Method for catalytically synthesizing biomimetic material hydroxyapatite from phosvitin and polypeptide thereof
A phosvitin and hydroxyapatite technology, applied in phosphorus compounds, chemical instruments and methods, inorganic chemistry, etc., can solve the problems of synthesis time limitation, long time, etc. active effect
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Embodiment 1
[0024] A method of utilizing phosvitin to catalyze the synthesis of biomimetic material hydroxyapatite:
[0025] After dissolving calcium chloride and potassium dihydrogen phosphate, react in a neutral solution under the catalysis of phosvitin, the molar ratio of calcium chloride and potassium dihydrogen phosphate is 3:1, and add 1 g of calcium ion per 3 mol of calcium ion Phosvitin. During the reaction process, 0.1 mol / L NaOH solution is continuously added dropwise to keep the pH of the system at 6.8-7.2. After 15 minutes of reaction, the precipitate is collected to obtain the hydroxyapatite mineralized material.
Embodiment 2
[0027] 1) Enzymatic hydrolysis of phosvitin: Dissolve phosvitin in 0.01mol / L NaOH solution, stir for 1 hour, adjust the pH of the solution to 2.2, add 1g of pepsin for every 50g of phosvitin, and perform enzymatic hydrolysis for 3 hours , and then adjust the pH of the solution to 7.5, then add 1 g of trypsin for every 20 g of phosvitin, and perform enzymatic hydrolysis for 5 hours. After the enzymatic solution is centrifuged, the supernatant is the phosvitin polypeptide mixture.
[0028] 2) Separation and purification of peptides: using Toyopearl DEAE-650M anion exchange chromatography, the filler balance buffer is Tris-HCl buffer with pH 7.2, after the supernatant is loaded, use sodium chloride concentrations of 0, 0.1, 0.2, 0.3, 0.4, 0.5 and 0.6 mol / L Tris-HCl buffer solution for gradient elution step by step, collect the eluate with a sodium chloride concentration of 0.2 mol / L, and perform desalination treatment according to the conventional ultrafiltration method. The mole...
Embodiment 3
[0031] (1) Enzymatic hydrolysis of phosvitin: take phosvitin and dissolve it in 0.1mol / L NaOH solution, stir for 0.5 hours, adjust the pH of the solution to 2.8, add 1g of pepsin per 100g of phosvitin, and enzymolyze 5 hour, then adjust the pH of the solution to 8.2, then add 1g of trypsin per 80g of phosvitin, and enzymatically hydrolyze for 8 hours. After the enzymatic solution is centrifuged, the supernatant is the phosvitin polypeptide mixture.
[0032] (2) Separation and purification of peptides: Q Sepharose FF anion exchange chromatography was used, and the filler equilibrium buffer was Tris-HCl buffer at pH 8.0. After loading the supernatant, Tris-HCl with a sodium chloride concentration of 0.5mol / L was used. The HCl buffer is used for elution, the eluate is collected, and after desalting treatment, the phosvitin polypeptide with biological activity is obtained.
[0033] (3) Catalytic synthesis: react calcium chloride and sodium dihydrogen phosphate under the catalysis ...
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