Production method for preparing isomahooligosaccharide from waste residues of sweet potatoes
A technology of isomaltooligosaccharides and sweet potato waste residues, which is applied in the field of preparation of isomaltooligosaccharides, can solve the problems of insufficient utilization of sweet potato residue resources, and achieve the effects of reducing enzyme addition costs, improving hydrolysis efficiency, and high purity
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[0050] Example 1:
[0051] Take 10kg of fresh potato residue (produced by processing sweet potato starch, with 88% water content, 50.5% starch content (dry basis), β-amylase activity 166U / g fresh potato residue, and 0.3g / kg of starch with α-amylase (BAN480L), After stirring uniformly, heat to 88℃, keep for 5min, measure DE value 22.0%, cool to 60±2℃, keep for 2 hours after saccharification, add α-glucosidyltransferase (enzyme activity 3×10 5 u / mL) 0.6mL, stir well and keep at 60±2℃ for 8h. After the incubation is over, the temperature is raised to 80°C and the temperature is kept for 10 minutes for enzyme inactivation. The potato residue after enzyme inactivation was separated by filtration, the residue was washed with a small amount of water, and the combined filtrate was 12.4L. The solid content is 4.6%. The sugar solution was concentrated under reduced pressure to a solid content of 22%. Add 6g of activated carbon to the concentrated sugar solution, heat up to 80°C, and dec...
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[0052] Example 2:
[0053] Take 20kg of fresh potato residue (produced by sweet potato starch processing, water content 89%, starch content 49.5%, β-amylase activity 137U / g), add α-amylase (BAN480L) 0.4g / kg starch, stir evenly, and heat to After incubating at 88°C for 10 minutes, the DE value was determined to be 24.5%. The temperature was lowered to 60°C. After saccharification was kept for 2 hours, 1.1 mL of α-glucosidase transferase was added. After stirring, the temperature was kept at 60°C for 10 hours. After the incubation, the enzyme was heated and the enzyme was inactivated, and the temperature was kept at 90°C for 5 minutes. The sugar solution of sweet potato residue after enzyme inactivation was filtered, the residue was washed with 1.5L of water, and the combined filtrate was 19.3L. The solid content is 5.6%. The sugar solution is concentrated to a solid content of 25%. The concentrated sugar solution is added with activated carbon, and the temperature is decolorize...
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[0054] Example 3:
[0055] Take 20kg of fresh potato residue (produced by sweet potato starch processing, water content 90%, starch content 50.2%, β-amylase activity 184U / g), add α-amylase (BAN480L) 0.5g / kg starch, heat to 90℃, keep warm After 5 minutes, the DE value was determined to be 28.2%, the temperature was lowered to 60°C, α-glucosidyltransferase was added, and the glycated transglycosidation was incubated for 10 hours. After the end of the incubation, the enzyme is heated to kill the enzyme. The sweet potato residue is filtered to obtain a sugar liquid. After the sugar solution is concentrated, it is decolorized and ion exchanged to remove impurities. The impurity-removing sugar liquid is pressurized and concentrated to a solid content of 80%. The ratio of isomalto-oligosaccharides to 52.8% was detected by HPLC. The filtered potato residue is dried to obtain crude fiber.
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