PreprintCited by 69Microbial Fuel Cells and BioremediationAdvanced Electron Microscopy Techniques and ApplicationsEnzyme Structure and Function

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Structure of Geobacter OmcZ filaments suggests extracellular cytochrome polymers evolved independently multiple times

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Preprint — published as 10.7554/elife.81551 · Paper page

Abstract

While early genetic and low resolution structural observations suggested that extracellular conductive filaments on metal reducing organisms such as Geobacter were composed of Type IV pili, it has now been established that bacterial c -type cytochromes can polymerize to form extracellular filaments capable of long-range electron transport. Atomic structures exist for two such cytochrome filaments, formed from the hexaheme cytochrome OmcS and the tetraheme cytochrome OmcE. Due to the highly conserved heme packing within the central OmcS and OmcE cores, and shared pattern of heme coordination between subunits, it has been suggested that these polymers have a common origin. We have now used cryo-EM to determine the structure of a third extracellular filament, formed from the Geobacter sulfurreducens octaheme cytochrome, OmcZ. In contrast to the linear heme chains in OmcS and OmcE, the packing of hemes, heme:heme angles, and between-subunit heme coordination is quite different in OmcZ. A branched heme arrangement within OmcZ leads to a highly surface exposed heme in every subunit, which may account for the formation of conductive biofilm networks, and explain the higher measured conductivity of OmcZ filaments. This new structural evidence suggests that conductive cytochrome polymers arose independently on more than one occasion from different ancestral multiheme proteins.

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Metadata

Authors
Wang, F., Chan, C. H., Suciu, V., Mustafa, K., Si, D., Hochbaum, A. I., Egelman, E. H., & Bond, D. R.
Affiliations
  • University of Virginia (US)
  • University of Minnesota (US)
  • University of Washington Bothell (US)
  • University of California, Irvine (US)
Corresponding author
  • Hochbaum, Allon I.
  • Egelman, Edward H.
  • Bond, Daniel R.
Venue
eLife
Publisher
openRxiv
Published
2022-07-17
Volume
11
ISSN
2050-084X (ISSN-L)
OpenAlex
W4294666866
Cited by
69
References
1
Citations by year
2026: 17 · 2025: 15 · 2024: 19 · 2023: 16 · 2022: 2
FWCI
3.94
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • eLife (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • eScholarship (California Digital Library) (submittedVersion, cc-by)
  • OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
Funders
  • National Science Foundation (2030381, G20-RR31199, GM122510)
  • U.S. Department of Energy (DESC0020322, DESC0020329)
  • University of Washington
  • University of Virginia (G20 RR31199)
  • National Institutes of Health (GM138756)
  • University of Washington Bothell
  • National Science Foundation of Sri Lanka (2030381)
  • Office of Naval Research (#N00014-18-1-2632, N00014-18, FA9550, N00014)
  • National Institute of General Medical Sciences (R00GM138756, K99GM138756, R35GM122510)
  • National Center for Research Resources (G20RR031199)
  • Air Force Office of Scientific Research (FA9550-, FA9550-19-1-0380)
Topics
  • Physical Sciences › Environmental Science › Environmental Engineering › Microbial Fuel Cells and Bioremediation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Advanced Electron Microscopy Techniques and Applications
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Enzyme Structure and Function
Keywords
Geobacter sulfurreducens, conductive filaments, multiheme cytochromes, heme coordination, electron transport, metal-reducing bacteria, OmcS, convergent evolution
MeSH terms
Bacterial Proteins, Cytochromes, Electron Transport, Heme, Oxidation-Reduction, Polymers, Cryoelectron Microscopy, Geobacter

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