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Beyond alcohol oxidase: the methylotrophic yeast Komagataella phaffii utilizes methanol also with its native alcohol dehydrogenase Adh2

Methylotrophic yeasts are considered to use alcohol oxidases to assimilate methanol, different to bacteria which employ alcohol dehydrogenases with better energy conservation. The yeast Komagataella phaffii carries two genes coding for alcohol oxidase, AOX1 and AOX2. The deletion of the AOX1 leads t...

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Autores principales: Zavec, Domen, Troyer, Christina, Maresch, Daniel, Altmann, Friedrich, Hann, Stephan, Gasser, Brigitte, Mattanovich, Diethard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7972947/
https://www.ncbi.nlm.nih.gov/pubmed/33599728
http://dx.doi.org/10.1093/femsyr/foab009
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author Zavec, Domen
Troyer, Christina
Maresch, Daniel
Altmann, Friedrich
Hann, Stephan
Gasser, Brigitte
Mattanovich, Diethard
author_facet Zavec, Domen
Troyer, Christina
Maresch, Daniel
Altmann, Friedrich
Hann, Stephan
Gasser, Brigitte
Mattanovich, Diethard
author_sort Zavec, Domen
collection PubMed
description Methylotrophic yeasts are considered to use alcohol oxidases to assimilate methanol, different to bacteria which employ alcohol dehydrogenases with better energy conservation. The yeast Komagataella phaffii carries two genes coding for alcohol oxidase, AOX1 and AOX2. The deletion of the AOX1 leads to the Mut(S) phenotype and the deletion of AOX1 and AOX2 to the Mut(–) phenotype. The Mut(–) phenotype is commonly regarded as unable to utilize methanol. In contrast to the literature, we found that the Mut(–) strain can consume methanol. This ability was based on the promiscuous activity of alcohol dehydrogenase Adh2, an enzyme ubiquitously found in yeast and normally responsible for ethanol consumption and production. Using (13)C labeled methanol as substrate we could show that to the largest part methanol is dissimilated to CO(2) and a small part is incorporated into metabolites, the biomass, and the secreted recombinant protein. Overexpression of the ADH2 gene in K. phaffii Mut(–) increased both the specific methanol uptake rate and recombinant protein production, even though the strain was still unable to grow. These findings imply that thermodynamic and kinetic constraints of the dehydrogenase reaction facilitated the evolution towards alcohol oxidase-based methanol metabolism in yeast.
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spelling pubmed-79729472021-03-23 Beyond alcohol oxidase: the methylotrophic yeast Komagataella phaffii utilizes methanol also with its native alcohol dehydrogenase Adh2 Zavec, Domen Troyer, Christina Maresch, Daniel Altmann, Friedrich Hann, Stephan Gasser, Brigitte Mattanovich, Diethard FEMS Yeast Res Research Article Methylotrophic yeasts are considered to use alcohol oxidases to assimilate methanol, different to bacteria which employ alcohol dehydrogenases with better energy conservation. The yeast Komagataella phaffii carries two genes coding for alcohol oxidase, AOX1 and AOX2. The deletion of the AOX1 leads to the Mut(S) phenotype and the deletion of AOX1 and AOX2 to the Mut(–) phenotype. The Mut(–) phenotype is commonly regarded as unable to utilize methanol. In contrast to the literature, we found that the Mut(–) strain can consume methanol. This ability was based on the promiscuous activity of alcohol dehydrogenase Adh2, an enzyme ubiquitously found in yeast and normally responsible for ethanol consumption and production. Using (13)C labeled methanol as substrate we could show that to the largest part methanol is dissimilated to CO(2) and a small part is incorporated into metabolites, the biomass, and the secreted recombinant protein. Overexpression of the ADH2 gene in K. phaffii Mut(–) increased both the specific methanol uptake rate and recombinant protein production, even though the strain was still unable to grow. These findings imply that thermodynamic and kinetic constraints of the dehydrogenase reaction facilitated the evolution towards alcohol oxidase-based methanol metabolism in yeast. Oxford University Press 2021-02-18 /pmc/articles/PMC7972947/ /pubmed/33599728 http://dx.doi.org/10.1093/femsyr/foab009 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of FEMS. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zavec, Domen
Troyer, Christina
Maresch, Daniel
Altmann, Friedrich
Hann, Stephan
Gasser, Brigitte
Mattanovich, Diethard
Beyond alcohol oxidase: the methylotrophic yeast Komagataella phaffii utilizes methanol also with its native alcohol dehydrogenase Adh2
title Beyond alcohol oxidase: the methylotrophic yeast Komagataella phaffii utilizes methanol also with its native alcohol dehydrogenase Adh2
title_full Beyond alcohol oxidase: the methylotrophic yeast Komagataella phaffii utilizes methanol also with its native alcohol dehydrogenase Adh2
title_fullStr Beyond alcohol oxidase: the methylotrophic yeast Komagataella phaffii utilizes methanol also with its native alcohol dehydrogenase Adh2
title_full_unstemmed Beyond alcohol oxidase: the methylotrophic yeast Komagataella phaffii utilizes methanol also with its native alcohol dehydrogenase Adh2
title_short Beyond alcohol oxidase: the methylotrophic yeast Komagataella phaffii utilizes methanol also with its native alcohol dehydrogenase Adh2
title_sort beyond alcohol oxidase: the methylotrophic yeast komagataella phaffii utilizes methanol also with its native alcohol dehydrogenase adh2
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7972947/
https://www.ncbi.nlm.nih.gov/pubmed/33599728
http://dx.doi.org/10.1093/femsyr/foab009
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