Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published April 2014 | Accepted Version
Journal Article Open

Phenazine redox cycling enhances anaerobic survival in Pseudomonas aeruginosa by facilitating generation of ATP and a proton-motive force

Abstract

While many studies have explored the growth of Pseudomonas aeruginosa, comparatively few have focused on its survival. Previously, we reported that endogenous phenazines support the anaerobic survival of P. aeruginosa, yet the physiological mechanism underpinning survival was unknown. Here, we demonstrate that phenazine redox cycling enables P. aeruginosa to oxidize glucose and pyruvate into acetate, which promotes survival by coupling acetate and ATP synthesis through the activity of acetate kinase. By measuring intracellular NAD(H) and ATP concentrations, we show that survival is correlated with ATP synthesis, which is tightly coupled to redox homeostasis during pyruvate fermentation but not during arginine fermentation. We also show that ATP hydrolysis is required to generate a proton-motive force using the ATP synthase complex during fermentation. Together, our results suggest that phenazines enable maintenance of the proton-motive force by promoting redox homeostasis and ATP synthesis. This work demonstrates the more general principle that extracellular redox-active molecules, such as phenazines, can broaden the metabolic versatility of microorganisms by facilitating energy generation.

Additional Information

© 2014 John Wiley & Sons Ltd. Article first published online: 19 March 2014; Accepted manuscript online: 25 February 2014 02:52AM EST; Manuscript Accepted: 22 February 2014. This work was supported by the Howard Hughes Medical Institute (HHMI). D.K.N. is an HHMI Investigator, and N.R.G. and S.E.K. were both supported by NSF graduate research fellowships. This work was supported in part by the National Research Service Award (T32GM07676) from the National Institute of General Medical Sciences. We thank Nathan Dalleska and the Environmental Analysis Center (Caltech) for help with metabolite analyses, Ron Grimm for help with electrodes, and Ian Booth and members of the Newman lab for helpful discussions. The authors declare no conflicts of interest.

Attached Files

Accepted Version - nihms573961.pdf

Files

nihms573961.pdf
Files (2.2 MB)
Name Size Download all
md5:8dfa35eba7a8b478ce50215cb308ed1c
2.2 MB Preview Download

Additional details

Created:
September 22, 2023
Modified:
October 23, 2023