Hydrogen Peroxide in Biocatalysis. A Dangerous Liaison


Autoria(s): Hernández, Karel; Berenguer-Murcia, Ángel; Rodrigues, Rafael C.; Fernández Lafuente, Roberto
Contribuinte(s)

Universidad de Alicante. Departamento de Química Inorgánica

Universidad de Alicante. Instituto Universitario de Materiales

Materiales Carbonosos y Medio Ambiente

Data(s)

11/09/2014

11/09/2014

01/11/2012

Resumo

Hydrogen peroxide is a substrate or side-product in many enzyme-catalyzed reactions. For example, it is a side-product of oxidases, resulting from the re-oxidation of FAD with molecular oxygen, and it is a substrate for peroxidases and other enzymes. However, hydrogen peroxide is able to chemically modify the peptide core of the enzymes it interacts with, and also to produce the oxidation of some cofactors and prostetic groups (e.g., the hemo group). Thus, the development of strategies that may permit to increase the stability of enzymes in the presence of this deleterious reagent is an interesting target. This enhancement in enzyme stability has been attempted following almost all available strategies: site-directed mutagenesis (eliminating the most reactive moieties), medium engineering (using stabilizers), immobilization and chemical modification (trying to generate hydrophobic environments surrounding the enzyme, to confer higher rigidity to the protein or to generate oxidation-resistant groups), or the use of systems capable of decomposing hydrogen peroxide under very mild conditions. If hydrogen peroxide is just a side-product, its immediate removal has been reported to be the best solution. In some cases, when hydrogen peroxide is the substrate and its decomposition is not a sensible solution, researchers coupled one enzyme generating hydrogen peroxide “in situ” to the target enzyme resulting in a continuous supply of this reagent at low concentrations thus preventing enzyme inactivation. This review will focus on the general role of hydrogen peroxide in biocatalysis, the main mechanisms of enzyme inactivation produced by this reactive and the different strategies used to prevent enzyme inactivation caused by this “dangerous liaison”.

This work has been supported by grant CTQ2009-07568 from Spanish Ministerio de Ciencia e Innovación. A. Berenguer-Murcia thanks the Spanish Ministerio de Ciencia e Innovación for a Ramon y Cajal fellowship (RyC-2009-03813). Mr. Hernandez is a holder of a MAEC-AECID fellowship.

Identificador

Current Organic Chemistry. 2012, 16(22): 2652-2672. doi:10.2174/138527212804004526

1385-2728 (Print)

1875-5348 (Online)

http://hdl.handle.net/10045/40212

10.2174/138527212804004526

Idioma(s)

eng

Publicador

Bentham Science Publishers

Relação

http://dx.doi.org/10.2174/138527212804004526

Direitos

© 2012 Bentham Science Publishers

info:eu-repo/semantics/openAccess

Palavras-Chave #Enzyme inactivation by oxidation #Catalase #Chemical modification #Genetic modification #Immobilization #Lipase #Oxidase #Partition effect #Química Inorgánica
Tipo

info:eu-repo/semantics/article