Method for concentrating and harvesting Porphyra and a method for coupling Porphyra cultivation and concentration and harvesting
A technology of cyanobacteria and cultivating pond, which is applied in the field of marine microorganisms, can solve the problems of high-speed operation, such as hidden safety hazards, existing processes, and large equipment investment, and achieves the advantages of increasing biomass productivity, reducing harvesting costs, and saving centrifugation time. Effect
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Embodiment 1
[0038] Under outdoor conditions, Porphyridum inoculated into 100L culture solution 5 (the formula of culture solution is: every liter contains sodium nitrate 1.5g, potassium dihydrogen phosphate 0.1g, iron trichloride 5mg and sodium bicarbonate 5.0g, Surplus is seawater) in the 120L culture tank 1, inoculum size is OD 750 =0.5, after culturing Porphyridium algae for 10 days at a temperature of 26°C and a light intensity of 22000Lux, the growth of Porphyridococcus reached a stable stage, and the cell density reached 3.6×10 7 cells / ml, and the exopolysaccharide content was 0.04g / L, reaching the harvest standard. Continuously input the algae liquid from the bottom of the cylindrical collection container 2 with a bottom diameter of 10 cm and a height of 100 cm into the cylindrical collection container 2 through a centrifugal pump or a diaphragm pump. The liquid flow rate is 1.0 L / min. ℃, and the light intensity is 22000Lux to continue the cultivation. When the algae liquid enters...
Embodiment 2
[0040] Under the outdoor conditions, Porphyridum inoculated into 800L culture solution 5 (the formula of culture solution is: every liter contains sodium nitrate 1.5g, potassium dihydrogen phosphate 0.1g, iron trichloride 5mg and sodium bicarbonate 5.0g, Surplus is seawater) in the 1000L culture pool 1, inoculum size is OD 750 =0.1, after culturing Porphyridium algae for 5 days at a temperature of 26°C and a light intensity of 22,000Lux, the growth of Porphyridococcus reached a stable stage, and the cell density reached 0.9×10 7 cells / ml, and the exopolysaccharide content was 0.02g / L, reaching the harvest standard. Through a centrifugal pump or a diaphragm pump, the algae liquid is continuously input from the bottom of a cylindrical collection container 2 with a diameter of 50 cm and a height of 100 cm into the cylindrical collection container 2 at a liquid flow rate of 10 L / min. ℃, and the light intensity is 22000Lux to continue the cultivation. When the algae liquid enters ...
Embodiment 3
[0042] Under outdoor conditions, Porphyridum inoculated into 100L culture solution 5 (the formula of culture solution is: every liter contains sodium nitrate 1.5g, potassium dihydrogen phosphate 0.1g, iron trichloride 5mg and sodium bicarbonate 5.0g, Surplus is seawater) in the 120L culture tank 1, inoculum size is OD 750 =0.5, after 13 days of culturing Porphyridium algae at a temperature of 26°C and a light intensity of 22000Lux, the growth of Porphyridococcus reached a stable stage, and the cell density reached 3.5×10 7 cells / ml, and the exopolysaccharide content was 0.1g / L, reaching the harvest standard. Continuously input the algae liquid from the bottom of the cylindrical collection container 2 with a diameter of 10 cm and a height of 100 cm into the cylindrical collection container 2 through a centrifugal pump or a diaphragm pump. Continue to cultivate, when the algae liquid enters the cylindrical collection container 2, the gas distributor at the bottom of the cylindr...
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