Bacterial strain with heterotrophic nitrification and aerobic denitrification function and application thereof
An aerobic denitrification and heterotrophic nitrification technology, which is applied in the field of environmental microorganisms, can solve the problems of water quality deterioration of water ecological balance, aquatic organisms poisoning, etc., and achieves obvious aerobic denitrification ability and good ammonia nitrogen removal effect.
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[0032] Example 1:
[0033] A strain having a heterotrophic nitrified oxygen-denddimized function, the strain is a pf1 of the Achromobacter Xylosoxidans, and the collection location is located in Anhui Lantian Special Town, Anhui Lantian, Wuhu City, Anhui Province. Its 2021 On March 25, he was deposited in China's Typical Casting Safety Center. The preservation of No. CCTCC NO: M2021273; Sales address is in Wuhan University, No. 299, Wuchang District, Wuhan, Hubei Province.
[0034] 1, separation and purification of strains
[0035] The water sample collected from the turtle breeding pond is enriched in a proportion of a volume ratio of 10% to the enriched, and the culture is cultured from 30 ° C, 150R / min shaker; 10% per 48 hours The volume ratio is replaced with fresh heterotrophic nitrification medium, continuous culture 20D.
[0036] Among them, the formulation of heterotrophic noduled enriched medium is: (NH 4 ) 2 SO 4 0.472 g, sodium succinate 4.052 g, 50 ml vitron salt sol...
Example Embodiment
[0046] Example 2, Culture and Nitrogen Performance Analysis of Nonorobacterium PF1
[0047] Picking the colonies of the complement of the complex mesenchyma separated from Example 1 to the R2A liquid medium, 30 ° C gas bath shaker 200 rpm culture for 18 h, centrifuge at 4000 R / min, collected by the bacteria, and resuspended with isometric The bacterium was inoculated with a 1% (volume ratio) inoculum, and DMA (nitrate nitrogen source) and DMB (nitrite as nitrogen source) were in liquid medium. At 30 ° C, 200 rpm shake flask culture, timing sample measurement cell light density (OD600), total nitrogen (TN), ammonia nitrogen (NH 4 + -N), nitrate (NO 3 - -N) and nitrite (NO 2 - The concentration of -N), according to the Growth curve of the OD600 value, by analyzing the nitrogen-nitrogen resistance of the strain by analyzing the removal rate of total nitrogen.
[0048] The R2A liquid medium formulation is: 0.5 g / l, yeast extract 0.5 g / L, starch 0.5 g / l, 0.5 g / l, glucose 0...
Example Embodiment
[0054] Example 3: Nonorobacterium pf1 actual denitrification application
[0055] Each of the 1000ml initial COD is 760mg / L of turtle plant breeding wastewater to add 3L beaker, add 15g of sodium citrate, add carbon supply, turtle factory cultured wastewater COD increase to 8160mg / L; add 0.5g The R2A medium in Example 2 enlarged the cultured PF1 wet bacteria, placed under room temperature (18 to 25 ° C), and the dissolved oxygen was maintained with a aeration device in 2 ppm or more. At the same time, the same treatment was carried out as a control group after breeding wastewater at the same time without the turtle of the PF1. After 24 hours, the sample was removed, centrifuged, and the total nitrogen, total phosphorus and COD content in the supernatant were detected. Specifically, as shown in the following table:
[0056] Table 1 Effect of Niogobacillus PF1 removes nitrogen phosphorus in wastewater
[0057]
[0058] Table 1 shows that the plant turtle breeding wastewater co...
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