Application of seaweed polypeptide in preparing health-care product for reducing blood fat and blood sugar as well as beverage containing polypeptide for reducing blood fat and blood sugar
A hypolipidemic and hypoglycemic technology, applied in the fields of hypoglycemic beverages, hypolipidemic, and seaweed polypeptides, can solve the problems of lack of a reliable and satisfactory treatment method, changes in liver function, muscle lysis, etc., and achieve the effect of lowering blood pressure. Significant effect, high vitamin and mineral content, and wide source of raw materials
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Embodiment 1
[0027] 1) Raw materials: choose the first stubble dried laver;
[0028] 2) Add water to soak: add water in the ratio of 1:25 (Porphyra haitanensis: water) and soak for 30 min;
[0029] 3) Colloidal grinding and grinding: Pass the laver soaking mixture through colloid milling to form a finer laver slurry;
[0030] 4) Heating and heat preservation: heat the seaweed slurry to the center temperature of 50℃;
[0031] 5) Protease enzymolysis: use AS.1398 neutral protease at 50℃, pH7.5, and enzyme amount E / S 10000U.g -1 , Under the condition of substrate concentration 5% (w / v), enzymatically hydrolyze Porphyra haitanensis slurry for 10 hours to obtain enzymatic hydrolysate;
[0032] 6) Centrifugation: Put the enzyme hydrolysate at 8000r.min -1 Centrifuge for 10 min to remove laver residue and obtain the supernatant;
[0033] 7) Supernatant dilution: the supernatant collected by centrifugation is thicker, first dilute it with water at a ratio of 1:1;
[0034] 8) Ul...
Embodiment 2
[0036] 1) Raw material: The raw material is selected from the third crop of dried laver;
[0037] 2) Add water to soak: add water in the ratio of 1:25 (Porphyra haitanensis: water) and soak for 30 min;
[0038] 3) Colloidal grinding and grinding: Pass the laver soaking mixture through colloid milling to form a finer laver slurry;
[0039] 4) Heating and heat preservation: heat the seaweed slurry to the core temperature of 45℃;
[0040] 5) Protease enzymolysis: use AS.1398 neutral protease at 45℃, pH7.2, and add enzyme amount E / S 8000U.g -1 , Under the condition of 3% (w / v) substrate concentration, enzymatically hydrolyze Porphyra haitanensis slurry for 10 hours to obtain enzymatic hydrolysate;
[0041] 6) Centrifugation: Put the enzyme hydrolysate at 8000r.min -1 Centrifuge for 10 min to remove laver residue and obtain the supernatant;
[0042] 7) Supernatant dilution: the supernatant collected by centrifugation is thicker, first dilute it with water at a ratio of...
Embodiment 3
[0045] 1) Raw material: choose the last dried laver as raw material;
[0046] 2) Add water to soak: add water at the ratio of 1:30 (Porphyra haitanensis: water) and soak for 30 min;
[0047] 3) Colloidal grinding and grinding: Pass the laver soaking mixture through colloid milling to form a finer laver slurry;
[0048] 4) Heating and heat preservation: heat the seaweed slurry to the core temperature of 55℃;
[0049] 5) Protease enzymolysis: use AS.1398 neutral protease at 55℃, pH7.8, and add enzyme amount E / S 12000U.g -1 , Under the condition of substrate concentration of 7% (w / v), enzymatically hydrolyze Porphyra haitanensis slurry for 5 hours to obtain enzymatic hydrolysate;
[0050] 6) Centrifugation: Put the enzyme hydrolysate at 8000r.min -1 Centrifuge for 10 min to remove laver residue and obtain the supernatant;
[0051] 7) Supernatant dilution: the supernatant collected by centrifugation is thicker, first dilute it with water at a ratio of 1:1;
[0052]...
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