| Literature DB >> 2995311 |
P V Attfield, F E Benson, R G Lloyd.
Abstract
The ruv gene of Escherichia coli, which is associated with inducible mechanisms of DNA repair and recombination, has been cloned into the low-copy plasmid vector pHSG415. The recombinant plasmid pPVA101 fully complements the DNA repair-deficient phenotype of ruv mutants. Restriction endonuclease analysis of this plasmid revealed a 10.6-kilobase (kb) HindIII DNA insert which contained a 7.7-kb PstI fragment identified as being from the chromosomal ruv region. Deletion analysis and Tn1000 insertional inactivation of ruv function located the ruv coding region to a 2.2-kb section of the cloned DNA fragment. A comparison of the proteins encoded by ruv wild-type and mutant plasmids identified the gene product as a protein of molecular weight 41,000.Entities:
Mesh:
Substances:
Year: 1985 PMID: 2995311 PMCID: PMC214240 DOI: 10.1128/jb.164.1.276-281.1985
Source DB: PubMed Journal: J Bacteriol ISSN: 0021-9193 Impact factor: 3.490