A kind of selenium-enriched tuna bone collagen peptide and preparation method thereof
A collagen peptide and tuna technology, which is applied to animal/human proteins, specific peptides, connective tissue peptides, etc., can solve the problem of different preparation processes of selenium-rich collagen peptides, low product yield and production cost, and unfavorable large-scale production. and other problems, to shorten the acid treatment time, avoid desorption, and be beneficial to human health.
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Embodiment 1
[0025] Tuna fish bones are cleaned after being broken by a bone cutter, then transported to a deashing tank, soaked for 4 hours with dilute hydrochloric acid (the molar concentration of hydrochloric acid in this embodiment is 1.2mol / L), soaked and washed with clear water after processing, soaked and washed for 3 hours -8 times, each soaking and washing time is 20-30min, soaking and washing with clear water until the pH value of the final soaking solution is 2 (the relationship between the final soaking and washing water and tuna bones is 5ml of water per 1g), the tuna bones and Purified water was thermally degraded at 60°C for 2 hours at a material-to-liquid ratio of 1:1 (w / v, g / ml); the pH value was adjusted to 5, and a compound neutral protease and alkaline protease with a fish bone weight of 1‰ were added to neutralize The mass ratio of protease to alkaline protease was 10:1, and after enzymolysis at 45°C for 2h, the enzyme was inactivated at 90°C for 10min; using acidic act...
Embodiment 2
[0028] Tuna fish bones are cleaned after being broken by a bone cutter, then transported to a deashing tank, soaked in dilute hydrochloric acid (the molar concentration of hydrochloric acid in this embodiment is 0.8mol / L) for 8 hours, soaked in clean water after treatment, and soaked and washed 3-8 times, soaking and washing for 20-30 minutes each time, soaking and washing with clean water until the pH value of the final soaking solution is 6 (the relationship between the amount of the final soaking washing water and the tuna bone is 5ml of water per 1g), and the tuna bone Thermally degrade at 90°C for 6 hours with purified water according to the material-liquid ratio of 1:3 (w / v, g / ml); adjust the pH value to 7, add compound neutral protease and alkaline protease with fish bone weight 5‰, The mass ratio of neutral protease to alkaline protease is 10:1, after enzymatic hydrolysis at 65°C for 6h, inactivate the enzyme at 90°C for 10min; add 10% of the weight of fish bone acidic ...
Embodiment 3
[0031] The tuna fish bones are cleaned after being broken by the bone cutter, then transported to the deashing tank, soaked with dilute hydrochloric acid (the molar concentration of hydrochloric acid in this embodiment is 1.0mol / L) for 8h, soaked and washed with clear water after processing, and soaked and washed for 3 hours. -8 times, each soaking and washing time is 20-30min, soaking and washing with clear water until the pH value of the final soaking solution is 4 (the relationship between the final soaking and washing water and tuna bones is 5ml of water per 1g), the tuna bones and Purified water is degraded in hot water at 80°C for 5 hours according to the ratio of material to liquid 1:3 (w / v, g / ml); the pH value is adjusted to 6.5, and a compound neutral protease and alkaline protease with a fish bone weight of 4‰ are added to The mass ratio of neutral protease to alkaline protease is 10:1. After enzymolysis at 50°C for 4 hours, the enzyme is inactivated at 90°C for 10 mi...
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