Team:Bielefeld-CeBiTec/Project/rMFC/Mediators

From 2014.igem.org

(Difference between revisions)
 
(27 intermediate revisions not shown)
Line 17: Line 17:
<html>
<html>
-
<h1> rMFC </h1>
+
<h1> Module I - Reverse Microbial Fuel Cell (rMFC) </h1>
<!-- Button begin -->
<!-- Button begin -->
-
<div id="main_menue" style="margin-left:25px; height:80px">
+
<div id="main_menue" style="margin-left:130px; height:80px">
<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/Theory"style="color:#000000">
<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/Theory"style="color:#000000">
   <div class="main_menueButton" style="width:100px">
   <div class="main_menueButton" style="width:100px">
               <p class="buttoncenter"><font color="#FFFFFF">Overview</font></p>
               <p class="buttoncenter"><font color="#FFFFFF">Overview</font></p>
 +
  </div>
 +
</a>
 +
 +
                        <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/GeneticalApproach"style="color:#000000">
 +
  <div class="main_menueButton" style="width:180px">
 +
              <p class="buttoncenter"><font color="#FFFFFF">Genetical Approach</font></p>
   </div>  
   </div>  
</a>
</a>
Line 45: Line 51:
   </div>  
   </div>  
</a>
</a>
 +
<!--
                         <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/Cultivation"style="color:#000000">
                         <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/Cultivation"style="color:#000000">
   <div class="main_menueButton" style="width:110px">
   <div class="main_menueButton" style="width:110px">
Line 50: Line 57:
   </div>  
   </div>  
</a>
</a>
-
 
+
-->
-
                        <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/GeneticalApproach"style="color:#000000">
+
                         <!--a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/Outlook"style="color:#000000">
-
  <div class="main_menueButton" style="width:180px">
+
-
              <p class="buttoncenter"><font color="#FFFFFF">Genetical Approach</font></p>
+
-
  </div>
+
-
</a>
+
-
 
+
-
                         <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/Outlook"style="color:#000000">
+
   <div class="main_menueButton" style="width:100px">
   <div class="main_menueButton" style="width:100px">
               <p class="buttoncenter"><font color="#FFFFFF">Outlook</font></p>
               <p class="buttoncenter"><font color="#FFFFFF">Outlook</font></p>
   </div>  
   </div>  
-
</a>
+
</a-->
 +
                        <br><br><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Results/rMFC"style="color:#000000">
 +
  <div class="main_menueButton" style="width:90px; float:right;margin-right:140px">
 +
              <p class="buttoncenter"><font color="#FFFFFF">Results</font></p>
 +
  </div>
 +
</a>
</div>
</div>
<!-- Button End -->
<!-- Button End -->
-
 
