Published September 2, 2011 | Version Accepted Version
Journal Article Open

Peptidoglycan Remodeling and Conversion of an Inner Membrane into an Outer Membrane during Sporulation

  • 1. ROR icon California Institute of Technology
  • 2. ROR icon Stanford University

Abstract

Two hallmarks of the Firmicute phylum, which includes the Bacilli and Clostridia classes, are their ability to form endospores and their "Gram-positive" single-membraned, thick-cell-wall envelope structure. Acetonema longum is part of a lesser-known family (the Veillonellaceae) of Clostridia that form endospores but that are surprisingly "Gram negative," possessing both an inner and outer membrane and a thin cell wall. Here, we present macromolecular resolution, 3D electron cryotomographic images of vegetative, sporulating, and germinating A. longum cells showing that during the sporulation process, the inner membrane of the mother cell is inverted and transformed to become the outer membrane of the germinating cell. Peptidoglycan persists throughout, leading to a revised, "continuous" model of its role in the process. Coupled with genomic analyses, these results point to sporulation as a mechanism by which the bacterial outer membrane may have arisen and A. longum as a potential "missing link" between single- and double-membraned bacteria.

Additional Information

© 2011 Elsevier Inc. Received 2 November 2010; revised 25 May 2011; Accepted 9 July 2011. Published: September 1, 2011. Available online 1 September 2011. We thank Alasdair McDowall and Mark Ladinsky for their help with the preparation of mature spores by traditional EM methods and Dr. Martin Pilhofer for helping with the immunofluorescence and western blotting experiments. The GC-MS analysis of LPS was performed at the Complex Carbohydrate Research Center and was supported by DOE grant DE-FG02-09ER20097. We thank Everett Kane for the generation of Movie S2 and Jane H. Ding for helping with the generation of Movie S1 and Movie S2. We thank Ivan Tochev for generating Figure 4B. We thank Dr. Stephen Quake and Richard White at Stanford University for performing the shotgun genome sequencing of A. longum. The authors gratefully acknowledge the IGS annotation engine. This work was supported by a Natural Sciences and Engineering Research Council of Canada Postdoctorate Fellowship (to E.I.T.), the Howard Hughes Medical Foundation, and gifts to Caltech from the Gordon and Betty Moore Foundation, including support for the Caltech Center for Integrative Study of Cell Regulation. E.G.M was supported by the Department of Energy (award DE-FG02-07ER64484 to J.R.L).

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Additional details

Identifiers

PMCID
PMC3176627
Eprint ID
25456
DOI
10.1016/j.cell.2011.07.029
Resolver ID
CaltechAUTHORS:20110928-072623751

Funding

Department of Energy (DOE)
DE-FG02-09ER20097
Natural Sciences and Engineering Research Council of Canada (NSERC)
Howard Hughes Medical Foundation
Gordon and Betty Moore Foundation
Department of Energy (DOE)
DE-FG02-07ER64484

Dates

Created
2011-09-28
Created from EPrint's datestamp field
Updated
2021-11-09
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