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Recombination deficient mutant of Caulobacter crescentus
Authors:Edward A. O'Neill   Robert H. Hynes  Robert A. Bender
Affiliation:(1) Department of Cellular and Molecular Biology, Division of Biological Sciences, The University of Michigan, 48109 Ann Arbor, MI, USA;(2) Present address: Department of Molecular Biology and Genetics, The Johns Hopkins University School of Medicine, 21205 Baltimore, MD, USA
Abstract:Summary A recombination-deficient (Rec-) strain of Caulobacter crescentus has been isolated from a collection of mutants sensitive to ultraviolet irradiation. The Rec- mutant fails to give recombinants following phivCr30-mediated generalized transduction or following RP4-mediated conjugation. The recombination frequency in the Rec- strain is at least 5000-fold lower than in the wild type strains. The Rec- mutant is indistinguishable from wild type in terms of morphology, growth rate, viability, and phage sensitivities, differing only in properties known to be associated with recA-type mutations in other organisms: recombination frequency, ultraviolet sensitivity, and Weigle reactivation. The map location of the rec-526 allele has not been identified, but rec-526 can be cotransferred with the fla-169 mutation by RP4-mediated conjugation at low frequency. This apparent linkage has been used to move the rec mutation to other strains. The Rec- mutant resembles recA strains of other organisms and provides a healthy strain severely deficient in recombination for use in complementation and cloning studies involving C. crescentus.
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