Pseudomonas denitrificans and microbial inoculum thereof, and application thereof in degradation of quinclorac
A technology of Pseudomonas denitrification and quinclorac, which is applied in the direction of bacteria, chemical instruments and methods, and methods based on microorganisms, can solve the problems of long residual period, pollution, soil damage, etc., and achieve fast growth, Simple operation, powerful effect
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Embodiment 1
[0051] This example is used to illustrate the tolerance and degradability of Pseudomonas denitrificans provided by the present invention to Quinclorac in the aqueous phase (LB liquid medium)
[0052] The strain W-7 was inserted into the sterilized LB liquid culture with the concentration of 30mg / L, 50mg / L, 100mg / L, 200mg / L and 300mg / L quinclorac at 1% by volume inoculum. 基中. Cultivated at 170rpm and 30±1℃ for 24h, the results showed that the strain W-7 showed good tolerance to Quinclorac, and the strain could grow in different media. The maximum OD value that the bacteria can reach and the degradation rate of Quinclorac are shown in Table 1.
Embodiment 2
[0060] This example is used to illustrate the tolerance and degradability of Pseudomonas denitrificans provided by the present invention to Quinclorac in the aqueous phase (inorganic salt medium)
[0061] The strain W-7 was cultured with an inoculum volume of 1% by volume and sterilized with an inorganic salt of quinclorac with a concentration of 30mg / L, 50mg / L, 100mg / L, 200mg / L and 300mg / L. 基中. Incubate at 170rpm and 30±1℃ for 24h. The results showed that the strain W-7 showed good tolerance to Quinclorac, and the strain could grow in different media. With Quinclorac as the sole carbon source, the maximum OD value that the bacteria can reach and the degradation rate of Quinclorac are shown in Table 1.
Embodiment 3
[0072] This example is used to illustrate the degradability of Quinclorac in the soil of Pseudomonas denitrificans provided by the present invention
[0073] Strain W-7 was inoculated into 100 mL of LB liquid medium at 1 vol% strain, 175rmp, 30±1°C for 24h, then the bacterial liquid was added to 5kg containing 20mg / kg quinclorac In the soil, stir evenly and cultivate for 7 days to ensure that the water content in the soil is about 20%. The content of quinclorac in the soil was measured on the 3rd, 5th and 7th days. The results are shown in Table 2.
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