Serveur d'exploration sur la détoxication des champignons

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YKL071W from Saccharomyces cerevisiae encodes a novel aldehyde reductase for detoxification of glycolaldehyde and furfural derived from lignocellulose.

Identifieur interne : 000A36 ( Main/Exploration ); précédent : 000A35; suivant : 000A37

YKL071W from Saccharomyces cerevisiae encodes a novel aldehyde reductase for detoxification of glycolaldehyde and furfural derived from lignocellulose.

Auteurs : Hanyu Wang [République populaire de Chine] ; Yidan Ouyang [République populaire de Chine] ; Chang Zhou [République populaire de Chine] ; Difan Xiao [République populaire de Chine] ; Yaping Guo [République populaire de Chine] ; Lan Wu [République populaire de Chine] ; Xi Li [République populaire de Chine] ; Yunfu Gu [République populaire de Chine] ; Quanju Xiang [République populaire de Chine] ; Ke Zhao [République populaire de Chine] ; Xiumei Yu [République populaire de Chine] ; Likou Zou [République populaire de Chine] ; Menggen Ma [République populaire de Chine]

Source :

RBID : pubmed:29034432

Descripteurs français

English descriptors

Abstract

Aldehydes generated as by-products during the pretreatment of lignocellulose are the key inhibitors to Saccharomyces cerevisiae, which is considered as the most promising microorganism for industrial production of biofuel, xylitol as well as other special chemicals from lignocellulose. S. cerevisiae has the inherent ability to in situ detoxify aldehydes to corresponding alcohols by multiple aldehyde reductases. Herein, we report that an uncharacterized open reading frame YKL071W from S. cerevisiae encodes a novel "classical" short-chain dehydrogenase/reductase (SDR) protein with NADH-dependent enzymatic activities for reduction of furfural (FF), glycolaldehyde (GA), formaldehyde (FA), and benzaldehyde (BZA). This enzyme showed much better specific activities for reduction of GA and FF than FA and BZA, and displayed much higher Km and Kcat/Km but lower Vmax and Kcat for reduction of GA than FF. For this enzyme, the optimum pH was 5.5 and 6.0 for reduction of GA and FF, and the optimum temperature was 30 °C for reduction of GA and FF. Both pH and temperature affected stability of this enzyme in a similar trend for reduction of GA and FF. Cu2+, Zn2+, Ni2+, and Fe3+ had severe inhibition effects on enzyme activities of Ykl071wp for reduction of GA and FF. Transcription of YKL071W in S. cerevisiae was significantly upregulated under GA and FF stress conditions, and its transcription is most probably regulated by transcription factor genes of YAP1, CAD1, PDR3, and STB5. This research provides guidelines to identify more uncharacterized genes with reductase activities for detoxification of aldehydes derived from lignocellulose in S. cerevisiae.

DOI: 10.1007/s00253-017-8567-z
PubMed: 29034432


Affiliations:


