Method for extracting microbial oil
A technology of microbial oil and extraction method, which is applied in the field of microbial oil extraction, can solve problems such as time-consuming, high energy consumption, and reduction of target fatty acid content, so as to achieve large-scale production, facilitate large-scale production, and improve oil extraction efficiency Effect
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Embodiment 1
[0029] (1) After inoculating the sloping surface with the dinoflagellate strain, perform liquid shake flask culture, and then transfer it to a 70L automatic fermentation tank. The composition of the medium is: tryptone 1g / L, yeast extract 2g / L, glucose 30g / L, KH 2 PO 4 3g / L, NaCl 30g / L, MgSO 4 .7H 2 O 10g / L, KCl 1g / L, CaCl 2 0.3g / L, NaHCO 3 1g / L, FeSO 4 0.01g / L, glutamic acid 40g / L, the rest is water, adjust the pH of the medium to 6~8, maintain the temperature of the fermenter at 25~28℃, and the air flow rate per minute is 0.8 times the volume of the fermentation broth , Culturing for 126h, the fermentation is over, the fermentation broth is obtained
[0030] (2) Adjust the temperature of the fermentation broth to 40°C, adjust the pH of the fermentation broth to 3.5 with phosphoric acid, and continue stirring for 6 hours to autolyze the microbial cells in the fermentation broth to obtain 50L of fermentation broth;
[0031] (3) Take 50L of fermentation broth obtained in step (...
Embodiment 2
[0037] (1) After inoculating the sloping surface with the dinoflagellate strain, perform liquid shake flask culture, and then transfer it to a 70L automatic fermentation tank. The composition of the medium is: tryptone 1g / L, yeast extract 2g / L, glucose 30g / L, KH 2 PO 4 3g / L, NaCl 30g / L, MgSO 4 .7H 2 O 10g / L, KCl 1g / L, CaCl 2 0.3g / L, NaHCO 3 1g / L, FeSO 4 0.01g / L, glutamic acid 40g / L, the rest is water, adjust the pH of the medium to 6~8, maintain the temperature of the fermenter at 25~28℃, and the air flow rate per minute is 0.8 times the volume of the fermentation broth , Culturing for 126h, the fermentation is over, the fermentation broth is obtained
[0038] (2) Adjust the temperature of the fermentation broth to 50°C, adjust the pH of the fermentation broth to 3.5 with sulfuric acid, and continue stirring for 6 hours to autolyze the microbial cells in the fermentation broth to obtain 50L of fermentation broth;
[0039] (3) Take 50L of fermentation broth obtained in step (2)...
Embodiment 3
[0046] (1) After inoculating the sloping surface with the dinoflagellate ampoule, perform liquid shake flask culture, then transfer to the first-level seed tank for culture, and then transfer to 50m 3 Fermentation tank culture, wherein the composition of the medium is: tryptone 1g / L, yeast extract 2g / L, glucose 30g / L, KH 2 PO 4 3g / L, NaCl 30g / L, MgSO 4 .7H 2 O 10g / L, KCl 1g / L, CaCl 2 0.3g / L, NaHCO 3 1g / L, FeSO 4 0.01g / L, glutamic acid 40g / L, the rest is water, adjust the pH of the medium to 6~8, maintain the temperature of the fermentation tank at 25~28℃, and the air flow rate per minute is 1.5 times the volume of the fermentation broth , Cultivate for 120h, the fermentation is over, and the fermentation broth is obtained;
[0047] (2) Adjust the temperature of the fermentation broth to 55°C, and adjust the pH of the fermentation broth to about 4.0 with hydrochloric acid for 12 hours to autolyze the microbial cells in the fermentation broth to obtain 40m 3 Fermentation broth
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