Method for screening algicidal bacteria and removing microcystis aeruginosa from Lake Tai branch river sediment
A technology of algae-lysing bacteria and Microcystis green, applied in the directions of microorganism-based methods, bacteria, chemical instruments and methods, etc., can solve the problems of unscaled application, in the laboratory stage, etc., and achieves low cost, algae-lysis The effect is ideal and the application prospect is broad
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Embodiment 1
[0054] In this example, 100 mL of fresh Microcystis aeruginosa liquid 1 was treated, and the concentration of chlorophyll a was 202.11 mg / m 3 , pH value is 7.2. The specific implementation steps are as follows: first, culture Bacillus lysinus at a temperature of 30°C and a shaker speed of 130 r / min until the logarithmic phase (16 h), and then, according to the bacteria-to-algae ratio of 1:2, the 50 mL of logarithmic phase bacterial liquid was inoculated into algae liquid, and sterile water was used as blank control, and the initial chlorophyll a concentration was determined to be 168.42 mg / m 3 , placed in a light incubator at 28°C, light intensity 2500 lux, and light cycle 12 h: 12 h for static culture, and samples were taken every 24 h to determine the concentration of chlorophyll a. After the algae liquid treated by the above method, the concentration of chlorophyll a was 8.68mg / m at 96 h 3 , the removal rate is 94.85%, which can dissolve algae cells well.
Embodiment 2
[0056] What this embodiment deals with is 100 mL of fresh Microcystis aeruginosa liquid 2, and the concentration of chlorophyll a is 220.93 mg / m 3 , pH value is 7.2. The specific implementation steps are as follows: firstly, the Bacillus lysinica was cultured to the logarithmic phase (16 h) at a temperature of 30 °C and a shaker speed of 130 r / min, and then the bacteria were injected at a bacterial ratio of 1:5. 20 mL of the logarithmic phase bacterial liquid was inoculated into the algae liquid, and sterile water was used as a blank control, and the initial chlorophyll a concentration was determined to be 189.62 mg / m 3 , placed in a light incubator at 28°C, light intensity 2500 lux, and light cycle 12 h: 12 h for static culture, and samples were taken every 24 h to determine the concentration of chlorophyll a. After the algae liquid treated by the above method, the chlorophyll a concentration was 21.6 mg / m at 96 h 3 , the removal rate reached 88.61%, and the algae-dissolvin...
Embodiment 3
[0058] In this example, 100 mL of fresh Microcystis aeruginosa liquid 3 was treated, and the concentration of chlorophyll a was 235.88 mg / m 3 , pH value is 7.2. The specific implementation steps are as follows: First, culture Bacillus lysinus at a temperature of 30°C and a shaker speed of 130 r / min until the logarithmic phase (16 h), and then, according to the bacteria-to-algae ratio of 1:10, the 10 mL of logarithmic phase bacterial liquid was inoculated into the algae liquid, and sterile water was used as a blank control, and the initial chlorophyll a concentration was determined to be 199.22 mg / m by sampling 3 , placed in a light incubator at 28°C, light intensity 2500 lux, and light cycle 12 h: 12 h for static culture, and samples were taken every 24 h to determine the concentration of chlorophyll a. After the algae liquid treated by the above method, the concentration of chlorophyll a was 25.28 mg / m at 96 h 3 , the removal rate reached 87.31%, and the algae-dissolving ef...
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