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Le document en format XML

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<name sortKey="Wu, Lan" sort="Wu, Lan" uniqKey="Wu L" first="Lan" last="Wu">Lan Wu</name>
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<name sortKey="Li, Xi" sort="Li, Xi" uniqKey="Li X" first="Xi" last="Li">Xi Li</name>
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<nlm:affiliation>College of Landscape Architecture, Sichuan Agricultural University, Wenjiang, 611130, Sichuan, People's Republic of China.</nlm:affiliation>
<country xml:lang="fr">République populaire de Chine</country>
<wicri:regionArea>College of Landscape Architecture, Sichuan Agricultural University, Wenjiang, 611130, Sichuan</wicri:regionArea>
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<name sortKey="Gu, Yunfu" sort="Gu, Yunfu" uniqKey="Gu Y" first="Yunfu" last="Gu">Yunfu Gu</name>
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<name sortKey="Xiang, Quanju" sort="Xiang, Quanju" uniqKey="Xiang Q" first="Quanju" last="Xiang">Quanju Xiang</name>
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<name sortKey="Zhao, Ke" sort="Zhao, Ke" uniqKey="Zhao K" first="Ke" last="Zhao">Ke Zhao</name>
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<name sortKey="Yu, Xiumei" sort="Yu, Xiumei" uniqKey="Yu X" first="Xiumei" last="Yu">Xiumei Yu</name>
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<nlm:affiliation>Department of Applied Microbiology, College of Resources, Sichuan Agricultural University, Wenjiang, 611130, Sichuan, People's Republic of China.</nlm:affiliation>
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<name sortKey="Zou, Likou" sort="Zou, Likou" uniqKey="Zou L" first="Likou" last="Zou">Likou Zou</name>
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<title level="j">Applied microbiology and biotechnology</title>
<idno type="eISSN">1432-0614</idno>
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<term>Acetaldehyde (analogs & derivatives)</term>
<term>Acetaldehyde (metabolism)</term>
<term>Alcohols (metabolism)</term>
<term>Aldehyde Reductase (chemistry)</term>
<term>Aldehyde Reductase (metabolism)</term>
<term>Benzaldehydes (metabolism)</term>
<term>Biotransformation (MeSH)</term>
<term>Enzyme Inhibitors (metabolism)</term>
<term>Enzyme Stability (MeSH)</term>
<term>Formaldehyde (metabolism)</term>
<term>Furaldehyde (metabolism)</term>
<term>Gene Expression Regulation, Fungal (MeSH)</term>
<term>Hydrogen-Ion Concentration (MeSH)</term>
<term>Kinetics (MeSH)</term>
<term>Lignin (chemistry)</term>
<term>Metals (metabolism)</term>
<term>Oxidation-Reduction (MeSH)</term>
<term>Oxidoreductases (chemistry)</term>
<term>Oxidoreductases (metabolism)</term>
<term>Saccharomyces cerevisiae (enzymology)</term>
<term>Saccharomyces cerevisiae (metabolism)</term>
<term>Saccharomyces cerevisiae Proteins (chemistry)</term>
<term>Saccharomyces cerevisiae Proteins (metabolism)</term>
<term>Temperature (MeSH)</term>
<term>Transcription, Genetic (MeSH)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Acétaldéhyde (analogues et dérivés)</term>
<term>Acétaldéhyde (métabolisme)</term>
<term>Alcools (métabolisme)</term>
<term>Aldose reductase (composition chimique)</term>
<term>Aldose reductase (métabolisme)</term>
<term>Antienzymes (métabolisme)</term>
<term>Benzaldéhydes (métabolisme)</term>
<term>Biotransformation (MeSH)</term>
<term>Cinétique (MeSH)</term>
<term>Concentration en ions d'hydrogène (MeSH)</term>
<term>Formaldéhyde (métabolisme)</term>
<term>Furfural (métabolisme)</term>
<term>Lignine (composition chimique)</term>
<term>Métaux (métabolisme)</term>
<term>Oxidoreductases (composition chimique)</term>
<term>Oxidoreductases (métabolisme)</term>
<term>Oxydoréduction (MeSH)</term>
<term>Protéines de Saccharomyces cerevisiae (composition chimique)</term>
<term>Protéines de Saccharomyces cerevisiae (métabolisme)</term>
<term>Régulation de l'expression des gènes fongiques (MeSH)</term>
<term>Saccharomyces cerevisiae (enzymologie)</term>
<term>Saccharomyces cerevisiae (métabolisme)</term>
<term>Stabilité enzymatique (MeSH)</term>
<term>Température (MeSH)</term>
<term>Transcription génétique (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analogs & derivatives" xml:lang="en">
<term>Acetaldehyde</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en">
<term>Aldehyde Reductase</term>
<term>Lignin</term>
<term>Oxidoreductases</term>
<term>Saccharomyces cerevisiae Proteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Acetaldehyde</term>
<term>Alcohols</term>
<term>Aldehyde Reductase</term>
<term>Benzaldehydes</term>
<term>Enzyme Inhibitors</term>
<term>Formaldehyde</term>
<term>Furaldehyde</term>
<term>Metals</term>
<term>Oxidoreductases</term>
<term>Saccharomyces cerevisiae Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="analogues et dérivés" xml:lang="fr">
