Anti AIDS 1 type virus compound preparation method
A typical, culture-based technology, applied in the direction of drug combination, allergic diseases, bacteria, etc., to achieve the effect of simple operation method
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Embodiment 1
[0027] Prepare 101X strain fermentation broth. Use MM medium for the deposited strain 101X: (NH4)2SO4 0.1%, K2HPO4 0.7%, KH2PO4 0.3%, sodium citrate 0.05%, MgSO4 0.01%, glucose 0.5%, agar 2.0%, distilled water Preparation. After activation, transfer to liquid 2216E medium, shake culture at 20°C to the exponential growth phase to obtain fermentation broth; centrifuge the fermentation broth, discard the precipitate, and store the supernatant at 4°C for later use; in the supernatant Add 1 / 2 volume of ethyl acetate for extraction, collect the aqueous phase, add 1 / 2 volume of ethyl acetate again for extraction, and collect the aqueous phase. The measured macroporous adsorption resin has an average pore diameter of 300mm. It is cleaned and activated according to the instructions and packed into the column. The measured macroporous adsorption resin is 1.7 times the aqueous solution on the column, and the amount used is 1.7 times the macroporous adsorption resin. The column was washed...
Embodiment 2
[0030] Similar to Example 1, the difference is that the 101X strain fermentation broth is prepared, and the deposited strain 101X uses MM medium: (NH4)2SO4 0.1%, K2HPO4 0.7%, KH2PO4 0.3%, sodium citrate 0.05%, MgSO4 0.01%, Prepared with 0.5% glucose, 1.5% agar and distilled water. After activation, transfer to liquid 2216E medium, shake culture at 15°C to the exponential growth phase to obtain fermentation broth; centrifuge the fermentation broth, discard the precipitate, and store the supernatant at 4°C for later use; in the supernatant Add 1 / 2 volume of ethyl acetate for extraction, collect the aqueous phase, add 1 / 2 volume of ethyl acetate again for extraction, and collect the aqueous phase. The measured macroporous adsorption resin has an average pore diameter of 280mm. It is cleaned and activated according to the instructions and packed into the column. The measured macroporous adsorption resin is 1.5 times the aqueous solution on the column, and the dosage is 2 times the ...
Embodiment 3
[0033] Similar to Example 1, the difference is that the 101X strain fermentation broth is prepared, and the deposited strain 101X uses MM medium: (NH4)2SO4 0.1%, K2HPO4 0.7%, KH2PO4 0.3%, sodium citrate 0.05%, MgSO4 0.01%, Prepared with 0.5% glucose, 1.8% agar and distilled water. After activation, transfer to liquid 2216E medium, shake culture at 30°C to the exponential growth phase to obtain fermentation broth; centrifuge the fermentation broth, discard the precipitate, and store the supernatant at 4°C for later use; in the supernatant Add 1 / 2 volume of ethyl acetate for extraction, collect the aqueous phase, add 1 / 2 volume of ethyl acetate again for extraction, and collect the aqueous phase. The measured macroporous adsorption resin has an average pore diameter of 330mm. It is cleaned and activated according to the instructions and packed into the column. The measured macroporous adsorption resin is twice as large as the aqueous solution on the column, and the dosage is 1 ti...
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