Affiliation:
1. Department of Radiology, Stanford University School of Medicine, Stanford, California 94305
Abstract
Mutants of
Escherichia coli
K-12 unable to excise pyrimidine dimers from their deoxyribonucleic acid (DNA) because of a
uvr
mutation show a higher survival when plated on a minimal salts medium after exposure to ultraviolet radiation than when plated on a complex medium such as nutrient agar containing yeast extract. This response has been called minimal medium recovery (MMR). Recovery of
uvr
mutants can take place in liquid as well as on solid medium, but not in buffer or under conditions of amino acid starvation that do not permit cell growth and normal DNA replication. MMR can thus be distinguished from the recovery of recombination-deficient (
rec
−
uvr
+
) derivatives of K-12 which can occur under conditions where growth is not possible. Because MMR is characteristic of excision-defective mutants, it evidently reflects a type of repair independent of excision. We have obtained genetic evidence that MMR is determined by the
rec
genes, which also control recombination in K-12. Cells carrying a
uvr
mutation together with
recA13, recA56, recB21
, or
recC22
failed to show MMR and were more sensitive to ultraviolet radiation than either their
rec
+
uvr
−
or
rec
−
uvr
+
parents. The
rec
+
uvr
−
derivatives obtained from
recA uvr
−
strains by transduction or by reversion regained the capacity for MMR. Our results indicate that inactivation of any one of the three genes,
recA, recB
, or
recC
, prevents cells from showing MMR.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
36 articles.
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