Method for preparing bactericidal agent using antagonizing bacteria M18 strain
A technology of fungicides and bacterial strains, applied in the field of microbial source pesticides, can solve the problems affecting the stability of plant disease control effects, and the content of active ingredients is easily affected by environmental conditions, so as to achieve broad-spectrum environmental compatibility and improve antibacterial effects , The effect of increasing the fermentation titer
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Embodiment 1
[0024]The derivative strain M18G of the growth-promoting antagonistic bacteria M18 was inoculated on a plate of glycerol medium, and activated and grown at 26°C for 24 hours, and then the activated M18G strain was transferred to a triangular flask containing glycerol culture medium, and incubated at 26°C. Shaking culture was carried out in a shaker for 14 hours, and the rotation speed of the shaker was 210 rpm. Then continue to transfer, and carry out 3-stage amplified fermentation culture in glycerol culture medium. Finally, it was transferred to the glucose culture solution for amplified fermentation culture, the temperature and rotational speed were unchanged, and the fermentation time was 74 hours to obtain the M18G strain fermentation solution. Wherein, the weight percent of the components contained in the glycerol culture medium and the glycerol culture solution is: peptone 1.8%, glycerin 1.3%, magnesium sulfate 0.07%, potassium dihydrogen phosphate 0.03%, pH7.0; the glu...
Embodiment 2
[0029] Inoculate the M18G strain, a derivative strain of the growth-promoting antagonistic bacteria M18, on a plate of glycerol medium, activate and grow at 28°C for 22 hours, and then transfer the activated M18G strain to a triangular flask containing glycerol culture medium for amplification. Cultivate with shaking in a shaker at ℃ for 12 hours, and the speed of the shaker is 220 rpm. Then continue to transfer, carry out 3 stages of amplified fermentation culture in glycerin nutrient solution, finally transfer to glucose nutrient solution and carry out amplified fermentation culture, fermentation temperature and rotating speed are constant, and fermentation time is extended to 72 hours, obtains M18G bacterial strain fermentation liquid. Wherein, the weight percent of the components contained in the glycerin medium and the glycerol culture solution is: peptone 2.0%, glycerin 1.7%, magnesium sulfate 0.1%, potassium dihydrogen phosphate 0.05%, pH7.2; the glucose culture solution...
Embodiment 3
[0035] Inoculate the M18G strain, a derivative strain of the growth-promoting antagonistic bacteria M18, on a plate of glycerol medium, activate and grow at 30°C for 20 hours, and then transfer the activated M18G strain to a triangular flask containing glycerol culture medium to amplify it at 28°C. Cultivate with shaking in a shaking table at ℃ for 12 hours, and the rotating speed of the shaking table is 220 rpm; then continue to transfer, and carry out 3-stage amplified fermentation culture in glycerol culture solution. Finally, it was transferred to the glucose culture solution for amplified fermentation culture, the temperature and rotation speed were constant, and the fermentation time was 70 hours to obtain the M18G strain fermentation solution. Wherein, the weight percent of the components contained in the glycerin medium and the glycerol culture solution is: peptone 2.2%, glycerol 1.7%, magnesium sulfate 0.05%, potassium dihydrogen phosphate 0.01%, pH6.8; the glucose cul...
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