Disruption of Autolysis in Bacillus subtilis using TiO2 Nanoparticles.

In contrast to many nanotoxicity studies where nanoparticles (NPs) are observed to be toxic or reduce viable cells in a population of bacteria, we observed that increasing concentration of TiO2 NPs increased the cell survival of Bacillus subtilis in autolysis-inducing buffer by 0.5 to 5 orders of magnitude over an 8 hour exposure. Molecular investigations revealed that TiO2 NPs prevent or delay cell autolysis, an important survival and growth-regulating process in bacterial populations. Overall, the results suggest two potential mechanisms for the disruption of autolysis by TiO2 NPs in a concentration dependent manner: (i) directly, through TiO2 NP deposition on the cell wall, delaying the collapse of the protonmotive-force and preventing the onset of autolysis; and (ii) indirectly, through adsorption of autolysins on TiO2 NP, limiting the activity of released autolysins and preventing further lytic activity. Enhanced darkfield microscopy coupled to hyperspectral analysis was used to map TiO2 deposition on B. subtilis cell walls and released enzymes, supporting both mechanisms of autolysis interference. The disruption of autolysis in B. subtilis cultures by TiO2 NPs suggests the mechanisms and kinetics of cell death may be influenced by nano-scale metal oxide materials, which are abundant in natural systems.

Exploring the impact of pore size distribution on the performance of carbon electrodes for capacitive deionization.

Capacitive deionization (CDI) removes charged ions from aqueous solutions through entrapment in the electric double layer (EDL) when the porous electrodes are polarized. In this study, three types of activated carbon cloth (ACC) with different pore-size distributions were used to study the effect of pore characteristics on electrosorption during CDI. Removal of seven different monovalent ions was examined for each ACC in batch reactors under 5 different combinations of applied potential and ionic strength. Results show underlying sorption mechanisms in the meso- and micro-pores were different. Electrosorption in the mesopores is influenced by partially-distorted EDL caused by EDL overlapping. Sorption capacity increased with increasing applied potential or ionic strength as overlapping effects were reduced. In contrast, EDL in the microporous regions could be highly distorted resulting in enhanced sorption capacity, which cannot be adequately described using the classic EDL theories. Electrosorption density (i.e., sorption capacity normalized by pore volume) decreased as the mesoporosity-to-microporosity ratio increased. These results are in agreement with those obtained using mathematical modeling by other recent CDI studies. Charge efficiency values were between 20% and 40% and appear to be substantially influenced by Faradaic reactions and ion desorption from the electrode surfaces. These findings suggest that pore-size distribution of electrode materials, especially the meso/microporosity ratio, should be optimized for the removal of targeted ions by CDI and well characterized to conduct more precise CDI modeling.