Heterotrophic nitrification-aerobic denitrification bacteria and identification method thereof
A technology of aerobic denitrification bacteria and heterotrophic nitrification, applied in the field of microorganisms, can solve the problems of long reaction time, low denitrification efficiency, poor sedimentation, etc., and achieve the effects of fast growth rate, simple denitrification process, and high cell yield
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Embodiment 1
[0042] Pick a single colony of MA1 and inoculate it in LB medium. The composition of LB medium is: casein 10g / L, yeast extract powder 5g / L, NaCl 10g / L, the same below, 30°C, 180rpm shaker for 8h-10h Then inoculate the seed solution in 100mL glucose medium with a ratio of 0.5%. The glucose medium consists of: glucose 5g / L, ammonium chloride 0.382g / L, dipotassium hydrogen phosphate 0.147g / L, EDTA 0.0025g / L, ZnSO 4 ·7H 2 O 0.011g / L, MnSO 4 ·H 2 O 0.00154g / L, CuSO 4 ·5H 2 O0.000392g / L, Co(NO 3 ) 2 ·6H 2 O 0.00025g / L, Na 2 B 4 o 7 10H 2 O 0.000177g / L, CaCl 2 2H 2 O0.0667g / L, MgSO 4 0.289g / L, (NH 4 ) 6 Mo 7 o 24 4H 2 O 0.000185g / L, KOH 0.146g / L, nitrilotriacetic acid 0.2g / L, FeSO 4 ·7H 2 O 0.00698g / L, the same below; in 30 ℃, 180rpm shaker culture 24h; according to water quality ammonia nitrogen determination Nessler's reagent spectrophotometry HJ535-2009 measured the initial ammonia nitrogen of the medium is 100ppm, cultured after 24h bacterial agent treatment ...
Embodiment 2
[0044] Pick a single colony of MA1 and inoculate it in LB medium, shake it in a shaker at 30°C and 180rpm for 8h-10h, then inoculate the seed solution with 1% in 100mL glucose medium and shake it in a shaker at 30°C and 180rpm for 24h; according to the water quality Determination of ammonia nitrogen Nessler's reagent spectrophotometry HJ535-2009 measured the initial ammonia nitrogen of the medium as 100ppm, and after 24 hours of bacterial agent treatment, the ammonia nitrogen of the medium was 29.9ppm, and the removal rate was 70.1%.
Embodiment 3
[0046] Pick a single colony of MA1 and inoculate it in LB medium, shake it in a shaker at 30°C and 180rpm for 8h-10h, then inoculate the seed solution with 5% in 100mL glucose medium and shake it in a shaker at 30°C and 180rpm for 24h; according to the water quality Determination of ammonia nitrogen Nessler's reagent spectrophotometry HJ535-2009 measured the initial ammonia nitrogen of the medium as 100ppm, and after 24 hours of bacterial agent treatment, the ammonia nitrogen of the medium was 27.8ppm, and the removal rate was 72.2%.
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