A Phage Bacteria and Its Application in Sludge Reduction
A technology of phage and bacteria, applied in the field of microorganisms, can solve the problems of high sludge treatment costs, etc., and achieve the goals of improving biodegradability and resource utilization, improving sludge dehydration and weight reduction performance, and improving dehydration and weight reduction performance Effect
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Embodiment 1
[0035] Embodiment 1: Separation and purification of phage type bacteria
[0036] The phage-type bacteria in the present invention are separated from the activated sludge of the secondary sedimentation tank of a sewage treatment plant in Jiangsu, and the specific process is as follows:
[0037]1) Isolation and identification of host bacteria: Take samples from the activated sludge of the secondary sedimentation tank of the municipal sewage treatment plant for preliminary treatment of the sludge. The sludge supernatant was diluted to 10 with Bacterial Phosphate Buffer 5 ~10 7 times, and then take 200 μL of each serial dilution and spread it on the peptone yeast extract solid medium. After the coating is completed, let it stand for 20 minutes, and then move it to a constant temperature incubator at 28° C. for upside-down cultivation. After culturing for 12-18 hours, streak and separate the isolated colonies that appear on the plate to obtain candidate host bacteria, and finall...
Embodiment 2
[0043] Embodiment 2: the gene identification of the 16S rRNA of SDWB01 bacterial strain
[0044] The 16S rRNA gene sequencing method was used to classify and identify the strain SDWB01, and the specific steps were as follows:
[0045] Sample DNA preparation: routine bacterial DNA extraction method was used for analysis.
[0046] PCR Primers: Use the following primers:
[0047] Upstream primer 1 (63F): 5'-CAGG CCTAACACATGCAAGTC-3'
[0048] Downstream primer 2 (Bdg842R): 5'-CGWCACTGAAGGGGTCAA-3'
[0049] PCR reaction system: 25 μL reaction system, reaction solution composition: 3 μL DNA template, 2 μL upstream primer, 2 μL downstream primer, 12.5 μL Taq enzyme and its mixture, and make up to 25 μL with ultrapure water.
[0050] PCR reaction conditions: pre-denaturation at 94°C for 3 min; main cycle of denaturation at 94°C for 1 min, annealing at 56°C for 45 s, extension at 72°C for 1 min, a total of 30 cycles; final extension at 72°C for 10 min. After the PCR reaction, the P...
Embodiment 3
[0053] Embodiment 3: Bacterial strain SDWB01 is to the phagocytosis of Gram-negative bacteria in sludge
[0054] 1) Separation, purification and screening of gram-negative bacteria: take samples from the activated sludge of the secondary sedimentation tank of the municipal sewage treatment plant and conduct preliminary treatment of the sludge. 20min, then the sludge supernatant was serially diluted to 10 with sterile phosphate buffer 5 ~10 7 times. The bacterium in the diluted sludge supernatant is coated and isolated for culture, and the specific steps are: take 200 μL of each gradient dilution solution and spread it on the solid medium of peptone yeast extract. After the coating is completed, let it stand for 20 minutes, and then move it to a constant temperature incubator at 28° C. for upside-down cultivation. Isolate and purify the strain obtained by coating and separating the above-mentioned solid medium with peptone yeast extract. The specific steps are: after the abo...
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