Chloramphenicol efficient degrading bacterium, efficient degrading bacterium agent and application thereof
A technology for efficiently degrading bacteria and chloramphenicol, applied in the direction of bacteria, biological water/sewage treatment, biochemical equipment and methods, etc., can solve the problems of harsh degradation conditions, low degradation efficiency, and difficulty in wide application
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Embodiment 1
[0040] Inoculate the colony of chloramphenicol highly efficient degrading bacteria SA-cd1 into 100ml of nutrient broth medium, culture it with shaking at 36°C for 24 hours at a shaking speed of 150r / min, and obtain the highly efficient chloramphenicol degrading bacterial agent.
Embodiment 2
[0042] Inoculate 100ml of nutrient broth culture medium with ceramic beads that preserve the high-efficiency chloramphenicol-degrading bacteria SA-cd1, and culture it with shaking at 36°C for 24 hours at a shaking speed of 150r / min to obtain the high-efficiency chloramphenicol-degrading bacterial agent.
Embodiment 3
[0044] Inoculate 100 μL of chloramphenicol-degrading bacterium SA-cd1 suspension into 100 ml of nutrient broth medium, shake and culture at 36°C for 12 hours at a shaking speed of 150 r / min, and obtain a chloramphenicol-efficient degrading bacterial agent.
[0045] 2. Degradation test of chloramphenicol by SA-cd1 bacterial agent
[0046] (1) The assay method of chloramphenicol content in the degradation reactant
[0047] Add ethyl acetate to the degradation reaction product to terminate the reaction, add 100ng chloramphenicol-D5 internal standard, add 5g anhydrous sodium sulfate, vortex for 5min, centrifuge at 4000r / min for 5min, take 0.5mL supernatant and put it in a water bath with nitrogen at 45℃ Blow dry, add 1mL water to reconstitute, bottle through 0.22μm filter membrane, measure with high-performance liquid chromatography-tandem mass spectrometer, the determination conditions and parameters refer to the literature (Wang Wenlong, Huang Daxin, Liu Junyi, Luo Zhaofei, Wu Y...
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