Bacillus cereus LY05 with efficient Butralin degradation function as well as application and use method of Bacillus cereus LY05
The technology of Bacillus cereus and fenbuterol, which is applied in the field of microorganisms, can solve the problems such as the inability to meet the bioremediation of pesticide residue pollution, and achieve the effects of protecting the ecological environment and human health, good removal effect and convenient use.
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Embodiment 1
[0026] Example 1 of the present invention: Isolation and identification of the butyrin-degrading bacteria LY05
[0027] 1) Isolation and screening of butylin-degrading bacteria LY05
[0028] Weigh 10 g of the long-term polluted soil with butylamine into a 250 mL conical flask, add 100 mL of inorganic salt medium, add butylline to a concentration of 100 mg / L, and place the conical flask on a shaker (30 Cultivate at 200 rpm for 7 days, inoculate 5 mL of the culture solution into fresh basal medium (100 mg / L secbutamyl), then culture in a shaker flask at 30°C for 7 days, and so on. The concentration gradient of mg / L increased, so that the concentration of secbutaline in the final enrichment medium reached 1000 mg / L, and the enrichment and degradation strains were obtained.
[0029] During the enrichment and separation of degrading bacteria, after every 2 transfers, the bacterial suspension was prepared into 10 -2 ~10 -6 Serial dilutions were separated on the solid separation a...
Embodiment 2
[0045] Embodiment 2 of the present invention: the preparation of Zhongbuling pesticide residue degradation bacterial agent:
[0046] Adopt the bacterial strain of bacillus cereus LY05 that efficiently degrades butyrin to produce the method for degrading butyrin preparation, comprising the steps:
[0047] 1) Cultivate the strain of Bacillus cereus LY05 in an inorganic salt medium at 30-35°C and 150-200 rpm to the logarithmic growth phase to obtain strains;
[0048] 2) Inoculate the above-mentioned strains into the seed bottle with an inoculum amount of 10% of the volume ratio of the inorganic salt medium, and vibrate at 30-35°C and 150-200 rpm until the logarithmic growth phase to obtain the seed liquid;
[0049] 3) Inoculate the obtained seed liquid into the fermentation medium according to the inoculation amount of 10% by volume, and ferment and cultivate it at 30-35°C and 150-200 rpm for 45-50h to obtain a fermentation liquid, the number of bacteria in the fermentation liqui...
Embodiment 3
[0051] Embodiment 3 of the present invention: Degradation bacteria LY05 is to the degradative performance of butaline:
[0052] Add secbutaline in the inorganic salt medium (same as Example 1) so that the final concentration is 50.0 mg / L; the inoculation concentration is 2.0×10 8 cfu / mL bacterial agent, and set the culture medium without inoculation as the control, culture in the dark at 30°C (200 rpm) for 0-7 days, and take samples regularly. The above-mentioned HPLC method was used to measure the residual amount of butaline and calculate the degradation rate. Degradation rate = (residual amount of control sample - residual amount of treated sample) / residual amount of control sample × 100%. see results figure 2 shown. The results showed that the degrading bacteria LGY06 could effectively degrade Zhongbuling in a short period of time, and the degradation rates of Zhongbuling reached 69.88% within 3 days, 85.84% within 5 days, and 85.84% within 7 days. The degradation rat...
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