Porphyridium extracellular polysaccharide adsorbent and preparation method thereof
A technology of extracellular polysaccharides and Porphyridium, applied in chemical instruments and methods, adsorption water/sewage treatment, other chemical processes, etc., can solve the problems of small adsorption capacity, poor regeneration ability, poor stress resistance, etc., and achieve adsorption capacity Larger, less contamination residues, and easier elution
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Embodiment 1
[0035] (1) Separation and purification of exopolysaccharide from Porphyridium algae:
[0036] 1) Take fresh Porphyridum algae and mix with distilled water or phosphate buffer solution, and perform ultrasonic crushing. The pH value of the phosphate buffer solution is 7.5, and the concentration is 60mmol / L;
[0037] 2) centrifuging the crushed liquid obtained in step 1), discarding the precipitate, and taking the supernatant;
[0038] 3) deproteinize the supernatant obtained in step 2);
[0039] 4) Add 2 times the volume of ethanol to the deproteinized supernatant obtained in step 3) for precipitation, collect the precipitate by centrifugation, wash with acetone, and dry to obtain crude polysaccharide;
[0040] 5) Dissolve the crude polysaccharide obtained in step 4) in distilled water to make a saturated solution, centrifuge and discard the precipitate, apply the supernatant to a DEAE-Sepharose FastFlow column, use Tris-HCl as the eluent, and perform NaCl gradient elution, Ph...
Embodiment 2
[0044] (1) Separation and purification of exopolysaccharide from Porphyridium algae:
[0045]1) Mix fresh Porphyridum algae with distilled water or phosphate buffer solution, and perform ultrasonic crushing. The pH value of the phosphate buffer solution is 7.5, and the concentration is 100mmol / L;
[0046] 2) centrifuging the crushed liquid obtained in step 1), discarding the precipitate, and taking the supernatant;
[0047] 3) deproteinize the supernatant obtained in step 2);
[0048] 4) adding 3 times the volume of ethanol to the deproteinized supernatant obtained in step 3) for precipitation, centrifuging to collect the precipitate, washing with acetone, and drying to obtain crude polysaccharide;
[0049] 5) Dissolve the crude polysaccharide obtained in step 4) in tris-hydrochloric acid buffer to make a saturated solution, centrifuge and discard the precipitate, put the supernatant on a DEAE-Sepharose FastFlow column, wash with Tris-HCl Deliquidation, NaCl gradient elution...
Embodiment 3
[0053] (1) Separation and purification of exopolysaccharide from Porphyridium algae:
[0054] 1) Take fresh Porphyridum algae and mix with distilled water or phosphate buffer solution, and perform ultrasonic crushing. The pH value of the phosphate buffer solution is 7.5, and the concentration is 40mmol / L;
[0055] 2) centrifuging the crushed liquid obtained in step 1), discarding the precipitate, and taking the supernatant;
[0056] 3) deproteinize the supernatant obtained in step 2);
[0057] 4) Add 2.5 times the volume of ethanol to the deproteinized supernatant obtained in step 3) for precipitation, collect the precipitate by centrifugation, wash with acetone, and dry to obtain crude polysaccharide;
[0058] 5) Dissolve the crude polysaccharide obtained in step 4) in tris-hydrochloric acid buffer to make a saturated solution, centrifuge and discard the precipitate, put the supernatant on a DEAE-Sepharose FastFlow column, wash with Tris-HCl Deliquidation, NaCl gradient elu...
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