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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-9151343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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