Method for extracting astragalus membranaceus lectin protein from astragalus membranaceus seeds
A technology of Astragalus membranaceus and lectin, which is applied in the biological field, can solve the problem of low extraction rate of Astragalus membranaceus seeds, and achieve the effect of increasing protein extraction rate and extraction amount
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Embodiment 1
[0029] The embodiment of the present invention provides a method for extracting the lectin protein of Astragalus membranaceus by using the seeds of Astragalus membranaceus, using the seeds of Astragalus membranaceus as the raw material, comprising the following steps:
[0030] S1. Preprocessing:
[0031] Rinse the raw materials with clean water at 25°C for 12 minutes, then shell and crush the seeds, soak them in warm water at 4°C for 1.5 days, and then stir them into a slurry;
[0032] S2, extraction:
[0033] Filter water through a 40um microporous membrane, then add agar powder with a volume of 2% of the slurry to the slurry, and stir evenly with the slurry, then place it in a centrifuge, centrifuge at 18000r / min for 20min, collect the supernatant, and then add 30ml of 20mmol / L, pH7.0 PBS buffer solution was dissolved, put into dialysis bags for dialysis, and the initial product was obtained after repeated dialysis;
[0034] S3, purification:
[0035] Separate and purify ...
Embodiment 2
[0045] The embodiment of the present invention provides a method for extracting the lectin protein of Astragalus membranaceus by using the seeds of Astragalus membranaceus, using the seeds of Astragalus membranaceus as the raw material, comprising the following steps:
[0046] S1. Preprocessing:
[0047] Rinse the raw materials with clean water at 35°C for 25 minutes, then shell and crush the seeds, soak them in warm water at 55°C for 3 days, and then stir them into a slurry;
[0048] S2, extraction:
[0049] Filter the water through a 40um microporous membrane, then add agar powder with a volume of 5% of the slurry to the slurry, and stir evenly with the slurry, then place it in a centrifuge, centrifuge at 18000r / min for 20min, collect the supernatant, and then add 30ml of 20mmol / L, pH7.0 PBS buffer solution was dissolved, put into dialysis bags for dialysis, and the initial product was obtained after repeated dialysis;
[0050] S3, purification:
[0051] Separate and puri...
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