2 research outputs found
Accumulation of Amorphous Cr(III)–Te(IV) Nanoparticles on the Surface of <i>Shewanella oneidensis</i> MR‑1 through Reduction of Cr(VI)
Industrial effluents
constitute a major source of metal pollution
of aquatic bodies. Moreover, due to their environmental persistence,
toxic metal pollution is of special concern. Microbial reduction is
considered a promising strategy for toxic metal removal among the
several methods available for metal remediation. Here, we describe
the coremediation of toxic CrÂ(VI) and TeÂ(IV) by the dissimilatory
metal reducing bacterium-<i>Shewanella oneidensis</i> MR-1.
In the presence of both CrÂ(VI) and TeÂ(IV), <i>S. oneidensis</i> MR-1 reduced CrÂ(VI) to the less toxic CrÂ(III) form, but not TeÂ(IV)
to Te(0). The reduced CrÂ(III) ions complexed rapidly with TeÂ(IV) ions
and were precipitated from the cell cultures. Electron microscopic
analyses revealed that the Cr–Te complexed nanoparticles localized
on the bacterial outer membranes. K-edge X-ray absorption spectrometric
analyses demonstrated that CrÂ(III) produced by <i>S. oneidensis</i> MR-1was rapidly complexed with TeÂ(IV) ions, followed by formation
of amorphous CrÂ(III)–TeÂ(IV) nanoparticles on the cell surface.
Our results could be applied for the simultaneous sequestration and
detoxification of both CrÂ(VI) and TeÂ(IV) as well as for the preparation
of nanomaterials through environmental friendly processes
Methanogenesis Facilitated by Geobiochemical Iron Cycle in a Novel Syntrophic Methanogenic Microbial Community
Production
and emission of methane have been increasing concerns
due to its significant effect on global climate change and the carbon
cycle. Here we report facilitated methane production from acetate
by a novel community of methanogens and acetate oxidizing bacteria
in the presence of poorly crystalline akaganeite slurry. Comparative
analyses showed that methanogenesis was significantly enhanced by
added akaganeite and acetate was mostly stoichiometrically converted
to methane. Electrons produced from anaerobic acetate oxidation are
transferred to akaganeite nanorods that likely prompt the transformation
into goethite nanofibers through a series of biogeochemical processes
of soluble FeÂ(II) readsorption and FeÂ(III) reprecipitation. The methanogenic
archaea likely harness the biotransformation of akaganeite to goethite
by the FeÂ(III)–FeÂ(II) cycle to facilitate production of methane.
These results provide new insights into biogeochemistry of iron minerals
and methanogenesis in the environment, as well as the development
of sustainable methods for microbial methane production