Pseudomonas aeruginosa with methylamine degrading capability and application thereof
A technology of Pseudomonas aeruginosa and methylamine, which is applied in the field of microorganisms and can solve problems such as no degradation of methylamine by Pseudomonas aeruginosa.
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Embodiment 1
[0030] A strain of Pseudomonas aeruginosa with the ability to degrade methylamine. The name of the strain is Pseudomonas aeruginosa (Pseudomonas aeruginosa) GDUTAN1. It is preserved in the China Center for Type Culture Collection, and the preservation address is Bayi, Wuchang District, Wuhan City, Hubei Province Wuhan University Campus, No. 299 Road; the preservation number is CCTCC NO: M 2017283, and the preservation date is May 24, 2017.
[0031] The Pseudomonas aeruginosa GDUTAN1 in this example was isolated and screened from a landfill leachate in Guangzhou City, Guangdong Province. Its separation and purification method is as follows: the acclimatization medium used is inorganic salt medium g / L (every 1000 mL inorganic salt medium contains: K 2 HPO 4 ·3H 2 O 1.2g, KH 2 PO 4 1.2g, NH 4 Cl 0.4g, MgSO 4 ·7H 2 O 0.2g, FeSO 4 ·7H 2 O 0.01g, 1mL trace element solution (g / L): CaCl 2 2H 2 O 0.2g, MnSO 4 4H 2 O 0.2g, CuSO 4 2H 2 O 0.01g, ZnSO 4 ·7H 2 O 0.2g, CoCl ...
Embodiment 2
[0051] This example is the application of Pseudomonas aeruginosa GDUTAN1 in environmental restoration, which can degrade methylamine in the environment. The environment includes the atmosphere, water body or soil.
[0052] The method that the methylamine degrading ability of the Pseudomonas aeruginosa (Pseudomonas aeruginosa) GDUTAN1 that the present invention screens obtains is tested and verified below is as follows:
[0053] Inoculate the Pseudomonas aeruginosa GDUTAN1 strain preserved on the slant into the LB enriched culture medium, activate the bacteria in a shaker at 35°C and 150 rpm for 24 hours, centrifuge the bacteria liquid, and collect the bacteria. And use 5mL inorganic salt solution (every 100mL inorganic salt solution contains: K 2 HPO 4 ·3H 2 O 0.12g, KH 2 PO 4 0.12g, NH 4 Cl 0.04g, MgSO 4 ·7H 2 O 0.02g, FeSO 4 ·7H 2 O0.001g, CaCl 2 2H 2 O 0.02g, MnSO 4 4H 2 O 0.02g, CuSO 4 2H 2 O 0.001g, ZnSO 4 ·7H 2 O 0.02g, CoCl 2 ·6H 2 O 0.009g, Na 2 M...
Embodiment 3
[0055] Inoculate the Pseudomonas aeruginosa GDUTAN1 strain preserved on the slant into the LB enriched culture medium, activate the bacteria in a shaker at 35°C and 150 rpm for 24 hours, centrifuge the bacteria liquid, and collect the bacteria. And resuspend with 5mL inorganic salt solution, inoculate 2.0mL bacterial liquid in the 100mL inorganic salt solution (same as embodiment 2) containing 50mg / L methylamine, wherein the pH value of inorganic salt is 8, shake table reaction at 35 ℃ 100rpm After 96 hours, samples were taken regularly to determine the degradation rate by spectrophotometry. The determination of the degradation rate is the same as in Example 1, and the degradation rate is 41.5%.
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