Abstract
The wild-type strain and mutants of Haemophilus influenzae, sensitive or resistant to ultraviolet light (UV) as defined by colony-forming ability, were examined for their ability to perform the incision and rejoining steps of the deoxyribonucleic acid (DNA) dark repair process. Although UV-induced pyrimidine dimers are excised by the wild-type Rd and a resistant mutant BC200, the expected single-strand DNA breaks could not be detected on alkaline sucrose gradients. Repair of the gap resulting from excision must be rapid when experimental conditions described by us are employed. Single-strand DNA breaks were not detected in a UV-irradiated sensitive mutant (BC100) incapable of excising pyrimidine dimers, indicating that this mutant may be defective in a dimer-recognizing endonuclease. No single-strand DNA breaks were detected in a lysogen BC100(HP1c1) irradiated with a UV dose large enough to induce phage development in 80% of the cells.
MeSH Terms
Bacteriophages
Carbon Isotopes
Centrifugation, Density Gradient
DNA Repair
DNA Viruses
DNA, Bacterial/analysis,biosynthesis,radiation effects
DNA, Single-Stranded/analysis,biosynthesis,radiation effects
Haemophilus influenzae/analysis,growth & development,metabolism,radiation effects
Lysogeny
Mutation
Radiation Effects
Thymidine/metabolism
Tritium
Ultraviolet Rays
Chemicals
Carbon Isotopes
DNA, Bacterial
DNA, Single-Stranded
Tritium
Thymidine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kantor G J
Barnhart B J
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17 references, click to expand
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