Albert T. Poortinga

Electric double layer interactions in bacterial adhesion to surfaces

The DLVO (Derjaguin, Landau, Verwey, Overbeek) theory was originally developed to describe interactions between non-biological lyophobic colloids such as polystyrene particles, but is also used to describe bacterial adhesion to surfaces. Despite the differences between the surface of bacteria and that of non-biological particles, DLVO-descriptions of bacterial adhesion have nearly always treated bacteria as if they were non-biological particles and consequently in many cases these descriptions have failed to describe bacterial adhesion adequately. This review summarizes recent advances in colloid and surface science regarding the electrokinetic characterization of biological colloids, most notably bacteria, and their electric double layer interactions with surfaces

Controlled electrophoretic deposition of bacteria to surfaces for the design of biofilms

In this report, the formation of ordered clusters of both spherical and rod-shaped bacteria on an electrode during electrophoretic deposition is described. Inside clusters, adhering bacteria are regularly spaced with an interbacterial distance that can be controlled by adjusting the ionic strength of the suspending solution and the DC density used. Formed clusters can be immobilized on the surface by applying a sufficiently high current density. This method enables the design of bacterial biofilms for biotechnological and biomedical applications. When AC fields were used, rod-shaped bacteria adhering on the electrode were seen to align parallel to the applied field.

Measurement of charge transfer during bacterial adhesion to an indium tin oxide surface in a parallel plate flow chamber

An experimental method is described for the measurement of charge transfer during bacterial adhesion in situ to a transparent, semiconducting indium tin oxide (ITO) coated glass plate in a parallel plate flow chamber. Bacterial adhesion is measured simultaneously with either the electric potential or the capacitance of the surface. Initial bacterial adhesion was accompanied by a change in electric potential of the surface with no measurable change in capacitance. Consequently, it can be assumed that the change in electric potential of the surface is due to charge transfer between bacteria and the surface, and it can be calculated that, on average, a charge of about 10(-14) C per bacterium is exchanged during initial adhesion, which corresponds to only several percent of the total surface charge of a bacterium. Charge transfer could either be to or from the bacterial cell surface, dependent on the bacterial strain involved and the ionic strength used.

Charge transfer during staphylococcal adhesion to TiNOX® coatings with different specific resistivity

Adhesion of the bacterial strain Staphylococcus epidermidis 3399 to titanium-oxy-nitride (TiNOX) substrata with different specific resistivities was studied in a parallel plate flow chamber, while simultaneously measuring the electric potential of the substrata. During adhesion, bacteria either donated or accepted electrons to the substrata depending on the specific resistivity of the substratum and bacteria that had donated electrons to the substratum adhered more strongly than bacteria that had accepted electrons from the substratum. These results demonstrate that electron transfer plays a role in bacterial adhesion to conducting surfaces, which has hitherto been neglected.

Electrostatic interactions in the adhesion of an ion-penetrable and ion-impenetrable bacterial strain to glass

Deposition to glass of Streptococcus salivarius HB-C12 and Staphylococcus epidermidis 3399 in a parallel plate flow chamber has been studied as a function of ionic strength. Electrophoretic mobility measurements revealed that S. epidermidis 3399 possesses a thick ion-penetrable layer, probably associated with its encapsulation, while S. salivarius HB-C12 has an ion-impenetrable surface. Streaming potential measurements indicated that also the glass surface was covered with a relatively thin, ion-penetrable layer. Theoretical initial deposition rates of both strains to glass were obtained by numerically solving the convective-diffusion equation, while accounting for the ion-penetrability of the interacting surfaces. Experimentally, the initial deposition rate of the ion-penetrable strain S. epidermidis 3399 was found to be higher and less dependent on ionic strength than of the ion-impenetrable S. salivarius HB-C12, in accordance with theoretical expectations. Agreement between theoretical and experimental deposition rates could be obtained when glass was considered ion-penetrable when interacting with the ion-penetrable organism S. epidermidis 3399, while glass behaved as an ion-impenetrable surface when interacting with the ion-impenetrable S. salivarius HB-C12. Probably, interaction with an ion-impenetrable strain drives the diffuse double layer charges into the limited volume of the thin ion-penetrable layer on the glass, readily filling it up and making it appear ion-impenetrable. During interaction of glass with another ion-penetrable surface, as of S. epidermidis 3399, diffuse double layer charges move into both ion-penetrable surfaces, resulting in a much lower mobile charge density in the ion-penetrable layer on the glass which consequently continues to behave as ion-penetrable.

