Method for increasing yield of ARA (arachidonic acid) produced through fermentation of Mortierella alpina by adding porphyridium
A technology of Mortierella alpina and arachidonic acid, applied in the direction of microorganism-based methods, biochemical equipment and methods, fermentation, etc., to achieve the effects of easier realization, simple operation, and increased yield
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Embodiment 1
[0033] 1) Preparation of porphyridium residues: insert the porphyridum strains into a petri dish containing fresh water, culture them at 10-15°C for 3-6 days under low-salt and low-light conditions, and then culture The liquid was sieved through an 80-mesh sieve, washed three times with distilled water, filtered with a vacuum pump, dried in vacuum for 24-48 hours, and ground into a powder for later use.
[0034] 2) Shake flask seed culture: under sterile conditions, take an appropriate amount of Mortierella alpina spores or mycelium and spread it on PDA medium, place it at 26-30°C for 6-12 days, and then scrape an appropriate amount of spores to contain shake flasks In the Erlenmeyer flask of the seed medium, culture on a shaker at 25-30°C, humidity 30%-60% for 36-48h, the shaker speed is 180-250rmp;
[0035] The PDA medium raw material is glucose 15-25g / L, potato 100-200g / L, agar powder 10-20g / L, K 2 PO 4 0.2-0.6 g / L ,MgSO 4 0.1-0.3 g / L, pH 7.0-7.5;
[0036] The seed cu...
Embodiment 2
[0048] 1) The preparation of purple ball residue is the same as in Example 1.
[0049] 2) The shake flask seed culture method is the same as in Example 1.
[0050] 3) Shake flask fermentation culture: put the seed liquid into the Erlenmeyer flask containing the fermentation medium according to the inoculum amount of 5%-10%, and culture it on a shaker at 25-30°C and humidity 30%-60% for 8-14 days. The shaker speed is 180-250rmp; 30 g / L, 45 g / L and 60 g / L of Porphyridium spp. residues were added to different fermentation bottles at one time during the 5 days of fermentation, and no Porphylocccus residues were added as a control group, pH 7.0-7.5, each group of experimental parallel fermentation bottles is 3, unseparated arachidonic acid oil fermentation product is obtained after fermentation;
[0051] The fermentation medium is 30-80g / L of glucose, 15-25g / L of yeast powder, and pH 7.0-7.5.
[0052] At the end of the fermentation, the percentage of cell oil and arachidonic acid...
Embodiment 3
[0055] 1) The preparation of the porphyrinous algae residue is the same as in Example 1.
[0056] 2) The shake flask seed culture method is the same as in Example 1.
[0057] 3) Shake flask fermentation culture: For shake flask fermentation culture, put the seed liquid into the triangular flask containing the fermentation medium according to the inoculum amount of 5%-10%, and cultivate it on a shaker under the conditions of 25-30°C and humidity 30%-60%. 8-14d, the shaker speed is 180-250rmp; at 10d, 30 g / L, 45 g / L and 60 g / L of Porphyridium residues were added to different fermentation bottles at one time, and there were no Porphyridium residues added As a control group, the pH is 7.0-7.5, and there are 3 parallel fermentation bottles for each group of experiments, and the arachidonic acid oil fermentation product is obtained after the fermentation is completed;
[0058] The fermentation medium is 30-80g / L of glucose, 15-25g / L of yeast powder, and pH 7.0-7.5.
[0059] At the...
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