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两种新型基于超氧化物歧化酶 MnSod 和 FeSod 的蓝细菌生物发光全细胞生物报告器,用于检测超氧阴离子。

Two novel cyanobacterial bioluminescent whole-cell bioreporters based on superoxide dismutases MnSod and FeSod to detect superoxide anion.

机构信息

Departamento de Biología, Facultad de Ciencias, Universidad Autónoma de Madrid, 28049 Madrid, Spain.

Departamento de Ingeniería Química, Universidad de Alcalá, E-28871 Alcalá de Henares, Madrid, Spain.

出版信息

Chemosphere. 2018 Jun;201:772-779. doi: 10.1016/j.chemosphere.2018.03.012. Epub 2018 Mar 3.

Abstract

This work describes the construction of two novel self-luminescent bioreporter strains of the cyanobacterium Nostoc sp. PCC 7120 by fusing the promoter region of the sodA and sodB genes (encoding the superoxide dismutases MnSod and FeSod, respectively) to luxCDABE from Photorhabdus luminescens aimed at detecting pollutants that generate reactive oxygen species (ROS), particularly O. Bioreporters were tested against methyl viologen (MV) as the inducer of superoxide anion (O). Both bioreporters were specific for O and Limits of detection (LODs) and Maximum Permissive Concentrations (MPCs) were calculated: Nostoc sp. PCC 7120 pBG2154 (sodA) had a range of detection from 400 to 1000 pM of MV and for Nostoc sp. PCC 7120 pBG2165 (sodB) the range of detection was from 500 to 1800 pM of MV after 5 h-exposure. To further validate the bioreporters, they were tested with the emerging pollutant Triclosan which induced bioluminescence in both strains. Furthermore, the bioreporters performance was tested in two real environmental samples with different water matrix complexity, spiked with MV. Both bioreporters were induced by O in these environmental samples. In the case of the river water sample, the amount of bioavailable MV as calculated from the bioreporters output was similar to that nominally added. For the waste water sample, the bioavailable MV concentration detected by the bioreporters was one order of magnitude lower than nominal. These differences could be due to MV complexation with organic matter and/or co-occurring organic contaminants. These results confirm their high sensitivity to O and their suitability to detect oxidative stress-generating pollutants in fresh-waters.

摘要

这项工作描述了通过融合 sodA 和 sodB 基因(分别编码超氧化物歧化酶 MnSod 和 FeSod)的启动子区域到 Photorhabdus luminescens 的 luxCDABE 来构建两种新型自发光生物报告株的方法,旨在检测产生活性氧物种(ROS)的污染物,特别是 O。生物报告株针对甲基紫精(MV)作为超氧阴离子(O)的诱导剂进行了测试。两种生物报告株均对 O 具有特异性,并且计算了检测限(LOD)和最大允许浓度(MPC): Nostoc sp. PCC 7120 pBG2154(sodA)的检测范围为 400 至 1000 pM MV,而 Nostoc sp. PCC 7120 pBG2165(sodB)的检测范围为 500 至 1800 pM MV,暴露 5 小时后。为了进一步验证生物报告株,用新兴污染物三氯生对其进行了测试,该污染物在两种菌株中均诱导了生物发光。此外,还在两种具有不同水基质复杂性的实际环境样品中用 MV 对生物报告株进行了测试。在这些环境样品中,O 诱导了两种生物报告株。在河水样品的情况下,根据生物报告株的输出计算出的可利用 MV 量与名义添加的量相似。对于废水样品,生物报告株检测到的可利用 MV 浓度比名义浓度低一个数量级。这些差异可能是由于 MV 与有机物的络合以及/或共存的有机污染物所致。这些结果证实了它们对 O 的高灵敏度及其适合检测淡水产生氧化应激的污染物。

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