Cy. Tai et Ct. Ho, INFLUENCE OF CYSTEINE OXIDATION ON THERMAL FORMATION OF MAILLARD AROMAS, Journal of agricultural and food chemistry, 45(9), 1997, pp. 3586-3589
Cysteic acid and cysteinesulfinic acid, which are oxidized forms of re
duced cysteine, were heated separately with D-glucose in an aqueous sy
stem of pH 6 at 160 degrees C for 2 h. The reaction products were extr
acted and analyzed. Among the identified compounds, pyrazines and fura
ns are the most predominant compounds and no or only trace amounts of
sulfur-containing compounds were identified in these two reaction syst
ems. In the same reaction condition, the reduced cysteine and D-glucos
e produced mainly sulfur-containing compounds; no pyrazines were found
in this system. The reaction mass of cysteic acid and D-glucose posse
ssed smoky, nutty, and yeasty aromas, while cysteinesulfinic acid with
D-glucose generated a strong coffee note. The reduced cysteine with g
lucose produced onion and garlic, as well as slightly meaty and sulfur
y, flavors.