Pseudomonas aeruginosa for denitrification and phosphorous removal under different dissolved oxygen conditions and application of pseudomonas aeruginosa
A Pseudomonas aeruginosa, conditional technology, applied in the direction of bacteria, microbial-based methods, biological water/sewage treatment, etc., can solve the problems of nitrification and denitrification and phosphorus release and phosphorus absorption that cannot be organically unified, and achieve broad application prospects. The effect of shortening the process flow and saving infrastructure costs
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Embodiment 1
[0037] Embodiment 1: Denitrification and phosphorus removal ability determination of Pseudomonas aeruginosa under anaerobic conditions
[0038] The strain preserved in glycerol at -20°C (preserved in the General Microbiology Center of China Committee for Microorganism Culture Collection (CGMCC for short) on January 21, 2010, the preservation number is CGMCC No.3602, the same below). Inoculate in sterilized 100mL medium (each L contains 5.0g sodium succinate, 0.607g NaNO 3 , 0.110g K 2 HPO 4 ·3H 2 O, 0.10g MgSO 4 ·7H 2 O, 0.006g FeSO 4 ·7H 2 O, 0.02g CaCl 2 2H 2 O, 0.10mL trace element mother solution (each L contains 3.5g EDTA, 2gZnSO 4 ·7H 2 O, 1g CuSO 4 ·5H 2 O, 1g MnSO 4 ·7H 2 O, 1 g Na 2 MoO 4 2H 2 O, 1g H 3 BO 3 , 0.2gCoCl 2 ·6H 2 O), pH 7.0~7.5) in a 250mL Erlenmeyer flask, placed in a 30°C, 150rpm shaker for 20~24h, so that the bacteria grew to the late logarithmic period, and the bacterial suspension was used for inoculation.
[0039] Take 5mL of ...
Embodiment 2
[0043] Embodiment 2: Nitrification and phosphorus removal ability determination of Pseudomonas aeruginosa under anoxic conditions
[0044] Inoculate the strains stored in glycerol at -20°C into 100 mL of sterilized medium (each L contains 5.0 g sodium succinate, 0.607 g NaNO 3 , 0.110g K 2 HPO 4 ·3H 2 O, 0.10g MgSO 4 ·7H 2 O, 0.006g FeSO 4 ·7H 2 O, 0.02g CaCl 2 2H 2 O, 0.10mL trace element mother solution (each L contains 3.5g EDTA, 2g ZnSO 4 ·7H 2 O, 1gCuSO 4 ·5H 2 O, 1gMnSO 4 ·7H 2 O, 1gNa 2 MoO 4 2H 2 O, 1gH 3 BO 3 , 0.2g CoCl 2 ·6H 2 O), pH 7.0~7.5) in a 250mL Erlenmeyer flask, placed in a shaker at 30°C and 150rpm for 20~24h, so that the bacteria grew to the late logarithmic period, and the bacterial suspension was used for inoculation.
[0045] Take 5mL of the above bacterial suspension and add it into a sterilized 250mL Erlenmeyer flask containing 100mL of the test medium (the composition is the same as the above medium), place it in a shaker at 30°...
Embodiment 3
[0049] Embodiment 3: Denitrification and phosphorus removal ability determination of Pseudomonas aeruginosa under anoxic conditions
[0050] Inoculate the strains stored in glycerol at -20°C into 100 mL of sterilized medium (each L contains 5.0 g sodium succinate, 0.607 g NaNO 3 , 0.110g K 2 HPO 4 ·3H 2 O, 0.10g MgSO 4 ·7H 2 O, 0.006g FeSO 4 ·7H 2 O, 0.02g CaCl 2 2H 2 O, 0.10mL trace element mother solution (each L contains 3.5g EDTA, 2g ZnSO 4 ·7H 2 O, 1gCuSO 4 ·5H 2 O, 1gMnSO 4 ·7H 2 O, 1gNa 2 MoO 4 2H 2 O, 1gH 3 BO 3 , 0.2g CoCl 2 ·6H 2 O), pH 7.0~7.5) in a 250mL Erlenmeyer flask, placed in a shaker at 30°C and 150rpm for 20~24h, so that the bacteria grew to the late logarithmic period, and the bacterial suspension was used for inoculation.
[0051] Take 5mL of the above bacterial suspension and add it into a sterilized 250mL Erlenmeyer flask containing 100mL of the test medium (the composition is the same as the above-mentioned pre-culture medium), pla...
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