PoplarV1, Main, Exploration, bibRecord, 003362

Biosynthesis of phenolic glycosides from phenylpropanoid and benzenoid precursors in populus.

Identifieur interne : 003362 ( Main/Exploration ); précédent : 003361; suivant : 003363

Biosynthesis of phenolic glycosides from phenylpropanoid and benzenoid precursors in populus.

Auteurs : Benjamin A. Babst [États-Unis] ; Scott A. Harding ; Chung-Jui Tsai

Source :

Journal of chemical ecology [ 1573-1561 ] ; 2010.

RBID : pubmed:20177744

Descripteurs français

KwdFr :
- Acide benzoïque (composition chimique), Acide benzoïque (pharmacologie), Alcools benzyliques (composition chimique), Alcools benzyliques (métabolisme), Aldéhydes (composition chimique), Aldéhydes (pharmacologie), Animaux (MeSH), Benzaldéhydes (composition chimique), Benzaldéhydes (pharmacologie), Glucosides (biosynthèse), Glucosides (composition chimique), Hétérosides (biosynthèse), Isotopes du carbone (métabolisme), Populus (métabolisme), Salicylates (composition chimique), Salicylates (pharmacologie).
MESH :
- biosynthèse : Glucosides, Hétérosides.
- composition chimique : Acide benzoïque, Alcools benzyliques, Aldéhydes, Benzaldéhydes, Glucosides, Salicylates.
- métabolisme : Alcools benzyliques, Isotopes du carbone, Populus.
- pharmacologie : Acide benzoïque, Aldéhydes, Benzaldéhydes, Salicylates.
- Animaux.

English descriptors

KwdEn :
- Aldehydes (chemistry), Aldehydes (pharmacology), Animals (MeSH), Benzaldehydes (chemistry), Benzaldehydes (pharmacology), Benzoic Acid (chemistry), Benzoic Acid (pharmacology), Benzyl Alcohols (chemistry), Benzyl Alcohols (metabolism), Carbon Isotopes (metabolism), Glucosides (biosynthesis), Glucosides (chemistry), Glycosides (biosynthesis), Populus (metabolism), Salicylates (chemistry), Salicylates (pharmacology).
MESH :
- chemical , biosynthesis : Glucosides, Glycosides.
- chemical , chemistry : Aldehydes, Benzaldehydes, Benzoic Acid, Benzyl Alcohols, Glucosides, Salicylates.
- chemical , metabolism : Benzyl Alcohols, Carbon Isotopes.
- chemical , pharmacology : Aldehydes, Benzaldehydes, Benzoic Acid, Salicylates.
- metabolism : Populus.
- Animals.

Abstract

Salicylate-containing phenolic glycosides (PGs) are abundant and often play a dominant role in plant-herbivore interactions of Populus and Salix species (family Salicaceae), but the biosynthetic pathway to PGs remains unclear. Cinnamic acid (CA) is thought to be a precursor of the salicyl moiety of PGs. However, the origin of the 6-hydroxy-2-cyclohexen-on-oyl (HCH) moiety found in certain PGs, such as salicortin, is not known. HCH is of interest because it confers toxicity and antifeedant properties against herbivores. We incubated Populus nigra leaf tissue with stable isotope-labeled CA, benzoates, and salicylates, and measured isotopic incorporation levels into both salicin, the simplest PG, and salicortin. Labeling of salicortin from [13C6]-CA provided the first evidence that HCH, like the salicyl moiety, is a phenylpropanoid derivative. Benzoic acid and benzaldehyde also labeled both salicyl and HCH, while benzyl alcohol labeled only the salicyl moiety in salicortin. Co-administration of unlabeled benzoates with [13C6]-CA confirmed their contribution to the biosynthesis of the salicyl but not the HCH moiety of salicortin. These data suggest that benzoate interconversions may modulate partitioning of phenylpropanoids to salicyl and HCH moieties, and hence toxicity of PGs. Surprisingly, labeled salicyl alcohol and salicylaldehyde were readily converted to salicin, but did not result in labeled salicortin. Co-administration of unlabeled salicylates with labeled CA suggested that salicyl alcohol and salicylaldehyde may have inhibited salicortin biosynthesis. A revised metabolic grid model of PG biosynthesis in Populus is proposed, providing a guide for functional genomic analysis of the PG biosynthetic pathway.

