Preparative isolation of anthocyanins by high-speed countercurrent chromatography and application of the color activity concept to red wine

Citation
A. Degenhardt et al., Preparative isolation of anthocyanins by high-speed countercurrent chromatography and application of the color activity concept to red wine, J AGR FOOD, 48(12), 2000, pp. 5812-5818
Citations number
30
Categorie Soggetti
Agricultural Chemistry","Chemistry & Analysis
Journal title
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
ISSN journal
00218561 → ACNP
Volume
48
Issue
12
Year of publication
2000
Pages
5812 - 5818
Database
ISI
SICI code
0021-8561(200012)48:12<5812:PIOABH>2.0.ZU;2-A
Abstract
Red pigments were isolated from wine and grape-skin extracts using preparat ive high-speed countercurrent chromatography (HSCCC) and identified by NMR and MS techniques. Four solvent systems were developed in order to separate anthocyanins with different polarities. Malvidin-3-glucoside was the major component present in young red wines, and up to 500 mg of pure malvidin-3- glucoside could be obtained from a single bottle of a red wine. Other isola ted pigments were the malvidin- and peonidin-3,5-diglucosides, as well as a cetyl-, coumaroyl-, and caffeoyl-derivatives of anthocyanins. Furthermore, condensed red wine pigments formed from malvidin-3-glueoside (vitisin A and acetylvitisin A) were isolated on a preparative scale. Isolated compounds were used as standards for quantification of anthocyanius in a range of red wines. The "color activity concept" was applied to red wine, and visual de tection thresholds were determined far some of the isolated anthocyanins. M ono-glucosides were found to exhibit lower visual detection thresholds than diglucosides and acylated anthocyanins.