Development of a set of simple bacterial biosensors for quantitative and rapid measurements of arsenite and arsenate in potable water

被引:248
作者
Stocker, J
Balluch, D
Gsell, M
Harms, H
Feliciano, J
Daunert, S
Malik, KA
Van der Meer, JR [1 ]
机构
[1] Swiss Fed Inst Environm Sci & Technol, CH-8600 Dubendorf, Switzerland
[2] Ecole Polytech, Lausanne, Switzerland
[3] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
[4] DSMZ, German Collect Microorganisms & Cell Cultures, D-38124 Braunschweig, Germany
关键词
D O I
10.1021/es034258b
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Testing for arsenic pollution is commonly performed with chemical test kits of unsatisfying accuracy. Bacterial biosensors are an interesting alternative as they are easily produced, simple, and highly accurate devices. Here, we describe the development of a set of bacterial biosensors based on a nonpathogenic laboratory strain of Escherichia coli, the natural resistance mechanism of E coli against arsenite and arsenate, and three reporter proteins: bacterial luciferase, beta-galactosidase and Green Fluorescent Protein (GFP). The biosensors were genetically optimized to reduce background expression in the absence of arsenic. In calibration experiments with the biosensors and arsenite-amended potable water, arsenite concentrations at 4 mug of As/L (0.05 muM) were routinely and accurately measured. The currently most quantitative system expressed the bacterial luciferase as reporter protein, responding proportional with a concentration range between 8 and 80 mug of As/L. Sensor cells could be stored as frozen batches, resuspended in plain media, and exposed to the aqueous test sample, and light emission was measured after 30-min incubation. Field testing for arsenite was achieved with a system that contained P-galactosidase, producing a visible blue color at arsenite concentrations above 8 mug/L. For this sensor, a protocol was developed in which the sensor cells were dried on a paper strip and placed in the aqueous test solution for 30 min after which time color development was allowed to take place. The GFP sensor showed good potential for continuous rather than end point measurements. In all cases, growth of the biosensors and production of the strip test was achieved by very simple means with common growth media, and quality control of the sensors was performed by isolating the respective plasmids with the genetic constructs according to simple standard genetic technologies. Therefore, the biosensor cells and protocols may offer a realistic alternative for measuring arsenic contamination in potable water.
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收藏
页码:4743 / 4750
页数:8
相关论文
共 25 条
[1]  
Abernathy C, 1999, ARSENIC EXPOSURE HLT
[2]  
[Anonymous], WC0019 BGS
[3]   THE ARS OPERON OF ESCHERICHIA-COLI CONFERS ARSENICAL AND ANTIMONIAL RESISTANCE [J].
CARLIN, A ;
SHI, WP ;
DEY, S ;
ROSEN, BP .
JOURNAL OF BACTERIOLOGY, 1995, 177 (04) :981-986
[4]   Genetically engineered whale-cell sensing systems: Coupling biological recognition with reporter genes [J].
Daunert, S ;
Barrett, G ;
Feliciano, JS ;
Shetty, RS ;
Shrestha, S ;
Smith-Spencer, W .
CHEMICAL REVIEWS, 2000, 100 (07) :2705-2738
[5]   Solar oxidation and removal of arsenic at circumneutral pH in iron containing waters [J].
Hug, SJ ;
Canonica, L ;
Wegelin, M ;
Gechter, D ;
Von Gunten, U .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (10) :2114-2121
[6]   HbpR, a new member of the XylR/DmpR subclass within the NtrC family of bacterial transcriptional activators, regulates expression of 2-hydroxybiphenyl metabolism in Pseudomonas azelaica HBP1 [J].
Jaspers, MCM ;
Suske, WA ;
Schmid, A ;
Goslings, DAM ;
Kohler, HPE ;
van der Meer, JR .
JOURNAL OF BACTERIOLOGY, 2000, 182 (02) :405-417
[7]   Measuring mass transfer processes of octane with the help of an alkS-alkB::gfp-tagged Escherichia coli [J].
Jaspers, MCM ;
Meier, C ;
Zehnder, AJB ;
Harms, H ;
van der Meer, JR .
ENVIRONMENTAL MICROBIOLOGY, 2001, 3 (08) :512-524
[8]   PLASMID-ENCODED RESISTANCE TO ARSENIC AND ANTIMONY [J].
KAUR, P ;
ROSEN, BP .
PLASMID, 1992, 27 (01) :29-40
[9]   STRUCTURE AND TRANSCRIPTIONAL REGULATION OF THE ESCHERICHIA-COLI ADAPTIVE RESPONSE GENE AIDB [J].
LANDINI, P ;
HAJEC, LI ;
VOLKERT, MR .
JOURNAL OF BACTERIOLOGY, 1994, 176 (21) :6583-6589
[10]   A SIMPLIFIED LIQUID-DRYING METHOD FOR THE PRESERVATION OF MICROORGANISMS SENSITIVE TO FREEZING AND FREEZE-DRYING [J].
MALIK, KA .
JOURNAL OF MICROBIOLOGICAL METHODS, 1990, 12 (02) :125-132