+
<br>
<div class="element" style="margin:10px 10px 10px 10px; padding:10px 10px 10px 10px">  
<div class="element" style="margin:10px 10px 10px 10px; padding:10px 10px 10px 10px">  
   <div id="text">
   <div id="text">
-
   <h6>Neutral Red</h6>
+
   <h6 id="NR">Neutral Red</h6>
-
     <p> Neutral red (3-Amino-7-dimethylamino-2-methylphenazine hydrochloride) is a phenazine-based dye which is normally used as pH-indicator due to the fact that it changes its colour from red (pH 6.8) to yellow (pH 8.0).<br> Besides that it could be shown that reduced neutral red is also capable as the sole source of reducing power for growth and metabolism of H2 consuming bacteria cultures.(<a href="#Park2000">Park, D. H. &amp; Zeikus, J. G. 2000</a>) <br>   
+
     <p> Neutral red (3-Amino-7-dimethylamino-2-methylphenazine hydrochloride) is a phenazine-based dye which is normally used as pH-indicator due to the fact that it changes its colour from red (pH 6.8) to yellow (pH 8.0).<br> It could be shown that reduced neutral red is also capable as the sole source of reducing power for growth and metabolism of H<sub>2</sub consuming bacteria cultures.((<a href="#Park2000">Park, D. H. &amp; Zeikus, J. G. 2000</a>) <br>   
The chemical structure is shown in figure 1.
The chemical structure is shown in figure 1.
Line 81: Line 87:
</div>
</div>
-
That indicates that based on its redox-potential it can function as an electron-shuttle from the electrode to the cells getting reduced by an one step two electron transfer.(<a href="#Azariah1998">Azariah, A. N. et al., 1998</a>)<br>  
+
That indicates that based on its redox-potential it can function as an electron-shuttle from the electrode to the cells getting reduced by an one step two electron transfer.(<a href="#Azariah1998">Azariah, A. N. et al., 1998</a>) In this case the literature value for the redox potential of neutral red accounts to -325 mV vs. NHE.(<a href="#Futz1982">Futz, M. L. & Durst, R. A., 1982</a>) <br>  
-
There is also evidence that electrically reduced neutral red can bind to the cell membrane and chemically reduces NAD. Furthermore it is not toxic to the cells  
+
There is also evidence that electrically reduced neutral red can bind to the cell membrane and chemically reduces NAD. Furthermore it is not toxic to the cells. (<a href="#Park1999">Park et al., 1999</a>)   
-
and can replace H<sub>2</sub> which is the natural electron shuttle for some bacteria species. (<a href="#Park1999">Park et al., 1999</a>)   
+
</div>
</div>
Line 91: Line 96:
<div class="element" style="margin:10px 10px 10px 10px; padding:10px 10px 10px 10px">  
<div class="element" style="margin:10px 10px 10px 10px; padding:10px 10px 10px 10px">  
   <div id="text">
   <div id="text">
-
   <h6>Bromophenol Blue</h6>
+
   <h6 id="BPB">Bromphenol Blue</h6>
-
Bromphenolblue is a triarylmethane dye that is similar to neutral red and also capable to function as mediator.
+
Bromphenol blue is a triarylmethane dye that is similar to neutral red and is normally used as a biological stain or as a pH indicator.(<a href="#Pubchem">NCBI:PubChem Compound</a>) Having a redox potential of -739 mV vs. SCE it is also capable to function as a mediator.(<a href="#Strehlitz1994">Strehlitz et al., 1994</a>)
 +
<br>Figure 2 shows the chemical structure of bromphenol blue.
<center>
<center>
Line 104: Line 110:
<div class="element" style="margin:10px 10px 10px 10px; padding:10px 10px 10px 10px">  
<div class="element" style="margin:10px 10px 10px 10px; padding:10px 10px 10px 10px">  
   <div id="text">
   <div id="text">
-
   <h6>Cytochromes</h6>
+
   <h6 id="Cytochromes">Cytochromes</h6>
-
Cytochromes are hemoproteins which act as a part of electron transport in the respiratory chain. Depending on the characteristics of the cytochrome it can be assigned to one of three main groups, called cytochrome <i>a</i>, <i>b</i> and <i>c</i>.<br> Members of the cytochrome <i>a</i> class are the reduction/oxidation units of the cytochrome-oxidase which catalyzes the electron transport from cytochrome <i>c</i> to oxygen as the final electron acceptor. <i>B</i>-type cytochromes are known to have the lowest redoxpotential of the respiratory chain and are located between ubichinon and cytochrome <i>c</i>. <br>However <i>c</i>-type cytochromes are the best studied and most abundant group of cytochromes. For metal-reducing bacteria it has been already shown that several of these <i>c</i>-type cytochromes are essential for electron transfer between an electrode and the cell. Therefore they can function as an electrondonor as well as an acceptor by changing the redox state of the iron atom of their porphyrin complex. <br> The heme group of cytochrome <i>c</i> is shwon in figure 3. <br>  
+
Apart from the synthetic mediators like neutral red or bromphenol blue there are naturally occuring mediators like cytochromes. Cytochromes are hemoproteins which are part of electron transport in the respiratory chain and therefore they play a role in <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/Theory"
 +
target="_blank">direct electron transfer</a> from an electrode to the cells. Depending on its characteristics cytochromes can be assigned to one of three main groups, cytochrome <i>a</i>, <i>b</i> and&nbsp;<i>c</i>.(<a href="#Spektrum2001">Spektrum,&nbsp;2001</a>)<br> Members of the cytochrome <i>a</i> class are the reduction/oxidation units of the cytochrome-oxidase which catalyzes the electron transport from cytochrome <i>c</i> to oxygen, the final electron acceptor. <i>B</i>-type cytochromes are known to have the lowest redoxpotential of the respiratory chain and are located between ubichinon and cytochrome <i>c</i>.(<a href="#Spektrum2001">Spektrum, 2001</a>) <br>However, <i>c</i>-type cytochromes are the best studied and most abundant group of cytochromes. For metal-reducing bacteria it has been already shown that several of these <i>c</i>-type cytochromes are essential for electron transfer between an electrode and the cell. Therefore they can function as an electron donor as well as an electron acceptor by changing the redox state of their heme group. The heme group consists of an iron atom surrounded by porphyrin rings and is shown in Figure 3.(<a href="#Qiao2010">Qiao et al., 2010</a><br>  
<center><div class="element" style="height:250px; width:250px; text-align:center">
<center><div class="element" style="height:250px; width:250px; text-align:center">
                       <a href="https://static.igem.org/mediawiki/2014/3/33/Bielefeld_CeBiTec_2014-09-24_csoS1-4_cPCR_08_22.png" target="_blank"><img src="https://static.igem.org/mediawiki/2014/4/4a/Bielefeld-CeBiTec_2014-10-14_Heme_group-01.png" height="230px"></a><br><font size="2"><b>Figure 3:</b>heme group of cytochrome <i>c</i></font>
                       <a href="https://static.igem.org/mediawiki/2014/3/33/Bielefeld_CeBiTec_2014-09-24_csoS1-4_cPCR_08_22.png" target="_blank"><img src="https://static.igem.org/mediawiki/2014/4/4a/Bielefeld-CeBiTec_2014-10-14_Heme_group-01.png" height="230px"></a><br><font size="2"><b>Figure 3:</b>heme group of cytochrome <i>c</i></font>
                     </div></center>
                     </div></center>
-
 
