Phytophthora austrocedri Elicitates Changes in Diterpene Profile of Austrocedrus chilensis.
Identifieur interne : 000E01 ( Main/Exploration ); précédent : 000E00; suivant : 000E02Phytophthora austrocedri Elicitates Changes in Diterpene Profile of Austrocedrus chilensis.
Auteurs : Ver Nica Rachel Olate [Chili] ; María Laura Vélez [Argentine] ; Alina Greslebin [Argentine] ; Guillermo Schmeda-Hirschmann [Chili]Source :
- Molecules (Basel, Switzerland) [ 1420-3049 ] ; 2015.
Descripteurs français
- KwdFr :
- Antifongiques (pharmacologie), Chromatographie gazeuse-spectrométrie de masse (MeSH), Chromatographie sur couche mince (MeSH), Cupressaceae (composition chimique), Cupressaceae (microbiologie), Diterpènes (analyse), Diterpènes (composition chimique), Diterpènes (isolement et purification), Phytophthora (physiologie), Résines synthétiques (analyse), Spectroscopie par résonance magnétique du proton (MeSH).
- MESH :
- analyse : Diterpènes, Résines synthétiques.
- composition chimique : Cupressaceae, Diterpènes.
- isolement et purification : Diterpènes.
- microbiologie : Cupressaceae.
- pharmacologie : Antifongiques.
- physiologie : Phytophthora.
- Chromatographie gazeuse-spectrométrie de masse, Chromatographie sur couche mince, Spectroscopie par résonance magnétique du proton.
English descriptors
- KwdEn :
- Antifungal Agents (pharmacology), Chromatography, Thin Layer (MeSH), Cupressaceae (chemistry), Cupressaceae (microbiology), Diterpenes (analysis), Diterpenes (chemistry), Diterpenes (isolation & purification), Gas Chromatography-Mass Spectrometry (MeSH), Phytophthora (physiology), Proton Magnetic Resonance Spectroscopy (MeSH), Resins, Synthetic (analysis).
- MESH :
- chemical , analysis : Diterpenes, Resins, Synthetic.
- chemical , chemistry : Diterpenes.
- chemical , isolation & purification : Diterpenes.
- chemical , pharmacology : Antifungal Agents.
- chemistry : Cupressaceae.
- microbiology : Cupressaceae.
- physiology : Phytophthora.
- Chromatography, Thin Layer, Gas Chromatography-Mass Spectrometry, Proton Magnetic Resonance Spectroscopy.
Abstract
The populations of the Andean Cupressaceae Austrocedrus chilensis have been severely affected by a disease caused by the phytopathogenic fungus Phytophthora austrocedri. A study was undertaken to disclose changes in the resin composition of P. austrocedri-infected individuals, including naturally infected and artificially inoculated trees, compared with healthy A. chilensis trees. GC-MS and (1)H-NMR studies showed a clear differentiation among healthy and infected resins, with the diterpene isopimara-8(9),15-dien-19-ol as a relevant constituent in resins from infected trees. The effect of resin fractions from P. austrocedri infected trees on the pathogen was assessed by measuring the mycelial growth in agar plates. The most active fractions from resin obtained from infected trees inhibited fungal growth by nearly 50% at 1 mg/dish (35.37 µg/cm(2)). The main constituent in the active fractions were 18-hydroxymanool and the aldehyde torulosal. Both compounds are oxidation products of manool and can be a chemical response of the tree to the pathogen or be formed from the pathogen as a biotransformation product of manool by microbial oxidation. While the diterpene profiles from A. chilensis tree resins can easily differentiate healthy and P. austrocedri infected individuals, the possible conversion of manool to the antifungal derivatives 4 and 6 by the microorganism remains to be established.
DOI: 10.3390/molecules200815084
PubMed: 26295220
PubMed Central: PMC6332227
Affiliations:
Links toward previous steps (curation, corpus...)
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qualifier="pharmacology" xml:lang="en"><term>Antifungal Agents</term></keywords><keywords scheme="MESH" qualifier="analyse" xml:lang="fr"><term>Diterpènes</term><term>Résines synthétiques</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Cupressaceae</term></keywords><keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr"><term>Cupressaceae</term><term>Diterpènes</term></keywords><keywords scheme="MESH" qualifier="isolement et purification" xml:lang="fr"><term>Diterpènes</term></keywords><keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr"><term>Cupressaceae</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Cupressaceae</term></keywords><keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Antifongiques</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Phytophthora</term></keywords><keywords scheme="MESH" qualifier="physiology" 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A study was undertaken to disclose changes in the resin composition of P. austrocedri-infected individuals, including naturally infected and artificially inoculated trees, compared with healthy A. chilensis trees. GC-MS and (1)H-NMR studies showed a clear differentiation among healthy and infected resins, with the diterpene isopimara-8(9),15-dien-19-ol as a relevant constituent in resins from infected trees. The effect of resin fractions from P. austrocedri infected trees on the pathogen was assessed by measuring the mycelial growth in agar plates. The most active fractions from resin obtained from infected trees inhibited fungal growth by nearly 50% at 1 mg/dish (35.37 µg/cm(2)). The main constituent in the active fractions were 18-hydroxymanool and the aldehyde torulosal. Both compounds are oxidation products of manool and can be a chemical response of the tree to the pathogen or be formed from the pathogen as a biotransformation product of manool by microbial oxidation. While the diterpene profiles from A. chilensis tree resins can easily differentiate healthy and P. austrocedri infected individuals, the possible conversion of manool to the antifungal derivatives 4 and 6 by the microorganism remains to be established. </div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">26295220</PMID><DateCompleted><Year>2016</Year><Month>05</Month><Day>31</Day></DateCompleted><DateRevised><Year>2020</Year><Month>02</Month><Day>25</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">1420-3049</ISSN><JournalIssue CitedMedium="Internet"><Volume>20</Volume><Issue>8</Issue><PubDate><Year>2015</Year><Month>Aug</Month><Day>18</Day></PubDate></JournalIssue><Title>Molecules (Basel, Switzerland)</Title><ISOAbbreviation>Molecules</ISOAbbreviation></Journal><ArticleTitle>Phytophthora austrocedri Elicitates Changes in Diterpene Profile of Austrocedrus chilensis.