Difference between revisions of "Team:UNITN-Trento/Description"

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<p style="margin-top:1em;">A typical MFC is composed of two separate chambers, the anode and the cathode, separated by a proton exchange membrane (PEM). Bacteria are grown in the anode <strong>under anaerobic condition</strong>.  The <strong>electrons</strong> are the product of the bacteria metabolism. The lack of oxygen as acceptor enables the electrons to be transferred to the electrode. In the cathode, electrons combine with oxygen and protons to form water.</p>
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<p style="margin-top:1em;">A typical MFC is composed of two separate chambers, the anode and the cathode, separated by a proton exchange membrane (PEM). Bacteria are grown in the anode under anaerobic condition.  The electrons are the product of the bacteria metabolism. The lack of oxygen as acceptor enables the electrons to be transferred to the electrode. In the cathode, electrons combine with oxygen and protons to form water.</p>
 
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<h4 class="header4  lateral-icon wow flipInX delay05"><span>Life in the anode</span> <i class="faabig flaticon-bacteria3"></i></h4>  
 
<h4 class="header4  lateral-icon wow flipInX delay05"><span>Life in the anode</span> <i class="faabig flaticon-bacteria3"></i></h4>  
 
 
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<p style="clear:both;">In the anode there is <strong>no oxygen</strong> and bacteria must survive under anaerobic conditions. Our system uses <span class="bacterium">E. coli</span>  as the model organism. <span class="bacterium">E. coli</span>  is a facultative anaerobic bacterium, able to live without oxygen undergoing fermentation. In these conditions, the  bacterial metabolism is <strong>slowed down</strong> and thus affecting the electrons production. Our idea is to increase <span class="bacterium">E. coli</span> viability in the anaerobic anode, in order to <strong>optimize electricity production</strong>.</p>
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<p style="clear:both;">In the anode there is no oxygen and bacteria must survive under anaerobic conditions. Our system uses <span class="bacterium">E. coli</span>  as the model organism. <span class="bacterium">E. coli</span>  is a facultative anaerobic bacterium, able to live without oxygen undergoing fermentation. In these conditions, the  bacterial metabolism is slowed down and thus affecting the electrons production. Our idea is to increase <span class="bacterium">E. coli</span> viability in the anaerobic anode, in order to optimize electricity production.</p>
 
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<h4 class="header4 lateral-icon wow flipInX delay05"> <span> Exploiting sunlight power: Proteorhodopsin </span><i class="faabig flaticon-sunbeam "></i> </h4>
 
<h4 class="header4 lateral-icon wow flipInX delay05"> <span> Exploiting sunlight power: Proteorhodopsin </span><i class="faabig flaticon-sunbeam "></i> </h4>
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<p style="clear:both;">Proteorhodopsin (PR) is a light-powered proton pump that belongs to the rhodopsin family. This 7-transmembrane protein exploits light to create an <strong>outward proton gradient</strong>, increasing the proton motive force (pmf) across the membrane. The generated pmf can subsequently <strong>power cellular processes</strong>. In particular, PR supports a <strong>light-driven ATP synthesis</strong> as proton reenter the cell through the H<sup>+</sup>-ATP synthetase complex. Therefore PR should increase the lifespan of <span class="bacterium">E. coli</span> and the electron flow under anaerobic conditions. Our new composite part (<a class="i_linker registry" href="http://parts.igem.org/Part:BBa_K1604010" target="_blank">BBa_K1604010</a>) is an <span class="i_enph">improvement</span> of the proteorhodopsin part that we extracted from the registry (<a href="http://parts.igem.org/Part:BBa_K773002" class="i_linker registry" target="_blank">BBa_K773002</a>). We added a strong RBS and placed the gene under an inducible promoter. We fully characterized the part to demonstrate that <span class="i_enph">the proton pump does work</span> when the bacteria are light exposed.</p>
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<p style="clear:both;">Proteorhodopsin (PR) is a light-powered proton pump that belongs to the rhodopsin family. This 7-transmembrane protein exploits light to create an outward proton gradient, increasing the proton motive force (pmf) across the membrane. The generated pmf can subsequently power cellular processes. In particular, PR supports a light-driven ATP synthesis as proton reenter the cell through the H<sup>+</sup>-ATP synthetase complex. Therefore PR should increase the lifespan of <span class="bacterium">E. coli</span> and the electron flow under anaerobic conditions.</p>
 
