Sphingomonas paucimobilis
A single cell, less motile sheath technology, applied in bacteria, water/sludge/sewage treatment, biochemical equipment and methods, etc., can solve the problem that the results cannot meet the actual needs of industrial production, and reduce nitrate nitrogen and nitrous nitrogen, the effect of obvious degradation
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Embodiment 1
[0009] Isolation screening and identification of embodiment 1 bacterial strain
[0010] 1. Culture medium:
[0011] Primary screening of BTB medium: beef extract 3.0g; peptone 10.0g; sucrose 15.0g; sodium chloride 20.0g; Teepol 1.0g; bromothymol blue 0.00006g; water 1000ml.
[0012] Nutrient broth medium: peptone 10g; beef powder 3g; sodium chloride 5.0g; glucose 1g; water 1000ml.
[0013] Screening medium: NaNO 2 0.1g (about 20mg / L NO 2 -N); Glucose 5.0g; K 2 HPO 4 1.0g; NaCl2.0g; MgSO 4 .7H 2 O0.5g; water 1000ml.
[0014] 2. Screening method
[0015] Dilute the sludge sample by the gradient dilution method, take 0.1mL and evenly spread it on the surface of the BTB medium, put it in a constant temperature incubator, and cultivate it at 30°C for 2-3 days, then pick it up with an inoculation loop to make the surrounding medium appear blue halo The single colonies in the circle were isolated and purified as the primary screening strains. A total of 13 single colonies we...
Embodiment 2
[0024] Example 2 Degradation experiment of sphingomonas paucimobilis NI1 to nitrite nitrogen
[0025] 1. Culture medium:
[0026] Activation medium: nutrient broth;
[0027] Screening medium: NaNO 2 0.1g (about 20mg / L NO 2 -N); Glucose 5.0g; K 2 HPO 4 1.0g; NaCl2.0g; MgSO 4 .7H 2 O0.5g; water 1000ml.
[0028] Detection medium:
[0029] High concentration nitrite nitrogen medium: NaNO 2 0.05g (about 10mg / L NO 2 -N); Glucose 5.0g; K 2 HPO 4 1.0g; NaCl2.0g; MgSO 4 .7H 2 O0.5g; water 1000ml.
[0030] Low concentration nitrite nitrogen medium: NaNO 2 0.025g (about 5mg / L NO 2 -N); Glucose 5.0g; K 2 HPO 4 1.0g; NaCl2.0g; MgSO 4 .7H 2 O0.5g; water 1000ml.
[0031] 2. Experimental method:
[0032] Pick a single colony of Sphingomonas paucimobilis NI1 on the plate and inoculate it into a test tube containing 8ml of nutrient broth, and place it in a shaker at 30°C and 205r / min for activation; transfer 5ml of the bacterial solution to 10ml without centrifuge at 4000...
Embodiment 3
[0036] Example 3 Sphingomonas paucimobilis NI1 treatment of aquaculture wastewater experiment
[0037] The NI1 strains screened by the present invention are activated and expanded, fermented in a nutrient broth medium in a liquid state, centrifuged to collect the bacteria sludge, added to a starch carrier, and dried to make 10 billion / g bacteria powder. The aquaculture wastewater was taken from loach pond aquaculture wastewater. Its nitrate nitrogen content was determined to be 45.62±1.15mg / L and nitrite nitrogen was 0.58±0.03mg / L. The experimental container was a plastic bucket, and the experimental water body was 10L. Add the bacteria powder of Sphingomonas paucimobilis NI1 at a mass ratio of 50ppm, and no bacteria powder is added to the control group. The experimental group and the control group are set up in three parallels, and the aeration is uninterrupted during the experiment, and the aeration volume of each container is adjusted to be consistent. , and the experimenta...
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