Comonas testosteroni with denitrification and dephosphorization functions and application thereof
A technology of Comamonas and testosterone, applied in the direction of bacteria, microbial-based methods, biological water/sewage treatment, etc., can solve the basic problems of single denitrification or phosphorus removal function research, and achieve slow value-added and growth rate Fast, high cell yield results
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Embodiment 1
[0032] Implementation Example 1: Phosphorus removal capacity determination of Comamonas testosteroni under aerobic conditions
[0033] Comamonas testosteroni strain (preserved on March 19, 2009 in the General Microbiology Center of China Committee for Microbial Culture Collection (CGMCC for short), the preservation number is CGMCC №2963, the same below) was inoculated 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 cultur...
Embodiment 2
[0036] Implementation Example 2: Determination of Optimal Phosphorus Removal Conditions for Comamonas testosteroni
[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 Comamonas testosteroni. 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 influence of four factors on the phosphorus removal effect of the strain was as follows: rotational speed>temperature>c...
Embodiment 3
[0042] Implementation example 3: Synchronous denitrification and dephosphorization ability determination of Comamonas testosteroni
[0043] Comamonas testosteroni strains were inoculated in 1 L of LB medium to prevent the invasion of miscellaneous bacteria and maintain the growth vigor of the bacteria for 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, 0.1911g NH 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 the same conditions. Take a...
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