Klebsiella capable of automatically generating biosurfactant and degrading benzene series and application of Klebsiella
A Klebsiella, biological surface technology, applied in the field of environmental restoration and microorganisms, to achieve good emulsification effect
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Embodiment 1
[0032] The isolation and screening of embodiment 1 Klebsiella HN02
[0033] Inorganic salt culture solution used: every 1000mL inorganic salt culture solution contains 1.2g K 2 HPO 4 ·3H 2 O, 1.2g KH 2 PO 4 , 0.2g MgSO 4 ·7H 2 O, 0.4g NH 4 Cl, 0.01g FeSO 4 ·7H 2 O and 1mL trace element aqueous solution. Among them, every 1000mL trace element aqueous solution contains 0.2g CaCl 2 , 0.2g MnSO4 4H 2 O, 0.1g CuSO 4 ·5H 2 O, 0.2g ZnSO 4 ·7H 2 O, 0.09g CoCl 2 ·6H 2 O, 0.12g Na 2 MoO 4 2H 2 O and 0.006g H 3 BO 3 .
[0034] The Klebsiella HN02 in this example was isolated and screened from the activated sludge in the aerobic pool of a papermaking wastewater treatment plant in Hainan Province. Take the sludge discharged from the aerobic tank of the papermaking sewage treatment plant, put it in a 500mL bottle, add 2 times the volume of papermaking black liquor to the sludge, adjust the pH to 8.3, seal the bottle, and culture it on a shaking table at a temperature ...
Embodiment 2
[0055] This example is the application of Klebsiella HN02 in environmental restoration, which can degrade p-xylene in the environment. The environment includes the atmosphere, water body or soil.
[0056] The p-xylene degradation ability of Klebsiella (Klebsiella) HN02 obtained by screening of the present invention is tested:
[0057] According to the needs of the degradation experiment, configure the inorganic salt medium: add 100 mL of inorganic salt solution to a 500 mL headspace bottle (every 1000 mL of inorganic salt culture solution contains: 1.2 g K 2 HPO 4 ·3H 2 O, 1.2g KH 2 PO 4 , 0.2g MgSO 4 ·7H 2 O, 0.4g NH 4 Cl, 0.01g FeSO 4 ·7H 2 O and 1mL trace element aqueous solution. Among them, every 1000mL trace element aqueous solution contains: 0.2g CaCl 2 , 0.2g MnSO 4 4H 2 O, 0.1g CuSO 4 ·5H 2 O, 0.2g ZnSO 4 ·7H 2 O, 0.09g CoCl 2 ·6H 2 O, 0.12g Na 2 MoO 4 2H 2 O and 0.006g H 3 BO 3 ). Autoclave at 121°C for 15 minutes. First, the screened Klebsi...
Embodiment 3
[0063] This example is a method for demonstrating the ability of Klebsiella HN02 to produce biosurfactants.
[0064] The biosurfactant ability produced by Klebsiella (Klebsiella) HN02 screened by the present invention is tested:
[0065] Klebsiella was cultured under the condition that the substrate concentration was 21 mg / L, and the culture conditions were referred to in Example 2. After p-xylene was completely degraded, the supernatant of the bacteria liquid was taken to measure the emulsifying ability. The specific method is to add 3mL peanut oil to the test tube, then add the same amount of cell-free supernatant obtained after centrifuging the bacterial liquid into the same test tube, shake the test tube vigorously for 2 minutes, then let it stand for 24 hours, and observe the height of the emulsified layer after 24 hours . Emulsification index = (height of emulsified layer / total height of liquid in test tube) × 100%.
[0066] After measuring, the emulsification index o...
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