Method for preparing wheat germ protein ACE inhibitory peptide by continuous enzymolysis and ultra-filtration separation coupling
An ultrafiltration separation and wheat germ protein technology is applied in the field of continuous enzymatic hydrolysis and ultrafiltration separation coupling technology to prepare wheat germ protein ACE inhibitory peptides, which can solve the problems of reducing product activity, excessive product degradation, and complicated purification methods, etc. Improve utilization, avoid enzyme inactivation, and achieve continuous effects
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Embodiment 1
[0014] Add defatted wheat germ powder into water at a concentration of 10% (w / v), stir at a pH value of 9.5 for 0.5 h, centrifuge to obtain a supernatant to adjust the pH value to 7.0, and use a medium-temperature amylase at 70° C. for 180 min to enzymatically hydrolyze. The amount of enzyme added is 3% (w / v); after enzymatically degrading the starch, adjust the pH to 4.5 to obtain a precipitate, dissolve and dilute with water, adjust the pH to neutral, and spray dry.
[0015] Weigh 5kg of wheat germ protein, add 50 times the weight of deionized water, stir and dissolve, configure a 2% solution, add 8% (w / w) alkaline protease of the wheat germ protein quality after homogenization, and maintain the reaction solution The pH value is 9.0, and the enzymatic hydrolysis reaction is carried out at 40°C. The enzymatic hydrolysis reaction solution is sent to the ultrafiltration device, the product solution passes through the ultrafiltration membrane, and the unreacted substrate and enz...
Embodiment 2
[0017] Add 8% (w / v) of defatted wheat germ powder into water, stir at pH 8.5 for 0.5 h, centrifuge to obtain the supernatant, adjust the pH to 6.5, use medium-temperature amylase at 60°C for 240 min, add The enzyme amount is 1% (w / v); after enzymatically degrading the starch, adjust the pH to 4 to obtain a precipitate, dissolve and dilute with water, adjust the pH value to neutral, and spray dry.
[0018] Take 5kg wheat germ protein, add 100 times of weight deionized water, stir and dissolve, configure 1% wheat germ solution, add alkaline protease after homogenization, the enzyme amount is 6% (w / w), maintaining the pH value of the reaction solution at 8.0, and performing the enzyme-membrane coupling reaction at 50°C. The enzymatic hydrolysis reaction solution is sent to the ultrafiltration device, the product solution passes through the ultrafiltration membrane, and the unreacted substrate and enzyme solution continue to return to the reactor for reaction. The molecular weigh...
Embodiment 3
[0020] Add defatted wheat germ powder at a concentration of 12% (w / v) to water, stir at pH 9.5 for 0.5 h, centrifuge to obtain the supernatant, adjust the pH to 7.5, use medium-temperature amylase at 70°C for 120 min, add The enzyme amount is 2.5% (w / v); after enzymatically degrading the starch, adjust the pH to 4 to obtain a precipitate, dissolve and dilute with water, adjust the pH to neutral, and spray dry.
[0021] Weigh 5kg of wheat germ protein, add 100 times the weight of deionized water, stir to dissolve, configure 1% wheat germ solution, add neutral protease after homogenization, the amount of enzyme added is 4% of the mass of wheat germ protein, and maintain the reaction The pH value of the solution was 7.0, and the enzyme-membrane coupling reaction was carried out at 45°C. The enzymatic hydrolysis reaction solution is sent to the ultrafiltration device, the product solution passes through the ultrafiltration membrane, and the unreacted substrate and enzyme solution ...
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