A kind of extraction method of chicken embryo egg yolk phosphoprotein phosphopeptide
A yolk protein and extraction method technology, which is applied in the preparation methods of peptides, chemical instruments and methods, peptides, etc., to achieve the effects of cost saving, high physiological activity, and promotion of mineral absorption
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Embodiment 1
[0022] Such as Figure 4 Shown, a kind of method for extracting the phosphoprotein phosphopeptide of egg yolk of chicken embryo, the steps are as follows:
[0023] (1) Incubation of fertilized eggs: select fertilized eggs that are not harmful to health, and put them in the incubator for incubation; after 12-15 days of incubation, take out the embryonic eggs, put them in a low temperature environment to end their life and save them for processing ;
[0024] (2) Extract phosvitin: Disinfect the surface of chicken embryo eggs, remove the eggshell and take out the chicken embryos, crush the chicken embryos with a tissue homogenizer, dilute with sterile water, adjust the pH to 3~6, and fully stir; Afterwards, the homogenate was centrifuged at 3000g for 20min, the precipitate was collected, and the mixed solution formed after mixing with n-hexane and ethanol in a volume ratio of 3:1 was fully degreased and filtered; the filtered retentate was washed with NaCl solution (1.74 M) D...
Embodiment 2
[0029] The prepared phosphopeptides were tested for promoting calcium absorption, promoting iron absorption and inhibiting linoleic acid oxidation. The specific experimental method is as follows:
[0030] Promote calcium absorption: different concentrations of phosphopeptide solutions (0 mg / L, 200 mg / L, 400 mg / L and 600 mg / L) with 5mM CaCl 2 Mix well with 20mM, 500mL sodium phosphate buffer (pH 8.0). React at 20°C for 30 min, titrate with NaOH to maintain the pH at 7.8, and then determine the soluble calcium content in the supernatant by atomic absorption chromatography. see attached results figure 1 .
[0031] To promote iron absorption: different concentrations of phosphopeptide solutions (0 mg / L, 200 mg / L, 400 mg / L and 600 mg / L) with 5mM FeCl 2 Mix well with 20mM, 500mL sodium phosphate buffer (pH 8.0). React at 20 °C for 30 min, titrate with NaOH to maintain the pH at 7.8, and then determine the soluble iron content in the supernatant by atomic absorption chromatograp...
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