Method for detecting subaqueous acute biological toxicity using photobacteria
A technology of luminescent bacteria and biotoxicity, which is applied in the direction of chemiluminescence/bioluminescence, biochemical equipment and methods, measurement/inspection of microorganisms, etc., which can solve cumbersome problems and achieve the goals of weakening toxicity, good stability and improving test sensitivity Effect
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[0024] 2.1 Preparation of fresh bacterial suspension of luminescent bacteria
[0025] (1) Screen strains: take the purchased luminescent bacterial strains and culture them for 48 hours, pick various bacterial colonies for microscopic examination, and select the desired luminescent bacterial colonies.
[0026] (2) Slant strain culture: Before the measurement, take the luminescent bacteria and pick out the first-generation slant on a fresh slant, and immediately transfer the second-generation slant after culturing at 20±0.5°C for 24 hours, and then culture at 20±0.5°C for 24 hours, and then pick up the second-generation slant The third-generation slant was cultured at 20±0.5°C for 12 hours before use. The amount of each inoculation should not exceed one inoculation loop.
[0027] (3) Cultivation of shake-flask bacterial culture: Take nearly one ring of the third-generation slant strain, inoculate it in a 250-mL Erlenmeyer flask filled with 50 mL of culture solution, and culture...
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