Pseudomonas stutzeri YZN-001 for removing ammoniacal nitrogen, nitrate nitrogen and nitrous nitrogen in water body and application
A technology of Pseudomonas stutzeri and nitrite nitrogen, which is applied in the direction of bacteria, water pollutants, water/sewage treatment, etc., can solve the problems of increasing water treatment costs, slow growth rate, and long reactor start-up time
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Embodiment 1
[0053] Embodiment 1. Isolation, screening and identification of Pseudomonas YZN-001 strain
[0054] 1. Isolation and screening of strains
[0055] 1. Culture medium preparation: Composition and ratio of liquid culture medium for heterotrophic nitrifying bacteria for separation and screening: (NH 4 ) 2 SO 4 0.5g, sodium succinate 7.12g, Vickers salt solution 50mL, add water to dissolve and add water to 1L, adjust the pH value of the medium to 7.5-8.0 (heterotrophic nitrifying bacteria solid medium components and proportions are the same as heterotrophic nitrifying bacteria). Liquid medium, just add 2% by weight of agar) to the medium, and sterilize by moist heat at 121°C for 30min.
[0056] Among them, the components and proportions of Vickers salt solution: K 2 HPO 4 5.0g, MgSO 4 ·7H 2 O 2.5g, NaCl 2.5g, FeSO 4 ·7H 2 O 0.05g, MnSO 4 ·4H 2 O, 0.05g, after dissolving, add water to dilute to 1L, and sterilize by moist heat at 121°C for 30 minutes.
[0057] 2. Selecti...
Embodiment 2
[0062] Example 2: Degradation test of ammonia nitrogen by Pseudomonas stutzeri YZN-001
[0063] Degradation experiment medium formula: (NH 4 ) 2 SO 4 0.5g, sodium succinate 5.95g, Vickers salt solution 50mL, add water to dissolve and make up to 1L, pH 7.5~8.0. Vickers salt solution: K 2 HPO 4 5.0g, MgSO 4 ·7H 2 O 2.5g, NaCl 2.5g, FeSO 4 ·7H 2 O 0.05g, MnSO 4 ·4H 2 O, 0.05g, after dissolving, add water to make up to 1L. The culture solution was put into a 250 mL conical flask, 100 mL per bottle, and sterilized by moist heat at 121°C for 30 min. According to the inoculum of 1%, the bacterial suspension of YZN-001 strain activated after 24 hours was inserted, cultured at 30°C, 150r / min shaker for 36h, sampling every 6 hours, and centrifuged at 10000r / min for 5min to determine the supernatant in The absorbance at 420nm was compared with the standard curve to calculate the ammonia nitrogen content in the culture solution at different times, and the degradation rate of...
Embodiment 3
[0065] Example 3. Degradation test of nitrate nitrogen and nitrite nitrogen by Pseudomonas stutzeri strain YZN-001
[0066] 1. Degradation of nitrate nitrogen
[0067] The medium formula used for degradation is (in volume of 1L): KNO 3 2g, sodium succinate 18.7g, Vickers salt solution 50mL, add water to dissolve and make up to 1L, adjust pH to 7.5-8.0, and sterilize by moist heat at 121°C for 30min. Vickers salt solution: K 2 HPO 4 5.0g, MgSO 4 ·7H 2 O 2.5g, NaCl 2.5g, FeSO 4 ·7H 2 O 0.05g, MnSO 4 ·4H 2 O, 0.05g, after dissolving, add water to make up to 1L. The culture solution was put into 250 mL conical flasks, each 100 mL, and sterilized by moist heat at 121° C. for 30 minutes. The bacterial suspension of YZN-001 strain activated for 24 hours was inserted at 3% of the inoculum, incubated at 30°C, 150r / min shaker for 36h, samples were taken every 6 hours, centrifuged at 10000r / min for 5min, and the supernatant was measured at 220nm and the absorbance value at 2...
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