and David H Figurski
Institution:(1) ICI Corporate Bioscience Group, The Heath, WA7 4QE Runcorn, Cheshire, UK;(2) Bacteriology Department, Royal Postgraduate Medical School, DuCane Road, W12 OHS London, UK;(3) Department of Microbiology and Cancer Centre, College of Physicians and Surgeons, 701 West 168th Street, 10032 New York, NY, USA;(4) Present address: Biochemistry Department, St. Mary's Hospital Medical School, W2 London, UK;(5) Present address: Department of Microbiology, The Public Health Research Institute of the City of New York, 10016 New York, NY, USA
Abstract:Summary Plasmid pRP761 is a derivative of the promiscuous plasmid RP4, which has a Tn76 insert 1.8 kb from its EcoRI site within the trfB region (Barth 1979). This mutation was pleiotropic, having three effects: the plasmid is unstably maintained in E. coli, it reduces the growth rate of its host and it has suffered a reduction in host-range. We show that pRP761 has reduced expression from both its korA and korB genes and that Tn76 has inserted between them. Fragment exchange experiments showed that this is the only mutant region in pRP761 and is therefore solely responsible for the pleiotropic effects. A spontaneous deletion derivative pRP761-6 has lost Tn76 and its adjacent kilA and korA genes: it has reacquired stability, does not inhibit host growth but is still reduced in its host-range. The provision of cloned korA + in trans complements the first two phenotypic effects in pRP761 to a large extent, but neither korA + alone nor korA + with korB + complements the host-range reduction in pRP761 or pRP761-6. A possible explanation for these results is that there is a site between korA and korB, affected by the Tn76 insert, that is essential to stable replication of these plasmids in some of their bacterial hosts.
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