利用克隆细菌荧光素酶编码基因的大肠杆菌评价化学毒性

J. Lampinen, M. Korpela, P. Saviranta, R. Kroneld, M. Karp
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引用次数: 20

摘要

基于基因工程大肠杆菌的使用,描述了一种评价水溶液毒性的方法。在lac启动子的控制下,从哈维弧菌中克隆出编码细菌荧光素酶的基因到大肠杆菌的深粗突变体中。通过优化几个影响基因表达的参数,使该菌株的产光量稳定下来。对选定的金属和有机溶剂进行毒性测量,以确定测试菌株的敏感性。根据这些测量计算出的有效浓度表明,该方法的灵敏度与其他常用方法相同。该测试可以使用低离子强度的缓冲液进行,而发射光的稳定性没有任何显著变化。此外,该方法不需要使用特殊设备或技能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Use of Escherichia coli cloned with genes encoding bacterial luciferase for evaluation of chemical toxicity
A method for evaluation of toxicity of aqueous solutions is described based on the use of genetically engineered Escherichia coli. The genes encoding bacterial luciferase have been cloned from Vibrio harveyi to a deep rough mutant of E. coli under the control of the lac promoter. Light production by this strain has been stabilized by optimizing several parameters having an effect on the gene expression. Toxicity measurements were performed for selected metals and organic solvents to determine the sensitivity of the test strain. Effective concentrations calculated from these measurements show that this method has a sensitivity equal to other normally used methods. The test can be performed using buffers with low ionic strength without any significant change in the stability of the light emitted. Moreover, the method does not necessitate the use of special equipment or skills.
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