Double-liquid-phase fermentation method of coupling in-situ extraction antrodia camphorate active product antrondin C
A two-liquid-phase, in-situ technology, applied in the field of fermentation engineering, can solve the problems of reducing the negative feedback inhibition of Antrodia camphorata physiologically active products, low yield of physiologically active products, and changing the permeability of cell membranes, so as to achieve good industrialization prospects and realize Large-scale industrial application, the effect of simple extraction and purification
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Embodiment 1
[0018] The culture medium formula of the present embodiment is:
[0019] Slant medium: potato 200g / L, glucose 20g / L, magnesium sulfate 0.1g / L, potassium dihydrogen phosphate 0.5g / L, peptone 5g / L, agar 20g / L.
[0020] Liquid seed medium: glucose 20g / L, soybean powder 4g / L, corn steep liquor powder 2g / L, magnesium sulfate 0.1g / L, potassium dihydrogen phosphate 0.5g / L.
[0021] Liquid fermentation medium: glucose 30g / L, soybean powder 5g / L, corn steep liquor powder 4g / L, magnesium sulfate 0.1g / L, potassium dihydrogen phosphate 0.5g / L.
[0022] Transfer the strains of Antrodia camphorata to the slant medium for cultivation at a temperature of 30°C and cultivate for 1 week to obtain fresh Antrodia camphorata bacteria, wash the spores from the slope with a certain amount of sterile water to prepare a spore suspension , with an inoculation volume of 10% by volume fraction into a 500ml Erlenmeyer flask containing 100ml of liquid seed medium, placed in a constant temperature shaker at...
Embodiment 2
[0024] The same as the steps of the above-mentioned Example 1, the difference is: when the cells were cultured for 48 hours, the surfactant Span-80 with a volume fraction of 0.1% was added to the culture solution, and the fermentation was continued for 8 days, and the active product Antrodin C output It was 200mg / L, which was increased by 50% compared with the blank control group.
Embodiment 3
[0026] The same as the steps of the above-mentioned Example 1, the difference is: when the cells were cultured for 48 hours, the surfactant Span-80 with a volume fraction of 0.3% was added to the culture solution, and the fermentation was continued for 8 days, and the active product Antrodin C output It was 250mg / L, which increased by 90% compared with the blank control group.
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