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Comparing divisome organization between vegetative and sporulating Bacillus subtilis at the nanoscale using DNA-PAINT

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Cramer,  Kimberly
IMPRS-ML: Martinsried, Max Planck Institute of Biochemistry, Max Planck Society;
Jungmann, Ralf / Molecular Imaging and Bionanotechnology, Max Planck Institute of Biochemistry, Max Planck Society;

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Reinhardt,  Susanne C. M.
IMPRS-ML: Martinsried, Max Planck Institute of Biochemistry, Max Planck Society;
Jungmann, Ralf / Molecular Imaging and Bionanotechnology, Max Planck Institute of Biochemistry, Max Planck Society;

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Auer,  Alexander
Jungmann, Ralf / Molecular Imaging and Bionanotechnology, Max Planck Institute of Biochemistry, Max Planck Society;

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Jungmann,  Ralf
Jungmann, Ralf / Molecular Imaging and Bionanotechnology, Max Planck Institute of Biochemistry, Max Planck Society;

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Citation

Cramer, K., Reinhardt, S. C. M., Auer, A., Shin, J. Y., & Jungmann, R. (2024). Comparing divisome organization between vegetative and sporulating Bacillus subtilis at the nanoscale using DNA-PAINT. Science Advances, 10(2): eadk5847. doi:10.1126/sciadv.adk5847.


Cite as: https://hdl.handle.net/21.11116/0000-000E-F552-1
Abstract
Spore-forming bacteria have two distinct division modes: sporulation and vegetative division. The placement of the foundational division machinery component (Z-ring) within the division plane is contingent on the division mode. However, investigating if and how division is performed differently between sporulating and vegetative cells remains challenging, particularly at the nanoscale. Here, we use DNA-PAINT super-resolution microscopy to compare the 3D assembly and distribution patterns of key division proteins SepF, ZapA, DivIVA, and FtsZ. We determine that ZapA and SepF placement within the division plane mimics that of the Z-ring in vegetative and sporulating cells. We find that DivIVA assemblies differ between vegetative and sporulating cells. Furthermore, we reveal that SepF assembles into similar to 50-nm arcs independent of division mode. We propose a nanoscale model in which symmetric or asymmetric placement of the Z-ring and early divisome proteins is a defining characteristic of vegetative or sporulating cells, respectively, and regulation of septal thickness differs between division modes.