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Roles of the Sodium-Translocating NADH:Quinone Oxidoreductase (Na⁺-NQR) on Vibrio cholerae Metabolism, Motility and Osmotic Stress Resistance

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Title Roles of the Sodium-Translocating NADH:Quinone Oxidoreductase (Na⁺-NQR) on Vibrio cholerae Metabolism, Motility and Osmotic Stress Resistance
Names Minato, Yusuke (creator)
Fassio, Sara R. (creator)
Kirkwood, Jay S. (creator)
Halang, Petra (creator)
Quinn, Matthew J. (creator)
Faulkner, Wyatt J. (creator)
Aagesen, Alisha M. (creator)
Steuber, Julia (creator)
Stevens, Jan F. (creator)
Häse, Claudia C. (creator)
Date Issued 2014-05-08 (iso8601)
Note This is the publisher’s final pdf. The published article is copyrighted by the author(s) and published by the Public Library of Science. The published article can be found at: http://www.plosone.org/.
Abstract The Na⁺ translocating NADH:quinone oxidoreductase (Na⁺-NQR) is a unique respiratory enzyme catalyzing the electron
transfer from NADH to quinone coupled with the translocation of sodium ions across the membrane. Typically, Vibrio spp.,
including Vibrio cholerae, have this enzyme but lack the proton-pumping NADH:ubiquinone oxidoreductase (Complex I).
Thus, Na⁺-NQR should significantly contribute to multiple aspects of V. cholerae physiology; however, no detailed
characterization of this aspect has been reported so far. In this study, we broadly investigated the effects of loss of Na⁺-NQR
on V. cholerae physiology by using Phenotype Microarray (Biolog), transcriptome and metabolomics analyses. We found
that the V. cholerae ΔnqrA-F mutant showed multiple defects in metabolism detected by Phenotype Microarray.
Transcriptome analysis revealed that the V. cholerae ΔnqrA-F mutant up-regulates 31 genes and down-regulates 55 genes in
both early and mid-growth phases. The most up-regulated genes included the cadA and cadB genes, encoding a lysine
decarboxylase and a lysine/cadaverine antiporter, respectively. Increased CadAB activity was further suggested by the
metabolomics analysis. The down-regulated genes include sialic acid catabolism genes. Metabolomic analysis also
suggested increased reductive pathway of TCA cycle and decreased purine metabolism in the V. cholerae ΔnqrA-F mutant.
Lack of Na⁺-NQR did not affect any of the Na+ pumping-related phenotypes of V. cholerae suggesting that other secondary
Na⁺ pump(s) can compensate for Na⁺ pumping activity of Na⁺-NQR. Overall, our study provides important insights into the
contribution of Na⁺-NQR to V. cholerae physiology.
Genre Article
Access Condition http://creativecommons.org/licenses/by/3.0/us/
Identifier Minato Y, Fassio SR, Kirkwood JS, Halang P, Quinn MJ, et al. (2014) Roles of the Sodium-Translocating NADH:Quinone Oxidoreductase (Na⁺-NQR) on Vibrio cholerae Metabolism, Motility and Osmotic Stress Resistance. PLoS ONE 9(5): e97083. doi:10.1371/journal.pone.0097083

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