Difference between revisions of "Team:UC San Diego/Description"
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<h2>Project Description</h2> | <h2>Project Description</h2> | ||
| − | + | <h4>Uses of Luciferase</h4> | |
| − | <p>The lux system’s | + | <p>The lux system’s bioluminescent reaction has been the subject of intense research. It is most often used as a reporter for gene expression and for tracking animal cells in vivo, and has more recently been utilized in synthetic biology for biosensor construction. As a result, it offers a powerful tool to researchers seeking to monitor a wide variety of biological and chemical processes.</p> |
| − | + | <h3>About the Lux System</h3> | |
| − | + | <p>The luminescent output of the lux system is jointly controlled by the activity of luciferase and a substrate-producing enzymatic complex. Firefly luminescence is the most well-known example of this type of reaction, but bioluminescent reactions also occur in beetles, marine bacteria, and other organisms. Between species, these reactions differ mechanistically and involve structurally distinct substrates and enzymes. We are studying the bacterial lux system, in which an enzyme complex converts fatty acids into an aldehyde. Catalyzed by luciferase, these aldehydes then react with FMNH2 and oxygen, emitting a photon and producing a fatty acid, FMN, and water. FMNH2 is then regenerated by a flavin reductase, allowing for continuous light production with oxygen input.</p> | |
| + | <h4>Our Approach</h4> | ||
| + | <p>Using existing approaches, mathematical models are limited in how they can predict and optimize metabolic pathways. We will be expressing several permutations of the bacterial lux system to empirically determine its rate limiting steps by measuring the resulting light production. The identification of rate-limiting steps will then allow us to optimize the pathway. With these findings, an improved and experimentally validated mathematical model of the pathway will be constructed. By strategically altering biosynthetic gene expression, we will gain both a generalizable method to rapidly optimize metabolic pathways and a means to tailor the reporter/sensor to better suit our needs (i.e. make it brighter).</p> | ||
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Revision as of 20:23, 13 July 2015
Project Description
Uses of Luciferase
The lux system’s bioluminescent reaction has been the subject of intense research. It is most often used as a reporter for gene expression and for tracking animal cells in vivo, and has more recently been utilized in synthetic biology for biosensor construction. As a result, it offers a powerful tool to researchers seeking to monitor a wide variety of biological and chemical processes.
About the Lux System
The luminescent output of the lux system is jointly controlled by the activity of luciferase and a substrate-producing enzymatic complex. Firefly luminescence is the most well-known example of this type of reaction, but bioluminescent reactions also occur in beetles, marine bacteria, and other organisms. Between species, these reactions differ mechanistically and involve structurally distinct substrates and enzymes. We are studying the bacterial lux system, in which an enzyme complex converts fatty acids into an aldehyde. Catalyzed by luciferase, these aldehydes then react with FMNH2 and oxygen, emitting a photon and producing a fatty acid, FMN, and water. FMNH2 is then regenerated by a flavin reductase, allowing for continuous light production with oxygen input.
Our Approach
Using existing approaches, mathematical models are limited in how they can predict and optimize metabolic pathways. We will be expressing several permutations of the bacterial lux system to empirically determine its rate limiting steps by measuring the resulting light production. The identification of rate-limiting steps will then allow us to optimize the pathway. With these findings, an improved and experimentally validated mathematical model of the pathway will be constructed. By strategically altering biosynthetic gene expression, we will gain both a generalizable method to rapidly optimize metabolic pathways and a means to tailor the reporter/sensor to better suit our needs (i.e. make it brighter).