Quinoline degrading bacteria QG6 with heterotrophic nitrification-aerobic denitrification function and phosphorous removal function and application thereof
A technology of aerobic denitrification and heterotrophic nitrification, which is applied in the direction of aerobic process treatment, bacteria, chemical instruments and methods, etc. It can solve the problems of unstable denitrification and phosphorus removal, high one-time cost, and insufficient effluent quality compliance rate, etc. problems, achieve good economic and environmental benefits, save equipment and investment costs, and shorten system response time
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0036] Implementation Example 1: Pseudomonas sp.QG6 Degradability Determination of Quinoline
[0037] Inoculate Pseudomonas sp.QG6 (preserved on November 9, 2012 in the General Microorganism Center of China Committee for Microbial Culture Collection (CGMCC for short), the preservation number is CGMCC No.6813, the same below) in 100ml of LB In the medium (yeast extract 5g / L, peptone 10g / L, NaCl 10g / L), add 100mg / L quinoline to prevent the invasion of miscellaneous bacteria and maintain the growth vitality of the bacteria, at 30°C, 120rpm, shake the shaker Enrichment culture. After 48 hours of shaking culture, centrifuge at 4000r / min for 10 minutes, collect the bacteria, and use inorganic salt medium (K 2 HPO 4 ·3H 2 O 0.0737g / L, MgSO 4 ·7H 2 O 0.2g / L, FeSO 4 ·7H 2 O 0.02g / L, CaCl 2 2H 2 O 0.002g / L, NaCl 1.0g / L, 0.1% spare trace element solution; trace element stock solution components are: MnSO 4 ·H 2 O 0.2g / L, CuSO 4 ·5H 2 O 0.1g / L, ZnSO4 7H 2 O 0.2g / L, CoCl 2 ·...
Embodiment 2
[0041] Implementation Example 2: Determination of Heterotrophic Nitrification-Aerobic Denitrification Performance of Pseudomonas sp.QG6
[0042] Get 5mL according to the Pseudomonas sp.QG6 bacterium suspension prepared by the method for example 1 and carry out 2 groups of experiments respectively, each group adds three containing 200mL test medium respectively (test medium 1:5.628g / L butanediol Sodium hexahydrate, 0.382g / L NH 4 Cl (C / N=10), 0.79g / L K 2 HPO 4 ·3H 2 O, 0.2g / L MgSO 4 ·7H 2 O, 0.02g / LFeSO 4 ·7H 2 O, 0.002g / L CaCl 2 2H 2 O, 1.0g / LNaCl, 0.1% standby trace element solution in Example 1:; test medium 2: 11.256g / L sodium succinate hexahydrate, 0.764g / LNH 4 Cl (C / N=10), 0.79g / L K 2 HPO 4 ·3H 2 O, 0.2g / L MgSO 4 ·7H 2 O, 0.02g / L FeSO 4 ·7H 2 O, 0.002g / L CaCl 2 2H 2 O, 1.0g / L NaCl, 0.1% of the spare trace element solution in Example 1; pH 7.5~8.0), sealed with 9 layers of gauze, and cultured in a shaker at 30°C and 150rpm. The test medium that was not in...
Embodiment 3
[0046] Implementation Example 3: Determination of the Synchronous Denitrification and Phosphorus Ability of Pseudomonas sp.QG6
[0047] Get 5mL according to the Pseudomonas sp.QG6 bacterium suspension prepared by the method for example 1 and carry out 2 groups of experiments respectively, each group adds three containing 200mL test medium respectively (test medium 1:5.628g / L butanediol Sodium hexahydrate, 0.382g / L NH 4 Cl, 0.0737g / L K 2 HPO 4 ·3H 2 O, 0.2g / L MgSO 4 ·7H 2 O, 0.02g / LFeSO 4 ·7H 2 O, 0.002g / L CaCl 2 2H 2 O, 1.0g / L NaCl, 0.1% spare trace element solution in Example 1; test medium 2: 5.628g / L sodium succinate hexahydrate, 0.382g / LNH 4 Cl, 0.1474g / L K 2 HPO 4 ·3H 2 O, 0.2g / LMgSO 4 ·7H 2 O, 0.02g / L FeSO 4 ·7H 2 O, 0.002g / L CaCl 2 2H 2 O, 1.0g / L NaCl, 0.1% of the spare trace element solution in Example 1; pH 7.5~8.0), sealed with 9 layers of gauze, and cultured in a shaker at 30°C and 150rpm. The test medium that was not inoculated with the bacterial...
PUM
| Property | Measurement | Unit |
|---|---|---|
| clearance rate | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 