Mucor circinelloides bacterial strain, cultivating method and application of the same in C21, C19 sterides and aza sterides biotransformation
A kind of technology of Mucor curcumae and steroid organisms, which is applied in the field of hydroxylated derivatives, can solve the problems such as no reports on the transformation of steroid substances, and achieves easy cultivation and preservation, reduced synthesis steps, and simple and convenient preparation method. Effect
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Embodiment 1
[0027] Collect soil samples from the northern suburbs of Zhengzhou City, Luoyang Luanchuan Mountain, Songshan and other places, weigh 10g of various soil samples, respectively suspend them in 0.9% NaCl solution, filter with 8 layers of gauze to remove larger impurity particles, inoculate and enrich Medium (yeast extract 0.15%, peptone 0.12%, glucose 3%, potassium dihydrogen phosphate 1%, pH 4.5, steroid mixture 0.5%), after 48 hours of culture, take 10 ml of culture solution and use the same method for secondary enrichment. Spread the selective plate (the composition is the same as the enrichment medium, containing 3% agar). After preliminary screening, 36 strains that can grow on the plate containing the substrate were obtained, and they were picked out and stored on the slant made by transferring the PDA medium and used for the transformation test.
[0028]Respectively inoculate 36 strains obtained from the above preliminary screening into transformation medium (yeast extract 0....
Embodiment 2
[0030] Optimize the fermentation medium for the selected Mucor circinelloides lusitanicus AY234877 CGMCC.NO.2256, and optimize the conditions such as carbon source, nitrogen source, metal ions, initial pH value, inoculation amount, liquid volume, etc. The composition of the fermentation medium was determined to be: maltose 50‰; peptone 18‰; yeast extract 1.5‰; magnesium sulfate 0.9‰; potassium dihydrogen phosphate 0.9‰; pH 6.0; inoculation volume 5%; liquid volume 80ml / 500ml bottle.
Embodiment 3
[0032] Configure 1L liquid medium according to the medium formula described in Example 2. After inserting the bacteria, culture at 28°C for 48h (shaker speed 220rpm), add 1.0g / L of substrate pregnenolone I, and then at 28°C Transformation for 96h. After TLC monitors the conversion termination (the raw material point disappears), the mycelium is removed by filtration, the fermentation broth is extracted 4 times with ethyl acetate, the organic phases are combined, concentrated under reduced pressure, and then washed 3 times with saturated sodium bicarbonate solution and saturated chlorinated Wash with sodium solution once, wash with water 3 times, and then dry with anhydrous sodium sulfate, and evaporate the solvent under reduced pressure to obtain 1.05 g of white solid, which is separated by column chromatography (ethyl acetate:chloroform 1:1) to obtain 1,256 mg of hydroxylated product , The yield is 24.38%, the compound 2 is 487mg, the yield is 46.38%, the structure is shown in th...
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