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Rex in Caldicellulosiruptor bescii: Novel regulon members and its effect on the production of ethanol and overflow metabolites

Rex is a global redox‐sensing transcription factor that senses and responds to the intracellular [NADH]/[NAD (+)] ratio to regulate genes for central metabolism, and a variety of metabolic processes in Gram‐positive bacteria. We decipher and validate four new members of the Rex regulon in Caldicellu...

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Autores principales: Sander, Kyle, Chung, Daehwan, Hyatt, Doug, Westpheling, Janet, Klingeman, Dawn M., Rodriguez, Miguel, Engle, Nancy L., Tschaplinski, Timothy J., Davison, Brian H., Brown, Steven D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391272/
https://www.ncbi.nlm.nih.gov/pubmed/29797457
http://dx.doi.org/10.1002/mbo3.639
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author Sander, Kyle
Chung, Daehwan
Hyatt, Doug
Westpheling, Janet
Klingeman, Dawn M.
Rodriguez, Miguel
Engle, Nancy L.
Tschaplinski, Timothy J.
Davison, Brian H.
Brown, Steven D.
author_facet Sander, Kyle
Chung, Daehwan
Hyatt, Doug
Westpheling, Janet
Klingeman, Dawn M.
Rodriguez, Miguel
Engle, Nancy L.
Tschaplinski, Timothy J.
Davison, Brian H.
Brown, Steven D.
author_sort Sander, Kyle
collection PubMed
description Rex is a global redox‐sensing transcription factor that senses and responds to the intracellular [NADH]/[NAD (+)] ratio to regulate genes for central metabolism, and a variety of metabolic processes in Gram‐positive bacteria. We decipher and validate four new members of the Rex regulon in Caldicellulosiruptor bescii; a gene encoding a class V aminotransferase, the HydG FeFe Hydrogenase maturation protein, an oxidoreductase, and a gene encoding a hypothetical protein. Structural genes for the NiFe and FeFe hydrogenases, pyruvate:ferredoxin oxidoreductase, as well as the rex gene itself are also members of this regulon, as has been predicted previously in different organisms. A C. bescii rex deletion strain constructed in an ethanol‐producing strain made 54% more ethanol (0.16 mmol/L) than its genetic parent after 36 hr of fermentation, though only under nitrogen limited conditions. Metabolomic interrogation shows this rex‐deficient ethanol‐producing strain synthesizes other reduced overflow metabolism products likely in response to more reduced intracellular redox conditions and the accumulation of pyruvate. These results suggest ethanol production is strongly dependent on the native intracellular redox state in C. bescii, and highlight the combined promise of using this gene and manipulation of culture conditions to yield strains capable of producing ethanol at higher yields and final titer.
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spelling pubmed-63912722019-03-07 Rex in Caldicellulosiruptor bescii: Novel regulon members and its effect on the production of ethanol and overflow metabolites Sander, Kyle Chung, Daehwan Hyatt, Doug Westpheling, Janet Klingeman, Dawn M. Rodriguez, Miguel Engle, Nancy L. Tschaplinski, Timothy J. Davison, Brian H. Brown, Steven D. Microbiologyopen Original Articles Rex is a global redox‐sensing transcription factor that senses and responds to the intracellular [NADH]/[NAD (+)] ratio to regulate genes for central metabolism, and a variety of metabolic processes in Gram‐positive bacteria. We decipher and validate four new members of the Rex regulon in Caldicellulosiruptor bescii; a gene encoding a class V aminotransferase, the HydG FeFe Hydrogenase maturation protein, an oxidoreductase, and a gene encoding a hypothetical protein. Structural genes for the NiFe and FeFe hydrogenases, pyruvate:ferredoxin oxidoreductase, as well as the rex gene itself are also members of this regulon, as has been predicted previously in different organisms. A C. bescii rex deletion strain constructed in an ethanol‐producing strain made 54% more ethanol (0.16 mmol/L) than its genetic parent after 36 hr of fermentation, though only under nitrogen limited conditions. Metabolomic interrogation shows this rex‐deficient ethanol‐producing strain synthesizes other reduced overflow metabolism products likely in response to more reduced intracellular redox conditions and the accumulation of pyruvate. These results suggest ethanol production is strongly dependent on the native intracellular redox state in C. bescii, and highlight the combined promise of using this gene and manipulation of culture conditions to yield strains capable of producing ethanol at higher yields and final titer. John Wiley and Sons Inc. 2018-05-23 /pmc/articles/PMC6391272/ /pubmed/29797457 http://dx.doi.org/10.1002/mbo3.639 Text en © 2018 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Sander, Kyle
Chung, Daehwan
Hyatt, Doug
Westpheling, Janet
Klingeman, Dawn M.
Rodriguez, Miguel
Engle, Nancy L.
Tschaplinski, Timothy J.
Davison, Brian H.
Brown, Steven D.
Rex in Caldicellulosiruptor bescii: Novel regulon members and its effect on the production of ethanol and overflow metabolites
title Rex in Caldicellulosiruptor bescii: Novel regulon members and its effect on the production of ethanol and overflow metabolites
title_full Rex in Caldicellulosiruptor bescii: Novel regulon members and its effect on the production of ethanol and overflow metabolites
title_fullStr Rex in Caldicellulosiruptor bescii: Novel regulon members and its effect on the production of ethanol and overflow metabolites
title_full_unstemmed Rex in Caldicellulosiruptor bescii: Novel regulon members and its effect on the production of ethanol and overflow metabolites
title_short Rex in Caldicellulosiruptor bescii: Novel regulon members and its effect on the production of ethanol and overflow metabolites
title_sort rex in caldicellulosiruptor bescii: novel regulon members and its effect on the production of ethanol and overflow metabolites
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391272/
https://www.ncbi.nlm.nih.gov/pubmed/29797457
http://dx.doi.org/10.1002/mbo3.639
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