Nanocomposite antimicrobials prevent bacterial growth through the enzyme-like activity of Bi-doped cerium dioxide (Ce1−xBixO2−δ). Issue 41 (19th October 2020)

• Record Type: Journal Article
• Authors: Frerichs, Hajo; Pütz, Eva; Pfitzner, Felix; Reich, Tobias; Gazanis, Athanasios; Panthöfer, Martin; Hartmann, Jens; Jegel, Olga; Heermann, Ralf; Tremel, Wolfgang
• Is Part Of: Nanoscale. Volume 12:Issue 41(2020)
• Page Start: 21344
• Page End: 21358
• Publication Date: 2020-10-19
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/d0nr06165d
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : Ce1− x Bi x O2− δ is an active halogenation catalyst with maximum activity for x ≈ 0.2 due to the effects of zeta-potential and BET surface area. Ce1− x Bi x O2− δ /polyethersulfone nanocomposites block bacterial biofilm formation of Gram-negative bacteria. Abstract : Preventing bacterial adhesion on materials surfaces is an important problem in marine, industrial, medical and environmental fields and a topic of major medical and societal importance. A defense strategy of marine organisms against bacterial colonization relies on the biohalogenation of signaling compounds that interfere with bacterial communication. These reactions are catalyzed by haloperoxidases, a class of metal-dependent enzymes, whose activity can be emulated by ceria nanoparticles. The enzyme-like activity of ceria was enhanced by a factor of 3 through bismuth substitution (Ce1− x Bi x O2− δ ). The solubility of Bi 3+ in CeO2 is confined to the range 0 < x < 0.25 under quasi-hydrothermal conditions. The Bi 3+ cations are located close to the nanoparticle surface because their ionic radii are larger than those of the tetravalent Ce 4+ ions. The synthesis of Ce1− x Bi x O2− δ (0 < x < 0.25) nanoparticles was upscaled to yields of ∼50 g. The halogenation activity of Ce1− x Bi x O2− δ was demonstrated with phenol red assays. The maximum activity for x ≈ 0.2 is related to the interplay of the ζ-potential of surface-engineered Ce1− x Bi x O2− δ nanoparticles and their BET surface area. Ce0.80 Bi0.20 O1.9 nanoparticles with optimized activity were incorporated in polyethersulfone beads, which are typical constituents of water filter membrane supports. Although Ce1− x Bi x O2− δ nanoparticles are not bactericidal on their own, naked Ce1− x Bi x O2− δ nanoparticles and polyethersulfone/Ce1− x Bi x O2− δ nanocomposites showed a strongly reduced bacterial coverage. We attribute the decreased adhesion of the Gram-negative soil bacterium Pseudomonas aeruginosa and of Phaeobacter gallaeciensis, a primary bacterial colonizer in marine biofilms, to the formation of halogenated signaling compounds. No biocides are needed, H2 O2 (formed in daylight) and halide are the only substrates required. The haloperoxidase-like activity of Ce1− x Bi x O2− δ may be a promising starting point for the development of environmentally friendly, "green" nanocomposites, when the use of conventional biocides is prohibited.