<term>Acétaldéhyde</term>
</keywords>
<keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr">
<term>Aldose reductase</term>
<term>Lignine</term>
<term>Oxidoreductases</term>
<term>Protéines de Saccharomyces cerevisiae</term>
</keywords>
<keywords scheme="MESH" qualifier="enzymologie" xml:lang="fr">
<term>Saccharomyces cerevisiae</term>
</keywords>
<keywords scheme="MESH" qualifier="enzymology" xml:lang="en">
<term>Saccharomyces cerevisiae</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Saccharomyces cerevisiae</term>
</keywords>
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<term>Acétaldéhyde</term>
<term>Alcools</term>
<term>Aldose reductase</term>
<term>Antienzymes</term>
<term>Benzaldéhydes</term>
<term>Formaldéhyde</term>
<term>Furfural</term>
<term>Métaux</term>
<term>Oxidoreductases</term>
<term>Protéines de Saccharomyces cerevisiae</term>
<term>Saccharomyces cerevisiae</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Biotransformation</term>
<term>Enzyme Stability</term>
<term>Gene Expression Regulation, Fungal</term>
<term>Hydrogen-Ion Concentration</term>
<term>Kinetics</term>
<term>Oxidation-Reduction</term>
<term>Temperature</term>
<term>Transcription, Genetic</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Biotransformation</term>
<term>Cinétique</term>
<term>Concentration en ions d'hydrogène</term>
<term>Oxydoréduction</term>
<term>Régulation de l'expression des gènes fongiques</term>
<term>Stabilité enzymatique</term>
<term>Température</term>
<term>Transcription génétique</term>
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<front>
<div type="abstract" xml:lang="en">Aldehydes generated as by-products during the pretreatment of lignocellulose are the key inhibitors to Saccharomyces cerevisiae, which is considered as the most promising microorganism for industrial production of biofuel, xylitol as well as other special chemicals from lignocellulose. S. cerevisiae has the inherent ability to in situ detoxify aldehydes to corresponding alcohols by multiple aldehyde reductases. Herein, we report that an uncharacterized open reading frame YKL071W from S. cerevisiae encodes a novel "classical" short-chain dehydrogenase/reductase (SDR) protein with NADH-dependent enzymatic activities for reduction of furfural (FF), glycolaldehyde (GA), formaldehyde (FA), and benzaldehyde (BZA). This enzyme showed much better specific activities for reduction of GA and FF than FA and BZA, and displayed much higher Km and Kcat/Km but lower Vmax and Kcat for reduction of GA than FF. For this enzyme, the optimum pH was 5.5 and 6.0 for reduction of GA and FF, and the optimum temperature was 30 °C for reduction of GA and FF. Both pH and temperature affected stability of this enzyme in a similar trend for reduction of GA and FF. Cu
<sup>2+</sup>
, Zn
<sup>2+</sup>
, Ni
<sup>2+</sup>
, and Fe
<sup>3+</sup>
had severe inhibition effects on enzyme activities of Ykl071wp for reduction of GA and FF. Transcription of YKL071W in S. cerevisiae was significantly upregulated under GA and FF stress conditions, and its transcription is most probably regulated by transcription factor genes of YAP1, CAD1, PDR3, and STB5. This research provides guidelines to identify more uncharacterized genes with reductase activities for detoxification of aldehydes derived from lignocellulose in S. cerevisiae.</div>
</front>
</TEI>
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<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">29034432</PMID>
<DateCompleted>
<Year>2018</Year>
<Month>06</Month>
<Day>22</Day>
</DateCompleted>
<DateRevised>
<Year>2018</Year>
<Month>07</Month>
<Day>10</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1432-0614</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>101</Volume>
<Issue>23-24</Issue>
<PubDate>
<Year>2017</Year>
<Month>Dec</Month>
</PubDate>
</JournalIssue>
<Title>Applied microbiology and biotechnology</Title>
<ISOAbbreviation>Appl Microbiol Biotechnol</ISOAbbreviation>
</Journal>
<ArticleTitle>YKL071W from Saccharomyces cerevisiae encodes a novel aldehyde reductase for detoxification of glycolaldehyde and furfural derived from lignocellulose.</ArticleTitle>
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<MedlinePgn>8405-8418</MedlinePgn>
</Pagination>
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<Abstract>
