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A Sodium-Translocating Module Linking Succinate Production to Formation of Membrane Potential in Prevotella bryantii
Ruminants such as cattle and sheep depend on the breakdown of carbohydrates from plant-based feedstuff, which is accomplished by the microbial community in the rumen. Roughly 40% of the members of the rumen microbiota belong to the family Prevotellaceae, which ferments sugars to organic acids such a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society for Microbiology
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516057/ https://www.ncbi.nlm.nih.gov/pubmed/34469197 http://dx.doi.org/10.1128/AEM.01211-21 |
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author | Schleicher, Lena Trautmann, Andrej Stegmann, Dennis P. Fritz, Günter Gätgens, Jochem Bott, Michael Hein, Sascha Simon, Jörg Seifert, Jana Steuber, Julia |
author_facet | Schleicher, Lena Trautmann, Andrej Stegmann, Dennis P. Fritz, Günter Gätgens, Jochem Bott, Michael Hein, Sascha Simon, Jörg Seifert, Jana Steuber, Julia |
author_sort | Schleicher, Lena |
collection | PubMed |
description | Ruminants such as cattle and sheep depend on the breakdown of carbohydrates from plant-based feedstuff, which is accomplished by the microbial community in the rumen. Roughly 40% of the members of the rumen microbiota belong to the family Prevotellaceae, which ferments sugars to organic acids such as acetate, propionate, and succinate. These substrates are important nutrients for the ruminant. In a metaproteome analysis of the rumen of cattle, proteins that are homologous to the Na(+)-translocating NADH:quinone oxidoreductase (NQR) and the quinone:fumarate reductase (QFR) were identified in different Prevotella species. Here, we show that fumarate reduction to succinate in anaerobically growing Prevotella bryantii is coupled to chemiosmotic energy conservation by a supercomplex composed of NQR and QFR. This sodium-translocating NADH:fumarate oxidoreductase (SNFR) supercomplex was enriched by blue native PAGE (BN-PAGE) and characterized by in-gel enzyme activity staining and mass spectrometry. High NADH oxidation (850 nmol min(−1 )mg(−1)), quinone reduction (490 nmol min(−1 )mg(−1)), and fumarate reduction (1,200 nmol min(−1 )mg(−1)) activities, together with high expression levels, demonstrate that SNFR represents a charge-separating unit in P. bryantii. Absorption spectroscopy of SNFR exposed to different substrates revealed intramolecular electron transfer from the flavin adenine dinucleotide (FAD) cofactor in NQR to heme b cofactors in QFR. SNFR catalyzed the stoichiometric conversion of NADH and fumarate to NAD(+) and succinate. We propose that the regeneration of NAD(+) in P. bryantii is intimately linked to the buildup of an electrochemical gradient which powers ATP synthesis by electron transport phosphorylation. IMPORTANCE Feeding strategies for ruminants are designed to optimize nutrient efficiency for animals and to prevent energy losses like enhanced methane production. Key to this are the fermentative reactions of the rumen microbiota, dominated by Prevotella spp. We show that succinate formation by P. bryantii is coupled to NADH oxidation and sodium gradient formation by a newly described supercomplex consisting of Na(+)-translocating NADH:quinone oxidoreductase (NQR) and fumarate reductase (QFR), representing the sodium-translocating NADH:fumarate oxidoreductase (SNFR) supercomplex. SNFR is the major charge-separating module, generating an electrochemical sodium gradient in P. bryantii. Our findings offer clues to the observation that use of fumarate as feed additive does not significantly increase succinate production, or decrease methanogenesis, by the microbial community in the rumen. |
format | Online Article Text |
