Team:Yale/Our Project

From 2010.igem.org

(Difference between revisions)
 
(80 intermediate revisions not shown)
Line 10: Line 10:
<p>
<p>
<ul id="proj-nav">
<ul id="proj-nav">
-
<li><b><a href="https://2010.igem.org/Team:Yale/Our Project">Project Overview</a></b></li>
+
<li><b><a href="https://2010.igem.org/Team:Yale/Our Project">introduction</a></b></li>
 +
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Applications">applications</a></li>
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Methods">methods</a></li>
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Methods">methods</a></li>
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Notebook">lab notebook</a></li>
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Notebook">lab notebook</a></li>
Line 16: Line 17:
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Safety">safety</a></li>
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Safety">safety</a></li>
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Future Work">future work</a></li>
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Future Work">future work</a></li>
-
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Applications">applications</a></li>
 
</ul>
</ul>
</p>
</p>
Line 23: Line 23:
<div id="right-col">
<div id="right-col">
<h5>
<h5>
-
introduction
+
Project Overview
</h5>
</h5>
<p>
<p>
-
<!------------- INTRODUCTION: NEEDS TO BE EDITED------------->
 
-
<a id="link" href="https://2010.igem.org/Team:Yale/Our Team">Yale-iGEM team </a> is doing great.
 
-
Welcome to Yale-iGEM 2010! In our inaugural year of iGEM competition, we have designed a system to harness biology to construct conductive circuits. <br/><br/>
+
<h6><i>What would it take to</i>...
 +
<br/>
 +
<br/>
 +
<b>Build a circuit using microbially catalyzed metal sulfide deposition?</b><h6/><hr /><br/>
-
<b>By enabling <i>E. coli</i> to affect local redox chemistry, we can use bacteria to construct circuit elements in a specified geometry. This could allow the manufacture of electrical components under biological conditions.</b><br/>
+
<img src="https://static.igem.org/mediawiki/2010/1/1a/Yale-bacteria-animation.gif">
-
<br/>
+
<br/>
 +
<p><h6>Background: SRB, H<sub>2</sub>S, and Copper Sulfides</h6>
 +
<p>The inspiration for this idea came from an ecological observation made of copper biomineralization by a species of Sulfate Reducing Bacteria. Sulfate Reducing Bacteria (<b>SRB</b>) comprise a family of chemolithotrophic bacteria that use sulfate as the terminal electron acceptor in anaerobic metabolism. As a result of sulfate reduction, these bacteria produce gaseous <b>H<sub>2</sub>S</b>. Subsequently, microbially generated H<sub>2</sub>S reduces copper in solution and precipitates soluble copper ions in the form of insoluble copper sulfide (<b>CuS</b>). It was discovered that by this method, some strains of SRB formed a CuS compound nearly identical to <b>covellite</b> - a natural superconductor (Weber, 2009). If this activity could be enhanced under spatial and temporal control, bacteria could be harnessed to deposit metal sulfide in specified geometries for manufacturing and engineering applications. <br/>
 +
 +
<h6>Building H<sub>2</sub>S Production Activity into <i>E. coli</i></h6>
 +
 +
<p>Investigation of H<sub>2</sub>S production in bacteria has been well documented in <i>E. coli</i>. Work by Dr. Jay Keasling at University of California, Berkeley, has shown that a gene encoding <b>Thiosulfate Reductase</b> from <i>Salmonella enterica</i> serovar Typhimurium has previously been expressed in <i>E. coli</i> to overproduce hydrogen sulfide from thiosulfate.
 +
 +
<p> The gene <a id="link" href="https://2010.igem.org/Team:Yale/Our_Project/Methods"><b>phsABC</b></a> functionally encodes Thiosulfate reductase. The gene itself contains an open reading frame for each of the three genes phsA, phsB, and phsC. The resulting complex of three transmembrane proteins constitutes Thiosulfate reductase and catalyzes the reduction of inorganic thiosulfate to hydrogen sulfide.
 +
 +
<br/>
 +
<br/>
 +
<img src="https://static.igem.org/mediawiki/2010/f/f4/Chemmechthiosulf.png" width="517.5" height="246.6"/>
 +
 +
<br/>
 +
<br/>
 +
 +
<p>This activity can be monitored by growing bacteria on
 +
<a id="link" href="https://2010.igem.org/Team:Yale/Our_Project/Methods/h2s_production"><b>Triple Sugar Iron (TSI) Agar</b></a>. Evolution of H<sub>2</sub>S as a gas, results in the reduction of Iron Sulfate to an Iron Sulfide. Iron sulfide precipitates as a black solid and can be easily identified visually on the macroscopic scale. Bacteria that are actively producing H<sub>2</sub>S will reduce the Iron in the medium, and turn the agar black.
 +
<br/>
 +
 +
<h6>Growing Bacteria In Copper Medium</h6>
 +
 +
<p> Bacteria expressing Thiosulfate Reductase can then be grown in media containing both a source of sulfur and free copper in solution. Some strains of <i>E. coli</i> exhibit robust growth in copper containing media, despite toxicity of high levels of copper in solution. By measuring cell growth and viability at varying concentrations of copper, we can maximize the reaction of H<sub>2</sub>S resulting from bacterial activity.
<br/>
<br/>
 +
<h6>Correlating Bacterial Growth to Copper Deposition</h6>
 +
<p>In this experimental system, the formation of the copper sulfide should be directly related to the disappearance of Cu2+ with time as the insoluble metal sulfide formed is a complex of copper and sulfur. As H<sub>2</sub>S production is turned on, there should be a subsequent decrease in soluble copper concentrations as copper is bound in the precipitated copper sulfide.
-
<b>Fabrication of Integrated Circuits (under construction!)</b><br/>
 
