A strain of Rhodococcus erythrococcus and its application in wastewater treatment containing organic pollutants
A technology of organic pollutants and Rhodococcus rubrum, applied in biological water/sewage treatment, water/sludge/sewage treatment, water pollutants, etc., can solve the problem of inhibiting environmental biological removal of organic pollutants, increasing the difficulty of sewage treatment, sewage Difficult to meet the standards and other problems, to achieve the effect of protecting health, low production and use costs, and good removal effect
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Embodiment 1
[0044] Obtaining and Identification of Example 1 Rhodococcus Erythrococcus ZHY1-6
[0045] 1. Acquisition and identification of strain ZHY1-6
[0046] Take oil-contaminated sludge from Changqing Oilfield, with a salt content of about 3% (mass percentage), take 2g of sludge and add it to basal salt medium, add 5g of crude oil to 100mL of basal salt medium, 37°C, 200 During the cultivation process, observe that the color of the black crude oil in the shake flask gradually becomes lighter until the crude oil is degraded to a minimum, then take 1 mL of the bacterial liquid and inoculate it in the same medium, and repeat the acclimatization and enrichment culture for 3 times.
[0047] Then inoculate 1mL of the enriched bacterial solution to inoculate the cells containing phenol, C 18 In the basal salt medium with alkanes and naphthalene as the only carbon source, the same enrichment culture was carried out for 3 times, and then 1 mL of the bacterial solution was taken for gradient...
Embodiment 2
[0063] Example 2 Degradation of different compounds by bacterial strain ZHY1-6 in high-salt basal liquid medium
[0064] Pick a single colony of strain ZHY1-6 and inoculate it in 100mL liquid medium (10g / L peptone, 5g / L yeast extract powder, 10g / L NaCl, 1g / L glucose, pH7.0-7.2), 37°C, 180 rpm Shake culture for 48 hours per minute to obtain fresh bacterial liquid.
[0065] In 100mL basal salt medium (same as the salt basal medium in Example 1), containing 2% NaCl (g / V), add phenol, 200mg / LC 18 Alkanes, 200mg / L naphthalene, inoculated with 5mL of fresh bacterial solution, 35°C, 180 rpm, cultured on a shaking table for 72 hours, and samples were taken to determine the degradation rate of the compound.
[0066] Table 1 Degradation rate of strain ZHY1-6 to different compounds
[0067] substrate
Embodiment 3
[0068] Example 3 Degradation effect of bacterial strain ZHY1-6 in high-salt phenol-containing pharmaceutical wastewater
[0069] Pick a single colony of strain ZHY1-6 and inoculate it in 100mL liquid medium (10g / L peptone, 5g / L yeast extract powder, 10g / L NaCl, 1g / L glucose, pH7.0-7.2), 37°C, 180 rpm Shake culture for 48 hours per minute to obtain fresh bacterial liquid.
[0070] Take 100mL of high-salt phenol-containing pharmaceutical wastewater with a salt content of about 2%, and detect that the phenol content is 181mg / L.
[0071] Insert 5mL of fresh bacterial solution, place it at 35°C, and culture it on a shaker at 160 rpm. Samples were taken to determine the degradation rate of the compound after 2 days, 3 days, and 4 days of culture.
[0072] Table 2 Removal of phenol by strain ZHY1-6 in high-salt phenol-containing wastewater
[0073] substrate
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