A Method for Assessing the Toxicity of Microcystins in Real Aquatic Environments
A microcystin, water environment technology, applied in the direction of biochemical equipment and methods, microbial measurement/inspection, material inspection products, etc., can solve the potential toxicity hazards of microcystin, and the research results are not convincing and other issues, to achieve the effects that are conducive to growth and survival, universal applicability, and wide application range
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Embodiment 1
[0048] This embodiment includes the following steps:
[0049] (1) The degradation strain M9 before irradiation was prepared into bacterial cell suspension and diluted to 10 9 each / mL; then prepare the stock solution where the degradation strain and MC-LR coexist;
[0050] The preparation method of the stock solution in which the degrading strain and MC-LR coexist is as follows: take 200 μL of 50 μM pure MC-LR stock solution and add the bacterial cell concentration to 10 9 In 800 μL cell suspension per mL, the volume ratio of cell suspension to MC-LR solution in the prepared solution is 4:1; shake evenly, and culture at room temperature in the dark for three days; then use a filter membrane with a pore size of 0.22 μm Filter and store in a -20°C refrigerator to prepare a stock solution in which the degrading strain and MC-LR coexist.
[0051] (2) Prepare MC-LR and strain coexisting working solution with concentrations of 1 μM and 0.1 μM, pure MC-LR working solution at 1 μM an...
Embodiment 2
[0062] Degraded strains after ion beam irradiation, prepared coexisting working solution with MC-LR, infected Hep G2 cells and carried out MTT experiment, and then detected its absorbance value, compared with the degraded strains before irradiation in Example 1. The strength of the degradation effect.
[0063] This embodiment includes the following steps:
[0064] (1) by N + Ion beam implantation technology was used to irradiate the degrading strain M9 to obtain degrading strains A1, A2 and A3 after irradiation;
[0065] A1: The radiation dose is 40 units, each unit is 2.6×10 13 N + / cm 2 ,
[0066] A2: The radiation dose is 60 units, each unit is 2.6×10 13 N + / cm 2 ,
[0067] A3: The radiation dose is 80 units, each unit is 2.6×10 13 N + / cm 2 ,
[0068] (2) The degradative strain M9 before irradiation and the degradative strain A1, A2, A3 after irradiation were prepared into bacterial cell suspension, and diluted to 10 9 each / mL; then prepare respectively the ...
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