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通过诱导热休克基因-生物发光基因融合实现快速灵敏的污染物检测。

Rapid and sensitive pollutant detection by induction of heat shock gene-bioluminescence gene fusions.

作者信息

Van Dyk T K, Majarian W R, Konstantinov K B, Young R M, Dhurjati P S, LaRossa R A

机构信息

DuPont Company, Wilmington, Delaware 19880.

出版信息

Appl Environ Microbiol. 1994 May;60(5):1414-20. doi: 10.1128/aem.60.5.1414-1420.1994.

DOI:10.1128/aem.60.5.1414-1420.1994
PMID:8017928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC201497/
Abstract

Heat shock gene expression is induced by a variety of environmental stresses, including the presence of many chemicals. To address the utility of this response for pollutant detection, two Escherichia coli heat shock promoters, dnaK and grpE, were fused to the lux genes of Vibrio fischeri. Metals, solvents, crop protection chemicals, and other organic molecules rapidly induced light production from E. coli strains containing these plasmid-borne fusions. Introduction of an outer membrane mutation, tolC, enhanced detection of a hydrophobic molecule, pentachlorophenol. The maximal response to pentachlorophenol in the tolC+ strain was at 38 ppm, while the maximal response in an otherwise isogenic tolC mutant was at 1.2 ppm. Stress responses were observed in both batch and chemostat cultures. It is suggested that biosensors constructed in this manner may have potential for environmental monitoring.

摘要

热休克基因表达可由多种环境压力诱导,包括许多化学物质的存在。为了探究这种反应在污染物检测中的效用,将两个大肠杆菌热休克启动子dnaK和grpE与费氏弧菌的lux基因融合。金属、溶剂、农作物保护化学品和其他有机分子能迅速诱导含有这些质粒携带融合体的大肠杆菌菌株发光。引入外膜突变tolC可增强对疏水分子五氯苯酚的检测。tolC+菌株对五氯苯酚的最大反应浓度为38 ppm,而在其他方面同基因的tolC突变体中的最大反应浓度为1.2 ppm。在分批培养和恒化器培养中均观察到应激反应。有人认为,以这种方式构建的生物传感器可能具有环境监测的潜力。

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本文引用的文献

1
The application of lux genes.lux基因的应用。
Biotechnol Appl Biochem. 1993 Feb;17(1):3-14.
2
An improved bacterial test system for the detection and classification of mutagens and carcinogens.一种用于检测诱变剂和致癌物并对其进行分类的改良细菌检测系统。
Proc Natl Acad Sci U S A. 1973 Mar;70(3):782-6. doi: 10.1073/pnas.70.3.782.
3
Consensus sequence for Escherichia coli heat shock gene promoters.大肠杆菌热休克基因启动子的共有序列。
Proc Natl Acad Sci U S A. 1985 May;82(9):2679-83. doi: 10.1073/pnas.82.9.2679.
4
Differential induction of heat shock, SOS, and oxidation stress regulons and accumulation of nucleotides in Escherichia coli.大肠杆菌中热休克、SOS和氧化应激调节子的差异诱导及核苷酸积累
J Bacteriol. 1987 Jan;169(1):26-32. doi: 10.1128/jb.169.1.26-32.1987.
5
The use of operon fusions in studies of the heat-shock response: effects of altered sigma 32 on heat-shock promoter function in Escherichia coli.操纵子融合在热休克反应研究中的应用:σ32改变对大肠杆菌热休克启动子功能的影响。
Mol Gen Genet. 1987 Apr;207(1):24-8. doi: 10.1007/BF00331486.
6
Sequence analysis and transcriptional regulation of the Escherichia coli grpE gene, encoding a heat shock protein.编码一种热休克蛋白的大肠杆菌grpE基因的序列分析及转录调控
Nucleic Acids Res. 1988 Aug 11;16(15):7545-62. doi: 10.1093/nar/16.15.7545.
7
The physical map of the whole E. coli chromosome: application of a new strategy for rapid analysis and sorting of a large genomic library.完整大肠杆菌染色体的物理图谱:一种用于大型基因组文库快速分析和分类的新策略的应用
Cell. 1987 Jul 31;50(3):495-508. doi: 10.1016/0092-8674(87)90503-4.
8
Functional identification of the fatty acid reductase components encoded in the luminescence operon of Vibrio fischeri.
J Bacteriol. 1985 Sep;163(3):1186-90. doi: 10.1128/jb.163.3.1186-1190.1985.
9
Regulation of the vir genes of Agrobacterium tumefaciens plasmid pTiC58.根癌土壤杆菌质粒pTiC58的vir基因调控
J Bacteriol. 1987 Nov;169(11):5101-12. doi: 10.1128/jb.169.11.5101-5112.1987.
10
The heat-shock-regulated grpE gene of Escherichia coli is required for bacterial growth at all temperatures but is dispensable in certain mutant backgrounds.大肠杆菌中受热激调节的grpE基因是细菌在所有温度下生长所必需的,但在某些突变背景下是可有可无的。
J Bacteriol. 1989 May;171(5):2748-55. doi: 10.1128/jb.171.5.2748-2755.1989.