id | pubmed-8516057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-85160572021-11-12 A Sodium-Translocating Module Linking Succinate Production to Formation of Membrane Potential in Prevotella bryantii Schleicher, Lena Trautmann, Andrej Stegmann, Dennis P. Fritz, Günter Gätgens, Jochem Bott, Michael Hein, Sascha Simon, Jörg Seifert, Jana Steuber, Julia Appl Environ Microbiol Environmental Microbiology Ruminants such as cattle and sheep depend on the breakdown of carbohydrates from plant-based feedstuff, which is accomplished by the microbial community in the rumen. Roughly 40% of the members of the rumen microbiota belong to the family Prevotellaceae, which ferments sugars to organic acids such as acetate, propionate, and succinate. These substrates are important nutrients for the ruminant. In a metaproteome analysis of the rumen of cattle, proteins that are homologous to the Na(+)-translocating NADH:quinone oxidoreductase (NQR) and the quinone:fumarate reductase (QFR) were identified in different Prevotella species. Here, we show that fumarate reduction to succinate in anaerobically growing Prevotella bryantii is coupled to chemiosmotic energy conservation by a supercomplex composed of NQR and QFR. This sodium-translocating NADH:fumarate oxidoreductase (SNFR) supercomplex was enriched by blue native PAGE (BN-PAGE) and characterized by in-gel enzyme activity staining and mass spectrometry. High NADH oxidation (850 nmol min(−1 )mg(−1)), quinone reduction (490 nmol min(−1 )mg(−1)), and fumarate reduction (1,200 nmol min(−1 )mg(−1)) activities, together with high expression levels, demonstrate that SNFR represents a charge-separating unit in P. bryantii. Absorption spectroscopy of SNFR exposed to different substrates revealed intramolecular electron transfer from the flavin adenine dinucleotide (FAD) cofactor in NQR to heme b cofactors in QFR. SNFR catalyzed the stoichiometric conversion of NADH and fumarate to NAD(+) and succinate. We propose that the regeneration of NAD(+) in P. bryantii is intimately linked to the buildup of an electrochemical gradient which powers ATP synthesis by electron transport phosphorylation. IMPORTANCE Feeding strategies for ruminants are designed to optimize nutrient efficiency for animals and to prevent energy losses like enhanced methane production. Key to this are the fermentative reactions of the rumen microbiota, dominated by Prevotella spp. We show that succinate formation by P. bryantii is coupled to NADH oxidation and sodium gradient formation by a newly described supercomplex consisting of Na(+)-translocating NADH:quinone oxidoreductase (NQR) and fumarate reductase (QFR), representing the sodium-translocating NADH:fumarate oxidoreductase (SNFR) supercomplex. SNFR is the major charge-separating module, generating an electrochemical sodium gradient in P. bryantii. Our findings offer clues to the observation that use of fumarate as feed additive does not significantly increase succinate production, or decrease methanogenesis, by the microbial community in the rumen. American Society for Microbiology 2021-10-14 /pmc/articles/PMC8516057/ /pubmed/34469197 http://dx.doi.org/10.1128/AEM.01211-21 Text en Copyright © 2021 Schleicher et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Environmental Microbiology Schleicher, Lena Trautmann, Andrej Stegmann, Dennis P. Fritz, Günter Gätgens, Jochem Bott, Michael Hein, Sascha Simon, Jörg Seifert, Jana Steuber, Julia A Sodium-Translocating Module Linking Succinate Production to Formation of Membrane Potential in Prevotella bryantii |
title | A Sodium-Translocating Module Linking Succinate Production to Formation of Membrane Potential in Prevotella bryantii |
title_full | A Sodium-Translocating Module Linking Succinate Production to Formation of Membrane Potential in Prevotella bryantii |
title_fullStr | A Sodium-Translocating Module Linking Succinate Production to Formation of Membrane Potential in Prevotella bryantii |
title_full_unstemmed | A Sodium-Translocating Module Linking Succinate Production to Formation of Membrane Potential in Prevotella bryantii |
title_short | A Sodium-Translocating Module Linking Succinate Production to Formation of Membrane Potential in Prevotella bryantii |
title_sort | sodium-translocating module linking succinate production to formation of membrane potential in prevotella bryantii |
topic | Environmental Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516057/ https://www.ncbi.nlm.nih.gov/pubmed/34469197 http://dx.doi.org/10.1128/AEM.01211-21 |
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