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Oxidative stress response and proteomic analysis reveal the mechanisms of toxicity of imidazolium-based ionic liquids against Arabidopsis thaliana.

Identifieur interne : 000078 ( Main/Exploration ); précédent : 000077; suivant : 000079

Oxidative stress response and proteomic analysis reveal the mechanisms of toxicity of imidazolium-based ionic liquids against Arabidopsis thaliana.

Auteurs : Mingkang Jin [République populaire de Chine] ; Huan Wang [République populaire de Chine] ; Huijun Liu [République populaire de Chine] ; Yilu Xia [République populaire de Chine] ; Songlin Ruan [République populaire de Chine] ; Yuqing Huang [République populaire de Chine] ; Jieren Qiu [République populaire de Chine] ; Shaoting Du [République populaire de Chine] ; Linglin Xu [République populaire de Chine]

Source :

RBID : pubmed:32000025

Descripteurs français

English descriptors

Abstract

Ionic liquids (ILs) are extensively used in various fields, posing a potential threat in the ecosystem because of their high stability, excellent solubility, and biological toxicity. In this study, the toxicity mechanism of three ILs, 1-octyl-3-methylimidazolium chloride ([C8MIM]Cl), 1-decyl-3-methylimidazolium chloride ([C10MIM]Cl), and 1-dodecyl-3-methylimidazolium chloride ([C12MIM]Cl) on Arabidopsis thaliana were revealed. Reactive oxygen species (ROS) level increased with higher concentration and longer carbon chain length of ILs, which led to the increase of malondialdehyde (MDA) content and antioxidase activity, including superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX) and peroxidase (POD) activities. SOD, CAT, and GPX activities decreased in high ILs concentration due to the excessive ROS. Differentially expressed protein was analyzed based on Gene ontology (GO) and KEGG pathways analysis. 70, 45, 84 up-regulated proteins, and 72, 104, 79 down-regulated proteins were identified in [C8MIM]Cl, [C10MIM]Cl, and [C12MIM]Cl treatment, respectively (fold change ≥ 1.5 with ≥95% confidence). Cellular aldehyde metabolic process, mitochondrial and mitochondrial respiratory chains, glutathione transferase and oxidoreductase activity were enriched as up-regulated proteins as the defense mechanism of A. thaliana to resist external stresses. Chloroplast, photosynthetic membrane and thylakoid, structural constituent of ribosome, and transmembrane transport were enriched as the down-regulated protein. Compared with the control, 8 and 14 KEGG pathways were identified forup-regulated and down-regulated proteins, respectively, in three IL treatments. Metabolic pathways, carbon metabolism, biosynthesis of amino acids, porphyrin and chlorophyll metabolism were significantly down-regulated. The GO terms annotation demonstrated the oxidative stress response and effects on photosynthesis of A. thaliana in ILs treatment from biological process, cellular component, and molecular function categories.

