Journal
CARBOHYDRATE POLYMERS
Volume 81, Issue 4, Pages 830-838Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.carbpol.2010.03.060
Keywords
TEMPO oxidation; Potato starch; Glucuronan; Acidic hydrolysis; Acidic methanolysis
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Funding
- European Union
- European Regional Development Fund
- The Northern Netherlands Provinces (Samenwerkingsverband Noord-Nederland), KOERS NOORD
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Chemical derivatization is often applied to improve polysaccharide functionality. Primary hydroxyl groups in starch can, for example, be oxidized to aldehydes by using a 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-mediated reaction. The major part of the aldehydo groups is subsequently converted to carboxyl groups by NaOCl. The exact structure of TEMPO-oxidized starch was studied to promote a better understanding of the TEMPO oxidation mechanism and the functionality of oxidized starches. By using weak and strong acidic hydrolysis, and methanolysis, at elevated temperatures, oxidized starches with different degrees of oxidation (DO) were broken down into oligomers and monomers. Analysis of the oligomers by chromatographic and mass spectrometric techniques revealed that blocks of glucuronic acid moieties are present in the oxidized starch polymers. The alpha(1 -> 4) glucuronic acid-glucuronic acid bond was found to be very resistant to breakdown by acids. The alpha(1 -> 4) glucuronic acid-glucose bond also showed increased resistance to acids compared to alpha(1 -> 4) glucose-glucose bonds. The size of the blocks of glucuronic acid moieties increased when DO increased. Furthermore, the presence of clusters of aldehydes close to carboxyl groups directly after oxidation was proven. This implies that TEMPO, which is positively charged in its active state, is apparently attracted by the negatively charged carboxyl groups. Because of this. TEMPO tends to be active in areas where carboxyl groups have already been formed, which leads to a block wise distribution of the glucuronic acid moieties. (C) 2010 Elsevier Ltd. All rights reserved.
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