DOI: 10.1007/s10886-010-9757-7
PubMed: 20177744

Affiliations:

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

to stream Main, to step Corpus: 003294
to stream Main, to step Curation: 003294

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Biosynthesis of phenolic glycosides from phenylpropanoid and benzenoid precursors in populus.</title>
<author><name sortKey="Babst, Benjamin A" sort="Babst, Benjamin A" uniqKey="Babst B" first="Benjamin A" last="Babst">Benjamin A. Babst</name>
<affiliation wicri:level="2"><nlm:affiliation>School of Forest Resources and Environmental Science, Michigan Technological University, Houghton, MI 49931, USA. benbabst@uga.edu</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>School of Forest Resources and Environmental Science, Michigan Technological University, Houghton, MI 49931</wicri:regionArea>
<placeName><region type="state">Michigan</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Harding, Scott A" sort="Harding, Scott A" uniqKey="Harding S" first="Scott A" last="Harding">Scott A. Harding</name>
</author>
<author><name sortKey="Tsai, Chung Jui" sort="Tsai, Chung Jui" uniqKey="Tsai C" first="Chung-Jui" last="Tsai">Chung-Jui Tsai</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2010">2010</date>
<idno type="RBID">pubmed:20177744</idno>
<idno type="pmid">20177744</idno>
<idno type="doi">10.1007/s10886-010-9757-7</idno>
<idno type="wicri:Area/Main/Corpus">003294</idno>
<idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">003294</idno>
<idno type="wicri:Area/Main/Curation">003294</idno>
<idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Curation">003294</idno>
<idno type="wicri:Area/Main/Exploration">003294</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Biosynthesis of phenolic glycosides from phenylpropanoid and benzenoid precursors in populus.</title>
<author><name sortKey="Babst, Benjamin A" sort="Babst, Benjamin A" uniqKey="Babst B" first="Benjamin A" last="Babst">Benjamin A. Babst</name>
<affiliation wicri:level="2"><nlm:affiliation>School of Forest Resources and Environmental Science, Michigan Technological University, Houghton, MI 49931, USA. benbabst@uga.edu</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>School of Forest Resources and Environmental Science, Michigan Technological University, Houghton, MI 49931</wicri:regionArea>
<placeName><region type="state">Michigan</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Harding, Scott A" sort="Harding, Scott A" uniqKey="Harding S" first="Scott A" last="Harding">Scott A. Harding</name>
</author>
<author><name sortKey="Tsai, Chung Jui" sort="Tsai, Chung Jui" uniqKey="Tsai C" first="Chung-Jui" last="Tsai">Chung-Jui Tsai</name>
</author>
</analytic>
<series><title level="j">Journal of chemical ecology</title>
<idno type="eISSN">1573-1561</idno>
<imprint><date when="2010" type="published">2010</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aldehydes (chemistry)</term>
<term>Aldehydes (pharmacology)</term>
<term>Animals (MeSH)</term>
<term>Benzaldehydes (chemistry)</term>
<term>Benzaldehydes (pharmacology)</term>
<term>Benzoic Acid (chemistry)</term>
<term>Benzoic Acid (pharmacology)</term>
<term>Benzyl Alcohols (chemistry)</term>
<term>Benzyl Alcohols (metabolism)</term>
<term>Carbon Isotopes (metabolism)</term>
<term>Glucosides (biosynthesis)</term>
<term>Glucosides (chemistry)</term>
<term>Glycosides (biosynthesis)</term>
<term>Populus (metabolism)</term>
<term>Salicylates (chemistry)</term>
<term>Salicylates (pharmacology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Acide benzoïque (composition chimique)</term>
<term>Acide benzoïque (pharmacologie)</term>
<term>Alcools benzyliques (composition chimique)</term>
<term>Alcools benzyliques (métabolisme)</term>
<term>Aldéhydes (composition chimique)</term>
<term>Aldéhydes (pharmacologie)</term>
<term>Animaux (MeSH)</term>
<term>Benzaldéhydes (composition chimique)</term>
<term>Benzaldéhydes (pharmacologie)</term>
<term>Glucosides (biosynthèse)</term>
<term>Glucosides (composition chimique)</term>
<term>Hétérosides (biosynthèse)</term>
<term>Isotopes du carbone (métabolisme)</term>
<term>Populus (métabolisme)</term>
<term>Salicylates (composition chimique)</term>
<term>Salicylates (pharmacologie)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Glucosides</term>
<term>Glycosides</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Aldehydes</term>
<term>Benzaldehydes</term>
<term>Benzoic Acid</term>
<term>Benzyl Alcohols</term>