+
These heme groups are located in the inner core of the protein which is an advantage for reduction/oxidation reactions as well as a problem at the same time. To avoid side reactions with gases like oxygen or carbon monoxide the position of the heme group is favourable, because it ensures that it is sufficiently protected from an unwanted reactant. However, it is assumed that the location in the inner core of the protein and the resulting poor accessibility could also be a reason for a limited or blocked  direct electron transfer between the electrode and the heme. For that reason the electrode material is key factor and different materials have to be tested to optimize the direct electron transfer via cytochromes.(<a href="#Qiao2010">Qiao et al., 2010</a>)<br>
-
Thus the fact that the heme groups of cytochromes are located in the inner core of the protein is an advantage for reduction/oxidation reactions as well as a problem at the same time. For the avoidance of unwanted reaction with gases like oxygen or carbon monoxide the structure of c-type cytochromes is favourable because it ensures that the heme group is sufficiently protected from these molecules. However it is assumed that this structure could also be a reason why the direct electron transfer between the electrode and the heme group could be limited or blocked because the heme group is poorly accessible. For that reason the electrode material is essential and different ones have to be tested for optimization of direct electron transfer via cytochromes.  
+
One of the best known organisms that are able to accept electrons from an electrode is <i>Geobacter sulfurreducens</i>. It has been demonstrated that current-consuming biofilms of this organism highly express a periplasmic key-type cytochrome <i>c</i> with one heme group. The deletion of the corresponding gene <i>GSU 3274</i> leads to a total inhibition of electron uptake.(<a href="#Strycharz2011">Strycharz et al., 2011</a>) <br> This indicates the importance of this <i>c</i>-type cytochrome for current-consuming biofilms and caused us to consider it as an potential alternative to realize enhanced electron uptake in <i>E. coli</i>.
</p>
</p>
   </div>
   </div>
</div>
</div>
 +
 +
 +
 +
<br>
 +
<!-- Button begin -->
 +
 +
<div id="main_menue" style="margin-left:130px; height:80px">
 +
<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/Theory"style="color:#000000">
 +
  <div class="main_menueButton" style="width:100px">
 +
              <p class="buttoncenter"><font color="#FFFFFF">Overview</font></p>
 +
  </div>
 +
</a>
 +
 +
                        <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/GeneticalApproach"style="color:#000000">
 +
  <div class="main_menueButton" style="width:180px">
 +
              <p class="buttoncenter"><font color="#FFFFFF">Genetical Approach</font></p>
 +
  </div>
 +
</a>
 +
 +
<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/ReactorSystem"style="color:#000000">
 +
  <div class="main_menueButton" style="width:150px">
 +
              <p class="buttoncenter"><font color="#FFFFFF">Reactor system</font></p>
 +
  </div>
 +
</a>
 +
 +
                        <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/MeasurementSystem"style="color:#000000">
 +
  <div class="main_menueButton" style="width:200px">
 +
              <p class="buttoncenter"><font color="#FFFFFF">Measurement System</font></p>
 +
  </div>
 +
</a>
 +
 +
                        <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/Mediators"style="color:#000000">
 +
