Whole-cell luminescence-based flow-through biodetector for toxicity testing

AbstractA new type of biodetector was designed based on a bioluminescence test with the bacterium Vibrio fischeri performed in a liquid continuous flow-through system. Here we describe the modification of a commercial tube luminescence detector to work in the flow mode by building a new flow cell holder and a new case including “top cover” to connect the flow cell with the waste and the incubation capillary in a light-proof manner. As different samples were injected successively it was necessary to keep the individual peaks separated. This was done using an air-segmented flow in the reaction coil. To afford fast screening, the incubation time of the sample and the Vibrio fischeri, which equaled the dead time of the detection system, was set at 5.6 min. Rapid monitoring of toxic substances is achieved by using 20 μL of sample and flow-rates of 110–150 μL min−1. As a proof-of-principle, we show results for the detection of five selected di-, tri- and tetrachlorophenols at different concentrations varying from 1 to 200 mg L−1. Calculation of inhibition rates and EC50 values were performed and compared with corresponding values from the DIN EN ISO 11348-2 microplate format. Compared with the latter, the inhibition rates obtained with our flow-through biodetector for the compounds tested were generally about twofold lower, but importantly, a much faster detection is possible. FigureFlow scheme of the biodetector setup

[1]  N. Christofi,et al.  Combination ecotoxicity and testing of common chemical discharges to sewer using the Vibrio fischeri luminescence bioassay , 2003, International microbiology : the official journal of the Spanish Society for Microbiology.

[2]  Oliver Fiehn,et al.  A modified method for the analysis of organics in industrial wastewater as directed by their toxicity to Vibrio fischeri , 1999 .

[3]  P. Dunlap,et al.  Regulation of luminescence by cyclic AMP in cya-like and crp-like mutants of Vibrio fischeri , 1989, Journal of bacteriology.

[4]  Oliver Fiehn,et al.  Toxicity‐directed Fractionation of Tannery Wastewater Using Solid‐phase Extraction and Luminescence Inhibition in Microtiter Plates , 1997 .

[5]  H. Okamura,et al.  Remarkable Synergistic Effects in Antifouling Chemicals against Vibrio fischeri in a Bioluminescent Assay , 2006 .

[6]  L. Skeggs An automatic method for colorimetric analysis. , 1957, American journal of clinical pathology.

[7]  V L Jennings,et al.  Assessing chemical toxicity with the bioluminescent photobacterium (Vibrio fischeri): a comparison of three commercial systems. , 2001, Water research.

[8]  P. Dunlap,et al.  Cell density-dependent modulation of the Vibrio fischeri luminescence system in the absence of autoinducer and LuxR protein , 1992, Journal of bacteriology.

[9]  D. Agar,et al.  The capillary-microreactor: a new reactor concept for the intensification of heat and mass transfer in liquid–liquid reactions , 2003 .

[10]  G. Shi,et al.  A water-soluble cationic oligopyrene derivative : Spectroscopic studies and sensing applications , 2009 .

[11]  Versatile device for on-line and in-situ measurement of growth and light production of bioluminescent cells , 2004 .

[12]  E. Ruby,et al.  Detection and quantification of Vibrio fischeri autoinducer from symbiotic squid light organs , 1995, Journal of bacteriology.

[13]  Reinhard Niessner,et al.  Effect-directed analysis by high-performance liquid chromatography with gas-segmented enzyme inhibition. , 2005, Journal of chromatography. A.

[14]  I. Tothill,et al.  Developments in bioassay methods for toxicity testing in water treatment , 1996 .

[15]  J. Etxebarria,et al.  A comparison of five rapid direct toxicity assessment methods to determine toxicity of pollutants to activated sludge. , 2002, Chemosphere.