Polyphosphate affects cytoplasmic and chromosomal dynamics in nitrogen-starved Pseudomonas aeruginosa

Author:

Magkiriadou Sofia1ORCID,Stepp Willi L.1,Newman Dianne K.23,Manley Suliana1ORCID,Racki Lisa R.4ORCID

Affiliation:

1. Laboratory of Experimental Biophysics, Institute of Physics, École Polytechnique Fédérale de Lausanne, Lausanne CH-1015, Switzerland

2. Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125

3. Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA 91125

4. Department of Integrative Structural and Computational Biology, The Scripps Research Institute, San Diego, CA 92037

Abstract

Polyphosphate (polyP) synthesis is a ubiquitous stress and starvation response in bacteria. In diverse species, mutants unable to make polyP have a wide variety of physiological defects, but the mechanisms by which this simple polyanion exerts its effects remain unclear. One possibility is that polyP’s many functions stem from global effects on the biophysical properties of the cell. We characterize the effect of polyphosphate on cytoplasmic mobility under nitrogen-starvation conditions in the opportunistic pathogen Pseudomonas aeruginosa . Using fluorescence microscopy and particle tracking, we quantify the motion of chromosomal loci and cytoplasmic tracer particles. In the absence of polyP and upon starvation, we observe a 2- to 10-fold increase in mean cytoplasmic diffusivity. Tracer particles reveal that polyP also modulates the partitioning between a “more mobile” and a “less mobile” population: Small particles in cells unable to make polyP are more likely to be “mobile” and explore more of the cytoplasm, particularly during starvation. Concomitant with this larger freedom of motion in polyP-deficient cells, we observe decompaction of the nucleoid and an increase in the steady-state concentration of ATP. The dramatic polyP-dependent effects we observe on cytoplasmic transport properties occur under nitrogen starvation, but not carbon starvation, suggesting that polyP may have distinct functions under different types of starvation.

Funder

HHS | NIH | National Institute of General Medical Sciences

EC | European Research Council

Swiss National Science Foundation

Donald E. and Delia B. Baxter Foundation

Publisher

Proceedings of the National Academy of Sciences

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