Method for accurately detecting toxicity of water quality by using photobacterium toxicity test
A technology of toxicity test and luminescent bacteria, which is applied in biochemical equipment and methods, measurement/inspection of microorganisms, etc., can solve the problems of comprehensive toxicity obstacles of luminescent bacteria toxicity test, and achieve the effects of high sensitivity, easy operation and risk reduction
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Embodiment 1
[0022] Taking Vibrio Qinghai as an example, the luminescence inhibition rate of the same substance was detected when it was pretreated and not treated:
[0023] Adopt the method of the present invention to prepare Qinghai Vibrio bacteria suspension: Qinghai Vibrio is cultured at 22 DEG C for 24 hours on LB solid medium, 30 single colony strains are inoculated in 150ml liquid LB medium, 22 DEG C shake culture 20h ; The liquid culture medium containing Vibrio qinghai was centrifuged under the centrifugation condition of 4000r / min, and then suspended with sterile normal saline to obtain a bacterial suspension with an OD value of 0.9;
[0024] Untreated Vibrio Qinghai was prepared directly into a bacterial suspension with an OD of 0.9.
[0025] Mix 0.1mg / L of chloroform, 0.02mg / L of deltamethrin, 0.02mg / L of carbon tetrachloride, and 0.25 mg / L of iron in the bacterial suspension at a volume ratio of 1:1, and detect after exposure for 10 minutes Luminescence inhibition rate, the r...
Embodiment 2
[0029] This specific embodiment adopts the following steps:
[0030] (1) Cultivate Vibrio Qinghai on LB solid medium at 22°C for 24h, inoculate 30 single colony strains into 150ml liquid LB medium, and culture with shaking at 22°C for 20h;
[0031] (2) Centrifuge the liquid medium containing luminescent bacteria under the centrifugation condition of 4000r / min, and then suspend it with sterile saline to obtain a bacterial suspension with an OD value of 0.9;
[0032] (3) Collect the factory water of the daily urban water plant, set up 3 parallels, mix the bacterial suspension and the water sample at a ratio of 1:1, control the exposure and reaction time of the bacteria at 10 minutes, and measure the luminescence after 10 minutes of reaction According to the determination, the luminescence inhibition rates of the three parallel samples of the water samples to be tested were 31.2%, 29%, and 30.7%, respectively, and the average luminescence inhibition rate was 30.3%.
[0033] Usin...
Embodiment 3
[0035] This specific embodiment adopts the following steps:
[0036] (1) Cultivate Vibrio Qinghai on LB solid medium at 20°C for 22 hours, inoculate single colony strains into liquid LB medium, and culture with shaking at 25°C for 16 hours. 5 -10 6 Between;
[0037] (2) Centrifuge the liquid medium containing luminescent bacteria under the centrifugation condition of 3500r / min, and then suspend it with sterile saline to obtain a bacterial suspension with an OD value of 0.7;
[0038] (3) Collect daily drinking water, set up 3 parallels, mix the bacterial suspension and the water sample at a ratio of 1:1, control the exposure reaction time of the bacteria at 15 minutes, and measure the luminescence after 15 minutes of reaction. The luminescence inhibition rates of the three parallel samples of the water sample to be tested were 42.4%, 43.5%, and 42.2%, respectively, and the average luminescence inhibition rate was 42.7%.
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Abstract
Description
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Application Information
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