A high temperature resistant nitrosomonas and its application in sewage treatment
A nitrosomonas, high temperature resistant technology, applied in biological water/sewage treatment, water/sludge/sewage treatment, polluted groundwater/leachate treatment, etc. population expansion and other problems, to achieve the effect of high-efficiency deamination
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Embodiment 1
[0018] Put 200 μL of sewage from the outlet of an aerobic pool in a domestic sewage treatment system in Wuhan City, Hubei Province into 5 mL of HNM medium, enrich and culture it on a shaker at 27°C and 190 rpm for 7 days, and then pass 3 rounds of streaking on the HNM solid A single colony was obtained on the culture medium (1.5% agar content).
[0019] The genomic DNA of the isolated strains was extracted using the Genomic Rapid Bacterial Genomic DNA Isolation Kit (Shanghai Sangon), and the 16S rDNA was amplified by PCR and sequenced for molecular biological identification. The upstream primers and downstream primers used in PCR amplification are:
[0020] Upstream primer 27F: 5'-AGA-GTTTGATCATGGCTCAG-3', (SEQ ID NO.1)
[0021] Downstream primer 1492R: 5'-TAC-GGTTACCTTGTTACGACTT-3'. (SEQ ID NO.2)
[0022] The purification and sequencing of the PCR products were completed by Shanghai Sangong, and the sequencing results are shown in SEQ ID NO.3. 16SrDNA sequencing results s...
Embodiment 2
[0024] Use an inoculation loop to pick 2 to 3 rings of Nitrosomonas WH-1 single colonies into 50mL liquid HNM medium, and culture it on a shaker at 39°C and 160rpm for 7 days to obtain the strain suspension (this suspension is defined as WH- 1 inoculum). Then 50 mL of the N. eutropha WH-1 strain suspension was inoculated into 1 L of HNM medium, and cultured on a shaker at 39° C. and 160 rpm for 72 hours to obtain an inoculum. The inoculation solutions in the following examples were all obtained through this condition.
[0025] figure 1 The implementation method is: after inoculation of WH-1 bacterial inoculum prepared in advance into 2000 mL HNM medium according to the volume ratio of 5%, it is then divided into 250 mL Erlenmeyer flasks (100 mL per bottle), At 32°C, 36°C, 39°C, 42°C and 45°C respectively, 160 r min -1 Cultivate on a shaking table for 40 hours, during which the concentration of nitrous nitrogen (D, mg·L -1 ), and accordingly calculate the specific growth r...
Embodiment 3
[0028] figure 2 The implementation method is: inoculate the WH-1 bacterial inoculum prepared in advance into 1000 mL of domestic sewage according to the volume ratio of 2.5%, and then divide it into 250 mL Erlenmeyer flasks (100 mL for each bottle), respectively. At 40°C and 45°C, 160r·min -1 Cultivate on a shaking table for 96 hours, no bacterial agent was added to the control group, during which the concentration of nitrous nitrogen was measured (D, mg·L -1 ), and accordingly calculate the specific growth rate (μ, h -1 ) and generation time (T, h): μ=(lnV n -lnV n-1 ) / 24, where V n is the accumulation rate of nitrite nitrogen (mg L -1 h -1 ), which is calculated as V n =(D t -D t-1 ) / 24; T = ln2 / μ.
[0029] according to figure 2 : It can be seen that in the range of 40°C~45°C, after adding WH-1 bacteria, there is an obvious ammonia oxidation effect (the maximum accumulation rate of nitrite nitrogen can reach 2.0 mg·L -1 h -1 ), the shortest generation time at...
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