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Gastrointestinal Release of β-Glucan and Pectin Using an In Vitro Method

July 2011 Volume 88 Number 4
Pages 385 — 390
Matilda Ulmius,1,2 Anna Johansson-Persson,1 Tina Immerstrand Nordén,3 Björn Bergenståhl,4 and Gunilla Önning1

1Biomedical Nutrition, Pure and Applied Biochemistry, Center for Applied Life Sciences, Department of Chemistry, Lund University, Lund, Sweden. 2Corresponding author. E-mail: matilda.ulmius@tbiokem.lth.se 3Applied Nutrition and Food Chemistry, Department of Food Technology, Engineering and Nutrition, Lund University, Lund, Sweden. 4Food Technology, Department of Food Technology, Engineering and Nutrition, Lund University, Lund, Sweden.


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Accepted May 9, 2011.
ABSTRACT

The release of soluble dietary fiber is a prerequisite for viscous effects and hence beneficial health properties. A simple in vitro method was adapted to follow the release during gastrointestinal digestion, and the percentage of solubilized fiber was measured over time. β-Glucan from oat bran was mainly released during gastric digestion while the release of pectin from sugar beet fiber continued in the small intestine. Unmilled fractions of sugar beet fiber released more soluble fiber than oat bran flakes, probably due to the porous structure of sugar beet fiber as a result of manufacturing processes, but also due to differences in source. Milling to smaller fiber particles significantly improved releasability (from 20 to 55% released β-glucan and from 50 to 70% released pectin, respectively, after digestion). When milled fibers were included in individual food matrices, the release was reduced by protein and starch matrices (5% β-glucan and 35% pectin released, respectively) and slowed by fat (45% β-glucan and 60% pectin released). This may result in a too low or too late release in the upper small intestine to be able to interfere with macronutrient uptake. The method may be suitable for predicting the gastrointestinal release of soluble dietary fibers from food matrices in the development of healthy food products.



© 2011 AACC International, Inc.