Biology subjects

Krasnopeeva, E.

Publications and source records attributed to Krasnopeeva, E..

6 recordsLinked to original sources

bioRxiv2026

Coupling of ATP and PMF in Escherichia coli is determined by growth conditions

The ATP molecule is the universal energy currency across all living organisms. There are two fundamental pathways of ATP synthesis: substrate-level and oxidative phosphorylation. While substrate-level phosphorylation generates ATP directly, in oxidative phosphorylation, proton motive force (PMF) is required to power ATP synthesis via the F1Fo ATP synthase. Using Escherichia coli, we show that due to simultaneous use of both pathways, the strength of coupling between ATP and PMF strongly depends on growth conditions: coupling is weak when requirements for independent generation of ATP and PMF are met, and becomes essential when not. We determine the conditions, under which PMF-ATP coupling becomes essential and show that PMF is required for bacterial growth irrespective of its ATP synthesis function. We propose that the main role of F1Fo in Escherichia coli, contrary to the canonical view, is not to generate ATP but to provide an auxiliary pathway that allows both, ATP and PMF, to be produced.

microbiology↗

bioRxiv2026

Metabolic feedback during bacterial fermentation is a motility brake

We study an unexpectedly fast decay of motility in dense suspensions of Escherichia coli bacteria supplied with excess glucose under anaerobic conditions. The decrease in swimming speed occurs on a timescale inversely proportional to the cell concentration, and is associated with the secretion of organic acids by the bacteria. We show that the decay is driven by the progressive accumulation of non-ionised organic acids in the medium, and develop a chemical kinetic model that successfully predicts the swimming speed variations over a range of conditions in the presence of these acids. We further measure the internal pH of E. coli cells exposed to organic acids, and find that the speed decay coincides with sharp declines in internal pH and metabolic rate. Our findings identify an additional layer of motility control that can arise in complex environments even when motility genes are expressed and energy sources are abundant. This mechanism is likely relevant for understanding bacterial motility in habitats such as the human gut, where high densities of bacteria and organic acids are common.

microbiology↗

bioRxiv2024

Nonlinear dependency of the bacterial flagellar motor speed on proton motive force and its consequences for swimming

The bacterial flagellar motor enables bacteria to swim by rotating helical flagellar filaments that form a bundle at the back of the cell. Escherichia colis motor uses the energy stored in the electrochemical gradient of protons, the proton motive force (PMF), to generate the torque driving this rotation. Until now, motor speed was thought to be proportional to the PMF, irrespective of the viscous load on the motor, and across the physiological range of PMF values. Here, we show that the PMF-speed relationship is non-linear in the high-torque regime. Because saturation in the relationship occurs in the physiologically relevant range, it challenges all current models of motor function that assume a tight coupling between the motor rotation and PMF across the entire physiological range. Furthermore, we experimentally determine the load on the motor experienced by swimming cells, and show that free swimming occurs close to or within the saturation regime, making the observed limiting torque evolutionary relevant.

microbiology↗

bioRxiv2022

Real-time dynamics of individual chemoreceptor mRNA molecules reveals translation hotspots at the inner membrane of Escherichia coli

Since bacteria lack a nucleus, the location of mRNA molecules is determined by the different characteristics of the encoded proteins, and the transcriptome is spatially arranged into cytosolic and membrane-associated mRNA. While translation of membrane protein-encoding mRNA has been studied in great mechanistic detail using biochemical methods, the spatiotemporal dynamics of this process remains poorly understood at the subcellular level. Here, we investigate the dynamics of individual fluorescently labelled mRNA molecules encoding the transmembrane serine chemoreceptor Tsr, to probe the mechanism of membrane protein translation. Analysis of tsr mRNA diffusion in the proximity of the plasma membrane revealed distinct diffusive modes that reflect the state of the mRNA molecule and its involvement in the process of active translation into the Sec secretion system. We find that the composition, and hence the fluidity of the membrane affects diffusion of membrane targeted mRNAs. Moreover, Tsr translation occurs in localized membrane regions, similar to eukaryotic hotspots. The hotspot localization coincides with the physical location of the transcribed gene, which itself is displaced towards the inner membrane. These findings suggest that inner membrane protein translation is a spatially defined process that occurs in hotspots, indicative of long-lived transertion sites. Our results show an additional layer of spatio-temporal structuring within the bacterial cell, thus revealing a qualitatively different understanding of the basic process of transcription and translation in bacteria. Significance StatementA large fraction of the bacterial proteome is directly synthesized into the inner membrane, and this process shapes the overall distribution of mRNA transcripts within the cell. Although highly dynamic in their nature, bacterial transcriptomes have mostly been studied in fixed cells. Here, we track individual mRNA molecules encoding the serine chemoreceptor in living bacterial cells and find that translation occurs in membrane hotspots that were previously exclusive to eukaryotes. Our results indicate an additional layer of spatio-temporal structuring within the bacterial cell that impacts our understanding of transcription and translation in bacteria.

microbiology↗

bioRxiv2021

The proton motive force determines Escherichia coli's robustness to extracellular pH

Maintaining intracellular homeostases is a hallmark of life, and key physiological variables, such as cytoplasmic pH, osmotic pressure, and proton motive force (PMF), are typically interdependent. Using a mathematical model, we argue that near neutral pH homeostasis implies that cells must export ions other than protons to generate physiological electrical potential across their plasma membrane. For Escherichia coli, proton:ion antiporters are the only known cation efflux pumps, and we therefore predict that principal function of antiporters is to generate an out-of-equilibrium plasma membrane potential and so maintain the PMF at the constant levels observed. Consequently, the strength of the PMF determines the range of extracellular pH over which the cell is able to preserve its near neutral cytoplasmic pH, and the non-zero PMF is needed to maintain membrane potential. In support, we concurrently measure the PMF and cytoplasmic pH in single cells and demonstrate both that decreasing the PMFs strength impairs E. colis ability to maintain its pH and that artificially collapsing the PMF destroys the out-of-equilibrium plasma membrane potential. We further predict the observed ranges of extracellular pH for which three of E. colis antiporters are expressed, through defining their cost by the rate at which they divert protons from being imported to generate ATP. Taken together, our results suggest a new perspective on bacterial electrophysiology, where cells regulate the plasma membrane potential to maintain

microbiology↗

bioRxiv2019

Comparison of Escherichia coli surface attachment methods for single-cell, in vivo microscopy

For in vivo, single-cell imaging bacterial cells are commonly immobilised via physical confinement or surface attachment. Different surface attachment methods have been used both for atomic force and optical microscopy (including super resolution), and some have been reported to affect bacterial physiology. However, a systematic comparison of the effects these attachment methods have on the bacterial physiology is lacking. Here we present such a comparison for bacterium Escherichia coli, and assess the growth rate, size and intracellular pH of cells growing attached to different, commonly used, surfaces. We demonstrate that E. coli grow at the same rate, length and internal pH on all the tested surfaces when in the same growth medium. The result suggests that tested attachment methods can be used interchangeably when studying E. coli physiology.

systems biology↗