Method for screening degradation bacteria strains by taking high-efficiency cyhalothrin as substrate
A technology of lambda-cyhalothrin and screening methods, which is applied in biochemical equipment and methods, measurement/testing of microorganisms, separation of microorganisms, etc., to achieve good application prospects, simple and feasible screening methods, and high feasibility
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Embodiment 1
[0025] Serratia marcescens can degrade lambda-cyhalothrin.
[0026] Screening of lambda-cyhalothrin-degrading bacteria:
[0027] 1) Bacteria sample collection: collected from the soil in the pesticide factory of Shahe Town, Sujiatun District, Shenyang City, Liaoning Province.
[0028] 2) Enrichment and acclimatization: 10 g of bacterial samples were inoculated into 100 ml enrichment medium containing lambda-cyhalothrin for transfer culture, and the culture conditions for each transfer were 30°C, 180r / min shaker culture for 7 days, A total of 4 transfers were made, and the transfer amount was calculated by volume percentage. 10% of each culture solution was inoculated in 100ml enrichment medium containing lambda-cyhalothrin, which was gradually increased. The / L gradually increased, and the lambda-cyhalothrin was 25, 50, 75, and 100 mg / L during the 4 transfers, and the bacteria samples were added to the enrichment medium for the first time and 15 glass beads were added at the ...
Embodiment 2
[0035] Identification of Degradative Ability of Strains
[0036] 1. UV spectrophotometry
[0037] 1) Standard curve drawing: Dissolve the efficient-cyhalothrin standard substance in n-hexane, prepare standard solutions with different concentrations (see Table 1), measure the absorbance at 278nm, and draw the standard curve as y=0.0041x+0.0012 R 2 =0.9999 (see figure 1 ).
[0038] Table 1 standard curve measured value
[0039] Concentration mg / l
Absorbance at 278nm
0.002202
0
0.110008
0.0066
0.05504
0.0023
0.2752
0.00325
1.376
0.0072
6.88
0.0265
34.4
0.1369
172
0.70115
[0040] 2) Identification of degradation activity: The 16 strains of degrading bacteria that were screened out using lambda-cyhalothrin as a substrate were shaken and cultivated in ordinary medium until OD600=1.0, and then 10% of the bacterial liquid was taken by volume p...
Embodiment 3
[0053] The difference from Example 1 is:
[0054] 1) Enrichment and acclimatization: Inoculate 5 g of bacterial samples into 80 ml enrichment medium containing lambda-cyhalothrin for transfer culture, and the conditions for each transfer culture are 25°C, 130r / min shaker culture for 5 days, A total of 7 transfers were made, and the transfer amount was calculated by volume percentage. 5% of each culture solution was inoculated in 80ml enrichment medium containing lambda-cyhalothrin, which was gradually increased, and was set aside; / L gradually increased, and lambda-cyhalothrin was 25, 55, 85, 115, 145, 175, and 205 mg / L during the 7 transfers, and the bacteria samples were added to the enrichment medium for the first time and 10 glass beads were added at the same time ; The enrichment medium is: peptone 8g, NaCl 0.8g, KH 2 PO 4 0.8g, glucose 1.0g, H 2 O 1000ml, pH=6.8.
[0055] 2) Screening: Inoculate the enriched culture solution in step 1) into 60 ml of basal medium con...
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