Multiresponse kinetic modelling of α-dicarbonyl compounds formation in fruit juices during storage

Food Chem. 2020 Aug 1:320:126620. doi: 10.1016/j.foodchem.2020.126620. Epub 2020 Mar 17.

Abstract

This study aims to investigate the formation of α-dicarbonyl compounds in fruit juices and nectars during storage using multi-response kinetic modeling approach. Changes in the concentrations of sugars, amino acids, α-dicarbonyl compounds (glucosone, 3-deoxyglucosone, threosone, methylglyoxal, glyoxal) and 5-hydroxymethylfurfural in apple juice, orange juice and peach nectar were monitored during storage. The concentrations of free amino acids showed no statistically significant change during storage. This suggested that sugar degradation reactions were found responsible for α-dicarbonyl compound formation. In apple and orange juices, the reaction rate constant of glucosone formation was found higher than that of 3-deoxyglucosone formation. Contrary, in peach nectar, 3-deoxyglucosone formation was the dominant. The contribution of fructose dehydration through fructofuranosyl cation on the formation of 5-hydroxymethylfurfural was significantly higher (p < 0.05) than 3-deoxyglucosone dehydration. The use of multi-response kinetic modeling provided better understanding the most possible pathway of sugar degradation reactions in fruit juices.

Keywords: 5-Hydroxymethylfurfural; Fruit juices; Multi-response kinetic modelling; Sugar degradations; α-Dicarbonyl compounds.

MeSH terms

  • Amino Acids / chemistry
  • Food Analysis
  • Fruit and Vegetable Juices / analysis*
  • Sugars / chemistry

Substances

  • Amino Acids
  • Sugars