EC Number   |
Application |
Reference |
|---|
    2.4.1.49 | synthesis |
biocatalytic production of cellodextrins with a degree of polymerization. Kinetic and thermodynamic restrictions upon alpha-Glc1-P utilization (200 mM; 45°C, pH 7.0) are effectively overcome by in situ removal of the phosphate released via precipitation with Mg2+. The product's degree of polymerization is controlled by the molar ratio of glucose/alpha-Glc1-P used in the reaction. In optimized conversion, 36 g/l soluble cellodextrins are obtained. By keeping the glucose concentration low, the reaction is shifted completely towards insoluble product formation |
756244 |
| 2.4.1.49 | synthesis |
enzyme is a good tool for the synthesis of cellodextrins |
489245 |
| 2.4.1.49 | synthesis |
simple procedures for synthesizing various sugar length radioactive cellodextrins (G2G6) are developed using the Clostridium thermocellum cellobiose and cellodextrin phosphorylases from small building blocks of nonradioactive glucose-1-phosphate and radioactive glucose |
671515 |
| 2.4.1.49 | synthesis |
synthesis of cellulase inhibitors from reaction of 4-O-beta-D-glucopyranosyl-1-deoxynojirimycin or 6-O-beta-cellobiosyl-1-deoxynojirimycin as acceptors with glucose 1-phosphate as donors |
489247 |
| 2.4.1.49 | synthesis |
to increase the reaction rate of cellodextrin phosphorolysis, synthetic enzyme complexes containing CDP and phosphoglucomutase are constructed to convert G1P to glucose 6-phosphate rapidly. The CDP-phosphoglucomutase enzyme complex with the highest enhancement of initial reaction rate is integrated into an in vitro synthetic enzymatic biosystem for generating bioelectricity from cellodextrin, exhibiting a much higher current density (3.35fold) and power density (2.14fold) than its counterpart biosystem containing free CDP and phosphoglucomutase mixture |
756255 |
