Method for producing arachidonic acid with fresh water green algae cultivation by photoautotroph mode
A technology of arachidonic acid and freshwater green algae, applied in the direction of unicellular algae, fermentation, etc., can solve the problem of low content of arachidonic acid, and achieve the effect of solving the problem of harvesting
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Embodiment 1
[0045] Put the sterilized fresh water into the pipeline photobioreactor of the first-level breeding, adjust the pH to 6-8, and the nutrient concentration to 1.5g / liter NaNO 3 , 36mg / L CaCl2, 20mg / L Na2CO3, 75mg / L MgSO4, 30mg / L K2HPO4, 1mg / L Fe-EDTA and trace element solution, inoculated according to 0.1g biomass / L, and washed into the solution containing 1-5% The filtered air of carbon dioxide makes the algae liquid circulate in the closed pipe. Breeding for 5-10 days; entering the second-level breeding stage, place the above-mentioned culture culture solution in the shallow waterway culture pond in the glass greenhouse, use natural light source for culture, and inoculate the culture solution from the above-mentioned first-level photobioreactor at an inoculation density of 0.1 g biomass / liter, cultured for 5-10 days; entering the third-level breeding stage, according to the density of 0.1g biomass / L, transfer the above-mentioned secondary seed expansion liquid to the above-men...
Embodiment 2
[0047] According to the steps described in Example 1, wherein the conditions for using the culture medium are: temperature at 25°C, pH value 6-8, 0.25g / L NaNO 3 , 2.5mg / L CaCl2, 25mg / L NaCl, 75mg / L MgSO4, 25mg / L K2HPO4, 12.5mg / LFeSO4-EDTA and trace element solution.
Embodiment 3
[0049] According to the steps described in Example 1, the conditions for using the culture medium are: the temperature is 15°C, the pH value is 6-8, and the nutrient concentration is 1.0 / liter NaNO 3 , 2.5mg / L CaCl2, 25mg / L NaCl, 75mg / L MgSO4, 25mg / L K2HPO4, 12.5mg / L FeSO4-EDTA and trace element solution.
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