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Micro‐aerobic production of isobutanol with engineered Pseudomonas putida
Pseudomonas putida KT2440 is emerging as a promising microbial host for biotechnological industry due to its broad range of substrate affinity and resilience to physicochemical stresses. Its natural tolerance towards aromatics and solvents qualifies this versatile microbe as promising candidate to p...
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/PMC8258000/ https://www.ncbi.nlm.nih.gov/pubmed/34257629 http://dx.doi.org/10.1002/elsc.202000116 |
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author | Ankenbauer, Andreas Nitschel, Robert Teleki, Attila Müller, Tobias Favilli, Lorenzo Blombach, Bastian Takors, Ralf |
author_facet | Ankenbauer, Andreas Nitschel, Robert Teleki, Attila Müller, Tobias Favilli, Lorenzo Blombach, Bastian Takors, Ralf |
author_sort | Ankenbauer, Andreas |
collection | PubMed |
description | Pseudomonas putida KT2440 is emerging as a promising microbial host for biotechnological industry due to its broad range of substrate affinity and resilience to physicochemical stresses. Its natural tolerance towards aromatics and solvents qualifies this versatile microbe as promising candidate to produce next generation biofuels such as isobutanol. In this study, we scaled‐up the production of isobutanol with P. putida from shake flask to fed‐batch cultivation in a 30 L bioreactor. The design of a two‐stage bioprocess with separated growth and production resulted in 3.35 g(isobutanol) L(–1). Flux analysis revealed that the NADPH expensive formation of isobutanol exceeded the cellular catabolic supply of NADPH finally causing growth retardation. Concomitantly, the cell counteracted to the redox imbalance by increased formation of 2‐ketogluconic thereby providing electrons for the respiratory ATP generation. Thus, P. putida partially uncoupled ATP formation from the availability of NADH. The quantitative analysis of intracellular pyridine nucleotides NAD(P)(+) and NAD(P)H revealed elevated catabolic and anabolic reducing power during aerobic production of isobutanol. Additionally, the installation of micro‐aerobic conditions during production doubled the integral glucose‐to‐isobutanol conversion yield to 60 mg(isobutanol) g(glucose) (–1) while preventing undesired carbon loss as 2‐ketogluconic acid. |
format | Online Article Text |
id | pubmed-8258000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82580002021-07-12 Micro‐aerobic production of isobutanol with engineered Pseudomonas putida Ankenbauer, Andreas Nitschel, Robert Teleki, Attila Müller, Tobias Favilli, Lorenzo Blombach, Bastian Takors, Ralf Eng Life Sci Research Articles Pseudomonas putida KT2440 is emerging as a promising microbial host for biotechnological industry due to its broad range of substrate affinity and resilience to physicochemical stresses. Its natural tolerance towards aromatics and solvents qualifies this versatile microbe as promising candidate to produce next generation biofuels such as isobutanol. In this study, we scaled‐up the production of isobutanol with P. putida from shake flask to fed‐batch cultivation in a 30 L bioreactor. The design of a two‐stage bioprocess with separated growth and production resulted in 3.35 g(isobutanol) L(–1). Flux analysis revealed that the NADPH expensive formation of isobutanol exceeded the cellular catabolic supply of NADPH finally causing growth retardation. Concomitantly, the cell counteracted to the redox imbalance by increased formation of 2‐ketogluconic thereby providing electrons for the respiratory ATP generation. Thus, P. putida partially uncoupled ATP formation from the availability of NADH. The quantitative analysis of intracellular pyridine nucleotides NAD(P)(+) and NAD(P)H revealed elevated catabolic and anabolic reducing power during aerobic production of isobutanol. Additionally, the installation of micro‐aerobic conditions during production doubled the integral glucose‐to‐isobutanol conversion yield to 60 mg(isobutanol) g(glucose) (–1) while preventing undesired carbon loss as 2‐ketogluconic acid. John Wiley and Sons Inc. 2021-03-13 /pmc/articles/PMC8258000/ /pubmed/34257629 http://dx.doi.org/10.1002/elsc.202000116 Text en © 2021 The Authors. Engineering in Life Sciences published by Wiley‐VCH GmbH 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 | Research Articles Ankenbauer, Andreas Nitschel, Robert Teleki, Attila Müller, Tobias Favilli, Lorenzo Blombach, Bastian Takors, Ralf Micro‐aerobic production of isobutanol with engineered Pseudomonas putida |
title | Micro‐aerobic production of isobutanol with engineered Pseudomonas putida
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title_full | Micro‐aerobic production of isobutanol with engineered Pseudomonas putida
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title_fullStr | Micro‐aerobic production of isobutanol with engineered Pseudomonas putida
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title_full_unstemmed | Micro‐aerobic production of isobutanol with engineered Pseudomonas putida
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title_short | Micro‐aerobic production of isobutanol with engineered Pseudomonas putida
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title_sort | micro‐aerobic production of isobutanol with engineered pseudomonas putida |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8258000/ https://www.ncbi.nlm.nih.gov/pubmed/34257629 http://dx.doi.org/10.1002/elsc.202000116 |
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