Guzzo J, Guzzo A, DuBow M S
McGill University, Department of Microbiology and Immunology, Montreal, Quebec, Canada.
Toxicol Lett. 1992 Dec;64-65 Spec No:687-93. doi: 10.1016/0378-4274(92)90248-i.
Luciferase-based biosensors are becoming increasingly used for environmental monitoring. A transcriptional fusion of the Vibrio harveyi luxAB genes (encoding bacterial luciferase) to the fliC gene of Escherichia coli was constructed and luminescence shown to be induced (in liquid media) in the presence of 1-10 micrograms/ml aluminum, but not copper, iron or nickel. Moreover, luminescence is markedly increased at pH 5.5, where aluminum is more soluble than at pH 7.0. However, aluminum also stimulated luciferase activity when the luxAB genes were located in the xyl operon. This suggests that aluminum stimulates luciferase enzyme activity in vivo. These results are specific to E. coli, as no such aluminum stimulation was observed in the luminescent bacterium V. harveyi. These results have important implications in the generalized use of these clones for environmental monitoring, where aluminum can be present at elevated concentrations.
基于荧光素酶的生物传感器正越来越多地用于环境监测。构建了哈维氏弧菌luxAB基因(编码细菌荧光素酶)与大肠杆菌fliC基因的转录融合体,并显示在存在1 - 10微克/毫升铝的情况下(在液体培养基中)发光被诱导,而在铜、铁或镍存在时则不发光。此外,在pH 5.5时发光明显增强,此时铝的溶解度比在pH 7.0时更高。然而,当luxAB基因位于木糖操纵子时,铝也刺激荧光素酶活性。这表明铝在体内刺激荧光素酶的酶活性。这些结果是大肠杆菌特有的,因为在发光细菌哈维氏弧菌中未观察到这种铝刺激现象。这些结果对于将这些克隆广泛用于环境监测具有重要意义,因为环境中铝的浓度可能会升高。