Aquaculture water body water purifying agent and preparation method thereof
A technology for aquaculture water and water purifiers, applied in biochemical equipment and methods, chemical instruments and methods, biological water/sewage treatment, etc., can solve problems such as unstable effects, increased application costs, and difficulty in obtaining, and achieve treatment effects Stabilization, maintenance of ecological balance, and the effect of strain acquisition
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[0035] Invent the preparation method of above-mentioned aquaculture water purifying agent, comprise the steps:
[0036] S1. Screen the pond water body in the late stage of intensive culture, collect 1.0g of water sample, put it into a 50mL triangular flask filled with 9mL sterile water and glass beads, shake it on a shaker for 20min to disperse the microbial cells, and let it stand for 30s. into 10 -1 Diluent;
[0037] S2. Use a 1mL sterile pipette to draw 10 -1 Dilute 1mL, transfer to a test tube filled with 9mL sterile water, suck and blow 3 times, mix the bacterial solution, and serve as 10 -2 Diluent; and so on, serially diluted to make 10 -3 、10 -4 、10 -5 、10 -6 、10 -7 、10 -8 A series of diluted bacterial solutions;
[0038] S3, from 10 -6 、10 -7 、10 -8 Take 1mL of each of the diluted bacterial solutions on the plate, pour into the medium that has been melted and cooled to 45-50°C, turn the plate gently to mix the bacterial liquid with the medium evenly; after...
Embodiment 1
[0042] A water purifying agent for aquaculture, comprising the following components with the ratio of bacteria numbers: Bacillus megaterium, Bacillus cereus, Thiobacillus denitrificans, Lactobacillus acidophilus, Nitrobacter victorii, the number ratio of bacteria is 2: 2:1:2:1, the addition amount is 5ppm.
[0043] The preparation method of the above-mentioned aquaculture water purifying agent is as follows:
[0044] S1. Screen the pond water body in the late stage of intensive culture, collect 1.0g of water sample, put it into a 50mL triangular flask filled with 9mL sterile water and glass beads, shake it on a shaker for 20min to disperse the microbial cells, and let it stand for 30s. into 10 -1 Diluent;
[0045] S2. Use a 1mL sterile pipette to draw 10 -1 Dilute 1mL, transfer to a test tube filled with 9mL sterile water, suck and blow 3 times, mix the bacterial solution, and serve as 10 -2 Diluent; and so on, serially diluted to make 10 -3 、10 -4 、10 -5 、10 -6 、10 -...
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