Production method of sea cucumber peptide extract
A production method and technology of extracting solution, which is applied in the field of sea cucumber peptide extracting solution, can solve the problems of deep color of sea cucumber peptide solution, large loss of sea cucumber peptide, and many side reactions, etc., and achieve small loss rate of sea cucumber peptide, strong biological activity, and simple operation Effect
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Embodiment 1
[0011] After the dried sea cucumber is desalted, remove the inner wall membrane and spit, wash, pulverize and homogenate; adjust the pH of the sea cucumber homogenate to 6.0 with food regulators such as hydrochloric acid, acetic acid or sodium hydroxide, and then add 3100U / g Bacillus subtilis neutral protease, 250U / g flavor protease, that is, add 3100U Bacillus subtilis neutral protease and 250U flavor protease to each gram of sea cucumber homogenate, control enzymolysis at 65°C for 3 hours, and heat at 100°C for 10 minutes , inactivate the enzyme, and cool to normal temperature; filter the enzymolysis mixture to remove the residue; use D280 anion resin to decolorize and deodorize the enzymolysis solution to obtain sea cucumber peptide extract. This product is light gray and has no fishy smell. The sea cucumber peptide content is 14 mg / ml determined by the biuret method, and the free amino acid nitrogen content is 0.6 mg / ml determined by the formaldehyde titration method.
Embodiment 2
[0013] After the dried sea cucumber is desalted, remove the inner wall membrane and spit, wash, pulverize and homogenate; adjust the pH of the sea cucumber homogenate to 6.5 with food regulators such as hydrochloric acid, acetic acid or sodium hydroxide, and then add 2400U / g Bacillus subtilis neutral protease, 400U / g flavor protease, that is, add 2400U Bacillus subtilis neutral protease and 400U flavor protease to each gram of sea cucumber homogenate, control enzymolysis at 50°C for 5 hours, and heat at 100°C for 10 minutes , inactivate the enzyme, and cool to normal temperature; filter the enzymolysis mixture to remove the residue; use D380 anion resin to decolorize the enzymolysis solution to obtain sea cucumber peptide extract. The product is light gray and has no fishy smell. The sea cucumber peptide content is 16 mg / ml determined by the biuret method, and the free amino acid nitrogen content is 0.7 mg / ml determined by the formaldehyde titration method.
Embodiment 3
[0015] For fresh sea cucumbers, remove the spit, viscera and inner wall membrane, wash, crush and homogenize; use hydrochloric acid, acetic acid or sodium hydroxide and other food regulators to adjust the pH of the sea cucumber homogenate to 7.0, add 1600U / g of Bacillus subtilis to neutralize Protease, 700U / g flavor protease, that is, add 1600U Bacillus subtilis neutral protease and 700U flavor protease to each gram of sea cucumber homogenate, control enzymolysis at 60°C for 3 hours, heat at 100°C for 10 minutes, inactivate the enzyme, and cool to Normal temperature; filter the enzymolysis mixture to remove residues; use D301T anion resin to decolorize and deodorize the enzymolysis solution to obtain sea cucumber peptide extract. This product is light gray and has no fishy smell. The sea cucumber peptide content is 13 mg / ml determined by the biuret method, and the free amino acid nitrogen content is 0.5 mg / ml determined by the formaldehyde titration method.
[0016] The sea cu...
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