A kind of pyrethroid pesticide degrading strain and its application
A technology of pyrethroids and pesticides, which is applied to non-decarboxylated Lucka strain Y4 and the bacteria agent and application field produced by it, can solve the problems of unsatisfactory effect and strain degradation, etc.
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Embodiment 1
[0035] Example 1 Isolation, screening and identification of pesticide degradation strain Y4
[0036] 1. Enrichment culture and isolation and screening of d-phenothrin-degrading bacteria:
[0037] From the farmland soil collected in the suburbs of Harbin, Heilongjiang, 5 g of soil samples were weighed and added to 50 mL of the above-mentioned MSM liquid medium containing d-phenothrin (50 mg / L). After culturing at 30°C and 200rpm for 7 days, the mass concentration of pesticides was sequentially increased from 50mg / L to 100mg / L, 200mg / L, 400mg / L, and 800mg / L at an inoculum size of 10% each time for continuous enrichment culture. Then, the culture medium transferred for 4 times was serially diluted and spread on the LB solid plate containing 50 mg / L d-phenothrin, and cultured upside down at 30°C for 2 days. After a single colony grows on the plate, pick a single colony and streak it several times for purification, and obtain a strain of bacteria, numbered Y4.
[0038] 2. Morphol...
Embodiment 2
[0043] Example 2 Decarboxylation Luckae Y4 Degradation Ability Determination of D-Phenothrin
[0044] 1. Experimental method
[0045] (1) Seed liquid preparation:
[0046] The purified strain Y4 was inserted into 5 mL of LB liquid medium for overnight activation to the logarithmic phase. After centrifugation at 4° C., the bacteria were washed with physiological saline (0.9% NaCl), and the resulting bacteria were used as inoculum.
[0047] (2) Degradation performance determination:
[0048] Press 1.0×10 7 The inoculum amount of CFU / mL wet thalline was inoculated into 50 mL of MM medium containing d-phenothrin (50 mg / L) respectively, and no inoculation was used as a control respectively, and each group was repeated three times. Incubate at 30°C, 200rpm constant temperature shaker for 7 days, take samples once on the 1st, 3rd, 5th, and 7th day respectively, and measure the OD with a spectrophotometer 600 The value represents the growth of strain Y4, and its degradation of d-phe...
Embodiment 3
[0074] Example 3 Decarboxylusella Y4 Degradation Effect of D-Phenothrin in Soil
[0075] 1. Soil sample for test
[0076] The topsoil (3-10 cm) of the farmland was taken from the experimental field of the teaching farm of South China Agricultural University.
[0077] After the soil samples were taken back, they were first placed in a cool and ventilated place to dry naturally, then ground after air drying, passed through a 2mm sieve, and a certain amount of d-phenothrin was dissolved in acetone, and then soaked in diatomaceous earth to make d-phenyl ether Permethrin is completely adsorbed. The soaked diatomaceous earth was placed in a fume hood to dry, and it was mixed into the soil so that the final concentration of d-phenothrin in the soil was 50 mg / kg. Take 500g of soil samples and culture them in a constant temperature and humidity incubator at 30°C, press 1.0×10 7 The inoculation amount of CFU / mL was inserted into the Y4 degrading bacteria suspension, and distilled wat...
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