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PMID: 5704812 Published · ppublish English Journal Article

The catalase-hydrogen peroxide system. A theoretical appraisal of the mechanism of catalase action.

The Biochemical journal ·Vol. 110 ·No. 4 ·1968-12-00 ·Pages 621-9

Jones P, Suggett A

Abstract

1. The mechanisms of catalase action advanced by Jones & Wynne-Jones (1962) and by Nicholls (1964) are compared in terms of their relative plausibilities and their utility for extension to accommodate more recent experimental information. 2. A revised formal mechanism is advanced that avoids the less satisfactory features of these mechanisms and attempts to account for the roles of catalase sub-units in both reversible and irreversible deactivation phenomena. 3. Theoretical studies of the redox chemistry of peroxides are used to provide the basis for a discussion of the mechanism of the redox act in catalatic action at the molecular level. It is suggested that an important feature of catalase action may be a mediation of the formation of a reactive intermediate by stereospecifically located acid-base functions in the active site. 4. A more detailed statement of this concept is attempted in terms of a hypothetical partial molecular model for the composition and stereochemistry of the active site of catalase. The utility of this model in describing the catalatic and peroxidatic actions of catalase is assessed.

MeSH Terms
Arginine Binding Sites Catalase Catalysis Hydrogen Peroxide Models, Chemical Molecular Biology Oxidation-Reduction Propionates Protons
Chemicals
Propionates Protons Arginine Hydrogen Peroxide Catalase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Jones P
Suggett A
References (13)
13 references, click to expand
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Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1968-12-00
Pages
621-9
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1187433
Subset
IM
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