Construction and characterization of novel dual stress-responsive bacterial biosensors

被引:30
|
作者
Mitchell, RJ [1 ]
Gu, MB [1 ]
机构
[1] Kwangju Inst Sci & Technol, Dept Environm Sci & Engn, Natl Res Lab Environm Biotechnol, Gwangju 500712, South Korea
来源
BIOSENSORS & BIOELECTRONICS | 2004年 / 19卷 / 09期
关键词
bacterial biosensor; bioluminescence; green fluorescent protein; genotoxin; oxidative damage; stress;
D O I
10.1016/j.bios.2003.09.002
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Using the genes for the green fluorescence protein and Xenorhabdus huninescens luciferase operon and the promoters for the recA and katG genes, two stress-responsive Escherichia coli biosensor strains have been constructed that can individually or concurrently respond to oxidative and genotoxic conditions. Strain DUO-1 carries the pRGDK1 plasmid, which has the recA::GFPuv4 and katG::luxCDABE fusion genes oriented divergently with each other, while in DUO-2, i.e., pRGDK2, they are in a tandem orientation, with the recA promoter showing run-though transcription of the katG::luxCDABE fusion. These two strains and their responses were characterized using several known hydroxyl radical-forming chemicals, e.g., hydrogen peroxide and cadmium chloride, along with some genotoxins, e.g., mitomycin C and methyl-N-nitro-N-nitrosoguanidine and sonic general toxicants. Both strains showed an induction of green fluorescent protein (GFP) and bioluminescence when they experienced DNA and oxidative damage, respectively, while the tandem orientation of the two fusion genes within DUO-2 allowed it to also sensitively respond to genotoxins via the production of bioluminescence. However, the characteristics of DUO-2's bioluminescent response to each stress were easily distinguishable, making it useful for the detection of both stresses. Furthermore, tests with mixtures of chemicals showed that both DUO-1 and DUO-2 were responsive when chemicals causing oxidative or genotoxic stress were present as a single chemical or within complex chemical mixtures. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:977 / 985
页数:9
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