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Published on: January 5, 2021
Linkage-resolved profiling of isomalto-oligosaccharides using porous graphitic carbon liquid chromatography-orbitrap
Chih-Chieh Lin1, Meng-Jui Lin2, Ju-Hua Chou2
1Institute of Food Science and Technology, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei 10617, Taiwan, ROC; Molecular and Cellular Glycoproteomics Research Group, Cellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba, Ibaraki 305-8565, Japan.
Abstract:
The digestibility and glycemic response of isomalto-oligosaccharides are determined by their glycosidic linkage and chain length. However, linkage-resolved profiling beyond tetrasaccharides remains limited. Herein, forty structures from disaccharides to hexasaccharides in eight commercial materials were characterized using porous graphitic carbon liquid chromatography-Orbitrap tandem mass spectrometry. Linkage profiles were dominated by α-1 → 6 and α-1 → 4, displaying a chain-length-dependent shift. Generally, α-1 → 4 linkages accounted for ∼10% of total linkages in disaccharides, rising to ∼80% in hexasaccharides. In one sample, α-1 → 4 linkages were 1.6-fold more abundant than α-1 → 6. With contents of 62.5-81.5%, no product met the European Food Safety Authority description for isomaltose plus trisaccharide-nonasaccharide content (≥90% dry basis). Even in products labeled "total isomalto-oligosaccharides ≥90% (dry basis)," α-1 → 6 linkages accounted for only ∼50% of glycosidic linkages. This suggests the need for linkage-resolved isomalto-oligosaccharide labeling frameworks that extend beyond total content claims to more precisely reflect the digestibility and glycemic impact.
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