Method for preparing crude phycobiliprotein and crude polysaccharide from porphyra yezoensis
A technology of laver and phycobiliprotein is applied in the field of preparation of phycobiliprotein and polysaccharide, and can solve the problems of protein denaturation, leftovers, affecting the extraction and activity of phycobiliprotein, etc.
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Embodiment 1
[0021] Embodiment 1, a method for preparing crude phycobiliprotein and crude polysaccharide by using Porphyra zebra, the main steps of the method include:
[0022] (1) Wash, drain, and centrifugally dehydrate the harvested Porphyra variegata to obtain fresh wet laver with a water content of 79.5%; add potassium dihydrogen phosphate-sodium hydroxide buffer solution with a pH of 8.0 to the fresh wet laver , the mass ratio of the buffer solution to the seaweed is 0.8:1; homogenize to a slurry state, and then swell the slurry material at 38° C. for 8 hours to obtain the first material.
[0023] (2) Treat the first material with a colloid mill, then dilute the treated material with an appropriate amount of water and then process it with a high-pressure homogenizer at 75Mpa to obtain the second material; centrifuge the second material to obtain the first supernatant and the first precipitate; add ammonium sulfate to the first supernatant, then stand at 4°C for 10 hours, then centrif...
Embodiment 2
[0025] Embodiment 2, a method for preparing crude phycobiliprotein and crude polysaccharide by using Porphyra zebra, the main steps of the method include:
[0026] (1) Wash, drain, and centrifugally dehydrate the harvested Porphyra variegata to obtain fresh wet laver with a water content of 81.2%; add potassium dihydrogen phosphate-sodium hydroxide buffer solution with a pH of 8.0 to the fresh wet laver , the mass ratio of the buffer solution to the seaweed is 1:1; homogenize to a slurry state, and then swell the slurry material at 42° C. for 10 hours to obtain the first material.
[0027] (2) Treat the first material with a colloid mill, then dilute the treated material with an appropriate amount of water and then process it with a high-pressure homogenizer at 100Mpa to obtain the second material; centrifuge the second material to obtain the first supernatant and the first precipitate; adding ammonium sulfate to the first supernatant, then standing at 10°C for 12 hours, and t...
Embodiment 3
[0029] Embodiment 3, a method for preparing crude phycobiliprotein and crude polysaccharide by using Porphyra zebra, the main steps of the method include:
[0030](1) Wash, drain, and centrifugally dehydrate the harvested Porphyra variegata to obtain fresh wet laver with a water content of 80%; add potassium dihydrogen phosphate-sodium hydroxide buffer solution with a pH of 8.0 to the fresh wet laver , the mass ratio of the buffer solution to the seaweed is 0.9:1; homogenize to a slurry state, and then swell the slurry material at 40° C. for 9 hours to obtain the first material.
[0031] (2) Treat the first material with a colloid mill, then dilute the treated material with an appropriate amount of water and then process it with a high-pressure homogenizer at 85Mpa to obtain the second material; centrifuge the second material to obtain the first supernatant and the first precipitate; adding ammonium sulfate to the first supernatant, then standing at 6°C for 11 hours, and then ...
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