Serveur d'exploration sur les maladies des plantes grimpantes

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Epoxynemanione A, nemanifuranones A-F, and nemanilactones A-C, from Nemania serpens, an endophytic fungus isolated from Riesling grapevines.

Identifieur interne : 000330 ( Main/Exploration ); précédent : 000329; suivant : 000331

Epoxynemanione A, nemanifuranones A-F, and nemanilactones A-C, from Nemania serpens, an endophytic fungus isolated from Riesling grapevines.

Auteurs : Ashraf Ibrahim [Canada] ; Dan S Rensen [Canada] ; Hilary A. Jenkins [Canada] ; Linda Ejim [Canada] ; Alfredo Capretta [Canada] ; Mark W. Sumarah [Canada]

Source :

RBID : pubmed:28441516

Descripteurs français

English descriptors

Abstract

Ten polyketide specialized metabolites, epoxynemanione A, nemanifuranones A-F, and nemanilactones A-C, were isolated from the culture filtrate of Nemania serpens (Pers.) Grey (1821), an endophytic fungus from a Riesling grapevine (Vitis vinifera) found in Canada's Niagara region. Additionally, four known metabolites 2-(hydroxymethyl)-3-methoxy-benzoic acid, phyllostine, 5-methylmellein and a nordammarane triterpenoid were isolated. A related known metabolite 2,3-dihydro-2-hydroxy-2,4-dimethyl-5-trans-propenylfuran-3-one has also been included for structural and biological comparison to the nemanifuranones. The latter was isolated from the culture filtrates of Mollisia nigrescens, an endophytic fungus from the leaves and stems of lowbush blueberry (Vaccinium angustifolium) found in the Acadian forest of Nova Scotia, Canada. Their structures were elucidated based on 1D and 2D NMR, HRESIMS measurements, X-ray crystallographic analysis of nemanifuranone A, the nordammarane triterpenoid and 2,3-dihydro-2-hydroxy-2,4-dimethyl-5-trans-propenylfuran-3-one compounds, and comparison of NOE and vicinal 1H-1H coupling constants to literature data for relative stereochemical assignments. Nemanifuranone A possesses a rare C2 hemiacetal and was active against both Gram-negative and Gram-positive bacteria.

