Team:Bielefeld-CeBiTec/Project/rMFC

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<h1> rMFC </h1>
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   <h6>Short summary</h6>
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     <p>In the first module we aim to identify possible mediators that are capable for electron transport. We want to use electricity to chemically reduce these mediators and transport them into the cells. The process takes place in a bioreactor called "reverse microbial fuel cell" (rMFC). One important requirement for a suitable mediator is that its reduction potential is high enough to restore reduction equivalents, like NAD(P)H (nicotinamide adenine dinucleotide (phosphate)). These reduction equivalents enter the respiratory chain where ATP (adenosine triphosphate) is produced which will be used in the <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/CO2-fixation">next module.</a></p>
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<p><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Results/rMFC">Here </a> you will find the results of the rMFC.</p>
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     <p>In the first module we aim to identify possible mediators that are capable for electron transport. We want to
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      use electricity to chemically reduce these mediators and transport them into the cells. The process takes  
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      place in a bioreactor called "reverse microbial fuel cell" (rMFC). One important requirement for a suitable  
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      mediator is that its reduction potential is high enough to restore reduction equivalents, like NAD(P)H  
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      (nicotinamide adenine dinucleotide (phosphate)). These reduction equivalents enter the respiratory chain where  
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      ATP (adenosine triphosphate) is produced which will be used in the <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/CO2-fixation">next module.</a>
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  <br><br>
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    <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Results/rMFC">Here </a> you will find the results of  
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          the rMFC.
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   <h6>Design of a electrobiochemical reactor system</h6>
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   <h6>References</h6>
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    <p>To perform our cultivation experiments under well defined conditions it was necessary to design a new bioreactor system. Besides the typically controlled parameters in bioreactors like the oxygen partial pressure, pH-signal, temperature and other parameters, it was indispensable to have the possibility to energize the reactor with a defined current. That is why we decided to build an H-cell reactor. This kind of reactor consits of two compartments which are connected by a glass flange. It is possible to fix a membrane in the middle of the flange connection so that the two compartments are seperated. We used a cation selective Nafion&reg; membrane which allowed the divison of the two compartments into an anode and cathode space. <br>
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For the investigation of electroactive microorganisms highly sensitive analytics are required. That is why we use a Potentiostat which allows to set and hold a defined electrode potential. Furthermore we tried out different media and buffer compositions and observed the effect of different electrode materials on the mediator oxidation and reduction peaks. <br>
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The H-cell reactor could be used for batch fermentations and is constructed for the electron transfer via a mediator. That is why we considered an alternative reactor design. The other reactor concept is named "scalable flow cell reactor" (SFC) and allows an continous mode of operation. In this reactor type the electron transfer must be realized by direct electron transfer. That is possible if the cells stay in direct contact to the electrode material. The electron transfer is carried out by cytochromes in the outer membrane. That is why we focused on different types of mediators and the expression of key type cytochromes.  
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  Lovley, Derek R., 2011. Powering microbes with electricity: direct electron transfer from electrodes to microbes. In: <a href="http://onlinelibrary.wiley.com/doi/10.1111/j.1758-2229.2010.00211.x/abstract"
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target="_blank">Environmental Microbiology Reports 3 (1)</a>, pp. 27–35.
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  Lovley, Derek R. & Nevin, Kelly P., 2013. Electrobiocommodities: powering microbial production of fuels and commodity chemicals from carbon dioxide with electricity. In: <a href="http://dx.doi.org/10.1016/j.copbio.2013.02.012"
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target="_blank">Current Opinion in Biotechnology</a>, 24, pp. 385-390.
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  Qiao, Yan; Bao, Shu-Juan; Li, Chang Ming (2010): Electrocatalysis in microbial fuel cells—from electrode material to direct electrochemistry. In: <a href="http://pubs.rsc.org/en/Content/ArticleLanding/2010/EE/b923503e#!divAbstract"
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target="_blank">Energy Environ. Sci.</a>, 3 (5), pp. 544.
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  Harnisch, F. & Freguia, S., 2012. A Basic Tutorial on Cyclic Voltammetry for the investigation of Electroactive Microbial Biofilms.
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In: <a href="http://www.ncbi.nlm.nih.gov/pubmed/22279004"
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target="_blank">Chemistry – An Asian Journal</a>, 7 (3), pp. 466–475.
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Latest revision as of 09:27, 15 October 2014


rMFC

Short summary

In the first module we aim to identify possible mediators that are capable for electron transport. We want to use electricity to chemically reduce these mediators and transport them into the cells. The process takes place in a bioreactor called "reverse microbial fuel cell" (rMFC). One important requirement for a suitable mediator is that its reduction potential is high enough to restore reduction equivalents, like NAD(P)H (nicotinamide adenine dinucleotide (phosphate)). These reduction equivalents enter the respiratory chain where ATP (adenosine triphosphate) is produced which will be used in the next module.

Here you will find the results of the rMFC.

References
  • Lovley, Derek R., 2011. Powering microbes with electricity: direct electron transfer from electrodes to microbes. In: Environmental Microbiology Reports 3 (1), pp. 27–35.
  • Lovley, Derek R. & Nevin, Kelly P., 2013. Electrobiocommodities: powering microbial production of fuels and commodity chemicals from carbon dioxide with electricity. In: Current Opinion in Biotechnology, 24, pp. 385-390.
  • Qiao, Yan; Bao, Shu-Juan; Li, Chang Ming (2010): Electrocatalysis in microbial fuel cells—from electrode material to direct electrochemistry. In: Energy Environ. Sci., 3 (5), pp. 544.
  • Harnisch, F. & Freguia, S., 2012. A Basic Tutorial on Cyclic Voltammetry for the investigation of Electroactive Microbial Biofilms. In: Chemistry – An Asian Journal, 7 (3), pp. 466–475.

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