Published July 2021 | Version Supplemental Material + Submitted + Published
Journal Article Open

Nitrate Reduction Stimulates and Is Stimulated by Phenazine-1-Carboxylic Acid Oxidation by Citrobacter portucalensis MBL

  • 1. ROR icon California Institute of Technology

Abstract

Phenazines are secreted metabolites that microbes use in diverse ways, from quorum sensing to antimicrobial warfare to energy conservation. Phenazines are able to contribute to these activities due to their redox activity. The physiological consequences of cellular phenazine reduction have been extensively studied, but the counterpart phenazine oxidation has been largely overlooked. Phenazine-1-carboxylic acid (PCA) is common in the environment and readily reduced by its producers. Here, we describe its anaerobic oxidation by Citrobacter portucalensis strain MBL, which was isolated from topsoil in Falmouth, MA, and which does not produce phenazines itself. This activity depends on the availability of a suitable terminal electron acceptor, specifically nitrate. When C. portucalensis MBL is provided reduced PCA and nitrate, it oxidizes the PCA at a rate that is environmentally relevant. We compared this terminal electron acceptor-dependent PCA-oxidizing activity of C. portucalensis MBL to that of several other gammaproteobacteria with various capacities to respire nitrate. We found that PCA oxidation by these strains in a nitrate-dependent manner is decoupled from growth and strain dependent. We infer that bacterial PCA oxidation is widespread and genetically determined. Notably, oxidizing PCA enhances the rate of nitrate reduction to nitrite by C. portucalensis MBL beyond the stoichiometric exchange of electrons from PCA to nitrate, which we attribute to C. portucalensis MBL's ability to also reduce oxidized PCA, thereby catalyzing a complete PCA redox cycle. This bidirectionality highlights the versatility of PCA as a biological redox agent.

Additional Information

© 2021 Tsypin and Newman. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license. Received 27 July 2021; Accepted 4 August 2021; Published 31 August 2021. We thank the members of the Newman lab, and especially Scott Saunders, Darcy McRose, Avi Flamholz, John Ciemniecki, Chelsey VanDrisse, and Justin Bois for their insight and helpful discussions throughout this work. We are grateful to Nathan Dalleska at the Water and Environment Laboratory at Caltech for training L.M.T. on the Dionex instrument and providing a facility for analytical chemistry. L.M.T. was supported by the Rosen Endowment Fellowship at Caltech and the National Science Foundation Graduate Research Fellowship (DGE‐1745301). Additional support to D.K.N. came from NIH (1R01AI127850-01A1 and 1R01HL152190-01) and ARO (W911NF-17-1-0024) grants.

Attached Files

Published - mBio.02265-21.pdf

Submitted - 2021.06.04.447179v1.full.pdf

Supplemental Material - mbio.02265-21-sf001.eps

Supplemental Material - mbio.02265-21-sf002.eps

Supplemental Material - mbio.02265-21-sf003.eps

Supplemental Material - mbio.02265-21-sf004.eps

Supplemental Material - mbio.02265-21-sf005.eps

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Additional details

Additional titles

Alternative title
C. portucalensis MBL links PCA and nitrate redox cycles

Identifiers

Eprint ID
109415
Resolver ID
CaltechAUTHORS:20210607-115053770

Funding

Donna and Benjamin M. Rosen Bioengineering Center
NSF Graduate Research Fellowship
DGE‐1745301
NIH
1R01AI127850-01A1
NIH
1R01HL152190-01
Army Research Office (ARO)
W911NF-17-1-0024

Dates

Created
2021-06-07
Created from EPrint's datestamp field
Updated
2021-09-13
Created from EPrint's last_modified field

Caltech Custom Metadata

Caltech groups
Rosen Bioengineering Center, Division of Geological and Planetary Sciences (GPS), Division of Biology and Biological Engineering (BBE)