Literature DB >> 3023322

On the molecular mechanism of lactoperoxidase-catalyzed H2O2 metabolism and irreversible enzyme inactivation.

H Jenzer, W Jones, H Kohler.   

Abstract

Lactoperoxidase-catalyzed H2O2 metabolism proceeds through one of three different pathways, depending on the nature and the concentration of the second substrate as an e- donor and/or on pH conditions. In the lactoperoxidase (LPO)-H2O2 system, at low H2O2 concentrations and/or alkaline conditions the peroxidatic cycle involves ferric LPO----compound I----compound II----ferric LPO conversion, whereas high H2O2 concentrations and/or acidic conditions favor the ferric LPO----compound I----compound II----compound III----ferrous LPO----ferric LPO pathway. The compound III/ferroperoxidase states are associated with irreversible enzyme inactivation by cleavage of the heme moiety and liberation of iron. It is likely that either singlet oxygen or superoxide and hydroxyl radicals are involved in the attack on heme iron, because inactivation correlates with oxygen production and can be decreased to a certain degree by scavengers such as ethanol, 1-propanol, 2-propanol, or mannitol. In the LPO-H2O2-I- system, the enzyme may also be inactivated by I2 generated in the course of enzymatic I- oxidation (i.e. during ferric LPO----compound I----ferric LPO cycles).

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Year:  1986        PMID: 3023322

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  8 in total

1.  Airway peroxidases catalyze nitration of the {beta}2-agonist salbutamol and decrease its pharmacological activity.

Authors:  Krzysztof J Reszka; Larry Sallans; Stephen Macha; Kari Brown; Dennis W McGraw; Melinda Butsch Kovacic; Bradley E Britigan
Journal:  J Pharmacol Exp Ther       Date:  2010-10-25       Impact factor: 4.030

2.  Catalase-like activity of horseradish peroxidase: relationship to enzyme inactivation by H2O2.

Authors:  J Hernández-Ruiz; M B Arnao; A N Hiner; F García-Cánovas; M Acosta
Journal:  Biochem J       Date:  2001-02-15       Impact factor: 3.857

3.  Peroxidase-promoted oxidation and peroxidation of the serotonergic neurotoxin 5,7-dihydroxytryptamine. A new pathway for its metabolic degradation.

Authors:  D Metodiewa; H B Dunford
Journal:  Mol Cell Biochem       Date:  1992-05-13       Impact factor: 3.396

4.  Doxorubicin inhibits oxidation of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) by a lactoperoxidase/H(2)O(2) system by reacting with ABTS-derived radical.

Authors:  Krzysztof J Reszka; Bradley E Britigan
Journal:  Arch Biochem Biophys       Date:  2007-07-10       Impact factor: 4.013

5.  Peroxidative metabolism of beta2-agonists salbutamol and fenoterol and their analogues.

Authors:  Krzysztof J Reszka; Dennis W McGraw; Bradley E Britigan
Journal:  Chem Res Toxicol       Date:  2009-06       Impact factor: 3.739

6.  Nutrigenomics-Associated Impacts of Nutrients on Genes and Enzymes With Special Consideration of Aromatase.

Authors:  Helena Jenzer; Leila Sadeghi-Reeves
Journal:  Front Nutr       Date:  2020-04-09

7.  Inactivation of human myeloperoxidase by hydrogen peroxide.

Authors:  Martina Paumann-Page; Paul G Furtmüller; Stefan Hofbauer; Louise N Paton; Christian Obinger; Anthony J Kettle
Journal:  Arch Biochem Biophys       Date:  2013-09-11       Impact factor: 4.013

Review 8.  Mode of action of lactoperoxidase as related to its antimicrobial activity: a review.

Authors:  F Bafort; O Parisi; J-P Perraudin; M H Jijakli
Journal:  Enzyme Res       Date:  2014-09-16
  8 in total

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