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Aroma extraction dilution analysis of Sauternes wines. Key role of polyfunctional thiols.
J Agric Food Chem. 2006 Sep 20; 54(19):7227-34.JA

Abstract

The aim of the present work was to investigate Sauternes wine aromas. In all wine extracts, polyfunctional thiols were revealed to have a huge impact. A very strong bacon-petroleum odor emerged at RI = 845 from a CP-Sil5-CB column. Two thiols proved to participate in this perception: 3-methyl-3-sulfanylbutanal and 2-methylfuran-3-thiol. A strong synergetic effect was evidenced between the two compounds. The former, never mentioned before in wines, and not found in the musts of this study, is most probably synthesized during fermentation. 3-Methylbut-2-ene-1-thiol, 3-sulfanylpropyl acetate, 3-sulfanylhexan-1-ol, and 3-sulfanylheptanal also contribute to the global aromas of Sauternes wines. Among other key odorants, the presence of a varietal aroma (alpha-terpineol), sotolon, fermentation alcohols (3-methylbutan-1-ol and 2-phenylethanol) and esters (ethyl butyrate, ethyl hexanoate, and ethyl isovalerate), carbonyls (trans-non-2-enal and beta-damascenone), and wood flavors (guaiacol, vanillin, eugenol, beta-methyl-gamma-octalactone, and Furaneol) is worth stressing.

Authors+Show Affiliations

Unité de Brasserie et des Industries Alimentaires, Faculté d'Ingénierie Biologique, Agronomique et Environnementale, Université catholique de Louvain, Croix du Sud, 2 bte 7, B-1348 Louvain-la-Neuve, Belgium.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

16968087

Citation

Bailly, Sabine, et al. "Aroma Extraction Dilution Analysis of Sauternes Wines. Key Role of Polyfunctional Thiols." Journal of Agricultural and Food Chemistry, vol. 54, no. 19, 2006, pp. 7227-34.
Bailly S, Jerkovic V, Marchand-Brynaert J, et al. Aroma extraction dilution analysis of Sauternes wines. Key role of polyfunctional thiols. J Agric Food Chem. 2006;54(19):7227-34.
Bailly, S., Jerkovic, V., Marchand-Brynaert, J., & Collin, S. (2006). Aroma extraction dilution analysis of Sauternes wines. Key role of polyfunctional thiols. Journal of Agricultural and Food Chemistry, 54(19), 7227-34.
Bailly S, et al. Aroma Extraction Dilution Analysis of Sauternes Wines. Key Role of Polyfunctional Thiols. J Agric Food Chem. 2006 Sep 20;54(19):7227-34. PubMed PMID: 16968087.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Aroma extraction dilution analysis of Sauternes wines. Key role of polyfunctional thiols. AU - Bailly,Sabine, AU - Jerkovic,Vesna, AU - Marchand-Brynaert,Jacqueline, AU - Collin,Sonia, PY - 2006/9/14/pubmed PY - 2006/11/3/medline PY - 2006/9/14/entrez SP - 7227 EP - 34 JF - Journal of agricultural and food chemistry JO - J Agric Food Chem VL - 54 IS - 19 N2 - The aim of the present work was to investigate Sauternes wine aromas. In all wine extracts, polyfunctional thiols were revealed to have a huge impact. A very strong bacon-petroleum odor emerged at RI = 845 from a CP-Sil5-CB column. Two thiols proved to participate in this perception: 3-methyl-3-sulfanylbutanal and 2-methylfuran-3-thiol. A strong synergetic effect was evidenced between the two compounds. The former, never mentioned before in wines, and not found in the musts of this study, is most probably synthesized during fermentation. 3-Methylbut-2-ene-1-thiol, 3-sulfanylpropyl acetate, 3-sulfanylhexan-1-ol, and 3-sulfanylheptanal also contribute to the global aromas of Sauternes wines. Among other key odorants, the presence of a varietal aroma (alpha-terpineol), sotolon, fermentation alcohols (3-methylbutan-1-ol and 2-phenylethanol) and esters (ethyl butyrate, ethyl hexanoate, and ethyl isovalerate), carbonyls (trans-non-2-enal and beta-damascenone), and wood flavors (guaiacol, vanillin, eugenol, beta-methyl-gamma-octalactone, and Furaneol) is worth stressing. SN - 0021-8561 UR - https://www.unboundmedicine.com/medline/citation/16968087/Aroma_extraction_dilution_analysis_of_Sauternes_wines__Key_role_of_polyfunctional_thiols_ L2 - https://doi.org/10.1021/jf060814k DB - PRIME DP - Unbound Medicine ER -