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Mitochondrial type II NAD(P)H dehydrogenases in fungal cell death

During aerobic respiration, cells produce energy through oxidative phosphorylation, which includes a specialized group of multi-subunit complexes in the inner mitochondrial membrane known as the electron transport chain. However, this canonical pathway is branched into single polypeptide alternative...

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Detalles Bibliográficos
Autores principales: Gonçalves, A. Pedro, Videira, Arnaldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shared Science Publishers OG 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349180/
https://www.ncbi.nlm.nih.gov/pubmed/28357279
http://dx.doi.org/10.15698/mic2015.03.192
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author Gonçalves, A. Pedro
Videira, Arnaldo
author_facet Gonçalves, A. Pedro
Videira, Arnaldo
author_sort Gonçalves, A. Pedro
collection PubMed
description During aerobic respiration, cells produce energy through oxidative phosphorylation, which includes a specialized group of multi-subunit complexes in the inner mitochondrial membrane known as the electron transport chain. However, this canonical pathway is branched into single polypeptide alternative routes in some fungi, plants, protists and bacteria. They confer metabolic plasticity, allowing cells to adapt to different environmental conditions and stresses. Type II NAD(P)H dehydrogenases (also called alternative NAD(P)H dehydrogenases) are non-proton pumping enzymes that bypass complex I. Recent evidence points to the involvement of fungal alternative NAD(P)H dehydrogenases in the process of programmed cell death, in addition to their action as overflow systems upon oxidative stress. Consistent with this, alternative NAD(P)H dehydrogenases are phylogenetically related to cell death - promoting proteins of the apoptosis-inducing factor (AIF)-family.
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spelling pubmed-53491802017-03-29 Mitochondrial type II NAD(P)H dehydrogenases in fungal cell death Gonçalves, A. Pedro Videira, Arnaldo Microb Cell Microbiology During aerobic respiration, cells produce energy through oxidative phosphorylation, which includes a specialized group of multi-subunit complexes in the inner mitochondrial membrane known as the electron transport chain. However, this canonical pathway is branched into single polypeptide alternative routes in some fungi, plants, protists and bacteria. They confer metabolic plasticity, allowing cells to adapt to different environmental conditions and stresses. Type II NAD(P)H dehydrogenases (also called alternative NAD(P)H dehydrogenases) are non-proton pumping enzymes that bypass complex I. Recent evidence points to the involvement of fungal alternative NAD(P)H dehydrogenases in the process of programmed cell death, in addition to their action as overflow systems upon oxidative stress. Consistent with this, alternative NAD(P)H dehydrogenases are phylogenetically related to cell death - promoting proteins of the apoptosis-inducing factor (AIF)-family. Shared Science Publishers OG 2015-03-02 /pmc/articles/PMC5349180/ /pubmed/28357279 http://dx.doi.org/10.15698/mic2015.03.192 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged.
spellingShingle Microbiology
Gonçalves, A. Pedro
Videira, Arnaldo
Mitochondrial type II NAD(P)H dehydrogenases in fungal cell death
title Mitochondrial type II NAD(P)H dehydrogenases in fungal cell death
title_full Mitochondrial type II NAD(P)H dehydrogenases in fungal cell death
title_fullStr Mitochondrial type II NAD(P)H dehydrogenases in fungal cell death
title_full_unstemmed Mitochondrial type II NAD(P)H dehydrogenases in fungal cell death
title_short Mitochondrial type II NAD(P)H dehydrogenases in fungal cell death
title_sort mitochondrial type ii nad(p)h dehydrogenases in fungal cell death
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349180/
https://www.ncbi.nlm.nih.gov/pubmed/28357279
http://dx.doi.org/10.15698/mic2015.03.192
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