A strain of Pseudomonas stutzeri with aerobic denitrification function and its application
A technology of Pseudomonas stutzeri and aerobic denitrification, applied in the field of microorganisms, can solve the problems of time consumption, complexity of sewage treatment system, low nitrification rate, etc., achieve fast metabolism, overcome intolerance to high organic load , The effect of short film growth time
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Embodiment 1
[0021] Embodiment 1: the screening method of strain
[0022] culture medium
[0023] Denitrification enrichment medium: Na 3 C 6 h 5 o 7 2H 2 O 1g / L, KNO 3 1g / L, KH 2 PO 4 1.5g / L, Na 2 HPO 4 0.42g / L, MgSO 4 ·7H 2 O 1.0g / L, CuSO 4 ·5H 2 O 4.0mg / L, FeSO 4 ·7H 2 O 0.7mg / L, FeCl 3 ·6H 2 O7.0mg / L, CoCl 3 ·6H 2O 0.2mg / L, Na 2 MO 4 2H 2 O 3.4mg / L, CaCl 2 2H 2 O 2.0g / L, pH 7.2.
[0024] Bromothymol blue (BTB) identification medium: Na 3 C 6 h 5 o 7 2H 2 O 1g / L, KNO 3 1.0g / L, FeSO 4 ·7H 2 O0.05 g / L, CaCl 2 2H 2 O 0.2g / L, MgSO 4 ·7H 2 O 1.0g / L, 1% BTB 1.0mL / L, pH 6.8.
[0025] Denitrification performance test medium: Na 3 C 6 h 5 o 7 2H 2 O 1.0g / L, KNO 3 1.0g / L, KH 2 PO 4 0.75g / L, MgSO 4 ·7H 2 O 0.4g / L, pH 7.2.
[0026] Ammonia nitrogen degradation performance test medium: NH 4 Cl 0.382g / L, CH 3 COONa 0.7g / L, MgSO 4 ·7H 2 O0.05g / L, K 2 HPO 4 0.2g / L, NaCl 0.12g / L, MnSO 4 4H 2 O 0.01g / L, FeSO 4 0.01g / L, pH 7.2.
[0027] Nitr...
Embodiment 2
[0042] Embodiment 2: Observation of strain morphology
[0043] Such as figure 1 As shown, the purified preferred strain was spread on the BTB solid medium, and the colony morphology of the strain was observed. The results of BTB plate identification show that ZH-14 can carry out denitrification and alkali production on the solid plate with potassium nitrate as the only nitrogen source, increase the pH value of the medium, and turn BTB from green to blue. The single colony of strain ZH-14 on the BTB plate was round, light yellow, smooth, opaque, raised, and easy to stir up in the early stage; light yellow folds were formed on the surface in the late growth period, and the surface area of the colony became larger.
Embodiment 3
[0044] Example 3: Nitrogen removal performance test
[0045] 1. Nitrogen removal performance test of aerobic denitrifying bacteria
[0046] Pick a single colony and inoculate them on the denitrification performance test medium, nitrite degradation test medium and ammonia nitrogen degradation test test medium respectively, and culture at constant temperature and shaking at 30°C and 160r / min for 1 day to obtain the corresponding seed solution.
[0047] Take the above-mentioned bacterial solution and inoculate them according to 1% (v / v) into 250mL Erlenmeyer flasks equipped with 100mL denitrification performance test medium, nitrite degradation test medium and ammonia nitrogen degradation test medium. Three repetitions were carried out at 30°C and 160r / min for constant temperature shaking culture. Among them, the denitrification performance measurement medium, the nitrite degradation performance measurement medium are sampled every 6h, the ammonia nitrogen degradation performanc...
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