Comamonas testosteroni strain for biological denitrificaion and application thereof
A Comamonas and biological denitrification technology, applied in the direction of microorganism-based methods, microorganisms, biological water/sewage treatment, etc., can solve problems such as blank and lengthy processes, achieve good social benefits, broad application prospects, simplify The effect of the process
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Embodiment 1
[0036] Example 1. Obtainment of strain GAD4 with heterotrophic nitrification-aerobic denitrification performance and biological denitrification experiment
[0037] 1. Isolation and purification method of bacterial strain GAD4 with heterotrophic nitrification-aerobic denitrification performance
[0038] The method has the following steps:
[0039] 1) Sludge samples were taken from the landfill leachate combined treatment system in Buji, Shenzhen;
[0040] 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, wherein the pH of the culture solution is 7.0-7.5;
[0041] 3) Wrap the mouth of the bottle with gauze, and culture it on a shaking table at 30°C and 140rpm for 4 days;
[0042] 4) Take the bacterial solution in the shake flask as the strain source, take out 10mL and inoculate it...
Embodiment 2
[0062] Embodiment 2. Biological denitrification experiment
[0063] The bacterial strain GAD4 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 prepared bacterial strain GAD4 bacterium suspension, add in three culture flasks 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 to measur...
Embodiment 3
[0071] Embodiment 3. Biological denitrification experiment
[0072]The bacterial strain GAD4 prepared by the method provided in Example 1 and its bacterial suspension were subjected to biological denitrification experiments.
[0073] 1. Ammonia nitrogen (NH 4 + -N) as nitrogen source biological denitrification experiments
[0074] Get 5mL prepared bacterial strain GAD4 bacterium suspension, add in 4 culture flasks containing 95ml test medium (each L medium contains 0.42g 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 O, 7.72 g anhydrous sodium acetate, pH 8.5). Seal with 9 layers of gauze, and culture at 40° C. in a shaker with a rotation speed of 100 rpm, 150 rpm, and 200 rpm (rotation radius: 15 mm), respectively. 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, the reaction solution in the shake flas...
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