An early salicylic acid-, pathogen- and elicitor-inducible tobacco glucosyltransferase: role in compartmentalization of phenolics and H2O2 metabolism.
Identifieur interne : 002941 ( Main/Exploration ); précédent : 002940; suivant : 002942An early salicylic acid-, pathogen- and elicitor-inducible tobacco glucosyltransferase: role in compartmentalization of phenolics and H2O2 metabolism.
Auteurs : J. Chong [France] ; R. Baltz ; B. Fritig ; P. SaindrenanSource :
- FEBS letters [ 0014-5793 ] ; 1999.
Descripteurs français
- KwdFr :
- Acide salicylique (pharmacologie), Acides caféiques (métabolisme), Acides coumariques (métabolisme), Cellules cultivées (MeSH), Compartimentation cellulaire (MeSH), Espace extracellulaire (métabolisme), Glucosyltransferases (biosynthèse), Glucosyltransferases (métabolisme), Glycoprotéines membranaires (pharmacologie), Induction enzymatique (MeSH), Liquide intracellulaire (métabolisme), Maladies des plantes (microbiologie), Oxydoréduction (MeSH), Peroxyde d'hydrogène (métabolisme), Phénols (métabolisme), Piégeurs de radicaux libres (métabolisme), Protéines fongiques (pharmacologie), Scopolétine (métabolisme), Tabac (cytologie), Tabac (enzymologie), Tabac (microbiologie), Tabac (métabolisme), Uridine diphosphate (métabolisme), Végétaux toxiques (MeSH).
- MESH :
- biosynthèse : Glucosyltransferases.
- cytologie : Tabac.
- enzymologie : Tabac.
- microbiologie : Maladies des plantes, Tabac.
- métabolisme : Acides caféiques, Acides coumariques, Espace extracellulaire, Glucosyltransferases, Liquide intracellulaire, Peroxyde d'hydrogène, Phénols, Piégeurs de radicaux libres, Scopolétine, Tabac, Uridine diphosphate.
- pharmacologie : Acide salicylique, Glycoprotéines membranaires, Protéines fongiques.
- Cellules cultivées, Compartimentation cellulaire, Induction enzymatique, Oxydoréduction, Végétaux toxiques.
English descriptors
- KwdEn :
- Caffeic Acids (metabolism), Cell Compartmentation (MeSH), Cells, Cultured (MeSH), Coumaric Acids (metabolism), Enzyme Induction (MeSH), Extracellular Space (metabolism), Free Radical Scavengers (metabolism), Fungal Proteins (pharmacology), Glucosyltransferases (biosynthesis), Glucosyltransferases (metabolism), Hydrogen Peroxide (metabolism), Intracellular Fluid (metabolism), Membrane Glycoproteins (pharmacology), Oxidation-Reduction (MeSH), Phenols (metabolism), Plant Diseases (microbiology), Plants, Toxic (MeSH), Salicylic Acid (pharmacology), Scopoletin (metabolism), Tobacco (cytology), Tobacco (enzymology), Tobacco (metabolism), Tobacco (microbiology), Uridine Diphosphate (metabolism).
- MESH :
- chemical , biosynthesis : Glucosyltransferases.
- chemical , metabolism : Caffeic Acids, Coumaric Acids, Free Radical Scavengers, Glucosyltransferases, Hydrogen Peroxide, Phenols, Scopoletin, Uridine Diphosphate.
- cytology : Tobacco.
- enzymology : Tobacco.
- metabolism : Extracellular Space, Intracellular Fluid, Tobacco.
- microbiology : Plant Diseases, Tobacco.
- chemical , pharmacology : Fungal Proteins, Membrane Glycoproteins, Salicylic Acid.
- Cell Compartmentation, Cells, Cultured, Enzyme Induction, Oxidation-Reduction, Plants, Toxic.
Abstract
Treatment of tobacco cell suspension cultures with a fungal elicitor of defense responses resulted in an early accumulation of the phenylpropanoid glucosyltransferase TOGT, along with the rapid synthesis and secretion of scopolin, the glucoside of scopoletin. Elicitor-triggered extracellular accumulation of the aglycone scopoletin and of free caffeic and ferulic acids could only be revealed in the presence of diphenylene iodonium, an inhibitor of extracellular H2O2 production. Our results strongly support a role for TOGT in the elicitor-stimulated production of transportable phenylpropanoid glucosides, followed by the release of free antioxidant phenolics into the extracellular medium and subsequent H2O2 scavenging.
