Method for regulating and controlling fermentation efficiency of clostridium butyricum
A technology of fermentation efficiency and butyric acid bacteria, applied in the biological field, can solve the problems of unstable active ingredient content, unfavorable fermentation efficiency of butyric acid bacteria, complex organic nitrogen source components, etc., and achieves an increase in the number of viable cells of butyric acid bacteria and high controllability of operation. , the effect of simple ingredients
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Embodiment 1
[0039] A method for regulating the fermentation efficiency of butyric acid bacteria, specifically comprising the following steps:
[0040] Step 1, preparation of culture medium
[0041] Prepare liquid culture medium, every liter of seed liquid medium is prepared according to the following formula: glucose 40g / L, peptone 50g / L, yeast powder 15g / L, dipotassium hydrogen phosphate 1.5g / L, magnesium sulfate heptahydrate 0.75g / L, Light calcium carbonate 1g / L, manganese sulfate monohydrate 0.02g / L, the balance is water, pH=7.3, deoxygenation and sterilization by conventional methods;
[0042] The anaerobic tube slant was prepared, and each liter of the anaerobic tube slant medium was prepared according to the following formula: 20 g of agar was added to 1 L of the seed liquid medium.
[0043] Step 2, prepare butyric acid bacteria seed solution
[0044] According to the requirements of aseptic and anaerobic operation, pick up the cells from the freeze-dried tube of butyric acid bact...
Embodiment 2
[0054] A method for regulating the fermentation efficiency of butyric acid bacteria, specifically comprising the following steps:
[0055] Step 1, preparation of culture medium
[0056] Same as Example 1
[0057] Step 2, prepare butyric acid bacteria seed solution
[0058] Same as Example 1
[0059] Step 3, fermentation culture
[0060] Except for the step of adding sodium formate solution, the rest of the fermentation conditions were the same as in Example 1.
[0061] Wherein, the addition condition of sodium formate solution is as follows:
[0062] Feed sterile, anaerobic sodium formate solution with a concentration of 10 g / L within 2 hours during the fermentation of butyric acid bacteria at a flow rate of 375 mL / h until the final concentration of sodium formate in the fermentation broth is 0.125 g / L.
[0063] Anaerobic fermentation 14h in the above-mentioned way, cell number (carry out colony CFU counting with Hungate rolling tube counting method) is 8.26 * 10 8 CFU / m...
Embodiment 3
[0065] A method for regulating the fermentation efficiency of butyric acid bacteria, specifically comprising the following steps:
[0066] Step 1, preparation of culture medium
[0067] Same as Example 1
[0068] Step 2, prepare butyric acid bacteria seed solution
[0069] Same as Example 1
[0070] Step 3, fermentation culture
[0071] Except for the step of adding sodium formate solution, the rest of the fermentation conditions were the same as in Example 1.
[0072] Wherein, the addition condition of sodium formate solution is as follows:
[0073] Feed a sterile, anaerobic sodium formate solution with a concentration of 10 g / L within 2 hours during the fermentation of butyric acid bacteria at a flow rate of 540 mL / h until the final concentration of sodium formate in the fermentation broth is 0.18 g / L.
[0074] Anaerobic fermentation 14h in the above-mentioned manner, cell number (carry out bacterial colony CFU counting with Hungate rolling tube counting method) is 8.12...
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