A kind of preparation method and application of pseudo sea dragon glycoprotein
A technology of glycoproteins and sea dragons, applied in the field of biochemistry, to achieve good repeatability, high product extraction rate, and ensure the integrity of the effect
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Embodiment 1
[0038] A preparation method of pseudo-hyronoprotein, comprising the following steps:
[0039] ①Pretreatment: Wash the pseudo sea dragon, put it in an oven, dry at 60°C for 4 hours, then pulverize and pass through a 10-mesh sieve to obtain pseudo sea dragon coarse powder, which is weighed;
[0040] ②Degreasing treatment: Add the quasi-sea dragon coarse powder obtained in step 1 and acetone equivalent to twice its volume into a rotary reflux apparatus, and rotate and reflux for 2 hours at 60 °C, carry out degreasing, and then filter, and repeat the rotary reflux extraction of the filter residue. drying the obtained degreasing coarse powder;
[0041]③Hot water extraction: add the degreasing coarse powder obtained in step ② and distilled water into a water bath at a material-to-liquid ratio of 1:20 (g / mL), stir evenly, extract at 100°C for 2.5 hours, filter, and the obtained filtrate is used for later use, The obtained filter residue is mixed and extracted with distilled water at...
Embodiment 2
[0047] The operation of embodiment 2 is basically the same as that of embodiment 1, and the difference is:
[0048] In step (3) hot water extraction: add the degreasing coarse powder obtained in step (2) and distilled water into a water bath at a material-to-liquid ratio of 1:25 (g / mL), stir evenly, extract at 80°C for 3h, filter, and the obtained filtrate For subsequent use, the obtained filter residue is mixed and extracted with distilled water at a material-to-liquid ratio of 1:25 (g / mL) for 1 h, filtered, and the filtrates of two times were merged to obtain a pseudo-hyronoprotein mixed solution;
[0049] In step 4. concentrated alcohol precipitation: add the mixed solution obtained in step 3 into a rotary evaporator, evaporate and concentrate to 1 / 5 of the original volume at 60 °C, add 3 times the volume of ethanol to the concentrated solution, and let stand at 4 °C for 12h, Carry out alcohol precipitation, collect the precipitate after centrifuging the alcohol precipitati...
Embodiment 3
[0051] The operation of embodiment 3 is basically the same as that of embodiment 1, and the difference is:
[0052] In step (3) hot water extraction: add the degreasing coarse powder obtained in step (2) and distilled water into a water bath at a material-to-liquid ratio of 1:30 (g / mL), stir evenly, extract at 90°C for 2h, filter, and the obtained filtrate For subsequent use, the obtained filter residue is mixed and extracted with distilled water at a material-to-liquid ratio of 1:30 (g / mL) for 1 h, filtered, and the filtrates of two times are combined to obtain a pseudo-hyronoprotein mixed solution;
[0053] In the concentrated alcohol precipitation in step 4: add the mixed solution obtained in step 3 into a rotary evaporator, evaporate and concentrate to 1 / 5 of the original volume at 70°C, add 3 times the volume of ethanol to the concentrated solution, and let stand at 4°C for 16h, Carry out alcohol precipitation, collect the precipitate after centrifuging the alcohol precip...
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