Enzyme method degumming method
A degumming method and enzymatic technology, applied in the direction of fat production, fat oil/fat refining, etc., can solve the problems of low product inhibition reaction efficiency, difficulty in continuous production, long reaction time, etc., to reduce enzyme loss and purification costs, Effects of cost reduction and short separation time
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Embodiment 1
[0024] Take an appropriate amount of Ultra phospholipase in a conical flask, add 100 times the volume of water, mix well, take 2g of crude enzyme solution (enzyme concentration 50U / mL), 1.5g of sodium citrate, mix well and add 1.5g poly Ethylene glycol 400 and 2.5g crude soybean oil were put into a stoppered Erlenmeyer flask and mixed evenly. The pH value of the mixed solution was 7.7, and placed on a constant temperature shaker with a rotation speed of 200rpm, controlled at 50°C for 3h. After the reaction is over, set the speed of centrifugation at 4600rpm for 5min and divide it into four layers, which are the upper liquid layer, the steroid layer, the middle liquid layer and the lower liquid layer. phase, and the middle liquid layer is the enzyme-rich phase. In addition, the middle and lower liquid layer was taken to measure its enzyme activity and the phosphorus content of the upper liquid layer. The phosphorus content in the oil phase was only 13.96mg / kg, and the removal r...
Embodiment 2
[0026] Take an appropriate amount of Ultra phospholipase in a conical flask, add 100 times the volume of water, mix well, take 5.2g of crude enzyme solution (enzyme concentration 50U / mL), add 1.6g of sodium citrate, mix well and add 3.2 g[BMIM]BF 4 and 5g of crude soybean oil were mixed evenly in a stoppered Erlenmeyer flask, the pH value of the mixed solution was 7.7, and placed on a constant temperature shaker with a rotation speed of 200rpm, controlled at 50°C for 10 minutes. Take another crude enzyme solution not less than the reaction volume, add 2.5g soybean crude oil, add water to the same volume as the experimental group, and react under the same conditions as a control. After the reaction finishes, set 4600rpm rotating speed centrifugation 5min, and experiment group is divided into four layers, is successively upper liquid layer, steroid layer, middle liquid layer and lower liquid layer, and upper liquid layer product is lipid product phase, and steroid layer is The ...
Embodiment 3
[0028] Take an appropriate amount of Ultra phospholipase in a conical flask, add 100 times the volume of water, mix well, take 2g of crude enzyme solution (enzyme concentration 50U / mL), add 1.5g of sodium citrate, mix well and add 1.5g Polyethylene glycol 400 and 2.5 g of crude soybean oil were put into a stoppered Erlenmeyer flask and mixed evenly. The pH value of the mixed solution was 7.7, and placed on a constant temperature shaker with a rotation speed of 200 rpm, controlled at 50° C. for 1 h. Take another crude enzyme solution not less than the reaction volume, add 2.5g soybean crude oil, add water to the same volume as the experimental group, and react under the same conditions as a control. After the reaction is over, set the speed of centrifugation at 4600rpm for 5min and divide it into four layers, which are the upper liquid layer, the steroid layer, the middle liquid layer and the lower liquid layer. phase, and the middle liquid layer is the enzyme-rich phase. In a...
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