Affiliations 

  • 1 Institute of Plant Science and Resources, Okayama University, 2-20-1, Chuo, Kurashiki, 710-0046, Japan; Southeast Asia Disaster Prevention Research Initiative (SEADPRI-UKM), Institute for Environment and Development (LESTARI), The National University of Malaysia, 43600, Bangi, Selangor, Malaysia. Electronic address: ooi@okayama-u.ac.jp
  • 2 Institute of Plant Science and Resources, Okayama University, 2-20-1, Chuo, Kurashiki, 710-0046, Japan
  • 3 Institute of Plant Science and Resources, Okayama University, 2-20-1, Chuo, Kurashiki, 710-0046, Japan; Product Stewardship & Toxicology Department, Group Health, Safety, Security & Environment, Petroliam Nasional Berhad (PETRONAS), 50088, Kuala Lumpur, Malaysia
  • 4 Southeast Asia Disaster Prevention Research Initiative (SEADPRI-UKM), Institute for Environment and Development (LESTARI), The National University of Malaysia, 43600, Bangi, Selangor, Malaysia; Faculty of Science and Technology, The National University of Malaysia, 43600, Bangi, Selangor, Malaysia
  • 5 Institute of Plant Science and Resources, Okayama University, 2-20-1, Chuo, Kurashiki, 710-0046, Japan. Electronic address: imori@okayama-u.ac.jp
Chemosphere, 2020 May;247:125933.
PMID: 32079055 DOI: 10.1016/j.chemosphere.2020.125933

Abstract

Toxicity Identification Evaluation (TIE) is a useful method for the classification and identification of toxicants in a composite environment water sample. However, its extension to a larger sample size has been restrained owing to the limited throughput of toxicity bioassays. Here we reported the development of a high-throughput method of TIE Phase I. This newly developed method was assisted by the fluorescence-based cellular oxidation (CO) biosensor fabricated with roGFP2-expressing bacterial cells in 96-well microplate format. The assessment of four river water samples from Langat river basin by this new method demonstrated that the contaminant composition of the four samples can be classified into two distinct groups. The entire toxicity assay consisted of 2338 tests was completed within 12 h with a fluorescence microplate reader. Concurrently, the sample volume for each assay was reduced to 50 μL, which is 600 to 4700 times lesser to compare with conventional bioassays. These imply that the throughput of the CO biosensor-assisted TIE Phase I is now feasible for constructing a large-scale toxicity monitoring system, which would cover a whole watershed scale.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.