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9HZE

CryoEM structure of F-ENA fibers on the spores of Bacillus thuringiensis serovar kurstaki

Summary for 9HZE
Entry DOI10.2210/pdb9hze/pdb
EMDB information52523
DescriptorDUF4183 domain-containing protein (1 entity in total)
Functional Keywordsena, endospore appendage, protein fiber, helical, protein fibril
Biological sourceBacillus thuringiensis serovar kurstaki
Total number of polymer chains24
Total formula weight232630.15
Authors
Sleutel, M.,Remaut, H. (deposition date: 2025-01-13, release date: 2025-03-12, Last modification date: 2025-09-10)
Primary citationSleutel, M.,Sogues, A.,Van Gerven, N.,Jonsmoen, U.L.,Van Molle, I.,Fislage, M.,Theunissen, L.D.,Bellis, N.F.,Baquero, D.P.,Egelman, E.H.,Krupovic, M.,Wang, F.,Aspholm, M.,Remaut, H.
Cryo-EM identifies F-ENA of Bacillus thuringiensis as a widespread family of endospore appendages across Firmicutes.
Nat Commun, 16:7652-7652, 2025
Cited by
PubMed Abstract: For over 100 years, Bacillus thuringiensis (Bt) has been used as an agricultural biopesticide to control pests caused by insect species in the orders of Lepidoptera, Diptera, and Coleoptera. Under nutrient starvation, Bt cells differentiate into spores and associated toxin crystals that can adopt biofilm-like aggregates. We reveal that such Bt spore/toxin biofilms are embedded in a fibrous extrasporal matrix, and using cryoID, we resolved the structure and molecular identity of an uncharacterized type of pili, referred to here as Fibrillar ENdospore Appendages or F-ENA. F-ENA are monomolecular protein filaments anchored to the exosporium and tipped with a flexible fibrillum. Phylogenetic and structural analyses reveal that F-ENA are conserved in Bacilli and Clostridia, featuring head-neck domains with β-barrel necks that interlock via N-terminal hook peptides. In Bacillus, two collagen-like proteins (F-Anchor and F-BclA), respectively, tether F-ENA and form the distal tip. Sedimentation assays suggest F-ENA promotes spore clustering via F-BclA contacts and/or filament bundling.
PubMed: 40818982
DOI: 10.1038/s41467-025-62896-3
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.23 Å)
Structure validation

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