Contribution of mozambioside roasting products to coffee's bitter taste

Roasting degrades the coffee compound mozambioside (1) into several products, including 17-O-β-D-glucosyl-11-hydroxycafestol-2-one (2), 11-O-β-D-glucosyl-16-desoxycafestol-2-one (3), 11-O-β-D-glucosyl-(S)-16-desoxy-17-oxocafestol-2-one (4), 11-O-β-D-glucosyl-15,16-dehydrocafestol-2-one (5), 11-O-β-D-glucosyl-(R)-16-desoxy-17-oxocafestol-2-one (6), bengalensol (7), and 11-hydroxycafestol-2-one (8). A UHPLC-MS/MS method was established to quantify 1-8 and monitor their formation during authentic coffee roasting. Concentrations of 1 and the dominant roasting products 4, 5, and 7 ranged from 21.0 to 170.4 nmol/g in coffee powders, with ∼41-128 % extracted into the brew. Human bitter taste thresholds of 1, 2, and 4-8 were determined. The major roasting products exhibited lower thresholds (27-80 μM) than 1 (132 μM). Genotyping of panelists revealed a correlation between sensitivity for mozambioside-derivatives and the presence of intact TAS2R43 gene loci. The combination of 1-8 in coffee concentrations elicited a bitter taste recognized in 80 % of the panelists, suggesting this compound class contributes to coffee's taste profile.

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Publication Details

Journal
Food Chemistry
Published
2024-12-18
DOI
https://doi.org/10.1016/j.foodchem.2024.142547
Citations
7
Primary Topic
Coffee research and impacts
Type
article
Field-Weighted Citation Impact
3.13
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article

Contribution of mozambioside roasting products to coffee's bitter taste

Maik Behrens, Roman Lang, Sonja Maria Fröhlich, Angelika Graßl et al.
7 citations
Food Chemistry
Coffee research and impacts
3.13
article

Contribution of mozambioside roasting products to coffee's bitter taste

Maik Behrens, Roman Lang, Sonja Maria Fröhlich, Angelika Graßl, Coline Bichlmaier, Valeria Brychcy
article en
7 citations

Abstract

Roasting degrades the coffee compound mozambioside (1) into several products, including 17-O-β-D-glucosyl-11-hydroxycafestol-2-one (2), 11-O-β-D-glucosyl-16-desoxycafestol-2-one (3), 11-O-β-D-glucosyl-(S)-16-desoxy-17-oxocafestol-2-one (4), 11-O-β-D-glucosyl-15,16-dehydrocafestol-2-one (5), 11-O-β-D-glucosyl-(R)-16-desoxy-17-oxocafestol-2-one (6), bengalensol (7), and 11-hydroxycafestol-2-one (8). A UHPLC-MS/MS method was established to quantify 1-8 and monitor their formation during authentic coffee roasting. Concentrations of 1 and the dominant roasting products 4, 5, and 7 ranged from 21.0 to 170.4 nmol/g in coffee powders, with ∼41-128 % extracted into the brew. Human bitter taste thresholds of 1, 2, and 4-8 were determined. The major roasting products exhibited lower thresholds (27-80 μM) than 1 (132 μM). Genotyping of panelists revealed a correlation between sensitivity for mozambioside-derivatives and the presence of intact TAS2R43 gene loci. The combination of 1-8 in coffee concentrations elicited a bitter taste recognized in 80 % of the panelists, suggesting this compound class contributes to coffee's taste profile.

Food ChemistryVol. 469
Leibniz-Institute for Food Systems Biology at the Technical University of Munich (DE), Technical University of Munich (DE)
Zero hunger
Openalex Percentile: Top 8%
Coffee research and impacts
3.13
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