Rhodopseudomonas spheroides strain and liquid inoculant thereof as well as preparation method and application thereof
A technology of Rhodopseudomonas and liquid inoculum, applied in biochemical equipment and methods, chemical instruments and methods, microorganism-based methods, etc., can solve the problem of high cost, achieve low production cost, reduce pesticide residues, The effect of protecting the ecological environment
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Embodiment 1
[0021] This example investigates the degradation of high-concentration pyrazosulfuron-methyl by the Rhodopseudomonas strain CCTCC M 2010144 of the present invention in a liquid medium.
[0022] First, pyrazosulfuron-methyl original drug is dissolved in acetone, and the dissolved pyrazosulfuron-methyl acetone solution is sterilized by filtering through a 0.22 μm filter membrane, and added to the sterilized seed liquid culture medium of the present invention until pyrazosulfuron-methyl The final concentration is 200mg / L. The seed liquid medium used was formulated from the following components: (NH 4 ) 2 SO 4 1g~2g, MgSO 4 ·7H 2 O 0.2g~0.5g, NaHCO 3 5g~6g, K 2 HPO 40.5g~1g, peptone 2g~2.5g, sodium acetate 2g~3g, NaCl 0.2g~0.5g and yeast extract 1.5g~1.7g, then dilute to 1000mL with distilled water, control the pH value to 7.0~7.2, after 121 It can be obtained after sterilization at ℃ for 30 minutes. In the above-mentioned seed liquid culture medium containing pyrazosul...
Embodiment 2
[0028] This example investigates the degradation of pyrazosulfuron-methyl by the liquid bacterial agent of Rhodopseudomonas strain CCTCC M 2010144 of the present invention in soil.
[0029] Weigh 100 g of sterilized paddy field soil, add pyrazosulfuron-methyl, so that the drug concentration in the soil is 20 mg / kg.
[0030] Adopt the following method to prepare a kind of liquid bacterial agent of rhodopseudomonas bacterial strain of the present invention:
[0031] (1) Activation: The Rhodopseudomonas strain CCTCC M 2010144 (containing 20% glycerol) obtained by screening and stored at -80°C was inoculated on a double-layer sandwich solid medium plate for activation. The solid medium used contained the following Concentration of components: (NH 4 ) 2 SO 4 0.1g / mL, MgSO 4 0.02g / mL, NaHCO 3 0.5g / mL, K 2 HPO 4 0.05g / mL, NaCl 0.02g / mL, yeast extract 0.15g / mL, agar 1.8g / mL; control the pH value of the solid medium to 7.0-7.2, control the activation temperature at 30°C-35...
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