Triple-element compound-specific stable isotope analysis of 1,2-dichloroethane for characterization of the underlying dehalogenation reaction in two Dehalococcoides mccartyi strains

Steffi Franke, Christina Lihl, Julian Renpenning, Martin Elsner, Ivonne Nijenhuis

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22 Scopus citations

Abstract

Chlorinated ethanes belong to the most common groundwater and soil contaminants. Of these, 1,2-dichloroethane (1,2-DCA) is a man-made, persistent and toxic contaminant, released due to improper waste treatment at versatile production sites. This study investigated the anaerobic transformation of 1,2-DCA by Dehalococcoides mccartyi strain 195 and strain BTF08 using triple-element compound-specific stable isotope analysis of carbon, chlorine and hydrogen for the first time. Isotope fractionation patterns for carbon (ϵCBTF08 =-28.4 ± 3.7‰; ϵC195 =-30.9 ± 3.6‰) and chlorine (ϵClBTF08 =-4.6 ± 0.7‰; ϵCl195 =-4.2 ± 0.5‰) within both investigated D. mccartyi strains, as well as the dual-element analysis (ΛBTF08 = 6.9 ± 1.2; Λ195 = 7.1 ± 0.2), supported identical reaction mechanisms for dehalogenation of 1,2-DCA. Hydrogen isotope fractionation analysis revealed dihaloelimination as prevalent reaction mechanism. Vinyl chloride as major intermediate could be excluded by performing the experiment in deuterated aqueous media. Furthermore, evaluation of the derived apparent kinetic isotope effects (AKIECBTF08 = 1.029/AKIEC195 = 1.031; AKIEClBTF08 = 1.005/AKIECl195 = 1.004) pointed towards simultaneous abstraction of both involved chlorine-substituents in a concerted matter. It was shown that D. mccartyi strain BTF08 and strain 195 are capable of complete, direct dihaloelimination of 1,2-DCA to ethene.

Original languageEnglish
Article numberfix137
JournalFEMS Microbiology Ecology
Volume93
Issue number12
DOIs
StatePublished - 1 Dec 2017

Keywords

  • 1,2-dichloroethane
  • Dehalococcoides
  • compound-specific stable isotope analysis
  • dihaloelimination
  • reductive dehalogenation

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