4.7 Article

Biotransformation of 6:2 fluorotelomer alcohol by the whole soybean (Glycine max L. Merrill) seedlings

Journal

ENVIRONMENTAL POLLUTION
Volume 257, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.envpol.2019.113513

Keywords

6:2 Fluorotelomer alcohol; Perfluorocarboxylic acid; Biotransformation; GSH-Conjugated metabolite; Soybean

Funding

  1. National Natural Science Foundation of China [41671465, 21537005, 21806134, 21621064]
  2. General Research Fund of Hong Kong Research Grants Council [12301518]

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Fluorotelomer alcohols (FTOHs) are important precursors of perfluorocarboxylic acids (PFCAs) in the environment and biota. With the growing application of 6:2 FTOH [F(CF2)(6)CH2CH2OH] in product formulation, it is becoming increasingly urgent to investigate its biological fates in different species. In this study, biotransformation of 6:2 FTOH by young soybean plants (Glycine max L Merrill) were investigated using hydroponic experiments. During the 144 h-exposure, 6:2 FTCA [F(CF2)(6)CH2COOH], 6:2 FTUCA [F(CF2)(5)CF=CHCOOH], 5:3 FTUCA [F(CF2)(5)CH=CHCOOH], 5:3 FTCA [F(CF2)(5)CH2CH2COOH}, PFHxA [F(CF2)(5)COOH] and PFPeA [F(CF2)(4)COOH] were phase I metabolites in soybean. At the end of exposure, 5:3 FTCA (5.08 mol%), PFHxA (234 mol%) and PFPeA (0.58 mol%) were three main metabolites in soybean-solution system. 5:3 FTCA was predominant in soybean roots and stems, while PFHxA was the most abundant product in leaves. PFBA [F(CF2)(3)COOH] and 4:3 FTCA [F(CF2)(4)CH2CH2COOH] detected in the hydroponic solution most-likely came from the transformation of 5:3 FTCA by root-associated microbes. Moreover, phase II metabolites of 6:2 FTOH were identified and monitored in soybean tissues. Alcohol dehydrogenase, aldehyde dehydrogenase and glutathione S-transferase were found to participate in 6:2 FTOH metabolism. Based on the phase I and phase II metabolism of 6:2 FTOH in soybean, this study for the first time provides evidences for the transformation pathways of 6:2 FTOH in plants. (C) 2019 Published by Elsevier Ltd.

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