Pile à bactéries | EPFL Graph Search

Une pile microbienne (ou biopile ou pile à bactéries) est une pile basée sur le principe des piles à combustible: la cathode est alimentée en oxygène (en général par l'air) et l'anode est constituée d'une électrode placée au sein d'une chambre contenant un biofilm de bactéries et de quoi les nourrir. Elles sont également désignées par l'acronyme MFC provenant de la dénomination anglo-saxonne : microbial fuel cell (littéralement : Pile à combustible microbienne). Principe Les molécules carbonées produites par les êtres vivants le sont sous des formes réduites qui peuvent être oxydées sous l'action du dioxygène de l'air. La chaîne respiratoire des êtres vivants est d'ailleurs basée sur ce principe. Il est donc possible de produire de l'énergie à partir de molécules carbonées. Il existe des piles fonctionnant sans bactéries, basée sur l'oxydation spontanée du glucose. Mais la bactérie grâce à son cycle catalytique, peut spectaculairement augmenter la cinétique de l

Insights into the microbial reduction of pentavalent and hexavalent uranium species by Shewanella oneidensis MR-1

Margaux Camille Andréa Molinas

Decades of uranium-related activities such as ore mining, nuclear power generation, weapon manufacture, storage of nuclear wastes, have contributed to the release of U in the environment. U occurrence is concerning, since in surface environments, U is typically found in the U(VI) oxidation state, as uranyl, complexed with various ligands, and is highly soluble. Therefore, this toxic metal is likely to leech into soils and contaminate surface waters and groundwaters. In addition, owing to the long half-lives of the predominant isotopes 238U and 235U, U is considered as a persistent contaminant over geological timescales. For several decades, efforts have focused on the development of in situ remediation solutions to tackle U pollution in the subsurface, and limit its mobility.With this aim, interest in the metabolic potential for U(VI)-respiration by dissimilatory metal-reducing bacteria (DMRB), such as Shewanella oneidensis MR-1, has seen a significant increase. This metabolically-versatile bacterium has been reported to reduce mobile U(VI) to typically insoluble crystalline and amorphous U(IV). The reduction of U(VI) in S. oneidensis MR-1 is coupled to the oxidation of an electron donor, which feeds electrons into an electron transport chain, extending from the cytoplasm to the outer-membrane of the cells. The microbially mediated reduction of U(VI) to U(IV) is the result of a two-step process. It is assumed that one electron is first transferred to U(VI) to form a pentavalent U(V) intermediate, followed by the abiotic disproportionation of two U(V) atoms into U(IV) and U(VI). However, evidence for this mechanism is limited to experimental systems rich in carbonate, which permits the rapid disproportionation of U(V). Thus, it remains unclear whether a second, biologically-mediated, electron transfer to U(V) is possible under conditions in which disproportionation is limited. To explore this, a novel U(V)-dpaea complex, that is stable in water at pH 7, was utilized to investigate the second step of the reduction mechanism. Here, we observed that U(V) can be biologically reduced by an additional one-electron transfer, resulting in the accumulation of U(IV) without the need for disproportionation. To improve our understanding of the molecular mechanism of U-dpaea reduction, we incubated mutant strains of S. oneidensis MR-1, lacking (i) only outer-membrane c-type cytochromes or (ii) all c-type cytochromes, with solid phase U(VI)-dpaea and aqueous U(V)-dpaea. We determined that U(VI)-dpaea reduction proceeds via the initial dissolution of the solid phase and that U(V)-dpaea reduction is mediated by outer-membrane c-type cytochromes. In particular, in vitro reactions between the purified outer-membrane c-type cytochrome MtrC and U(V)-dpaea demonstrated that MtrC can directly transfer electrons to U(V)-dpaea.Finally, we sought to determine the factors that influence electron transfer kinetics between DMRB and U. To this end, we reacted U(VI) coordinated by various aminocarboxylate ligands with purified MtrC. Here, U speciation significantly impacted reduction rates and appeared to be related to the binding strength of the U-MtrC interaction, i.e., hydrogen bonding versus electrostatic.All together, these findings provide further insights in the reduction mechanism of U by DMRB, and underline the importance of U speciation in controlling the pathway and rate of electron transfer.

EPFL2021

Scale-up of phosphate remobilization from sewage sludge in a microbial fuel cell

Christos Comninellis, Thomas Egli, Fabian Fischer, Alain-François Grogg, Marc Sugnaux, Géraldine Zufferey

Phosphate remobilization from digested sewage sludge containing iron phosphate was scaled-up in a microbial fuel cell (MFC). A 3 litre triple chambered MFC was constructed. This reactor was operated as a microbial fuel cell and later as a microbial electrolysis cell to accelerate cathodic phosphate remobilization. Applying an additional voltage and exceeding native MFC power accelerated chemical base formation and the related phosphate remobilization rate. The electrolysis approach was extended using a platinum-RVC cathode. The pH rose to 12.6 and phosphate was recovered by 67% in 26 h. This was significantly faster than using microbial fuel cell conditions. Shrinking core modelling particle fluid kinetics showed that the reaction resistance has to move inside the sewage sludge particle for considerable rate enhancement. Remobilized phosphate was subsequently precipitated as struvite and inductively coupled plasma mass spectrometry indicated low levels of cadmium, lead, and other metals as required by law for recycling fertilizers. (C) 2015 Elsevier Ltd. All rights reserved.

Elsevier Sci Ltd2016

Microbial bioelectrochemical cells for hydrogen generation based on irradiated semiconductor photoelectrodes

Fabian Fischer, Ulf Anders Hagfeldt, Michele Morgante, Nikolaos Vlachopoulos

In recent years, one of the most important challenges of the 21st century is to satisfy the ever-increasing world's energy demand. Many efforts are being undertaken to find alternative renewable energy sources, which ideally should outcompete fossil fuel use in all its aspects. In this respect, photo-assisted microbial bioelectrochemical cells (MBECs) in which the reduction of water to hydrogen takes place have been of considerable interest in recent years. Two categories of such systems have been investigated: MBECs with a semiconductor photocathode or photoanode, and hybrid systems, in which an MBEC cell with dark electrodes is coupled to an electrochemical photovoltaic cell. A common denominator of all these systems is the need of microorganisms at the anode, the action of which results in the generation of an electron flow by organic matter oxidation. The aim of this review is to describe the general working principles, with respect to both biochemical and electrochemical aspects, and the performance of various categories of hydrogen-generating photo-assisted MBECs.

IOP PUBLISHING LTD2021

Insights into the microbial reduction of pentavalent and hexavalent uranium species by Shewanella oneidensis MR-1

Margaux Camille Andréa Molinas

EPFL2021