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Metabolic engineering of Vibrio natriegens for anaerobic succinate production

The biotechnological production of succinate bears serious potential to fully replace existing petrochemical approaches in the future. In order to establish an economically viable bioprocess, obtaining high titre, yield and productivity is of central importance. In this study, we present a straightf...

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Autores principales: Thoma, Felix, Schulze, Clarissa, Gutierrez‐Coto, Carolina, Hädrich, Maurice, Huber, Janine, Gunkel, Christoph, Thoma, Rebecca, Blombach, Bastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9151343/
https://www.ncbi.nlm.nih.gov/pubmed/34843164
http://dx.doi.org/10.1111/1751-7915.13983
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author Thoma, Felix
Schulze, Clarissa
Gutierrez‐Coto, Carolina
Hädrich, Maurice
Huber, Janine
Gunkel, Christoph
Thoma, Rebecca
Blombach, Bastian
author_facet Thoma, Felix
Schulze, Clarissa
Gutierrez‐Coto, Carolina
Hädrich, Maurice
Huber, Janine
Gunkel, Christoph
Thoma, Rebecca
Blombach, Bastian
author_sort Thoma, Felix
collection PubMed
description The biotechnological production of succinate bears serious potential to fully replace existing petrochemical approaches in the future. In order to establish an economically viable bioprocess, obtaining high titre, yield and productivity is of central importance. In this study, we present a straightforward engineering approach for anaerobic succinate production with Vibrio natriegens, consisting of essential metabolic engineering and optimization of process conditions. The final producer strain V. natriegens Δlldh Δdldh Δpfl Δald Δdns::pyc (Cg) (Succ1) yielded 1.46 mol of succinate per mol of glucose under anaerobic conditions (85% of the theoretical maximum) and revealed a particularly high biomass‐specific succinate production rate of 1.33 g(Succ) g(CDW) (−1) h(−1) compared with well‐established production systems. By applying carbon and redox balancing, we determined the intracellular flux distribution and show that under the tested conditions the reductive TCA as well as the oxidative TCA/glyoxylate pathway contributed to succinate formation. In a zero‐growth bioprocess using minimal medium devoid of complex additives and expensive supplements, we obtained a final titre of 60.4 g(Succ) l(−1) with a maximum productivity of 20.8 g(Succ) l(−1) h(−1) and an overall volumetric productivity of 8.6 g(Succ) l(−1) h(−1) during the 7 h fermentation. The key performance indicators (titre, yield and productivity) of this first engineering approach in V. natriegens are encouraging and compete with costly tailored microbial production systems.
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spelling pubmed-91513432022-06-04 Metabolic engineering of Vibrio natriegens for anaerobic succinate production Thoma, Felix Schulze, Clarissa Gutierrez‐Coto, Carolina Hädrich, Maurice Huber, Janine Gunkel, Christoph Thoma, Rebecca Blombach, Bastian Microb Biotechnol Lilliput The biotechnological production of succinate bears serious potential to fully replace existing petrochemical approaches in the future. In order to establish an economically viable bioprocess, obtaining high titre, yield and productivity is of central importance. In this study, we present a straightforward engineering approach for anaerobic succinate production with Vibrio natriegens, consisting of essential metabolic engineering and optimization of process conditions. The final producer strain V. natriegens Δlldh Δdldh Δpfl Δald Δdns::pyc (Cg) (Succ1) yielded 1.46 mol of succinate per mol of glucose under anaerobic conditions (85% of the theoretical maximum) and revealed a particularly high biomass‐specific succinate production rate of 1.33 g(Succ) g(CDW) (−1) h(−1) compared with well‐established production systems. By applying carbon and redox balancing, we determined the intracellular flux distribution and show that under the tested conditions the reductive TCA as well as the oxidative TCA/glyoxylate pathway contributed to succinate formation. In a zero‐growth bioprocess using minimal medium devoid of complex additives and expensive supplements, we obtained a final titre of 60.4 g(Succ) l(−1) with a maximum productivity of 20.8 g(Succ) l(−1) h(−1) and an overall volumetric productivity of 8.6 g(Succ) l(−1) h(−1) during the 7 h fermentation. The key performance indicators (titre, yield and productivity) of this first engineering approach in V. natriegens are encouraging and compete with costly tailored microbial production systems. John Wiley and Sons Inc. 2021-11-29 /pmc/articles/PMC9151343/ /pubmed/34843164 http://dx.doi.org/10.1111/1751-7915.13983 Text en © 2021 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Lilliput
Thoma, Felix
Schulze, Clarissa
Gutierrez‐Coto, Carolina
Hädrich, Maurice
Huber, Janine
Gunkel, Christoph
Thoma, Rebecca
Blombach, Bastian
Metabolic engineering of Vibrio natriegens for anaerobic succinate production
title Metabolic engineering of Vibrio natriegens for anaerobic succinate production
title_full Metabolic engineering of Vibrio natriegens for anaerobic succinate production
title_fullStr Metabolic engineering of Vibrio natriegens for anaerobic succinate production
title_full_unstemmed Metabolic engineering of Vibrio natriegens for anaerobic succinate production
title_short Metabolic engineering of Vibrio natriegens for anaerobic succinate production
title_sort metabolic engineering of vibrio natriegens for anaerobic succinate production
topic Lilliput
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9151343/
https://www.ncbi.nlm.nih.gov/pubmed/34843164
http://dx.doi.org/10.1111/1751-7915.13983
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