<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>38(3)</volume><submitter>Sako K</submitter><pubmed_abstract>Abiotic stresses, such as high light and salinity, are major factors that limit crop productivity and sustainability worldwide. Chemical priming is a promising strategy for improving the abiotic stress tolerance of plants. Recently, we discovered that ethanol enhances high-salinity stress tolerance in &lt;i>Arabidopsis thaliana&lt;/i> and rice by detoxifying reactive oxygen species (ROS). However, the effect of ethanol on other abiotic stress responses is unclear. Therefore, we investigated the effect of ethanol on the high-light stress response. Measurement of chlorophyll fluorescence showed that ethanol mitigates photoinhibition under high-light stress. Staining with 3,3'-diaminobenzidine (DAB) showed that the accumulation of hydrogen peroxide (H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>) was inhibited by ethanol under high-light stress conditions in &lt;i>A. thaliana&lt;/i>. We found that ethanol increased the gene expressions and enzymatic activities of antioxidative enzymes, including &lt;i>ASCORBATE PEROXIDASE1&lt;/i> (&lt;i>AtAPX1&lt;/i>), &lt;i&gt;Catalase (AtCAT1 and AtCAT2)&lt;/i>. Moreover, the expression of flavonoid biosynthetic genes and anthocyanin contents were upregulated by ethanol treatment during exposure to high-light stress. These results imply that ethanol alleviates oxidative damage from high-light stress in &lt;i>A. thaliana&lt;/i> by suppressing ROS accumulation. Our findings support the hypothesis that ethanol improves tolerance to multiple stresses in field-grown crops.</pubmed_abstract><journal>Plant biotechnology (Tokyo, Japan)</journal><pagination>339-344</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8562572</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Exogenous ethanol treatment alleviates oxidative damage of &lt;i>Arabidopsis thaliana&lt;/i> under conditions of high-light stress.</pubmed_title><pmcid>PMC8562572</pmcid><pubmed_authors>Nagashima R</pubmed_authors><pubmed_authors>Tamoi M</pubmed_authors><pubmed_authors>Sako K</pubmed_authors><pubmed_authors>Seki M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exogenous ethanol treatment alleviates oxidative damage of &lt;i>Arabidopsis thaliana&lt;/i> under conditions of high-light stress.</name><description>Abiotic stresses, such as high light and salinity, are major factors that limit crop productivity and sustainability worldwide. Chemical priming is a promising strategy for improving the abiotic stress tolerance of plants. Recently, we discovered that ethanol enhances high-salinity stress tolerance in &lt;i>Arabidopsis thaliana&lt;/i> and rice by detoxifying reactive oxygen species (ROS). However, the effect of ethanol on other abiotic stress responses is unclear. Therefore, we investigated the effect of ethanol on the high-light stress response. Measurement of chlorophyll fluorescence showed that ethanol mitigates photoinhibition under high-light stress. Staining with 3,3'-diaminobenzidine (DAB) showed that the accumulation of hydrogen peroxide (H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>) was inhibited by ethanol under high-light stress conditions in &lt;i>A. thaliana&lt;/i>. We found that ethanol increased the gene expressions and enzymatic activities of antioxidative enzymes, including &lt;i>ASCORBATE PEROXIDASE1&lt;/i> (&lt;i>AtAPX1&lt;/i>), &lt;i&gt;Catalase (AtCAT1 and AtCAT2)&lt;/i>. Moreover, the expression of flavonoid biosynthetic genes and anthocyanin contents were upregulated by ethanol treatment during exposure to high-light stress. These results imply that ethanol alleviates oxidative damage from high-light stress in &lt;i>A. thaliana&lt;/i> by suppressing ROS accumulation. Our findings support the hypothesis that ethanol improves tolerance to multiple stresses in field-grown crops.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2024-02-15T15:02:25.489Z</modification><creation>2022-02-11T12:51:55.639Z</creation></dates><accession>S-EPMC8562572</accession><cross_references><pubmed>34782821</pubmed><doi>10.5511/plantbiotechnology.21.0715a</doi></cross_references></HashMap>