Salt-tolerant, heterotrophic and aerobic nitrifying bacterium strain, culture method, bacterial liquid and application
A nitrifying bacteria strain and heterotrophic nitrification technology, applied in the field of salt-tolerant heterotrophic aerobic nitrifying bacteria strains, can solve problems such as poisoning and achieve good market application prospects
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Embodiment 1
[0039] The isolation and enrichment screening steps of heterotrophic nitrifying strains are as follows:
[0040] (1) Activated sludge was collected from China Petroleum Dagang Petrochemical Company in Tianjin, and the sludge sample was inoculated into sterilized nitrification medium by dilution and plate coating method. The initial NH 4 + -N concentration is 100 mg / L, and the formula of nitrification medium is as follows (g / L): ammonium chloride 0.3, sodium acetate 1, disodium hydrogen phosphate 0.2, potassium chloride 0.1, sodium chloride 10, magnesium sulfate 0.05, and 1 mL Trace element solution, pH 7.0, cultivated on a shaker at 30°C to obtain isolated strains;
[0041] (2) Place the strain isolated in (1) in the culture medium for NH 4 + -N removal experiment, NH 4 + The strain with the highest removal rate of -N was the desired strain.
Embodiment 2
[0043] Molecular biological identification of strains
[0044] 30 strains were screened from the activated sludge, and the HQXH-21 strain with the best ammonia nitrogen removal effect was selected for 16S rRNA identification, and it was identified as Pseudomonas by using 16S rRNA ( Pseudomonas sp. ), and named Pseudomonas sp. HQXH-21, the single colony of this strain in LB medium is regular round, moist, yellow in color, opaque, and viscous. See the appendix for the sequence list in the 16S rRNA identification of the bacterial strain of the present invention.
Embodiment 3
[0046] Pseudomonas sp. The cultivation method of HQXH-21
[0047] The above-mentioned isolated bacterial strains are cultivated in a nitrifying medium, which consists of: 0.3g / L ammonium chloride, 1g / L sodium acetate, 0.2g / L disodium hydrogen phosphate, 0.1g / L potassium chloride, and 10g sodium chloride / L, magnesium sulfate 0.05g / L and 1mL trace element solution; culture temperature is 30°C; pH is 7;
[0048] Inoculate 5% of the inoculum in the nitrification medium, culture at 37°C and 150 r / min on a shaker; every 48 h, replace with fresh heterotrophic nitrification medium at a volume ratio of 10%; continuously culture for more than 30 h.
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