Preparation method of glycosylated silybum marianum protein isolate
A technology for separating protein and milk thistle, which is applied in the field of protein preparation, can solve the problems that the functional properties of milk thistle protein are not particularly good, and achieve the effects of improving the comprehensive utilization of resources, mild reaction conditions, and simple operation
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[0022] A method for preparing glycosylated milk thistle protein isolate, which comprises the following steps:
[0023] (1) Take milk thistle protein and dissolve it in deionized water to make the mass concentration 1.2g / 100mL.
[0024] (2) Adjust the pH value of (1) to 11 with 0.1mol / L NaOH, then heat to 50°C, stir magnetically for 30min, and cool at room temperature.
[0025] (3) Add sugar according to the ratio, stir for 30 minutes and adjust the pH value of the system with 0.1mol / L HCl solution until precipitation occurs.
[0026] (4) After magnetically stirring for another 30 minutes, centrifuge, remove the supernatant precipitate, and freeze-dry to obtain a freeze-dried powder of a mixture of milk thistle protein and sugar.
[0027] (5) Put the freeze-dried powder in a desiccator (filled with saturated KI solution), and take a sample after a period of reaction, which is the silymarin protein glycosylation complex.
[0028] The milk thistle protein isolate described in s...
Embodiment 1
[0036] Under the conditions of setting the temperature at 60°C, the material mass ratio (silymarin / glucan) at 1:3, and the reaction time at 30 hours, prepare glycosylated milk thistle according to the method described in claims 1-7 protein isolate. The obtained product has better appearance and luster, and the grafting degree of the compound is the highest.
Embodiment 2
[0038] Combined with single factor experiment, through response surface analysis, the optimal preparation conditions of glycosylated milk thistle protein were obtained: material mass ratio (silymarin / dextran) was 1:3.02, reaction time was 42.98h, reaction temperature was 59.82 °C, the degree of grafting of the glycosylation complex obtained under this condition was 42.55%, and the browning index was 0.931.
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