  <div class="main_menueButtonActual" style="width:100px">
 +
              <p class="buttoncenter"><font color="#FFFFFF">Mediators</font></p>
 +
  </div>
 +
</a>
 +
<!--
 +
                        <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/Cultivation"style="color:#000000">
 +
  <div class="main_menueButton" style="width:110px">
 +
              <p class="buttoncenter"><font color="#FFFFFF">Cultivation</font></p>
 +
  </div>
 +
</a>
 +
-->
 +
                        <!--a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Project/rMFC/Outlook"style="color:#000000">
 +
  <div class="main_menueButton" style="width:100px">
 +
              <p class="buttoncenter"><font color="#FFFFFF">Outlook</font></p>
 +
  </div>
 +
</a-->
 +
 +
</div>
 +
 +
<!-- Button End -->
 +
 +
<div class="element">  
<div class="element">  
Line 141: Line 202:
</li>
</li>
</ul>
</ul>
 +
 +
<ul>
 +
<li id="Fultz1982">
 +
<div class="element" style="margin:10px 10px 10px 10px; padding:10px 10px 10px 10px">
 +
  <div id="text">
 +
    Fultz, M. L., Durst, R. A. (1982): Mediator compounds for the electrochemical study of biological redox systems: a compilation <a href="http://www.sciencedirect.com/science/article/pii/S0003267001954479#" target="_blank">Analytica Chimica Acta. </a> ,140, pp. 1-18
 +
  </div>
 +
</div>
 +
</li>
 +
</ul>
 +
<ul>
<ul>
Line 154: Line 226:
</ul>
</ul>
 +
<ul>
 +
<li id="Pubchem">
 +
<div class="element" style="margin_10px 10px 10px 10px; padding:10px 10px 10px 10px">
 +
<div id="text">
 +
  <a href="http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=8272&loc=ec_rcs#itabs-2d" target="_blank">NCBI:PubChem Compound</a>: Bromphenol Blue
 +
</div>
 +
</div>
 +
</li>
 +
</ul>
 +
<ul>
 +
<li id="Strehlitz1994">
 +
<div class="element" style="margin_10px 10px 10px 10px; padding:10px 10px 10px 10px">
 +
<div id="text"> Strehlitz, B., Gründig, B., Vorlop, K.-D., Bartholmes, P., Kotte, H., Stottmeister, U. (1994) Artificial electron donors for nitrate and nitrite reductases usable as mediators in amperometric biosensors.
 +
In: <a href="http://link.springer.com/article/10.1007%2FBF00323479"
 +
target="_blank">Fresenius' Journal of Analytical Chemistry</a>, 349, pp. 676-678.
 +
</div>
 +
</div>
 +
</li>
 +
</ul>
 +
 +
<ul>
 +
<li id="Spektrum2001">
 +
<div class="element" style="margin_10px 10px 10px 10px; padding:10px 10px 10px 10px">
 +
<div id="text">
 +
  <a href="http://spektrum.de/lexikon/biologie-kompakt/cytochrome/2817" target="_blank">Spektrum Akademischer Verlag (2001)</a>: Kompaktlexikon der Biologie - Cytochrome
 +
</div>
 +
</div>
 +
</li>
 +
</ul>
 +
 +
<ul>
 +
<li id="Qiao2010">
 +
<div class="element" style="margin_10px 10px 10px 10px; padding:10px 10px 10px 10px">
 +
<div id="text">
 +
  Qiao, Y., Bao, S. &amp; Li, C. M. (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"
 +
target="_blank">Energy Environ. Sci.</a> 3 (5), pp. 544 - 553.
 +
</div>
 +
</div>
 +
</li>
 +
</ul>
 +
 +
 +
 +
<ul>
 +
<li id="Strycharz2011">
 +
<div class="element" style="margin_10px 10px 10px 10px; padding:10px 10px 10px 10px">
 +
<div id="text">
 +
Stycharz, S. M., Glaven, R. H., Coppi, M. V., Gannon, S. M., Perpetua, L. A., Liu, A., Nevin, K. P. &amp. Lovley, D. R. (2011):Gene expression and deletion analysis of mechanisms for electron transfer from
 +
electrodes to <i>Geobacter sulfurreducens</i>.
 +
In: <a href="http://www.sciencedirect.com/science/article/pii/S1567539410001167"
 +
target="_blank">Bioelectrochemistry</a> 80, pp. 142 - 150.
 +
</div>
 +
</div>
 +
</li>
</html>
</html>