DOI: 10.1016/s0014-5793(99)01154-0
PubMed: 10481066
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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<author><name sortKey="Baltz, R" sort="Baltz, R" uniqKey="Baltz R" first="R" last="Baltz">R. Baltz</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Caffeic Acids (metabolism)</term>
<term>Cell Compartmentation (MeSH)</term>
<term>Cells, Cultured (MeSH)</term>
<term>Coumaric Acids (metabolism)</term>
<term>Enzyme Induction (MeSH)</term>
<term>Extracellular Space (metabolism)</term>
<term>Free Radical Scavengers (metabolism)</term>
<term>Fungal Proteins (pharmacology)</term>
<term>Glucosyltransferases (biosynthesis)</term>
<term>Glucosyltransferases (metabolism)</term>
<term>Hydrogen Peroxide (metabolism)</term>
<term>Intracellular Fluid (metabolism)</term>
<term>Membrane Glycoproteins (pharmacology)</term>
<term>Oxidation-Reduction (MeSH)</term>
<term>Phenols (metabolism)</term>
<term>Plant Diseases (microbiology)</term>
<term>Plants, Toxic (MeSH)</term>
<term>Salicylic Acid (pharmacology)</term>
<term>Scopoletin (metabolism)</term>
<term>Tobacco (cytology)</term>
<term>Tobacco (enzymology)</term>
<term>Tobacco (metabolism)</term>
<term>Tobacco (microbiology)</term>
<term>Uridine Diphosphate (metabolism)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Acide salicylique (pharmacologie)</term>
<term>Acides caféiques (métabolisme)</term>
<term>Acides coumariques (métabolisme)</term>
<term>Cellules cultivées (MeSH)</term>
<term>Compartimentation cellulaire (MeSH)</term>
<term>Espace extracellulaire (métabolisme)</term>
<term>Glucosyltransferases (biosynthèse)</term>
<term>Glucosyltransferases (métabolisme)</term>
<term>Glycoprotéines membranaires (pharmacologie)</term>
<term>Induction enzymatique (MeSH)</term>
<term>Liquide intracellulaire (métabolisme)</term>
<term>Maladies des plantes (microbiologie)</term>
<term>Oxydoréduction (MeSH)</term>
<term>Peroxyde d'hydrogène (métabolisme)</term>
<term>Phénols (métabolisme)</term>
<term>Piégeurs de radicaux libres (métabolisme)</term>
<term>Protéines fongiques (pharmacologie)</term>
<term>Scopolétine (métabolisme)</term>
<term>Tabac (cytologie)</term>
<term>Tabac (enzymologie)</term>
<term>Tabac (microbiologie)</term>
<term>Tabac (métabolisme)</term>
<term>Uridine diphosphate (métabolisme)</term>
<term>Végétaux toxiques (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Glucosyltransferases</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Caffeic Acids</term>
<term>Coumaric Acids</term>
<term>Free Radical Scavengers</term>
<term>Glucosyltransferases</term>
<term>Hydrogen Peroxide</term>
<term>Phenols</term>
<term>Scopoletin</term>
<term>Uridine Diphosphate</term>
</keywords>
<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>Glucosyltransferases</term>
</keywords>
<keywords scheme="MESH" qualifier="cytologie" xml:lang="fr"><term>Tabac</term>
</keywords>
<keywords scheme="MESH" qualifier="cytology" xml:lang="en"><term>Tobacco</term>
</keywords>
<keywords scheme="MESH" qualifier="enzymologie" xml:lang="fr"><term>Tabac</term>
</keywords>
<keywords scheme="MESH" qualifier="enzymology" xml:lang="en"><term>Tobacco</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Extracellular Space</term>
<term>Intracellular Fluid</term>
<term>Tobacco</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr"><term>Maladies des plantes</term>
<term>Tabac</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Plant Diseases</term>
<term>Tobacco</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Acides caféiques</term>
<term>Acides coumariques</term>
<term>Espace extracellulaire</term>
<term>Glucosyltransferases</term>
<term>Liquide intracellulaire</term>
<term>Peroxyde d'hydrogène</term>
<term>Phénols</term>
<term>Piégeurs de radicaux libres</term>
<term>Scopolétine</term>
<term>Tabac</term>
<term>Uridine diphosphate</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Acide salicylique</term>
<term>Glycoprotéines membranaires</term>
<term>Protéines fongiques</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Fungal Proteins</term>
<term>Membrane Glycoproteins</term>
<term>Salicylic Acid</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Cell Compartmentation</term>
<term>Cells, Cultured</term>
<term>Enzyme Induction</term>
<term>Oxidation-Reduction</term>
<term>Plants, Toxic</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Cellules cultivées</term>
<term>Compartimentation cellulaire</term>
<term>Induction enzymatique</term>
<term>Oxydoréduction</term>
<term>Végétaux toxiques</term>
