Achromobacter xylosoxidans with denitrification and dephosphorization function and application of Achromobacter xylosoxidans
An achromobacter, xylose technology, applied in bacteria, aerobic process treatment, chemical instruments and methods, etc., can solve the problem of single denitrification or phosphorus removal function research basis, etc., to solve the problem of slow value-added and high cell yield , the effect of fast growth rate
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Embodiment 1
[0032] Implementation Example 1: Phosphorus removal capacity determination of Achromobacter xylosoxidans under aerobic conditions
[0033] Inoculate the Achromobacter xylosoxidans strain (preserved in the General Microbiology Center of China Committee for Microbial Culture Collection (CGMCC) on March 19, 2009, the preservation number is CGMCC№2964, the same below) in 1L In the LB medium, to prevent the invasion of miscellaneous bacteria and maintain the growth vigor of the bacteria, carry out enrichment culture. The cultured bacterial solution was centrifuged, washed three times with sterile water, and the optical density (OD 600 ) is the bacterial suspension of 1-2.
[0034] Take 5mL of the above bacterial suspension and add two test media containing 120mL (each L contains 5g sodium succinate, 0.1911gNH 4 Cl, 0.044g KH 2 PO 4 , 0.2g CaCl 2 2H 2 O, 0.5g MgSO 4 ·7H 2 O, 0.006g FeSO 4 ·7H 2 (0, pH7.0~7.5) Erlenmeyer flasks, sealed with 9 layers of gauze, and cultured i...
Embodiment 2
[0036] Implementation Example 2: Determination of Optimal Phosphorus Removal Conditions for Achromobacter xylosoxidans
[0037] Using the shaking flask experiment mode, according to the principle of orthogonal experiment, with pH value, shaker culture temperature, shaker speed and carbon-nitrogen ratio as the influencing factors, a total of 9 orthogonal experiments with 4 factors and 3 levels were established to determine Optimal phosphorus removal conditions for the strain Achromobacter xylosoxidans. The medium used in the experiment was the same as in Example 1 except that the content of sodium succinate was changed as needed.
[0038] Orthogonal experimental design and results are shown in Table 1.
[0039] Table 1 Orthogonal experiment design and results
[0040]
[0041] Through the analysis of the results of the orthogonal experiment, it was found that the strength of the influence of four factors on the phosphorus removal effect of the strain was: pH>carbon-nitroge...
Embodiment 3
[0042] Implementation example 3: Determination of simultaneous denitrification and phosphorus removal ability of Achromobacter xylosoxidans
[0043] The Achromobacter xylosoxidans strain was inoculated in 1 L of LB medium to prevent the invasion of miscellaneous bacteria and maintain the growth activity of the bacteria, and carry out enrichment culture. The cultured bacterial solution was centrifuged, washed three times with sterile water, and the optical density (OD 600 ) is the bacterial suspension of 1-2.
[0044] Take 2.5mL of the above bacterial suspension and add to two test media containing 120mL (each L contains 5g sodium succinate, 0.1911gNH 4 Cl, 0.044g KH 2 PO 4 , 0.2g CaCl 2 2H 2 O, 0.5g MgSO 4 ·7H 2 O, 0.006g FeSO 4 ·7H 2 (0, pH 7.0-7.2) Erlenmeyer flasks, sealed with 9 layers of gauze, and cultured in a shaker at 30° C. at 150 rpm. The culture medium that was not inoculated with the bacterial suspension was used as a blank control for experiments under ...
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