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35results about "Pollution detectors" patented technology

Transgenic animals for monitoring water quality

InactiveUS20060143718A1Reduce cost per sampleIncreases time required data acquisitionPollution detectorsChemiluminescene/bioluminescenceLuciferase GeneWater quality
The present invention provides methods and systems that uses transgenic zebrafish with an easily assessable reporter gene under the control of pollutant-inducible DNA response elements. Transgenic zebrafish, carrying pollution-inducible response elements, are placed in the water to be tested, and the contaminants become bioconcentrated (generally 1,000- to 40,000-fold, relative to the water) in the tissues of the fish thereby activating specific response elements, which up-regulate the LUC reporter gene. Fish are then removed from the test water and placed immediately in a luminometer cuvette and incubated with luciferin. Luciferin is rapidly taken up into the tissues of the fish, oxidized by luciferase, and light is produced. The luminescence is proportional to the environmental concentration of the pollutant (to which the fish had been exposed), which drives the expression of the LUC gene by means of the various DNA motifs. The luminescence is quantitated in the luminometer. In each response element-containing construct, a specific class of polluting chemicals, allowing for differential identification of pollutants in a complex mixture activates the expression of the LUC gene. This assay does not require killing the fish and allows for repeated analysis of the same site with the same fish. The sensitivity of the system can be manipulated by varying the sequence of the response element.
Owner:NEBERT DANIEL

Immobilized microbial system as well as preparation method thereof and water toxicity detection method

The invention provides an immobilized microbial system, which comprises a microbial carrier and microorganisms attached to the surface of the microbial carrier, wherein the microbial carrier is prepared by carbonizing plant tissues. The invention also provides a preparation method of the immobilized microbial system and a water toxicity detection method. The preparation method disclosed by the invention, which prepares the immobilized microbial system from the plant carbonized tissues by virtue of a one-step method, is simple to implement; moreover, according to the immobilized microbial system provided by the invention, the microorganisms are immobilized by virtue of an attachment process, so that the microorganisms naturally deposit on pore surfaces of a carrier material, and a cross-linking curing process is avoided; and in addition, the adopted microbial carrier, which is of a three-dimensional spatial reticular structure, is relatively good in mass transfer performance. Therefore, the immobilized microbial system provided by the invention is relatively good in activity in a process of detecting the water toxicity; the immobilized microbial system can be repeatedly applicable to water toxicity detection; and the immobilized microbial system is relatively good in detection effect.
Owner:CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI

Method for testing toxicity of high algae-laden aquatic organisms

InactiveCN105483202AFacile apoptosis rateSimple death ratePollution detectorsMicrobiological testing/measurementTesting toxicityPhosphate
The invention discloses a method for testing the toxicity of high algae-laden aquatic organisms. The method comprises the steps that saccharomyces cerevisiae is cultured in a solid medium containing 5% of YPD and 1.5% of agar firstly, after clone is grown out, a YPD fluid medium of 5% is inoculated with monoclone, and overnight shake cultivation is conducted based on 180-250 rpm and 25-58 DEG C; phosphate buffer is added to a culture solution with the OD value of 1.5-1.8 to obtain a blank sample A, a high algae-laden water sample is added to the culture solution with the OD value of 1.5-1.8 to obtain a detection sample B, and the two samples are placed on a mixer for oscillation lasting 2 h; cell washing is conducted on the sample A and the sample B twice by means of PBS, and cell suspension with the concentration of 1*105-1*106 cel ls/mL is prepared; the sample A and the sample B are both added to Annexin V-FITC of 5 mug/mL to be evenly mixed, and then propidium iodide of 5 mug/mL is added to be evenly mixed; reaction is conducted at the room temperature away from light for 5-15 min; flow cytometry detection is conducted within 1 h; the proportion of dead cells, the proportion of living cells and the proportion of apoptotic cells are detected by means of flow cytometry; the apoptosis rate and the death rate of the sample B are compared with those of the blank sample A, so that water toxicity is judged. Early warning technical support is provided for high algae-laden water pollution, so that high water supply quality is guaranteed.
Owner:上海艾耐基科技股份有限公司 +1
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