Pseudomonas putida capable of metabolizing nicotine and application thereof
A technology of Pseudomonas putida and nicotine, which is applied in the direction of bacteria, microbial-based methods, biological water/sewage treatment, etc., can solve the problems of weak resistance to nicotine toxicity, limited application, and weak metabolism
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Embodiment 1
[0072] Example 1: Screening of Pseudomonas putida (Pseudomonas putida) XPSN CCTCC NO.M205038 strain
[0073] Collect soil samples from long-term tobacco-growing fields in Weifang, Shandong, etc., take 2-4g and add them to the liquid basic medium containing 1g / L nicotine, shake and cultivate on a shaker at 30°C for 2-4 days, and then transfer to Then transfer 5mL to the same culture medium and transfer 3 to 5 times in succession according to this method. Dilute the obtained culture solution and spread it on the basic medium of solid plate containing 1g / L nicotine. Culture at 30℃ for 1 ~3 days, after the colonies grow, pick large colonies and streak them continuously on the same nicotine solid plate basic medium to confirm that the strains have the ability to degrade nicotine and are pure cultures, and then pick single colonies to contain 1g / L nicotine on a solid slant basic medium, cultured at 30°C for 1 to 3 days to obtain the Pseudomonas putida XPSN of the present invention, ...
Embodiment 2
[0079] Example 2: Acquisition of the above-mentioned Pseudomonas putida (Pseudomonas putida) XPSN CCTCC NO.M205038 strain 16SrDNA
[0080] Collect 2 mL of the culture of Pseudomonas putida (Pseudomonas putida) XPSN CCTCC NO.M205038 that has grown to the stationary phase, centrifuge at 6,000 rpm for 5 minutes, and remove the supernatant; add 565 μL of TE solution to the precipitate, and the formula of the TE solution is : Tris (Tris) of 10mmol / L, ethylenediaminetetraacetic acid (EDTA) of 1mmol / L, adjust the pH to 8.0 with hydrochloric acid; blow repeatedly with a pipette to suspend the sediment, and then add 30 μL of mass-volume ratio Concentration of 10% sodium dodecylsulfonate (SDS) and 5 μL 20 mg / mL proteinase K (Merck, USA), mix well, and put in a water bath at 37 ° C for 1 hour; add 100 μL 5mol / L NaCl, fully Mix well, then add 80 μL of CTAB / NaCl solution, the formula of CTAB / NaCl solution is: the mass volume ratio concentration is 10% cetyltriethylammonium bromide (CTAB) i...
Embodiment 3
[0107] Embodiment 3: Utilize the method for the intact cell of Pseudomonas putida (Pseudomonas putida) to process tobacco processing wastewater, wherein the final concentration of nicotine in the tobacco processing wastewater is 0.8g / L
[0108] (1) Microbial strain: select Pseudomonas putida XPSN CCTCC NO.M205038;
[0109] (2) Slant culture: inoculate the above-mentioned strains on a solid slant basic medium containing 0.02% nicotine in a mass volume ratio, and culture at 20°C for 24 hours;
[0110] (3) Seed culture: the bacterial strain cultivated in step (2) was placed in 20 mL of nicotine liquid basic medium containing 0.02% mass volume ratio with an inoculation loop under aseptic conditions, and was shaken at 20° C. Shake culture on the bed for 6 hours to obtain first-grade seeds;
[0111] (4) Expansion cultivation: with the inoculum amount of 5% by volume, connect the primary seeds in 200 mL of nicotine liquid basic medium containing 0.02% by mass volume ratio, and cultu...
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