Bacillus coagulans solid-state fermentation production method
A technology of Bacillus coagulans and solid-state fermentation, applied in the field of microbial fermentation, can solve the problems of post-treatment sewage discharge, low spore formation rate, long fermentation period, etc., and achieve the effects of cost saving, simple process and high bacterial count.
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Embodiment 1
[0023] (1) First-level seed preparation: take 0.5ml of a bacterial strain preserved in a glycerol tube, put it into a bottle of YPD liquid medium (300ml / 1000ml), prepare 5 bottles of a total of 1500ml seed liquid; cultivate at 40°C and 150r / min 17h, that is, the first-class seed liquid.
[0024] (2) Secondary solid seed medium preparation: prepare 2.5kg solid seed medium: weigh 2250g of bran, 250g of soybean meal and mix for later use; weigh 25g of glucose, 50g of urea, and 50g of calcium carbonate; ℃ hot water, pour it into the weighed solid material and mix well until it is completely wet, put it into a cloth bag, tie it up, and sterilize it in a laboratory sterilizer at 121 ℃ for 50 minutes.
[0025] (3) Two-stage solid seed inoculation method: naturally cool the sterilized solid material to about 50°C, and at the same time put the plastic film and 35cm*45cm*15cm white pot under the ultraviolet light for 30 minutes to sterilize, and wait for the solid material to cool down ...
Embodiment 2
[0031] In order to better prove that the fermentation formula can stabilize the pH value in the fermentation process, the formulas with and without urea were compared.
[0032] (1) The process of adding urea formula: Weigh 900g of bran and 100g of soybean meal and mix them for use. First, dissolve 1.4g of manganese sulfate in 400ml, then add 10g of glucose and 20g of urea to dissolve, and finally add 20g of calcium carbonate. Mix well with the solid material until it is completely wet, put it in a cloth bag, sterilize at 121°C for 50 minutes, cool the sterilized solid material to about 50°C naturally, pour it into the fermentation container after the solid material is cooled, and take 600ml of the primary liquid seed in Example 1, adjust the pH value to 8.0, mix with the solid material, put it into the cultivation room for cultivation at 45°C, monitor the change of the pH value during the cultivation process, cultivate it for 3 days, and dry it at low temperature for detection....
Embodiment 3
[0039] (1) First-level seed preparation: take 0.5ml of a bacterial strain preserved in a glycerol tube, put it into a bottle of YPD liquid medium (300ml / 1000ml), prepare 5 bottles of a total of 1500ml seed liquid; cultivate at 40°C and 150r / min 17h, that is, the first-class seed liquid.
[0040] (2) Secondary solid seed medium preparation: prepare 2.5kg solid seed medium: weigh 2250g of bran, 250g of soybean meal and mix for later use, weigh 2.5g of glucose, 2.5g of urea, and 2.5g of calcium carbonate, dissolve in 1250ml In hot water at 50-60°C, pour it into the weighed solid material and mix well until it is completely wet, put it into a cloth bag, tie it up, and sterilize it in a laboratory sterilizer at 121°C for 50 minutes.
[0041] (3) Two-stage solid seed inoculation method: naturally cool the sterilized solid material to about 50°C, and at the same time put the plastic film and 35cm*45cm*15cm white pot under the ultraviolet light for 30 minutes to sterilize, and wait fo...
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