Acinetobacter johnson aj-3 strain and use thereof
A technology of AJ-3 and bacteria strains, applied in the field of environmental microorganisms, can solve the problems of large amount of chemical sludge, high treatment costs, and large dosage of chemicals, and achieve high phosphorus removal efficiency, strong environmental adaptability, and stable phosphorus removal efficiency Effect
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Embodiment 1
[0022] Example 1 Isolation, Screening and Identification of High-efficiency Phosphorus Accumulating Bacteria Acinetobacter Johnson AJ-3
[0023] (1) Medium
[0024] Beef extract peptone solid medium: beef extract 3g / L, peptone 10g / L, NaCl5g / L, agar 20g / L, pH7.0-7.2 (liquid medium without agar);
[0025] Phosphorus-limited (phosphorus-rich) solid medium: Dissolve 8.372g 3-morpholinopropanesulfonic acid and 0.717g N-tris(hydroxymethyl)methylglycine in 30mL deionized water, adjust the pH to 7.4 with 10mol / L KOH, press Add the solution in the following order: 0.01mL1.830%FeSO 4 Solution (now equipped), 5mL1.9mol / LNH 4 Cl, 1mL0.276mol / LK 2 SO 4 , 0.025mL0.02mol / LCaCl 2 ·2H 2 O, 0.42mL1.25mol / LMgCl 2 ·6H 2 O, 20mL2.5mol / LNaCl, 0.02mL trace element mixture (ammonium heptamolybdate 3×10 -6 mol / L, H 3 BO 3 4×10 -4 mol / L, CoCl 2 3×10 -5 mol / L, CuSO 4 10 -5 mol / L, MnCl 2 8×10 -5 mol / L, ZnSO 4 10 -5 mol / L), 10mL1% glucose, 0.4mL1.686% vitamin B1, 250μL 6.928%K 2 HPO 4 (Add 5mL for rich phospho...
Embodiment 2
[0037] Example 2 Determination of the growth curve of Acinetobacter johnsonii AJ-3 strain
[0038] (1) Strains: AJ-3 strain.
[0039] (2) Medium
[0040] Beef extract peptone solid medium: the formula is the same as in Example 1
[0041] Synthetic sewage liquid culture medium: sodium acetate 0.925g / L, peptone 0.1g / L, yeast extract 0.01g / L, NaCl0.05g / L, KH 2 PO 4 0.0655g / L, MgCl 2 ·6H 2 O0.1412g / L, CaCl 2 0.025g / L, pH7.0-7.2.
[0042] (3) Method
[0043] Take 20μL of glycerol bacteria stored at -20℃ and spread it on the plate of beef extract peptone solid medium. After incubating at 28℃ for 24h, pick a single colony and mix it with 0.3mL sterile water. Take 100μL and spread it on beef extract peptone solid culture. Use a punch (aperture 0.5cm) to take 2 holes into 15mL beef extract peptone liquid medium, place them in a shaker at 28℃, 170r / min for 24h (OD 600 ≈0.9) Activated and used as seed solution; then 8% of the inoculum was inserted into a 250mL Erlenmeyer flask containing 100mL...
Embodiment 3
[0046] Example 3 The influence of the liquid volume on the biological phosphorus removal effect of Acinetobacter johnsonii AJ-3 strain.
[0047] (One) Strain: AJ-3 strain.
[0048] (2) Medium
[0049] Beef extract peptone solid medium: the formula is the same as in Example 1;
[0050] Synthetic sewage liquid culture medium: the formula is the same as in Example 2.
[0051] (3) Method
[0052] Take 20μL of glycerol bacteria stored at -20℃ and spread it on the plate of beef extract peptone solid medium. After incubating at 28℃ for 24h, pick a single colony and mix it with 0.3mL sterile water. Take 100μL and spread it on beef extract peptone solid culture. Use a punch (aperture 0.5cm) to take 2 holes into 15mL beef extract peptone liquid medium, place them in a shaker at 28℃, 170r / min for 24h (OD 600 ≈0.9) activated and used as a seed solution; then 8% of the inoculum was inserted into a 250mL Erlenmeyer flask containing different amounts of synthetic sewage liquid culture medium (the...
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