The Uppsala methodology for rapid analysis and characterization of tot
al 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 amyloglucos
idase. Neutral DFP residues were quantified by gas chromatography as a
lditol acetates after acid hydrolysis of this residue, and the acid-in
soluble fraction, Klason lignin, was determined gravimetrically. Uroni
c acid residues were quantified by decarboxylation of the original sam
ple. The efficacy of the Uppsala methodology was tested with foods var
ying 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 t
he main fiber components. Fiber contents determined with the method we
re higher than those determined with a similar method that excludes Kl
ason lignin and starch resistant to amylases but soluble in dimethyl s
ulfoxide and lower than those determined with an enzymatic/gravimetric
method. Important aspects of fiber analysis, like enzyme purity and t
he recovery of soluble fiber on ethanol precipitation, also were inves
tigated.