A kind of heterotrophic nitrifying aerobic denitrifying Acinetobacter and its application
A bacillus and expanded culture technology, applied in the field of environmental microorganisms, can solve the problems of lack of efficient denitrification, lack of simultaneous multi-resistance, etc.
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Embodiment 1
[0037]Example 1 Screening and isolation of heterotrophic nitrification-aerobic denitrification strains
[0038] Take the activated sludge from the sewage treatment tank of the No. 1 Sewage Treatment Plant in Zhuyuan, Pudong, Shanghai, and take 5mL of mud-water mixture from the activated sludge into 45mL of sterilized NSM enrichment medium.
[0039] Then placed at 30°C, 200rpm air bath shaker enrichment culture for 12h. After gradient dilution of the enriched solution, spread evenly on NSM separation medium (agar 20g / L, other components are the same as NSM). 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.
[0040] Wherein, the formula of NSM medium is, by every liter: (NH 4 ) 2 SO 4 0.945g, sodium citrate 16.34g, MgSO 4 ·7H 2 O 1.0g, NaCl 0.12g, MnSO 4 ·H 2 O 0.01g, FeSO 4 ·7H 2 O0.02g, phosphate ...
Embodiment 2
[0045] Example 2 Molecular biology identification
[0046] Genomic DNA of YN-3 was extracted using a kit from Axygen, and 16S rDNA was amplified using this as a template. Primers: 16S rDNA-8F: AGAGTTTGATCCTGGCTCA, 1492R: GGTTACCTTGTTACGACTT.
[0047] PCR reaction system (50 μL): template DNA 1 μL, PCR Taq mix 25 μL, upstream and downstream primers 1.5 μL, DMSO 2 μL, add ddH 2 O to 50 μL of the reaction system. PCR program: 94°C for 5min, 94°C for 30s, 50°C for 1min, 72°C for 2min, 72°C for 5min, 72°C for 10min; 30 cycles. The purification and sequencing of PCR products were completed by Meiji Biomedical Technology Co., Ltd., and the sequencing sequences were registered in NCBI for homologous sequence search (Blastn analysis), and the obtained sequences were imported into the bioinformatics software Mega6 for genetic tree analysis.
[0048] The effective sequence length of the 16S rDNA of the amplified strain YN-3 is 1437bp, as shown in SEQ ID NO.1 in the sequence table. Aft...
Embodiment 3
[0049] Embodiment 3 (Acinetobacter sp.) The growth adaptability of (Acinetobacter sp.) YN-3 and the effect analysis of removing ammonia nitrogen
[0050] NM medium was used to cultivate strain YN3, and YN3 was inoculated into LB medium, and cultured at 30° C. on an air-bath shaker at 200 rpm for 12 hours. Then get the centrifugal washing of bacterium liquid respectively, inoculate in the NM liquid nutrient solution of 50mL respectively, inoculum amount is 0.3g / L by thalline wet weight, and the acidity and alkalinity (pH) of nutrient solution is respectively 4.0,4.5,5.0,6.0, 7.0, 8.0, 9.0, 10.0, 10.5, 11.0. At 30°C, 200rpm air bath shake flask cultured for 24h, the results are as follows: image 3 shown.
[0051] And by image 3 It can be seen that YN3 can grow between pH 5.0 and 10.0. Although the growth slows down at pH 5.0 or 10.0, the growth of the strain still continues; There is no growth phenomenon or the growth is extremely slow, and when the pH value is 5.0-10.0, t...
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