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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...

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Autores principales: Ankenbauer, Andreas, Nitschel, Robert, Teleki, Attila, Müller, Tobias, Favilli, Lorenzo, Blombach, Bastian, Takors, Ralf
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/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.
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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
title_full Micro‐aerobic production of isobutanol with engineered Pseudomonas putida
title_fullStr Micro‐aerobic production of isobutanol with engineered Pseudomonas putida
title_full_unstemmed Micro‐aerobic production of isobutanol with engineered Pseudomonas putida
title_short Micro‐aerobic production of isobutanol with engineered Pseudomonas putida
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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