The elicitor cryptogein blocks glucose transport in tobacco cells.
Identifieur interne : 002544 ( Main/Exploration ); précédent : 002543; suivant : 002545The elicitor cryptogein blocks glucose transport in tobacco cells.
Auteurs : Stéphane Bourque [France] ; Rémi Lemoine ; Anabelle Sequeira-Legrand ; Léon Fayolle ; Serge Delrot ; Alain PuginSource :
- Plant physiology [ 0032-0889 ] ; 2002.
Descripteurs français
- KwdFr :
- Apoptose (effets des médicaments et des substances chimiques), Calcium (métabolisme), Cellules cultivées (MeSH), Espèces réactives de l'oxygène (métabolisme), Glucose (métabolisme), Immunité innée (effets des médicaments et des substances chimiques), Maladies des plantes (microbiologie), Oxygène (métabolisme), Phosphorylation (effets des médicaments et des substances chimiques), Phytophthora (composition chimique), Phytophthora (croissance et développement), Protéines d'algue (pharmacologie), Protéines de transport de la membrane mitochondriale (métabolisme), Protéines fongiques (MeSH), Tabac (cytologie), Tabac (microbiologie), Tabac (métabolisme), Transduction du signal (effets des médicaments et des substances chimiques), Transport biologique (effets des médicaments et des substances chimiques), Transporteurs de monosaccharides (métabolisme).
- MESH :
- composition chimique : Phytophthora.
- croissance et développement : Phytophthora.
- cytologie : Tabac.
- effets des médicaments et des substances chimiques : Apoptose, Immunité innée, Phosphorylation, Transduction du signal, Transport biologique.
- microbiologie : Maladies des plantes, Tabac.
- métabolisme : Calcium, Espèces réactives de l'oxygène, Glucose, Oxygène, Protéines de transport de la membrane mitochondriale, Tabac, Transporteurs de monosaccharides.
- pharmacologie : Protéines d'algue.
- Cellules cultivées, Protéines fongiques.
English descriptors
- KwdEn :
- Algal Proteins (pharmacology), Apoptosis (drug effects), Biological Transport (drug effects), Calcium (metabolism), Cells, Cultured (MeSH), Fungal Proteins (MeSH), Glucose (metabolism), Immunity, Innate (drug effects), Mitochondrial Membrane Transport Proteins (metabolism), Monosaccharide Transport Proteins (metabolism), Oxygen (metabolism), Phosphorylation (drug effects), Phytophthora (chemistry), Phytophthora (growth & development), Plant Diseases (microbiology), Reactive Oxygen Species (metabolism), Signal Transduction (drug effects), Tobacco (cytology), Tobacco (metabolism), Tobacco (microbiology).
- MESH :
- chemical , metabolism : Calcium, Glucose, Mitochondrial Membrane Transport Proteins, Monosaccharide Transport Proteins, Oxygen, Reactive Oxygen Species.
- chemical , pharmacology : Algal Proteins.
- chemistry : Phytophthora.
- cytology : Tobacco.
- drug effects : Apoptosis, Biological Transport, Immunity, Innate, Phosphorylation, Signal Transduction.
- growth & development : Phytophthora.
- metabolism : Tobacco.
- microbiology : Plant Diseases, Tobacco.
- Cells, Cultured, Fungal Proteins.
Abstract
Cryptogein is a 10-kD protein secreted by the oomycete Phytophthora cryptogea that induces a hypersensitive response on tobacco (Nicotiana tabacum var. Xanthi) plants and a systemic acquired resistance against various pathogens. The mode of action of this elicitor has been studied using tobacco cell suspensions. Our previous data indicated that within minutes, cryptogein signaling involves various events including changes in ion fluxes, protein phosphorylation, sugar metabolism, and, eventually, cell death. These results suggested that transport of sugars could be affected and, thus, involved in the complex relationships between plant and microorganisms via elicitors. This led us to investigate the effects of cryptogein on glucose (Glc) uptake and mitochondrial activity in tobacco cells. Cryptogein induces an immediate inhibition of Glc uptake, which is not attributable to plasma membrane (PM) depolarization. Conversely, cryptogein-induced valine uptake is because of PM depolarization. Inhibition of the PM Glc transporter(s) was shown to be mediated by a calcium-dependent phosphorylation process, and is independent of active oxygen species production. This inhibition was associated with a strong decrease in O(2) uptake rate by cells and a large mitochondrial membrane depolarization. Thus, inhibition of Glc uptake accompanied by inhibition of phosphorylative oxidation may participate in hypersensitive cell death. These results are discussed in the context of competition between plants and microorganisms for apoplastic sugars.
