4.7 Article

Genome Sequence, Proteome Profile, and Identification of a Multiprotein Reductive Dehalogenase Complex in Dehalogenimonas alkenigignens Strain BRE15M

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 20, Issue 1, Pages 613-623

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jproteome.0c00569

Keywords

organohalide respiration; dihaloelimination; Dehalogenimonas alkenigignens strain BRE15M; Dehalococcoidia; genome sequencing; 1,2-dichloropropane; proteome profiling

Funding

  1. Spanish Ministry of Economy and Competitiveness State Research Agency - European Union through the European Regional Development Fund (ERDF) [CTM2016-75587-C2-1-R, PID2019-103989RB-100]
  2. Generalitat de Catalunya (Consolidate Research Group) [2017-SGR-14]
  3. MINECO [BES-2014070817]
  4. German Academic Exchange Service (DAAD) scholarship [91726320]
  5. Austrian Science Fund (FWF) [P29246-B29]
  6. European regional development funds (EFRE-Europe Funds Saxony)
  7. Helmholtz Association
  8. German Research Council (DFG) [FOR1530, SPP1927]
  9. Biomedical Sequencing Facility (BSF) of Vienna, Austria

Ask authors/readers for more resources

The study focused on the respiratory mechanism of Dehalogenimonas bacteria, specifically how they respire with vicinally halogenated alkanes. Genomic and proteomic analyses revealed a complex system involving various proteins, with the discovery of new protein components in protein complexes. The proposed quinone-independent respiration in Dehalogenimonas suggests a unique pathway for organohalide respiration.
Bacteria of the genus Dehalogenimonas respire with vicinally halogenated alkanes via dihaloelimination. We aimed to describe involved proteins and their supermolecular organization. Metagenomic sequencing of a Dehalogenimonas-containing culture resulted in a 1.65 Mbp draft genome of Dehalogenimonas alkenigignens strain BRE15M. It contained 31 full-length reductive dehalogenase homologous genes (rdhA), but only eight had cognate rdhB gene coding for membrane-anchoring proteins. Shotgun proteomics of cells grown with 1,2-dichloropropane as an electron acceptor identified 1152 proteins representing more than 60% of the total proteome. Ten RdhA proteins were detected, including a DcpA ortholog, which was the strongest expressed RdhA. Blue native gel electrophoresis (BNE) demonstrating maximum activity was localized in a protein complex of 146-242 kDa. Protein mass spectrometry revealed the presence of DcpA, its membrane-anchoring protein DcpB, two hydrogen uptake hydrogenase subunits (HupL and HupS), an iron-sulfur protein (HupX), and subunits of a redox protein with a molybdopterin-binding motif (OmeA and OmeB) in the complex. BNE after protein solubilization with different detergent concentrations revealed no evidence for an interaction between the putative respiratory electron input module (HupLS) and the OmeA/OmeB/HupX module. All detected RdhAs comigrated with the organohalide respiration complex. Based on genomic and proteomic analysis, we propose quinoneindependent respiration in Dehalogenimonas.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available