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pubmed-article:11052755rdf:typepubmed:Citationlld:pubmed
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pubmed-article:11052755pubmed:abstractTextIn extracts prepared from various fruits as well as in fruit juices a single tryptophan glycoconjugate was detected by HPLC-MS analysis. Product ion spectra demonstrated the N-glycosidic linkage of a hexose moiety to the indole nitrogen. For structure elucidation, the novel tryptophan glycoside was isolated from pear juice and identified as N(1)-(beta-D-glucopyranosyl-(4)C(1))-L-tryptophan by (1)H, HH-COSY and (13)C NMR spectroscopy. Finally, we disclosed the biosynthetic origin of the novel tryptophan metabolite by demonstrating the enzymatic glycosylation of deuterium-labeled tryptophan, which was applied to pear fruit.lld:pubmed
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pubmed-article:11052755pubmed:issn0021-8561lld:pubmed
pubmed-article:11052755pubmed:authorpubmed-author:DietJJlld:pubmed
pubmed-article:11052755pubmed:authorpubmed-author:BergmannJJlld:pubmed
pubmed-article:11052755pubmed:authorpubmed-author:HerderichMMlld:pubmed
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pubmed-article:11052755pubmed:volume48lld:pubmed
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pubmed-article:11052755pubmed:pagination4913-7lld:pubmed
pubmed-article:11052755pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:11052755pubmed:year2000lld:pubmed
pubmed-article:11052755pubmed:articleTitleTryptophan-N-glucoside in fruits and fruit juices.lld:pubmed
pubmed-article:11052755pubmed:affiliationLehrstuhl für Lebensmittelchemie, Universität Würzburg, Am Hubland, 97074 Würzburg, Germany.lld:pubmed
pubmed-article:11052755pubmed:publicationTypeJournal Articlelld:pubmed