Heterotrophic nitrification and aerobic denitrification bacterium and application thereof in pig raising wastewater treatment
An aerobic denitrifying bacteria and heterotrophic nitrification technology, applied in the field of environmental microorganisms, can solve the problems of increased investment cost, low biomass concentration, slow growth, etc., and achieve the effects of good application value, simple operation and mild reaction.
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Embodiment 1
[0058] Example 1 Screening and isolation and identification of heterotrophic nitrification-aerobic denitrification strains
[0059] Take samples from the pig farm manure composting fermentation tank in Zhubian Town, Junan County, Linyi City, Shandong Province, and mix 5 g of the compost samples into 45 mL of sterilized VM enrichment medium.
[0060] Then placed at 30°C, 150rpm constant temperature shaker for enrichment culture for 12h. After gradient dilution of the enriched solution, evenly spread on VM separation medium (agar 20g / L, other components are the same as VM). After culturing in a constant temperature incubator at 30°C for 1 day, single clones with different shapes and sizes were picked, streaked and purified, and numbered and stored to obtain the strains for primary screening. Put the isolated strains into 300ml wide-mouth Erlenmeyer flasks containing 100ml of nitrifying medium, place them in a shaker at 30°C and 150rpm for 16 hours, then take the bacterial liqui...
Embodiment 2
[0066] Example 2 Analysis of Influencing Factors for the Removal of Ammonia Nitrogen by Delftia tsuruhatensis SDU2
[0067] 1. The effect of carbon source on the removal of ammonia nitrogen by Delftia tsuruhatensis SDU2
[0068] Glucose, sucrose, methanol, glycerol, sodium acetate, sodium citrate, and sodium succinate were selected as the sole carbon source of the nitration medium, and the carbon-nitrogen ratio in the medium was C / N=10. The activated bacterial liquid in the LB medium was inserted into the nitrification medium according to the inoculum amount of 10%, and after culturing for 32 hours at 30°C and 150rpm, the calculation was carried out according to the implementation case 1, and the results were as follows figure 2 shown. The results show that the ammonia nitrogen removal rate of Delftia tsuruhatensis SDU2 using sodium acetate, sodium succinate and sodium citrate can reach more than 60%, and the ammonia nitrogen removal rate of sodium citrate can reach more tha...
Embodiment 3
[0083] Embodiment 3 is suitable for (Delftia tsuruhatensis) SDU2 ammonia nitrogen removes optimal culture medium and optimal culture condition
[0084] Based on the screening results of Example 2, determine the optimal medium suitable for Crane Haneda Delftia (Delftia tsuruhatensis) SDU2: 4.07g sodium citrate; 0.47g (NH 4 ) 2 SO 4 ; 7.9 g Na 2 HPO 4 ·7H 2 O; 1.5 g KH 2 PO 4 ,0.1g MgSO 4 ·7H 2 O and 2mL trace element solution; make up to 1L with distilled water. Among them, trace element solution: 50.0gNa 2 EDTA; 2.2 g ZnSO 4 ·7H 2 O; 5.5 g CaCl 2 ; 5.06g MnCl 2 4H 2 O; 5.0 g FeSO 4 ; 1.57g CuSO 4 ·5H 2 O; 1.60g CoCl 2 ·6H 2 O; distilled water to 1L.
[0085]Optimal culture conditions suitable for Delftia tsuruhatensis SDU2: 30° C., 150 rpm, pH=7, cultured for 168 hours, and the removal rate of ammonia nitrogen is over 90%.
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