DOI: 10.1104/pp.009449
PubMed: 12481101
PubMed Central: PMC166729
Affiliations:
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effects)</term><term>Mitochondrial Membrane Transport Proteins (metabolism)</term><term>Monosaccharide Transport Proteins (metabolism)</term><term>Oxygen (metabolism)</term><term>Phosphorylation (drug effects)</term><term>Phytophthora (chemistry)</term><term>Phytophthora (growth & development)</term><term>Plant Diseases (microbiology)</term><term>Reactive Oxygen Species (metabolism)</term><term>Signal Transduction (drug effects)</term><term>Tobacco (cytology)</term><term>Tobacco (metabolism)</term><term>Tobacco (microbiology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Apoptose (effets des médicaments et des substances chimiques)</term><term>Calcium (métabolisme)</term><term>Cellules cultivées (MeSH)</term><term>Espèces réactives de l'oxygène (métabolisme)</term><term>Glucose (métabolisme)</term><term>Immunité innée (effets des médicaments et des substances chimiques)</term><term>Maladies des plantes (microbiologie)</term><term>Oxygène (métabolisme)</term><term>Phosphorylation (effets des médicaments et des substances chimiques)</term><term>Phytophthora (composition chimique)</term><term>Phytophthora (croissance et développement)</term><term>Protéines d'algue (pharmacologie)</term><term>Protéines de transport de la membrane mitochondriale (métabolisme)</term><term>Protéines fongiques (MeSH)</term><term>Tabac (cytologie)</term><term>Tabac (microbiologie)</term><term>Tabac (métabolisme)</term><term>Transduction du signal (effets des médicaments et des substances chimiques)</term><term>Transport biologique (effets des médicaments et des substances chimiques)</term><term>Transporteurs de monosaccharides (métabolisme)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Calcium</term><term>Glucose</term><term>Mitochondrial Membrane Transport Proteins</term><term>Monosaccharide Transport Proteins</term><term>Oxygen</term><term>Reactive Oxygen Species</term></keywords><keywords 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xml:lang="en"><term>Cells, Cultured</term><term>Fungal Proteins</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Cellules cultivées</term><term>Protéines fongiques</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Cryptogein is a 10-kD protein secreted by the oomycete Phytophthora cryptogea that induces a hypersensitive response on tobacco (Nicotiana tabacum var. Xanthi) plants and a systemic acquired resistance against various pathogens. The mode of action of this elicitor has been studied using tobacco cell suspensions. Our previous data indicated that within minutes, cryptogein signaling involves various events including changes in ion fluxes, protein phosphorylation, sugar metabolism, and, eventually, cell death. These results suggested that transport of sugars could be affected and, thus, involved in the complex relationships between plant and microorganisms via elicitors. This led us to investigate the effects of cryptogein on glucose (Glc) uptake and mitochondrial activity in tobacco cells. Cryptogein induces an immediate inhibition of Glc uptake, which is not attributable to plasma membrane (PM) depolarization. Conversely, cryptogein-induced valine uptake is because of PM depolarization. Inhibition of the PM Glc transporter(s) was shown to be mediated by a calcium-dependent phosphorylation process, and is independent of active oxygen species production. This inhibition was associated with a strong decrease in O(2) uptake rate by cells and a large mitochondrial membrane depolarization. Thus, inhibition of Glc uptake accompanied by inhibition of phosphorylative oxidation may participate in hypersensitive cell death. These results are discussed in the context of competition between plants and microorganisms for apoplastic sugars.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">12481101</PMID><DateCompleted><Year>2003</Year><Month>05</Month><Day>30</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0032-0889</ISSN><JournalIssue CitedMedium="Print"><Volume>130</Volume><Issue>4</Issue><PubDate><Year>2002</Year><Month>Dec</Month></PubDate></JournalIssue><Title>Plant physiology</Title><ISOAbbreviation>Plant Physiol</ISOAbbreviation></Journal><ArticleTitle>The elicitor cryptogein blocks glucose transport in tobacco cells.</ArticleTitle><Pagination><MedlinePgn>2177-87</MedlinePgn></Pagination><Abstract><AbstractText>Cryptogein is a 10-kD protein secreted by the oomycete Phytophthora cryptogea that induces a hypersensitive response on tobacco (Nicotiana tabacum var. Xanthi) plants and a systemic acquired resistance against various pathogens. The mode of action of this elicitor has been studied using tobacco cell suspensions. Our previous data indicated that within minutes, cryptogein signaling involves various events including changes in ion fluxes, protein phosphorylation, sugar metabolism, and, eventually, cell death. These results suggested that transport of sugars could be affected and, thus, involved in the complex relationships between plant and microorganisms via elicitors. This led us to investigate the effects of cryptogein on glucose (Glc) uptake and mitochondrial activity in tobacco cells. Cryptogein induces an immediate inhibition of Glc uptake, which is not attributable to plasma membrane (PM) depolarization. Conversely, cryptogein-induced valine uptake is because of PM depolarization. Inhibition of the PM Glc transporter(s) was shown to be mediated by a calcium-dependent phosphorylation process, and is independent of active oxygen species production. This inhibition was associated with a strong decrease in O(2) uptake rate by cells and a large mitochondrial membrane depolarization. Thus, inhibition of Glc uptake accompanied by inhibition of phosphorylative oxidation may participate in hypersensitive cell death. These results are discussed in the context of competition between plants and microorganisms for apoplastic sugars.