4.6 Article

Characterization of phenolic profile in dried grape skin of Vitis vinifera L. cv. Pinot Blanc with UHPLC-MS/MS and its development during ripening

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jfca.2022.104731

关键词

Flavonolglycosides; Myricetinglycosides; Massspectrometry; Chemotaxonomicalclassification; Metabolomics; Grapepomace

资金

  1. European Regional Development Fund [FESR1010, CUPH32F16000410009]

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This study reports the comprehensive phenolic composition of dried grape skin from cv. Pinot Blanc and its development during ripening, with a focus on flavonol glycosides profile. The extraction procedure and UHPLC-QqQ-MS/MS method were optimized and validated for the determination of 39 phenolic compounds belonging to different groups. The major flavonol component was found to be quercetin-3-O-rutinoside, and rutinosides for kaempferol and isorhamnetin structures were also quantifiable. Various myricetin derivatives were identified, with myricetin-3-O-glucoside being quantifiable at all ripening time points. The dihydroquercetins profile was highly complex, and the ratio between caftaric and coutaric acid and between isomers of coutaric acid at harvest was uncommon compared to other white cultivars.
Comprehensive phenolic composition of dried grape skin from cv. Pinot Blanc and its development during ripening is reported, with particular emphasis on flavonol glycosides profile. Extraction procedure and reversed -phase ultra-high-performance liquid chromatography-triple quadrupole mass spectrometry (UHPLC-QqQ-MS/ MS) method were optimized and validated for the determination of 39 phenolic compounds belonging to different groups (flavonols, dihydroflavonols, benzoic and hydroxycinnamic acids, flavan-3-ols). Beside selected reaction monitoring (SRM) for analytes available as standards, flavonols and dihydroflavonols profile was fur-therly explored performing precursor ion scan (PIS) with neutral loss (NL) for unavailable compounds. Quer-cetin-3-O-rutinoside occurred as major flavonol component, and rutinosides for kaempferol-and isorhamnetin-structures were also quantitable. Presence of different myricetin derivatives was unveiled, with myricetin-3-O- glucoside being quantifiable at all ripening time points. Besides high levels of astilbin, dihydroquercetins profile resulted highly complex. Moreover, ratio between caftaric and coutaric acid and between isomers of coutaric acid at harvest was uncommon if compared to other white cultivars.

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