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<h4 class="header4 lateral-icon wow flipInX delay05"> <span>Retinal-producer: blh</span> <i class="faabig flaticon-atom27"></i></h4>
 
<h4 class="header4 lateral-icon wow flipInX delay05"> <span>Retinal-producer: blh</span> <i class="faabig flaticon-atom27"></i></h4>
 
 
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<p>Proteorhodopsin needs retinal as chromophore. In the MFC, PR-engineered <span class="bacterium">E. coli</span> can be supplemented with all-trans-retinal. A cheaper solution is to engineer a retinal-producer <span class="bacterium">E. coli</span> with <strong>&beta;-carotene 15,15’-dioxygenase</strong> (encoded by the gene blh), an enzyme that splits one molecule of &beta;-carotene into two molecules of retinal.(<a class="i_linker registry" href="http://parts.igem.org/Part:BBa_K1604022" target="_blank">BBa_K1604022</a>)  We also engineered <span class="bacterium">E. coli</span> with enzymes required for <strong>&beta;-carotene production</strong>.
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<p>Proteorhodopsin needs retinal as chromophore. In the MFC, PR-engineered E. coli can be supplemented with all-trans-retinal. A cheaper solution is to engineer a retinal-producer <span class="bacterium">E. coli</span> with <strong>&beta;-carotene 15,15’-dioxygenase</strong> (encoded by the gene blh), an enzyme that splits one molecule of &beta;-carotene into two molecules of retinal. We also engineered <span class="bacterium">E. coli</span> with enzymes required for <strong>&beta;-carotene production</strong>.
 
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<h4 class="header4 lateral-icon wow flipInX delay05"> <span>How can electrons be stolen?</span><i class="faabig flaticon-chemistry33"></i></h4>
 
<h4 class="header4 lateral-icon wow flipInX delay05"> <span>How can electrons be stolen?</span><i class="faabig flaticon-chemistry33"></i></h4>
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<p style="clear:both;">Electrons can be stolen by <strong>exogenous mediators</strong> or by expressing <strong>heterologous-cytochrome</strong> in <span class="bacterium">E. coli</span>. <i>Shewanella odenensis</i> Mtr electrons transport pathway transfers metabolic electrons across the double membrane. Electrons are transported from CymA to MtrA and from MtrA to MtrC through the MtrCAB complex. The electrons coming out from MtrC are in direct contact with the electrodes. Alternatively, electrons can be transferred to the electrodes by exogenous chemical redox molecules called mediators (e.g. neutral red and methylen blue).</p>
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<p style="clear:both;">Electrons can be stolen by exogenous mediators or by expressing heterologous-cytochrome in <span class="bacterium">E. coli</span>. <i>Shewanella odenensis</i> Mtr electrons transport pathway transfers metabolic electrons across the double membrane. Electrons are transported from CymA to MtrA and from MtrA to MtrC through the MtrCAB complex. The electrons coming out from MtrC are in direct contact with the electrodes. Alternatively, electrons can be transferred to the electrodes by exogenous chemical redox molecules called mediators (e.g. neutral red and methylen blue).</p>
 
 
 
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<h4 class="header4 lateral-icon wow flipInX delay05">  <span>pncB: an electron producer booster</span> <i class="faabig flaticon-atomic4"></i></h4>
 
<h4 class="header4 lateral-icon wow flipInX delay05">  <span>pncB: an electron producer booster</span> <i class="faabig flaticon-atomic4"></i></h4>
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<p style="clear:both;">We planned to increase electrons production by <strong>over-expressing pncB</strong>. This gene encodes for the enzyme NAPRTase (nicotinic acid phosphorbosyl-transferase) that catalyzes the formation of nicotinate mono-nucleotide, a direct precursor of NAD, starting from NA.(<a class="i_linker registry" href="http://parts.igem.org/Part:BBa_K1604031" target="_blank">BBa_K1604031</a>)  The presence of higher levels of NAD should push the cell to produce more electron carriers molecules (NADH), thus <strong>increasing electricity</strong>.</p>
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<p style="clear:both;">We planned to increase electrons production by over-expressing pncB. This gene encodes for the enzyme NAPRTase (nicotinic acid phosphorbosyl-transferase) that catalyzes the formation of nicotinate mono-nucleotide, a direct precursor of NAD, starting from NA. The presence of higher levels of NAD should push the cell to produce more electron carriers molecules (NADH), thus increasing electricity.</p>
 
