Enterobacter ludwig with quinclorac degrading function and application thereof
A technology of Enterobacter ludwigii and Enterobacter dervii is applied in the field of degrading quinclorac, which can solve the problems of adverse effects on growth and quality of flue-cured tobacco, economic loss of tobacco leaf production, etc., and achieve high tolerance and degradation ability , the effect of strong vitality and fast growth
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Embodiment 1
[0045] This example is used to illustrate the tolerance and degradation of Enterobacter ludwig provided by the present invention to quinclorac in water
[0046] The bacterial strain LZ-1 is inserted into the LB liquid culture medium of 10mg / L, 20mg / L, 50mg / L, 100mg / L, and 200mg / L quinclorac after sterilization with the inoculation amount of 1 volume % middle. Cultured at 170rpm, 30±1°C for 24h, the results showed that the strain LZ-1 showed good tolerance to quinclorac, and the strains 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
[0048] This example is used to illustrate the tolerance and degradation of Enterobacter ludwig provided by the present invention to quinclorac in water
[0049] Inoculate bacterial strain LZ-1 with the inoculum of 1 volume % into the sterilized inorganic salt culture of quinclorac with a concentration of 10mg / L, 20mg / L, 50mg / L, 100mg / L, and 200mg / L respectively Base. Cultivate at 170rpm, 30±1°C for 24h. The results showed that the strain LZ-1 showed good tolerance to quinclorac, and the strains could grow in different media. In the case of using quinclorac as the only carbon source, the maximum OD value that the bacteria can achieve and the degradation rate of quinclorac are shown in Table 1.
Embodiment 3
[0057] This embodiment is used to illustrate the degradability of Enterobacter ludwig provided by the present invention to quinclorac in soil
[0058] Bacterial strain LZ-1 is inoculated in 100mL LB liquid culture medium with 1 volume % strain quantity, after 175rmp, 30 ± 1 ℃ under cultivation 24h, add bacterial solution to the contamination of 5kg containing 20mg / kg quinclorac In the soil, stir evenly, cultivate for 7 days, and ensure that the water content in the soil is about 20%, and finally detect the content of quinclorac in the soil, and the results are shown in Table 2.
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