Latest revision as of 03:52, 18 October 2014


Module I - Reverse Microbial Fuel Cell (rMFC)


Neutral Red

Neutral red (3-Amino-7-dimethylamino-2-methylphenazine hydrochloride) is a phenazine-based dye which is normally used as pH-indicator due to the fact that it changes its colour from red (pH 6.8) to yellow (pH 8.0).
It could be shown that reduced neutral red is also capable as the sole source of reducing power for growth and metabolism of H2Park, D. H. & Zeikus, J. G. 2000)
The chemical structure is shown in figure 1.


Figure 1: Chemical structure of the triphenylmethane dye neutral red.
That indicates that based on its redox-potential it can function as an electron-shuttle from the electrode to the cells getting reduced by an one step two electron transfer.(Azariah, A. N. et al., 1998) In this case the literature value for the redox potential of neutral red accounts to -325 mV vs. NHE.(Futz, M. L. & Durst, R. A., 1982)
There is also evidence that electrically reduced neutral red can bind to the cell membrane and chemically reduces NAD. Furthermore it is not toxic to the cells. (Park et al., 1999)
Bromphenol Blue
Bromphenol blue is a triarylmethane dye that is similar to neutral red and is normally used as a biological stain or as a pH indicator.(NCBI:PubChem Compound) Having a redox potential of -739 mV vs. SCE it is also capable to function as a mediator.(Strehlitz et al., 1994)
Figure 2 shows the chemical structure of bromphenol blue.

Figure 2: Chemical structure of the triphenylmethane dye bromphenol blue.
Cytochromes
Apart from the synthetic mediators like neutral red or bromphenol blue there are naturally occuring mediators like cytochromes. Cytochromes are hemoproteins which are part of electron transport in the respiratory chain and therefore they play a role in direct electron transfer from an electrode to the cells. Depending on its characteristics cytochromes can be assigned to one of three main groups, cytochrome a, b and c.(Spektrum, 2001)
Members of the cytochrome a class are the reduction/oxidation units of the cytochrome-oxidase which catalyzes the electron transport from cytochrome c to oxygen, the final electron acceptor. B-type cytochromes are known to have the lowest redoxpotential of the respiratory chain and are located between ubichinon and cytochrome c.(Spektrum, 2001)
However, c-type cytochromes are the best studied and most abundant group of cytochromes. For metal-reducing bacteria it has been already shown that several of these c-type cytochromes are essential for electron transfer between an electrode and the cell. Therefore they can function as an electron donor as well as an electron acceptor by changing the redox state of their heme group. The heme group consists of an iron atom surrounded by porphyrin rings and is shown in Figure 3.(Qiao et al., 2010)

Figure 3:heme group of cytochrome c
These heme groups are located in the inner core of the protein which is an advantage for reduction/oxidation reactions as well as a problem at the same time. To avoid side reactions with gases like oxygen or carbon monoxide the position of the heme group is favourable, because it ensures that it is sufficiently protected from an unwanted reactant. However, it is assumed that the location in the inner core of the protein and the resulting poor accessibility could also be a reason for a limited or blocked direct electron transfer between the electrode and the heme. For that reason the electrode material is key factor and different materials have to be tested to optimize the direct electron transfer via cytochromes.(Qiao et al., 2010)
One of the best known organisms that are able to accept electrons from an electrode is Geobacter sulfurreducens. It has been demonstrated that current-consuming biofilms of this organism highly express a periplasmic key-type cytochrome c with one heme group. The deletion of the corresponding gene GSU 3274 leads to a total inhibition of electron uptake.(Strycharz et al., 2011)
This indicates the importance of this c-type cytochrome for current-consuming biofilms and caused us to consider it as an potential alternative to realize enhanced electron uptake in E. coli.


References
  • Park, D. H. & Zeikus, J. G. (2000) Electricity generation in microbial fuel cells using neutral red as an electronophore. In: Applied and Environmental Microbiology, 66 (4), pp. 1292 - 1297.
  • Fultz, M. L., Durst, R. A. (1982): Mediator compounds for the electrochemical study of biological redox systems: a compilation Analytica Chimica Acta. ,140, pp. 1-18
  • Park, D. H.,Laivenieks, M., Guettler, M. V., Jain, M. K. & Zeikus, J. G. (1999) Microbial utilization of electrically reduced neutral red as the sole electron donor for growth and metabolic production. In: Appl. Environ. Microbiol., 65 (7), pp. 2912 - 2917.
  • Strehlitz, B., Gründig, B., Vorlop, K.-D., Bartholmes, P., Kotte, H., Stottmeister, U. (1994) Artificial electron donors for nitrate and nitrite reductases usable as mediators in amperometric biosensors. In: Fresenius' Journal of Analytical Chemistry, 349, pp. 676-678.
  • Qiao, Y., Bao, S. & Li, C. M. (2010): Electrocatalysis in microbial fuel cells—from electrode material to direct electrochemistry. In: Energy Environ. Sci. 3 (5), pp. 544 - 553.