Method for preparing red algae phycoerythrin
A technology for red algae and algae, which is applied in the preparation methods of peptides, chemical instruments and methods, algae/moss peptides, etc., can solve the problems of long time, high cost, low yield and the like, and achieves a simple method and high recovery rate. , the effect of high purity
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Embodiment 1
[0007] (1) Pretreatment: The dried laver is pulverized with a pulverizer, and passed through an 80-mesh sieve to obtain dry laver powder for later use.
[0008] (2) Fully mix the laver powder in step (1) with 0.1M phosphate buffer solution with pH 6.8-7.2 at a ratio of 1:30 to obtain a mixed solution for later use.
[0009] (3) Add 0.02% β-agarase and 0.02% cellulase in sequence to the cell suspension obtained in step (2), and enzymolyze at 30°C for 5 h under low-speed stirring to obtain a wall-breaking solution.
[0010] (4) Refrigerate and centrifuge the porphyra wall-broken liquid obtained in step (3) at 8000 r / min for 10 min to obtain the supernatant.
[0011] (5) Add ammonium sulfate with a saturation of 50% to the supernatant in step (4), let it stand overnight at low temperature, then refrigerate and centrifuge at 8000 r / min for 10 min, take the precipitate and add 0.1 pH 6.8-7.2 M Phosphate buffer reconstituted.
[0012] (6) Concentrate the protein solution reconstit...
Embodiment 2
[0015] (1) Pretreatment: Wash the fresh algal bodies with water, drain and set aside.
[0016] (2) Homogenize fresh algae from step (1) with 0.1M phosphate buffer at pH 6.8-7.2 at a ratio of 1:2-3 for later use.
[0017] (3) Add 0.01% β-agarase and 0.01% cellulase to the cell suspension obtained in step (2) in sequence, and enzymatically hydrolyze at 30°C for 5 h under low-speed stirring to obtain a wall-breaking solution.
[0018] (4) The porphyra wall-broken liquid obtained in step (3) was centrifuged at 8000 r / min for 10 min at low temperature to obtain the supernatant.
[0019] (5) Concentrate the supernatant in step (4) to 1 / 5 of the original volume, add ammonium sulfate with a saturation of 50%, let stand overnight at low temperature, and then refrigerate and centrifuge at 8000 r / min After 10 min, the precipitate was taken and redissolved in 0.1M phosphate buffer with pH 6.8-7.2.
[0020] (6) Concentrate the protein solution reconstituted in step (5) by ultrafiltration...
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