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Surface‐catalysed disinfection of thick Pseudomonas aeruginosa biofilms
Author(s) -
; Wood,
CaldweII,
Mark D. Evans,
; Jones,
Korber,
Wolfhaardt,
Wilson Marcelo,
Frédéric Gilbert
Publication year - 1998
Publication title -
journal of applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.889
H-Index - 156
eISSN - 1365-2672
pISSN - 1364-5072
DOI - 10.1046/j.1365-2672.1998.00446.x
Subject(s) - biofilm , pseudomonas aeruginosa , chemistry , diffusion , microbiology and biotechnology , bacteria , biology , physics , genetics , thermodynamics
Transition metal catalysts were incorporated into polymers which formed the surface for bacterial attachment and biofilm formation in a constant depth film fermenter (100 μm thickness), flow chamber (about 30 μm thickness) and in batch culture (<30 μm thickness). The catalysts drive the breakdown of persulphates to reactive oxygen species. When Pseudomonas aeruginosa biofilms were exposed to dilute solutions of potassium monopersulphate (20 μg ml −1 –1 mg ml −1 ), significant enhancement of killing was notable for catalyst‐containing surfaces over that of controls. The degree of enhancement was greatest for thin films, but was nevertheless significant for the 100 μm thick biofilms. Fluorescence probes and viability staining, in conjunction with laser confocal microscopy, showed that reactive species were generated at the biofilm–substratum interface and killed the biofilm from the inside. Reaction‐diffusion limitation now concentrates the active species within the biofilm rather than protecting it, and a diffusion pump is established whereby further treatment agent is drawn to the substratum enabling relatively thick biofilms to be disinfected.