As previously reported, ultraviolet-inactivated bacterial transforming DNA can be restored to activity by an enzyme-like agent from bakers' yeast which requires light for its activity. Kinetics of this reaction, in the presence and absence of inhibitors, are found consistent with the Michaelis-Menten reaction scheme, with the sites of ultraviolet damage on the DNA serving as substrate and the repaired structure as product. Kinetic studies with different light intensities suggest that the necessary illumination causes photolysis of the enzyme-substrate complex with concurrent repair of the DNA. Competitive inhibition of irradiated transforming DNA repair, which occurs when irradiated non-transforming DNA is present in the same reaction mixture, permits ultraviolet damage (of the kind capable of being photoreactivated) to be detected in any type of DNA.
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1 March 1962
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March 01 1962
Photoenzymatic Repair of Ultraviolet Damage in DNA : I. Kinetics of the reaction
Claud S. Rupert
Claud S. Rupert
From The Department of Biochemistry, The Johns Hopkins University School of Hygiene and Public Health, Baltimore.
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Claud S. Rupert
From The Department of Biochemistry, The Johns Hopkins University School of Hygiene and Public Health, Baltimore.
Dr. Rupert's present address is University Institute of Microbiology, Copenhagen, Denmark
Received:
August 22 1961
Online ISSN: 1540-7748
Print ISSN: 0022-1295
Copyright, 1962, by The Rockefeller Institute Press
1962
J Gen Physiol (1962) 45 (4): 703–724.
Article history
Received:
August 22 1961
Citation
Claud S. Rupert; Photoenzymatic Repair of Ultraviolet Damage in DNA : I. Kinetics of the reaction . J Gen Physiol 1 March 1962; 45 (4): 703–724. doi: https://doi.org/10.1085/jgp.45.4.703
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