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R-Type Fonticins Produced by Pragia fontium Form Large Pores with High Conductance

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Látrová, KláraORCiD Profile - 0000-0003-4757-5795WoS Profile - Q-1910-2017Scopus Profile - 57217848403
Dolejšová, TerezaORCiD Profile - 0000-0003-0231-1518WoS Profile - Q-9294-2017Scopus Profile - 57210217030
Motlová, LuciaORCiD Profile - 0000-0002-5581-8737WoS Profile - Q-9469-2017Scopus Profile - 57188711497
Mikušová, GabrielaORCiD Profile - 0000-0001-8424-9249WoS Profile - H-2050-2014Scopus Profile - 23487250200
Bosák, Juraj
Snopková, Kateřina
Šmajs, David
Konopásek, IvoORCiD Profile - 0000-0002-6824-5974WoS Profile - AAE-9034-2021Scopus Profile - 56018797900
Fišer, RadovanORCiD Profile - 0000-0003-4516-0086WoS Profile - E-4908-2012Scopus Profile - 16506945200

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Publication date
2023
Published in
Journal of Bacteriology
Volume / Issue
205 (1)
ISBN / ISSN
ISSN: 0021-9193
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This publication has a published version with DOI 10.1128/jb.00315-22

Abstract
Fonticins are phage tail-like bacteriocins produced by the Gram-negative bacterium Pragia fontium from the family Budviciaceae. This bacterium produces contractile-type particles that adsorb on the surface of sensitive bacteria and penetrate the cell wall, probably during contraction, in a way similar to the type VI secretion system. We characterized the pore-forming activity of fonticins using both living cells and in vitro model membranes. Using a potassium leakage assay, we show that fonticins are able to permeabilize sensitive cells. On black lipid membranes, single-pore conductance is about 0.78 nS in 1 M NaCl and appears to be linearly dependent on the increasing molar strength of NaCl solution, which is a property of considerably large pores. In agreement with these findings, fonticins are not ion selective for Na+, K+, and Cl-. Polyethylene glycol 3350 (PEG 3350) molecules of about 3.5 nm in diameter can enter the fonticin pore lumen, whereas the larger molecules cannot pass the pore. The size of fonticin pores was confirmed by transmission electron microscopy. The terminal membrane-piercing complex of the fonticin tube probably creates a selective barrier restricting passage of macromolecules. IMPORTANCE Phage tail-like bacteriocins are now the subject of research as potent antibacterial agents due to their narrow host specificity and single-hit mode of action. In this work, we focused on the structure and mode of action of fonticins. According to some theories, related particles were initially adapted for passage of double-stranded DNA (dsDNA) molecules, but fonticins changed their function during the evolution; they are able to form large pores through the bacterial envelope of Gram-negative bacteria. As various pore-forming proteins are extensively used for nanopore sequencing and stochastic sensing, we decided to investigate the pore-forming properties of fonticin protein complexes on artificial lipid membranes. Our research revealed remarkable structural properties of these particles that may have a potential application as a nanodevice.
Keywords
fonticin, phage tail-like bacteriocins, black lipid membranes, membrane pore formation, conductance, electric current, electron microscopy, single-pore conductance
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https://hdl.handle.net/20.500.14178/2026
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WOS:000901435900002
SCOPUS:2-s2.0-85147046924
PUBMED:36541812
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