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Published July 15, 2019 | Supplemental Material + Accepted Version + Submitted
Journal Article Open

In situ imaging of the bacterial flagellar motor disassembly and assembly processes

Abstract

The self‐assembly of cellular macromolecular machines such as the bacterial flagellar motor requires the spatio‐temporal synchronization of gene expression with proper protein localization and association of dozens of protein components. In Salmonella and Escherichia coli, a sequential, outward assembly mechanism has been proposed for the flagellar motor starting from the inner membrane, with the addition of each new component stabilizing the previous one. However, very little is known about flagellar disassembly. Here, using electron cryo‐tomography and sub‐tomogram averaging of intact Legionella pneumophila, Pseudomonas aeruginosa, and Shewanella oneidensis cells, we study flagellar motor disassembly and assembly in situ. We first show that motor disassembly results in stable outer membrane‐embedded sub‐complexes. These sub‐complexes consist of the periplasmic embellished P‐ and L‐rings, and bend the membrane inward while it remains apparently sealed. Additionally, we also observe various intermediates of the assembly process including an inner‐membrane sub‐complex consisting of the C‐ring, MS‐ring, and export apparatus. Finally, we show that the L‐ring is responsible for reshaping the outer membrane, a crucial step in the flagellar assembly process.

Additional Information

© 2019 The Authors. Received 18 October 2018; Revised 11 April 2019; Accepted 18 April 2019. This work was supported by the National Institutes of Health (NIH, grant R01 AI127401 to G.J.J.). M.K. is supported by a postdoctoral Rubicon fellowship from De Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO). S.P. and M.Y.E.‐N. are supported by the Air Force Office of Scientific Research Presidential Early Career Award for Scientists and Engineers (FA955014‐1‐0294, to M.Y.E.‐N.). R.S.L. and J.A.G acknowledge support from the Office of Naval Research (N00014‐18‐1‐2632 to J.A.G.). We would like to thank Dr. Spiros Garbis, Dr. Annie Moradian, Dr. Michael Sweredoski, and Dr. Brett Lomenick from the Caltech Proteome Exploration Laboratory for their help in mass spectrometry experiments and data analysis. All P. aeruginosa mutants were kindly supplied by Dianne Newman's laboratory at Caltech. ECT was performed in the Beckman Institute Resource Center for Cryo‐EM. Author contributions: MK and GJJ designed research. MK, PS, DG, and RS-L prepared samples. MK, PS, and DG recorded ECT data. MK performed MS experiments. MK and DRO performed bioinformatics analysis. SP, SKM, JAG, and MYE-N supplied reagents. MK, CMO, and GJJ analyzed data. MK, CMO, and GJJ wrote the manuscript, and all authors edited it. The authors declare that they have no conflict of interest.

Attached Files

Accepted Version - embj.2018100957-2.pdf

Submitted - 369405.full.pdf

Supplemental Material - embj.2018100957.reviewer-comments.pdf

Supplemental Material - inline-supplementary-material-1.docx

Supplemental Material - inline-supplementary-material-2.xlsx

Supplemental Material - inline-supplementary-material-3.xlsx

Supplemental Material - inline-supplementary-material-4.xlsx

Supplemental Material - inline-supplementary-material-5.zip

Supplemental Material - inline-supplementary-material-6.zip

Supplemental Material - inline-supplementary-material-7.zip

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Additional details

Created:
August 22, 2023
Modified:
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