A kind of perilla seed antioxidant dipeptide and its preparation method and application
A technology for oxidizing dipeptides and anti-oxidizing peptides, which is applied in the field of food biology and can solve the problems of less research on protein development and utilization, and no reports on the pharmacology of active peptides.
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Embodiment 1
[0028] The separation and purification of the antioxidant dipeptide in the present invention includes two steps of Sephadex G-25 gel filtration chromatography and reverse phase high performance liquid chromatography (RP-HPLC).
[0029]Preparation of perilla seed crude protein enzymatic hydrolysis product: first degrease perilla seed with petroleum ether, then use alkali extraction and acid precipitation method to obtain perilla seed crude protein, use alkaline protease to enzymatically hydrolyze perilla seed crude protein, use alkali Protease under its optimum enzymolysis conditions: pH 9.80, enzyme addition 3000U / g, substrate concentration 3% (w / v), hydrolysis time 5.00h, inactivated in boiling water bath for 10min, centrifuged at 12000rpm for 10min, take the The clear liquid is freeze-dried, which is the enzymatic hydrolyzate of perilla seed protein;
[0030] Sephadex G-25 Gel Filtration Chromatography: Dissolve the freeze-dried powder of perilla seed enzymatic hydrolyzate i...
Embodiment 2
[0035] The natural antioxidant dipeptide activity obtained in Example 1 is studied:
[0036] ABTS free radical scavenging effect: prepare 7 mmol / L ABTS with distilled water + solution and 2.45 mmol / L potassium persulfate solution (must be placed at room temperature for 16 h before use), ABTS + Mix with potassium persulfate solution at a volume ratio of 1:1, and dilute the mixture to the absorbance value A with pH 7.4, 5 mmol / L phosphate buffer solution before use 734 is 0.70±0.02. Take 0.5 mL of samples with different concentrations and 0.5 mL of ABTS radical solution, mix and let stand for 10 min, then measure the absorbance at 734 nm. Deionized water and reduced glutathione were used instead of samples as blank control and positive control, respectively. ABTS free radical scavenging activity is calculated according to the following formula (1):
[0037] (1)
[0038] In the formula, A 0 : Absorbance value of blank control group; A s : Absorbance value of the sample ...
Embodiment 3
[0058] The natural antioxidative dipeptide obtained in embodiment 1 is carried out cytotoxicity and antioxidant research:
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