Pseudomonas sp. GY13 and application of pseudomonas sp. GY13 in sewage treatment
A technology of pseudomonas and resin, which is applied in the field of microbial and microbial wastewater treatment, can solve the problems of increased investment and operation costs, limited application of denitrification, and harsh growth conditions, so as to save treatment space and cost, and simplify the denitrification process , the effect of wide pH adaptability
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Embodiment 1
[0023] Isolation and identification of strains:
[0024] Enrichment culture: The sample is the aerobic activated sludge collected by Cao Xianhe from a sewage treatment plant in Beijing in April 2020. Take 20mL of fully mixed activated sludge and suspend it in 180mL0.2% sodium chloride solution. Take 5mL The suspension was placed in a 250mL Erlenmeyer flask filled with 100mL heterotrophic nitrification medium, and acclimatization and enrichment culture was carried out at 30°C and 180rpm. Acclimatization takes 48h as a cycle. After each cycle, take 10 mL of the enrichment solution and add it to a new 100 mL heterotrophic nitrification medium to continue the enrichment culture, and thus continue the enrichment culture for 5 cycles. During this period, the removal of ammonia nitrogen in the culture medium was detected.
[0025] Take the culture solution after enrichment for 5 generations, and use sterile water according to 10 -3 -10 -7 Different proportions of gradient dilutio...
Embodiment 2
[0036] Growth and heterotrophic nitrification characteristics of strain GY13:
[0037]After the bacterial strain GY13 was activated and cultured in the LB liquid test tube for 24 hours, a certain amount of bacterial solution was drawn according to the inoculum amount (v / v) of 2%, and the bacterial cells were collected after centrifugation at 4000 rpm for 5 minutes, washed with sterile water and inoculated in the container. In a 150mL Erlenmeyer flask with 50mL of sterilized heterotrophic nitrification medium (initial ammonia nitrogen concentration 100mg / L, C / N=20), cultivate it in a shaker at 30°C and 180rpm for 72h, during which time samples were taken every 4h to measure OD600 value, and the sample was centrifuged at 10000rpm for 10min to remove the bacteria, and then the supernatant was taken to detect COD and NH in the water sample 4 -N, NO 2 -N, NO 3 -N, TN content.
[0038] The results are as follows and figure 1 shown. The strain began to grow rapidly 4h after inoc...
Embodiment 3
[0041] Effect of pH on growth and denitrification of strain GY13:
[0042] Adjust the pH of the heterotrophic nitrification medium to be 3, 4, 5, 7, 8.5, 9.5, 10.5, 11.5 respectively, after activating the bacterial strain GY13 according to the conventional method, draw a certain amount of The bacteria solution was centrifuged at 4000rpm for 5min to collect the bacteria, washed with sterile water, inoculated in the heterotrophic nitrification medium after adjusting the pH, cultured in a shaker at 30°C and 180rpm for 72h, and tested the final pH value under each pH condition. OD600 value, and the sample was centrifuged at 10000rpm for 10min to remove the bacteria, and then the supernatant was taken to detect COD and NH in the water sample 4 -N content.
[0043] The results are as follows and figure 2 shown. Strain GY13 can grow well and perform heterotrophic nitrification in the pH range of 4-11.5. When the pH is 5, 6, 7, 9, and 10.5, the removal rates of ammonia nitrogen ar...
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