Styrene degrading bacterium and application thereof
A technology of styrene and degrading bacteria, applied in the field of bioengineering, can solve the problems of harmfulness to human health, air and water pollution, etc., and achieve the effect of improving the efficiency of biochemical treatment
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Embodiment 1
[0035] The preparation of embodiment 1 styrene degrading bacterial agent
[0036] (1) Strain activation: take out the strains of Pseudomonas mutans stored at 4°C and place them at room temperature for 3 hours of activation. Since the strains are stored on nutrient agar medium on a test tube slant, there is no need to add nutrients during the activation process;
[0037] (2) Preparation of liquid seeds: In the aseptic operating table, use a pipette gun to take 10ml of sterile water and add it to the strain preservation tube, and use the pipette to repeatedly blow to prepare the bacterial suspension, and then inoculate the bacterial suspension into 200ml of liquid culture medium, shaking culture for 20 hours, the culture conditions are: temperature 35°C, shaking speed 170r / min;
[0038] (3) High-density fermentation: Pseudomonas mutans liquid seeds are inoculated in the corresponding fermentation medium with an inoculum size of 1.5% by volume to carry out liquid submerged fermen...
Embodiment 2
[0043] The tolerance test of embodiment 2 styrene degrading bacteria agent
[0044] Establish inorganic salt medium systems with styrene concentrations of 5,000, 10,000, 20,000, 30,000, 40,000, 50,000, 60,000, 70,000, 80,000, 90,000, 100,000, 110,000, 120,000, 130,000, 140,000, and 150,000 mg / L respectively, and set up without adding benzene Blank system of ethylene, inoculum amount of 1%, 30°C, 110r / min constant temperature shaking for 24h, OD after 24h 600 determination.
[0045] The result is as figure 1 As shown, with the increase of styrene concentration, OD 600 It showed a trend of increasing first and then decreasing, and the OD concentration was 100000mg / L 600 Reaching the maximum shows that the strain propagation speed is faster under this concentration, and the growth of the strain shows certain inhibition when the concentration exceeds 100000mg / L.
Embodiment 3
[0046] Embodiment 3 Styrene degradation effect test
[0047] The specific verification method is as follows: put the preserved Pseudomonas mutans into the sterile LB liquid medium in the ultra-clean workbench, 35°C, 180rpm shaking culture for 16-20h, the cultured bacterial liquid is 5% by volume The amount of inoculum was inserted into the LB liquid culture medium containing styrene 60000mg / L, 30 DEG C, 110r / min constant temperature vibration 24h, every 12h sampling detects the mass concentration of remaining styrene in the shaking flask, calculates the deformity of the present invention Degradation rate of styrene by Monas.
[0048] The results are shown in Table 1. The degradation rate of Pseudomonas mutans of the present invention to a solution containing 60000 mg / L styrene in 24 hours was 99.97%.
[0049] Table 1 Verification of bacterial strains on the degradation effect of styrene
[0050]
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