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PMID: 2842317 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Activation of recF-dependent recombination in Escherichia coli by bacteriophage lambda- and P22-encoded functions.

Journal of bacteriology ·Vol. 170 ·No. 9 ·1988-09-00 ·Pages 4379-81

Poteete AR, Volkert MR

Abstract

Escherichia coli strains bearing wild-type and mutant alleles of various recombination genes, as well as plasmids that express recombination-related genes of bacteriophages lambda and P22, were tested for their proficiency as recipients in Hfr-mediated conjugation. It was found that the homologous recombination systems of both phages could promote recombination in a recB recC mutant host. In addition, the Abc function of P22, but not the Gam function of lambda, was found to inhibit recombination in a wild-type host; however, both Abc and Gam inhibited recombination in a recF mutant host. These observations are interpreted as indicating that the recombination systems of both phages, as well as the RecBCD-modulating functions Abc and Gam, all activate the RecF recombination pathway of E. coli.

MeSH Terms
Alleles Bacterial Proteins/genetics Bacteriophage lambda/genetics Conjugation, Genetic Escherichia coli/genetics Genes, Bacterial Genes, Viral Mutation Plasmids Recombination, Genetic Salmonella Phages/genetics
Chemicals
Bacterial Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Poteete A R
Department of Molecular Genetics and Microbiology, University of Massachusetts, Worcester 01655.
Volkert M R
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16 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1988-09-00
Pages
4379-81
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC211454
Subset
IM
Grants
NIAID NIH HHS · AI18234 · United States
NIGMS NIH HHS · GM37052 · United States
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