Preparation and application of compound for inhabiting aspergillus fumigatus activity
A compound, the technology of Aspergillus fumigatus, applied in the field of medicine, can solve the problem of no compound inhibiting the activity of Aspergillus fumigatus and other problems, and achieve the effect of inhibiting the activity of Aspergillus fumigatus
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Embodiment 1
[0027] Embodiment 1: Preparation of Compound Methyl Esterui
[0028] a. Solid state fermentation of strain Geomyces sp.
[0029] Activation of strain Geomyces sp. PDA medium: 200g of potatoes, 20g of glucose, 15g of agar, 1000mL of water, sterilized by high-pressure steam at 121°C for 30 minutes, made into a test tube slant, picked mycelium and inoculated it on the test tube slant, and cultured at 25°C for 7 days;
[0030] Solid state fermentation of strain Geomyces sp. Preparation of rice culture medium (add 100g rice and 100mL water into a 500mL Erlenmeyer flask, soak overnight, sterilize with high pressure steam at 121°C for 30min, cool for later use); 6 Individuals / mL) 5 mL was inoculated on rice culture medium, and cultured in a sterile culture room at 25°C for 40 days.
[0031] b. Extraction of Methyl Estrela
[0032] After the fermentation was completed, ethyl acetate was added into the Erlenmeyer flask for extraction three times, and the organic solvent was distill...
Embodiment 2
[0044] Embodiment 2: The inhibition of the activity of Aspergillis fumigatus (Aspergillis fumigatus) detected by Alamar Blue fluorescence detection method
[0045] 1. Test reagents:
[0046] Use dimethyl sulfoxide (DMSO) as a solvent to prepare 4, 2, 1, 0.5, 0.2, 0.1, 0.05, 0.02, 0.01, 0.005 and 0.002mg / mL of the tested solution;
[0047] The positive control substance fluconazole (purchased from Sigma Company) was prepared into a 4 mg / mL solution with DMSO;
[0048] 2. Cultivation of Aspergillis fumigatus
[0049] Aspergillus fumigatus (Aspergillis fumigatus 48238E, which was provided by the Culture Collection Center of the Institute of Microbiology, Chinese Academy of Sciences) was inoculated on PDB medium (starch 40 g / L, glucose 20 g / L), cultured on a shaker at 28 ° C for 2 days and then Count the number of spores under a microscope and adjust the number of spores to 1×10 5 individual / mL.
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