Preparation method of cordyceps militaris natto product
A soy product, the technology of Cordyceps militaris, applied in the field of microorganisms, can solve the problems that the production process of natto has not been reported yet, and achieve the effect of enhancing the immune function of the body, inhibiting cancer cells, and having a good taste
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Embodiment 1
[0022] (1) Mix and dissolve 5 g of peptone, 3 g of beef extract, 5 g of NaCl, 15 g of agar and 1000 ml of water, and then adjust the pH value to 7.0 with sodium bicarbonate solution to obtain a bacterial culture medium. Put the melted bacterial culture medium into 18mm×180mm test tubes, 7ml in each test tube, stuff them with cotton plugs, sterilize at 0.14MPa for 30min, and place them on an inclined plane. After inoculating the pure Bacillus natto in the ultra-clean workbench, cultivate it at a constant temperature of 37°C until the slant is covered with bacteria to obtain the slant strain.
[0023] (2) Mix 5 g of peptone, 3 g of beef extract, 5 g of NaCl and 1000 ml of water, and then adjust the pH value to 7.0 with sodium bicarbonate solution to obtain a liquid medium. Fill 100ml of liquid medium in a 500ml glass bottle, seal it with a cotton plug, sterilize at 0.14MPa for 30min, cool to 35°C and inoculate slant strains, inoculate 0.3cm per 500ml of liquid medium 2 , and th...
Embodiment 2
[0031] (1) Mix and dissolve 5 g of peptone, 3 g of beef extract, 5 g of NaCl, 15 g of agar and 1000 ml of water, and then adjust the pH value to 7.0 with sodium bicarbonate solution to obtain a bacterial culture medium. Put the melted bacterial culture medium into 18mm×180mm test tubes, 7ml in each test tube, stuff them with cotton plugs, sterilize at 0.12MPa for 40min, and place them on an inclined plane. After inoculating the pure Bacillus natto in the ultra-clean workbench, cultivate it at a constant temperature of 37°C until the slant is covered with bacteria to obtain the slant strain.
[0032] (2) Mix 5 g of peptone, 3 g of beef extract, 5 g of NaCl and 1000 ml of water, and then adjust the pH value to 7.0 with sodium bicarbonate solution to obtain a liquid medium. Fill 100ml of liquid culture medium in a 500ml glass bottle, seal it with a cotton plug, sterilize at 0.12MPa for 40min, cool to 37°C and inoculate slant strains, inoculate 0.2cm per 500ml of liquid culture me...
Embodiment 3
[0040] (1) Mix and dissolve 5 g of peptone, 3 g of beef extract, 5 g of NaCl, 15 g of agar and 1000 ml of water, and then adjust the pH value to 7.2 with sodium bicarbonate solution to obtain a bacterial culture medium. Put the melted bacterial culture medium into 15mm×150mm test tubes, 4ml in each test tube, stuffed with cotton plugs, sterilized at 0.1MPa for 50min, and placed on a slope. After inoculating the pure Bacillus natto in the ultra-clean workbench, cultivate it at a constant temperature of 36°C until the slope is covered with bacteria to obtain the slope strain.
[0041] (2) Mix 2 g of peptone, 3 g of beef extract, 4 g of NaCl and 1000 ml of water, and then adjust the pH value to 7.2 with sodium bicarbonate solution to obtain a liquid medium. Fill 100ml of liquid medium in a 500ml glass bottle, seal it with a cotton plug, sterilize at 0.14MPa for 40min, cool to 35°C and inoculate slant strains, inoculate 0.4cm per 500ml of liquid medium 2 , and then use a reciproc...
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