Enzymatic synthesis method of straight-chain dextrin
A technology of linear dextrin and enzymatic synthesis, applied in the food field, can solve the problems of high production cost, complicated operation process, unsuitable for industrialized large-scale production, etc., achieve narrow polymerization degree distribution, simplify the purification process, and reduce production cost Effect
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Embodiment 1
[0026] Accurately weigh 0.02g of sucrose, absorb 1.0mL of 0.1mol / L phosphate buffer (pH 6.7), absorb 0.1mL of 34U / mL sucrose phosphorylase and add it to the reaction system. At this time, the concentration of sucrose in the system is 0.05mol / L, with an enzyme activity of 3.0 U, reacted in a constant temperature water bath at 40°C for 6 hours, and measured the yield of the intermediate product glucose-1-phosphate by the phosphorus determination method.
[0027] On the basis of the above reaction, add 0.01 g of maltotetraose, adjust the pH to 5.5, and absorb 0.18 mL of 37 U / mL glucan phosphorylase. At this time, the concentration of maltotetraose in the system is 0.01 mol / L, and the enzyme in the system The activity is about 4.5U / mL, react in a constant temperature water bath at 40°C for 6h, and use LC-MS and anion chromatography to detect the formation of linear dextrin.
Embodiment 2
[0029] Accurately weigh 0.018g of sucrose, absorb 1.0mL of 0.1mol / L phosphate buffer (pH 7.0), absorb 0.08mL of 34U / mL sucrose phosphorylase and add it to the reaction system. At this time, the concentration of sucrose in the system is 0.048mol / L, the enzyme activity is 2.5U, reacted in a constant temperature water bath at 40°C for 6 hours, and measured the yield of the intermediate product glucose-1-phosphate by the phosphorus determination method.
[0030] On the basis of the above reaction, add 0.012 g of maltotetraose, adjust the pH to 5.0, absorb 0.20 mL of glucan phosphorylase at 37 U / mL, and at this time, the concentration of maltotetraose in the system is 0.012 mol / L, and the enzyme in the system The activity is about 5.0U / mL, react in a constant temperature water bath at 40°C for 6h, and use LC-MS and anion chromatography to detect the formation of linear dextrin.
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