Theander O, Aman P, Westerlund E, Graham H
Swedish University of Agricultural Sciences, Department of Chemistry, Uppsala.
J AOAC Int. 1994 May-Jun;77(3):703-9.
The Uppsala methodology for rapid analysis and characterization of total dietary fiber, defined as the sum of dietary fiber polysaccharides (DFP) and Klason lignin, was studied. A sugar- and starch-free residue was prepared by treatment with a thermostable amylase and amyloglucosidase. Neutral DFP residues were quantified by gas chromatography as alditol acetates after acid hydrolysis of this residue, and the acid-insoluble fraction, Klason lignin, was determined gravimetrically. Uronic acid residues were quantified by decarboxylation of the original sample. The efficacy of the Uppsala methodology was tested with foods varying in fiber content and composition, including heat-treated samples. The present method allowed the analysis of up to 40 samples per week. It had good repeatability and coefficients of variation of 3-5% for the main fiber components. Fiber contents determined with the method were higher than those determined with a similar method that excludes Klason lignin and starch resistant to amylases but soluble in dimethyl sulfoxide and lower than those determined with an enzymatic/gravimetric method. Important aspects of fiber analysis, like enzyme purity and the recovery of soluble fiber on ethanol precipitation, also were investigated.
对乌普萨拉总膳食纤维快速分析与表征方法进行了研究,总膳食纤维定义为膳食纤维多糖(DFP)与克拉斯森木质素之和。通过用热稳定淀粉酶和淀粉葡萄糖苷酶处理制备无糖和无淀粉残渣。该残渣经酸水解后,中性DFP残渣以糖醇乙酸酯形式通过气相色谱法定量,酸不溶部分即克拉斯森木质素通过重量法测定。糖醛酸残基通过原始样品的脱羧作用进行定量。使用纤维含量和组成各异的食品(包括热处理样品)对乌普萨拉方法的有效性进行了测试。本方法每周可分析多达40个样品。它具有良好的重复性,主要纤维成分的变异系数为3 - 5%。用该方法测定的纤维含量高于用类似方法(排除克拉斯森木质素和抗淀粉酶但可溶于二甲基亚砜的淀粉)测定的结果,且低于用酶法/重量法测定的结果。还对纤维分析的重要方面,如酶纯度和乙醇沉淀时可溶性纤维的回收率进行了研究。