TY - JOUR
T1 - Identification of key aroma compounds generated from cysteine and carbohydrates under roasting conditions
AU - Hofmann, T.
AU - Schieberle, P.
PY - 1998
Y1 - 1998
N2 - Application of the aroma extract dilution analysis to volatile fractions obtained from dry-heated (180°C for 6 min on silica) mixtures of cysteine and ribose (I), glucose (II) or rhamnose (III) revealed the following compounds with the highest flavour dilution factors: 2-furfurylthiol (FFT) and 2-acetyl-2-thiazoline in I; 2-acetyl-2-thiazoline, 2-propionyl-2-thiazoline and FFT in II; 5-methyl-2-furfurylthiol, 4-hydroxy-2,5-dimethyl-3(2H)-furanone, 2-acetyl-2-thiazoline, 2-propionyl-2-thiazoline and (Z)-2-propenyl-3,5- dimethylpyrazine in III. A comparison of the data with results of previous studies, in which the same mixtures had been reacted under aqueous conditions (145°C, 20 min) revealed that the dry-heating process favoured the formation of the roasty, popcorn-like smelling 2-acetyl- and 2-propionyl-2-thiazoline as well as the potato-chip-like 2-ethyl-3,5-dimethylpyrazine and 2,3-diethyl-5-methylpyrazine in all three reaction systems. 2-Ethenyl- and (Z)-2-propenyl-3,5-dimethylpyrazine, both having an intense roast potato smell were, however, selectively formed in the presence of ribose or rhamnose, respectively. Based on quantitative data, pathways generating the latter two pyrazines via their 1-desoxyosones as key intermediates are discussed.
AB - Application of the aroma extract dilution analysis to volatile fractions obtained from dry-heated (180°C for 6 min on silica) mixtures of cysteine and ribose (I), glucose (II) or rhamnose (III) revealed the following compounds with the highest flavour dilution factors: 2-furfurylthiol (FFT) and 2-acetyl-2-thiazoline in I; 2-acetyl-2-thiazoline, 2-propionyl-2-thiazoline and FFT in II; 5-methyl-2-furfurylthiol, 4-hydroxy-2,5-dimethyl-3(2H)-furanone, 2-acetyl-2-thiazoline, 2-propionyl-2-thiazoline and (Z)-2-propenyl-3,5- dimethylpyrazine in III. A comparison of the data with results of previous studies, in which the same mixtures had been reacted under aqueous conditions (145°C, 20 min) revealed that the dry-heating process favoured the formation of the roasty, popcorn-like smelling 2-acetyl- and 2-propionyl-2-thiazoline as well as the potato-chip-like 2-ethyl-3,5-dimethylpyrazine and 2,3-diethyl-5-methylpyrazine in all three reaction systems. 2-Ethenyl- and (Z)-2-propenyl-3,5-dimethylpyrazine, both having an intense roast potato smell were, however, selectively formed in the presence of ribose or rhamnose, respectively. Based on quantitative data, pathways generating the latter two pyrazines via their 1-desoxyosones as key intermediates are discussed.
KW - (Z)-2-propenyl-3,5-dimethylpyrazine
KW - Aroma extract dilution analysis
KW - Cysteine
KW - Flavour
KW - Maillard reaction
UR - https://www.scopus.com/pages/publications/54749143937
U2 - 10.1007/s002170050324
DO - 10.1007/s002170050324
M3 - Article
AN - SCOPUS:54749143937
SN - 1438-2377
VL - 207
SP - 229
EP - 236
JO - European Food Research and Technology
JF - European Food Research and Technology
IS - 3
ER -