Method for preparing rapeseed dreg protein antioxidative peptide solution by gastrointestinal simulated digestion
A technology for simulating digestion and anti-oxidative peptides, applied in the field of food processing technology and protein utilization, can solve the problems of unclear correlation between the activity of the enzymatic hydrolyzate product and the molecular weight of the polypeptide, and the low efficiency of single-enzyme enzymatic hydrolysis, so as to make full use of raw materials and improve The effect of high hydrolysis efficiency and enzymatic hydrolysis efficiency
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Embodiment 1
[0051] Add 25 mL of simulated gastric digestion solution into a 100 mL Erlenmeyer flask, and place in a constant temperature water bath at 37°C for 5 minutes. Add rapeseed meal accounting for 4% of the mass ratio of gastric digestive juice, quickly vortex and oscillate, quickly place in a 37°C water bath, and stir for 4 hours for enzymatic hydrolysis. Then 35 mL of simulated intestinal digestion solution was added, the pH was adjusted to 6.4, and the enzyme was hydrolyzed for 1 h at a constant temperature of 37°C. Boiling water bath for 10 min to terminate the reaction; centrifuge at 4500r / min for 10min, take the supernatant to adjust the pH to 4.2, centrifuge at 4500r / min for 30min to remove macromolecular protein, and obtain the antioxidant rapeseed meal peptide solution. The scavenging rate of DPPH was 72.99±0.32%, and the scavenging rate of OH (hydroxyl radical) was 93.98±0.19%. Peptides with a molecular weight distribution of 211-5000Da in the peptide solution accounted ...
Embodiment 2
[0055] Add 25 mL of simulated gastric digestion solution into a 100 mL Erlenmeyer flask, and place in a constant temperature water bath at 37°C for 5 minutes. Add 2% rapeseed meal in the mass ratio of gastric digestive juice, quickly vortex and oscillate, quickly place in a 37°C water bath, and stir for 4 hours for enzymatic hydrolysis. Then 35 mL of simulated intestinal digestion solution was added, the pH was adjusted to 6.4, and the enzyme was hydrolyzed for 1 h at a constant temperature of 37°C. Boiling water bath for 10 min to terminate the reaction; centrifuge at 4500r / min for 10min, take the supernatant to adjust the pH to 4.2, centrifuge at 4500r / min for 30min to remove macromolecular protein, and obtain the antioxidant rapeseed meal peptide solution. The scavenging rate of DPPH was 71.65±0.78%, and the scavenging rate of OH (hydroxyl radical) was 93.21±0.65%.
Embodiment 3
[0057] Add 25 mL of simulated gastric digestion solution into a 100 mL Erlenmeyer flask, and place in a constant temperature water bath at 37°C for 5 minutes. Add 1% rapeseed meal in the mass ratio of gastric digestive juice, vortex and shake rapidly, place in a 37°C water bath, and stir for 4 hours for enzymatic hydrolysis. Then 35 mL of simulated intestinal digestion solution was added, the pH was adjusted to 6.4, and the enzyme was hydrolyzed for 1 h at a constant temperature of 37°C. Boiling water bath for 10 min to terminate the reaction; centrifuge at 4500r / min for 10min, take the supernatant to adjust the pH to 4.2, centrifuge at 4500r / min for 30min to remove macromolecular protein, and obtain the antioxidant rapeseed meal peptide liquid. The scavenging rate of DPPH was 71.12±0.28%, and the scavenging rate of OH (hydroxyl radical) was 90.23±0.73%.
[0058] Table 1 Composition and content of free amino acids in rapeseed meal raw materials and rapeseed meal antioxidant p...
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