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转糖基化反应,酚类物质掺入咖啡类黑素的主要机制:美拉德反应的抑制作用

Transglycosylation reactions, a main mechanism of phenolics incorporation in coffee melanoidins: Inhibition by Maillard reaction.

作者信息

Moreira Ana S P, Nunes Fernando M, Simões Cristiana, Maciel Elisabete, Domingues Pedro, Domingues M Rosário M, Coimbra Manuel A

机构信息

QOPNA, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal.

CQ-VR, Chemistry Research Centre, Department of Chemistry, University of Trás-os-Montes e Alto Douro, 5001-801 Vila Real, Portugal.

出版信息

Food Chem. 2017 Jul 15;227:422-431. doi: 10.1016/j.foodchem.2017.01.107. Epub 2017 Jan 23.

DOI:10.1016/j.foodchem.2017.01.107
PMID:28274453
Abstract

Under roasting conditions, polysaccharides depolymerize and also are able to polymerize, forming new polymers through non-enzymatic transglycosylation reactions (TGRs). TGRs can also occur between carbohydrates and aglycones, such as the phenolic compounds present in daily consumed foods like coffee. In this study, glycosidically-linked phenolic compounds were quantified in coffee melanoidins, the polymeric nitrogenous brown-colored compounds formed during roasting, defined as end-products of Maillard reaction. One third of the phenolics present were in glycosidically-linked form. In addition, the roasting of solid-state mixtures mimicking coffee beans composition allowed the conclusion that proteins play a regulatory role in TGRs extension and, consequently, modulate melanoidins composition. Overall, the results obtained showed that TGRs are a main mechanism of phenolics incorporation in melanoidins and are inhibited by amino groups through Maillard reaction.

摘要

在烘焙条件下,多糖会发生解聚,同时也能够聚合,通过非酶转糖基化反应(TGRs)形成新的聚合物。TGRs也可能发生在碳水化合物和糖苷配基之间,比如日常食用的食物(如咖啡)中存在的酚类化合物。在本研究中,对咖啡黑素中的糖苷键连接的酚类化合物进行了定量分析,咖啡黑素是烘焙过程中形成的聚合含氮棕色化合物,被定义为美拉德反应的终产物。所呈现的酚类物质中有三分之一是以糖苷键连接的形式存在。此外,对模拟咖啡豆成分的固态混合物进行烘焙后得出结论:蛋白质在TGRs的扩展过程中起调节作用,因此会调节黑素的组成。总体而言,所获得的结果表明,TGRs是酚类物质掺入黑素的主要机制,并且会被氨基通过美拉德反应所抑制。

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