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1.
Environ Pollut ; 142(1): 17-23, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16298031

ABSTRACT

A green fluorescent protein (GFP)-based bacterial biosensor Escherichia coli DH5alpha (pVLCD1) was developed based on the expression of gfp under the control of the cad promoter and the cadC gene of Staphylococcus aureus plasmid pI258. DH5alpha (pVLCD1) mainly responded to Cd(II), Pb(II), and Sb(III), the lowest detectable concentrations being 0.1 nmol L(-1), 10 nmol L(-1), and 0.1 nmol L(-1), respectively, with 2h exposure. The biosensor was field-tested to measure the relative bioavailability of the heavy metals in contaminated sediments and soil samples. The results showed that the majority of heavy metals remained adsorbed to soil particles: Cd(II)/Pb(II) was only partially available to the biosensor in soil-water extracts. Our results demonstrate that the GFP-based bacterial biosensor is useful and applicable in determining the bioavailability of heavy metals with high sensitivity in contaminated sediment and soil samples and suggests a potential for its inexpensive application in environmentally relevant sample tests.


Subject(s)
Biosensing Techniques , Environmental Monitoring/methods , Escherichia coli/metabolism , Green Fluorescent Proteins , Metals, Heavy/analysis , Soil Pollutants/analysis , Biological Availability , Cadmium/analysis , Geologic Sediments , Lead/analysis , Microscopy, Fluorescence , Soil , Tin/analysis , Zinc/analysis
2.
Environ Toxicol Chem ; 24(7): 1624-31, 2005 Jul.
Article in English | MEDLINE | ID: mdl-16050578

ABSTRACT

A green fluorescent protein (GFP)-based bacterial biosensor for the detection of bioavailable As(III), As(V), and Sb(III) was developed and characterized. The biosensor strain Escherichia coli DH5alpha (pVLAS1) was developed based on the expression of gfp under the control of the ars promoter and the arsR gene of Staphylococcus aureus plasmid pI258. Strain DH5alpha (pVLAS1) responded mainly to As(III), As(V), and Sb(III), with the lowest detectable concentrations being 0.4, 1, and 0.75 microM, respectively, during a 2-h exposure and 0.1 microM for all three metal ions with an 8-h induction period. To assess its applicability for analyzing environmentally relevant samples, the biosensor was field-tested on shallow-well groundwater for which contaminant levels were known. Our results demonstrate that the nonpathogenic bacterial biosensor developed in the present study is useful and applicable in determining the bioavailability of arsenic with high sensitivity in contaminated groundwater samples, and they suggest a potential for its inexpensive application in field-ready tests.


Subject(s)
Arsenic/pharmacokinetics , Biosensing Techniques , Green Fluorescent Proteins/chemistry , Water Pollutants, Chemical/pharmacokinetics , Base Sequence , Biological Availability , DNA Primers , Escherichia coli , Kinetics , Plasmids , Sensitivity and Specificity , Staphylococcus aureus
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