A kind of Pseudomonas aeruginosa bacterial strain and application thereof
A technology of Pseudomonas aeruginosa and strains, applied in the field of microorganisms, can solve the problems of mancozeb residues and other problems, and achieve the effects of fast growth, low mutation and high vitality
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Embodiment 1
[0026] Example 1 Bacterial cell culture: Use an inoculating needle to pick out the hyphae of Pseudomonas aeruginosa and inoculate them into the above-mentioned strain activation medium plate, and cultivate in an incubator at 37°C for 4 days. The colony is Non-capsular, non-spore, and mobile Gram-negative bacteria, with different shapes, arranged in pairs or short chains, are obligate aerobes. Scrape the bacterial cells with a scalpel, and inoculate them into a 500ml conical flask containing a culture solution that has been autoclaved at 121°C and 0.1MPa for 20 minutes. Then place it at 37° C., rotate at 240 rpm / min, shake culture on a shaker for 4 days, and obtain a mixture of hyphae and bacterial liquid.
Embodiment 2
[0027] Example 2 Degradation of mancozeb residues in solid medium supplemented with carbon sources: When the bacteria activation medium is sterilized and cooled to 40°C, the mancozeb pesticide that has been sterilized by ultraviolet for 30 minutes is mixed with the concentration of 5mg / L, after mixing well, pour it into a petri dish with a diameter of 60ml, 3ml medium per petri dish, the medium is pink. The hyphae cultured in Example 1 were punched into small pieces along the edge of the colony with a 6 mm diameter puncher. After the culture medium mixed with mancozeb pesticide is condensed, the small pieces of hyphae are connected, and the hyphae are pressed down against the surface of the culture medium. Placed in a 37°C incubator for 10 days, the pink color in the medium has faded, the molecular structure of mancozeb pesticide is degraded, and the medium is cream-colored and translucent.
Embodiment 3
[0028] Example 3: Degradation of high-concentration mancozeb pesticide residues by degrading bacteria
[0029] (1) Add 5 mg / L of mancozeb pesticide to 100 ml of the cultured medium, and culture at 37°C with a rotating speed of 240 rpm / min, shaking on a shaker, and add an equal concentration of generation to the uninoculated medium. Mancozeb pesticide as a control group;
[0030] (2) Sampling once every 12h, take 3ml sample and place it in 50ml of the described Pseudomonasaeruginosa (Pseudomonasaeruginosa) strain to degrade mancozeb pesticide residues: proceed as follows:
[0031] (1) Add mancozeb pesticide at a final concentration of 5-10 mg / L to 100-150 ml of the cultured medium, and culture at 30-37°C with a rotation speed of 240-260rmp / min. Add the same concentration of mancozeb pesticide to the inoculated culture solution as a control group;
[0032] (2) Sampling every 12h, take 2-3ml sample in a 5-10ml plastic centrifuge tube, add 10-12ml of acetonitrile, shake for 20-30min, cen...
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