Cargando…
Fermentation of oxidized hexose derivatives by Clostridium acetobutylicum
BACKGROUND: Clostridium acetobutylicum fermentations are promising for production of commodity chemicals from heterogeneous biomass due to the wide range of substrates the organism can metabolize. Much work has been done to elucidate the pathways for utilization of aldoses, but little is known about...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4179846/ https://www.ncbi.nlm.nih.gov/pubmed/25231163 http://dx.doi.org/10.1186/s12934-014-0139-7 |
_version_ | 1782337151469355008 |
---|---|
author | Servinsky, Matthew D Liu, Sanchao Gerlach, Elliot S Germane, Katherine L Sund, Christian J |
author_facet | Servinsky, Matthew D Liu, Sanchao Gerlach, Elliot S Germane, Katherine L Sund, Christian J |
author_sort | Servinsky, Matthew D |
collection | PubMed |
description | BACKGROUND: Clostridium acetobutylicum fermentations are promising for production of commodity chemicals from heterogeneous biomass due to the wide range of substrates the organism can metabolize. Much work has been done to elucidate the pathways for utilization of aldoses, but little is known about metabolism of more oxidized substrates. Two oxidized hexose derivatives, gluconate and galacturonate, are present in low cost feedstocks, and their metabolism will contribute to overall metabolic output of these substrates. RESULTS: A complete metabolic network for glucose, gluconate, and galacturonate utilization was generated using online databases, previous studies, genomic context, and experimental data. Gluconate appears to be metabolized via the Entner-Doudoroff pathway, and is likely dehydrated to 2-keto-3-deoxy-gluconate before phosphorylation to 2-keto-3-deoxy-6-P-gluconate. Galacturonate appears to be processed via the Ashwell pathway, converging on a common metabolite for gluconate and galacturonate metabolism, 2-keto-3-deoxygluconate. As expected, increasingly oxidized substrates resulted in increasingly oxidized products with galacturonate fermentations being nearly homoacetic. Calculations of expected ATP and reducing equivalent yields and experimental data suggested galacturonate fermentations were reductant limited. Galacturonate fermentation was incomplete, which was not due solely to product inhibition or the inability to utilize low concentrations of galacturonate. Removal of H(2) and CO(2) by agitation resulted in faster growth, higher cell densities, formation of relatively more oxidized products, and higher product yields for cultures grown on glucose or gluconate. In contrast, cells grown on galacturonate showed reduced growth rates upon agitation, which was likely due to loss in reductant in the form of H(2). The growth advantage seen on agitated glucose or gluconate cultures could not be solely attributed to improved ATP economics, thereby indicating other factors are also important. CONCLUSIONS: The metabolic network presented in this work should facilitate similar reconstructions in other organisms, and provides a further understanding of the pathways involved in metabolism of oxidized feedstocks and carbohydrate mixtures. The nearly homoacetic fermentation during growth on galacturonate indicates further optimization of this and related organisms could provide a route to an effective biologically derived acetic acid production platform. Furthermore, the pathways could be targeted to decrease production of undesirable products during fermentations of heterogeneous biomass. |
format | Online Article Text |
id | pubmed-4179846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41798462014-10-01 Fermentation of oxidized hexose derivatives by Clostridium acetobutylicum Servinsky, Matthew D Liu, Sanchao Gerlach, Elliot S Germane, Katherine L Sund, Christian J Microb Cell Fact Research BACKGROUND: Clostridium acetobutylicum fermentations are promising for production of commodity chemicals from heterogeneous biomass due to the wide range of substrates the organism can metabolize. Much work has been done to elucidate the pathways for utilization of aldoses, but little is known about metabolism of more oxidized substrates. Two oxidized hexose derivatives, gluconate and galacturonate, are present in low cost feedstocks, and their metabolism will contribute to overall metabolic output of these substrates. RESULTS: A complete metabolic network for glucose, gluconate, and galacturonate utilization was generated using online databases, previous studies, genomic context, and experimental data. Gluconate appears to be metabolized via the Entner-Doudoroff pathway, and is likely dehydrated to 2-keto-3-deoxy-gluconate before phosphorylation to 2-keto-3-deoxy-6-P-gluconate. Galacturonate appears to be processed via the Ashwell pathway, converging on a common metabolite for gluconate and galacturonate metabolism, 2-keto-3-deoxygluconate. As expected, increasingly oxidized substrates resulted in increasingly oxidized products with galacturonate fermentations being nearly homoacetic. Calculations of expected ATP and reducing equivalent yields and experimental data suggested galacturonate fermentations were reductant limited. Galacturonate fermentation was incomplete, which was not due solely to product inhibition or the inability to utilize low concentrations of galacturonate. Removal of H(2) and CO(2) by agitation resulted in faster growth, higher cell densities, formation of relatively more oxidized products, and higher product yields for cultures grown on glucose or gluconate. In contrast, cells grown on galacturonate showed reduced growth rates upon agitation, which was likely due to loss in reductant in the form of H(2). The growth advantage seen on agitated glucose or gluconate cultures could not be solely attributed to improved ATP economics, thereby indicating other factors are also important. CONCLUSIONS: The metabolic network presented in this work should facilitate similar reconstructions in other organisms, and provides a further understanding of the pathways involved in metabolism of oxidized feedstocks and carbohydrate mixtures. The nearly homoacetic fermentation during growth on galacturonate indicates further optimization of this and related organisms could provide a route to an effective biologically derived acetic acid production platform. Furthermore, the pathways could be targeted to decrease production of undesirable products during fermentations of heterogeneous biomass. BioMed Central 2014-09-18 /pmc/articles/PMC4179846/ /pubmed/25231163 http://dx.doi.org/10.1186/s12934-014-0139-7 Text en © Servinsky et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Servinsky, Matthew D Liu, Sanchao Gerlach, Elliot S Germane, Katherine L Sund, Christian J Fermentation of oxidized hexose derivatives by Clostridium acetobutylicum |
title | Fermentation of oxidized hexose derivatives by Clostridium acetobutylicum |
title_full | Fermentation of oxidized hexose derivatives by Clostridium acetobutylicum |
title_fullStr | Fermentation of oxidized hexose derivatives by Clostridium acetobutylicum |
title_full_unstemmed | Fermentation of oxidized hexose derivatives by Clostridium acetobutylicum |
title_short | Fermentation of oxidized hexose derivatives by Clostridium acetobutylicum |
title_sort | fermentation of oxidized hexose derivatives by clostridium acetobutylicum |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4179846/ https://www.ncbi.nlm.nih.gov/pubmed/25231163 http://dx.doi.org/10.1186/s12934-014-0139-7 |
work_keys_str_mv | AT servinskymatthewd fermentationofoxidizedhexosederivativesbyclostridiumacetobutylicum AT liusanchao fermentationofoxidizedhexosederivativesbyclostridiumacetobutylicum AT gerlachelliots fermentationofoxidizedhexosederivativesbyclostridiumacetobutylicum AT germanekatherinel fermentationofoxidizedhexosederivativesbyclostridiumacetobutylicum AT sundchristianj fermentationofoxidizedhexosederivativesbyclostridiumacetobutylicum |