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pmid:32903289

Dual Element (C/Cl) Isotope Analysis Indicates Distinct Mechanisms of Reductive Dehalogenation of Chlorinated Ethenes and Dichloroethane in Dehalococcoides mccartyi Strain BTF08 With Defined Reductive Dehalogenase Inventories.

Steffi Franke · Katja Seidel · Lorenz Adrian · Ivonne Nijenhuis

Frontiers in microbiology · 2020 doi:10.3389/fmicb.2020.01507

Paper

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Experiment

complete

Data

partial

Analysis

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Execution

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title
Dual Element (C/Cl) Isotope Analysis Indicates Distinct Mechanisms of Reductive Dehalogenation of Chlorinated Ethenes and Dichloroethane in Dehalococcoides mccartyi Strain BTF08 With Defined Reductive Dehalogenase Inventories.
doi
10.3389/fmicb.2020.01507
pmid
32903289
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[0]
Steffi Franke
[1]
Katja Seidel
[2]
Lorenz Adrian
[3]
Ivonne Nijenhuis
journal
Frontiers in microbiology
year
2020
abstract
Dehalococcoides mccartyi strain BTF08 has the unique property to couple complete dechlorination of tetrachloroethene and 1,2-dichloroethane to ethene with growth by using the halogenated compounds as terminal electron acceptor. The genome of strain BTF08 encodes 20 genes for reductive dehalogenase homologous proteins (RdhA) including those described for dehalogenation of tetrachloroethene (PceA, PteA), trichloroethene (TceA) and vinyl chloride (VcrA). Thus far it is unknown under which conditions the different RdhAs are expressed, what their substrate specificity is and if different reaction mechanisms are employed. Here we found by proteomic analysis from differentially activated batches that PteA and VcrA were expressed during dechlorination of tetrachloroethene to ethene, while TceA was expressed during 1,2-dichloroethane dehalogenation. Carbon and chlorine compound-specific stable isotope analysis suggested distinct reaction mechanisms for the dechlorination of (i) cis-dichloroethene and vinyl chloride versus (ii) tetrachloroethene. This differentiation was observed independent of the expressed RdhA proteins. Differently, two stable isotope fractionation patterns were observed for 1,2-dichloroethane transformation, for cells with distinct RdhA inventories. Conclusively, we could link specific RdhA expression with functions and provide an insight into the apparently substrate-specific reaction mechanisms in the pathway of reductive dehalogenation in D. mccartyi strain BTF08. Data are available via ProteomeXchange with identifiers PXD018558 and PXD018595.
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Based on the slope of the regression a two-tailed T-test was uses to calculate the 95% confidence interval (data evaluation in Microsoft Excel).
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Dual element (C/Cl) isotope analysis indicates distinct mechanisms of reductive dehalogenation of chlorinated ethenes and dichloroethane in Dehalococcoides mccartyi strain BTF08 with defined reductive dehalogenase inventories
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Part2: Dual element (C/Cl) isotope analysis indicates distinct mechanisms of reductive dehalogenation of chlorinated ethenes and dichloroethane in Dehalococcoides mccartyi strain BTF08 with defined reductive dehalogenase inventories
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Dehalogenation Activity in Growing Cultures Correlates With Electron Acceptor Change
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Analysis of the Expression of RdhA Proteins in vivo in Response to Electron Acceptor Change
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Substrate specificity of expressed reductive dehalogenases.
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Stable Isotope Fractionation Patterns Suggest Distinct Dehalogenation Mechanisms
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PCE
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12.2 ± 2.5
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1,2-DCA
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0.89
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0.95
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0.94
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0.74
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0.63
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on mechanisms are employed. Here we found by proteomic analysis from differentially activated batch
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. Cell Harvesting and Sample Preparation for Proteomic Analysis Dehalococcoides mccartyi strain BTF
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Ratios by Gas Chromatography – Isotope Ratio Mass Spectrometry Carbon isotope ratios were determined via co
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able isotope analyses using GC-isotope ratio mass spectrometry (IRMS). The organic mixture was separated by
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Analysis of the Expression of RdhA Proteins in vivo in Response to Electron Acceptor Change The
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Complete file
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The genome of strain BTF08 encodes 20 genes for reductive dehalogenase homologous proteins (RdhA) including those described for dehalogenation of tetrachloroethene (PceA, PteA), trichloroethene (TceA) and vinyl chloride (VcrA). Thus far it is unknown under which conditions the different RdhAs are expressed, what their substrate specificity is and if different reaction mechanisms are employed. Here we found by proteomic analysis from differentially activated batches that PteA and VcrA were expressed during dechlorination of tetrachloroethene to ethene, while TceA was expressed during 1,2-dichloroethane dehalogenation. Carbon and chlorine compound-specific stable isotope analysis suggested distinct reaction mechanisms for the dechlorination of (i) cis-dichloroethene and vinyl chloride versus (ii) tetrachloroethene. This differentiation was observed independent of the expressed RdhA proteins. Differently, two stable isotope fractionation patterns were observed for 1,2-dichloroethane transformation, for cells with distinct RdhA inventories. Conclusively, we could link specific RdhA expression with functions and provide an insight into the apparently substrate-specific reaction mechanisms in the pathway of reductive dehalogenation in D. mccartyi strain BTF08. 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Here we found by proteomic analysis from differentially activated batch", ". Cell Harvesting and Sample Preparation for Proteomic Analysis Dehalococcoides mccartyi strain BTF", "Ratios by Gas Chromatography – Isotope Ratio Mass Spectrometry Carbon isotope ratios were determined via co", "able isotope analyses using GC-isotope ratio mass spectrometry (IRMS). The organic mixture was separated by"], "order_basis": "paper_text_order:823", "id": "assay:1"}, {"role": "data_generation", "definition_id": "animal_model", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.77, "evidence": ["Analysis of the Expression of RdhA Proteins in vivo in Response to Electron Acceptor Change The"], "order_basis": "paper_text_order:5983", "id": "assay:2"}]}