Method for co-producing glucose and dietary fibers from multiple high-solid enzymes of sweet potato residues through synergetic enzymatic hydrolysis
A technology for dietary fiber and sweet potato dregs, applied in food science, fermentation and other directions, can solve the problems of low-end, short industrial chain and low-value deep processing technology of sweet potato dregs, achieve high value-added resource utilization and simplify units Operation, the effect of saving equipment cost
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Embodiment 1
[0027] Remove impurities such as soil and fine stones from the sweet potato dregs, and crush them to 40 mesh; add water to the crushed sweet potato dregs to adjust the solid-liquid ratio to 1:2.5 (w / v), add 20 U / g substrate acid cellulase and 5 U / g substrate Pectinase, after stirring evenly, oscillating enzymolysis at 150 rpm at 50°C for 16 hours at natural pH value to obtain a pre-enzymolysis solution; adjust the pH of the pre-enzymolysis solution to about 5.5, and add 20U / g substrate α-amylase , liquefied at 90°C for 2 hours, after cooling the liquefied solution, add 60 U / g substrate glucoamylase, and saccharify at 60°C for 4 hours to obtain a saccharified solution;
[0028] The enzymatic hydrolysis and saccharification liquid of sweet potato dregs after saccharification was centrifuged at 4000rpm, and 7.5% (w / w) powdered activated carbon and diatomaceous earth mixed at a ratio of 1:1 (w / w) were added to the obtained liquid crude sugar liquid, and the mixture was heated at 50...
Embodiment 2
[0031]Remove impurities such as soil and fine stones from sweet potato dregs, and crush them to 10 meshes; add water to the crushed sweet potato dregs to adjust the solid-liquid ratio to 1:3 (w / v), add 30 U / g substrate acid cellulase and 10 U / g substrate Pectinase, stirred evenly, placed in a drum reactor at natural pH value, and enzymatically hydrolyzed at 50°C for 24 hours to obtain a pre-enzymolyzed solution; adjust the pH of the pre-enzymolyzed solution to about 5.0, and add 40U / g at the end The α-amylase of the substrate was liquefied at 85°C for 3 hours. After the liquefied liquid was cooled, 40 U / g of substrate glucoamylase was added, and saccharified at 60°C for 16 hours to obtain a saccharified liquid;
[0032] After saccharification, the enzymatic hydrolysis and saccharification liquid of sweet potato dregs is suction-filtered, and the filtrate is crude sugar liquid, which is mixed with 10% (w / w) powdered activated carbon and diatomaceous earth at a ratio of 1:1 (w / w)...
Embodiment 3
[0035] Remove impurities such as soil and fine stones from the sweet potato dregs, and crush them to 20 meshes; add water to the crushed sweet potato dregs to adjust the solid-liquid ratio to 1:2.5 (w / v), add 40U / g substrate acid cellulase and 10U / g substrate Pectinase, stirred evenly, placed in a drum reactor at the natural pH value, and enzymatically hydrolyzed at 50°C for 12 hours to obtain a pre-enzymolyzed solution; adjust the pH of the pre-enzymolyzed solution to about 6.0, and add 20U / g at the end The α-amylase of the substrate was liquefied at 90°C for 2 hours. After the liquefied solution was cooled, 100 U / g of substrate glucoamylase was added and saccharified at 60°C for 24 hours to obtain a saccharified solution;
[0036] After saccharification, the enzymatic hydrolysis and saccharification liquid of sweet potato dregs was filtered by plate and frame filter, and 12.5% (w / w) of powdery activated carbon and diatomite mixture mixed with 1:1 (w / w) were added to the fil...
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