<term>Glucosides</term>
<term>Salicylates</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Benzyl Alcohols</term>
<term>Carbon Isotopes</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Aldehydes</term>
<term>Benzaldehydes</term>
<term>Benzoic Acid</term>
<term>Salicylates</term>
</keywords>
<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>Glucosides</term>
<term>Hétérosides</term>
</keywords>
<keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr"><term>Acide benzoïque</term>
<term>Alcools benzyliques</term>
<term>Aldéhydes</term>
<term>Benzaldéhydes</term>
<term>Glucosides</term>
<term>Salicylates</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Populus</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Alcools benzyliques</term>
<term>Isotopes du carbone</term>
<term>Populus</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Acide benzoïque</term>
<term>Aldéhydes</term>
<term>Benzaldéhydes</term>
<term>Salicylates</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Animaux</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Salicylate-containing phenolic glycosides (PGs) are abundant and often play a dominant role in plant-herbivore interactions of Populus and Salix species (family Salicaceae), but the biosynthetic pathway to PGs remains unclear. Cinnamic acid (CA) is thought to be a precursor of the salicyl moiety of PGs. However, the origin of the 6-hydroxy-2-cyclohexen-on-oyl (HCH) moiety found in certain PGs, such as salicortin, is not known. HCH is of interest because it confers toxicity and antifeedant properties against herbivores. We incubated Populus nigra leaf tissue with stable isotope-labeled CA, benzoates, and salicylates, and measured isotopic incorporation levels into both salicin, the simplest PG, and salicortin. Labeling of salicortin from [13C6]-CA provided the first evidence that HCH, like the salicyl moiety, is a phenylpropanoid derivative. Benzoic acid and benzaldehyde also labeled both salicyl and HCH, while benzyl alcohol labeled only the salicyl moiety in salicortin. Co-administration of unlabeled benzoates with [13C6]-CA confirmed their contribution to the biosynthesis of the salicyl but not the HCH moiety of salicortin. These data suggest that benzoate interconversions may modulate partitioning of phenylpropanoids to salicyl and HCH moieties, and hence toxicity of PGs. Surprisingly, labeled salicyl alcohol and salicylaldehyde were readily converted to salicin, but did not result in labeled salicortin. Co-administration of unlabeled salicylates with labeled CA suggested that salicyl alcohol and salicylaldehyde may have inhibited salicortin biosynthesis. A revised metabolic grid model of PG biosynthesis in Populus is proposed, providing a guide for functional genomic analysis of the PG biosynthetic pathway.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">20177744</PMID>
<DateCompleted><Year>2010</Year>
<Month>06</Month>
<Day>03</Day>
</DateCompleted>
<DateRevised><Year>2018</Year>
<Month>11</Month>
<Day>13</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1573-1561</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>36</Volume>
<Issue>3</Issue>
<PubDate><Year>2010</Year>
<Month>Mar</Month>
</PubDate>
</JournalIssue>
<Title>Journal of chemical ecology</Title>
<ISOAbbreviation>J Chem Ecol</ISOAbbreviation>
</Journal>
<ArticleTitle>Biosynthesis of phenolic glycosides from phenylpropanoid and benzenoid precursors in populus.</ArticleTitle>
<Pagination><MedlinePgn>286-97</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1007/s10886-010-9757-7</ELocationID>
<Abstract><AbstractText>Salicylate-containing phenolic glycosides (PGs) are abundant and often play a dominant role in plant-herbivore interactions of Populus and Salix species (family Salicaceae), but the biosynthetic pathway to PGs remains unclear. Cinnamic acid (CA) is thought to be a precursor of the salicyl moiety of PGs. However, the origin of the 6-hydroxy-2-cyclohexen-on-oyl (HCH) moiety found in certain PGs, such as salicortin, is not known. HCH is of interest because it confers toxicity and antifeedant properties against herbivores. We incubated Populus nigra leaf tissue with stable isotope-labeled CA, benzoates, and salicylates, and measured isotopic incorporation levels into both salicin, the simplest PG, and salicortin. Labeling of salicortin from [13C6]-CA provided the first evidence that HCH, like the salicyl moiety, is a phenylpropanoid derivative. Benzoic acid and