Synthesis by a α-Glucosidase of Glycosyl-trehaloses with an Isomaltosyl Residue

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タイトル別名
  • Synthesis by an .ALPHA.-Glucosidase of Glycosyl-trehaloses with an Isomaltosyl Residue.
  • Synthesis by a アルファ Glucosidase of Glyc
  • Synthesis by an<i>α</i>-Glucosidase of Glycosyl-trehaloses with an Isomaltosyl Residue
  • Synthesis by an α-glucosidase of glycosyl-trehaloses with an isomaltosyl residue

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Glycosyl-trehaloses with an isomaltosyl residue were synthesized by α-glucosidase from Aspergillus niger by using maltotetraose as a glucosyl donor and trehalose as the acceptor. The one trisaccharide and two tetrasaccharides formed were isolated by successive column chromatography. The results of an enzymatic digestion, methylation analysis, and 13C-NMR studies indicated that these oligosaccharides were α-isomaltosyl α-glucoside, α-isomaltotriosyl α-glucoside and α-isomaltosyl α-isomaltoside. These oligosaccharides were not fermented to an acid by Streptococcus mutans, and they effectively inhibited water-insoluble glucan synthesis from sucrose by glucosyltransferase. In an in vitro utilization test with human intestinal bacteria, these oligosaccharides were predominantly utilized by Bifidobacteria.

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