Lateral and Perpendicular Interaction Forces Involved in Mobile and Immobile Adhesion of Microorganisms on Model Solid Surfaces

Abstract. Gliding and near-surface swimming of microorganisms are described as a mobile form of microbial adhesion that need not necessarily be reversible. It is argued that the reversibility of microbial adhesion depends on the depth of the secondary interaction minimum, calculated from the forces between an organism and a substratum acting in a direction perpendicular to the substratum surface. The mobility of adhering microorganisms depends on lateral interactions between the organisms. On ideally homogeneous and smooth model surfaces, only mobile adhesion occurs because the multibody, lateral interactions are weak compared with the thermal or Brownian motion energy of the organisms. Minor chemical or structural heterogeneities, which exist on all real-life surfaces, yield a lateral interaction on adhering microorganisms. This causes their immobilization, which helps to explain the physicochemical nature of microbial gliding or near-surface swimming. Moreover, these lateral interaction energies are one order of magnitude smaller than the Lifshitz-Van der Waals, electrostatic, and acid-base forces acting perpendicular to substratum surfaces that are responsible for adhesion.

Influence of oral detergents and chlorhexidine on soft-layer electrokinetic parameters of the acquired enamel pellicle

Electron microscopy has described the salivary pellicle as an ‘uneven, knotted structure’. This study describes a novel soft-layer model of salivary pellicles, based on measured electrophoretic mobilities and the influence of dentifrices and a chlorhexidine mouthwash on the parameters of the model. The enamel surface was found to possess a high number of fixed, negative charges (zN = –62 mM) and to be electrophoretically hard (1/λ = 0.6 nm), i.e. impenetrable to fluid flow. Adsorption of a salivary pellicle resulted in a fourfold reduction in the surface fixed charge density (zN = –15 mM) along with an increase in electrophoretic softness (1/λ = 2.3 nm). Exposure of pellicles to various dentifrices containing sodium fluoride as an active component and sodium lauryl sulfate as a detergent had little effect on the surface fixed charge densities (varying between –15 and –30 mM, depending on the dentifrice involved) and electrophoretic softnesses (varying between 2.3 and 3.4 nm). Exposure of pellicles to a dentifrice containing sodium fluoride and hexametaphosphate as an additional detergent yielded soft (8.0 nm) pellicles, penetrable to fluid flow, with few fixed, negative charges (1 mM). This is opposite to the effects of chlorhexidine, which created an electrophoretically hard pellicle (1.7 nm). This soft-layer electrokinetic model quantitatively shows that the degree to which pellicles are penetrable to fluid flow differs upon exposure to dentifrices, with relevance for plaque formation, de- and remineralization and staining processes.

Lack of effect of an externally applied electric field on bacterial adhesion to glass

Deposition to glass of Streptococcus salivarius HB-C12 and Staphylococcus epidermidis 3399 in a parallel plate flow chamber in the absence and presence of an externally applied electric field has been studied experimentally. No effect on bacterial adhesion, including initial deposition rates, numbers of adhering bacteria after 4 h, spatial distributions of adhering bacteria and air bubble induced detachment, was found. A theoretical analysis shows that electric fields applied over a 150 µm thin glass substratum do not have a sufficiently strong effect on its surface potential to influence bacterial adhesion.