benzaldehyde also labeled both salicyl and HCH, while benzyl alcohol labeled only the salicyl moiety in salicortin. Co-administration of unlabeled benzoates with [13C6]-CA confirmed their contribution to the biosynthesis of the salicyl but not the HCH moiety of salicortin. These data suggest that benzoate interconversions may modulate partitioning of phenylpropanoids to salicyl and HCH moieties, and hence toxicity of PGs. Surprisingly, labeled salicyl alcohol and salicylaldehyde were readily converted to salicin, but did not result in labeled salicortin. Co-administration of unlabeled salicylates with labeled CA suggested that salicyl alcohol and salicylaldehyde may have inhibited salicortin biosynthesis. A revised metabolic grid model of PG biosynthesis in Populus is proposed, providing a guide for functional genomic analysis of the PG biosynthetic pathway.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Babst</LastName>
<ForeName>Benjamin A</ForeName>
<Initials>BA</Initials>
<AffiliationInfo><Affiliation>School of Forest Resources and Environmental Science, Michigan Technological University, Houghton, MI 49931, USA. benbabst@uga.edu</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Harding</LastName>
<ForeName>Scott A</ForeName>
<Initials>SA</Initials>
</Author>
<Author ValidYN="Y"><LastName>Tsai</LastName>
<ForeName>Chung-Jui</ForeName>
<Initials>CJ</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013486">Research Support, U.S. Gov't, Non-P.H.S.</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2010</Year>
<Month>02</Month>
<Day>23</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>J Chem Ecol</MedlineTA>
<NlmUniqueID>7505563</NlmUniqueID>
<ISSNLinking>0098-0331</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D000447">Aldehydes</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D001547">Benzaldehydes</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D001592">Benzyl Alcohols</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D002247">Carbon Isotopes</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D005960">Glucosides</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D006027">Glycosides</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D012459">Salicylates</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>17K64GZH20</RegistryNumber>
<NameOfSubstance UI="C013243">salicylaldehyde</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>4649620TBZ</RegistryNumber>
<NameOfSubstance UI="C005696">salicin</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>8SKN0B0MIM</RegistryNumber>
<NameOfSubstance UI="D019817">Benzoic Acid</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>TA269SD04T</RegistryNumber>
<NameOfSubstance UI="C032175">benzaldehyde</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>YI29948E0Q</RegistryNumber>
<NameOfSubstance UI="C113068">salicortin</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000447" MajorTopicYN="N">Aldehydes</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D001547" MajorTopicYN="N">Benzaldehydes</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D019817" MajorTopicYN="N">Benzoic Acid</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D001592" MajorTopicYN="N">Benzyl Alcohols</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002247" MajorTopicYN="N">Carbon Isotopes</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005960" MajorTopicYN="N">Glucosides</DescriptorName>
<QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006027" MajorTopicYN="N">Glycosides</DescriptorName>
<QualifierName UI="Q000096" MajorTopicYN="Y">biosynthesis</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D032107" MajorTopicYN="N">Populus</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012459" MajorTopicYN="N">Salicylates</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2009</Year>
<Month>12</Month>
<Day>01</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2010</Year>
<Month>02</Month>
<Day>02</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised"><Year>2010</Year>
<Month>02</Month>
<Day>01</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>2010</Year>
<Month>2</Month>
<Day>24</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2010</Year>
<Month>2</Month>
<Day>24</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2010</Year>
<Month>6</Month>
<Day>4</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">20177744</ArticleId>
<ArticleId IdType="doi">10.1007/s10886-010-9757-7</ArticleId>
</ArticleIdList>
