Nestlé Product Technology Centre Orbe, Nestec Ltd. , CH-1350 Orbe , Switzerland.
Nestlé Research Centre , P.O. Box 44, CH-1000 Lausanne 26 , Switzerland.
J Agric Food Chem. 2018 Mar 14;66(10):2422-2431. doi: 10.1021/acs.jafc.6b04849. Epub 2017 Jan 18.
The origin and formation pathways of the buttery-smelling α-diketones 2,3-butanedione and 2,3-pentanedione upon coffee roasting were studied by means of biomimetic in-bean experiments combined with labeling experiments. For this purpose natural sucrose in the coffee bean was replaced by fully or partially C-labeled sucrose or by a mixture of unlabeled and fully C-labeled sucrose (CAMOLA approach). The obtained data point out that sucrose contributes to both α-diketones; however, its importance and reaction pathways clearly differ. Whereas the major part of 2,3-pentanedione originates from sucrose (about 76%), its contribution to 2,3-butanedione is much lower (about 35%). Formation from intact sugar skeleton is the major pathway generating 2,3-pentanedione from sucrose, whereas 2,3-butanedione is mainly generated by recombination of sucrose fragments. The contribution of glucose and fructose moieties of sucrose to both α-diketones is comparable. Finally, kinetic experiments with fully labeled sucrose showed that the contribution of sucrose changes during roasting.
通过豆内模拟实验与示踪实验相结合的方法,研究了咖啡烘焙过程中具有黄油香味的α-二酮(2,3-丁二酮和 2,3-戊二酮)的起源和形成途径。为此,将咖啡豆中的天然蔗糖用完全或部分 C 标记的蔗糖或用未标记和完全 C 标记的蔗糖混合物(CAMOLA 方法)代替。所得数据表明,蔗糖对两种α-二酮都有贡献;然而,其重要性和反应途径明显不同。虽然 2,3-戊二酮的主要来源是蔗糖(约 76%),但其对 2,3-丁二酮的贡献要低得多(约 35%)。从完整的糖骨架形成是生成 2,3-戊二酮的主要途径,而 2,3-丁二酮主要是由蔗糖片段的重组生成的。蔗糖中葡萄糖和果糖部分对两种α-二酮的贡献相当。最后,用完全标记的蔗糖进行的动力学实验表明,在烘焙过程中,蔗糖的贡献会发生变化。