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Improved Itaconate Production with Ustilago cynodontis via Co-Metabolism of CO(2)-Derived Formate

In recent years, it was shown that itaconic acid can be produced from glucose with Ustilago strains at up to maximum theoretical yield. The use of acetate and formate as co-feedstocks can boost the efficiency of itaconate production with Ustilaginaceae wild-type strains by reducing the glucose amoun...

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Autores principales: Ullmann, Lena, Guntermann, Nils, Kohl, Philipp, Schröders, Gereon, Müsgens, Andreas, Franciò, Giancarlo, Leitner, Walter, Blank, Lars M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9784962/
https://www.ncbi.nlm.nih.gov/pubmed/36547610
http://dx.doi.org/10.3390/jof8121277
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author Ullmann, Lena
Guntermann, Nils
Kohl, Philipp
Schröders, Gereon
Müsgens, Andreas
Franciò, Giancarlo
Leitner, Walter
Blank, Lars M.
author_facet Ullmann, Lena
Guntermann, Nils
Kohl, Philipp
Schröders, Gereon
Müsgens, Andreas
Franciò, Giancarlo
Leitner, Walter
Blank, Lars M.
author_sort Ullmann, Lena
collection PubMed
description In recent years, it was shown that itaconic acid can be produced from glucose with Ustilago strains at up to maximum theoretical yield. The use of acetate and formate as co-feedstocks can boost the efficiency of itaconate production with Ustilaginaceae wild-type strains by reducing the glucose amount and thus the agricultural land required for the biotechnological production of this chemical. Metabolically engineered strains (U. cynodontis Δfuz7 Δcyp3 ↑P(ria1) and U. cynodontis Δfuz7 Δcyp3 P(etef)mttA ↑P(ria1)) were applied in itaconate production, obtaining a titer of 56.1 g L(−1) and a yield of 0.55 g(itaconate) per g(substrate). Both improved titer and yield (increase of 5.2 g L(−1) and 0.04 g(itaconate) per g(substrate), respectively) were achieved when using sodium formate as an auxiliary substrate. By applying the design-of-experiments (DoE) methodology, cultivation parameters (glucose, sodium formate and ammonium chloride concentrations) were optimized, resulting in two empirical models predicting itaconate titer and yield for U. cynodontis Δfuz7 Δcyp3 P(etef)mttA ↑P(ria1). Thereby, an almost doubled itaconate titer of 138 g L(−1) was obtained and a yield of 0.62 g(itaconate) per g(substrate) was reached during confirmation experiments corresponding to 86% of the theoretical maximum. In order to close the carbon cycle by production of the co-feed via a “power-to-X” route, the biphasic Ru-catalysed hydrogenation of CO(2) to formate could be integrated into the bioprocess directly using the obtained aqueous solution of formates as co-feedstock without any purification steps, demonstrating the (bio)compatibility of the two processes.
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spelling pubmed-97849622022-12-24 Improved Itaconate Production with Ustilago cynodontis via Co-Metabolism of CO(2)-Derived Formate Ullmann, Lena Guntermann, Nils Kohl, Philipp Schröders, Gereon Müsgens, Andreas Franciò, Giancarlo Leitner, Walter Blank, Lars M. J Fungi (Basel) Article In recent years, it was shown that itaconic acid can be produced from glucose with Ustilago strains at up to maximum theoretical yield. The use of acetate and formate as co-feedstocks can boost the efficiency of itaconate production with Ustilaginaceae wild-type strains by reducing the glucose amount and thus the agricultural land required for the biotechnological production of this chemical. Metabolically engineered strains (U. cynodontis Δfuz7 Δcyp3 ↑P(ria1) and U. cynodontis Δfuz7 Δcyp3 P(etef)mttA ↑P(ria1)) were applied in itaconate production, obtaining a titer of 56.1 g L(−1) and a yield of 0.55 g(itaconate) per g(substrate). Both improved titer and yield (increase of 5.2 g L(−1) and 0.04 g(itaconate) per g(substrate), respectively) were achieved when using sodium formate as an auxiliary substrate. By applying the design-of-experiments (DoE) methodology, cultivation parameters (glucose, sodium formate and ammonium chloride concentrations) were optimized, resulting in two empirical models predicting itaconate titer and yield for U. cynodontis Δfuz7 Δcyp3 P(etef)mttA ↑P(ria1). Thereby, an almost doubled itaconate titer of 138 g L(−1) was obtained and a yield of 0.62 g(itaconate) per g(substrate) was reached during confirmation experiments corresponding to 86% of the theoretical maximum. In order to close the carbon cycle by production of the co-feed via a “power-to-X” route, the biphasic Ru-catalysed hydrogenation of CO(2) to formate could be integrated into the bioprocess directly using the obtained aqueous solution of formates as co-feedstock without any purification steps, demonstrating the (bio)compatibility of the two processes. MDPI 2022-12-05 /pmc/articles/PMC9784962/ /pubmed/36547610 http://dx.doi.org/10.3390/jof8121277 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ullmann, Lena
Guntermann, Nils
Kohl, Philipp
Schröders, Gereon
Müsgens, Andreas
Franciò, Giancarlo
Leitner, Walter
Blank, Lars M.
Improved Itaconate Production with Ustilago cynodontis via Co-Metabolism of CO(2)-Derived Formate
title Improved Itaconate Production with Ustilago cynodontis via Co-Metabolism of CO(2)-Derived Formate
title_full Improved Itaconate Production with Ustilago cynodontis via Co-Metabolism of CO(2)-Derived Formate
title_fullStr Improved Itaconate Production with Ustilago cynodontis via Co-Metabolism of CO(2)-Derived Formate
title_full_unstemmed Improved Itaconate Production with Ustilago cynodontis via Co-Metabolism of CO(2)-Derived Formate
title_short Improved Itaconate Production with Ustilago cynodontis via Co-Metabolism of CO(2)-Derived Formate
title_sort improved itaconate production with ustilago cynodontis via co-metabolism of co(2)-derived formate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9784962/
https://www.ncbi.nlm.nih.gov/pubmed/36547610
http://dx.doi.org/10.3390/jof8121277
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