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Aeration mitigates endoplasmic reticulum stress in Saccharomyces cerevisiae even without mitochondrial respiration

Saccharomyces cerevisiae is a facultative anaerobic organism that grows well under both aerobic and hypoxic conditions in media containing abundant fermentable nutrients such as glucose. In order to deeply understand the physiological dependence of S. cerevisiae on aeration, we checked endoplasmic r...

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Autores principales: Phuong, Huong Thi, Ishiwata-Kimata, Yuki, Nishi, Yuki, Oguchi, Norie, Takagi, Hiroshi, Kimata, Yukio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shared Science Publishers OG 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010904/
https://www.ncbi.nlm.nih.gov/pubmed/33816593
http://dx.doi.org/10.15698/mic2021.04.746
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author Phuong, Huong Thi
Ishiwata-Kimata, Yuki
Nishi, Yuki
Oguchi, Norie
Takagi, Hiroshi
Kimata, Yukio
author_facet Phuong, Huong Thi
Ishiwata-Kimata, Yuki
Nishi, Yuki
Oguchi, Norie
Takagi, Hiroshi
Kimata, Yukio
author_sort Phuong, Huong Thi
collection PubMed
description Saccharomyces cerevisiae is a facultative anaerobic organism that grows well under both aerobic and hypoxic conditions in media containing abundant fermentable nutrients such as glucose. In order to deeply understand the physiological dependence of S. cerevisiae on aeration, we checked endoplasmic reticulum (ER)-stress status by monitoring the splicing of HAC1 mRNA, which is promoted by the ER stress-sensor protein, Ire1. HAC1-mRNA splicing that was caused by conventional ER-stressing agents, including low concentrations of dithiothreitol (DTT), was more potent in hypoxic cultures than in aerated cultures. Moreover, growth retardation was observed by adding low-dose DTT into hypoxic cultures of ire1Δ cells. Unexpectedly, aeration mitigated ER stress and DTT-induced impairment of ER oxidative protein folding even when mitochondrial respiration was halted by the ρ(o) mutation. An ER-located protein Ero1 is known to directly consume molecular oxygen to initiate the ER protein oxidation cascade, which promotes oxidative protein folding of ER client proteins. Our further study using ero1-mutant strains suggested that, in addition to mitochondrial respiration, this Ero1-medaited reaction contributes to mitigation of ER stress by molecular oxygen. Taken together, here we demonstrate a scenario in which aeration acts beneficially on S. cerevisiae cells even under fermentative conditions.
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spelling pubmed-80109042021-04-02 Aeration mitigates endoplasmic reticulum stress in Saccharomyces cerevisiae even without mitochondrial respiration Phuong, Huong Thi Ishiwata-Kimata, Yuki Nishi, Yuki Oguchi, Norie Takagi, Hiroshi Kimata, Yukio Microb Cell Research Article Saccharomyces cerevisiae is a facultative anaerobic organism that grows well under both aerobic and hypoxic conditions in media containing abundant fermentable nutrients such as glucose. In order to deeply understand the physiological dependence of S. cerevisiae on aeration, we checked endoplasmic reticulum (ER)-stress status by monitoring the splicing of HAC1 mRNA, which is promoted by the ER stress-sensor protein, Ire1. HAC1-mRNA splicing that was caused by conventional ER-stressing agents, including low concentrations of dithiothreitol (DTT), was more potent in hypoxic cultures than in aerated cultures. Moreover, growth retardation was observed by adding low-dose DTT into hypoxic cultures of ire1Δ cells. Unexpectedly, aeration mitigated ER stress and DTT-induced impairment of ER oxidative protein folding even when mitochondrial respiration was halted by the ρ(o) mutation. An ER-located protein Ero1 is known to directly consume molecular oxygen to initiate the ER protein oxidation cascade, which promotes oxidative protein folding of ER client proteins. Our further study using ero1-mutant strains suggested that, in addition to mitochondrial respiration, this Ero1-medaited reaction contributes to mitigation of ER stress by molecular oxygen. Taken together, here we demonstrate a scenario in which aeration acts beneficially on S. cerevisiae cells even under fermentative conditions. Shared Science Publishers OG 2021-03-31 /pmc/articles/PMC8010904/ /pubmed/33816593 http://dx.doi.org/10.15698/mic2021.04.746 Text en Copyright: © 2021 Phuong et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged.
spellingShingle Research Article
Phuong, Huong Thi
Ishiwata-Kimata, Yuki
Nishi, Yuki
Oguchi, Norie
Takagi, Hiroshi
Kimata, Yukio
Aeration mitigates endoplasmic reticulum stress in Saccharomyces cerevisiae even without mitochondrial respiration
title Aeration mitigates endoplasmic reticulum stress in Saccharomyces cerevisiae even without mitochondrial respiration
title_full Aeration mitigates endoplasmic reticulum stress in Saccharomyces cerevisiae even without mitochondrial respiration
title_fullStr Aeration mitigates endoplasmic reticulum stress in Saccharomyces cerevisiae even without mitochondrial respiration
title_full_unstemmed Aeration mitigates endoplasmic reticulum stress in Saccharomyces cerevisiae even without mitochondrial respiration
title_short Aeration mitigates endoplasmic reticulum stress in Saccharomyces cerevisiae even without mitochondrial respiration
title_sort aeration mitigates endoplasmic reticulum stress in saccharomyces cerevisiae even without mitochondrial respiration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010904/
https://www.ncbi.nlm.nih.gov/pubmed/33816593
http://dx.doi.org/10.15698/mic2021.04.746
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