Accumulation of apocarotenoids in mycorrhizal roots of Ornithogalum umbellatum.
Identifieur interne : 003238 ( Main/Corpus ); précédent : 003237; suivant : 003239Accumulation of apocarotenoids in mycorrhizal roots of Ornithogalum umbellatum.
Auteurs : Willibald Schliemann ; Jürgen Schmidt ; Manfred Nimtz ; Victor Wray ; Thomas Fester ; Dieter StrackSource :
- Phytochemistry [ 0031-9422 ] ; 2006.
English descriptors
- KwdEn :
- Carotenoids (biosynthesis), Cyclohexanones (chemistry), Cyclohexanones (metabolism), Kinetics (MeSH), Magnetic Resonance Spectroscopy (MeSH), Mass Spectrometry (MeSH), Molecular Structure (MeSH), Mycorrhizae (chemistry), Mycorrhizae (metabolism), Ornithogalum (chemistry), Ornithogalum (metabolism), Pigments, Biological (biosynthesis), Plant Roots (chemistry), Plant Roots (metabolism), Plant Roots (microbiology).
- MESH :
- chemical , biosynthesis : Carotenoids, Pigments, Biological.
- chemical , chemistry : Cyclohexanones.
- chemical , metabolism : Cyclohexanones.
- chemistry : Mycorrhizae, Ornithogalum, Plant Roots.
- metabolism : Mycorrhizae, Ornithogalum, Plant Roots.
- microbiology : Plant Roots.
- Kinetics, Magnetic Resonance Spectroscopy, Mass Spectrometry, Molecular Structure.
Abstract
Colonization of roots of Ornithogalum umbellatum by the arbuscular mycorrhizal fungus Glomus intraradices induced the accumulation of different types of apocarotenoids. In addition to the mycorrhiza-specific occurrence of cyclohexenone derivatives and the "yellow pigment" described earlier, free mycorradicin and numerous mycorradicin derivatives were detected in a complex apocarotenoid mixture for the first time. From the accumulation pattern of the mycorradicin derivatives their possible integration into the continuously accumulating "yellow pigment" is suggested. Structure analyses of the cyclohexenone derivatives by MS and NMR revealed that they are mono-, di- and branched triglycosides of blumenol C, 13-hydroxyblumenol C, and 13-nor-5-carboxy-blumenol C, some of which contain terminal rhamnose as sugar moiety.
DOI: 10.1016/j.phytochem.2006.05.005
PubMed: 16790253
Links to Exploration step
pubmed:16790253Le document en format XML
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In addition to the mycorrhiza-specific occurrence of cyclohexenone derivatives and the "yellow pigment" described earlier, free mycorradicin and numerous mycorradicin derivatives were detected in a complex apocarotenoid mixture for the first time. From the accumulation pattern of the mycorradicin derivatives their possible integration into the continuously accumulating "yellow pigment" is suggested. Structure analyses of the cyclohexenone derivatives by MS and NMR revealed that they are mono-, di- and branched triglycosides of blumenol C, 13-hydroxyblumenol C, and 13-nor-5-carboxy-blumenol C, some of which contain terminal rhamnose as sugar moiety.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">16790253</PMID><DateCompleted><Year>2006</Year><Month>11</Month><Day>09</Day></DateCompleted><DateRevised><Year>2006</Year><Month>11</Month><Day>17</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0031-9422</ISSN><JournalIssue CitedMedium="Print"><Volume>67</Volume><Issue>12</Issue><PubDate><Year>2006</Year><Month>Jun</Month></PubDate></JournalIssue><Title>Phytochemistry</Title><ISOAbbreviation>Phytochemistry</ISOAbbreviation></Journal><ArticleTitle>Accumulation of apocarotenoids in mycorrhizal roots of Ornithogalum umbellatum.</ArticleTitle><Pagination><MedlinePgn>1196-205</MedlinePgn></Pagination><Abstract><AbstractText>Colonization of roots of Ornithogalum umbellatum by the arbuscular mycorrhizal fungus Glomus intraradices induced the accumulation of different types of apocarotenoids. In addition to the mycorrhiza-specific occurrence of cyclohexenone derivatives and the "yellow pigment" described earlier, free mycorradicin and numerous mycorradicin derivatives were detected in a complex apocarotenoid mixture for the first time. From the accumulation pattern of the mycorradicin derivatives their possible integration into the continuously accumulating "yellow pigment" is suggested. Structure analyses of the cyclohexenone derivatives by MS and NMR revealed that they are mono-, di- and branched triglycosides of blumenol C, 13-hydroxyblumenol C, and 13-nor-5-carboxy-blumenol C, some of which contain terminal rhamnose as sugar moiety.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Schliemann</LastName><ForeName>Willibald</ForeName><Initials>W</Initials><AffiliationInfo><Affiliation>Department of Secondary Metabolism, Leibniz Institute of Plant Biochemistry, Weinberg 3, D-06120 Halle (Saale), Germany. willibald.schliemann@ipb-halle.de</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Schmidt</LastName><ForeName>Jürgen</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Nimtz</LastName><ForeName>Manfred</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Wray</LastName><ForeName>Victor</ForeName><Initials>V</Initials></Author><Author 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RefType="ErratumIn"><RefSource>Phytochemistry. 2006 Sep;67(18):2090</RefSource></CommentsCorrections></CommentsCorrectionsList><MeshHeadingList><MeshHeading><DescriptorName UI="D002338" MajorTopicYN="N">Carotenoids</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="Y">biosynthesis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003512" MajorTopicYN="N">Cyclohexanones</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007700" MajorTopicYN="N">Kinetics</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009682" MajorTopicYN="N">Magnetic Resonance Spectroscopy</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013058" MajorTopicYN="N">Mass Spectrometry</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015394" MajorTopicYN="N">Molecular 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MajorTopicYN="Y">microbiology</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2006</Year><Month>03</Month><Day>22</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2006</Year><Month>05</Month><Day>04</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2006</Year><Month>05</Month><Day>05</Day></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2006</Year><Month>6</Month><Day>23</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2006</Year><Month>11</Month><Day>11</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2006</Year><Month>6</Month><Day>23</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">16790253</ArticleId><ArticleId IdType="pii">S0031-9422(06)00237-8</ArticleId><ArticleId 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