Method for cleanly and efficiently producing microorganism bactericide
A technology of microbial agent and production method, which is applied in the direction of microorganisms, microorganisms, biochemical equipment and methods, etc., can solve the problems of difficult product extraction and high energy consumption, and achieve the reduction of organic matter content, high utilization rate of nutrients, and high yield of products. high rate effect
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Embodiment 1
[0030] Fermentation of Bacillus subtilis by adding a composite carrier with a particle size of less than 10um in the fermentation medium
[0031] The specific steps are:
[0032] (1) Activate the freeze-dried bacteria stored at 4°C or the liquid bacteria stored at -80°C. Mark Bacillus subtilis ACCC10619 on the LB (peptone 10 g / L, yeast extract powder 5 g / L, sodium chloride 5 g / L) solid culture dish prepared in advance, and then place it in the Incubate for 18 hours in a biochemical incubator.
[0033] (2) Preparation of primary seed solution. Pick a typical uniform single colony from the activated culture dish and inoculate it into the prepared LB liquid sterile medium, then place it in a constant temperature shaking incubator, set the temperature at 37°C, and the rotation speed at 150rpm, and cultivate for 18 hours . Obtain first-class seed liquid.
[0034] (3) Preparation of secondary seed solution. Firstly, the air filter, air duct and fermenter of the fermentation sy...
Embodiment 2
[0042] Fermentation of Bacillus licheniformis by adding a composite carrier with a particle size of less than 50um in the fermentation medium
[0043] The specific steps are:
[0044] (1) Activate the freeze-dried bacteria stored at 4°C or the liquid bacteria stored at -80°C. Bacillus licheniformis CICC23584 was streaked on the LB solid culture dish prepared in advance, and then placed in a biochemical incubator set at 35°C for 24 hours.
[0045] (2) Preparation of primary seed solution. Pick a typical uniform single colony from the activated culture dish and inoculate it into the LB liquid sterile medium prepared in advance, then place it in a constant temperature shaking incubator, set the temperature at 32°C and rotate at 150rpm, and incubate for 22 hours . Obtain first-class seed liquid.
[0046] (3) Preparation of secondary seed solution. Firstly, the air filter, air duct and fermenter of the fermentation system for making the seed liquid are sterilized with steam, a...
Embodiment 3
[0055] Fermentation of Pseudomonas stutzeri by adding zeolite powder with particle size less than 50um in the fermentation medium
[0056] The specific steps are:
[0057] (1) Activate the freeze-dried bacteria stored at 4°C or the liquid bacteria stored at -80°C. Pseudomonas stutzeri CICC23621 was streaked on the LB solid culture dish prepared in advance, and then placed in a biochemical incubator set at 30°C for 24 hours.
[0058] (2) Preparation of primary seed solution. Pick a typical uniform single colony from the activated petri dish and inoculate it into the prepared LB liquid sterile medium, then place it in a constant temperature shaking incubator, set the temperature at 30°C, and the rotation speed at 150rpm, and incubate for 22 hours . Obtain first-class seed liquid.
[0059] (3) Preparation of secondary seed solution. Firstly, the air filter, air duct and fermenter of the fermentation system for making the seed liquid are sterilized with steam, and then the pr...
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