Epigenetic modification method of Enteromorpha-derived fungi and its secondary metabolite
A modification method, fungal technology, applied in the direction of microorganism-based methods, fungi, metabolic diseases, etc., can solve the problems of poor understanding, and achieve the effects of preventing hyperglycemia, easy absorption, and enhancing the degree of acetylation
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[0030] The preparation method of above-mentioned secondary metabolite is:
[0031] 1) the fermentation broth is filtered through cheesecloth to separate the filtrate and mycelia, the filtrate is extracted three times with an equivalent volume of ethyl acetate to obtain an ethyl acetate solution, the mycelium is extracted three times with 80% acetone, the acetone solution is concentrated under reduced pressure, and then Extract with ethyl acetate three times to obtain an ethyl acetate solution, combine the above two ethyl acetate solutions together, and concentrate under reduced pressure to obtain an ethyl acetate solution extract;
[0032] 2) The ethyl acetate extract was eluted step by step by vacuum silica gel column chromatography, and the eluent was petroleum ether-CH 2 Cl 2 (1:1 and 0:1) and CH 2 Cl 2 - Yield gradient of MeOH (100% ~ 0%) 6 main fractions (fraction 1 ~ 6), fraction 4 was further purified by Sephadex LH-20 (MeOH) to obtain fractions 4.2, 4.3, 4.4, fracti...
Embodiment 1
[0035] A preparation method for the appearance modification method of enteromorpha-derived fungi, comprising:
[0036] 1) Fungal material: The fungal strain Aspergillus terreus OUCMDZ-2739 was isolated from Enteromorpha samples from Shilaoren Beach in Qingdao, and the Enteromorpha samples were washed with sterile seawater, 75% ethanol and sterile water in sequence. Then, the samples were crushed with a mortar and pestle, and then stored in PDA medium (containing 200 g of potato extract, 20 g of glucose, 15 g of agar, and 1 L of seawater per liter) containing 100 mg / mL chloramphenicol at 28 ° C. After cultured until a single strain appeared, the strain was transferred to another PDA medium and stored at 4°C. Through multiphase taxonomic studies, colony morphology and 18S rRNA sequence analysis, and establishment of strain development trees, it was identified as soil Aspergillus OUCMDZ-2739;
[0037] 2) Expansion cultivation: inoculate the Enteromorpha-derived fungus Aspergillu...
Embodiment 2
[0046] A preparation method for the appearance modification method of Enteromorpha-derived fungi, comprising:
[0047] 1) Fungal material: The fungal strain Aspergillus terreus OUCMDZ-2739 was isolated from Enteromorpha samples from Shilaoren Beach in Qingdao, and the Enteromorpha samples were washed with sterile seawater, 75% ethanol and sterile water in sequence. Then, the samples were crushed with a mortar and pestle, and then stored in PDA medium (containing 200 g of potato extract, 20 g of glucose, 15 g of agar, and 1 L of seawater per liter) containing 100 mg / mL chloramphenicol at 28 ° C. After cultured until a single strain appeared, the strain was transferred to another PDA medium and stored at 4°C. Through multiphase taxonomic studies, colony morphology and 18S rRNA sequence analysis, and establishment of strain development trees, it was identified as soil Aspergillus OUCMDZ-2739;
[0048] 2) Expansion cultivation: inoculate the Enteromorpha-derived fungus Aspergillu...
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