A method for effectively degrading drug resistance genes in citrus processing wastewater
A technology for drug-resistant genes and processing wastewater, which is applied in the food industry wastewater treatment, chemical instruments and methods, biochemical equipment and methods, etc., can solve the problems of increasing drug-resistant genes and difficult to eliminate high-resistant drug-resistant bacteria, etc. Achieve the effect of promoting industrial application, reducing the possibility of drug resistance gene transmission, and optimizing wastewater treatment process
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Embodiment 1
[0023] A low-temperature plasma technology treatment
[0024] (1) drug resistance gene suspension
[0025] Escherichia coli strain DH5α was inoculated in common broth medium and cultured on a shaker at 37°C until logarithmic growth phase. The ampicillin-resistant and tetracycline-resistant gene plasmids in Escherichia coli were extracted using a plasmid mini-extraction kit, and the ampicillin-resistant and tetracycline-resistant genes were dissolved in the citrus processing wastewater at a concentration of 8-9 log copy number / mL.
[0026] (2) Low temperature plasma treatment
[0027] Experimental group: use double dielectric barrier discharge low-temperature plasma CTP-2000K device to treat citrus processing wastewater containing drug-resistant genes, specific steps: put 3mL of citrus processing wastewater containing drug-resistant genes into a quartz glass with a diameter of 50mm for cultivation In the dish, the air gap distance between the upper medium and the liquid surfa...
Embodiment 2
[0039] A low-temperature plasma technology treatment
[0040] (1) The drug-resistant gene suspension is the same as the method of step (1) in Example 1.
[0041] (2) Low temperature plasma treatment
[0042] The method of one step (2) in embodiment 1 is basically the same, only the processing time is changed to 6min.
[0043] Two detection
[0044] Same as the method of two in embodiment 1.
[0045]The results are as follows: the gene level of ampicillin resistance in the control group was 8.48log copy number / mL, and the gene level of tetracycline resistance was 8.68log copy number / mL. The gene level of ampicillin resistance in the experimental group was 5.22 log copy number / mL, and the gene level of tetracycline resistance was 5.55 log copy number / mL. Therefore, the ampicillin-resistant gene level was degraded to 3.26 log copy number / mL, and the degradation rate was 99.9%, and the tetracycline-resistant gene level was degraded to 3.14 log copy number / mL, and the degradati...
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