Xylose oxidation achromatous bacillus SY8 for purifying arsenic contamination and usage thereof
A colorless bacillus and arsenic-polluted technology, applied in the field of environmental microorganisms, to achieve the effect of easy to harm the environment, strong mobility, and reduce the harm of arsenic
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Embodiment 1
[0023] Example 1: Isolation of Achromobacter xyloseoxidizing SY8 from arsenic-contaminated soil
[0024] The experimental soil was taken from arsenic-contaminated topsoil in Shayang County, Hubei Province, China. The specific operation steps are as follows:
[0025] (1) Sample enrichment: Accurately weigh 100g of soil sample into a 250ml sterilized conical flask, add 5ml of 80mM NaAsO 2 , Gently stir well and place in a 28°C incubator for one week, pay attention to adding sterile water to ensure that the samples are not dry.
[0026] (2) Isolation of arsenic-resistant bacteria: accurately weigh NaAsO 2 10g of enriched soil samples were placed in a triangular flask containing 90ml of sterile physiological saline, shaken in a shaker at 28°C for half an hour, and then 1ml to 9ml of sterile physiological saline was gradually diluted to 10 -3 , 10 -4 , 10 -5 , respectively take 0.1ml of coating containing 800uM NaAsO 2 The CDM solid medium plates of 100% were coated with 3 pla...
Embodiment 2
[0030] Example 2: Arsenic oxidation curve of Achromobacter xylose oxidizing SY8
[0031] Pick Achromobacter xylose oxidizing bacteria SY8 monoclone and inoculate it into 100ml CDM liquid medium, and place it in a shaker at 28°C for 48 hours of shaking culture. At this time, the cell density is OD. 600 is about 0.15, stored in a refrigerator at 4°C, and used as a seed bacterial solution for inoculation. Pipette 1ml into 100ml of fresh CDM liquid medium at 1% inoculum volume, place it in a shaker at 28°C for 12 hours and then add NaAsO 2 The mother liquor was made to have a final concentration of 800 uM, and after culturing for 9 hours, sampling was started, and samples were taken every 1 hour until NaAsO 2 Until complete oxidation, take 1.2ml and 0.6ml each time, respectively, and then measure the cell density (OD) by spectrophotometry. 600 ) and pentavalent arsenic concentration (OD 838 ), all cash out. The specific methods are as follows: First, measure the cell density (...
Embodiment 3
[0032] Example 3: The oxidation effect of Achromobacter xylose oxidizing bacteria SY8 on trivalent arsenic in simulated arsenic-polluted water
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