<AbstractText>Aldehydes generated as by-products during the pretreatment of lignocellulose are the key inhibitors to Saccharomyces cerevisiae, which is considered as the most promising microorganism for industrial production of biofuel, xylitol as well as other special chemicals from lignocellulose. S. cerevisiae has the inherent ability to in situ detoxify aldehydes to corresponding alcohols by multiple aldehyde reductases. Herein, we report that an uncharacterized open reading frame YKL071W from S. cerevisiae encodes a novel "classical" short-chain dehydrogenase/reductase (SDR) protein with NADH-dependent enzymatic activities for reduction of furfural (FF), glycolaldehyde (GA), formaldehyde (FA), and benzaldehyde (BZA). This enzyme showed much better specific activities for reduction of GA and FF than FA and BZA, and displayed much higher Km and Kcat/Km but lower Vmax and Kcat for reduction of GA than FF. For this enzyme, the optimum pH was 5.5 and 6.0 for reduction of GA and FF, and the optimum temperature was 30 °C for reduction of GA and FF. Both pH and temperature affected stability of this enzyme in a similar trend for reduction of GA and FF. Cu
<sup>2+</sup>
, Zn
<sup>2+</sup>
, Ni
<sup>2+</sup>
, and Fe
<sup>3+</sup>
had severe inhibition effects on enzyme activities of Ykl071wp for reduction of GA and FF. Transcription of YKL071W in S. cerevisiae was significantly upregulated under GA and FF stress conditions, and its transcription is most probably regulated by transcription factor genes of YAP1, CAD1, PDR3, and STB5. This research provides guidelines to identify more uncharacterized genes with reductase activities for detoxification of aldehydes derived from lignocellulose in S. cerevisiae.</AbstractText>
</Abstract>
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<Author ValidYN="Y">
<LastName>Wang</LastName>
<ForeName>Hanyu</ForeName>
<Initials>H</Initials>
<AffiliationInfo>
<Affiliation>Institute of Natural Resources and Geographic Information Technology, College of Resources, Sichuan Agricultural University, No. 211 Huimin Road, Wenjiang, 611130, Sichuan, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Ouyang</LastName>
<ForeName>Yidan</ForeName>
<Initials>Y</Initials>
<AffiliationInfo>
<Affiliation>College of Environmental Sciences, Sichuan Agricultural University, Wenjiang, 611130, Sichuan, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Zhou</LastName>
<ForeName>Chang</ForeName>
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<AffiliationInfo>
<Affiliation>Institute of Natural Resources and Geographic Information Technology, College of Resources, Sichuan Agricultural University, No. 211 Huimin Road, Wenjiang, 611130, Sichuan, People's Republic of China.</Affiliation>
</AffiliationInfo>
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<Initials>D</Initials>
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<Affiliation>Institute of Natural Resources and Geographic Information Technology, College of Resources, Sichuan Agricultural University, No. 211 Huimin Road, Wenjiang, 611130, Sichuan, People's Republic of China.</Affiliation>
</AffiliationInfo>
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<LastName>Guo</LastName>
<ForeName>Yaping</ForeName>
<Initials>Y</Initials>
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</AffiliationInfo>
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<Initials>L</Initials>
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<Affiliation>Institute of Natural Resources and Geographic Information Technology, College of Resources, Sichuan Agricultural University, No. 211 Huimin Road, Wenjiang, 611130, Sichuan, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Li</LastName>
<ForeName>Xi</ForeName>
<Initials>X</Initials>
<AffiliationInfo>
<Affiliation>College of Landscape Architecture, Sichuan Agricultural University, Wenjiang, 611130, Sichuan, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gu</LastName>
<ForeName>Yunfu</ForeName>
<Initials>Y</Initials>
<AffiliationInfo>
<Affiliation>Department of Applied Microbiology, College of Resources, Sichuan Agricultural University, Wenjiang, 611130, Sichuan, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Xiang</LastName>
<ForeName>Quanju</ForeName>
<Initials>Q</Initials>
<AffiliationInfo>
<Affiliation>Department of Applied Microbiology, College of Resources, Sichuan Agricultural University, Wenjiang, 611130, Sichuan, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Zhao</LastName>
<ForeName>Ke</ForeName>
<Initials>K</Initials>
<AffiliationInfo>
<Affiliation>Department of Applied Microbiology, College of Resources, Sichuan Agricultural University, Wenjiang, 611130, Sichuan, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Yu</LastName>
<ForeName>Xiumei</ForeName>
<Initials>X</Initials>
<AffiliationInfo>
<Affiliation>Department of Applied Microbiology, College of Resources, Sichuan Agricultural University, Wenjiang, 611130, Sichuan, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Zou</LastName>
<ForeName>Likou</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Department of Applied Microbiology, College of Resources, Sichuan Agricultural University, Wenjiang, 611130, Sichuan, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Ma</LastName>
<ForeName>Menggen</ForeName>