<br/>
<br/>
-
Nano/Micro scale circuits have been instrumental development of new concepts and technologies like the lab-in-a-chip. The wire deposition technique invented by the Yale team can be used to fabricate such circuits by depositing copper wire a substrate in a controlled fashion (Fig 1)
+
<h6>Localizing Copper Deposition</h6><br/>
-
[[Image:Example.jpg]]<br/>
+
 
 +
<img src="https://static.igem.org/mediawiki/2010/8/8b/Yalechannels3.gif" width="517.5" height="246.6"/>  
<br/>
<br/>
 +
<p> With bacteria able to affect CuS deposition, the next logical step is to control this activity spatially and temporally. Inspired by the work of Christine Jacobs-Wagner (Yale, MCDB), we built a mold for constructing agar channels in which to grow and constrain the active bacteria. A master mold was designed and constructed out of the polymer PDMS. This could then be used to iteratively create indented agar channels in our solid growth medium.
 +
 +
<p> When bacteria are washed over these channels, they become trapped in the indentation. By imposing a physical restraint prior to the induction of metal deposition activity, it is possible to control where the metal sulfide is deposited. This is a necessary requirement in the construction of a circuit.
 +
 +
<br/>
 +
<h6>Modeling the Construction of Metal Sulfides</h6>
 +
 +
<p>The metal sulfide can self-associate to form clusters of a mineral called covellite. This Copper Sulfide has a specific arrangements of unit cells. In an effort to model this, we used CAD to construct an idealized computer model for how this mineral deposition would effectively create a circuit.
 +
 +
<p> This method can then be applied for the construction and manufacture of innumerable microscale structures, ranging from electrical components to microfluidic devices. Read on to find out more about our <a id="link" href="https://2010.igem.org/Team:Yale/Our_Project/Applications"><b>applications!</b></a>
 +
<!------------- INTRODUCTION: NEEDS TO BE EDITED ------------->
<!------------- INTRODUCTION: NEEDS TO BE EDITED ------------->

Latest revision as of 03:53, 28 October 2010

iGEM Yale

Project Overview

What would it take to...

Build a circuit using microbially catalyzed metal sulfide deposition?



Background: SRB, H2S, and Copper Sulfides

The inspiration for this idea came from an ecological observation made of copper biomineralization by a species of Sulfate Reducing Bacteria. Sulfate Reducing Bacteria (SRB) comprise a family of chemolithotrophic bacteria that use sulfate as the terminal electron acceptor in anaerobic metabolism. As a result of sulfate reduction, these bacteria produce gaseous H2S. Subsequently, microbially generated H2S reduces copper in solution and precipitates soluble copper ions in the form of insoluble copper sulfide (CuS). It was discovered that by this method, some strains of SRB formed a CuS compound nearly identical to covellite - a natural superconductor (Weber, 2009). If this activity could be enhanced under spatial and temporal control, bacteria could be harnessed to deposit metal sulfide in specified geometries for manufacturing and engineering applications.

Building H2S Production Activity into E. coli

Investigation of H2S production in bacteria has been well documented in E. coli. Work by Dr. Jay Keasling at University of California, Berkeley, has shown that a gene encoding Thiosulfate Reductase from Salmonella enterica serovar Typhimurium has previously been expressed in E. coli to overproduce hydrogen sulfide from thiosulfate.

The gene phsABC functionally encodes Thiosulfate reductase. The gene itself contains an open reading frame for each of the three genes phsA, phsB, and phsC. The resulting complex of three transmembrane proteins constitutes Thiosulfate reductase and catalyzes the reduction of inorganic thiosulfate to hydrogen sulfide.



This activity can be monitored by growing bacteria on Triple Sugar Iron (TSI) Agar. Evolution of H2S as a gas, results in the reduction of Iron Sulfate to an Iron Sulfide. Iron sulfide precipitates as a black solid and can be easily identified visually on the macroscopic scale. Bacteria that are actively producing H2S will reduce the Iron in the medium, and turn the agar black.

Growing Bacteria In Copper Medium

Bacteria expressing Thiosulfate Reductase can then be grown in media containing both a source of sulfur and free copper in solution. Some strains of E. coli exhibit robust growth in copper containing media, despite toxicity of high levels of copper in solution. By measuring cell growth and viability at varying concentrations of copper, we can maximize the reaction of H2S resulting from bacterial activity.

Correlating Bacterial Growth to Copper Deposition

In this experimental system, the formation of the copper sulfide should be directly related to the disappearance of Cu2+ with time as the insoluble metal sulfide formed is a complex of copper and sulfur. As H2S production is turned on, there should be a subsequent decrease in soluble copper concentrations as copper is bound in the precipitated copper sulfide.

Localizing Copper Deposition


With bacteria able to affect CuS deposition, the next logical step is to control this activity spatially and temporally. Inspired by the work of Christine Jacobs-Wagner (Yale, MCDB), we built a mold for constructing agar channels in which to grow and constrain the active bacteria. A master mold was designed and constructed out of the polymer PDMS. This could then be used to iteratively create indented agar channels in our solid growth medium.

When bacteria are washed over these channels, they become trapped in the indentation. By imposing a physical restraint prior to the induction of metal deposition activity, it is possible to control where the metal sulfide is deposited. This is a necessary requirement in the construction of a circuit.

Modeling the Construction of Metal Sulfides

The metal sulfide can self-associate to form clusters of a mineral called covellite. This Copper Sulfide has a specific arrangements of unit cells. In an effort to model this, we used CAD to construct an idealized computer model for how this mineral deposition would effectively create a circuit.

This method can then be applied for the construction and manufacture of innumerable microscale structures, ranging from electrical components to microfluidic devices. Read on to find out more about our applications!