Kinetics of 3-Deoxy-D-Erythro-Hexos-2-Ulose in Unifloral Honeys

被引:8
作者
Arena, Elena [1 ]
Ballistreri, Gabriele [1 ]
Fallico, Biagio [1 ]
机构
[1] Univ Catania, Dipartimento GeSA, I-95123 Catania, Italy
关键词
1,2-dicarbonyl compounds; 3-deoxyglucosulose synthesis; 5-hydroxymethylfurfural; honey; safety; ALPHA-DICARBONYL COMPOUNDS; MAILLARD REACTION; SOY-SAUCE; FUROSINE; HMF; MODEL; 3-DEOXYGLUCOSONE; MELANOIDINS; PRODUCTS; ASSAYS;
D O I
10.1111/j.1750-3841.2011.02329.x
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In this study, for the first time, the amount of 3-deoxy-d-erythro-hexos-2-ulose (3-DG) in fresh citrus and chestnut honeys was determined. 3-DG was measured as the corresponding quinoxalines after derivatization with orthophenylenediamine using reverse-phase high-performance liquid chromatography (RP-HPLC). Notwithstanding the freshness of the samples, high levels of 3-DG were detected in both honeys. The comparison of 3-DG and 5-hydroxymethylfurfural (HMF) concentrations, which was also quantified by RP-HPLC, showed that citrus honeys had the lowest amount of 3-DG (107 mg/kg) and the highest of HMF (16.7 mg/kg), while chestnut honeys had the opposite (398 and 1.2 mg/kg, respectively). During thermal treatment, different 3-DG and HMF trends were highlighted between the citrus and chestnut honeys; at the end, 3-DG formation was more favored with respect to HMF formation. Moreover, in citrus honeys, a good correlation between 3-DG and HMF levels was observed, which was not found in chestnut honeys, suggesting a role of the high pH values of these honeys on the degradation routes. The kinetic analysis showed the highest k value for 3-DG and HMF formation in chestnut and citrus honeys, respectively. The lowest Ea values related to 3-DG formation and the highest to HMF formation, indicating that the key intermediate 3-DG is easily formed at low temperatures, whilst the formation of HMF requires higher temperatures. For this reason, 3-DG seems to be an aging index rather than a thermal index and its use, at least for honeys at high pH values, together with HMF, could improve their quality assessment.
引用
收藏
页码:C1044 / C1049
页数:6
相关论文
共 42 条
[1]  
ALLEN BH, 1980, J ASSOC OFF ANA CHEM, V63, P1074
[2]  
[Anonymous], 2002, OFFICIAL J EUROPEAN
[3]  
*AOAC, 1980, OFF METH AN
[4]   Thermal damage in blood orange juice: kinetics of 5-hydroxymethyl-2-furancarboxaldehyde formation [J].
Arena, E ;
Fallico, B ;
Maccarone, E .
INTERNATIONAL JOURNAL OF FOOD SCIENCE AND TECHNOLOGY, 2001, 36 (02) :145-151
[5]  
ARENA E, 2010, J FOOD SCI UNPUB
[6]  
Belitz H.-D., 2009, Food Chemistry, V4th, P374
[7]   Standardization of antioxidant properties of honey by a combination of spectrophotometric/fluorimetric assays and chemometrics [J].
Beretta, G ;
Granata, P ;
Ferrero, M ;
Orioli, M ;
Facino, RM .
ANALYTICA CHIMICA ACTA, 2005, 533 (02) :185-191
[8]   Formation of α-dicarbonyl compounds in beer during storage of Pilsner [J].
Bravo, Adriana ;
Herrera, Julio C. ;
Scherer, Erika ;
Ju-Nam, Yon ;
Ruebsam, Heinrich ;
Madrid, Jorge ;
Zufall, Carsten ;
Rangel-Aldao, Rafael .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2008, 56 (11) :4134-4144
[9]   Determination of furosine in honey [J].
Cárdenas-Ruiz, J ;
García-Villanova, B ;
Guerra-Hernández, E .
JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 2003, 26 (02) :317-326
[10]  
*CODEX, 121981 CODEX STAN, P1