A preparation method of fish egg glycoprotein with anti-osteoporosis effect
A technology for osteoporosis and glycoproteins, applied in food preparation, hydrolyzed protein components, applications, etc., to achieve strong anti-osteoporosis activity, no environmental pollution, and simple process steps
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Embodiment 1
[0018] Take 2.0 kg of fresh or thawed crucian carp roe at room temperature, remove impurities, wash 3 times, colloid mill homogenate, and freeze-dry, add 3L of 95% ethanol to degrease for 15 hours, and change ethanol 4 times during this period. Centrifuge at 3500 rpm for 10 minutes, remove the supernatant, and the precipitate is defatted roe protein. Freeze-dry the defatted fish egg protein, add 6L of distilled water and preheat to 50°C. Under constant temperature stirring, add 3g of neutral protease and 3g of alkaline protease for hydrolysis for 5 hours, and the pH is 7.0. Then inactivate the enzyme activity at 100°C for 7 minutes. The enzymatic solution was cooled to room temperature and centrifuged at 5000 rpm for 5 min. The supernatant was taken, subjected to ultrafiltration with an ultrafiltration membrane with a molecular weight cut-off of 10KD, and the filtrate was freeze-dried to obtain a fish egg glycopeptide sample.
Embodiment 2
[0020] Take 2.0 kg of fresh cod roe or thawed at room temperature, remove impurities, wash 3 times, colloid mill homogenate, freeze-dry, add 3L of 95% ethanol to degrease for 18 hours, and change ethanol 3 times during this period. Centrifuge at 3500 rpm for 10 minutes, remove the supernatant, and the precipitate is defatted roe protein. Freeze-dry the defatted fish egg protein, add 6L of distilled water and preheat to 50°C. Under constant temperature stirring, add 4g of neutral protease and 4g of alkaline protease for hydrolysis for 4 hours, and the pH is 7.0. Then inactivate the enzyme activity at 100°C for 7 minutes. The enzymatic solution was cooled to room temperature and centrifuged at 5000 rpm for 5 min. The supernatant was taken, subjected to ultrafiltration with an ultrafiltration membrane with a molecular weight cut-off of 10KD, and the filtrate was freeze-dried to obtain a fish egg glycopeptide sample.
[0021] The 95% ethanol degreasing 15h described in the prep...
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