Hericium erinaceus glycoprotein with anti-tumor and agglutination activity and preparation method thereof
A technology of glycoprotein and Hericium erinaceus, which is applied in the field of Hericium erinaceus glycoprotein and its preparation, achieves the effects of high extraction rate, broad application prospects, and simple preparation process
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Embodiment 1
[0036] Cultivate the strain Hericium erinaceus ACCC 50011 preserved in the China Agricultural Microorganism Culture Collection and Management Center on the substrates such as soybean straw powder, corn stalk powder, wheat bran, broad-leaved tree bran, sugar beet bagasse, sugarcane bagasse or cottonseed hulls, etc., for 20-30 days. oC After culturing for 15-30 days, the fruiting bodies of Hericium erinaceus were collected.
Embodiment 2
[0038] Activate the strain Hericium erinaceus ACCC 50011 preserved in the China Agricultural Microbiological Culture Collection Management Center, boil it in PDA slant medium (200 g potato in boiling water for 20 min, filter the filtrate, add 20 g glucose and 20 g agar, and add water to 1 L, pH natural). The test tubes and tampons used for culture need to be kept at 121 oC Sterilize for 30 min, then fill with medium 121 oC Sterilize for 30 minutes, and cool down on an inclined plane to make it solidify into an inclined plane. Then the ultra-clean bench was inoculated. The slant was cultured at a constant temperature of 25 oC Left and right, for a period of 7 days. Cut the slant bacteria into small pieces and inoculate them into the seed culture medium. After the medium is divided, put a cotton plug on the Erlenmeyer flask to prevent external microorganisms from entering the medium and cause pollution, and ensure good ventilation performance. . The composition of the s...
Embodiment 3
[0040] After 500 g Hericium erinaceus fruiting bodies were added to 0.8 times the volume of water, the homogenate was broken, 4 o C leaching, centrifugation, discarding the insoluble matter, collecting the supernatant, adding ammonium sulfate to 80% saturation after the supernatant was concentrated, standing for 24 hours, high-speed centrifugation to take the precipitate, adding a small amount of water to redissolve the above precipitate, and reconstituted The solution was placed in a dialysis bag of 8000-14000 Da, dialyzed with deionized water, the dialysate was collected, concentrated, subjected to DEAE-Sepharose Fast Flow column chromatography, unbound components were eluted with distilled water, and 0.1 mol / L, 0.3 mol / L and 0.5 mol / L NaCl were used as the eluent for gradient elution, and the glycoprotein fractions eluted at each stage of the NaCl solution were collected, and each collected solution was freeze-dried; among them, the HE-1 fraction was subjected to Superdex T...
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