Funding Information This research was supported in part by the Samaria and Jordan Rift Valley Regional R and D Center, the Research Authority of the Ariel University Center and the Rappaport Foundation for Medical Microbiology, Bar-Ilan University (to Y.N.).
Special Issue Article
Current production in a microbial fuel cell using a pure culture of Cupriavidus basilensis growing in acetate or phenol as a carbon source
Article first published online: 10 JAN 2013
DOI: 10.1111/1751-7915.12026
© 2013 The Authors. Published by Society for Applied Microbiology and Blackwell Publishing Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Issue

Microbial Biotechnology
Early View (Online Version of Record published before inclusion in an issue)
Total views since publication: 270
Additional Information
How to Cite
Friman, H., Schechter, A., Ioffe, Y., Nitzan, Y. and Cahan, R. (2013), Current production in a microbial fuel cell using a pure culture of Cupriavidus basilensis growing in acetate or phenol as a carbon source. Microbial Biotechnology. doi: 10.1111/1751-7915.12026
Publication History
- Article first published online: 10 JAN 2013
- Manuscript Accepted: 30 NOV 2012
- Manuscript Revised: 27 NOV 2012
- Manuscript Received: 27 JUL 2012
Funded by
- Samaria and Jordan Rift Valley Regional R and D Center
- Research Authority of the Ariel University Center
- Rappaport Foundation for Medical Microbiology, Bar-Ilan University
Summary
A microbial fuel cell (MFC) was operated with a pure culture of Cupriavidus basilensis bacterial cells growing in the anode compartment in a defined medium containing acetate or phenol. Operating this mediator-less MFC under a constant external resistor of 1 kΩ with acetate or phenol led to current generation of 902 and 310 mA m−2 respectively. In the MFC which was operated using acetate or phenol, the current density measured from the plankton bacterial cells with a fresh electrode was 125 and 109 mA m−2, respectively, whereas the current obtained with biofilm-covered electrodes in sterile medium was 541 and 228 mA m−2 respectively. After 72 h in the MFC, 86% of the initial phenol concentration was removed, while only 64% was removed after the same time in the control MFC which was held at an open circuit potential (OCP). Furthermore, SEM and confocal microscopy analyses demonstrated a developed biofilm with a live C. basilensis population. In conclusion, in this study we demonstrated, for the first time, use of C. basilensis facultative aerobe bacterial cells in a MFC using acetate or phenol as the sole carbon source which led to electricity generation.

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