Title of article
Glucosylation of raffinose via alternansucrase acceptor reactions Original Research Article
Author/Authors
Gregory L. Côté، نويسنده , , Christopher A. Dunlap، نويسنده , , Karl E. Vermillion، نويسنده ,
Issue Information
دوهفته نامه با شماره پیاپی سال 2009
Pages
9
From page
1951
To page
1959
Abstract
The glucansucrase known as alternansucrase [EC 2.4.1.140] can transfer glucosyl units from sucrose to raffinose to give good yields of oligosaccharides, which may serve as prebiotics. The main products were the tetrasaccharides α-d-Glcp-(1→3)-α-d-Galp-(1→6)-α-d-Glcp-(1↔2)-β-d-Fruf and α-d-Glcp-(1→4)-α-d-Galp-(1→6)-α-d-Glcp-(1↔2)-β-d-Fruf in ratios ranging from 4:1 to 9:1, along with lesser amounts of α-d-Glcp-(1→6)-α-d-Galp-(1→6)-α-d-Glcp-(1↔2)-β-d-Fruf. Ten unusual pentasaccharide structures were isolated. Three of these arose from glucosylation of the major tetrasaccharide product, two each from the minor tetrasaccharides, and three were the result of glucosylations of the fructose acceptor product leucrose or isomaltulose. The major pentasaccharide product arose from glucosylation of the major tetrasaccharide at position 4 of the fructofuranosyl unit, to give a subunit structure analogous to that of maltulose. A number of hexasaccharides and higher oligosaccharides were also produced. Unlike alternansucrase, dextransucrase [EC 2.4.1.5] gave only a single tetrasaccharide product in low yield, and no significant amounts of higher oligosaccharides. The tetrasaccharide structure from dextransucrase was found to be α-d-Glcp-(1→4)-α-d-Galp-(1→6)-α-d-Glcp-(1↔2)-β-d-Fruf, which is at odds with the previously published structure.
Keywords
Raffinose , Oligosaccharides , Alternansucrase , Prebiotics , Dextransucrase
Journal title
Carbohydrate Research
Serial Year
2009
Journal title
Carbohydrate Research
Record number
966535
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