Paraquat quick detoxifying liquid and method
A paraquat and fast technology, which is applied in the field of paraquat rapid detoxification solution, can solve the problems such as difficult to meet fast detoxification, unsatisfactory fast detoxification, slow response, etc., and achieves the effect of low cost, simple preparation method and detoxification
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Embodiment 1
[0037] Paraquat antidote ( 1 ) preparation
[0038] Using strict aseptic operation, add Fe(III) humus-reducing bacteria (Kukia rosea) to the 100mL vial Kocuria rosea HN01, strain preservation number CGMCC No.5810) bacterial suspension, anthraquinone (9,10-anthraquinone-2,6-disulfonic acid, referred to as AQDS), sucrose, liquid medium, phosphate buffer solution, make the culture medium The total volume is 100 mL, and the initial concentration of each reactant is: 10mmol / L anthraquinone, 10mmol / L sucrose, 0.4mol / L phosphate buffer solution (provides buffer capacity, pH=6.0); then use high-purity nitrogen to inflate for 20min , discharge the oxygen in the culture medium of the vial, cover the rubber cap immediately after inflating, pressurize the aluminum cap to seal, and culture at 30°C in the dark for 5 days; become.
[0039] Paraquat solution and antidote ( 1 )reaction
[0040] Prepare a paraquat solution with a concentration of 200mg / L (pH6) with paraquat mothe...
Embodiment 2
[0046] Paraquat antidote ( 2 ) preparation
[0047] Using strict aseptic operation, add Fe(III) humus-reducing bacteria (Pseudomonas flexiformis) in the 100mL vial Pseudomonas geniculata PQ01 strain preservation number CCTCC NO: M 2014107) bacterial suspension, anthraquinone (AQDS), sucrose, liquid medium, phosphate buffer solution, so that the total volume of the culture medium is 100mL, and the initial concentration of each reactant is: 10mmol / L Anthraquinone, 10mmol / L sucrose, 0.4mol / L phosphate buffer solution (provide buffer capacity, pH=6.0); then inflate with high-purity nitrogen for 20min to discharge oxygen in the culture medium of the vial, cover the rubber cap immediately after inflating and add Press the aluminum cover to seal, and culture at 30°C in the dark for 5 days; finally, the vial is autoclaved (115°C, 20min), and the detoxification solution is prepared.
[0048] Paraquat solution and antidote ( 2 )reaction
[0049] Prepare a paraquat solution ...
Embodiment 3
[0055] Paraquat antidote ( 3 ) preparation
[0056] Using strict aseptic operation, add Fe(III) humus-reducing bacteria ( Kocuria rosea HN01) bacterial suspension, anthraquinone (9,10-anthraquinone-2-carboxylic acid, referred to as AQC), sucrose, liquid medium, phosphate buffer solution, so that the total volume of the culture medium is 100 mL, and the initial The concentration is: 10mmol / L anthraquinone, 10mmol / L sucrose, 0.4mol / L phosphate buffer solution (provide buffer capacity, pH=6.0); then use high-purity nitrogen to inflate for 20min, discharge the oxygen in the culture medium of the vial, and inflate completely Immediately cover the rubber cap and pressurize the aluminum cap to seal it, and incubate at 30°C in the dark for 5 days; finally, autoclave the vial (115°C, 20min) to prepare the detoxification solution.
[0057] Paraquat solution and antidote ( 3 )reaction
[0058] Prepare a paraquat solution with a concentration of 200mg / L (pH6) with paraquat m...
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