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dc.rights.licenseopenen_US
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorCRETIN, Blandine N
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorSALLEMBIEN, Quentin
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorSINDT, Lauriane
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorDAUGEY, Nicolas
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorBUFFETEAU, Thierry
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorWAFFO TEGUO, Pierre
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorDUBOURDIEU, Denis
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorMARCHAL, Axel
dc.date.accessioned2020-10-19T10:19:39Z
dc.date.available2020-10-19T10:19:39Z
dc.date.issued2015-08-12
dc.identifier.issn1873-4324en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/11418
dc.description.abstractEnWine expresses its beauty by sending a sensory message to the taster through molecules coming from grapes, yeast metabolism or oak wood. Among the compounds released during barrel aging, lyoniresinol has been recently reported as a relevant contributor to wine bitterness. As this lignan contains three stereogenic carbons, this work aimed at investigating the influence of stereochemistry on wine taste by combining analytical and sensorial techniques. First, an oak wood extract was screened by Liquid Chromatography-High Resolution Mass Spectrometry to target isomers separable in a symmetric environment and a diastereoisomer called epi-lyoniresinol was isolated for the first time. Then, an original racemic resolution based on natural xylose-derivatives was carried out to obtain lyoniresinol enantiomers. Chiroptical spectroscopic measurements associated with theoretical calculations allowed the unambiguous determination of their absolute configuration. The taste properties of all these stereoisomers revealed that only one lyoniresinol enantiomer is strongly bitter whereas the other one is tasteless and the diastereoisomer is slightly sweet. The presence of these three compounds was established in an oaked Bordeaux wine by chiral and non-chiral chromatography, suggesting the significant influence of stereochemistry on wine taste.
dc.language.isoENen_US
dc.subject.enBitterness
dc.subject.enChiral Liquid Chromatography–High Resolution Mass Spectrometry
dc.subject.enCounter Current Chromatography
dc.subject.enLignan
dc.subject.enOak wood
dc.subject.enVibrational circular dichroism
dc.subject.enAnisoles
dc.subject.enChromatography Liquid
dc.subject.enCountercurrent Distribution
dc.subject.enHumans
dc.subject.enMass Spectrometry
dc.subject.enNaphthalenes
dc.subject.enPlant Extracts
dc.subject.enQuercus
dc.subject.enStereoisomerism
dc.subject.enTaste
dc.subject.enTaste Perception
dc.subject.enWine
dc.subject.enWood
dc.title.enHow stereochemistry influences the taste of wine: Isolation, characterization and sensory evaluation of lyoniresinol stereoisomers.
dc.title.alternativeAnal Chim Actaen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.aca.2015.06.061en_US
dc.subject.halSciences du Vivant [q-bio]/Biologie végétaleen_US
dc.identifier.pubmed26320975en_US
bordeaux.journalAnalytica Chimica Actaen_US
bordeaux.page191-8en_US
bordeaux.volume888en_US
bordeaux.hal.laboratoriesOenologie - EA 4577en_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.exportfalse
workflow.import.sourcepubmed
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