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Evolution of Complex Maillard Chemical Reactions Resolved in Time

机译:及时解决的复杂美拉德化学反应的演变

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摘要

In this study, we monitored the thermal formation of early ribose-glycine Maillard reaction products over time by ion cyclotron resonance mass spectrometry. Here, we considered sugar decomposition (caramelization) apart from compounds that could only be produced in the presence of the amino acid. More than 300 intermediates as a result of the two initial reactants were found after ten hours (100 °C) to participate in the interplay of the Maillard reaction cascade. Despite the large numerical variety the majority of intermediates follow simple and repetitive reaction patterns. Dehydration, carbonyl cleavage, and redox reactions turned out to have a large impact on the diversity the Maillard reaction causes. Although the Amadori breakdown is considered as the main Maillard reaction pathway, other reactive intermediates, often of higher molecular weight than the Amadori rearrangement product, contribute to a large extent to the multitude of intermediates we observed.
机译:在这项研究中,我们通过离子回旋共振质谱法监测了早期核糖-甘氨酸美拉德反应产物随时间的热形成。在这里,我们考虑了糖分解(焦糖化)和仅在氨基酸存在下才能产生的化合物。十小时(100°C)后,发现两种初始反应物导致的300多种中间体参与了美拉德反应级联反应。尽管数值差异很大,但大多数中间体仍遵循简单且重复的反应模式。事实证明,脱水,羰基裂解和氧化还原反应对美拉德反应引起的多样性有很大影响。尽管Amadori分解被认为是主要的美拉德反应途径,但其他反应性中间体(通常比Amadori重排产物的分子量更高)在很大程度上有助于我们观察到许多中间体。

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