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<AffiliationInfo>
<Affiliation>Institute of Natural Resources and Geographic Information Technology, College of Resources, Sichuan Agricultural University, No. 211 Huimin Road, Wenjiang, 611130, Sichuan, People's Republic of China. mgen@sicau.edu.cn.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Applied Microbiology, College of Resources, Sichuan Agricultural University, Wenjiang, 611130, Sichuan, People's Republic of China. mgen@sicau.edu.cn.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y">
<Grant>
<GrantID>31570086</GrantID>
<Agency>National Natural Science Foundation of China</Agency>
<Country></Country>
</Grant>
<Grant>
<GrantID>01426100</GrantID>
<Agency>Sichuan Agricultural University</Agency>
<Country></Country>
</Grant>
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<Year>2017</Year>
<Month>10</Month>
<Day>15</Day>
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<Country>Germany</Country>
<MedlineTA>Appl Microbiol Biotechnol</MedlineTA>
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<ISSNLinking>0175-7598</ISSNLinking>
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<RegistryNumber>0</RegistryNumber>
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<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D001547">Benzaldehydes</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
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<Chemical>
<RegistryNumber>11132-73-3</RegistryNumber>
<NameOfSubstance UI="C036909">lignocellulose</NameOfSubstance>
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<Chemical>
<RegistryNumber>1HG84L3525</RegistryNumber>
<NameOfSubstance UI="D005557">Formaldehyde</NameOfSubstance>
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<Chemical>
<RegistryNumber>9005-53-2</RegistryNumber>
<NameOfSubstance UI="D008031">Lignin</NameOfSubstance>
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<Chemical>
<RegistryNumber>DJ1HGI319P</RegistryNumber>
<NameOfSubstance UI="D005662">Furaldehyde</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 1.-</RegistryNumber>
<NameOfSubstance UI="C000626873">OSI1 protein, S cerevisiae</NameOfSubstance>
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<Chemical>
<RegistryNumber>EC 1.-</RegistryNumber>
<NameOfSubstance UI="D010088">Oxidoreductases</NameOfSubstance>
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<Chemical>
<RegistryNumber>GO1N1ZPR3B</RegistryNumber>
<NameOfSubstance UI="D000079">Acetaldehyde</NameOfSubstance>
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<Chemical>
<RegistryNumber>TA269SD04T</RegistryNumber>
<NameOfSubstance UI="C032175">benzaldehyde</NameOfSubstance>
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<Chemical>
<RegistryNumber>W0A0XPU08U</RegistryNumber>
<NameOfSubstance UI="C010972">glycolaldehyde</NameOfSubstance>
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<MeshHeading>
<DescriptorName UI="D000079" MajorTopicYN="N">Acetaldehyde</DescriptorName>
<QualifierName UI="Q000031" MajorTopicYN="Y">analogs & derivatives</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000438" MajorTopicYN="N">Alcohols</DescriptorName>
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</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000449" MajorTopicYN="N">Aldehyde Reductase</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
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</MeshHeading>
<MeshHeading>
<DescriptorName UI="D001547" MajorTopicYN="N">Benzaldehydes</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D001711" MajorTopicYN="N">Biotransformation</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D004791" MajorTopicYN="N">Enzyme Inhibitors</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D004795" MajorTopicYN="N">Enzyme Stability</DescriptorName>
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<MeshHeading>
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<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
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<MeshHeading>
<DescriptorName UI="D008670" MajorTopicYN="N">Metals</DescriptorName>
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<MeshHeading>
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<name sortKey="Ma, Menggen" sort="Ma, Menggen" uniqKey="Ma M" first="Menggen" last="Ma">Menggen Ma</name>
<name sortKey="Ouyang, Yidan" sort="Ouyang, Yidan" uniqKey="Ouyang Y" first="Yidan" last="Ouyang">Yidan Ouyang</name>
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<name sortKey="Xiang, Quanju" sort="Xiang, Quanju" uniqKey="Xiang Q" first="Quanju" last="Xiang">Quanju Xiang</name>
<name sortKey="Xiao, Difan" sort="Xiao, Difan" uniqKey="Xiao D" first="Difan" last="Xiao">Difan Xiao</name>
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