DOI: 10.1016/j.phytochem.2017.04.009
PubMed: 28441516


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Epoxynemanione A, nemanifuranones A-F, and nemanilactones A-C, from Nemania serpens, an endophytic fungus isolated from Riesling grapevines.</title>
<author>
<name sortKey="Ibrahim, Ashraf" sort="Ibrahim, Ashraf" uniqKey="Ibrahim A" first="Ashraf" last="Ibrahim">Ashraf Ibrahim</name>
<affiliation wicri:level="4">
<nlm:affiliation>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1</wicri:regionArea>
<orgName type="university">Université McMaster</orgName>
<placeName>
<settlement type="city">Hamilton (Ontario)</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="S Rensen, Dan" sort="S Rensen, Dan" uniqKey="S Rensen D" first="Dan" last="S Rensen">Dan S Rensen</name>
<affiliation wicri:level="4">
<nlm:affiliation>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1</wicri:regionArea>
<orgName type="university">Université McMaster</orgName>
<placeName>
<settlement type="city">Hamilton (Ontario)</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Jenkins, Hilary A" sort="Jenkins, Hilary A" uniqKey="Jenkins H" first="Hilary A" last="Jenkins">Hilary A. Jenkins</name>
<affiliation wicri:level="4">
<nlm:affiliation>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1</wicri:regionArea>
<orgName type="university">Université McMaster</orgName>
<placeName>
<settlement type="city">Hamilton (Ontario)</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Ejim, Linda" sort="Ejim, Linda" uniqKey="Ejim L" first="Linda" last="Ejim">Linda Ejim</name>
<affiliation wicri:level="4">
<nlm:affiliation>Department of Biochemistry and Biomedical Sciences, M.G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Biochemistry and Biomedical Sciences, M.G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, L8S 4M1</wicri:regionArea>
<orgName type="university">Université McMaster</orgName>
<placeName>
<settlement type="city">Hamilton (Ontario)</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Capretta, Alfredo" sort="Capretta, Alfredo" uniqKey="Capretta A" first="Alfredo" last="Capretta">Alfredo Capretta</name>
<affiliation wicri:level="4">
<nlm:affiliation>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1</wicri:regionArea>
<orgName type="university">Université McMaster</orgName>
<placeName>
<settlement type="city">Hamilton (Ontario)</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Sumarah, Mark W" sort="Sumarah, Mark W" uniqKey="Sumarah M" first="Mark W" last="Sumarah">Mark W. Sumarah</name>
<affiliation wicri:level="1">
<nlm:affiliation>London Research and Development Centre, Agriculture and Agri-Food Canada, London, Ontario, N5V 4T3, Canada. Electronic address: mark.sumarah@agr.gc.ca.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>London Research and Development Centre, Agriculture and Agri-Food Canada, London, Ontario, N5V 4T3</wicri:regionArea>
<wicri:noRegion>N5V 4T3</wicri:noRegion>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PubMed</idno>
<date when="2017">2017</date>
<idno type="RBID">pubmed:28441516</idno>
<idno type="pmid">28441516</idno>
<idno type="doi">10.1016/j.phytochem.2017.04.009</idno>
<idno type="wicri:Area/Main/Corpus">000317</idno>
<idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">000317</idno>
<idno type="wicri:Area/Main/Curation">000317</idno>
<idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Curation">000317</idno>
<idno type="wicri:Area/Main/Exploration">000317</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en">Epoxynemanione A, nemanifuranones A-F, and nemanilactones A-C, from Nemania serpens, an endophytic fungus isolated from Riesling grapevines.</title>
<author>
<name sortKey="Ibrahim, Ashraf" sort="Ibrahim, Ashraf" uniqKey="Ibrahim A" first="Ashraf" last="Ibrahim">Ashraf Ibrahim</name>
<affiliation wicri:level="4">
<nlm:affiliation>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1</wicri:regionArea>
<orgName type="university">Université McMaster</orgName>
<placeName>
<settlement type="city">Hamilton (Ontario)</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="S Rensen, Dan" sort="S Rensen, Dan" uniqKey="S Rensen D" first="Dan" last="S Rensen">Dan S Rensen</name>
<affiliation wicri:level="4">
<nlm:affiliation>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1</wicri:regionArea>
<orgName type="university">Université McMaster</orgName>
<placeName>
<settlement type="city">Hamilton (Ontario)</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Jenkins, Hilary A" sort="Jenkins, Hilary A" uniqKey="Jenkins H" first="Hilary A" last="Jenkins">Hilary A. Jenkins</name>
<affiliation wicri:level="4">