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<front><div type="abstract" xml:lang="en">Treatment of tobacco cell suspension cultures with a fungal elicitor of defense responses resulted in an early accumulation of the phenylpropanoid glucosyltransferase TOGT, along with the rapid synthesis and secretion of scopolin, the glucoside of scopoletin. Elicitor-triggered extracellular accumulation of the aglycone scopoletin and of free caffeic and ferulic acids could only be revealed in the presence of diphenylene iodonium, an inhibitor of extracellular H2O2 production. Our results strongly support a role for TOGT in the elicitor-stimulated production of transportable phenylpropanoid glucosides, followed by the release of free antioxidant phenolics into the extracellular medium and subsequent H2O2 scavenging.</div>
</front>
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<Month>06</Month>
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<Title>FEBS letters</Title>
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<ArticleTitle>An early salicylic acid-, pathogen- and elicitor-inducible tobacco glucosyltransferase: role in compartmentalization of phenolics and H2O2 metabolism.</ArticleTitle>
<Pagination><MedlinePgn>204-8</MedlinePgn>
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<Abstract><AbstractText>Treatment of tobacco cell suspension cultures with a fungal elicitor of defense responses resulted in an early accumulation of the phenylpropanoid glucosyltransferase TOGT, along with the rapid synthesis and secretion of scopolin, the glucoside of scopoletin. Elicitor-triggered extracellular accumulation of the aglycone scopoletin and of free caffeic and ferulic acids could only be revealed in the presence of diphenylene iodonium, an inhibitor of extracellular H2O2 production. Our results strongly support a role for TOGT in the elicitor-stimulated production of transportable phenylpropanoid glucosides, followed by the release of free antioxidant phenolics into the extracellular medium and subsequent H2O2 scavenging.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Chong</LastName>
<ForeName>J</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Institut de Biologie Moléculaire des Plantes du CNRS, Université Louis Pasteur, Strasbourg, France.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Baltz</LastName>
<ForeName>R</ForeName>
<Initials>R</Initials>
</Author>
<Author ValidYN="Y"><LastName>Fritig</LastName>
<ForeName>B</ForeName>
<Initials>B</Initials>
</Author>
<Author ValidYN="Y"><LastName>Saindrenan</LastName>
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<Initials>P</Initials>
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<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
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<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D003373">Coumaric Acids</NameOfSubstance>
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<NameOfSubstance UI="C091510">elicitor protein, Phytophthora megasperma</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>58-98-0</RegistryNumber>
<NameOfSubstance UI="D014530">Uridine Diphosphate</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>AVM951ZWST</RegistryNumber>
<NameOfSubstance UI="C004999">ferulic acid</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>BBX060AN9V</RegistryNumber>
<NameOfSubstance UI="D006861">Hydrogen Peroxide</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 2.4.1.-</RegistryNumber>
<NameOfSubstance UI="D005964">Glucosyltransferases</NameOfSubstance>
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<MeshHeading><DescriptorName UI="D010636" MajorTopicYN="N">Phenols</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
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<MeshHeading><DescriptorName UI="D010935" MajorTopicYN="N">Plant Diseases</DescriptorName>
<QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010947" MajorTopicYN="Y">Plants, Toxic</DescriptorName>
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<MeshHeading><DescriptorName UI="D020156" MajorTopicYN="N">Salicylic Acid</DescriptorName>
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<MeshHeading><DescriptorName UI="D012603" MajorTopicYN="N">Scopoletin</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014026" MajorTopicYN="N">Tobacco</DescriptorName>
<QualifierName UI="Q000166" MajorTopicYN="N">cytology</QualifierName>
<QualifierName UI="Q000201" MajorTopicYN="Y">enzymology</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
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<MeshHeading><DescriptorName UI="D014530" MajorTopicYN="N">Uridine Diphosphate</DescriptorName>
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