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Photoenzymatic Repair of Ultraviolet Damage in DNA : II. Formation of an enzyme-substrate complex

The photoenzyme from bakers' yeast which repairs ultraviolet-inactivated transforming DNA is mechanically bound to ultraviolet-irradiated DNA in the dark, but not to unirradiated DNA. In the bound condition it is stabilized against inactivation by heat and heavy metals. Both the mechanical bind...

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Autor principal: Rupert, Claud S.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1962
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2195215/
https://www.ncbi.nlm.nih.gov/pubmed/14495309
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author Rupert, Claud S.
author_facet Rupert, Claud S.
author_sort Rupert, Claud S.
collection PubMed
description The photoenzyme from bakers' yeast which repairs ultraviolet-inactivated transforming DNA is mechanically bound to ultraviolet-irradiated DNA in the dark, but not to unirradiated DNA. In the bound condition it is stabilized against inactivation by heat and heavy metals. Both the mechanical binding and stabilization are eliminated by illumination. These observations are consistent with the reaction scheme suggested by kinetic studies, in which the enzyme combines with the ultraviolet lesions in DNA and the complex absorbs light, producing repair and subsequent liberation of the enzyme. The approximately exponential decrease of heat stabilization during illumination gives the first order rate constant for the light-dependent step at the corresponding light intensity. This quantity in turn sets limits on the possible magnitude of the molar absorption coefficient of the enzyme-substrate complex and on the quantum yield of the process.
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spelling pubmed-21952152008-04-23 Photoenzymatic Repair of Ultraviolet Damage in DNA : II. Formation of an enzyme-substrate complex Rupert, Claud S. J Gen Physiol Article The photoenzyme from bakers' yeast which repairs ultraviolet-inactivated transforming DNA is mechanically bound to ultraviolet-irradiated DNA in the dark, but not to unirradiated DNA. In the bound condition it is stabilized against inactivation by heat and heavy metals. Both the mechanical binding and stabilization are eliminated by illumination. These observations are consistent with the reaction scheme suggested by kinetic studies, in which the enzyme combines with the ultraviolet lesions in DNA and the complex absorbs light, producing repair and subsequent liberation of the enzyme. The approximately exponential decrease of heat stabilization during illumination gives the first order rate constant for the light-dependent step at the corresponding light intensity. This quantity in turn sets limits on the possible magnitude of the molar absorption coefficient of the enzyme-substrate complex and on the quantum yield of the process. The Rockefeller University Press 1962-03-01 /pmc/articles/PMC2195215/ /pubmed/14495309 Text en Copyright © Copyright, 1962, by The Rockefeller Institute Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Rupert, Claud S.
Photoenzymatic Repair of Ultraviolet Damage in DNA : II. Formation of an enzyme-substrate complex
title Photoenzymatic Repair of Ultraviolet Damage in DNA : II. Formation of an enzyme-substrate complex
title_full Photoenzymatic Repair of Ultraviolet Damage in DNA : II. Formation of an enzyme-substrate complex
title_fullStr Photoenzymatic Repair of Ultraviolet Damage in DNA : II. Formation of an enzyme-substrate complex
title_full_unstemmed Photoenzymatic Repair of Ultraviolet Damage in DNA : II. Formation of an enzyme-substrate complex
title_short Photoenzymatic Repair of Ultraviolet Damage in DNA : II. Formation of an enzyme-substrate complex
title_sort photoenzymatic repair of ultraviolet damage in dna : ii. formation of an enzyme-substrate complex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2195215/
https://www.ncbi.nlm.nih.gov/pubmed/14495309
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