<nlm:affiliation>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1</wicri:regionArea>
<orgName type="university">Université McMaster</orgName>
<placeName>
<settlement type="city">Hamilton (Ontario)</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Ejim, Linda" sort="Ejim, Linda" uniqKey="Ejim L" first="Linda" last="Ejim">Linda Ejim</name>
<affiliation wicri:level="4">
<nlm:affiliation>Department of Biochemistry and Biomedical Sciences, M.G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Biochemistry and Biomedical Sciences, M.G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, L8S 4M1</wicri:regionArea>
<orgName type="university">Université McMaster</orgName>
<placeName>
<settlement type="city">Hamilton (Ontario)</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Capretta, Alfredo" sort="Capretta, Alfredo" uniqKey="Capretta A" first="Alfredo" last="Capretta">Alfredo Capretta</name>
<affiliation wicri:level="4">
<nlm:affiliation>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1</wicri:regionArea>
<orgName type="university">Université McMaster</orgName>
<placeName>
<settlement type="city">Hamilton (Ontario)</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Sumarah, Mark W" sort="Sumarah, Mark W" uniqKey="Sumarah M" first="Mark W" last="Sumarah">Mark W. Sumarah</name>
<affiliation wicri:level="1">
<nlm:affiliation>London Research and Development Centre, Agriculture and Agri-Food Canada, London, Ontario, N5V 4T3, Canada. Electronic address: mark.sumarah@agr.gc.ca.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>London Research and Development Centre, Agriculture and Agri-Food Canada, London, Ontario, N5V 4T3</wicri:regionArea>
<wicri:noRegion>N5V 4T3</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Phytochemistry</title>
<idno type="eISSN">1873-3700</idno>
<imprint>
<date when="2017" type="published">2017</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Anti-Bacterial Agents (chemistry)</term>
<term>Anti-Bacterial Agents (isolation & purification)</term>
<term>Antifungal Agents (chemistry)</term>
<term>Antifungal Agents (isolation & purification)</term>
<term>Canada (MeSH)</term>
<term>Endophytes (chemistry)</term>
<term>Microbial Sensitivity Tests (MeSH)</term>
<term>Molecular Structure (MeSH)</term>
<term>Plant Leaves (microbiology)</term>
<term>Plant Stems (microbiology)</term>
<term>Polyketides (chemistry)</term>
<term>Polyketides (isolation & purification)</term>
<term>Vitis (microbiology)</term>
<term>Xylariales (chemistry)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Antibactériens (composition chimique)</term>
<term>Antibactériens (isolement et purification)</term>
<term>Antifongiques (composition chimique)</term>
<term>Antifongiques (isolement et purification)</term>
<term>Canada (MeSH)</term>
<term>Endophytes (composition chimique)</term>
<term>Feuilles de plante (microbiologie)</term>
<term>Polycétides (composition chimique)</term>
<term>Polycétides (isolement et purification)</term>
<term>Structure moléculaire (MeSH)</term>
<term>Tests de sensibilité microbienne (MeSH)</term>
<term>Tiges de plante (microbiologie)</term>
<term>Vitis (microbiologie)</term>
<term>Xylariales (composition chimique)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en">
<term>Anti-Bacterial Agents</term>
<term>Antifungal Agents</term>
<term>Polyketides</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="isolation & purification" xml:lang="en">
<term>Anti-Bacterial Agents</term>
<term>Antifungal Agents</term>
<term>Polyketides</term>
</keywords>
<keywords scheme="MESH" qualifier="chemistry" xml:lang="en">
<term>Endophytes</term>
<term>Xylariales</term>
</keywords>
<keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr">
<term>Antibactériens</term>
<term>Antifongiques</term>
<term>Endophytes</term>
<term>Polycétides</term>
<term>Xylariales</term>
</keywords>
<keywords scheme="MESH" qualifier="isolement et purification" xml:lang="fr">
<term>Antibactériens</term>
<term>Antifongiques</term>
<term>Polycétides</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr">
<term>Feuilles de plante</term>
<term>Tiges de plante</term>
<term>Vitis</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en">
<term>Plant Leaves</term>
<term>Plant Stems</term>
<term>Vitis</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Canada</term>
<term>Microbial Sensitivity Tests</term>
<term>Molecular Structure</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Canada</term>
<term>Structure moléculaire</term>
