Process for biologically synthesizing extracellular cholesterol oxidase from Brevibacterium and its transferred product cholest-4-ene-3-one
A technology of cholesterol oxidase and Brevibacterium, applied in the direction of oxidoreductase, fermentation, etc., can solve the problems that have not been reported in the public literature, so as to reduce the absorption of cholesterol, increase high-density lipoprotein, and reduce low-density lipoprotein. Effect
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Embodiment 1
[0054] Shake Flask Fermentation of Cholesterol Oxidase:
[0055] Using the above-mentioned medium in this manual, DGCDC-82 was used as the production bacteria, cultured on a slant, 30°C, 48hr. Seed liquid culture: Take the slant bacteria into a 250ml Erlenmeyer flask containing 30ml of seed medium, 30°C, 220r / min, and cultivate for 12hrs as the seed liquid.
[0056] Fermentation broth culture: Add 3ml of seed solution into a 250ml Erlenmeyer flask containing 30ml of fermentation medium, 30°C, 220r / min, and after 36hrs of cultivation, the cholesterol oxidase production is as high as 700U / L.
Embodiment 2
[0058] 15L tank fermentation of cholesterol oxidase:
[0059] Fermentation medium conditions are the same as above, seed liquid medium conditions are the same as above, 5% inoculum size, culture temperature 33°C, 500r / min, ventilation rate 1vvm, liquid volume 6-7L, culture in 15L automatic fermenter for 28-32hr, fermented liquid Enzyme activity is over 1000U / L.
Embodiment 3
[0061] A two-phase system utilizes cholesterol oxidase to convert free cholesterol to cholestenone:
[0062] With 30ml pH7.5 potassium phosphate buffer as the aqueous phase and 20ml n-octane as the organic phase, add 2g cholesterol and 16U cholesterol oxidase, and react in a 250ml three-necked flask. The reaction conditions are: oxygen flow rate 40L / hr, temperature 40°C, stirring speed 300r / min. After 40 minutes, the conversion rate of cholesterol reaches over 92%.
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