Strain for biosynthesis of 3beta, 7alpha, 15alpha-trihydroxyandrost-5-ene-17-one and application thereof
A technology of hydroxyandrosteroids and microbial strains, applied in the biological field, can solve the problems of low feed concentration, low general conversion rate, high industrial cost, etc.
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Embodiment 1
[0018] Example 1 Activation and screening of strains.
[0019] Add the glycerol tubes of strains stored at -80°C in the laboratory to 10 mL of seed medium for activation culture. Then transfer to the seed medium, the liquid volume is 250 mL Erlenmeyer flask filled with 30 mL of seed liquid cultured for 2 days. Inoculate 4% of the inoculum into the fermentation medium, fill 30 mL in a 250 mL Erlenmeyer flask, and incubate at 30°C and 220 r / min for 24 hours. Accurately weigh 3g / L of DHEA and put it into the cell culture solution, and transform under the same conditions for 60 hours. The conversion solution was extracted and analyzed by HPLC. The results showed that only Gibberella ( Gibberella intermedia ) CA3-1 has the ability to transform DHEA, and can generate the product 3β, 7α, 15α-trihydroxyandrost-5-en-17-one.
Embodiment 2
[0020] Embodiment 2 Gibberella ( Gibberella intermedia ) CA3-1 converts DHEA.
[0021] (1) Place the PDA slant of the inoculated strain in a constant temperature incubator at 30°C, and cultivate it for 4 days to obtain mature spores. Use an inoculation loop to pick a ring of mycelium and inoculate it into a 500mL shake flask containing 100mL of seed medium , at 28°C, cultivated on a shaker at 220rpm for 1 day to obtain a seed culture solution suitable for inoculation;
[0022] (2) Put the seed culture solution into a 250mL shake flask with 30mL of fermentation medium at an inoculum amount of 4%, and continue to cultivate for 20 hours under the same conditions to obtain the cell fermentation solution;
[0023] (3) Put dehydroepiandrosterone into the fermentation broth of the bacteria, the feeding concentration is 3.0g / L, transform under the same conditions for 60 hours and put in the bottle. The extracted product was analyzed by HPLC, and the conversion rate was 90.08%.
Embodiment 3
[0025] (1) Slope culture, seed culture and fermentation culture are the same as in Example 1.
[0026] (2) Put dehydroepiandrosterone into the fermentation broth of the bacteria, the feeding concentration is 5.0g / L, transform under the same conditions for 60 hours and release the bottle. The extracted product was analyzed by HPLC, and the conversion rate was 84.08%.
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