Institute of Science, Nirma University, Sarkhej-Gandhinagar Highway, Ahmedabad, 382481, Gujarat, India.
Division of Biotechnology and Phycology, CSIR Central Salt and Marine Chemicals Research Institute, Bhavnagar, Gujarat, India.
Ecotoxicol Environ Saf. 2019 Oct 30;182:109450. doi: 10.1016/j.ecoenv.2019.109450. Epub 2019 Jul 23.
The major sources for release of hydrocarbons into the environment include the effluents generated from chemical processing industries and ports. The introduction of such hazardous compounds into natural water bodies creates considerable disturbances in aquatic life and causes a threat to humans. Thus, it is essential to detect and quantify pollutants at various stages of the wastewater generation and treatment before they reach natural aquatic environments and contaminate them. This study reports the development of "biosensing strains" by cloning hydrocarbon recognizing promoter-operator and a reporter gene in bacterial strains for sensing the presence of pollutants at their lowest possible concentration. So far, various biosensing strains have been constructed with a fused promoter-operator region of the hydrocarbon degrading operons, but most of them use luxAB as a reporter gene. A novel approach in the present study aimed at constructing strains harboring two different fluorescent protein (FP)-based reporter genes for the quantification of multiple pollutants at a time. Two vectors were designed with a fusion of tbuT-gfp and phnR-cfp for the quantification of mono- and poly-aromatic hydrocarbons, respectively. The designed vectors were transformed into E. coli DH5α, and these strains were designated as E. coli DH5α 2296-gfp (containing pPROBE-Tbut-RBS-gfp-npt) and E. coli DH5α 2301-cfp (containing pPROBE-phn-RBS-cfp-npt). Both the developed recombinant strains were capable of successfully detecting mono- and poly-aromatic hydrocarbons in the range of 1-100 μM. The sensing capacity of recombinant strains was successfully validated with actual wastewater samples against available physico-chemical analytical techniques. The development of such recombinant microbial strains indicates the future for online contaminant detection, treatment quality monitoring and protection of aquatic flora and fauna.
烃类向环境中释放的主要来源包括化学加工工业和港口产生的废水。这些危险化合物被引入天然水体中,会对水生生物造成严重干扰,并对人类构成威胁。因此,在这些废水到达自然水生环境并造成污染之前,有必要在各个生成和处理阶段检测和量化污染物。本研究报告了通过克隆烃类识别启动子-操纵子和报告基因,在细菌菌株中开发“生物感应菌株”的方法,以在最低可能浓度下检测污染物的存在。到目前为止,已经构建了各种带有烃类降解操纵子融合启动子-操纵子区域的生物感应菌株,但大多数都使用 luxAB 作为报告基因。本研究的一个新方法旨在构建同时定量多种污染物的两个不同荧光蛋白(FP)-基于报告基因的菌株。设计了两个带有 tbuT-gfp 和 phnR-cfp 融合的载体,分别用于单环和多环芳烃的定量。设计的载体被转化为大肠杆菌 DH5α,这些菌株被命名为大肠杆菌 DH5α 2296-gfp(含有 pPROBE-Tbut-RBS-gfp-npt)和大肠杆菌 DH5α 2301-cfp(含有 pPROBE-phn-RBS-cfp-npt)。这两个开发的重组菌株都能够成功地检测 1-100μM 范围内的单环和多环芳烃。通过与现有物理化学分析技术相比,对实际废水样品对重组菌株的感应能力进行了成功验证。这种重组微生物菌株的开发为在线污染物检测、处理质量监测以及保护水生动植物提供了未来的方向。