Unravelling caramelization and Maillard reactions in glucose and glucose + leucine model cakes: Formation and degradation kinetics of precursors, α-dicarbonyl intermediates and furanic compounds during baking

美拉德反应 化学 糠醛 羟甲基糠醛 有机化学 果糖 降级(电信) 乙二醛 动力学 食品科学 催化作用 电信 物理 量子力学 计算机科学
作者
Jeehyun Lee,Stéphanie Roux,Even Le Roux,Séverine Keller,Barbara Rega,Catherine Bonazzi
出处
期刊:Food Chemistry [Elsevier BV]
卷期号:376: 131917-131917 被引量:26
标识
DOI:10.1016/j.foodchem.2021.131917
摘要

Understanding the mechanisms leading to the multitude of newly–formed compounds generated during the thermal processing of food is important for the reasoned construction of quality. Thanks to a solid food model with a structure and technological history comparable to that of a real sponge cake and containing only known amounts of precursors (glucose with or without leucine), an adapted reaction scheme unravelling Maillard and caramelization reactions was built and then compared to experimental kinetic data measured on numerous reaction markers (precursors, α–dicarbonyl intermediates and furanic compounds). For caramelization, this study showed that glucose mainly formed 1,2–enediol and then fructose rather than glucosone and glyoxal. 5–hydroxymethylfurfural started to form when there were sufficient quantities of fructose, and 3,4–dideoxyoglucosone was not generated until after this step. Furfural was mainly formed via 3–deoxyglucosone. The involvement of leucine tended to accelerate the breakdown of sugars as more degradation pathways (via enaminols) were added.
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