<ReferenceList><Reference><Citation>New Phytol. 2006;172(1):47-62</Citation>
<ArticleIdList><ArticleId IdType="pubmed">16945088</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Phytochemistry. 2007 Aug;68(15):2043-52</Citation>
<ArticleIdList><ArticleId IdType="pubmed">17599371</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Annu Rev Plant Biol. 2004;55:85-107</Citation>
<ArticleIdList><ArticleId IdType="pubmed">15725058</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Chem Ecol. 1984 Mar;10(3):499-520</Citation>
<ArticleIdList><ArticleId IdType="pubmed">24318555</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Physiol. 2004 Aug;135(4):1993-2011</Citation>
<ArticleIdList><ArticleId IdType="pubmed">15286288</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Phytochem Anal. 2005 Nov-Dec;16(6):470-8</Citation>
<ArticleIdList><ArticleId IdType="pubmed">16315493</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Chem Ecol. 2003 May;29(5):1083-97</Citation>
<ArticleIdList><ArticleId IdType="pubmed">12857023</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Chem Ecol. 2003 Jul;29(7):1565-88</Citation>
<ArticleIdList><ArticleId IdType="pubmed">12921436</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Oecologia. 1997 Jun;111(1):99-108</Citation>
<ArticleIdList><ArticleId IdType="pubmed">28307511</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Trends Plant Sci. 2000 Sep;5(9):380-6</Citation>
<ArticleIdList><ArticleId IdType="pubmed">10973093</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Chem Ecol. 2001 Aug;27(8):1595-615</Citation>
<ArticleIdList><ArticleId IdType="pubmed">11521399</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>New Phytol. 2006;169(3):561-70</Citation>
<ArticleIdList><ArticleId IdType="pubmed">16411958</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Planta. 2000 Dec;212(1):119-26</Citation>
<ArticleIdList><ArticleId IdType="pubmed">11219576</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Chem Ecol. 2001 Jul;27(7):1289-313</Citation>
<ArticleIdList><ArticleId IdType="pubmed">11504029</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Science. 2006 Sep 15;313(5793):1596-604</Citation>
<ArticleIdList><ArticleId IdType="pubmed">16973872</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Cell. 2006 Dec;18(12):3458-75</Citation>
<ArticleIdList><ArticleId IdType="pubmed">17194766</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant J. 2009 Jul;59(2):256-65</Citation>
<ArticleIdList><ArticleId IdType="pubmed">19292760</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
</PubmedData>
</pubmed>
<affiliations><list><country><li>États-Unis</li>
</country>
<region><li>Michigan</li>
</region>
</list>
<tree><noCountry><name sortKey="Harding, Scott A" sort="Harding, Scott A" uniqKey="Harding S" first="Scott A" last="Harding">Scott A. Harding</name>
<name sortKey="Tsai, Chung Jui" sort="Tsai, Chung Jui" uniqKey="Tsai C" first="Chung-Jui" last="Tsai">Chung-Jui Tsai</name>
</noCountry>
<country name="États-Unis"><region name="Michigan"><name sortKey="Babst, Benjamin A" sort="Babst, Benjamin A" uniqKey="Babst B" first="Benjamin A" last="Babst">Benjamin A. Babst</name>
</region>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Bois/explor/PoplarV1/Data/Main/Exploration

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003362 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 003362 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Bois
   |area=    PoplarV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     pubmed:20177744
   |texte=   Biosynthesis of phenolic glycosides from phenylpropanoid and benzenoid precursors in populus.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i   -Sk "pubmed:20177744" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd   \
       | NlmPubMed2Wicri -a PoplarV1

This area was generated with Dilib version V0.6.37.
Data generation: Wed Nov 18 12:07:19 2020. Site generation: Wed Nov 18 12:16:31 2020

	Serveur d'exploration sur le peuplier
	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.

Serveur d'exploration sur le peuplier

Biosynthesis of phenolic glycosides from phenylpropanoid and benzenoid precursors in populus.

Biosynthesis of phenolic glycosides from phenylpropanoid and benzenoid precursors in populus.

Source :

Descripteurs français

English descriptors

Abstract

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

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki