D. Grasso et al., IMPACT OF PHYSIOLOGICAL-STATE ON SURFACE THERMODYNAMICS AND ADHESION OF PSEUDOMONAS-AERUGINOSA, Environmental science & technology, 30(12), 1996, pp. 3604-3608
A quantitative understanding of microorganism migration in geological
formations is critical to predict the dissemination of microorganisms
in the environment and to evaluate the efficacy of microbially mediate
d in situ pollutant degradation. The key event that retards the moveme
nt of microorganisms in the saturated zone with respect to the convect
ive water flow is the interaction between microorganisms and the matri
x surfaces. This interaction may result in adhesion and concomitant re
tardation. Interactions are determined by the surface thermodynamics o
f the microorganism and the matrix. Whereas the nature of the matrix s
ubstratum surface may be considered temporally invariant, the nature o
f bacterial cell surfaces is a function of its physiological state. Th
e work presented here explored quantitatively the impact of the physio
logical state of Pseudomonas aeruginosa Olin on its surface thermodyna
mic characteristics and its adhesion to dolomite. Lewis acid/base (hyd
rophobic), Lifshitz-van der Waals (electrodynamic), and Coulombic (ele
ctrostatic) forces were measured via contact angle measurements and el
ectrophoretic mobility assays. It was found that P. aeruginosa Olin ex
hibited a decreased electron-donating potential (gamma(i)(-)) and incr
eased zeta-potential in the stationary phase as compared with logarith
mic growth and decay phases. These changes in surface thermodynamic pr
operties were clearly manifested in subsequent partitioning experiment
s with dolomite. P. aeruginosa Olin was found to partition onto dolomi
te to a significantly larger extent in the stationary phase than in th
e logarithmic growth or decay phases. This observation further corrobo
rates the need to include Lewis acid/base interactions in the evaluati
on of bacterium/surface interactions. The reported results indicate th
e clear impact of physiological state on surface thermodynamics and ad
hesion.