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General acid/base catalysis of sugar anomerization

机译:一般酸/碱催化糖的异构化

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Based on theoretical and mechanistical considerations, an equation is presented that describes the observed rate of a pH sensitive reaction. In contrast to the commonly used catalytic catenary, the new approach enables the calculation of non-biased thermodynamic activation parameters. Applying this model, the general acid/base catalysis of the ring opening of beta-D-fructopyranose was analyzed polarimetrically. Thereby, it could be shown that acids (bases) catalyze the ring opening of anionic (cationic) sugar species. Since anomerization rate constants correlate with the rate of sugar degradation, catalysts of anomerization will increase the sugars reactivity as well. The most effective catalysts of the ring opening of beta-D-fructopyranose in the food relevant pH milieu are weak acids and their conjugated bases. Consequently, the enhanced reactivity of reducing sugars in the presence of amino acids is not solely due to classical Maillard reaction but primarily due to carboxylic acid catalysis of degradation reactions.
机译:基于理论和机械方面的考虑,提出了一个方程,该方程描述了观察到的pH敏感反应的速率。与常用的催化链相反,这种新方法能够计算出无偏热力学活化参数。应用该模型,以极化方式分析了β-D-果糖吡喃糖开环的一般酸/碱催化作用。因此,可以表明酸(碱)催化阴离子(阳离子)糖种类的开环。由于阴离子化速率常数与糖的降解速率相关,所以阴离子化的催化剂也将增加糖的反应性。在食品相关的pH环境中,β-D-果糖吡喃糖开环最有效的催化剂是弱酸及其共轭碱。因此,在氨基酸存在下还原糖的增强的反应性不仅是由于经典的美拉德反应,还主要归因于降解反应的羧酸催化。

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