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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-8313246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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
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title_full | Metabolic regulation adapting to high methanol environment in the methylotrophic yeast Ogataea methanolica
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title_fullStr | Metabolic regulation adapting to high methanol environment in the methylotrophic yeast Ogataea methanolica
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title_full_unstemmed | Metabolic regulation adapting to high methanol environment in the methylotrophic yeast Ogataea methanolica
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title_short | Metabolic regulation adapting to high methanol environment in the methylotrophic yeast Ogataea methanolica
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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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