</ArticleTitle><Pagination><MedlinePgn>15084-97</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.3390/molecules200815084</ELocationID><Abstract><AbstractText>The populations of the Andean Cupressaceae Austrocedrus chilensis have been severely affected by a disease caused by the phytopathogenic fungus Phytophthora austrocedri. A study was undertaken to disclose changes in the resin composition of P. austrocedri-infected individuals, including naturally infected and artificially inoculated trees, compared with healthy A. chilensis trees. GC-MS and (1)H-NMR studies showed a clear differentiation among healthy and infected resins, with the diterpene isopimara-8(9),15-dien-19-ol as a relevant constituent in resins from infected trees. The effect of resin fractions from P. austrocedri infected trees on the pathogen was assessed by measuring the mycelial growth in agar plates. The most active fractions from resin obtained from infected trees inhibited fungal growth by nearly 50% at 1 mg/dish (35.37 µg/cm(2)). The main constituent in the active fractions were 18-hydroxymanool and the aldehyde torulosal. Both compounds are oxidation products of manool and can be a chemical response of the tree to the pathogen or be formed from the pathogen as a biotransformation product of manool by microbial oxidation. While the diterpene profiles from A. chilensis tree resins can easily differentiate healthy and P. austrocedri infected individuals, the possible conversion of manool to the antifungal derivatives 4 and 6 by the microorganism remains to be established. </AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Olate</LastName><ForeName>Verónica Rachel</ForeName><Initials>VR</Initials><AffiliationInfo><Affiliation>Laboratorio de Química de Productos Naturales, Instituto de Química de Recursos Naturales, Universidad de Talca, Casilla 747, 3460000 Talca, Chile. volate@utalca.cl.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Vélez</LastName><ForeName>María Laura</ForeName><Initials>ML</Initials><AffiliationInfo><Affiliation>CONICET-Área de Protección Forestal, Centro de Investigación y Extensión Forestal Andino Patagónico (CIEFAP), 9200 Esquel, Chubut, Argentina. mvelez@ciefap.org.ar.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Greslebin</LastName><ForeName>Alina</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>CONICET-Facultad de Ciencias Naturales, Universidad Nacional de la Patagonia, 9200 Esquel, Chubut, Argentina. agreslebin@unpata.edu.ar.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Schmeda-Hirschmann</LastName><ForeName>Guillermo</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>Laboratorio de Química de Productos Naturales, Instituto de Química de Recursos Naturales, Universidad de Talca, Casilla 747, 3460000 Talca, Chile. schmeda@utalca.cl.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2015</Year><Month>08</Month><Day>18</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Molecules</MedlineTA><NlmUniqueID>100964009</NlmUniqueID><ISSNLinking>1420-3049</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000935">Antifungal Agents</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D004224">Diterpenes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012117">Resins, Synthetic</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000935" MajorTopicYN="N">Antifungal Agents</DescriptorName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002855" MajorTopicYN="N">Chromatography, Thin Layer</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D029779" MajorTopicYN="N">Cupressaceae</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004224" MajorTopicYN="N">Diterpenes</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="Y">analysis</QualifierName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008401" MajorTopicYN="N">Gas Chromatography-Mass Spectrometry</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010838" MajorTopicYN="N">Phytophthora</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D066244" MajorTopicYN="N">Proton Magnetic Resonance Spectroscopy</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012117" MajorTopicYN="N">Resins, Synthetic</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Austrocedrus chilensis</Keyword><Keyword MajorTopicYN="N">Cupressaceae</Keyword><Keyword MajorTopicYN="N">Phytophthora austrocedri</Keyword><Keyword MajorTopicYN="N">resin diterpenes</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2015</Year><Month>06</Month><Day>24</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2015</Year><Month>06</Month><Day>24</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2015</Year><Month>08</Month><Day>08</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2015</Year><Month>8</Month><Day>22</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2015</Year><Month>8</Month><Day>22</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2016</Year><Month>6</Month><Day>1</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">26295220</ArticleId><ArticleId IdType="pii">molecules200815084</ArticleId><ArticleId IdType="doi">10.3390/molecules200815084</ArticleId><ArticleId IdType="pmc">PMC6332227</ArticleId></ArticleIdList><ReferenceList><Reference><Citation>Trends Plant Sci. 1999 May;4(5):184-190</Citation><ArticleIdList><ArticleId IdType="pubmed">10322558</ArticleId></ArticleIdList></Reference><Reference><Citation>Plant Physiol. 2002 Jul;129(3):1003-18</Citation><ArticleIdList><ArticleId IdType="pubmed">12114556</ArticleId></ArticleIdList></Reference><Reference><Citation>J Mass Spectrom. 2004 Nov;39(11):1337-47</Citation><ArticleIdList><ArticleId 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uniqKey="Velez M" first="María Laura" last="Vélez">María Laura Vélez</name></noRegion><name sortKey="Greslebin, Alina" sort="Greslebin, Alina" uniqKey="Greslebin A" first="Alina" last="Greslebin">Alina Greslebin</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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