Evidence map›Paper›PMID 25259857›Full record

ArticlePloS one2014

Architecture and assembly of the Bacillus subtilis spore coat.

Marco Plomp, Alicia Monroe Carroll, Peter Setlow, Alexander J Malkin

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

  1. Article
  2. Review
  3. Sporulation at reduced water activity impairs germination kinetics ofApplied and environmental microbiology · 2025
    Article
  4. Disruption of Spore Coat Integrity inCurrent issues in molecular biology · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Computational and structural biotechnology journal · 2023
    Article
  10. Multiscale X-ray study ofProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. A 2-dimensional ratchet model describes assembly initiation of a specialized bacterial cell surface.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  16. Accumulation and Release of Rare Earth Ions by Spores ofApplied and environmental microbiology · 2019
    Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Marco PlompBiosciences and Biotechnology Division, Physical and Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, California, United States of America.
Alicia Monroe CarrollDepartment of Molecular Biology and Biophysics, University of Connecticut Health Center, Farmington, Connecticut, United States of America.
Peter SetlowDepartment of Molecular Biology and Biophysics, University of Connecticut Health Center, Farmington, Connecticut, United States of America.
Alexander J MalkinBiosciences and Biotechnology Division, Physical and Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, California, United States of America.

Funding

DEGRADATION REACTIONS IN SPORE GERMINATIONR01GM019698 · NIGMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI SETLOW, PETER · 1985 to 2007
$1.9M
DEGRADATION REACTIONS IN SPORE GERMINATIONR37GM019698 · NIGMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI SETLOW, PETER · 1994 to 2003
$1.7M
NIGMS NIH HHS GM-19698NIGMS NIH HHS R01 GM019698NIGMS NIH HHS R37 GM019698PHS HHS W-7405
6 · The paper itself

Abstract

Bacillus spores are encased in a multilayer, proteinaceous self-assembled coat structure that assists in protecting the bacterial genome from stresses and consists of at least 70 proteins. The elucidation of Bacillus spore coat assembly, architecture, and function is critical to determining mechanisms of spore pathogenesis, environmental resistance, immune response, and physicochemical properties. Recently, genetic, biochemical and microscopy methods have provided new insight into spore coat architecture, assembly, structure and function. However, detailed spore coat architecture and assembly, comprehensive understanding of the proteomic composition of coat layers, and specific roles of coat proteins in coat assembly and their precise localization within the coat remain in question. In this study, atomic force microscopy was used to probe the coat structure of Bacillus subtilis wild type and cotA, cotB, safA, cotH, cotO, cotE, gerE, and cotE gerE spores. This approach provided high-resolution visualization of the various spore coat structures, new insight into the function of specific coat proteins, and enabled the development of a detailed model of spore coat architecture. This model is consistent with a recently reported four-layer coat assembly and further adds several coat layers not reported previously. The coat is organized starting from the outside into an outermost amorphous (crust) layer, a rodlet layer, a honeycomb layer, a fibrous layer, a layer of "nanodot" particles, a multilayer assembly, and finally the undercoat/basement layer. We propose that the assembly of the previously unreported fibrous layer, which we link to the darkly stained outer coat seen by electron microscopy, and the nanodot layer are cotH- and cotE- dependent and cotE-specific respectively. We further propose that the inner coat multilayer structure is crystalline with its apparent two-dimensional (2D) nuclei being the first example of a non-mineral 2D nucleation crystallization pattern in a biological organism.

Indexed as

Bacillus subtilisBacterial ProteinsCell WallMicroscopy, Atomic ForceSpores, BacterialBacterial Proteins

Identifiers

PMID25259857
PMCPMC4178626

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.