The isomeric sugar-branched cyclodextrin (CD) derivatives of 6-O-glucosyl-betaCD (G1-betaCD) and 6,6-di-O-glucosyl-alphaCD (G1, G1-alphaCD) were analyzed by matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry at the different acceleration voltages of 20 and 8 kV.
Influence of different glycosidic linkages on relative ion intensities in post-source decay fragmentation of a xyloglucan heptaoligosaccharide using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
โ Scribed by Tohru Yamagaki; Yasushi Mitsuishi; Hiroshi Nakanishi
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 169 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0951-4198
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โฆ Synopsis
Post-source decay fragment analysis using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) has been applied to a highly branched xyloglucan heptasaccharide from tamarind seed. All fragment ions were produced by cleavage of the glycosidic linkages, including multi-site cleavages. The relative intensities of fragment ions that originated from one-site cleavages of the glycosidic linkages were much higher than those arising from two-site cleavages of the same kind of glycosidic linkage, which were in turn higher than those from three-site cleavages. The types of glycosidic linkages were an important factor which influenced the relative intensities of the MALDI-PSD (post-source decay) fragment ions. In the MALDI-PSD fragment spectrum of the xyloglucan heptasaccharide, the relative intensities of the ions produced by the cleavage of an a1-6 glycosidic linkage were much higher than those arising from cleavage of the b1-4 glycosidic linkage.
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