A strain of Aspergillus oryzae and its application
A technology of Aspergillus oryzae and atrazine, applied in the biological field, can solve the problems of metabolic process disorder, difficulty, genetic damage of mouse germ cells, etc., and achieve high application value and strong removal ability
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Embodiment 1
[0042] The medium (separation medium) used in the present invention:
[0043] Beef extract glucose medium: beef extract 5g, glucose 10g, sodium chloride 10g, atrazine 200mg, distilled water 1000mL, agar powder 20g.
[0044] The fermentation medium used in the present invention: 5g of beef extract, 10g of glucose, 10g of sodium chloride, 1000mL of distilled water, pH 7±0.2.
[0045] The original bacterial strain ECUST-TXZC2018 of the present invention is obtained by separating and screening from atrazine-contaminated soil; the method for isolating and cultivating the bacterial strain comprises the following steps:
[0046] Isolation of strain Aspergillus oryzae: 10g of soil from atrazine-contaminated area was put into 90mL liquid beef extract glucose medium containing 200mg / L atrazine and 500mg / L atrazine for enrichment culture , after 48h, the enriched culture solution was taken for 10 -4 、10 -5 、10 -6 For gradient dilution, 0.1 mL each was spread on the atrazine-containin...
Embodiment 2
[0056] The cultivation method of Aspergillus oryzae: the strain Aspergillus oryzae is inoculated into the fermentation medium, and cultured with shaking at 30±2°C and 220 rpm for 4-5 days. The composition of the fermentation medium is 5g of beef extract, 10g of glucose, 10g of NaCl and 1000mL of distilled water, pH 7±0.2.
Embodiment 3
[0058] Research on the characteristics of strains adsorbing atrazine: the experiment of the influence of pH, adsorption time and temperature on the adsorption effect.
[0059] The strain was expanded and cultivated in beef extract glucose medium at 28°C and 220rpm for 6h, the obtained activated strain was centrifuged at 8000rpm for 10min, the obtained pure strain was washed 2-3 times with sterile water / dilute nitric acid, and prepared as Concentrated bacteria solution for use. Using 1mol / L NaOH and HCl to adjust the pH of the solution containing 200mg / L atrazine to be 1, 3, 5, 7, 9 respectively; the temperature is 15, 20, 25, 30, 35°C; v / v) The prepared concentrated bacterial liquid is placed in the atrazine-containing bacterial liquid prepared above, and the supernatant is taken regularly to measure the atrazine content.
[0060] (1) Adsorption time: the result is as follows Figure 4 as shown, Figure 4 is the schematic diagram of the effect of time on the adsorption rate...
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