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明胶与戊二醛交联的替代反应机制。

Alternative reaction mechanism for the cross-linking of gelatin with glutaraldehyde.

机构信息

Department of Food Science and Microbiology, University of Milan, Via Celoria 2, 20133 Milano, Italy.

出版信息

J Agric Food Chem. 2010 Jan 27;58(2):998-1003. doi: 10.1021/jf9031603.

DOI:10.1021/jf9031603
PMID:20043635
Abstract

FT-IR, in combination with residual amino group determination using a fluorescence technique, has been used to investigate the chemical functional groups involved in the cross-linking reaction between glutaraldehyde and gelatin molecules. The results suggest that, at high pH values (i.e., close to the pK(a) of lysine), the cross-linking reaction is mainly governed by the well-known Schiff base formation, whereas at low pH (i.e., when the amino groups of lysine are protonated), the reaction may also involve the -OH groups of hydroxyproline and hydroxylysine, leading to the formation of hemiacetals.

摘要

傅里叶变换红外光谱(FT-IR)结合荧光技术测定残留氨基基团的方法,被用于研究戊二醛与明胶分子交联反应中涉及的化学官能团。结果表明,在高 pH 值条件下(即接近赖氨酸的 pKa 值),交联反应主要受众所周知的希夫碱形成所控制;而在低 pH 值条件下(即赖氨酸的氨基被质子化时),反应可能还涉及羟脯氨酸和羟赖氨酸的 -OH 基团,从而形成半缩醛。

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