Published March 21, 2006 | Version Published
Journal Article Open

Extracellular respiration of dimethyl sulfoxide by Shewanella oneidensis strain MR-1

  • 1. ROR icon McGill University
  • 2. ROR icon California Institute of Technology

Abstract

Shewanella species are renowned for their respiratory versatility, including their ability to respire poorly soluble substrates by using enzymatic machinery that is localized to the outside of the cell. The ability to engage in "extracellular respiration" to date has focused primarily on respiration of minerals. Here, we identify two gene clusters in Shewanella oneidensis strain MR-1 that each contain homologs of genes required for metal reduction and genes that are predicted to encode dimethyl sulfoxide (DMSO) reductase subunits. Molecular and genetic analyses of these clusters indicate that one (SO1427–SO1432) is required for anaerobic respiration of DMSO. We show that DMSO respiration is an extracellular respiratory process through the analysis of mutants defective in type II secretion, which is required for transporting proteins to the outer membrane in Shewanella. Moreover, immunogold labeling of DMSO reductase subunits reveals that they reside on the outer leaflet of the outer membrane under anaerobic conditions. The extracellular localization of the DMSO reductase in S. oneidensis suggests these organisms may perceive DMSO in the environment as an insoluble compound.

Additional Information

© 2006 by the National Academy of Sciences Edited by Harry B. Gray, California Institute of Technology, Pasadena, CA, and approved January 30, 2006 (received for review July 14, 2005) Published online before print March 14, 2006, 10.1073/pnas.0505959103 We thank the University of Southern California/Agouron Institute 2003 International Geobiology class for technical assistance in isolating type II secretion mutants and Drs. A. Komeili and L. Dietrich for helpful discussions and suggestions. We also thank J. Mui and Dr. S. K. Sears (both of the Facility for Electron Microscopy Research, McGill University) for assistance. This work was supported by grants from the Office of Naval Research, Henry Luce Foundation, Packard Foundation, and the Howard Hughes Medical Institute (to D.K.N.). H.V. acknowledges financial support from the Natural Sciences and Engineering Research Council (NSERC) of Canada. Author contributions: J.A.G., D.P.L., and D.K.N. designed research; J.A.G., H.V., and D.P.L. performed research; H.V. contributed new reagents/analytic tools; J.A.G., H.V., D.P.L., and D.K.N. analyzed data; and J.A.G. H.V., D.P.L., and D.K.N. wrote the paper. Conflict of interest statement: No conflicts declared. This paper was submitted directly (Track II) to the PNAS office.

Attached Files

Published - GRApnas06b.pdf

Files

GRApnas06b.pdf

Files (1.4 MB)

Name Size Download all
md5:6bf51bf9a9e779481a7d103271fb2bab
1.4 MB Preview Download

Additional details

Identifiers

PMCID
PMC1450229
Eprint ID
5442
Resolver ID
CaltechAUTHORS:GRApnas06b

Funding

Office of Naval Research (ONR)
Henry Luce Foundation
David and Lucile Packard Foundation
Howard Hughes Medical Institute (HHMI)
Natural Sciences and Engineering Research Council of Canada (NSERC)

Dates

Created
2006-10-17
Created from EPrint's datestamp field
Updated
2023-06-01
Created from EPrint's last_modified field

Caltech Custom Metadata

Caltech groups
Division of Geological and Planetary Sciences (GPS)