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PMID: 6348024 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Escherichia coli RecBC pseudorevertants lacking chi recombinational hotspot activity.

Journal of bacteriology ·Vol. 155 ·No. 2 ·1983-08-00 ·Pages 664-80

Schultz DW, Taylor AF, Smith GR

Abstract

Pseudorevertants of an Escherichia coli exonuclease V (RecBC enzyme)-negative mutant have been isolated after ethyl methane sulfonate mutagenesis of a recC73 (presumed missense) mutant. The remedial mutations in each of the four pseudorevertants studied in detail map and complement as recC mutations. By several criteria, such as recombination proficiency, support of phage growth, RecBC nuclease activity, and cell viability, the pseudorevertants appear to have regained partially or completely various aspects of RecBC activity. However, chi recombinational hotspots, which stimulate exclusively the RecBC pathway of recombination, have no detectable activity in lambda vegetative crosses in the pseudorevertants. The properties of these mutants, in which the RecBC pathway of recombination is active yet in which chi is not active, are consistent with the hypothesis that wild-type RecBC enzyme directly interacts with chi sites; alternatively, the mutants may block or bypass the productive interaction of another recombinational enzyme with chi.

MeSH Terms
Coliphages/genetics Escherichia coli/genetics Escherichia coli Proteins Exodeoxyribonuclease V Exodeoxyribonucleases/genetics Genes, Bacterial Genes, Dominant Genetic Complementation Test Lysogeny Mutation Phenotype Recombination, Genetic
Chemicals
Escherichia coli Proteins Exodeoxyribonucleases Exodeoxyribonuclease V exodeoxyribonuclease V, E coli
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Schultz D W
Taylor A F
Smith G R
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39 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1983-08-00
Pages
664-80
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC217737
Subset
IM
Grants
NIAID NIH HHS · AI 00385 · United States
NIGMS NIH HHS · GM 26798 · United States
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