Method for preparing antioxidant active peptide by hydrolyzing fish scale collagen with co-immobilized double enzymes
A technology of fish scale collagen and antioxidant active peptide is applied in the preparation method of peptide, chemical instrument and method, fixed on/in organic carrier, etc., to achieve non-toxic side effect, easy purification and high enzymatic hydrolysis efficiency. Effect
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Embodiment 1
[0028] (1) Dissolve papain and Alcalase alkaline protease in phosphate buffer at a ratio of 1:1 to prepare a protease solution with a mass concentration of 1.0%; meanwhile, prepare a pH 7.0 mass concentration of 2.0% alginic acid Sodium solution, take the prepared protease solution and add it to the sodium alginate solution. The volume ratio of the protease solution to the sodium alginate solution is 1:1. After fully stirring, add 0.5% CaCl 2 In the solution, transfer it to a 4℃ refrigerator to harden for 6 h, filter and wash. Then add 0.1% glutaraldehyde solution in volume fraction, shake for 0.5 h, let stand for 4 h at 25℃, wash away residual glutaraldehyde and unimmobilized enzyme with phosphate buffer, and blow dry with cold air Surface water has to co-immobilize the dual enzyme.
[0029] (2) Using fresh grass carp fish scales as raw materials, soak and wash the surface adhesions of the fish scales, dry at 40°C, then crush the washed and dried fish scales into fine powder, a...
Embodiment 2
[0038] (1) Dissolve the neutral protease and Alcalase alkaline protease in the phosphate buffer at a ratio of 1:2 to prepare a protease solution with a mass concentration of 3.0%; meanwhile, prepare a pH 9.0 mass concentration of 4.0% seaweed Sodium solution, add the prepared protease solution to the sodium alginate solution, the volume ratio of the protease solution to the sodium alginate solution is 1:3. After stirring well, add CaCl with a mass concentration of 2.5% 2 In the solution, transfer to a 4℃ refrigerator to harden for 4 h, filter and wash. Then add 1.5% glutaraldehyde solution with volume fraction, shake for 0.5 h, stand for 5 h at 15℃ for cross-linking, wash away residual glutaraldehyde and unimmobilized enzyme with phosphate buffer, and blow dry with cold air The surface moisture has to be co-immobilized dual enzymes.
[0039] (2) Using fresh grass carp fish scales as raw materials, wash the surface adhesions of the fish scales by immersion, dry at 40°C, then crus...
Embodiment 3
[0048] (1) Dissolve the neutral protease and papain in the phosphate buffer in the ratio of activity ratio of 1:3, prepare a protease solution with a mass concentration of 5.0%; meanwhile, prepare a pH 6.0 with a mass concentration of 6.0% sodium alginate Solution: Take the prepared protease solution and add it to the sodium alginate solution. The volume ratio of the protease solution to the sodium alginate solution is 1:5. After stirring well, add CaCl with mass concentration of 5.0% 2 In the solution, transfer to a 4℃ refrigerator to harden for 2 hours, filter and wash. Then add the volume fraction of 3.0% glutaraldehyde solution, shake for 0.5 h, let stand for 6 h at 4℃, wash away residual glutaraldehyde and unimmobilized enzyme with phosphate buffer, and blow dry with cold air The surface moisture has to be co-immobilized dual enzymes.
[0049] (2) Using fresh grass carp fish scales as raw materials, wash the surface adhesions of the fish scales by immersion, dry at 40°C, th...
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