Acinetobacter johnsonii AJ-3 strain and application thereof
A technology of AJ-3 and bacteria strains, applied in the field of environmental microorganisms, can solve the problems of high treatment costs, large dosage, large amount of chemical sludge, etc., and achieve strong environmental adaptability, high phosphorus removal efficiency, and low requirements for dissolved oxygen Effect
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Embodiment 1
[0022] Example 1 Isolation, screening and identification of high-efficiency phosphorus-accumulating bacterium Acinetobacter johnsonii AJ-3 strain
[0023] (1) Medium
[0024] Beef extract peptone solid medium: beef extract 3 g / L, peptone 10 g / L, NaCl 5 g / L, agar 20 g / L, pH 7.0-7.2 (liquid medium without agar);
[0025] Phosphorus-limited (phosphorus-rich) solid medium: Dissolve 8.372 g of 3-morpholine propanesulfonic acid and 0.717 g of N-tris(hydroxymethyl)methylglycine in 30 mL of deionized water, and adjust the pH with 10 mol / L KOH To 7.4, add solutions in the following order: 0.01 mL 1.830% FeSO 4 solution (prepared), 5 mL 1.9 mol / L NH 4 Cl, 1 mL 0.276 mol / L K 2 SO 4 , 0.025 mL 0.02 mol / L CaCl 2 2H 2 O, 0.42 mL of 1.25 mol / L MgCl 2 6H 2 O, 20 mL 2.5 mol / L NaCl, 0.02 mL trace element mixed solution (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)...
Embodiment 2
[0037] The growth curve determination of embodiment 2 Johnson's Acinetobacter AJ-3 bacterial strain
[0038] (1) Strain: 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 medium: sodium acetate 0.925 g / L, peptone 0.1 g / L, yeast extract 0.01 g / L, NaCl 0.05 g / L, KH 2 PO 4 0.0655 g / L, MgCl 2 ·6H 2 O 0.1412 g / L, CaCl 2 0.025 g / L, pH7.0-7.2.
[0042] (3) Method
[0043] Take 20 μL of glycerol bacteria stored at -20°C and spread it on the plate of beef extract peptone solid medium, culture it at 28°C for 24 hours, pick a single colony and mix it with 0.3 mL sterile water, take 100 μL and spread it on beef extract On the plate of peptone solid medium, use a hole puncher (pore diameter 0.5 cm) to take 2 holes and connect it to 15 mL beef extract peptone liquid medium, and culture it in a shaker at 28 °C and 170 r / min for 24 h (OD 600 ≈0.9) was activated as seed solution; the...
Embodiment 3
[0046] Example 3 The effect of liquid volume on the biological phosphorus removal effect of Acinetobacter johnsonii strain AJ-3.
[0047] (1) 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: formula is the same as embodiment 2.
[0051] (3) Method
[0052] Take 20 μL of glycerol bacteria stored at -20°C and spread it on the plate of beef extract peptone solid medium, culture it at 28°C for 24 hours, pick a single colony and mix it with 0.3 mL sterile water, take 100 μL and spread it on beef extract On the plate of peptone solid medium, use a hole puncher (pore diameter 0.5 cm) to take 2 holes and connect it to 15 mL beef extract peptone liquid medium, and culture it in a shaker at 28 °C and 170 r / min for 24 h (OD 600 ≈0.9) to be activated as seed solution; then 8% of the inoculum volume was inserted into liquid medium containing different amounts of...
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