Investigations on the formation of α-dicarbonyl compounds and 5-hydroxymethylfurfural in apple juice, orange juice and peach puree under industrial processing conditions

被引:0
作者
Işıl Gürsul Aktağ
Vural Gökmen
机构
[1] Hacettepe University,Food Quality and Safety Research Group, Department of Food Engineering
来源
European Food Research and Technology | 2021年 / 247卷
关键词
α-Dicarbonyl compounds; 5-Hydroxymethylfurfural; Fruit process; Apple juice concentrate; Orange juice; Peach puree concentrate;
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学科分类号
摘要
The formation of α-dicarbonyl compounds and 5-hydroxymethylfurfural during industrial processing of apple juice, orange juice, and peach puree samples was investigated in this study. Changes in the concentrations of sugars, free amino acids, α-dicarbonyl compounds, and 5-hydroxymethylfurfural in the samples from the critical process stages such as pasteurization, enzyme treatment, concentration, were monitored. The concentrations of sugars and free amino acids showed no statistically significant change during processing. 3-deoxyglucosone was identified as the dominant dicarbonyl compound formed during orange juice and peach puree processes, while glucosone was the main one formed in apple juice samples at all sampling points. In general, total dicarbonyl compounds significantly increased (p < 0.05) in apple juice, orange juice, and peach puree samples during processing, varied between 2.04 and 28.09 mg/L, 9.16 and 31.2 mg/L, and 8.9 and 48.31 mg/kg, respectively. The concentration of 5-hydroxymethylfurfural was found to be low in apple and orange samples and not detected in peach puree samples. The presence of molecular oxygen, the temperature and the duration of the process were determined as the remarkable processing parameters that affect the formation of α-dicarbonyl compounds.
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页码:797 / 805
页数:8
相关论文
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[1]  
Babsky NE(1986)Influence of storage on the composition of clarified apple juice concentrate J Food Sci 51 564-567
[2]  
Toribio JL(1994)Caramelisation in food and beverages Food Chem 51 373-379
[3]  
Lozano JE(2020)Multiresponse kinetic modelling of alpha-dicarbonyl compounds formation in fruit juices during storage Food Chem 320 126620-369
[4]  
Kroh LW(1994)Chemistry of amadori rearrangement products: analysis, synthesis, kinetics, reactions, and spectroscopic properties Crit Rev Food Sci Nutr 34 321-401
[5]  
Gursul Aktag I(1998)Reactive intermediates and carbohydrate fragmentation in Maillard chemistry Food Chem 62 393-6723
[6]  
Gokmen V(2008)Isotope labeling studies on the formation of 5-(hydroxymethyl)-2-furaldehyde (HMF) from sucrose by pyrolysis-GC/MS J Agric Food Chem 56 6717-1084
[7]  
Yaylayan VA(2007)Dietary advanced glycation endproducts (AGEs) and their health effects—PRO MolNutr Food Res 51 1079-902
[8]  
Huyghues-Despointes A(2016)Multiresponse kinetic modelling of Maillard reaction and caramelisation in a heated glucose/wheat flour system Food Chem 211 892-7720
[9]  
Weenen H(2014)Investigation of α-dicarbonyl compounds in baby foods by high-performance liquid chromatography coupled with electrospray ionization mass spectrometry J Agric Food Chem 62 7714-68
[10]  
Locas CP(2019)Lactose hydrolysis and protein fortification pose an increased risk for the formation of Maillard reaction products in UHT treated milk products J Food Compos Anal 84 103308-288