Algicidal bacteria and method for removing microcystis aeruginosa
A technology of Microcystis aeruginosa and algae-dissolving bacteria, applied in the direction of microorganism-based methods, bacteria, chemical instruments and methods, etc., can solve problems such as no effective solutions, cyanobacteria bloom pollution, etc., and achieve low cost and high application promising effect
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Embodiment 1
[0047] In this example, 100 mL of fresh Microcystis aeruginosa liquid 1 was treated, and the concentration of chlorophyll a was 91.72 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 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 61.2 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 34.2 mg / m at 96 h 3 , the removal rate was 44.12%, which can dissolve algae cells well.
Embodiment 2
[0049] What this embodiment deals with is 100 mL of fresh Microcystis aeruginosa liquid 2, and the concentration of chlorophyll a is 74.76 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 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 62.3 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 40.64 mg / m at 96 h 3 , the removal rate reached 34.77%, and the algae-dissolving e...
Embodiment 3
[0051] In this example, 100 mL of fresh Microcystis aeruginosa liquid 3 was treated, and the concentration of chlorophyll a was 71.17 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 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 64.71 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 51.45 mg / m at 96 h 3 , The removal rate is up to 20.49%. At this time, the algae-dissolving e...
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