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Bourque</LastName><ForeName>Stéphane</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Unité Mixte de Recherche-Institut National de la Recherche Agronomique/Université de Bourgogne, Biochimie, Biologie Cellulaire, et Ecologie des Interactions Plantes/Micro-organismes, 17 Rue Sully, BV 86510-21065 Dijon cedex, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Lemoine</LastName><ForeName>Rémi</ForeName><Initials>R</Initials></Author><Author ValidYN="Y"><LastName>Sequeira-Legrand</LastName><ForeName>Anabelle</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Fayolle</LastName><ForeName>Léon</ForeName><Initials>L</Initials></Author><Author ValidYN="Y"><LastName>Delrot</LastName><ForeName>Serge</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Pugin</LastName><ForeName>Alain</ForeName><Initials>A</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Plant Physiol</MedlineTA><NlmUniqueID>0401224</NlmUniqueID><ISSNLinking>0032-0889</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D020418">Algal Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005656">Fungal Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D033681">Mitochondrial Membrane Transport Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D009004">Monosaccharide Transport Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D017382">Reactive Oxygen Species</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C061032">cryptogein protein, Phytophthora cryptogea</NameOfSubstance></Chemical><Chemical><RegistryNumber>IY9XDZ35W2</RegistryNumber><NameOfSubstance UI="D005947">Glucose</NameOfSubstance></Chemical><Chemical><RegistryNumber>S88TT14065</RegistryNumber><NameOfSubstance UI="D010100">Oxygen</NameOfSubstance></Chemical><Chemical><RegistryNumber>SY7Q814VUP</RegistryNumber><NameOfSubstance UI="D002118">Calcium</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D020418" MajorTopicYN="N">Algal Proteins</DescriptorName><QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017209" MajorTopicYN="N">Apoptosis</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001692" MajorTopicYN="N">Biological Transport</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002118" MajorTopicYN="N">Calcium</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002478" MajorTopicYN="N">Cells, Cultured</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005656" MajorTopicYN="N">Fungal Proteins</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005947" MajorTopicYN="N">Glucose</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007113" MajorTopicYN="N">Immunity, Innate</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D033681" MajorTopicYN="N">Mitochondrial Membrane Transport Proteins</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009004" MajorTopicYN="N">Monosaccharide Transport Proteins</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010100" MajorTopicYN="N">Oxygen</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010766" MajorTopicYN="N">Phosphorylation</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010838" MajorTopicYN="N">Phytophthora</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010935" MajorTopicYN="N">Plant Diseases</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017382" MajorTopicYN="N">Reactive Oxygen Species</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015398" MajorTopicYN="N">Signal Transduction</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014026" MajorTopicYN="N">Tobacco</DescriptorName><QualifierName UI="Q000166" MajorTopicYN="N">cytology</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName><QualifierName UI="Q000382" 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IdType="pubmed">9847105</ArticleId></ArticleIdList></Reference></ReferenceList></PubmedData></pubmed><affiliations><list><country><li>France</li></country><region><li>Nouvelle-Aquitaine</li><li>Poitou-Charentes</li></region><settlement><li>Dijon</li></settlement><orgName><li>Université de Bourgogne</li></orgName></list><tree><noCountry><name sortKey="Delrot, Serge" sort="Delrot, Serge" uniqKey="Delrot S" first="Serge" last="Delrot">Serge Delrot</name><name sortKey="Fayolle, Leon" sort="Fayolle, Leon" uniqKey="Fayolle L" first="Léon" last="Fayolle">Léon Fayolle</name><name sortKey="Lemoine, Remi" sort="Lemoine, Remi" uniqKey="Lemoine R" first="Rémi" last="Lemoine">Rémi Lemoine</name><name sortKey="Pugin, Alain" sort="Pugin, Alain" uniqKey="Pugin A" first="Alain" last="Pugin">Alain Pugin</name><name sortKey="Sequeira Legrand, Anabelle" sort="Sequeira Legrand, Anabelle" uniqKey="Sequeira Legrand A" first="Anabelle" last="Sequeira-Legrand">Anabelle Sequeira-Legrand</name></noCountry><country name="France"><region name="Nouvelle-Aquitaine"><name sortKey="Bourque, Stephane" sort="Bourque, Stephane" uniqKey="Bourque S" first="Stéphane" last="Bourque">Stéphane Bourque</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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