Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/17265

TitleKinetic study of the redox processes in carbon electrodes with Geobacter sulfurreducens at different growth temperatures
Author(s)Peixoto, L.
Santos, Andréa F. S.
Machado, Idalina
Sousa, A. M. M.
Brito, A. G.
Parpot, Pier
Pereira, Maria Olívia
Nogueira, R.
Issue dateJul-2011
Abstract(s)Geobacter sulfurreducens is a bacteria that can transfer electrons directly to the electrode from different external membrane cytochromes. Each cytochrome is associated with a range of electrical potentials, being energetically more favourable than some others. Different growth conditions of the bacteria, such as temperature, may influence the prevalence of certain cytochromes in the external membrane. The aim of this work was to evaluate the difference in the kinetic parameters of the electronic transfer in G. sulfurreducens that growth at different temperatures (25 ºC and 37 ºC). The cyclic voltammetry is an electrochemical technique that can be used to assess the redox reactions between bacteria and electrode and was used to compare different cultures of G. sulfurreducens. With these studies it can be concluded that at different temperatures the oxidation peaks potentials and current intensities were different. The current intensity increased in bacteria that growth at higher temperatures but the potential of the oxidation peak was more anodic, thus more energy was required. The oxidation reaction was limited by diffusion. An irreversible electronic transfer is noticed. At 25ºC the kinetic of the reaction had a mixed control and charge transfer was reversible for lower sweep scan rates. SDS-Page was used to characterize the membrane protein complexes. The membrane proteins extracted from bacteria that growth at different temperatures migrated differently in the gel, revealing proteins of different molecular weights. G. sulfurreducens may provide an interesting model for structural comparison of proteins since the two samples revealed different profiles. The separation of the membrane proteins was obtained from sucrose gradient centrifugation and 2D electrophoresis. The complete proteins characterization is already being developed in our laboratories.
TypeAbstract
URIhttp://hdl.handle.net/1822/17265
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CEB - Resumos em Livros de Atas / Abstracts in Proceedings

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