Culturing method for improving ammoxidation capability of nitrobacteria
A technology for nitrifying bacteria and culturing methods, applied in microorganism-based methods, biochemical equipment and methods, and adding compounds to stimulate growth, etc., can solve the problems of increasing difficulty in nitrifying bacteria culturing, large environmental factors, and slow growth. , to achieve the effect of promoting rapid proliferation, solving growth inhibition and enhancing vitality
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Embodiment 1
[0021] Dissolve 1.0g of sodium bicarbonate, 0.5g of ammonium sulfate, 0.3g of sodium carbonate, 0.1g of sodium chloride, 0.1g of potassium dihydrogen phosphate, 0.1g of magnesium sulfate, 0.01g of ferrous sulfate and 0.1mL of trace elements (FeCl) in 1000mL of water. 3 ·6H 2 O 1.5g / L, H 3 BO 3 0.15g / L, CuSO 4 ·5H 2 O 0.03g / L, KI 0.18g / L, MnCl 2 4H 2 O 0.12g / L, Na 2 MoO 4 2H 2 O 0.06g / L, ZnSO 4 7H2O 0.12g / L, CoCl 6 ·H 2 O 0.15g / L and disodium EDTA 10g / L. ) to make a culture medium for nitrifying bacteria, adjust the pH to 6.8 with 0.1M HCl, and add tourmaline with a particle size of 0.1 μm to the culture medium at a mass ratio of 0.5%. The nitrifying bacteria were mixed at a volume ratio of 10% (OD 600 0.5) inoculum amount was inoculated into the culture medium, and cultured for 7 days at 28°C and 4.0 mg / L dissolved oxygen. After 7 days, the cell mass and ammonia oxidation capacity of the nitrifying bacteria were detected, and the results were compared with the ...
Embodiment 2
[0023] Dissolve 4.0g of sodium bicarbonate, 1.2g of ammonium sulfate, 0.8g of sodium carbonate, 0.5g of sodium chloride, 0.5g of potassium dihydrogen phosphate, 0.5g of magnesium sulfate, 0.05g of ferrous sulfate and 1.0mL of trace elements (FeCl) in 1000mL of water. 3 ·6H 2 O 1.5g / L, H 3 BO 3 0.15g / L, CuSO 4 ·5H 2 O 0.03g / L, KI 0.18g / L, MnCl 2 4H 2 O 0.12g / L, Na 2 MoO 4 2H 2 O 0.06g / L, ZnSO 4 7H2O 0.12g / L, CoCl 6 ·H 2 O 0.15g / L and disodium EDTA 10g / L. ) formula to make a culture medium for nitrifying bacteria, adjust the pH to 8.0 with 0.1M HCl, and add tourmaline with a particle size of 0.5 μm to the culture medium at a mass ratio of 5%. The nitrifying bacteria were mixed at a volume ratio of 15% (OD 6000.5) was inoculated into the culture medium, and cultured for 7 days at 34°C and 4.0 mg / L dissolved oxygen. After 7 days, the cell mass and ammonia oxidation ability of nitrifying bacteria were detected, and the results were compared with the cell mass and amm...
Embodiment 3
[0025] Dissolve 2.0g of sodium bicarbonate, 1.0g of ammonium sulfate, 0.4g of sodium carbonate, 0.3g of sodium chloride, 0.3g of potassium dihydrogen phosphate, 0.3g of magnesium sulfate, 0.03g of ferrous sulfate and 0.5mL of trace elements (FeCl) in 1000mL of water. 3 ·6H 2 O 1.5g / L, H 3 BO 3 0.15g / L, CuSO 4 ·5H 2 O 0.03g / L, KI 0.18g / L, MnCl 2 4H 2 O 0.12g / L, Na 2 MoO 4 2H 2 O 0.06g / L, ZnSO 4 7H2O 0.12g / L, CoCl 6 ·H 2 O 0.15g / L and disodium EDTA 10g / L. ) formula to make a culture medium for nitrifying bacteria, adjust the pH to 7.4 with 0.1M HCl, and add tourmaline with a particle size of 0.8 μm to the culture medium with a mass ratio of 2%. The nitrifying bacteria were mixed at a volume ratio of 12% (OD 600 0.5), and cultivated for 7 days at 30°C and 4.0 mg / L dissolved oxygen. After 7 days, the cell mass and ammonia oxidation ability of nitrifying bacteria were detected, and the results were compared with the cell mass and ammonia oxidation capacity of nitrif...
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