<term>Tests de sensibilité microbienne</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Ten polyketide specialized metabolites, epoxynemanione A, nemanifuranones A-F, and nemanilactones A-C, were isolated from the culture filtrate of Nemania serpens (Pers.) Grey (1821), an endophytic fungus from a Riesling grapevine (Vitis vinifera) found in Canada's Niagara region. Additionally, four known metabolites 2-(hydroxymethyl)-3-methoxy-benzoic acid, phyllostine, 5-methylmellein and a nordammarane triterpenoid were isolated. A related known metabolite 2,3-dihydro-2-hydroxy-2,4-dimethyl-5-trans-propenylfuran-3-one has also been included for structural and biological comparison to the nemanifuranones. The latter was isolated from the culture filtrates of Mollisia nigrescens, an endophytic fungus from the leaves and stems of lowbush blueberry (Vaccinium angustifolium) found in the Acadian forest of Nova Scotia, Canada. Their structures were elucidated based on 1D and 2D NMR, HRESIMS measurements, X-ray crystallographic analysis of nemanifuranone A, the nordammarane triterpenoid and 2,3-dihydro-2-hydroxy-2,4-dimethyl-5-trans-propenylfuran-3-one compounds, and comparison of NOE and vicinal
<sup>1</sup>
H-
<sup>1</sup>
H coupling constants to literature data for relative stereochemical assignments. Nemanifuranone A possesses a rare C2 hemiacetal and was active against both Gram-negative and Gram-positive bacteria.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">28441516</PMID>
<DateCompleted>
<Year>2017</Year>
<Month>07</Month>
<Day>17</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>07</Month>
<Day>17</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1873-3700</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>140</Volume>
<PubDate>
<Year>2017</Year>
<Month>Aug</Month>
</PubDate>
</JournalIssue>
<Title>Phytochemistry</Title>
<ISOAbbreviation>Phytochemistry</ISOAbbreviation>
</Journal>
<ArticleTitle>Epoxynemanione A, nemanifuranones A-F, and nemanilactones A-C, from Nemania serpens, an endophytic fungus isolated from Riesling grapevines.</ArticleTitle>
<Pagination>
<MedlinePgn>16-26</MedlinePgn>
</Pagination>
<ELocationID EIdType="pii" ValidYN="Y">S0031-9422(17)30158-9</ELocationID>
<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.phytochem.2017.04.009</ELocationID>
<Abstract>
<AbstractText>Ten polyketide specialized metabolites, epoxynemanione A, nemanifuranones A-F, and nemanilactones A-C, were isolated from the culture filtrate of Nemania serpens (Pers.) Grey (1821), an endophytic fungus from a Riesling grapevine (Vitis vinifera) found in Canada's Niagara region. Additionally, four known metabolites 2-(hydroxymethyl)-3-methoxy-benzoic acid, phyllostine, 5-methylmellein and a nordammarane triterpenoid were isolated. A related known metabolite 2,3-dihydro-2-hydroxy-2,4-dimethyl-5-trans-propenylfuran-3-one has also been included for structural and biological comparison to the nemanifuranones. The latter was isolated from the culture filtrates of Mollisia nigrescens, an endophytic fungus from the leaves and stems of lowbush blueberry (Vaccinium angustifolium) found in the Acadian forest of Nova Scotia, Canada. Their structures were elucidated based on 1D and 2D NMR, HRESIMS measurements, X-ray crystallographic analysis of nemanifuranone A, the nordammarane triterpenoid and 2,3-dihydro-2-hydroxy-2,4-dimethyl-5-trans-propenylfuran-3-one compounds, and comparison of NOE and vicinal
<sup>1</sup>
H-
<sup>1</sup>
H coupling constants to literature data for relative stereochemical assignments. Nemanifuranone A possesses a rare C2 hemiacetal and was active against both Gram-negative and Gram-positive bacteria.</AbstractText>
<CopyrightInformation>Crown Copyright © 2017. Published by Elsevier Ltd. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Ibrahim</LastName>
<ForeName>Ashraf</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Sørensen</LastName>
<ForeName>Dan</ForeName>
<Initials>D</Initials>
<AffiliationInfo>
<Affiliation>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Jenkins</LastName>
<ForeName>Hilary A</ForeName>
<Initials>HA</Initials>
<AffiliationInfo>
<Affiliation>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Ejim</LastName>
<ForeName>Linda</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Department of Biochemistry and Biomedical Sciences, M.G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Capretta</LastName>
<ForeName>Alfredo</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Sumarah</LastName>
<ForeName>Mark W</ForeName>
<Initials>MW</Initials>
<AffiliationInfo>
<Affiliation>London Research and Development Centre, Agriculture and Agri-Food Canada, London, Ontario, N5V 4T3, Canada. Electronic address: mark.sumarah@agr.gc.ca.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2017</Year>
<Month>04</Month>
<Day>22</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>England</Country>
