The fermentations, at a commercial winery, of six different grape musts encompassing the varieties Riesling, Chardonnay, Sauvignon blanc, Shiraz, Grenache, and Pinot noir were monitored for damascenone concentration. In every case, the concentration of damascenone increased during fermentation from low or undetectable levels to concentrations of several parts per billion. Further increases in damascenone concentration were observed during barrel aging of three of these wines. Two ketones, megastigma-4,6,7-triene-3,9-dione (4) and 3-hydroxymegastigma-4,6,7-trien-9-one (5), were synthesized and subjected to fermentation conditions using two yeasts, AWRI 796, and AWRI 1537. In the case of the former compound, 4, synthesis confirmed the original, tentative assignment of the structure and confirmed 4 as a natural product, isolated from honey. Both compounds, under the action of both yeasts, produced appreciable amounts of damascenone (1), with ketone 5 and AWRI 796 yeast yielding the highest concentration of 1. © 2011 American Chemical Society.

Formation of damascenone under both commercial and model fermentation conditions

Ugliano, Maurizio;
2011-01-01

Abstract

The fermentations, at a commercial winery, of six different grape musts encompassing the varieties Riesling, Chardonnay, Sauvignon blanc, Shiraz, Grenache, and Pinot noir were monitored for damascenone concentration. In every case, the concentration of damascenone increased during fermentation from low or undetectable levels to concentrations of several parts per billion. Further increases in damascenone concentration were observed during barrel aging of three of these wines. Two ketones, megastigma-4,6,7-triene-3,9-dione (4) and 3-hydroxymegastigma-4,6,7-trien-9-one (5), were synthesized and subjected to fermentation conditions using two yeasts, AWRI 796, and AWRI 1537. In the case of the former compound, 4, synthesis confirmed the original, tentative assignment of the structure and confirmed 4 as a natural product, isolated from honey. Both compounds, under the action of both yeasts, produced appreciable amounts of damascenone (1), with ketone 5 and AWRI 796 yeast yielding the highest concentration of 1. © 2011 American Chemical Society.
2011
commercial; Damascenone; grasshopper ketone; honey; norisoprenoids; reductase; Saccharomyces cerevisiae, Concentration (process); Fermentation; Food products; Ketones; Organic compounds; Wine, Yeast, alkene; cyclohexane derivative; damascenone; ketone, article; chemistry; fermentation; fruit; grape; metabolism; microbiology; odor; Saccharomyces cerevisiae; wine, Alkenes; Cyclohexanes; Fermentation; Fruit; Ketones; Odors; Saccharomyces cerevisiae; Vitis; Wine, Saccharomyces cerevisiae; Vitaceae; commercial; Damascenone; fermentations; grasshopper ketone; honey; norisoprenoids; reductase; Saccharomyces cerevisiae
File in questo prodotto:
File Dimensione Formato  
Lloyd et al.pdf

solo utenti autorizzati

Tipologia: Documento in Post-print
Licenza: Accesso ristretto
Dimensione 895.44 kB
Formato Adobe PDF
895.44 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/929321
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 31
  • ???jsp.display-item.citation.isi??? 28
social impact