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<p>MFCs provide new opportunities for the <strong>sustainable energy production</strong>, a rapidly evolving technology. In particular, our controlled and self-sustainable platform could have many future applications. We envision that our Solar pMFCs will become a valid <strong>cheaper</strong> and <strong>greener</strong> alternative to modern photovoltaic panels. Solar energy activates the system, that provides electricity to sustain domestic needs.</p>  
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<p>MFCs provide new opportunities for the sustainable energy production, a rapidly evolving technology. In particular, our controlled and self-sustainable platform could have many future applications. We envision that our Solar pMFCs will become a valid cheaper and greener alternative to modern photovoltaic panels. Solar energy activates the system, that provides electricity to sustain domestic needs.</p>  
 
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Revision as of 15:15, 16 September 2015

Solar pMFC

A Microbial Fuel Cell with a light-driven E. coli engine.

Solar pMFC

Microbial Fuel Cells (MFCs) are bio-electrochemical systems that drive current by using bacteria, that are isolated often times from waste waters or soil. Modeling the metabolism and electron transfer strategies of the bacteria living in waste waters through a controlled system based on a single species can help to optimize and enhance the MFCs technological landscape. Our idea is to optimize MFC’s platform using an engineered E. coli that exploits sunlight to live better under stressful conditions and that has an increased electron production.

A typical MFC is composed of two separate chambers, the anode and the cathode, separated by a proton exchange membrane (PEM). Bacteria are grown in the anode under anaerobic condition. The electrons are the product of the bacteria metabolism. The lack of oxygen as acceptor enables the electrons to be transferred to the electrode. In the cathode, electrons combine with oxygen and protons to form water.

How it works

Life in the anode

In the anode there is no oxygen and bacteria must survive under anaerobic conditions. Our system uses E. coli as the model organism. E. coli is a facultative anaerobic bacterium, able to live without oxygen undergoing fermentation. In these conditions, the bacterial metabolism is slowed down and thus affecting the electrons production. Our idea is to increase E. coli viability in the anaerobic anode, in order to optimize electricity production.

Exploiting sunlight power: Proteorhodopsin

Proteorhodopsin (PR) is a light-powered proton pump that belongs to the rhodopsin family. This 7-transmembrane protein exploits light to create an outward proton gradient, increasing the proton motive force (pmf) across the membrane. The generated pmf can subsequently power cellular processes. In particular, PR supports a light-driven ATP synthesis as proton reenter the cell through the H+-ATP synthetase complex. Therefore PR should increase the lifespan of E. coli and the electron flow under anaerobic conditions.

Retinal-producer: blh

Proteorhodopsin needs retinal as chromophore. In the MFC, PR-engineered E. coli can be supplemented with all-trans-retinal. A cheaper solution is to engineer a retinal-producer E. coli with β-carotene 15,15’-dioxygenase (encoded by the gene blh), an enzyme that splits one molecule of β-carotene into two molecules of retinal. We also engineered E. coli with enzymes required for β-carotene production.

How can electrons be stolen?

Electrons can be stolen by exogenous mediators or by expressing heterologous-cytochrome in E. coli. Shewanella odenensis Mtr electrons transport pathway transfers metabolic electrons across the double membrane. Electrons are transported from CymA to MtrA and from MtrA to MtrC through the MtrCAB complex. The electrons coming out from MtrC are in direct contact with the electrodes. Alternatively, electrons can be transferred to the electrodes by exogenous chemical redox molecules called mediators (e.g. neutral red and methylen blue).

pncB: an electron producer booster

We planned to increase electrons production by over-expressing pncB. This gene encodes for the enzyme NAPRTase (nicotinic acid phosphorbosyl-transferase) that catalyzes the formation of nicotinate mono-nucleotide, a direct precursor of NAD, starting from NA. The presence of higher levels of NAD should push the cell to produce more electron carriers molecules (NADH), thus increasing electricity.

Explore our idea!

Bla la la

A glance into the future

MFCs provide new opportunities for the sustainable energy production, a rapidly evolving technology. In particular, our controlled and self-sustainable platform could have many future applications. We envision that our Solar pMFCs will become a valid cheaper and greener alternative to modern photovoltaic panels. Solar energy activates the system, that provides electricity to sustain domestic needs.