A phenanthrene-degrading bacterium, Sphingomonas paucimobilis EPA505 was used to construct two fluorescence-based reporter strains. Strain D harboring gfp gene was constructed to generate green fluorescence when the strain started to biodegrade phenanthrene. Strain S possessing gef gene was designed to die once phenanthrene biodegradation was initiated and thus to lose green fluorescence when visualized by a live/dead cell staining. Confocal laser scanning microscopic observation followed by image analysis demonstrates that the fluorescence intensity generated by strain D increased and the intensity by strain S decreased linearly at the phenanthrene concentration of up to 200 mg/L Such quantitative increase and decrease of fluorescence intensity in strain D (i.e., from 1 to 11.90 +/- 0.72) and strain S (from 1 to 0.40 +/- 0.07) were also evident in the presence of Ottawa sand spiked with the phenanthrene up to 1000 mg/kg. The potential use of the reporter strains in quantitatively determining biodegradable or toxic phenanthrene was discussed. (C) 2010 Elsevier Ltd. All rights reserved.
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Univ Technol MARA Selangor, Fac Pharm, Puncak Alam, Malaysia
Univ Queensland, QAEHS, Brisbane, Qld, AustraliaUniv Technol MARA Selangor, Fac Pharm, Puncak Alam, Malaysia
Abu-Bakar, A'edah
Hu, Hao
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NIEHS, Pharmacogenet Sect, Reprod & Dev Biol Lab, NIH, POB 12233, Res Triangle Pk, NC 27709 USAUniv Technol MARA Selangor, Fac Pharm, Puncak Alam, Malaysia
Hu, Hao
Lang, Matti A.
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Alar Consultants, Ctr Mol Genet, Espoo, FinlandUniv Technol MARA Selangor, Fac Pharm, Puncak Alam, Malaysia