Pseudomonas and application of the same in biological removal of nitrogenous heterocyclic compounds
A technology of nitrogen heterocyclic compounds and pseudomonas, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of microbial growth and biological removal, and achieve the effect of broad application prospects
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Embodiment 1
[0023] Example 1, Isolation, Purification and Identification of Pseudomonas sp. BC001
[0024] 1. Isolation and purification of Pseudomonas sp. BC001
[0025] Pseudomonas sp. BC001 is a Gram-negative bacterium obtained by sampling from the activated sludge in the secondary sedimentation tank of the sewage treatment system of Shougang Coking Plant, after domestication, isolation and purification. Specific steps are as follows:
[0026] Activated sludge samples were taken from the wastewater treatment system of Shougang Coking Plant, and intermittently aerated in a container (about 2 L) sealed with multiple layers of gauze. Regularly add 10mL pyridine (50-300mg / L), 10mL quinoline (50-300mg / L) and about 50mL coking wastewater raw water, and add 2mL phosphate buffer (each L contains 8.5gKH 2 PO 4 , 21.75g K 2 HPO 4 , 33.4 g Na 2 HPO 4 ·7H 2 O, 1.7 g NH 4 Cl, pH 7.2) and 2mL trace element solution (1.5g FeCl per L 3 ·6H 2 O, 0.024g NiCl 2 ·6H 2 O, 0.19g CoCl 2 ·6H ...
Embodiment 2
[0038] Example 2, Pseudomonas sp. (Pseudomonas sp.) BC001 CGMCC No. 2223 adsorption and degradation detection of nitrogen-containing heterocyclic compounds
[0039] 1. Detection of Pseudomonas sp. BC001 for bioremoval of pyridine and quinoline
[0040] Under the conditions of pyridine single substrate, quinoline single substrate, pyridine-quinoline double substrate, pyridine-glucose double substrate, quinoline-glucose double substrate, implement Pseudomonas sp. BC001 CGMCC №.2223 on pyridine, Biological removal of quinolines. It was found that the bioremoval of pyridine by Pseudomonas sp. BC001 CGMCC №.2223 was mainly biosorption, while the bioremoval of quinoline included biosorption and biodegradation, adding an appropriate amount of carbon source could promote the degradation of quinoline. The specific implementation steps are as follows:
[0041] 1) Preparation of Pseudomonas sp. BC001 CGMCC №.2223 bacterial suspension
[0042] Inoculate Pseudomonas sp. BC001 CGMCC №.22...
Embodiment 3
[0067] Embodiment 3, the plasmid detection of pseudomonas (Pseudomonas sp.) BC001
[0068] The plasmid of Pseudomonas sp. BC001 was extracted by improved alkaline lysis method, and it was found that Pseudomonas sp. BC001 did not carry the plasmid.
[0069] Reagents used:
[0070] P1: Dissolve 6.06g Tris base and 3.72g Na 2 EDTA·2H 2 O in 800mL distilled water, adjust the pH to 8.0, dilute to 1 liter, and then add 100mg RNase A.
[0071] P2: Add 8.0g NaOH and 50mL SDS solution with a concentration of 20% (g / mL) in 950mL distilled water, mix well, and dilute to 1 liter.
[0072] P3: Add 294.5 g of potassium acetate to 500 mL of distilled water, adjust the pH to 5.5 with glacial acetic acid (about 110 mL), and dilute to 1 liter.
[0073] TE: Add 1.576g Tris·Cl per liter of distilled water to adjust the pH to 8.0; add 0.3722g EDTA·Na 2 .
[0074] The specific implementation is as follows:
[0075] 1. Use LB medium to cultivate Pseudomonas sp. BC001 to logarithmic growth pha...
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