Cargando…

The Relationship of NADPH Oxidases and Heme Peroxidases: Fallin' in and Out

Peroxidase enzymes can oxidize a multitude of substrates in diverse biological processes. According to the latest phylogenetic analysis, there are four major heme peroxidase superfamilies. In this review, we focus on certain members of the cyclooxygenase-peroxidase superfamily (also labeled as anima...

Descripción completa

Detalles Bibliográficos
Autores principales: Sirokmány, Gábor, Geiszt, Miklós
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411640/
https://www.ncbi.nlm.nih.gov/pubmed/30891045
http://dx.doi.org/10.3389/fimmu.2019.00394
_version_ 1783402419982434304
author Sirokmány, Gábor
Geiszt, Miklós
author_facet Sirokmány, Gábor
Geiszt, Miklós
author_sort Sirokmány, Gábor
collection PubMed
description Peroxidase enzymes can oxidize a multitude of substrates in diverse biological processes. According to the latest phylogenetic analysis, there are four major heme peroxidase superfamilies. In this review, we focus on certain members of the cyclooxygenase-peroxidase superfamily (also labeled as animal heme peroxidases) and their connection to specific NADPH oxidase enzymes which provide H(2)O(2) for the one- and two-electron oxidation of various peroxidase substrates. The family of NADPH oxidases is a group of enzymes dedicated to the production of superoxide and hydrogen peroxide. There is a handful of known and important physiological functions where one of the seven known human NADPH oxidases plays an essential role. In most of these functions NADPH oxidases provide H(2)O(2) for specific heme peroxidases and the concerted action of the two enzymes is indispensable for the accomplishment of the biological function. We discuss human and other metazoan examples of such cooperation between oxidases and peroxidases and analyze the biological importance of their functional interaction. We also review those oxidases and peroxidases where this kind of partnership has not been identified yet.
format Online
Article
Text
id pubmed-6411640
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-64116402019-03-19 The Relationship of NADPH Oxidases and Heme Peroxidases: Fallin' in and Out Sirokmány, Gábor Geiszt, Miklós Front Immunol Immunology Peroxidase enzymes can oxidize a multitude of substrates in diverse biological processes. According to the latest phylogenetic analysis, there are four major heme peroxidase superfamilies. In this review, we focus on certain members of the cyclooxygenase-peroxidase superfamily (also labeled as animal heme peroxidases) and their connection to specific NADPH oxidase enzymes which provide H(2)O(2) for the one- and two-electron oxidation of various peroxidase substrates. The family of NADPH oxidases is a group of enzymes dedicated to the production of superoxide and hydrogen peroxide. There is a handful of known and important physiological functions where one of the seven known human NADPH oxidases plays an essential role. In most of these functions NADPH oxidases provide H(2)O(2) for specific heme peroxidases and the concerted action of the two enzymes is indispensable for the accomplishment of the biological function. We discuss human and other metazoan examples of such cooperation between oxidases and peroxidases and analyze the biological importance of their functional interaction. We also review those oxidases and peroxidases where this kind of partnership has not been identified yet. Frontiers Media S.A. 2019-03-05 /pmc/articles/PMC6411640/ /pubmed/30891045 http://dx.doi.org/10.3389/fimmu.2019.00394 Text en Copyright © 2019 Sirokmány and Geiszt. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Sirokmány, Gábor
Geiszt, Miklós
The Relationship of NADPH Oxidases and Heme Peroxidases: Fallin' in and Out
title The Relationship of NADPH Oxidases and Heme Peroxidases: Fallin' in and Out
title_full The Relationship of NADPH Oxidases and Heme Peroxidases: Fallin' in and Out
title_fullStr The Relationship of NADPH Oxidases and Heme Peroxidases: Fallin' in and Out
title_full_unstemmed The Relationship of NADPH Oxidases and Heme Peroxidases: Fallin' in and Out
title_short The Relationship of NADPH Oxidases and Heme Peroxidases: Fallin' in and Out
title_sort relationship of nadph oxidases and heme peroxidases: fallin' in and out
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411640/
https://www.ncbi.nlm.nih.gov/pubmed/30891045
http://dx.doi.org/10.3389/fimmu.2019.00394
work_keys_str_mv AT sirokmanygabor therelationshipofnadphoxidasesandhemeperoxidasesfallininandout
AT geisztmiklos therelationshipofnadphoxidasesandhemeperoxidasesfallininandout
AT sirokmanygabor relationshipofnadphoxidasesandhemeperoxidasesfallininandout
AT geisztmiklos relationshipofnadphoxidasesandhemeperoxidasesfallininandout