Method of degrading surface-source petroleum hydrocarbon in water body through microorganisms
A microbial degradation and biodegradation technology is applied in the field of using microorganisms to degrade non-point source petroleum hydrocarbons in water bodies, which can solve the problems of secondary environmental pollution, poor treatment effect and high cost, and achieves increased contact area, good application prospects and low cost. Effect
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Embodiment 1
[0025] 1) In waters heavily polluted by petroleum hydrocarbons, 5 g of water samples were collected, and the samples were added to LB liquid medium, and shaken in a constant temperature shaking incubator at 30 °C and a speed of 200 r / min for 12 h.
[0026] The preparation method of LB liquid medium: Weigh 5g of tryptone, 2.5g of yeast extract, and 5g of NaCl respectively, then use deionized water to make up to 300mL, adjust the pH to 7.0 with 5mol / L NaOH solution, and use 121℃ Steam sterilize for 20 min.
[0027] 2) Spread the bacterial liquid obtained in step 1) on an LB plate, and separate and purify a single bacterial strain. Through the identification of 16sRNA, 5 kinds of rapid petroleum hydrocarbon degrading bacteria were obtained: Pseudomonas, Paleobacterium, Bordetella, Gordonia and Pseudomonas aeruginosa, bacteria preservation, standby.
[0028] 3) Inoculate the screened and enriched Pseudomonas, Pseudomonas pallidum, Bordetella, Gordonia and Pseudomonas aeruginosa i...
Embodiment 2
[0035] 1) In waters heavily polluted by petroleum hydrocarbons, 5 g of water samples were collected, and the samples were added to LB liquid medium, and shaken in a constant temperature shaking incubator at 30 °C and a speed of 200 r / min for 12 h.
[0036] 2) Spread the bacterial liquid obtained in step 1) on an LB plate, and separate and purify a single bacterial strain. Through the identification of 16sRNA, 4 kinds of rapid petroleum hydrocarbon degrading bacteria were obtained: Paleobacterium pallidus, Bordetella, Gordonella and Pseudomonas aeruginosa, bacteria preservation, standby.
[0037] 3) Inoculate the screened and enriched Pseudomonas pallidum, Bordetella, Gordonia and Pseudomonas aeruginosa into LB liquid medium respectively, and then place them at a constant temperature of 30°C and 200r / min Shaking culture in a shaking incubator for 36 hours;
[0038] 4) Centrifuge the bacteria cultured in step 3), remove the supernatant, collect the bacteria, and then resuspend ...
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