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Metabolic Engineering of Fusarium oxysporum to Improve Its Ethanol-Producing Capability

Fusarium oxysporum is one of the few filamentous fungi capable of fermenting ethanol directly from plant cell wall biomass. It has the enzymatic toolbox necessary to break down biomass to its monosaccharides and, under anaerobic and microaerobic conditions, ferments them to ethanol. Although these t...

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Autores principales: Anasontzis, George E., Kourtoglou, Elisavet, Villas-Boâs, Silas G., Hatzinikolaou, Dimitris G., Christakopoulos, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854878/
https://www.ncbi.nlm.nih.gov/pubmed/27199958
http://dx.doi.org/10.3389/fmicb.2016.00632
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author Anasontzis, George E.
Kourtoglou, Elisavet
Villas-Boâs, Silas G.
Hatzinikolaou, Dimitris G.
Christakopoulos, Paul
author_facet Anasontzis, George E.
Kourtoglou, Elisavet
Villas-Boâs, Silas G.
Hatzinikolaou, Dimitris G.
Christakopoulos, Paul
author_sort Anasontzis, George E.
collection PubMed
description Fusarium oxysporum is one of the few filamentous fungi capable of fermenting ethanol directly from plant cell wall biomass. It has the enzymatic toolbox necessary to break down biomass to its monosaccharides and, under anaerobic and microaerobic conditions, ferments them to ethanol. Although these traits could enable its use in consolidated processes and thus bypass some of the bottlenecks encountered in ethanol production from lignocellulosic material when Saccharomyces cerevisiae is used—namely its inability to degrade lignocellulose and to consume pentoses—two major disadvantages of F. oxysporum compared to the yeast—its low growth rate and low ethanol productivity—hinder the further development of this process. We had previously identified phosphoglucomutase and transaldolase, two major enzymes of glucose catabolism and the pentose phosphate pathway, as possible bottlenecks in the metabolism of the fungus and we had reported the effect of their constitutive production on the growth characteristics of the fungus. In this study, we investigated the effect of their constitutive production on ethanol productivity under anaerobic conditions. We report an increase in ethanol yield and a concomitant decrease in acetic acid production. Metabolomics analysis revealed that the genetic modifications applied did not simply accelerate the metabolic rate of the microorganism; they also affected the relative concentrations of the various metabolites suggesting an increased channeling toward the chorismate pathway, an activation of the γ-aminobutyric acid shunt, and an excess in NADPH regeneration.
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spelling pubmed-48548782016-05-19 Metabolic Engineering of Fusarium oxysporum to Improve Its Ethanol-Producing Capability Anasontzis, George E. Kourtoglou, Elisavet Villas-Boâs, Silas G. Hatzinikolaou, Dimitris G. Christakopoulos, Paul Front Microbiol Microbiology Fusarium oxysporum is one of the few filamentous fungi capable of fermenting ethanol directly from plant cell wall biomass. It has the enzymatic toolbox necessary to break down biomass to its monosaccharides and, under anaerobic and microaerobic conditions, ferments them to ethanol. Although these traits could enable its use in consolidated processes and thus bypass some of the bottlenecks encountered in ethanol production from lignocellulosic material when Saccharomyces cerevisiae is used—namely its inability to degrade lignocellulose and to consume pentoses—two major disadvantages of F. oxysporum compared to the yeast—its low growth rate and low ethanol productivity—hinder the further development of this process. We had previously identified phosphoglucomutase and transaldolase, two major enzymes of glucose catabolism and the pentose phosphate pathway, as possible bottlenecks in the metabolism of the fungus and we had reported the effect of their constitutive production on the growth characteristics of the fungus. In this study, we investigated the effect of their constitutive production on ethanol productivity under anaerobic conditions. We report an increase in ethanol yield and a concomitant decrease in acetic acid production. Metabolomics analysis revealed that the genetic modifications applied did not simply accelerate the metabolic rate of the microorganism; they also affected the relative concentrations of the various metabolites suggesting an increased channeling toward the chorismate pathway, an activation of the γ-aminobutyric acid shunt, and an excess in NADPH regeneration. Frontiers Media S.A. 2016-05-04 /pmc/articles/PMC4854878/ /pubmed/27199958 http://dx.doi.org/10.3389/fmicb.2016.00632 Text en Copyright © 2016 Anasontzis, Kourtoglou, Villas-Boâs, Hatzinikolaou and Christakopoulos. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Anasontzis, George E.
Kourtoglou, Elisavet
Villas-Boâs, Silas G.
Hatzinikolaou, Dimitris G.
Christakopoulos, Paul
Metabolic Engineering of Fusarium oxysporum to Improve Its Ethanol-Producing Capability
title Metabolic Engineering of Fusarium oxysporum to Improve Its Ethanol-Producing Capability
title_full Metabolic Engineering of Fusarium oxysporum to Improve Its Ethanol-Producing Capability
title_fullStr Metabolic Engineering of Fusarium oxysporum to Improve Its Ethanol-Producing Capability
title_full_unstemmed Metabolic Engineering of Fusarium oxysporum to Improve Its Ethanol-Producing Capability
title_short Metabolic Engineering of Fusarium oxysporum to Improve Its Ethanol-Producing Capability
title_sort metabolic engineering of fusarium oxysporum to improve its ethanol-producing capability
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854878/
https://www.ncbi.nlm.nih.gov/pubmed/27199958
http://dx.doi.org/10.3389/fmicb.2016.00632
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