Phlebia acerina strain and application thereof in degrading metalaxyl pesticide residue
A technology of P. aceriformis and pesticide residues, applied in the field of environmental microorganisms, can solve the problems of phytotoxicity of plants, entry into the human body, and human hazards, and achieve the effects of not easy to mutate, fast growth, and simple cultivation methods
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Embodiment 1
[0028] The culture of embodiment 1 thalline: pick the mycelia of Phlebia acerinaY3667 with an inoculation needle and inoculate it into the above-mentioned bacterial species activation medium plate, and cultivate it in a 28°C incubator for 4 days, and the colony is loose and snowy. White, cottony. Scrape the loose hyphae with a scalpel and inoculate them into a conical flask filled with 500ml of culture medium that was autoclaved at 121°C and 0.1MPa for 20min. Then place it at 30° C., rotate at 140 rpm / min, and culture on a shaking table for 4 days to obtain a mixed bacterial agent of mycelium and bacterial liquid.
Embodiment 2
[0029] Example 2 Degradation of metalaxyl residues in supplemented carbon source solid medium: when the strain activation medium was sterilized and cooled to 40°C, mixed with metalaxyl pesticide sterilized by ultraviolet light for 30 minutes, the concentration was 5mg / L, After mixing well, pour it into a petri dish with a diameter of 60 mm, with 3 mL of culture medium per dish, and the culture medium is pink. The mycelia cultivated in Example 1 were punched into small pieces along the edge of the colony with a puncher with a diameter of 6 mm. After the medium mixed with metalaxyl pesticide is condensed, a small piece of mycelium is inserted, and the mycelium is close to the surface of the medium downward. Placed in a 30°C incubator for 10 days, the pink color in the medium has faded, the molecular structure of metalaxyl pesticide has been degraded, and the medium is creamy translucent.
Embodiment 3
[0030] Example 3: Degradation of high-concentration metalaxyl pesticide residues by degrading bacteria agent
[0031] (1) Add 5mg / L of metalaxyl pesticide to 100ml of the culture medium cultivated in claim 3, and culture it on a shaking table at 30°C with a rotation speed of 140rmp / min, and add an equal concentration to the uninoculated culture medium The metalaxyl pesticide was used as the control group;
[0032](2) Take a sample every 12 hours, take 3ml of the sample and place it in a 50mL plastic centrifuge tube, add 10mL of acetonitrile, shake on the shaker for 30min, centrifuge at 3000rmp / min, take out the supernatant, repeat 3 times, and combine the supernatant , after extracting the metalaxyl pesticide residues in the culture solution, it was purified by a Florisil solid-phase extraction column (specification: 500mg3ml) in a solid-phase extraction device, concentrated by a rotary evaporator (below 40°C), and stored at -20°C After freeze-drying, the extracted pesticide ...
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