4.7 Article

Transformation of short-chain chlorinated paraffins by the bacterial haloalkane dehalogenase LinB - Formation of mono- and di-hydroxylated metabolites

Journal

CHEMOSPHERE
Volume 262, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2020.128288

Keywords

Haloalkane dehalogenase LinB; Chlorinated olefins (COs); Chlorinated paraffins (CPs); Hydroxylated chlorinated paraffins; Persistent organic pollutants (POPs)

Funding

  1. Swiss Federal Office for the Environment (BAFU) [19.0011, PJ/S113-1600]

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Short-chain chlorinated paraffins (SCCPs) are persistent organic pollutants listed under the Stockholm Convention. Certain bacterial strains can degrade SCCPs, with the enzyme LinB catalyzing the conversion of chlorinated tridecanes to hydroxylated compounds. LC-MS analysis revealed the formation of various hydroxylated products after exposure to LinB, suggesting its potential for environmental remediation.
Short-chain chlorinated paraffins (SCCPs) are listed as persistent organic pollutants (POPs) under the Stockholm Convention. Such substances are toxic, bioaccumulating, transported over long distances and degrade slowly in the environment. Certain bacterial strains of the Sphingomonadacea family are able to degrade POPs, such as hexachlorocyclohexanes (HCHs) and hexabromocyclododecanes (HBCDs). The haloalkane dehalogenase LinB, expressed in certain Sphingomonadacea, is able to catalyze the transformation of haloalkanes to hydroxylated compounds. Therefore, LinB is a promising candidate for conversion of SCCPs. Hence, a mixture of chlorinated tridecanes was exposed in vitro to LinB, which was obtained through heterologous expression in Escherichia coli. Liquid chromatography mass spectrometry (LC-MS) was used to analyze chlorinated tridecanes and their transformation products. A chloride-enhanced soft ionization method, which favors the formation of chloride adducts [M+Cl](-) without fragmentation, was applied. Mathematical deconvolution was used to distinguish interfering mass spectra of paraffinic, mono-olefinic and di-olefinic compounds. Several mono- and di-hydroxylated products including paraffinic, mono-olefinic and di-olefinic compounds were found after LinB exposure. Mono- (rt = 5.9-6.9 min) and di-hydroxylated (rt = 3.2-4.5 min) compounds were separated from starting material (rt = 7.7-8.5 min) by reversed phase LC. Chlorination degrees of chlorinated tridecanes increased during LinB-exposure from n(Cl )= 8.80 to 9.07, indicating a preferential transformation of lower chlorinated (Cl-<9) tridecanes. Thus, LinB indeed catalyzed a dehalohydroxylation of chlorinated tridecanes, tridecenes and tridecadienes. The observed hydroxylated compounds are relevant CP transformation products whose environmental and toxicological effects should be further investigated. (C) 2020 The Author(s). Published by Elsevier Ltd.

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