Heat-induced degradation of inulin

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • A Bohm - , TUD Dresden University of Technology (Author)
  • Julia Kaiser - , TUD Dresden University of Technology (Author)
  • A Trebstein - , TUD Dresden University of Technology (Author)
  • T Henle - , Chair of Food Chemistry (Author)

Abstract

Dry heating of inulin from chicory for up to 60 min at temperatures between 135 and 195 degrees C resulted in a significant degradation of the fructan ranging from 20 to 100%. The choice of the analytical method has a significant influence on inulin quantification especially in heat-treated samples. The amount of inulin found after thermal treatment measured as fructose after acidic hydrolysis was significantly higher compared with corresponding data obtained with a method based on enzymatic hydrolysis. Using high-performance anion-exchange chromatography with pulsed amperometric detection as well as high-performance thin-layer chromatography, it was found that thermal treatment of inulin leads to a degradation of the long fructose chains and formation of new products, most likely di-D-fructose dianhydrides. These degradation products of inulin are cleavable by acid to fructose monomers, but their glycosidic bonds are no longer accessible for beta-fructosidase, thus explaining the discrepancies in inulin quantification with respect to the method used. Inulin degradation must be taken into account when fructan is used as a prebiotic ingredient in thermally treated foods like bakery products.

Details

Original languageEnglish
Pages (from-to)466-471
Number of pages6
JournalEuropean Food Research and Technology
Volume220
Issue number5-6
Publication statusPublished - May 2005
Peer-reviewedYes

External IDs

WOS 000229094300003
Scopus 18744396074

Keywords

Keywords

  • inulin, thermal treatment, fructose, Di-D-fructose dianhydrides, high-performance thin-layer chromatography, high-performance anion-exchange chromatography with pulsed amperometric detection, D-FRUCTOSE DIANHYDRIDES, ENZYMATIC DETERMINATION, OLIGOFRUCTOSE, FOOD, PYROLYSIS