Denitrifying bacterium and application thereof
A technology of denitrifying bacteria and Stenotrophomonas, which is applied in the field of environmental microorganisms, can solve the problems of denitrification effect, low denitrification efficiency, low tolerance of nitrate and nitrite, and achieve tolerance High and good denitrification effect
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Embodiment 1
[0050] Example 1 Isolation and identification of Stenotrophomonas maltophilia CCTCC M 2012455
[0051] (1) Liquid medium
[0052] CH 3 COONa, 2.5g / L; NaNO 3 , 1.2g / L; K 2 HPO 4 , 0.5g / L; MgSO 4 ·7H 2 O, 0.1g / L; trace element solution, 2mL / L; pH adjusted to 7.2-7.6, sterilized at 121°C for 20 minutes;
[0053] Wherein, the trace element solution components are:
[0054] EDTA, 2.06g / L; FeSO 4 ·7H 2 O, 1.54g / L; MnCl 2 4H 2 O, 0.2g / L; ZnSO 4 ·7H 2 O, 0.1g / L; CuSO 4 ·5H 2 O, 0.02g / L; Na 2 MnO 4 , 0.1g / L; CoCl 2 ·6H 2 O, 0.002g / L.
[0055] The solid medium is the agar with 1.5-2% added to the above-mentioned liquid medium components.
[0056] (2) Strain isolation and screening
[0057] The bacterial strain of the present invention is obtained by separating and obtaining from filler biofilm in a continuously operating moving bed biofilm (MBBR) reactor of Jiaxing Sewage Treatment Plant.
[0058] ① Take the sludge samples on the filler biofilm and serially dilute ...
Embodiment 2
[0077] Embodiment 2 The cultivation of Stenotrophomonas maltophilia CCTCC M 2012455
[0078] (1) Liquid medium
[0079] CH 3 COONa, 2.5g / L; NaNO 3 , 1.2g / L; K 2 HPO 4 , 0.5g / L; MgSO 4 ·7H 2 O, 0.1g / L; trace element solution, 2mL / L; pH adjusted to 7.2-7.6, sterilized at 121°C for 20 minutes;
[0080] Wherein, the trace element solution components are:
[0081] EDTA, 2.06g / L; FeSO 4 ·7H 2 O, 1.54g / L; MnCl 2 4H 2 O, 0.2g / L; ZnSO 4 ·7H2 O, 0.1g / L; CuSO 4 ·5H 2 O, 0.02g / L; Na 2 MnO 4 , 0.1g / L; CoCl 2 ·6H 2 O, 0.002g / L.
[0082] The solid medium is agar powder with 1.5% (w / v) added to the above medium components.
[0083] (2) Inoculate the bacterial strain of the present invention stored at -86°C with 50% glycerol onto the above solid medium, and place it in an anaerobic incubator at 33.5°C for upside-down activation for 36 to 48 hours for later use.
[0084] (3) Inoculate the activated strain into a 110mL serum bottle filled with 50mL of liquid medium, and shake...
Embodiment 3
[0087] Example 3 Denitrification ability test of Stenotrophomonas maltophilia CCTCC M 2012455
[0088] NaNO 3 and NaNO 2 As a nitrogen source, the strain growth and denitrification ability were investigated.
[0089] Denitrification medium: CH 3 COONa, 2.5g / L; NaNO 3 / NaNO 2 (according to test requirements); K 2 HPO 4 , 0.5g / L; MgSO 4 ·7H 2 O, 0.1g / L; trace element solution, 2mL / L; sterilized at 121°C for 20 minutes;
[0090] Wherein, the trace element solution components are:
[0091] EDTA, 2.06g / L; FeSO 4 ·7H 2 O, 1.54g / L; MnCl 2 4H 2 O, 0.2g / L; ZnSO 4 ·7H 2 O, 0.1g / L; CuSO 4 ·5H 2 O, 0.02g / L; Na 2 MnO 4 , 0.1g / L; CoCl 2 ·6H 2 O, 0.002g / L.
[0092] In the 110mL serum bottle, add 50mL denitrification culture solution, 2mL embodiment 2 expands the bacterial solution after cultivating, wherein NO 3 - -N and NO 2 - -N concentrations were respectively set to 70mg / L, 140mg / L, 210mg / L, 280mg / L and 350mg / L, the initial pH value was controlled at 7.5, and cu...
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