Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1783666743741251584 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7972947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT zavecdomen beyondalcoholoxidasethemethylotrophicyeastkomagataellaphaffiiutilizesmethanolalsowithitsnativealcoholdehydrogenaseadh2 AT troyerchristina beyondalcoholoxidasethemethylotrophicyeastkomagataellaphaffiiutilizesmethanolalsowithitsnativealcoholdehydrogenaseadh2 AT mareschdaniel beyondalcoholoxidasethemethylotrophicyeastkomagataellaphaffiiutilizesmethanolalsowithitsnativealcoholdehydrogenaseadh2 AT altmannfriedrich beyondalcoholoxidasethemethylotrophicyeastkomagataellaphaffiiutilizesmethanolalsowithitsnativealcoholdehydrogenaseadh2 AT hannstephan beyondalcoholoxidasethemethylotrophicyeastkomagataellaphaffiiutilizesmethanolalsowithitsnativealcoholdehydrogenaseadh2 AT gasserbrigitte beyondalcoholoxidasethemethylotrophicyeastkomagataellaphaffiiutilizesmethanolalsowithitsnativealcoholdehydrogenaseadh2 AT mattanovichdiethard beyondalcoholoxidasethemethylotrophicyeastkomagataellaphaffiiutilizesmethanolalsowithitsnativealcoholdehydrogenaseadh2 |