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Metabolic regulation adapting to high methanol environment in the methylotrophic yeast Ogataea methanolica

Since methylotrophic yeasts such as Ogataea methanolica can use methanol as a sole carbon feedstock, they could be applied to produce valuable products from methanol, a next‐generation energy source synthesized from natural gases, using genetic engineering tools. In this study, metabolite profiling...

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Autores principales: Cai, Hao‐Liang, Doi, Ryohei, Shimada, Masaya, Hayakawa, Takashi, Nakagawa, Tomoyuki
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/PMC8313246/
https://www.ncbi.nlm.nih.gov/pubmed/33939325
http://dx.doi.org/10.1111/1751-7915.13811
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author Cai, Hao‐Liang
Doi, Ryohei
Shimada, Masaya
Hayakawa, Takashi
Nakagawa, Tomoyuki
author_facet Cai, Hao‐Liang
Doi, Ryohei
Shimada, Masaya
Hayakawa, Takashi
Nakagawa, Tomoyuki
author_sort Cai, Hao‐Liang
collection PubMed
description Since methylotrophic yeasts such as Ogataea methanolica can use methanol as a sole carbon feedstock, they could be applied to produce valuable products from methanol, a next‐generation energy source synthesized from natural gases, using genetic engineering tools. In this study, metabolite profiling of O. methanolica was conducted under glucose (Glc) and low and high methanol (L‐ and H‐MeOH) conditions to show the adaptation mechanism to a H‐MeOH environment. The yeast strain responded not only to the presence of methanol but also to its concentration based on the growth condition. Under H‐MeOH conditions, O. methanolica downregulated the methanol utilization, glycolytic pathway and alcohol oxidase (AOD) isozymes and dihydroxyacetone synthase (DAS) expression compared with L‐MeOH‐grown cells. However, levels of energy carriers, such as ATP, were maintained to support cell survival. In H‐MeOH‐grown cells, reactive oxygen species (ROS) levels were significantly elevated. Along with increasing ROS levels, ROS scavenging system expression was significantly increased in H‐MeOH‐grown cells. Thus, we concluded that formaldehyde and H(2)O(2), which are products of methanol oxidation by AOD isozymes in the peroxisome, are overproduced in H‐MeOH‐grown cells, and excessive ROS derived from these cells is generated in the cytosol, resulting in upregulation of the antioxidant system and downregulation of the methanol‐utilizing pathway to suppress overproduction of toxic intermediates.
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spelling pubmed-83132462021-07-30 Metabolic regulation adapting to high methanol environment in the methylotrophic yeast Ogataea methanolica Cai, Hao‐Liang Doi, Ryohei Shimada, Masaya Hayakawa, Takashi Nakagawa, Tomoyuki Microb Biotechnol Research Articles Since methylotrophic yeasts such as Ogataea methanolica can use methanol as a sole carbon feedstock, they could be applied to produce valuable products from methanol, a next‐generation energy source synthesized from natural gases, using genetic engineering tools. In this study, metabolite profiling of O. methanolica was conducted under glucose (Glc) and low and high methanol (L‐ and H‐MeOH) conditions to show the adaptation mechanism to a H‐MeOH environment. The yeast strain responded not only to the presence of methanol but also to its concentration based on the growth condition. Under H‐MeOH conditions, O. methanolica downregulated the methanol utilization, glycolytic pathway and alcohol oxidase (AOD) isozymes and dihydroxyacetone synthase (DAS) expression compared with L‐MeOH‐grown cells. However, levels of energy carriers, such as ATP, were maintained to support cell survival. In H‐MeOH‐grown cells, reactive oxygen species (ROS) levels were significantly elevated. Along with increasing ROS levels, ROS scavenging system expression was significantly increased in H‐MeOH‐grown cells. Thus, we concluded that formaldehyde and H(2)O(2), which are products of methanol oxidation by AOD isozymes in the peroxisome, are overproduced in H‐MeOH‐grown cells, and excessive ROS derived from these cells is generated in the cytosol, resulting in upregulation of the antioxidant system and downregulation of the methanol‐utilizing pathway to suppress overproduction of toxic intermediates. John Wiley and Sons Inc. 2021-05-03 /pmc/articles/PMC8313246/ /pubmed/33939325 http://dx.doi.org/10.1111/1751-7915.13811 Text en © 2021 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Cai, Hao‐Liang
Doi, Ryohei
Shimada, Masaya
Hayakawa, Takashi
Nakagawa, Tomoyuki
Metabolic regulation adapting to high methanol environment in the methylotrophic yeast Ogataea methanolica
title Metabolic regulation adapting to high methanol environment in the methylotrophic yeast Ogataea methanolica
title_full Metabolic regulation adapting to high methanol environment in the methylotrophic yeast Ogataea methanolica
title_fullStr Metabolic regulation adapting to high methanol environment in the methylotrophic yeast Ogataea methanolica
title_full_unstemmed Metabolic regulation adapting to high methanol environment in the methylotrophic yeast Ogataea methanolica
title_short Metabolic regulation adapting to high methanol environment in the methylotrophic yeast Ogataea methanolica
title_sort metabolic regulation adapting to high methanol environment in the methylotrophic yeast ogataea methanolica
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313246/
https://www.ncbi.nlm.nih.gov/pubmed/33939325
http://dx.doi.org/10.1111/1751-7915.13811
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