Abstract

Single-celled organisms must adapt their physiology to persist and propagate across a wide range of environmental conditions. The growth and division of bacterial cells depend on continuous synthesis of an essential extracellular barrier: the peptidoglycan cell wall, a polysaccharide matrix that counteracts turgor pressure and confers cell shape. Unlike many other essential processes and structures within the bacterial cell, the peptidoglycan cell wall and its synthesis machinery reside at the cell surface and are thus uniquely vulnerable to the physicochemical environment and exogenous threats. In addition to the diversity of stressors endangering cell wall integrity, defects in peptidoglycan metabolism require rapid repair in order to prevent osmotic lysis, which can occur within minutes. Here, we review recent work that illuminates mechanisms that ensure robust peptidoglycan metabolism in response to persistent and acute environmental stress. Advances in our understanding of bacterial cell wall quality control promise to inform the development and use of antimicrobial agents that target the synthesis and remodeling of this essential macromolecule.IMPORTANCE Nearly all bacteria are encased in a peptidoglycan cell wall, an essential polysaccharide structure that protects the cell from osmotic rupture and reinforces cell shape. The integrity of this protective barrier must be maintained across the diversity of environmental conditions wherein bacteria replicate. However, at the cell surface, the cell wall and its synthesis machinery face unique challenges that threaten their integrity. Directly exposed to the extracellular environment, the peptidoglycan synthesis machinery encounters dynamic and extreme physicochemical conditions, which may impair enzymatic activity and critical protein-protein interactions. Biotic and abiotic stressors-including host defenses, cell wall active antibiotics, and predatory bacteria and phage-also jeopardize peptidoglycan integrity by introducing lesions, which must be rapidly repaired to prevent cell lysis. Here, we review recently discovered mechanisms that promote robust peptidoglycan synthesis during environmental and acute stress and highlight the opportunities and challenges for the development of cell wall active therapeutics.

Highlights

  • Single-celled organisms must adapt their physiology to persist and propagate across a wide range of environmental conditions

  • We focus on strategies in Escherichia coli because it is the predominant model organism for studying cell wall biogenesis and is an environmental generalist, but we draw examples from other bacteria to highlight conservation and diversity when relevant

  • Several pieces of evidence implicate a role for the bifunctional class A penicillin binding proteins (PBPs), and specially PBP1b, in E. coli cell wall quality control. (i) Class A PBP dynamics suggest a unique role in cell wall synthesis compared to other PBPs [11, 95]. (ii) PBP1b activity is elevated in response to cell envelope stress [95, 96]. (iii) PBP1b is required for survival and recovery from cell wall damage [95, 97, 98]

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Summary

Introduction

Single-celled organisms must adapt their physiology to persist and propagate across a wide range of environmental conditions. E. coli genes encode two essential class B PBP/SEDS enzyme pairs—PBP2/RodA and PBP3/FtsW—that function as parts of multicomponent PG synthesis complexes involved in cell elongation and cell division, respectively. We focus on two of the adaptations that promote PG homeostasis during steady-state growth in nonstandard conditions (i.e., constant stress): (i) plasticity within the active repertoire of cell wall enzymes, and (ii) production of modulatory factors that stabilize multicomponent cell wall synthesis complexes.

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