Serratia strain and method for disposing methidathion pesticide residues on surfaces of soil and fruits/vegetables
A technology for the degradation of Serratia and pesticide residues, applied in the direction of microorganism-based methods, restoration of contaminated soil, biochemical equipment and methods, etc., can solve problems such as pesticide residue pollution, achieve low production costs, and protect the ecology The effect of environment and ease of use
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Embodiment 1
[0024] The surface soil of peach orchards in Nongquanyi District, Chengdu, which had been treated with chlorpyrifos for several years, was collected. Weigh 5g of the collected pesticide-contaminated soil sample, pass it through a 20-mesh sieve, and add it to 100ml sterilized basal salt medium containing 50mg / l methapon. The formula of the basal salt medium is (all g / L): NH 4 NO 3 1.0, MgSO 4 ·7H 2 O 0.5, (NH 4 ) 2 SO 4 0.5, KH 2 PO 4 0.5, NaCl 0.5, K 2 HPO 4 1.5, PH: 7.0-7.2, cultured at 37°C with 180r / min shaking. After 7 days, take 5ml of the bacterial liquid and insert it into the same medium for cultivation at 37°C. During the subculture process, the concentration of methionin was gradually increased to 400 mg / l, and the subculture was carried out 6 times, and once in about 7 days. Make a 10-fold gradient of the enriched pesticide-degrading bacteria solution with sterile water (10 - 7 、10 - 8 、10 - 9 ) dilution, respectively take 0.1mL bacterial suspensio...
Embodiment 2
[0026] The slant of Serratia spp. in Example 1 with negative Gram staining was inoculated in 100ml LB medium, and the formula of LB medium (g / l) was as follows: peptone 10, yeast extract 5, NaCl 10, pH 7.0-7.2 , constant temperature shaking culture to the logarithmic phase, to obtain bacterial liquid. Transfer the above-mentioned cultivated bacterial solution into a seed tank that has been autoclaved at 121°C and cooled to about 35°C according to the inoculation amount of 15% by volume. The formula of the seed tank medium is: glucose 5g / L, NH 4 NO 3 10g / L , K 2 HPO 4 2 g / L, MgSO 4 ·7H 2 O 0.5 g / L, Na2 HPO 4 2 g / L, CaCO 3 3g / L, NaCl 1.0 g / L, yeast extract 0.5 g / L, pH: 7.0-7.2; continue to cultivate until the logarithmic growth phase, the ventilation rate of sterile air during the cultivation is 1:1.5, and the stirring speed is 200 revolutions per minute, and the incubation temperature was 35°C. The seed solution that has reached the logarithmic growth phase is inser...
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