Microbial method capable of efficiently decolorizing gentian violet in dye wastewater
A technology for dye wastewater and gentian violet, applied in the field of microbial engineering, can solve the problems of low safety and high cost, and achieve the effects of reducing pollution, no secondary pollution, and avoiding environmental pollution
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[0018] The preparation of LB high-salt liquid culture medium of the present invention is: yeast powder 10g, peptone 5g, sodium chloride 5g, pH7.0, water is settled to 1L, 121 ℃ of sterilization 30min, cooling;
[0019] The preparation of gentian violet dye aqueous solution of the present invention is: 1ml of gentian violet dye storage solution is fixed to 1L with double-distilled water, and sterilized by 450nm membrane filtration;
[0020] The preparation of gentian violet dye storage liquid of the present invention is: 10 g of gentian violet, 100 ml of double distilled water, natural pH, fully dissolved, 450nm membrane filter sterilization, storage for later use;
[0021] The preparation of the strain culture solution of the present invention is as follows: inoculate Comamonas testosteroni (Comamonastestosteroni) CT1 strain in LB high-salt liquid medium, and shake the flask at 37° C. for 24 hours;
[0022] The pH of the shake flask culture of the present invention is 7.0.
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experiment example 1
[0024] Activation of experimental example 1 bacterial strain and biological decolorization of gentian violet dye
[0025] 1. Strain activation
[0026] Comamonas testosteroni CT1 and KF-1, Vibrio H5, Buttiauxella S19-1, Pseudomonas sp LY1, Acinetobacter calcoacetate ( Acinetobacter calcoaceticus) LM1, Rhodococcus sp. P14, Pseudomonas sp. JP1, the above 8 strains were screened from the natural environment and proved to be harmless to humans;
[0027] The above-mentioned strains were taken out from the -80°C refrigerator, thawed at room temperature, added to LB medium, and cultured overnight at 37°C in a 180r / min shake flask to complete the activation of the bacteria. Carry out subculture the next day (method is the same as above);
[0028] The composition of described LB high-salt liquid culture medium is: yeast powder 10g, peptone 5g, sodium chloride 5g, pH 7.0, water is settled to 1L. Sterilize at 121°C for 30 minutes and cool down.
[0029] 2. Degradation experiment of s...
experiment example 2
[0032] Experimental example 2 Comamonas testosteroni (Comamonas testosteroni) CT1 decolorization effect experiment on gentian violet at different temperatures
[0033] 1. Inoculate the bacterial strain of Comamonas testosteroni (Comamonas testosteroni) CT1 in a liquid medium, and culture it on a shaker at 37° C. and 180 rpm for 24 hours to obtain the culture medium of the strain; the composition of the liquid medium is: Yeast powder 10g, peptone 5g, sodium chloride 10g, pH 7.0, water to 1L;
[0034] 2. Take CT1 culture medium and adjust OD 600 =1.0, according to the inoculum amount of 1:100, insert it into the aqueous solution containing 100mg / L gentian violet, respectively place it at different temperatures (22°C, 27°C, 32°C, 37°C), and cultivate it at 180rpm (three parallel experiments) , measure the absorbance value every 1d;
[0035] 3. The decolorization ability of CT1 is calculated by the decolorization rate. Above-mentioned solution was centrifuged at 3000rpm 10 minu...
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