Shewanella decolorationis
A technology of shewanelladecolorationis and decolorizing Shewanella, which is applied in the direction of bacteria, microorganisms, biochemical equipment and methods, etc., can solve the problem of the ability of Shewanella to degrade dyes that has not been found, and achieve the improvement of water ecological environment quality and simple equipment , the effect of improving efficiency
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Embodiment 1
[0024] Add Na to 200 mL deionized water 2 HPO 4 .7H 2 O 2.56g, KH 2 PO 4 0.6g, NaCl 0.1g, NH 4 Cl 0.2g, Acid Scarlet GR (C.I.27290) 0.01g, sterilized at 211°C for 20 minutes as a dye culture solution. Inoculate the LB liquid medium from the slant where Shewanella depigmentation was preserved, and activate the bacteria on a shaking table at 30°C and 150r / min to make the number of bacteria reach the order of 108, and inoculate the activated bacteria solution with an inoculation amount of 1 / 10 In the dye culture solution, culture at 30°C, observe the color change of the culture solution, take 10mL of the dye culture solution every 30 minutes and centrifuge at 6000r / min to remove the bacteria, use DU640 ultraviolet spectrophotometer (BECKMAN) at 503nm Measure the absorbance value of Acid Scarlet GR (C.I.27290) in the dye culture solution, and calculate the degradation rate of the dye with the dye culture solution without adding bacteria as the control. After 2 hours, the re...
Embodiment 2
[0026] Add Na to 200 mL deionized water 2 HPO 4 .7H 2 O 2.56g, KH 2 PO 4 0.6g, NaCl 0.1g, NH 4 Cl 0.2g, Acid Scarlet GR (C.I.27290) 0.1g, sterilized at 211°C for 20 minutes as a dye culture solution. Inoculate the LB liquid medium from the slant where Shewanella depigmentation was preserved, and activate the bacteria on a shaking table at 30°C and 150r / min to make the number of bacteria reach the order of 108, and inoculate the activated bacteria solution with an inoculation amount of 1 / 10 In the dye culture solution, culture at 30°C, observe the color change of the culture solution, take 10mL of the dye culture solution every 30 minutes and centrifuge at 6000r / min to remove the bacteria, use DU640 ultraviolet spectrophotometer (BECKMAN) at 503nm Measure the absorbance value of Acid Scarlet GR (C.I.27290) in the dye culture solution, and calculate the degradation rate of the dye with the dye culture solution without adding bacteria as the control. After 4 days, the remo...
Embodiment 3
[0028] Add Na to 200 mL deionized water 2 HPO 4 .7H2 O 2.56g, KH 2 PO 4 0.6g, NaCl 0.1g, NH 4 Cl 0.2g, Reactive Brilliant Blue (C.I.612051) 0.01g, sterilized at 211°C for 20 minutes as dye culture solution. Inoculate the LB liquid medium from the slant where Shewanella depigmentation was preserved, and activate the bacteria on a shaking table at 30°C and 150r / min to make the number of bacteria reach the order of 108, and inoculate the activated bacteria solution with an inoculation amount of 1 / 10 In the dye culture solution, culture at 30°C, observe the color change of the culture solution, take 10mL of the dye culture solution every 30 minutes and centrifuge at 6000r / min to remove the bacteria, use DU640 ultraviolet spectrophotometer (BECKMAN) at 592nm Measure the absorbance of reactive brilliant blue (C.I.612051) in the dye culture solution, and use the dye culture solution without bacteria as a control to calculate the degradation rate of the dye. After 15 hours, the ...
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