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A Third Way of Energy Conservation in Acetogenic Bacteria

Acetogenic bacteria are a group of strictly anaerobic bacteria that make a living from acetate formation from two molecules of CO(2) via the Wood-Ljungdahl pathway (WLP). The free energy change of this reaction is very small and allows the synthesis of only a fraction of an ATP. How this pathway is...

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Detalles Bibliográficos
Autores principales: Kremp, Florian, Roth, Jennifer, Müller, Volker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9430772/
https://www.ncbi.nlm.nih.gov/pubmed/35699467
http://dx.doi.org/10.1128/spectrum.01385-22
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author Kremp, Florian
Roth, Jennifer
Müller, Volker
author_facet Kremp, Florian
Roth, Jennifer
Müller, Volker
author_sort Kremp, Florian
collection PubMed
description Acetogenic bacteria are a group of strictly anaerobic bacteria that make a living from acetate formation from two molecules of CO(2) via the Wood-Ljungdahl pathway (WLP). The free energy change of this reaction is very small and allows the synthesis of only a fraction of an ATP. How this pathway is coupled to energy conservation has been an enigma since its discovery ~90 years ago. Here, we describe an electron transport chain in the cytochrome- and quinone-containing acetogen Sporomusa ovata that leads from molecular hydrogen as an electron donor to an intermediate of the WLP, methylenetetrahydrofolate (methylene-tetrahydrofolate [THF]), as an electron acceptor. The catalytic site of the hydrogenase is periplasmic and likely linked cytochrome b to the membrane. We provide evidence that the MetVF-type methylenetetrahydrofolate reductase is linked proteins MvhD and HdrCBA to the cytoplasmic membrane. Membrane preparations catalyzed the H(2)-dependent reduction of methylene-THF to methyl-THF. In our model, a transmembrane electrochemical H(+) gradient is established by both scalar and vectorial protons that leads to the synthesis of 0.5 mol ATP/mol methylene-THF by a H(+)-F(1)F(o) ATP synthase. This H(2)- and methylene-THF-dependent electron transport chain may be present in other cytochrome-containing acetogens as well and represents a third way of chemiosmotic energy conservation in acetogens, but only in addition to the well-established respiratory enzymes Rnf and Ech. IMPORTANCE Acetogenic bacteria grow by making acetate from CO(2) and are considered the first life forms on Earth since they couple CO(2) reduction to the conservation of energy. How this is achieved has been an enigma ever since. Recently, two respiratory enzymes, a ferredoxin:NAD(+) oxidoreductase (Rnf) and a ferredoxin:H(+) oxidoreductase (Ech), have been found in cytochrome-free acetogenic model bacteria. However, some acetogens contain cytochromes in addition, and there has been a long-standing assumption of a cytochrome-containing electron transport chain in those acetogens. Here, we provide evidence for a respiratory chain in Sporomusa ovata that has a cytochrome-containing hydrogenase as the electron donor and a methylenetetrahydrofolate reductase as the terminal electron acceptor. This is the third way of chemiosmotic energy conservation found in acetogens.
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spelling pubmed-94307722022-09-01 A Third Way of Energy Conservation in Acetogenic Bacteria Kremp, Florian Roth, Jennifer Müller, Volker Microbiol Spectr Research Article Acetogenic bacteria are a group of strictly anaerobic bacteria that make a living from acetate formation from two molecules of CO(2) via the Wood-Ljungdahl pathway (WLP). The free energy change of this reaction is very small and allows the synthesis of only a fraction of an ATP. How this pathway is coupled to energy conservation has been an enigma since its discovery ~90 years ago. Here, we describe an electron transport chain in the cytochrome- and quinone-containing acetogen Sporomusa ovata that leads from molecular hydrogen as an electron donor to an intermediate of the WLP, methylenetetrahydrofolate (methylene-tetrahydrofolate [THF]), as an electron acceptor. The catalytic site of the hydrogenase is periplasmic and likely linked cytochrome b to the membrane. We provide evidence that the MetVF-type methylenetetrahydrofolate reductase is linked proteins MvhD and HdrCBA to the cytoplasmic membrane. Membrane preparations catalyzed the H(2)-dependent reduction of methylene-THF to methyl-THF. In our model, a transmembrane electrochemical H(+) gradient is established by both scalar and vectorial protons that leads to the synthesis of 0.5 mol ATP/mol methylene-THF by a H(+)-F(1)F(o) ATP synthase. This H(2)- and methylene-THF-dependent electron transport chain may be present in other cytochrome-containing acetogens as well and represents a third way of chemiosmotic energy conservation in acetogens, but only in addition to the well-established respiratory enzymes Rnf and Ech. IMPORTANCE Acetogenic bacteria grow by making acetate from CO(2) and are considered the first life forms on Earth since they couple CO(2) reduction to the conservation of energy. How this is achieved has been an enigma ever since. Recently, two respiratory enzymes, a ferredoxin:NAD(+) oxidoreductase (Rnf) and a ferredoxin:H(+) oxidoreductase (Ech), have been found in cytochrome-free acetogenic model bacteria. However, some acetogens contain cytochromes in addition, and there has been a long-standing assumption of a cytochrome-containing electron transport chain in those acetogens. Here, we provide evidence for a respiratory chain in Sporomusa ovata that has a cytochrome-containing hydrogenase as the electron donor and a methylenetetrahydrofolate reductase as the terminal electron acceptor. This is the third way of chemiosmotic energy conservation found in acetogens. American Society for Microbiology 2022-06-14 /pmc/articles/PMC9430772/ /pubmed/35699467 http://dx.doi.org/10.1128/spectrum.01385-22 Text en Copyright © 2022 Kremp 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 Research Article
Kremp, Florian
Roth, Jennifer
Müller, Volker
A Third Way of Energy Conservation in Acetogenic Bacteria
title A Third Way of Energy Conservation in Acetogenic Bacteria
title_full A Third Way of Energy Conservation in Acetogenic Bacteria
title_fullStr A Third Way of Energy Conservation in Acetogenic Bacteria
title_full_unstemmed A Third Way of Energy Conservation in Acetogenic Bacteria
title_short A Third Way of Energy Conservation in Acetogenic Bacteria
title_sort third way of energy conservation in acetogenic bacteria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9430772/
https://www.ncbi.nlm.nih.gov/pubmed/35699467
http://dx.doi.org/10.1128/spectrum.01385-22
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