Adsorption of a cationic polyelectrolyte on Escherichia coli bacteria: 2. Interactions between the bacterial surfaces covered with the polymer

Citation
X. Chatellier et al., Adsorption of a cationic polyelectrolyte on Escherichia coli bacteria: 2. Interactions between the bacterial surfaces covered with the polymer, LANGMUIR, 17(9), 2001, pp. 2791-2800
Citations number
31
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
LANGMUIR
ISSN journal
07437463 → ACNP
Volume
17
Issue
9
Year of publication
2001
Pages
2791 - 2800
Database
ISI
SICI code
0743-7463(20010501)17:9<2791:AOACPO>2.0.ZU;2-C
Abstract
Quaternized polyvinylpyridine (PVPQ) was used as a cationic polymer to dest abilize an Escherichia coli bacterial suspension. The optical density and t he fraction of free cells, obtained by light scattering measurements, were recorded as a function of the introduced polymer amount, as a way to monito r the stability of the suspension. The flocculation was almost complete for polymer dosages ranging from about 28 to 47 mg of carbon of PVPQ per dry g of bacteria. These dosages correspond to still negatively charged cells, a s shown by xi potential measurements. At low polymer coverages, a less effi cient flocculation is observed. At higher dosages, the suspension restabili zes. We interpret these results using our previous study on the adsorption of the polymer chains. We argue that the flocculation at low dosages is ren dered possible by the strong inhomogeneities of charge on the bacterial sur faces because of the self-similar configuration of the adsorbed polymer lay er and that the restabilization at large dosages is due to the small mesh s ize of the polymer network on the surface as well as to the Coulombic repul sion between the cells. The properties of the bacterial aggregates were inv estigated by light scattering. Destabilized suspensions produce aggregates with sizes decreasing as the quantity of adsorbed polymer increases. At the optimum of flocculation, the polydispersity of the aggregates is low, sugg esting a diffusion-limited aggregation mechanism (DLA). The presence of the characteristic self-similar structure of DLA aggregates, with a fractal di mension on the order of 1.9, is suggested by some of the light diffusion ex periments. On the other hand, at low coverages, that is, when only some reg ions on the surfaces are covered with polymers, the flocculation seems to o bey a reaction-limited aggregation, with a large polydispersity in the size of the aggregates.