Pseudomonas aeruginosa and inoculant containing Pseudomonas aeruginosa, application thereof, and TNT degradation method
A technology of Pseudomonas aeruginosa and bacterial agents, applied in the field of bioremediation of organic matter pollution, to achieve high TNT degradation ability, high degradation rate, and good tolerance
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[0040] The present invention will be described in detail below through examples and comparative examples, but the present invention is not limited thereby.
[0041] The experimental methods in the following examples and comparative examples are conventional methods in the art unless otherwise specified. The experimental materials used in the following examples and comparative examples were purchased from conventional biochemical reagent stores unless otherwise specified.
Embodiment 1
[0045] This example is used to illustrate the liquid-phase TNT (with TNT as the single nitrogen source) degradation ability of Pseudomonas aeruginosa with the deposit number CGMCC NO: 10842 of the present invention.
[0046] Centrifuge the bacterial solution obtained in the preparation example to obtain the bacterial cells, then wash the bacterial cells with physiological saline and resuspend to obtain OD 600 3.0 normal saline bacterium liquid, the 1mL preservation number of the present invention obtained above is the physiological saline bacterium liquid (OD) of Pseudomonas aeruginosa NO:10842 600 =3.0) were inoculated into 100 mL of liquid medium M, and cultured at 37° C. in a shaker at 170 rpm, wherein the composition of liquid medium M was 5 g / L glucose+100 ppm TNT. Use high-performance liquid chromatography (the model of high-performance liquid chromatography is LC-20A, purchased from Shimadzu Corporation, Japan, the chromatographic column is Agilent ZORBAXSB-Aq (4.6mm × ...
Embodiment 2
[0048] This example is used to illustrate the liquid-phase TNT (containing ammonium salt in the liquid phase) degradation ability of Pseudomonas aeruginosa with the preservation number of CGMCC NO: 10842 of the present invention.
[0049] Centrifuge the bacterial solution obtained in the preparation example to obtain the bacterial cells, then wash the bacterial cells with physiological saline and resuspend to obtain OD 600 3.0 normal saline bacterium liquid, the 1mL preservation number of the present invention obtained above is the physiological saline bacterium liquid (OD) of Pseudomonas aeruginosa NO:10842 600 =3.0) were inoculated into 100mL liquid medium A, B, C, D respectively, and cultivated at 37°C in a 170rpm shaker, wherein the composition of liquid medium A was 5g / L glucose+100ppm TNT+1g / L (NH 4 ) 2 SO 4 . The composition of liquid medium B is 5g / L glucose+100ppm TNT+1g / L NH 4 Cl. The composition of liquid medium C is 5g / L glucose+100ppm TNT+1g / L NH 4 NO 3 . ...
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