Fluoroglycofen-ethyl degradation pseudomonas YS-03 and application thereof
A technology of acifluorfen and YS-03, which is applied to acifluorfen-degrading Pseudomonas YS-03 and its application field, can solve problems such as residues, achieve low production and use costs, good removal effect, Ease of use
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Embodiment 1
[0025] Example 1 Screening and isolation of acifluorfen-degrading Pseudomonas YS-03
[0026] Get 5.0ml of activated sludge obtained from the wastewater treatment tank of a certain pesticide factory production workshop that produces acetoxyfen and add it into 100ml of inorganic salt liquid culture that the concentration of acetoxyfen is 100mg / L, and its formula is: Liter contains 1.50 g K 2 HPO 4 , 0.50 g KH 2 PO 4 , 0.20 g MgSO 4 ×7H 2 O, 1.00 g NaCl, 1.00 g (NH 4 ) 2 SO 4 , pH 7.0, cultured with shaking at 160r / min, 30°C, transferred to fresh inorganic salt medium at 5% inoculum every 5 days, and transferred 5 times in a row.
[0027] Take 1.0ml of the enriched bacteria solution obtained above, add 9.0ml of sterile water, and make 10 -1 The rich solution, and then draw 1.0ml prepared 10 -1 The enrichment solution was added to 9.0ml sterile water, mixed thoroughly to make 10 -2 The enrichment solution, and so on, carry out gradient dilution on the enrichment solutio...
Embodiment 2
[0029] Example 2 Shake Flask Degradation Experiment of Pseudomonas YS-03
[0030] In the inorganic salt medium containing 100 mg / L acifluorfen, the formula is: 1.50 g K per liter 2 HPO 4 , 0.50g KH 2 PO 4 , 0.20g MgSO 4 ×7H 2 O, 1.00g NaCl, 1.00g (NH 4 ) 2 SO 4 , pH 7.0, inoculate YS-03 according to 5% inoculum size, culture with shaking at 30°C, and take samples for measurement after 72 hours. Compared with the blank, the absorption peak of the treated sample decreased significantly, and acifluorfen was degraded by more than 90%.
Embodiment 3
[0031] Embodiment 3 Contains the preparation of Pseudomonas YS-03 bacterial agent
[0032] The original species of Pseudomonas acifluorfen-degrading Pseudomonas YS-03 screened and isolated in Example 1 were activated on a petri dish, and the degradation performance was measured, and inoculated on the inclined surface of the test tube for later use. The test tube was inoculated in a 1000ml shake flask containing 200ml LB medium. The formula of LB medium was: yeast extract 5.00g / L, peptone 10.00g / L, NaCl 10.00g / L, pH 7.0, constant temperature shaking culture to logarithmic phase , ready to inoculate the seed pot. The seed tank is 500 liters, the feeding volume is 400 liters, the medium formula is: glucose 0.8%, (NH 4 ) 2 SO 4 1%, K 2 HPO 4 0.2%, MgSO 4 0.05%, NaCl 0.01%, CaCO 3 0.3%, yeast extract 0.02%, pH 7.2-7.5. After the feeding is completed, 121°C high-pressure damp heat sterilization, after cooling to 33°C, inoculate the above-mentioned cultivated shake flask ...
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