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Calvin Cycle Flux, Pathway Constraints, and Substrate Oxidation State Together Determine the H(2) Biofuel Yield in Photoheterotrophic Bacteria

Hydrogen gas (H(2)) is a possible future transportation fuel that can be produced by anoxygenic phototrophic bacteria via nitrogenase. The electrons for H(2) are usually derived from organic compounds. Thus, one would expect more H(2) to be produced when anoxygenic phototrophs are supplied with incr...

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Autores principales: McKinlay, James B., Harwood, Caroline S.
Formato: Texto
Lenguaje:English
Publicado: American Society of Microbiology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063381/
https://www.ncbi.nlm.nih.gov/pubmed/21427286
http://dx.doi.org/10.1128/mBio.00323-10
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author McKinlay, James B.
Harwood, Caroline S.
author_facet McKinlay, James B.
Harwood, Caroline S.
author_sort McKinlay, James B.
collection PubMed
description Hydrogen gas (H(2)) is a possible future transportation fuel that can be produced by anoxygenic phototrophic bacteria via nitrogenase. The electrons for H(2) are usually derived from organic compounds. Thus, one would expect more H(2) to be produced when anoxygenic phototrophs are supplied with increasingly reduced (electron-rich) organic compounds. However, the H(2) yield does not always differ according to the substrate oxidation state. To understand other factors that influence the H(2) yield, we determined metabolic fluxes in Rhodopseudomonas palustris grown on (13)C-labeled fumarate, succinate, acetate, and butyrate (in order from most oxidized to most reduced). The flux maps revealed that the H(2) yield was influenced by two main factors in addition to substrate oxidation state. The first factor was the route that a substrate took to biosynthetic precursors. For example, succinate took a different route to acetyl-coenzyme A (CoA) than acetate. As a result, R. palustris generated similar amounts of reducing equivalents and similar amounts of H(2) from both succinate and acetate, even though succinate is more oxidized than acetate. The second factor affecting the H(2) yield was the amount of Calvin cycle flux competing for electrons. When nitrogenase was active, electrons were diverted away from the Calvin cycle towards H(2), but to various extents, depending on the substrate. When Calvin cycle flux was blocked, the H(2) yield increased during growth on all substrates. In general, this increase in H(2) yield could be predicted from the initial Calvin cycle flux.
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spelling pubmed-30633812011-03-28 Calvin Cycle Flux, Pathway Constraints, and Substrate Oxidation State Together Determine the H(2) Biofuel Yield in Photoheterotrophic Bacteria McKinlay, James B. Harwood, Caroline S. mBio Research Article Hydrogen gas (H(2)) is a possible future transportation fuel that can be produced by anoxygenic phototrophic bacteria via nitrogenase. The electrons for H(2) are usually derived from organic compounds. Thus, one would expect more H(2) to be produced when anoxygenic phototrophs are supplied with increasingly reduced (electron-rich) organic compounds. However, the H(2) yield does not always differ according to the substrate oxidation state. To understand other factors that influence the H(2) yield, we determined metabolic fluxes in Rhodopseudomonas palustris grown on (13)C-labeled fumarate, succinate, acetate, and butyrate (in order from most oxidized to most reduced). The flux maps revealed that the H(2) yield was influenced by two main factors in addition to substrate oxidation state. The first factor was the route that a substrate took to biosynthetic precursors. For example, succinate took a different route to acetyl-coenzyme A (CoA) than acetate. As a result, R. palustris generated similar amounts of reducing equivalents and similar amounts of H(2) from both succinate and acetate, even though succinate is more oxidized than acetate. The second factor affecting the H(2) yield was the amount of Calvin cycle flux competing for electrons. When nitrogenase was active, electrons were diverted away from the Calvin cycle towards H(2), but to various extents, depending on the substrate. When Calvin cycle flux was blocked, the H(2) yield increased during growth on all substrates. In general, this increase in H(2) yield could be predicted from the initial Calvin cycle flux. American Society of Microbiology 2011-03-22 /pmc/articles/PMC3063381/ /pubmed/21427286 http://dx.doi.org/10.1128/mBio.00323-10 Text en Copyright © 2011 McKinlay and Harwood http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
McKinlay, James B.
Harwood, Caroline S.
Calvin Cycle Flux, Pathway Constraints, and Substrate Oxidation State Together Determine the H(2) Biofuel Yield in Photoheterotrophic Bacteria
title Calvin Cycle Flux, Pathway Constraints, and Substrate Oxidation State Together Determine the H(2) Biofuel Yield in Photoheterotrophic Bacteria
title_full Calvin Cycle Flux, Pathway Constraints, and Substrate Oxidation State Together Determine the H(2) Biofuel Yield in Photoheterotrophic Bacteria
title_fullStr Calvin Cycle Flux, Pathway Constraints, and Substrate Oxidation State Together Determine the H(2) Biofuel Yield in Photoheterotrophic Bacteria
title_full_unstemmed Calvin Cycle Flux, Pathway Constraints, and Substrate Oxidation State Together Determine the H(2) Biofuel Yield in Photoheterotrophic Bacteria
title_short Calvin Cycle Flux, Pathway Constraints, and Substrate Oxidation State Together Determine the H(2) Biofuel Yield in Photoheterotrophic Bacteria
title_sort calvin cycle flux, pathway constraints, and substrate oxidation state together determine the h(2) biofuel yield in photoheterotrophic bacteria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063381/
https://www.ncbi.nlm.nih.gov/pubmed/21427286
http://dx.doi.org/10.1128/mBio.00323-10
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