Chloro acetamide herbicide degrading bacteria as well as bactericide prepared thereby and application thereof
A chloroacetamide and herbicide technology, which is applied in the field of environmental pollution bioremediation, can solve problems such as simultaneous degradation that cannot be seen, and achieves the effect of protecting health, reducing the phytotoxicity of herbicides to crops, and having a good removal effect.
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Embodiment 1
[0031] Example 1 Isolation and identification of strains
[0032] The enrichment matrix used to enrich the chloroacetamide herbicide-degrading strains was taken from the activated sludge in the pesticide wastewater biochemical treatment pond of the Lvlilai Pesticide Plant in Kunshan City, Jiangsu Province, and 5.0g of the activated sludge was added to 100ml of basic salt medium , Add 50mg·L -1 Butachlor, 30℃, 180r·min -1 Cultivate for 7 days, transfer 5% of the inoculum to the same medium, transfer 3 times in a row, dilute the enrichment solution stepwise, and take 10 -4 ~10 -7 Diluted enrichment solution 0.1mL each coated with 100mg·L -1 On a solid medium plate of butachlor, cultured at 30°C for 4 days, pick out the single colonies that grow and inoculate them with 100 mg·L -1 In the culture medium of various chloroacetamide herbicides (butachlor, acetochlor, alachlor and metolachlor), 30℃, 180r·min -1 Incubate on a shaker for 5 days to verify the degradation effect. The basic sa...
Embodiment 2
[0036] Example 2 Fermentation of repairing bacteria
[0037] The process of using the above-mentioned strain DC-2 to produce the repairing inoculum is: slant seed-shake flask seed liquid-seed tank-product (the packaging formulation is liquid inoculum).
[0038] 1) Inoculate the test tube of DC-2 (CCTCC NO: M 2012190) in the fermentation medium, and shake culture to the logarithmic phase;
[0039] 2) Inoculate the above-mentioned cultured strains at an inoculum of 10% (v / v, based on the volume of the culture medium) into a filling volume of 70% (v / v, based on the volume of the fermenter, the same below) 500 liters of seed tanks, cultivated to the logarithmic growth phase;
[0040] 3) The seed liquid is cultured in a production tank with a volume of 70% of the inoculum of 10% (v / v, based on the volume of the medium, the same below);
[0041] 4) During the cultivation process of the seed tank and the production tank, the aeration rate of sterile air is 1:1.0, the stirring speed is 220 rpm...
Embodiment 3
[0043] Example 3 Experiment on the biodegradation of chloroacetamide herbicides by DC-2 in the culture medium
[0044] Add alachlor, acetochlor and butachlor at a final concentration of 100mg / L to the basic salt medium (same as Example 1), and 1% of the inoculum is connected to DC-2 (CCTCC NO: M 2012190) bacteria Solution, set up inoculation inactivated DC-2 (CCTCC NO: M 2012190) control, culture in a 30 ℃ constant temperature incubator. Regular samples were taken to detect the degradation of alachlor, acetochlor and butachlor by the strains. The results are shown in Table 1. The degradation rate of strain DC-2 (CCTCC NO: M 2012190) to alachlor, acetochlor and butachlor reached 93.4%, 96.7% and 90.5% within 3 days, and to alachlor and acetochlor within 5 days The degradation rates of and butachlor reached 98.2%, 99.6% and 95.7%, respectively.
[0045] Table 1 The effect of strain DC-2 on alachlor, acetochlor and butachlor in the medium
[0046]
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