Evidence map›Paper›PMID 26994074›Full record

ArticleApplied and environmental microbiology2016

Vacuolar H+-ATPase Protects Saccharomyces cerevisiae Cells against Ethanol-Induced Oxidative and Cell Wall Stresses.

Sirikarn Charoenbhakdi, Thanittra Dokpikul, Thanawat Burphan, Todsapol Techo, Choowong Auesukaree

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Applied and environmental microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 72 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Sirikarn CharoenbhakdiDepartment of Biology, Faculty of Science, Mahidol University, and Center of Excellence on Environmental Health and Toxicology, CHE, Ministry of Education, Bangkok, Thailand.
Thanittra DokpikulDepartment of Biology, Faculty of Science, Mahidol University, and Center of Excellence on Environmental Health and Toxicology, CHE, Ministry of Education, Bangkok, Thailand.
Thanawat BurphanDepartment of Biology, Faculty of Science, Mahidol University, and Center of Excellence on Environmental Health and Toxicology, CHE, Ministry of Education, Bangkok, Thailand.
Todsapol TechoDepartment of Biology, Faculty of Science, Mahidol University, and Center of Excellence on Environmental Health and Toxicology, CHE, Ministry of Education, Bangkok, Thailand.
Choowong AuesukareeDepartment of Biology, Faculty of Science, Mahidol University, and Center of Excellence on Environmental Health and Toxicology, CHE, Ministry of Education, Bangkok, Thailand choowong.aue@mahidol.ac.th.
Mahidol University · THMinistry of Education · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledDuring fermentation, increased ethanol concentration is a major stress for yeast cells. Vacuolar H(+)-ATPase (V-ATPase), which plays an important role in the maintenance of intracellular pH homeostasis through vacuolar acidification, has been shown to be required for tolerance to straight-chain alcohols, including ethanol. Since ethanol is known to increase membrane permeability to protons, which then promotes intracellular acidification, it is possible that the V-ATPase is required for recovery from alcohol-induced intracellular acidification. In this study, we show that the effects of straight-chain alcohols on membrane permeabilization and acidification of the cytosol and vacuole are strongly dependent on their lipophilicity. These findings suggest that the membrane-permeabilizing effect of straight-chain alcohols induces cytosolic and vacuolar acidification in a lipophilicity-dependent manner. Surprisingly, after ethanol challenge, the cytosolic pH in Δvma2 and Δvma3 mutants lacking V-ATPase activity was similar to that of the wild-type strain. It is therefore unlikely that the ethanol-sensitive phenotype of vma mutants resulted from severe cytosolic acidification. Interestingly, the vma mutants exposed to ethanol exhibited a delay in cell wall remodeling and a significant increase in intracellular reactive oxygen species (ROS). These findings suggest a role for V-ATPase in the regulation of the cell wall stress response and the prevention of endogenous oxidative stress in response to ethanol. IMPORTANCE: The yeast Saccharomyces cerevisiae has been widely used in the alcoholic fermentation industry. Among the environmental stresses that yeast cells encounter during the process of alcoholic fermentation, ethanol is a major stress factor that inhibits yeast growth and viability, eventually leading to fermentation arrest. This study provides evidence for the molecular mechanisms of ethanol tolerance, which is a desirable characteristic for yeast strains used in alcoholic fermentation. The results revealed that straight-chain alcohols induced cytosolic and vacuolar acidification through their membrane-permeabilizing effects. Contrary to expectations, a role for V-ATPase in the regulation of the cell wall stress response and the prevention of endogenous oxidative stress, but not in the maintenance of intracellular pH, seems to be important for protecting yeast cells against ethanol stress. These findings will expand our understanding of the mechanisms of ethanol tolerance and provide promising clues for the development of ethanol-tolerant yeast strains.

Indexed as

Oxidative StressAnti-Infective Agents, LocalCell MembraneCell WallCytosolEthanolGene DeletionHydrogen-Ion ConcentrationPermeabilitySaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsStress, PhysiologicalVacuolar Proton-Translocating ATPasesAnti-Infective Agents, LocalEthanolSaccharomyces cerevisiae ProteinsVacuolar Proton-Translocating ATPasesVMA2 protein, S cerevisiaeVMA3 protein, S cerevisiae

Identifiers

PMID26994074
PMCPMC4959079
OpenAlexW2300882872

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.