Single-molecule imaging reveals modulation of cell wall synthesis dynamics in live bacterial cells

Timothy K. Lee, Kevin Meng, Handuo Shi and Kerwyn Casey Huang ()
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Timothy K. Lee: Stanford University
Kevin Meng: Stanford University School of Medicine
Handuo Shi: Stanford University
Kerwyn Casey Huang: Stanford University

Nature Communications, 2016, vol. 7, issue 1, 1-9

Abstract: Abstract The peptidoglycan cell wall is an integral organelle critical for bacterial cell shape and stability. Proper cell wall construction requires the interaction of synthesis enzymes and the cytoskeleton, but it is unclear how the activities of individual proteins are coordinated to preserve the morphology and integrity of the cell wall during growth. To elucidate this coordination, we used single-molecule imaging to follow the behaviours of the two major peptidoglycan synthases in live, elongating Escherichia coli cells and after perturbation. We observed heterogeneous localization dynamics of penicillin-binding protein (PBP) 1A, the synthase predominantly associated with cell wall elongation, with individual PBP1A molecules distributed between mobile and immobile populations. Perturbations to PBP1A activity, either directly through antibiotics or indirectly through PBP1A’s interaction with its lipoprotein activator or other synthases, shifted the fraction of mobile molecules. Our results suggest that multiple levels of regulation control the activity of enzymes to coordinate peptidoglycan synthesis.

Date: 2016
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DOI: 10.1038/ncomms13170

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