Preparation method of high-content sisomicin fermentation liquor
A technology of sisomycin and fermented liquid, which is applied in the field of preparation of high-content sisomycin fermented liquid, can solve the problems of low biological potency, high purification yield, and large difference between high and low, and achieve high biological potency, High purification yield and easy operation
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example 1
[0019] In terms of percentage by weight, take 30 parts of sucrose, 25 parts of agar, 15 parts of potassium nitrate solution with a mass fraction of 10%, 12 parts of a sodium chloride solution with a mass fraction of 12%, and 18 parts of glucose. Adjust the pH to 7.0 with a 5% sodium hydroxide solution, and sterilize at 120°C for 30 minutes to obtain a slant medium; use an inoculation loop to inoculate Micromonospora innio into the above slant medium, and inoculate once. Place the inoculated slant culture medium at 32°C in a sterile environment, and after cultivating for 7 days, move the culture medium to a refrigerator at 0°C for storage for 4 days to obtain the cultured strains on the slant for future use; parts by weight , get 35 parts of starch, 18 parts of bean curd residue, 32 parts of beef extract, 4 parts of L-proline, 10 parts of magnesium sulfate solution with a mass fraction of 10%, 1.2 parts of dipotassium hydrogen phosphate and 0.8 part of potassium dihydrogen phosp...
example 2
[0022]In terms of percentage by weight, take 35 parts of sucrose, 22 parts of agar, 13 parts of potassium nitrate solution with a mass fraction of 10%, 10 parts of a sodium chloride solution with a mass fraction of 12% and 20 parts of glucose. Adjust the pH to 7.0 with a sodium hydroxide solution with a fraction of 5%, and sterilize at 130°C for 40 minutes to obtain a slant medium; use an inoculation loop to inoculate Micromonospora ineosus into the above slant medium, inoculate 3 times, Place the inoculated slant medium at 35°C in a sterile environment, and after culturing for 9 days, move the medium to a refrigerator at 4°C and store it for 6 days to obtain the cultured strains on the slant for future use; parts by weight , get 42 parts of starch, 15 parts of bean curd residue, 30 parts of beef extract, 3 parts of L-proline, 8 parts of magnesium sulfate solution with a mass fraction of 10%, 1.2 parts of dipotassium hydrogen phosphate and 0.8 part of potassium dihydrogen phosp...
example 3
[0025] In terms of percentage by weight, take 34 parts of sucrose, 24 parts of agar, 13 parts of potassium nitrate solution with a mass fraction of 10%, 11 parts of a sodium chloride solution with a mass fraction of 12%, and 18 parts of glucose. Adjust the pH to 7.0 with a sodium hydroxide solution with a fraction of 5%, and sterilize at 130°C for 35 minutes to obtain a slant medium; use an inoculation loop to inoculate Micromonospora ineosus into the above slant medium, inoculate twice, Place the inoculated slant culture medium at 35°C in a sterile environment. After cultivating for 8 days, move the culture medium to a refrigerator at 2°C and store it for 5 days to obtain the cultured strains on the slant for future use; parts by weight , get 40 parts of starch, 17 parts of bean curd residue, 31 parts of beef extract, 3 parts of L-proline, 8 parts of magnesium sulfate solution with a mass fraction of 10%, 0.6 part of dipotassium hydrogen phosphate and 0.4 part of potassium dih...
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