Abstract

In nature, bacteria must survive long periods of nutrient deprivation while maintaining the ability to recover and grow when conditions improve. This quiescent state is called stationary phase. The biochemistry of Escherichia coli in stationary phase is reasonably well understood. Much less is known about the biophysical state of the cytoplasm. Earlier studies of harvested nucleoids concluded that the stationary-phase nucleoid is "compacted" or "supercompacted," and there are suggestions that the cytoplasm is "glass-like." Nevertheless, stationary-phase bacteria support active transcription and translation. Here, we present results of a quantitative superresolution fluorescence study comparing the spatial distributions and diffusive properties of key components of the transcription-translation machinery in intact E. coli cells that were either maintained in 2-day stationary phase or undergoing moderately fast exponential growth. Stationary-phase cells are shorter and exhibit strong heterogeneity in cell length, nucleoid volume, and biopolymer diffusive properties. As in exponential growth, the nucleoid and ribosomes are strongly segregated. The chromosomal DNA is locally more rigid in stationary phase. The population-weighted average of diffusion coefficients estimated from mean-square displacement plots is 2-fold higher in stationary phase for both RNA polymerase (RNAP) and ribosomal species. The average DNA density is roughly twice as high as that in cells undergoing slow exponential growth. The data indicate that the stationary-phase nucleoid is permeable to RNAP and suggest that it is permeable to ribosomal subunits. There appears to be no need to postulate migration of actively transcribed genes to the nucleoid periphery.IMPORTANCE Bacteria in nature usually lack sufficient nutrients to enable growth and replication. Such starved bacteria adapt into a quiescent state known as the stationary phase. The chromosomal DNA is protected against oxidative damage, and ribosomes are stored in a dimeric structure impervious to digestion. Stationary-phase bacteria can recover and grow quickly when better nutrient conditions arise. The biochemistry of stationary-phase E. coli is reasonably well understood. Here, we present results from a study of the biophysical state of starved E. coli Superresolution fluorescence microscopy enables high-resolution location and tracking of a DNA locus and of single copies of RNA polymerase (the transcription machine) and ribosomes (the translation machine) in intact E. coli cells maintained in stationary phase. Evidently, the chromosomal DNA remains sufficiently permeable to enable transcription and translation to occur. This description contrasts with the usual picture of a rigid stationary-phase cytoplasm with highly condensed DNA.

Highlights

  • Background strainMG1655 VH1000 VH1000 VH1000 VH1000 VH1000 VH1000Expression method PlasmidPlasmid Chromosome Chromosome Chromosome Plasmid distributions for the other strains in stationary phase are similar

  • In contrast to the usual picture of the stationary-phase nucleoid as a supercompacted, relatively impermeable structure, we found that RNA polymerase (RNAP) (450 kDa), Kaede tetramer (110 kDa), and the more rapidly diffusing ribosomal species readily permeated the 2-day stationary-phase nucleoid

  • We begin with a qualitative comparison of overall cell and nucleoid morphology in fairly rapid exponential growth (45 min doubling time at 30°C) versus 2-day stationary phase

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Summary

Introduction

Plasmid Chromosome Chromosome Chromosome Plasmid distributions for the other strains in stationary phase are similar (see Fig. S2A in the supplemental material). The WT cells are much shorter in 2-day stationary phase than in exponential phase. The mean cell length in 2-day stationary phase is 2.6 Ϯ 0.5 ␮m (Ϯ 1 standard deviation). This compares favorably with two previous results: 2.7 Ϯ 0.2 ␮m for an overnight culture [22] and ϳ2.2 ␮m for a 1-day stationary-phase culture (see Fig. S1 in reference 23). All cells remain spherocylindrical in stationary phase; 10% have aspect ratios of Ͻ2.0 (Fig. S2C). Cell widths determined from Oufti are compared with

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