Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1191005 | Food Chemistry | 2009 | 4 Pages |
Abstract
A highly purified type I arabinogalactan (AG) from soybean meal was prepared. It contained galactose, arabinose, galacturonic acid and rhamnose in a 52:41:4:3 molar ratio and had Mw 124,000 g/mol. Methylation analysis and 13C NMR spectroscopy indicated that AG is constituted by a (1→4)-linked β-Galp main chain with substituents of α-Araf at O-3, which are in turn substituted at O-5, O-3,5, and O-2,5. It is probably linked to O-4 of some rhamnosyl units of a type I rhamnogalacturonan, formed by repeating (1→4)-α-D-GalpA-(1→2)-α-L-Rhap groups. AG significantly inhibited ethanol-induced gastric lesions in rats at an ED50 of 35 mg/kg, indicating that it has a gastroprotective effect.
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Thales R. Cipriani, Caroline G. Mellinger, Maria L.C. Bertolini, Cristiane H. Baggio, Cristina S. Freitas, Maria Consuelo A. Marques, Philip A.J. Gorin, Guilherme L. Sassaki, Marcello Iacomini,