Team:Wisconsin-Madison
From 2012.igem.org
Line 127: | Line 127: | ||
In synthetic biology, one of the most powerful tools a research has is the ability to express heterologous genes in Escherichia coli. Unfortunately this does not always work. A common challenge when using non-native genes in metabolic engineering is determining if they are being properly expressed. To address this issue, we have constructed a BioFusion compatible system for diagnosing the failure of a gene expression at the translational level. This system couples the translation of the target gene to a fluorescent reporter gene. Fluorescence will only be detected when the target gene is entirely translated. This construct enables synthetic biologists to quickly determine if a gene is being expressed without the need for costly antibiodies or analytical instruments. | In synthetic biology, one of the most powerful tools a research has is the ability to express heterologous genes in Escherichia coli. Unfortunately this does not always work. A common challenge when using non-native genes in metabolic engineering is determining if they are being properly expressed. To address this issue, we have constructed a BioFusion compatible system for diagnosing the failure of a gene expression at the translational level. This system couples the translation of the target gene to a fluorescent reporter gene. Fluorescence will only be detected when the target gene is entirely translated. This construct enables synthetic biologists to quickly determine if a gene is being expressed without the need for costly antibiodies or analytical instruments. | ||
</p> | </p> | ||
- | <p class="classtheinlinecontent" style="font-style:italic">This tool is based on a phenomenon known as translational coupling. </p> | + | <p align="center" class="classtheinlinecontent" style="font-style:italic">This tool is based on a phenomenon known as translational coupling. </p> |
</div> | </div> | ||
<!--div close description2!--> | <!--div close description2!--> |
Revision as of 15:16, 23 September 2012
Engineering the limonene production metabolic pathway: TCC.
Creating a tool to evaluate the translation of heterologous genes in Eschericia coli.
TCC
Translational couplding cassette
In synthetic biology, one of the most powerful tools a research has is the ability to express heterologous genes in Escherichia coli. Unfortunately this does not always work. A common challenge when using non-native genes in metabolic engineering is determining if they are being properly expressed. To address this issue, we have constructed a BioFusion compatible system for diagnosing the failure of a gene expression at the translational level. This system couples the translation of the target gene to a fluorescent reporter gene. Fluorescence will only be detected when the target gene is entirely translated. This construct enables synthetic biologists to quickly determine if a gene is being expressed without the need for costly antibiodies or analytical instruments.
This tool is based on a phenomenon known as translational coupling.