Distribution and organoleptic impact of sotolon enantiomers in dry white wines

被引:42
作者
Pons, Alexandre [1 ,3 ]
Lavigne, Valerie [1 ,3 ]
Landais, Yannick [2 ]
Darriet, Philippe [3 ]
Dubourdieu, Denis [3 ]
机构
[1] Seguin Moreau France, F-16103 Cognac, France
[2] Univ Bordeaux 1, Inst Mol Sci, CNRS, UMR 5255, F-33405 Talence, France
[3] Univ Bordeaux 2, Inst Sci Vigne & Vin, F-33405 Talence, France
关键词
sotolon; enantiomers; wine; racemization; chiral GC;
D O I
10.1021/jf072337r
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The enantiomers of sotolon, a flavor compound typical of oxidized white wines, were separated by preparative HPLC to determine their perception thresholds and distribution in wines. The enantiomeric ratios of chiral sotolon were evaluated in several dry white wines using gas chromatography and a chiral column (beta-cyclodextrin). connected to a 2 m precolumn (BP20). The perception threshold of (S)-sotolon (0.8 mu g/L) in model wine solution was 100 times lower than that of the (R) form (89 mu g/L), indicating that (S)-sotolon contributes to the characteristic aroma of prematurely aged dry white wines. Both enantiomers; are detected in white wines. Analysis of commercial dry white wines from various vintages and origins revealed three types of distribution patterns: the racemic form, an excess of R, and an excess of S. The proportions found in these wines may be partially explained by the slow racemization kinetics (20 months) of optically active sotolon.
引用
收藏
页码:1606 / 1610
页数:5
相关论文
共 27 条
[1]   Formation of 3-hydroxy-4,5-dimethyl-2(5H)-furanone (sotolone) from 4-hydroxy-L-isoleucine and 3-amino-4,5-dimethyl-3,4-dihydro-2(5H)-furanone [J].
Blank, I ;
Lin, JM ;
Fumeaux, R ;
Welti, DH ;
Fay, LB .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1996, 44 (07) :1851-1856
[2]   Enantioselective perception of chiral odorants [J].
Brenna, E ;
Fuganti, C ;
Serra, S .
TETRAHEDRON-ASYMMETRY, 2003, 14 (01) :1-42
[3]   TAUTOMERISM OF THE MONOHYDROXY DERIVATIVES OF 5-MEMBERED O, N, AND S HETEROCYCLES [J].
CAPON, B ;
KWOK, FC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (14) :5346-5356
[4]  
Cutzach Isabelle, 1998, Journal International des Sciences de la Vigne et du Vin, V32, P223
[5]   Stability of sotolon in acidic and basic aqueous solutions - Application to the synthesis of a deuterated analogue for its quantitative determination in wine [J].
Dagan, L ;
Schneider, R ;
Lepoutre, JP ;
Baumes, R .
ANALYTICA CHIMICA ACTA, 2006, 563 (1-2) :365-374
[6]  
DUBOIS P, 1976, LEBENSM WISS TECHNOL, V9, P366
[7]   Controlled racemization of optically active organic compounds: Prospects for asymmetric transformation [J].
Ebbers, EJ ;
Ariaans, GJA ;
Houbiers, JPM ;
Bruggink, A ;
Zwanenburg, B .
TETRAHEDRON, 1997, 53 (28) :9417-9476
[8]  
Eliel E.L., 1994, Stereochemistry of Organic Compounds
[9]   Isolation and identification of odorants generated in wine during its oxidation: a gas chromatography-olfactometric study [J].
Escudero, A ;
Cacho, J ;
Ferreira, V .
EUROPEAN FOOD RESEARCH AND TECHNOLOGY, 2000, 211 (02) :105-110
[10]   3-hydroxy-4,5-dimethyl-2(5H)-furanone:: A key odorant of the typical aroma of oxidative aged Port wine [J].
Ferreira, ACS ;
Barbe, JC ;
Bertrand, A .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2003, 51 (15) :4356-4363