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Continuous succinic acid production by Actinobacillus succinogenes on xylose-enriched hydrolysate

BACKGROUND: Bio-manufacturing of high-value chemicals in parallel to renewable biofuels has the potential to dramatically improve the overall economic landscape of integrated lignocellulosic biorefineries. However, this will require the generation of carbohydrate streams from lignocellulose in a for...

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Autores principales: Bradfield, Michael F. A., Mohagheghi, Ali, Salvachúa, Davinia, Smith, Holly, Black, Brenna A., Dowe, Nancy, Beckham, Gregg T., Nicol, Willie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650334/
https://www.ncbi.nlm.nih.gov/pubmed/26581168
http://dx.doi.org/10.1186/s13068-015-0363-3
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author Bradfield, Michael F. A.
Mohagheghi, Ali
Salvachúa, Davinia
Smith, Holly
Black, Brenna A.
Dowe, Nancy
Beckham, Gregg T.
Nicol, Willie
author_facet Bradfield, Michael F. A.
Mohagheghi, Ali
Salvachúa, Davinia
Smith, Holly
Black, Brenna A.
Dowe, Nancy
Beckham, Gregg T.
Nicol, Willie
author_sort Bradfield, Michael F. A.
collection PubMed
description BACKGROUND: Bio-manufacturing of high-value chemicals in parallel to renewable biofuels has the potential to dramatically improve the overall economic landscape of integrated lignocellulosic biorefineries. However, this will require the generation of carbohydrate streams from lignocellulose in a form suitable for efficient microbial conversion and downstream processing appropriate to the desired end use, making overall process development, along with selection of appropriate target molecules, crucial to the integrated biorefinery. Succinic acid (SA), a high-value target molecule, can be biologically produced from sugars and has the potential to serve as a platform chemical for various chemical and polymer applications. However, the feasibility of microbial SA production at industrially relevant productivities and yields from lignocellulosic biorefinery streams has not yet been reported. RESULTS: Actinobacillus succinogenes 130Z was immobilised in a custom continuous fermentation setup to produce SA on the xylose-enriched fraction of a non-detoxified, xylose-rich corn stover hydrolysate stream produced from deacetylation and dilute acid pretreatment. Effective biofilm attachment, which serves as a natural cell retention strategy to increase cell densities, productivities and resistance to toxicity, was accomplished by means of a novel agitator fitting. A maximum SA titre, yield and productivity of 39.6 g L(−1), 0.78 g g(−1) and 1.77 g L(−1) h(−1) were achieved, respectively. Steady states were obtained at dilution rates of 0.02, 0.03, 0.04, and 0.05 h(−1) and the stirred biofilm reactor was stable over prolonged periods of operation with a combined fermentation time of 1550 h. Furthermore, it was found that a gradual increase in the dilution rate was required to facilitate adaptation of the culture to the hydrolysate, suggesting a strong evolutionary response to the toxic compounds in the hydrolysate. Moreover, the two primary suspected fermentation inhibitors, furfural and HMF, were metabolised during fermentation with the concentration of each remaining at zero across all steady states. CONCLUSIONS: The results demonstrate that immobilised A. succinogenes has the potential for effective conversion of an industrially relevant, biomass-derived feed stream to succinic acid. Furthermore, due to the attractive yields, productivities and titres achieved in this study, the process has the potential to serve as a means for value-added chemical manufacturing in the integrated biorefinery.
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spelling pubmed-46503342015-11-19 Continuous succinic acid production by Actinobacillus succinogenes on xylose-enriched hydrolysate Bradfield, Michael F. A. Mohagheghi, Ali Salvachúa, Davinia Smith, Holly Black, Brenna A. Dowe, Nancy Beckham, Gregg T. Nicol, Willie Biotechnol Biofuels Research BACKGROUND: Bio-manufacturing of high-value chemicals in parallel to renewable biofuels has the potential to dramatically improve the overall economic landscape of integrated lignocellulosic biorefineries. However, this will require the generation of carbohydrate streams from lignocellulose in a form suitable for efficient microbial conversion and downstream processing appropriate to the desired end use, making overall process development, along with selection of appropriate target molecules, crucial to the integrated biorefinery. Succinic acid (SA), a high-value target molecule, can be biologically produced from sugars and has the potential to serve as a platform chemical for various chemical and polymer applications. However, the feasibility of microbial SA production at industrially relevant productivities and yields from lignocellulosic biorefinery streams has not yet been reported. RESULTS: Actinobacillus succinogenes 130Z was immobilised in a custom continuous fermentation setup to produce SA on the xylose-enriched fraction of a non-detoxified, xylose-rich corn stover hydrolysate stream produced from deacetylation and dilute acid pretreatment. Effective biofilm attachment, which serves as a natural cell retention strategy to increase cell densities, productivities and resistance to toxicity, was accomplished by means of a novel agitator fitting. A maximum SA titre, yield and productivity of 39.6 g L(−1), 0.78 g g(−1) and 1.77 g L(−1) h(−1) were achieved, respectively. Steady states were obtained at dilution rates of 0.02, 0.03, 0.04, and 0.05 h(−1) and the stirred biofilm reactor was stable over prolonged periods of operation with a combined fermentation time of 1550 h. Furthermore, it was found that a gradual increase in the dilution rate was required to facilitate adaptation of the culture to the hydrolysate, suggesting a strong evolutionary response to the toxic compounds in the hydrolysate. Moreover, the two primary suspected fermentation inhibitors, furfural and HMF, were metabolised during fermentation with the concentration of each remaining at zero across all steady states. CONCLUSIONS: The results demonstrate that immobilised A. succinogenes has the potential for effective conversion of an industrially relevant, biomass-derived feed stream to succinic acid. Furthermore, due to the attractive yields, productivities and titres achieved in this study, the process has the potential to serve as a means for value-added chemical manufacturing in the integrated biorefinery. BioMed Central 2015-11-14 /pmc/articles/PMC4650334/ /pubmed/26581168 http://dx.doi.org/10.1186/s13068-015-0363-3 Text en © Bradfield et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Bradfield, Michael F. A.
Mohagheghi, Ali
Salvachúa, Davinia
Smith, Holly
Black, Brenna A.
Dowe, Nancy
Beckham, Gregg T.
Nicol, Willie
Continuous succinic acid production by Actinobacillus succinogenes on xylose-enriched hydrolysate
title Continuous succinic acid production by Actinobacillus succinogenes on xylose-enriched hydrolysate
title_full Continuous succinic acid production by Actinobacillus succinogenes on xylose-enriched hydrolysate
title_fullStr Continuous succinic acid production by Actinobacillus succinogenes on xylose-enriched hydrolysate
title_full_unstemmed Continuous succinic acid production by Actinobacillus succinogenes on xylose-enriched hydrolysate
title_short Continuous succinic acid production by Actinobacillus succinogenes on xylose-enriched hydrolysate
title_sort continuous succinic acid production by actinobacillus succinogenes on xylose-enriched hydrolysate
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650334/
https://www.ncbi.nlm.nih.gov/pubmed/26581168
http://dx.doi.org/10.1186/s13068-015-0363-3
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