Method for producing oligopeptides and glycosaminoglycans by using scallop processing by-products
A technology of scallops and glycosaminoglycans, which is applied in the field of preparation of oligopeptides and glycosaminoglycans, can solve the problems of waste of resources, environment, pollution, etc., and achieve high production safety, improved safety, and small molecular weight Effect
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Embodiment 1
[0026] A method for preparing scallop oligopeptides and glycosaminoglycans by using scallop processing by-products, comprising the following steps:
[0027] (1) With the scallop skirt of Ezo as raw material, get 200kg of scallop edge and prepare homogenate liquid with a meat grinder;
[0028] (2) Put the homogenate into a reaction tank, add distilled water with 5 times the weight of the homogenate, and autolyze at 40° C. for 3 hours to obtain the scallop liquid;
[0029] (3) Add the composite protease of 0.2% of the weight of the scallop liquid, adjust pH 3 with mass concentration 10% HCl, enzymolysis 4h under the condition of 45 DEG C, the mass ratio of the composite protease is as follows, pepsin: trypsin: Subtilisin = 4:4:2.
[0030] (4) After the enzymolysis is completed, boil to kill the enzyme for 15 minutes, cool to room temperature, centrifuge at 16000r / min with a swing-type tubular separator, discard impurities, and collect the supernatant;
[0031] (5) Use NaOH wit...
Embodiment 2
[0037] A method for preparing scallop oligopeptides and glycosaminoglycans by using scallop processing by-products, comprising the following steps:
[0038] (1) Using the cooking liquid of Ezo scallop as raw material;
[0039] (2) Take 4 tons of cooking liquid of Ezo scallop and put it into the reaction tank, and stir for 10 minutes.
[0040] (3) Add 0.2% compound protease by weight in the cooking liquid of scallop, adjust the pH to 3 with mass concentration of 10% HCl, and enzymatically hydrolyze for 4 hours at 45°C. The mass ratio of the compound protease is as follows, pepsin: trypsin : subtilisin=4:3:3.
[0041] (4) After the enzymolysis is completed, boil to kill the enzyme for 15 minutes, cool to room temperature, centrifuge at 16000r / min with a swing-type tubular separator, discard impurities, and collect the supernatant;
[0042](5) Use 10% NaOH in the mass concentration to adjust the pH of the clear liquid to 9.5, add 0.2% hydrogen peroxide in the volume of the clea...
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