Method of preparing microbial oil and microbial oil
A technology for microbial oil and oil-producing microorganisms, which is applied in the production of fat, fat oil/fat production, fermentation, etc., to achieve the effect of reducing surface oil content, promoting emulsification process, and reducing preparation process
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Embodiment 1
[0016] With dinoflagellation as the fermentation strain, follow the following steps successively:
[0017] (1) fermentation to obtain a microbial fermentation broth rich in docosahexaenoic acid;
[0018] (2) After the above-mentioned fermented liquid is processed by a centrifuge, the concentrated fermented liquid obtained with a solids content of 25.1%;
[0019] (3) Take 500g of the concentrated fermentation broth and put it into a 1L glass reaction bottle, adjust the pH value to 8.01, add 1.01g of alkaline protease, control the temperature at 45°C, cut for 2h, then add 2.5g of phospholipase C, and stir further React for 2 hours to obtain the enzymolysis solution.
[0020] (4) The above enzymolysis solution was heated to 97° C., and then centrifuged with a high-speed centrifuge at 10,000 rpm to separate the upper oil phase for vacuum dehydration to obtain 41.3 g of microbial oil rich in docosahexaenoic acid.
[0021] (5) After testing, the phosphorus content in the microbial...
Embodiment 2
[0023] Using Microella as the fermentation strain, follow the steps below:
[0024] (1) fermentation to obtain a microbial fermentation broth rich in eicosapentaenoic acid;
[0025] (2) After the above-mentioned fermented liquid is separated by membrane, the concentrated fermented liquid obtained with a solids content of 17.1%;
[0026] (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, 10g phospholipase C, stir and shear React for 4 hours to obtain the enzymolysis solution.
[0027] (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.
[0028] (5) After testing, the phosphorus content in the microbial oil ...
Embodiment 3
[0030] Using yeast as the fermentation strain, follow the steps below:
[0031] (1) Fermentation obtains a microbial fermentation broth rich in linolenic acid;
[0032] (2) After the above-mentioned fermented liquid is centrifuged, the concentrated fermented liquid obtained with a solids content of 29.7%;
[0033] (3) Take 51kg of the concentrated fermentation broth and put it into a 300L reactor, adjust the pH value to 5, control the temperature at 48°C, add 100.5g of helicase and 127.5g of phospholipase C, stir and cut for 2 hours to obtain an enzymolysis solution.
[0034] (4) Add 100L of n-hexane and 50L of ethanol to the above enzymatic hydrolysis solution for extraction for 1.5h, settle and separate to obtain the extract, and vacuum precipitate the extract to obtain 4179.1g of microbial oil rich in linolenic acid.
[0035] (5) After testing, the phosphorus content in the microbial oil is 2.9ppm, the triglyceride content is 94.1%, and the diglyceride content is 3.9%.
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