Abstract
In Escherichia coli K-12 strains infected with phage T4 which is defective in gene 30 [deoxyribonucleic acid (DNA) ligase] and in the rII gene (product unknown), near normal levels of DNA and viable phage were produced. Growth of such T4 ligase-rII double mutants was less efficient in E. coli B strains which show the "rapidlysis" phenotype of rII mutations. In pulse-chase experiments coupled with temperature shifts and with inhibition of DNA synthesis, it was observed that DNA synthesized by gene 30-defective phage is more susceptible to breakdown in vivo when the phage is carrying a wild-type rII gene. Breakdown was delayed or inhibited by continued DNA synthesis. Mutations of the rII gene decreased but did not completely abolish the breakdown. T4 ligase-rII double mutants had normal sensitivity to ultraviolet irradiation.
MeSH Terms
Coliphages/enzymology,growth & development,metabolism,radiation effects
Culture Media
DNA Nucleotidyltransferases/biosynthesis
DNA Repair
DNA Replication
DNA, Bacterial/biosynthesis
DNA, Viral/biosynthesis
Escherichia coli/growth & development,metabolism
Genes
Genetics, Microbial
Molecular Biology
Mutation
Radiation Effects
Thymidine/metabolism
Tritium
Ultraviolet Rays
Virus Replication
Chemicals
Culture Media
DNA, Bacterial
DNA, Viral
Tritium
DNA Nucleotidyltransferases
Thymidine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Karam J D
Barker B
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31 references, click to expand
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