Sea squirt antioxidant polypeptide and preparation method thereof
A technology of antioxidant peptides and sea squirts, applied in the biological field, can solve the problems of less research on antioxidant active peptides, and achieve the effect of increasing added value and broadening research
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Embodiment 1
[0034] The preparation of sea squirt antioxidant polypeptide comprises the following steps:
[0035] 1) Treatment of true sea squirts: after thawing, remove the outer shell of true sea squirts to take the inner capsule, remove the viscera and fascia in the inner capsule, add ultrapure water to boil at 100°C for 15 minutes to inactivate enzymes, and prepare meat pieces of the sea squirt inner capsule for use.
[0036] 2) Impurity removal: After the meat pieces are crushed, they are placed in petroleum ether to remove fat, and ethanol is added to remove pigment to obtain ascidian crude protein, which is ready for use.
[0037] 3) Enzymatic hydrolysis of ascidian internal capsule protein: use complex protease to enzymolyze the internal capsule protein of sea squirt, pH is 7.0, keep the temperature in a water bath at 50°C, the ratio of enzyme to substrate is 1:4, enzymatic hydrolysis for 7 hours, then boil in water bath for 15 minutes Inactivate the enzyme, quickly cool to room te...
Embodiment 2
[0049] Example 2 Determination of antioxidant activity
[0050] 1) DPPH free radical scavenging ability
[0051] 95% ethanol prepared DPPH radical solution with a concentration of 0.1mM. Samples with different concentrations were mixed with DPPH at a ratio of 1:1, and the absorbance was measured at 517nm after reacting at room temperature for 30 minutes in the dark. The blank group replaced the sample with the same volume of 95% ethanol, and the DPPH free radical scavenging ability of the sample was calculated according to the following formula:
[0052]
[0053] In the formula, A control Absorbance value of the blank group, A sample is the absorbance value of the experimental group.
[0054] 2) ABTS free radical scavenging ability
[0055] ABTS solution with a concentration of 7mM and potassium persulfate solution with a concentration of 2.45mM were prepared in ultrapure water, mixed at a ratio of 1:1, and incubated at room temperature in the dark for 12-16 hours to ob...
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