Short-cut nitrifying bacteria pseudomonad and application thereof
A Pseudomonas, short-range nitrification technology, applied in the direction of bacteria, chemical instruments and methods, biochemical equipment and methods, etc.
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Embodiment 1
[0033] Screening and identification of Pseudomonas sp. YH-01.
[0034] The experimental materials come from the silt on the banks of the Yi River in Linyi City, Shandong Province.
[0035] Take 0.1ml of the sludge dilution, spread it on the screening medium plate, culture it in a 30°C incubator, pick a single blue colony and repeat the streak purification 2-3 times to obtain the purified strain. After 16S rDNA identification, it belongs to Pseudomonas sp., see the phylogenetic tree figure 1 , having the sequence shown in 1 in the sequence table.
Embodiment 2
[0037] Experiment 1 of removing ammonia nitrogen by Pseudomonas sp. YH-01.
[0038] The processing object is the screening medium, and the operation mode is shaking culture in shake flasks.
[0039] The specific implementation steps are as follows: the strains are inoculated into LB medium, and cultured with shaking at 30°C until the bacterial concentration is O.D. 600 =2.0, inoculate in high ammonia nitrogen wastewater with 5% inoculum amount, culture at 25°C for 2 days, maintain dissolved oxygen above 3.0mg / L; centrifuge to take supernatant, according to "Nessler's reagent colorimetric method (GB7479-87)" Determination of ammonia nitrogen, according to "N-1-Naphthylethylenediamine Spectrophotometry (GB7493-87)" Determination of nitrite nitrogen, according to "Ultraviolet Spectrophotometry (DZ / T 0064.59-1993)" Determination of nitrate nitrogen, according to "Alkaline potassium persulfate digestion ultraviolet spectrophotometry (GB11894-89)" was used to determine total nitrog...
Embodiment 3
[0043] Experiment 2 of removing ammonia nitrogen by Pseudomonas sp. YH-01.
[0044] The treatment object is artificial high-nitrogen wastewater, and the operation mode is aeration cultivation in a 3L SBR (sequencing batch bioreactor) system.
[0045] The specific implementation steps are as follows: the strains are inoculated into LB medium, and cultured with shaking at 30°C until the bacterial concentration is O.D. 600 =2.0, inoculate in high ammonia nitrogen waste water with 1-5% inoculum size, cultivate 1 day at 20 ℃, maintain dissolved oxygen 2.5mg / L; The results are shown in Table 2 below.
[0046] Table 2
[0047]
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