Chicken bone antioxidant peptides and preparation method thereof
An antioxidant peptide and chicken bone technology, applied in the field of chicken bone antioxidant peptide and its preparation, can solve the problems of weak chicken bone research, low comprehensive utilization rate, environmental pollution, etc., so as to improve comprehensive antioxidant capacity and reduce resource waste. and pollution, strong antioxidant effect
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Embodiment 1
[0023] The preparation method of antioxidant peptide of the present invention is as follows:
[0024] Chicken bone pretreatment: Wash the chicken bone, remove the flesh, cut into pieces, dry in a constant temperature drying oven at 50°C for 48 hours, pulverize with a pulverizer, degrease with petroleum ether, and pass through a 40-mesh sieve to obtain the raw material of chicken bone powder .
[0025] Extraction of chicken bone protein: Soak the chicken bone powder in distilled water, the substrate protein concentration is 8% (w / v), put it in the ultrasonic microwave combination reaction system, the corresponding ultrasonic wave and microwave treatment conditions are ultrasonic power 500W, ultrasonic time 30min, Microwave power 520W, microwave time 7.9min.
[0026] Enzymatic hydrolysis of chicken bone protein: papain and flavor protease are used to compound enzymatic hydrolysis of chicken bone protein with an enzyme activity ratio of 1:4. The amount of enzyme added is 9000U / g...
Embodiment 2
[0033] The activity of the natural antioxidant peptide obtained in Example 1 is studied:
[0034] Reducing power: Weigh the freeze-dried sample and prepare a 5mg / mL sample solution. Take 1.2mL sample solution for reducing power measurement, add 3mL 0.2mol / L phosphate buffer solution and 3ml 1% potassium ferricyanide solution, and bathe in water at 50°C for 20min. Take it out after the water bath, and after returning to room temperature, add 3 mL of 10% trichloroacetic acid, and centrifuge at 3000 r / min for 10 min. Mix 2 mL of supernatant with 2 mL of distilled water, add 0.5 mL of 0.1% ferric chloride solution, let stand for 10 min, and measure absorbance at a wavelength of 700 nm. At the same time, 1.2 mL of distilled water was used instead of the enzymatic solution as a blank control.
[0035] DPPH free radical scavenging rate: Accurately weigh 3.94mg DPPH, dissolve in 95% ethanol, dilute to 100mL, and make 0.1mmol / L DPPH solution. Weigh the freeze-dried sample and prepar...
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