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PMID: 8218289 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Substrate specificity of the Escherichia coli endonuclease III: excision of thymine- and cytosine-derived lesions in DNA produced by radiation-generated free radicals.

Biochemistry ·Vol. 32 ·No. 45 ·1993-11-16 ·Pages 12105-11

Dizdaroglu M, Laval J, Boiteux S

Abstract

The excision of modified bases from DNA by Escherichia coli endonuclease III was investigated. Modified bases were produced in DNA by exposure of dilute buffered solutions of DNA to ionizing radiation under oxic or anoxic conditions. The technique of gas chromatography/mass spectrometry (GC/MS) was used to identify and quantify 16 pyrimidine- and purine-derived DNA lesions. DNA substrates were incubated either with the native enzyme or with the heat-inactivated enzyme. Subsequently, DNA was precipitated. Pellets were analyzed by GC/MS after hydrolysis and derivatization. Supernatant fractions were analyzed after derivatization without hydrolysis. The results provided unequivocal evidence for the excision by E. coli endonuclease III of a number of thymine- and cytosine-derived lesions from DNA. These were 5,6-dihydrothymine, 5-hydroxy-5-methylhydantoin, thymine glycol, 5-hydroxy-6-hydrothymine, 5,6-dihydrouracil, alloxan, uracil glycol, and 5-hydroxy-6-hydrouracil. None of the purine-derived lesions was excised by endonuclease III. The present work extends the substrate specificity of E. coli endonuclease III to another thymine-derived and four cytosine-derived lesions. It is the first investigation of the substrate specificity of this repair enzyme in the context of a large number of pyrimidine- and purine-derived lesions in DNA.

MeSH Terms
Animals Cattle Cytosine DNA Damage/radiation effects Deoxyribonuclease (Pyrimidine Dimer) Endodeoxyribonucleases/metabolism Escherichia coli/enzymology Escherichia coli Proteins Free Radicals Gas Chromatography-Mass Spectrometry Substrate Specificity Thymine
Chemicals
Escherichia coli Proteins Free Radicals Cytosine Endodeoxyribonucleases Deoxyribonuclease (Pyrimidine Dimer) NTH protein, E coli Thymine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Dizdaroglu M
Chemical Science and Technology Laboratory, National Institute of Standards and Technology, Gaithersburg, Maryland 20899.
Laval J
Boiteux S
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1993-11-16
Pages
12105-11
Language
English
Region
United States
NLM ID
0370623
Subset
IM
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