Achromobacter xylosoxidans strain for biological denitrificaion and application thereof
A colorless bacillus and biological denitrification technology, applied in the field of biological denitrification, can solve problems such as lengthy process, achieve broad application prospects, save equipment and investment costs, and simplify the process flow
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Embodiment 1
[0037] Example 1. Obtainment of strain GAD3 with heterotrophic nitrification-aerobic denitrification performance and biological denitrification experiment
[0038] 1. Isolation and purification method of bacterial strain GAD3 with heterotrophic nitrification-aerobic denitrification performance
[0039] The method has the following steps:
[0040] 1) Sludge samples were taken from the landfill leachate combined treatment system in Buji, Shenzhen;
[0041] 2) Inoculate into a 500mL Erlenmeyer flask containing 100mL enriched culture medium: each L contains 0.95g NaNO 3 , 0.7g peptone, 0.5g beef extract, 0.15g urea, 0.04g NaCl, 0.15g KH 2 PO 4 , 0.02g KCl, 0.03g MgSO 4 ·7H 2 O, 0.20g CaCl2 2H 2 O, pH 7.0-7.5;
[0042] 3) Wrap the mouth of the bottle with gauze, and culture it on a shaker at 30° C. and 140 rpm for 4 days;
[0043] 4) Take the bacterial solution in the shake flask as the strain source, take out 10mL and inoculate it into a fresh Erlenmeyer flask containing 1...
Embodiment 2
[0062] Embodiment 2. Biological denitrification experiment
[0063] The bacterial strain GAD3 prepared by the method provided in Example 1 and its bacterial suspension were subjected to biological denitrification experiments.
[0064] 1. Ammonia nitrogen (NH 4 + -N) as nitrogen source biological denitrification experiments
[0065] Get 5mL of the prepared bacterial strain GAD3 bacterium suspension, add in three culture bottles containing 95ml test medium (each L medium contains 1.52g NH 4 Cl, 1.0g KH 2 PO 4 , 0.06g FeSO 4 ·7H 2 O, 0.2g CaCl 2 2H 2 O, 1.0g MgSO 4 ·7H 2 (0, 8.1 g sodium citrate, pH is 8.0), sealed with 9 layers of gauze, and incubated at 15° C. in a shaker at 160 rpm (radius of rotation: 15 mm). The culture medium that was not inoculated with the bacterial suspension was used as a blank control for experiments under the same conditions. The reaction solution was taken the next day, and centrifuged at 4000rpm for 10min, and the supernatant was taken t...
Embodiment 3
[0071] Embodiment 3. Biological denitrification condition experiment
[0072] The bacterial strain GAD3 prepared by the method provided in Example 1 and its bacterial suspension were subjected to biological denitrification condition experiments.
[0073] 1. Ammonia nitrogen (NH 4 + -N) as nitrogen source biological denitrification condition experiment
[0074] Get 5mL prepared bacterial strain GAD3 bacterium suspension, add in 9 culture flasks containing 95ml test medium (each L medium contains 0.57g NH 4 Cl, 1.0g KH 2 PO 4 , 0.06g FeSO 4 ·7H 2 O, 0.2g CaCl 2 2H 2 O, 1.0g MgSO 4 ·7H 2 (2, 7.72g anhydrous sodium acetate), the initial pH is respectively 5.0, 6.0, 7.0, 8.0, 9.0, 10.0, 11.0. Seal it with 9 layers of gauze, and cultivate it in a shaker at 40° C. and 160 rpm (rotation radius: 15 mm). The culture medium that was not inoculated with the bacterial suspension was used as a blank control for experiments under the same conditions. After culturing for 24 hours, ...
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