Microbacterium and application thereof in degradation for organic pollutants
A technology of organic pollutants and microbacteria, applied in the field of microorganisms, can solve problems such as endocrine disorders, threats to the health of fetuses and children, and achieve the effect of no secondary pollution and low cost
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Embodiment 1
[0026] The microbacteria ( Exiguobacterium profundum ) L20 is isolated and purified from sea mud in the South China Sea.
[0027] The separation and purification method is as follows: the acclimatization medium used is inorganic salt medium, and the composition is (g / L): 6.2g Na 2 HPO 4 , 3.0g KH 2 PO 4 , 0.5g NaCl, 1.0g NH 4 Cl, pH 7.0. First, add 3g of sludge to 100mL inorganic salt medium containing 20mg / L bisphenol A, and after acclimatization at 37°C for 60 days, add 10% by volume inoculum to the inorganic salt medium containing 40mg / L bisphenol A and then acclimate for one week , and so on to gradually increase the concentration of bisphenol A for domestication, the concentration of bisphenol A is 40mg / L, 60mg / L, 80mg / L respectively. After the acclimatization, spread the acclimatization solution on the agar plate (beef extract 3g / L, peptone 10g / L, sodium chloride 5g / L, agar powder 20g / L, pH7.0) and culture at 37°C for 48h, and select a single colony on Beef extra...
Embodiment 2
[0035] microbacteria ( Exiguobacterium profundum ) L20 single colony was inoculated in 3mL beef extract peptone medium, cultured for 18h (OD 600 0.45) with an inoculum volume of 20% by volume, it was inserted into the inorganic salt medium with a bisphenol A concentration of 20 mg / L and a pH of 8.0, and reacted for 96 hours at 37 ° C on a shaker at 150 rpm. Determine the degradation rate. The mensuration of degradation rate is the same as embodiment 1, and detection result is that degradation rate is 92%.
Embodiment 3
[0037] microbacteria ( Exiguobacterium profundum ) L20 single colony was inoculated in 3mL beef extract peptone medium, and the culture cultured for 18h was inserted into the inorganic salt medium with a bisphenol A concentration of 60mg / L and a pH of 7.0 at an inoculation volume of 40% by volume. ℃, 100rpm shaker reaction for 108h, the degradation rate was measured by high performance liquid chromatography, and the determination method was the same as in Example 1. The test result showed that the degradation rate was 89%.
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