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At groundwater sites contaminated with chlorinated ethenes, fermentable substrates are often added to promote reductive dehalogenation by indigenous or augmented microorganisms. Contemporary bioremediation performance monitoring relies on nucleic acid biomarkers of key organohalide-respiring bacteria, such as (). Metagenome sequencing of the commercial, -containing consortium, SDC-9, identified 12 reductive dehalogenase (RDase) genes, including (two copies), , and , and allowed for specific detection and quantification of RDase peptides using liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS). Shotgun (i.e., untargeted) proteomics applied to the SDC-9 consortium grown with tetrachloroethene (PCE) and lactate identified 143 RDase peptides, and 36 distinct peptides that covered greater than 99% of the protein-coding sequences of the PceA, TceA, and VcrA RDases. Quantification of RDase peptides using multiple reaction monitoring (MRM) assays with C-/N-labeled peptides determined 1.8 × 10 TceA and 1.2 × 10 VcrA RDase molecules per cell. The MRM mass spectrometry approach allowed for sensitive detection and accurate quantification of relevant RDases and has potential utility in bioremediation monitoring regimes.
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http://dx.doi.org/10.1021/acs.jproteome.0c00072 | DOI Listing |
J Proteome Res
April 2020
Department of Microbiology, University of Tennessee, 1311 Cumberland Avenue, Knoxville, Tennessee 37996, United States.
At groundwater sites contaminated with chlorinated ethenes, fermentable substrates are often added to promote reductive dehalogenation by indigenous or augmented microorganisms. Contemporary bioremediation performance monitoring relies on nucleic acid biomarkers of key organohalide-respiring bacteria, such as (). Metagenome sequencing of the commercial, -containing consortium, SDC-9, identified 12 reductive dehalogenase (RDase) genes, including (two copies), , and , and allowed for specific detection and quantification of RDase peptides using liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS).
View Article and Find Full Text PDFSci Rep
July 2019
Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee, 37831, United States.
Dehalococcoides mccartyi (Dhc) bacterial strains expressing active reductive dehalogenase (RDase) enzymes play key roles in the transformation and detoxification of chlorinated pollutants, including chlorinated ethenes. Site monitoring regimes traditionally rely on qPCR to assess the presence of Dhc biomarker genes; however, this technique alone cannot directly inform about dechlorination activity. To supplement gene-centric approaches and provide a more reliable proxy for dechlorination activity, we sought to demonstrate a targeted proteomics approach that can characterize Dhc mediated dechlorination in groundwater contaminated with chlorinated ethenes.
View Article and Find Full Text PDFAppl Environ Microbiol
July 2015
Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, Ontario, Canada
Many reductive dehalogenases (RDases) have been identified in organohalide-respiring microorganisms, and yet their substrates, specific activities, and conditions for expression are not well understood. We tested whether RDase expression varied depending on the substrate-exposure history of reductive dechlorinating communities. For this purpose, we used the enrichment culture KB-1 maintained on trichloroethene (TCE), as well as subcultures maintained on the intermediates cis-dichloroethene (cDCE) and vinyl chloride (VC).
View Article and Find Full Text PDFPhilos Trans R Soc Lond B Biol Sci
April 2013
Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, Ontario, Canada.
Two novel reductive dehalogenases (RDases) that are highly similar to each other but catalyse distinct dechlorination reactions were identified from Dehalobacter-containing mixed cultures. These two RDases were partially purified from crude protein extracts of anaerobic dechlorinating enrichment cultures using blue native polyacrylamide gel electrophoresis. Gel slices were assayed for dechlorinating activity, and associated proteins were identified using liquid chromatography tandem mass spectrometry with the metagenome of the parent culture as the reference database.
View Article and Find Full Text PDFAppl Environ Microbiol
January 2007
Civil and Environmental Engineering, Cornell University, Ithaca, NY 14853, USA.
Anaerobic reductive dehalogenation by Dehalococcoides spp. is an ideal system for studying functional diversity of closely related strains of bacteria. In Dehalococcoides spp.
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