Microbial oil preparation method
A technology of microbial oil and oil-producing microorganisms, applied in the direction of fat production, fat oil/fat production, fermentation, etc., to achieve the effect of reducing production costs, reducing preparation processes, and high quality crude oil
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Embodiment 1
[0014] With dinoflagellation as the fermentation strain, follow the following steps successively:
[0015] (1) fermentation to obtain a microbial fermentation broth rich in docosahexaenoic acid;
[0016] (2) After the above-mentioned fermented liquid is processed by a centrifuge, the solid content obtained is 23.1% concentrated fermented liquid;
[0017] (3) Take 1000g of the concentrated fermentation broth and put it into a 1L glass reaction bottle, adjust the pH value to 8.1, add 1.01g of alkaline protease, control the temperature at 45°C, cut for 2h, then add 1.0g of phospholipase A, and stir further React for 3 hours to obtain the enzymolysis solution.
[0018] (4) Boil the above-mentioned enzymolysis solution, then centrifuge with a high-speed centrifuge at 10000 rpm, separate the upper oil phase and carry out vacuum dehydration to obtain 81.1 g of microbial oil rich in docosahexaenoic acid.
[0019] (5) After testing, the phosphorus content in the microbial oil is 4.1p...
Embodiment 2
[0021] Using Microella as the fermentation strain, follow the steps below:
[0022] (1) fermentation to obtain a microbial fermentation broth rich in eicosapentaenoic acid;
[0023] (2) After the above-mentioned fermented liquid is separated by membrane, the concentrated fermented liquid obtained with a solids content of 18.5%;
[0024] (3) Take 5kg of the concentrated fermentation broth and put it into a 25L glass reactor, adjust the pH value to 7.01, add 5.1g alkaline protease, 5.1g helicase, control the temperature at 51°C, 25g phospholipase A, stir and shear React for 2 hours to obtain the enzymolysis solution.
[0025] (4) 10 L of n-hexane and 5 L of ethanol were added to the enzymolysis solution for extraction for 1 hour, and the extract was separated by sedimentation to obtain an extract, which was subjected to vacuum precipitation to obtain 377.3 g of microbial oil rich in eicosapentaenoic acid.
[0026] (5) After testing, the phosphorus content in the microbial oil ...
Embodiment 3
[0028] Using yeast as the fermentation strain, follow the steps below:
[0029] (1) Fermentation obtains a microbial fermentation broth rich in linolenic acid;
[0030] (2) After centrifuging the above-mentioned fermented liquid, the concentrated fermented liquid obtained with a solids content of 28.3%;
[0031] (3) Take 51kg of the concentrated fermentation broth and put it into a 300L reaction kettle, adjust the pH value to 5, control the temperature at 48°C, add 100.1g of helicase and 127.5g of phospholipase A, stir and cut for 5 hours to obtain an enzymolysis solution.
[0032] (4) Add 100 L of n-hexane and 50 L of ethanol to the above enzymolysis solution to extract for 1.5 h, settle and separate to obtain the extract, and vacuum precipitate the extract to obtain 4171.3 g of microbial oil rich in linolenic acid.
[0033] (5) After testing, the phosphorus content in the microbial oil is 2.9ppm.
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