Oligosaccharides with α-
d-galactosidic linkages, especially each positional isomer of α-galactobiose (α-Gal2), participate in such biological process as immunity and pathogen-to-cell adhesion on the basis of molecular mechanisms for ligand-receptor interaction. α-Linked galactooligosaccharide (α-GOS) containing positional isomers of α-Gal2 produced from galactose by the reverse reaction of α-galactosidase, is a potential food to be used in the prevention of infections by pathogens, neutralization of toxins, and regulation of the immune system.
α-GOS was produced from galactose (prepared from lactose hydrolyzate) by the reverse reaction of α-galactosidase from
Aspergillus niger APC-9319. α -GOS contained 58% disaccharide, 28% trisaccharide, and 14% oligosaccharides larger than trisaccharide. The disaccharide in α-GOS consisted largely of α-1,6-galactobiose.
α-GOS was stable at neutral and acidic pHs, and high temperatures. The sweetness of α-GOS was 25% of that of sucrose. The taste of α-GOS was mild and mellow. α-GOS reduced acid taste, bitterness, astringency, and harsh taste without spoiling the original taste in various fruit juices, and emphasized the original flavor of food materials in various cooking foods. α-GOS was not hydrolyzed in an
in vitro digestion method. In oral tolerance tests of α-GOS, the blood glucose level did not change at all. α-GOS had a strong selective growth activity for
Bifidobacterium sp. and
Clostridium butyricum. An α-GOS intake in rats made the contents of lactate and
n-butyrate in the cecum higher, and pH in the cecum lower than for a control intake. In young female students who defecated 3 to 5 times /week, the investigation of α -GOS (3 g) increased the defecation frequency and fecal volume, and improved the condition of feces by promoting the proliferation of
Bifidobacterium sp. The maximum non-effective dose of α-GOS was estimated at 0.25 g/kg body weight for males and 0.33 g/kg body weight for females. The viable count of
Candida albicans in the cecum and colon of mouse was decreased by an α-GOS intake more than a raffinose intake. Dietary α-GOS ameliorated allergic airway eosinophilia at least partly via post-absorptive mechanisms in Brown Norway rats. Therapeutic oral treatment with α-GOS had a potent inhibitory effect on adjuvant arthritis in Wister rats and type II collagen-induced arthritis in DBA/1J mice.
抄録全体を表示