Abstract

The rising concern about the potential toxicity of synthetic gold nanoparticles (AuNPs) in aquatic environments requires a rigorous estimation of physico-chemical parameters of reactions between AuNPs and major freshwater microorganisms. This study addresses the interaction of 10-nm size, positively charged AuNPs with periphytic freshwater diatoms (Eolimna minima). The adsorption experiments on viable cells were performed in 10 mM NaCl and 5 mM NaCl + 5 mM NaHCO3 solution at a variable pH (3–10), at an AuNPs concentration from 1 µg/L to 10,000 µg/L, and an exposure time from a few minutes to 55 days. Three types of experiments, adsorption as a function of time (kinetics), pH-dependent adsorption edge, and constant-pH “Langmuirian” type isotherms, were conducted. In addition, long-term interactions (days to weeks) of live diatoms (under light and in the darkness) were performed. The adsorption was maximal at a pH from 3 to 6 and sizably decreased at a pH of 6 to 10. Results of adsorption experiments were modeled using a second order kinetic model, a Linear Programming Model, Freundlich isotherm, and a ligand binding equation for one site competition. The adsorption of AuNPs(+) most likely occurred on negatively-charged surface sites of diatom cell walls such as carboxylates or phosphorylates, similar to previously studied metal cations. Under light exposure, the AuNPs were stabilized in aqueous solution in the presence of live cells, probably due to the production of exometabolites by diatoms. The adsorbed amount of AuNPs decreased after several days of reaction, suggesting some AuNPs desorption. In the darkness, the adsorption and assimilation were stronger than under light. Overall, the behavior of positively charged AuNPs at the diatom–aqueous solution interface is similar to that of metal cations, but the affinity of aqueous AuNPs to cell exometabolites is higher, which leads to the stabilization of nanoparticles in solution in the presence of diatoms and their exudates. During photosynthetic activity and the pH rising above 9 in the vicinity of diatom cells, the adsorption of AuNPs strongly decreases, which indicates a decreasing potential toxicity of AuNPs for photosynthesizing cells. The present study demonstrates the efficiency of a thermodynamic and kinetic approach for understanding gold nanoparticles interaction with aquatic freshwater peryphytic microorganisms.

Highlights

  • The rapid growth of the nanotechnology industry has led to the wide-scale production and application of engineered nanoparticles (NP)

  • It is known that these particles, and in particular amine coated gold nanoparticles, are able to penetrate a high variety of cells [11,12], and are recognized to be highly stable in aqueous solution [5]

  • In order to understand the impact of AuNPs on freshwater microbial ecosystems, the adsorption of AuNPs on cell surfaces should be studied as the first step before AuNPs internalization

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Summary

Introduction

The rapid growth of the nanotechnology industry has led to the wide-scale production and application of engineered nanoparticles (NP). Coagulation or flocculation techniques of nanoparticles by organic molecules have been developed [6,7,8], and the efficiency of gold nanoparticles as low-molecular-weight-chelators in aqueous suspensions has been demonstrated [9]. Their harmless nature has yet to be proven for living organisms in the natural environment. In order to understand the impact of AuNPs on freshwater microbial ecosystems, the adsorption of AuNPs on cell surfaces should be studied as the first step before AuNPs internalization

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