A kind of preparation method of cholesterol-lowering protein
A cholesterol-lowering, protein-based technology, applied in peptide preparation methods, chemical instruments and methods, metabolic diseases, etc., to achieve the effect of increasing cholesterol-lowering activity
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Embodiment 1
[0028] Measure 3L of milk, adjust its temperature to 50°C for preheating, and use high-intensity ultrasound for protein modification. The modification time is 5 minutes, and the power density is 50W / L; S-neutral protease performs low-intensity ultrasound-enzyme hydrolysis coupling modification on the protein, keeps the temperature and pH constant, and the ultrasound power density is 5W / L. When the cholesterol-lowering activity of the modified protein reaches the highest value of 41.63% after the in vitro simulated gastrointestinal digestion, the enzymatic hydrolysis reaction is terminated, and the modified protein product is obtained through inactivation, concentration and spray drying. After reconstitution by adding water (keep the protein content unchanged), the cholesterol-lowering activity after the in vitro simulated gastrointestinal tract digestion was determined to be 21.56%, and the activity remained 51.79% after spray-drying.
Embodiment 2
[0030] Measure 3L of milk, adjust its temperature to 50°C to preheat, and use high-intensity ultrasound to modify the protein. The modification time is 20 minutes, and the power density is 200W / L; S-neutral protease performs low-intensity ultrasound-enzyme hydrolysis coupling modification on the protein, keeps the temperature and pH constant, and the ultrasound power density is 10W / L. When the cholesterol-lowering activity of the modified protein reaches the highest value of 53.28% after the in vitro simulated gastrointestinal digestion, the enzymatic hydrolysis reaction is terminated, and the modified protein product is obtained through inactivation, concentration and spray drying. After reconstitution by adding water (keep the protein content unchanged), the cholesterol-lowering activity after the in vitro simulated gastrointestinal digestion was determined to be 32.43%, and the activity remained 60.87% after spray-drying.
Embodiment 3
[0032] Measure 3L of milk, adjust its temperature to 50°C for preheating, and use high-intensity ultrasound to modify the protein. The modification time is 60 minutes, and the power density is 500W / L; S-neutral protease performs low-intensity ultrasound-enzyme hydrolysis coupling modification on the protein, keeps the temperature and pH constant, and the ultrasound power density is 20W / L. When the cholesterol-lowering activity of the modified protein reaches the highest value of 48.29% after in vitro simulated gastrointestinal digestion, the enzymatic hydrolysis reaction is terminated, and the modified protein product is obtained through inactivation, concentration and spray drying. After reconstitution by adding water (keep the protein content unchanged), the cholesterol-lowering activity after the in vitro simulated gastrointestinal tract digestion was determined to be 26.72%, and the activity remained 55.33% after spray-drying.
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