TY - JOUR
T1 - Identification of characteristic aroma components of Thai fried chili paste
AU - Rotsatchakul, Premsiri
AU - Chaiseri, Siree
AU - Cadwallader, Keith R.
N1 - Funding Information:
The bibliographic research accomplished by Caria Vinals has greatly helped the documentation of this work. We appreciate friendly and useful comments of Steve Sprang and Bob Flettenck. We would like to thank Biosym Technologies. San Diego, where an important part of this work has been achieved. We are indebted to Arme Hagier, Don McKay and Judy Hempel who improved an original cliques-finding algorithm and Eva Meirovitch and Rick Lee for their scientific collaboration. This work has been partially supported by a grant of the Belgian Fonds National de la Recherche Scientifique (FNRS) Source programs (Fortran 77) may be obtained on request by electronic mail at: EDEPIER-EUX@BNANDP51 .BITNET.
PY - 2008/1/23
Y1 - 2008/1/23
N2 - Three forms of Thai fried chili pastes (CP) were prepared, consisting of an unheated CP (UH-CP), a CP heated at 100°C for 25 min (H25-CP, typical product), and a CP excessively heated for 50 min (H50-CP). The potent odorants in the CPs were investigated by two gas chromatography-olfactometry methods: dynamic headspace dilution analysis (DHDA) and aroma extract dilution analysis (AEDA). DHDA revealed that the predominant odorants in heated CPs were mainly sulfur-containing compounds, followed by lipid-derived compounds, Strecker aldehydes, and Maillard reaction products. Dimethyl sulfide, allyl mercaptan, 2- (or 3-) methylbutanal, ally methyl sulfide, 2,3-butanedione, 3,3′-thiobis(1-propene), and methyl propyl disulfide were among the most potent headspace odorants detected by DHDA. By AEDA, 2-vinyl-4H-1,3-dithiin and diallyl trisulfide had the highest FD factors in H25-CP. On the basis of their high FD factors by both GCO methods, the predominant odorants in H25-CP were 3-vinyl-4H-1,2-dithiin, allyl methyl disulfide, and allyl methyl trisulfide. Furthermore, dimethyl trisulfide and diallyl disulfide had the highest odor activity values in H25-CP, suggesting that these were also potent odorants in CP. In addition, methional, 3-methylbutanoic acid, 4-hydroxy-2,5-dimethyl-3-(2H) -furanone, and 3-hydroxy-4,5-dimethyl-2(5H)-furanone (sotolon) were indicated as potent thermally derived odorants of H25-CP.
AB - Three forms of Thai fried chili pastes (CP) were prepared, consisting of an unheated CP (UH-CP), a CP heated at 100°C for 25 min (H25-CP, typical product), and a CP excessively heated for 50 min (H50-CP). The potent odorants in the CPs were investigated by two gas chromatography-olfactometry methods: dynamic headspace dilution analysis (DHDA) and aroma extract dilution analysis (AEDA). DHDA revealed that the predominant odorants in heated CPs were mainly sulfur-containing compounds, followed by lipid-derived compounds, Strecker aldehydes, and Maillard reaction products. Dimethyl sulfide, allyl mercaptan, 2- (or 3-) methylbutanal, ally methyl sulfide, 2,3-butanedione, 3,3′-thiobis(1-propene), and methyl propyl disulfide were among the most potent headspace odorants detected by DHDA. By AEDA, 2-vinyl-4H-1,3-dithiin and diallyl trisulfide had the highest FD factors in H25-CP. On the basis of their high FD factors by both GCO methods, the predominant odorants in H25-CP were 3-vinyl-4H-1,2-dithiin, allyl methyl disulfide, and allyl methyl trisulfide. Furthermore, dimethyl trisulfide and diallyl disulfide had the highest odor activity values in H25-CP, suggesting that these were also potent odorants in CP. In addition, methional, 3-methylbutanoic acid, 4-hydroxy-2,5-dimethyl-3-(2H) -furanone, and 3-hydroxy-4,5-dimethyl-2(5H)-furanone (sotolon) were indicated as potent thermally derived odorants of H25-CP.
KW - Aroma extract dilution analysis
KW - Aroma-active
KW - Dynamic headspace dilution analysis
KW - Gas chromatography-olfactometry
KW - Odorant
KW - Thai fried chili paste (nam phrikphao)
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U2 - 10.1021/jf072499n
DO - 10.1021/jf072499n
M3 - Article
C2 - 18163558
AN - SCOPUS:38949155842
SN - 0021-8561
VL - 56
SP - 528
EP - 536
JO - Journal of Agricultural and Food Chemistry
JF - Journal of Agricultural and Food Chemistry
IS - 2
ER -