A method for degrading triphenyl phosphate by Bacillus brevis and its application
A technology of Bacillus brevis, triphenyl phosphate, applied in chemical instruments and methods, water/sludge/sewage treatment, biological water/sewage treatment, etc., can solve the problem of low efficiency and achieve low cost and environmental adaptation Strong performance and good degradation effect
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Embodiment 1
[0023] 1. Screening of degrading strains
[0024] (1) Collect the sediment in the water body of the polluted site, weigh 1g of the sediment sample, add it to the enrichment medium containing triphenyl phosphate with a concentration of 5mg / L, and cultivate it in a constant temperature shaker at 30°C and 150rpm. The main components of enrichment medium are: 5g / L beef extract, 10g / L peptone, 5g / L NaCl, 1000 mL distilled water, pH 7.0.
[0025] (2) Transfer once every 2 days, increase the concentration of triphenyl phosphate by 5mg / L at the same time of each transfer, until the concentration of triphenyl phosphate reaches 40mg / L, inoculate with 40mg / L triphenyl phosphate ester as the only carbon source in inorganic salt medium. The main components of the inorganic salt medium are: 1g / L NH 4 NO 3 , 1.5 g / L KH 2 PO 4 , 3 g / L K 2 HPO 4 , 40 mg / L triphenyl phosphate, 2mL / L trace element solution, 1000mL distilled water, pH 7.0. The composition of trace elements is: 4g / L MgSO ...
Embodiment 2
[0032] Example 2 Degradation analysis of Bacillus brevis to triphenyl phosphate
[0033] Inoculate Bacillus brevis into a 1000mL Erlenmeyer flask containing 500mL of sterilized enrichment medium, place it in a constant temperature shaker, and cultivate it at 30°C and 150rpm for 24h. The main component of the enrichment medium is: 5g / L beef extract, 10g / L peptone, 5g / L NaCl, 1000 mL distilled water, pH 7.0.
[0034] Place the enriched cultured bacterial solution in a 50mL sterilized centrifuge tube at 6000 g After centrifugation at the speed of 5 min, the bacteria were collected and washed repeatedly with sterile normal saline and centrifuged for 3 times, and finally added normal saline to make a certain concentration (OD 600 =0.6) of the bacterial suspension, add 1mL of the prepared bacterial suspension to 19mL of sterilized degradation medium for degradation experiment, 30℃, 150rpm, after 5 days of incubation, the sample is determined by GC-MS, analysis Degradation effect ...
Embodiment 3
[0053] Same as Example 2, except that during the enrichment culture process, the pH of the enrichment medium is 6.5, the culture conditions are: the temperature is 20°C, the rotation speed of the shaking table is 120 rpm, and the culture time is 16h, and finally Bacillus brevis triphenyl phosphate The degradation rate of ester was 94.8%.
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