Title of article
Optimized synthesis of specific sizes of maltodextrin glycosides by the coupling reactions of Bacillus macerans cyclomaltodextrin glucanyltransferase Original Research Article
Author/Authors
James S.S. Gray، نويسنده , , Rex Montgomery، نويسنده ,
Issue Information
دوهفته نامه با شماره پیاپی سال 2006
Pages
8
From page
210
To page
217
Abstract
Bacillus macerans cyclomaltodextrin glucanyltransferase (CGTase, EC 2.4.1.19), in reaction with cyclomaltohexaose and methyl α-d-glucopyranoside, methyl β-d-glucopyranoside, phenyl α-d-glucopyranoside, and phenyl β-d-glucopyranoside gave four kinds of maltodextrin glycosides. The reactions were optimized by using different ratios of the individual d-glucopyranosides to cyclomaltohexaose, from 0.5 to 5.0, to obtain the maximum molar percent yields of products, which were from 68.3% to 78.6%, depending on the particular d-glucopyranoside, and also to obtain different maltodextrin chain lengths. The lower ratios of 0.5–1.0 gave a wide range of sizes from d.p. 2–17 and higher. As the molar ratio was increased from 1.0 to 3.0, the larger sizes, d.p. 9–17, decreased, and the small and intermediate sizes, d.p. 2–8, increased; as the molar ratios were increased further from 3.0 to 5.0, the large sizes completely disappeared, the intermediate sizes, d.p. 4–8, decreased, and the small sizes, d.p. 2 and 3 became predominant. A comparison is made with the synthesis of maltodextrins by the reaction of CGTase with different molar ratios of d-glucose to cyclomaltohexaose.
Keywords
Acceptor reactions , Coupling reactions , Cyclomaltodextrin glucanyltransferase , Synthesis of maltodextrin glycosides , Reaction optimization , Cyclomaltohexaose , Phenyl ?-d-glucopyranoside , Methyl ?-d-glucopyranoside , Transglycosylation reactions , Phenyl ?-d-glucopyranoside , Methyl ?-d-glucopyranoside
Journal title
Carbohydrate Research
Serial Year
2006
Journal title
Carbohydrate Research
Record number
964673
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