Team:Wisconsin-Madison/biosensor

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Both the ethanol (EtOH) and n-alkane sensors rely on an arabinose inducible two plasmid system for either EtOH or n-alkane detection. The first plasmid contains genes for producing a protein controlled the pBAD promoter, which turns on transcription of the <a href="https://2011.igem.org/Team:Wisconsin-Madison/genes">genes</a> in the presence of arabinose. The second plasmid has the EtOH or n-alkane promoter which turns on the transcription of our RFP. The production of the RFP is then measured with a plate reader.  
Both the ethanol (EtOH) and n-alkane sensors rely on an arabinose inducible two plasmid system for either EtOH or n-alkane detection. The first plasmid contains genes for producing a protein controlled the pBAD promoter, which turns on transcription of the <a href="https://2011.igem.org/Team:Wisconsin-Madison/genes">genes</a> in the presence of arabinose. The second plasmid has the EtOH or n-alkane promoter which turns on the transcription of our RFP. The production of the RFP is then measured with a plate reader.  
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In the <a href="https://2011.igem.org/Team:Wisconsin-Madison/directedevolution">directed evolution</a> construct, this two plasmid system is all put on a single plasmid, which the first plasmid’s parts being put on the reverse strand (5’ to 3’) of the DNA.  
In the <a href="https://2011.igem.org/Team:Wisconsin-Madison/directedevolution">directed evolution</a> construct, this two plasmid system is all put on a single plasmid, which the first plasmid’s parts being put on the reverse strand (5’ to 3’) of the DNA.  

Revision as of 11:20, 19 September 2011









Project >> Overview, Ethanol Sensor, Alkane Sensor, Microcompartment

Biosensors

Both the ethanol (EtOH) and n-alkane sensors rely on an arabinose inducible two plasmid system for either EtOH or n-alkane detection. The first plasmid contains genes for producing a protein controlled the pBAD promoter, which turns on transcription of the genes in the presence of arabinose. The second plasmid has the EtOH or n-alkane promoter which turns on the transcription of our RFP. The production of the RFP is then measured with a plate reader.


In the directed evolution construct, this two plasmid system is all put on a single plasmid, which the first plasmid’s parts being put on the reverse strand (5’ to 3’) of the DNA.


Learn more about biofuels, genes.