DOI: 10.1016/j.envpol.2020.114013
PubMed: 32000025


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<div type="abstract" xml:lang="en">Ionic liquids (ILs) are extensively used in various fields, posing a potential threat in the ecosystem because of their high stability, excellent solubility, and biological toxicity. In this study, the toxicity mechanism of three ILs, 1-octyl-3-methylimidazolium chloride ([C
<sub>8</sub>
MIM]Cl), 1-decyl-3-methylimidazolium chloride ([C
<sub>10</sub>
MIM]Cl), and 1-dodecyl-3-methylimidazolium chloride ([C
<sub>12</sub>
MIM]Cl) on Arabidopsis thaliana were revealed. Reactive oxygen species (ROS) level increased with higher concentration and longer carbon chain length of ILs, which led to the increase of malondialdehyde (MDA) content and antioxidase activity, including superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX) and peroxidase (POD) activities. SOD, CAT, and GPX activities decreased in high ILs concentration due to the excessive ROS. Differentially expressed protein was analyzed based on Gene ontology (GO) and KEGG pathways analysis. 70, 45, 84 up-regulated proteins, and 72, 104, 79 down-regulated proteins were identified in [C
<sub>8</sub>
MIM]Cl, [C
<sub>10</sub>
MIM]Cl, and [C
<sub>12</sub>
MIM]Cl treatment, respectively (fold change ≥ 1.5 with ≥95% confidence). Cellular aldehyde metabolic process, mitochondrial and mitochondrial respiratory chains, glutathione transferase and oxidoreductase activity were enriched as up-regulated proteins as the defense mechanism of A. thaliana to resist external stresses. Chloroplast, photosynthetic membrane and thylakoid, structural constituent of ribosome, and transmembrane transport were enriched as the down-regulated protein. Compared with the control, 8 and 14 KEGG pathways were identified forup-regulated and down-regulated proteins, respectively, in three IL treatments. Metabolic pathways, carbon metabolism, biosynthesis of amino acids, porphyrin and chlorophyll metabolism were significantly down-regulated. The GO terms annotation demonstrated the oxidative stress response and effects on photosynthesis of A. thaliana in ILs treatment from biological process, cellular component, and molecular function categories.</div>
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<AbstractText>Ionic liquids (ILs) are extensively used in various fields, posing a potential threat in the ecosystem because of their high stability, excellent solubility, and biological toxicity. In this study, the toxicity mechanism of three ILs, 1-octyl-3-methylimidazolium chloride ([C
<sub>8</sub>
MIM]Cl), 1-decyl-3-methylimidazolium chloride ([C
<sub>10</sub>
MIM]Cl), and 1-dodecyl-3-methylimidazolium chloride ([C
<sub>12</sub>
MIM]Cl) on Arabidopsis thaliana were revealed. Reactive oxygen species (ROS) level increased with higher concentration and longer carbon chain length of ILs, which led to the increase of malondialdehyde (MDA) content and antioxidase activity, including superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX) and peroxidase (POD) activities. SOD, CAT, and GPX activities decreased in high ILs concentration due to the excessive ROS. Differentially expressed protein was analyzed based on Gene ontology (GO) and KEGG pathways analysis. 70, 45, 84 up-regulated proteins, and 72, 104, 79 down-regulated proteins were identified in [C
<sub>8</sub>
MIM]Cl, [C
<sub>10</sub>
MIM]Cl, and [C
<sub>12</sub>
MIM]Cl treatment, respectively (fold change ≥ 1.5 with ≥95% confidence). Cellular aldehyde metabolic process, mitochondrial and mitochondrial respiratory chains, glutathione transferase and oxidoreductase activity were enriched as up-regulated proteins as the defense mechanism of A. thaliana to resist external stresses. Chloroplast, photosynthetic membrane and thylakoid, structural constituent of ribosome, and transmembrane transport were enriched as the down-regulated protein. Compared with the control, 8 and 14 KEGG pathways were identified forup-regulated and down-regulated proteins, respectively, in three IL treatments. Metabolic pathways, carbon metabolism, biosynthesis of amino acids, porphyrin and chlorophyll metabolism were significantly down-regulated. The GO terms annotation demonstrated the oxidative stress response and effects on photosynthesis of A. thaliana in ILs treatment from biological process, cellular component, and molecular function categories.</AbstractText>
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<LastName>Xu</LastName>
<ForeName>Linglin</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou, 310018, Zhejiang Province, China.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2020</Year>
<Month>01</Month>
<Day>21</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>England</Country>
<MedlineTA>Environ Pollut</MedlineTA>
<NlmUniqueID>8804476</NlmUniqueID>
<ISSNLinking>0269-7491</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D052578">Ionic Liquids</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D017360" MajorTopicYN="Y">Arabidopsis</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D017753" MajorTopicYN="N">Ecosystem</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D052578" MajorTopicYN="N">Ionic Liquids</DescriptorName>
<QualifierName UI="Q000633" MajorTopicYN="Y">toxicity</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018384" MajorTopicYN="N">Oxidative Stress</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D040901" MajorTopicYN="N">Proteomics</DescriptorName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Arabidopsis thaliana</Keyword>
<Keyword MajorTopicYN="N">Gene ontology</Keyword>
<Keyword MajorTopicYN="N">Ionic liquid</Keyword>
<Keyword MajorTopicYN="N">KEGG pathways</Keyword>
<Keyword MajorTopicYN="N">Oxidative stress response</Keyword>
</KeywordList>
<CoiStatement>Declaration of competing interest We declare that we do not have any conflicts of interest in connection with the work submitted.</CoiStatement>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="received">
<Year>2019</Year>
<Month>11</Month>
<Day>16</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised">
<Year>2019</Year>
<Month>12</Month>
<Day>29</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted">
<Year>2020</Year>
<Month>01</Month>
<Day>16</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed">
<Year>2020</Year>
<Month>1</Month>
<Day>31</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2020</Year>
<Month>6</Month>
<Day>13</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2020</Year>
<Month>1</Month>
<Day>31</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">32000025</ArticleId>
<ArticleId IdType="pii">S0269-7491(19)36805-8</ArticleId>
<ArticleId IdType="doi">10.1016/j.envpol.2020.114013</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations>
<list>
<country>
<li>République populaire de Chine</li>
</country>
</list>
<tree>
<country name="République populaire de Chine">
<noRegion>
<name sortKey="Jin, Mingkang" sort="Jin, Mingkang" uniqKey="Jin M" first="Mingkang" last="Jin">Mingkang Jin</name>
</noRegion>
<name sortKey="Du, Shaoting" sort="Du, Shaoting" uniqKey="Du S" first="Shaoting" last="Du">Shaoting Du</name>
<name sortKey="Huang, Yuqing" sort="Huang, Yuqing" uniqKey="Huang Y" first="Yuqing" last="Huang">Yuqing Huang</name>
<name sortKey="Liu, Huijun" sort="Liu, Huijun" uniqKey="Liu H" first="Huijun" last="Liu">Huijun Liu</name>
<name sortKey="Qiu, Jieren" sort="Qiu, Jieren" uniqKey="Qiu J" first="Jieren" last="Qiu">Jieren Qiu</name>
<name sortKey="Ruan, Songlin" sort="Ruan, Songlin" uniqKey="Ruan S" first="Songlin" last="Ruan">Songlin Ruan</name>
<name sortKey="Wang, Huan" sort="Wang, Huan" uniqKey="Wang H" first="Huan" last="Wang">Huan Wang</name>
<name sortKey="Xia, Yilu" sort="Xia, Yilu" uniqKey="Xia Y" first="Yilu" last="Xia">Yilu Xia</name>
<name sortKey="Xu, Linglin" sort="Xu, Linglin" uniqKey="Xu L" first="Linglin" last="Xu">Linglin Xu</name>
</country>
</tree>
</affiliations>
</record>

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