Degrading bacterium capable of eliminating plant fungicide residues and application of degrading bacterium
A plant fungicide, degrading bacteria technology, applied in the direction of application, microbe-based methods, bacteria, etc., can solve the problem of decreased control effect, achieve the effect of increasing added value, good removal effect, and solving the problem of excessive pesticide residues
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Embodiment 1
[0019] Example 1 Screening and isolation of ectacazole degrading Providencia rettgeri CS-7
[0020] Get 3.0 ml of activated sludge obtained from the waste water treatment tank of a certain pesticide factory production workshop that produces eclozazole and add it into 100 ml of inorganic salt liquid culture that has a concentration of 100 mg / L of ebacazole. The formula is: 1.50 g K 2 HPO 4 , 0.50 gKH 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, shake culture at 160 r / min, 30°C, transfer to fresh inorganic salt medium every 5 days at 3% inoculum size, and transfer 5 times in a row.
[0021] Take 1.0 ml of the enriched bacterial solution obtained above, add it into 9.0 ml sterile water, and make 10 -1 enriched solution, and then draw 1.0 ml prepared 10 -1 The enrichment solution was added to 9.0 ml sterile water, mixed thoroughly to make 10 -2 The enrichment solution, and so on, carry out gradient dilution on the enrichment solution. Dr...
Embodiment 2
[0023] Embodiment 2 Shake flask degradation experiment of Providencia rettgeri CS-7
[0024] In the inorganic salt medium containing 100 mg / L eubazole, the formula is: 1.50 g K per liter 2 HPO 4 , 0.50gKH 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, inoculate CS-7 at 3% inoculum size, culture at 30°C with shaking, and take samples every 12 h for determination. Depend on figure 2 It can be seen that the absorption peak of the treated sample decreased significantly, and eubazole was degraded by more than 90%.
Embodiment 3
[0025] Embodiment 3 Contains the preparation of Providencia rettgeri CS-7 bacterial agent
[0026] Activate the original species of eubazole-degrading Providencia rettgeri CS-7 on a petri dish, measure its degradation performance, and inoculate it on the inclined surface of a test tube for later use. The test tube seed was inoculated in a 1000 ml shake flask containing 200 ml LB medium. The formula of LB medium was: yeast extract 5.00 g / L, peptone 10.00 g / L, NaCl 10.00 g / L, pH 7.0, constant temperature shaking culture until In several phases, prepare the seed pots for inoculation. The seed tank is 500 L, the feeding volume is 400 L, and 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 7.0. After the feeding is completed, sterilize under high pressure at 121°C, cool to 33°C, inoculate 10% of the cultured shake flask strains into a 500 L seed tank, and cultivate to the logarithmic gr...
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