<MedlineTA>Phytochemistry</MedlineTA>
<NlmUniqueID>0151434</NlmUniqueID>
<ISSNLinking>0031-9422</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D000900">Anti-Bacterial Agents</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D000935">Antifungal Agents</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D061065">Polyketides</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000900" MajorTopicYN="N">Anti-Bacterial Agents</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000935" MajorTopicYN="N">Antifungal Agents</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D002170" MajorTopicYN="N">Canada</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D060026" MajorTopicYN="N">Endophytes</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008826" MajorTopicYN="N">Microbial Sensitivity Tests</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D015394" MajorTopicYN="N">Molecular Structure</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018515" MajorTopicYN="N">Plant Leaves</DescriptorName>
<QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018547" MajorTopicYN="N">Plant Stems</DescriptorName>
<QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D061065" MajorTopicYN="N">Polyketides</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D027843" MajorTopicYN="N">Vitis</DescriptorName>
<QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D013098" MajorTopicYN="N">Xylariales</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Antibiotic</Keyword>
<Keyword MajorTopicYN="N">Epoxynemanione</Keyword>
<Keyword MajorTopicYN="N">Fungal endophyte</Keyword>
<Keyword MajorTopicYN="N">Nemania serpens</Keyword>
<Keyword MajorTopicYN="N">Nemanifuranone</Keyword>
<Keyword MajorTopicYN="N">Nemanilactone</Keyword>
<Keyword MajorTopicYN="N">Specialized metabolites</Keyword>
<Keyword MajorTopicYN="N">Vitaceae</Keyword>
<Keyword MajorTopicYN="N">Vitis vinifera</Keyword>
<Keyword MajorTopicYN="N">Xylariaceae</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="received">
<Year>2016</Year>
<Month>08</Month>
<Day>24</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised">
<Year>2017</Year>
<Month>04</Month>
<Day>10</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted">
<Year>2017</Year>
<Month>04</Month>
<Day>12</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed">
<Year>2017</Year>
<Month>4</Month>
<Day>26</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2017</Year>
<Month>7</Month>
<Day>18</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2017</Year>
<Month>4</Month>
<Day>26</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">28441516</ArticleId>
<ArticleId IdType="pii">S0031-9422(17)30158-9</ArticleId>
<ArticleId IdType="doi">10.1016/j.phytochem.2017.04.009</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations>
<list>
<country>
<li>Canada</li>
</country>
<region>
<li>Ontario</li>
</region>
<settlement>
<li>Hamilton (Ontario)</li>
</settlement>
<orgName>
<li>Université McMaster</li>
</orgName>
</list>
<tree>
<country name="Canada">
<region name="Ontario">
<name sortKey="Ibrahim, Ashraf" sort="Ibrahim, Ashraf" uniqKey="Ibrahim A" first="Ashraf" last="Ibrahim">Ashraf Ibrahim</name>
</region>
<name sortKey="Capretta, Alfredo" sort="Capretta, Alfredo" uniqKey="Capretta A" first="Alfredo" last="Capretta">Alfredo Capretta</name>
<name sortKey="Ejim, Linda" sort="Ejim, Linda" uniqKey="Ejim L" first="Linda" last="Ejim">Linda Ejim</name>
<name sortKey="Jenkins, Hilary A" sort="Jenkins, Hilary A" uniqKey="Jenkins H" first="Hilary A" last="Jenkins">Hilary A. Jenkins</name>
<name sortKey="S Rensen, Dan" sort="S Rensen, Dan" uniqKey="S Rensen D" first="Dan" last="S Rensen">Dan S Rensen</name>
<name sortKey="Sumarah, Mark W" sort="Sumarah, Mark W" uniqKey="Sumarah M" first="Mark W" last="Sumarah">Mark W. Sumarah</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Bois/explor/GrapevineDiseaseV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000330 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000330 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Bois
   |area=    GrapevineDiseaseV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     pubmed:28441516
   |texte=   Epoxynemanione A, nemanifuranones A-F, and nemanilactones A-C, from Nemania serpens, an endophytic fungus isolated from Riesling grapevines.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i   -Sk "pubmed:28441516" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd   \
       | NlmPubMed2Wicri -a GrapevineDiseaseV1 

Wicri

This area was generated with Dilib version V0.6.37.
Data generation: Wed Nov 18 16:11:34 2020. Site generation: Wed Nov 18 16:12:50 2020