IGEM:Cambridge/2008/Notebook/Voltage/Gene Design: Difference between revisions

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==Amplification from E.coli MG1655==
==Amplification from E.coli MG1655==
*This was performed via PCR amplification of the genome template using the following primers:
*This was performed via PCR amplification of the genome template using the following primers:
           -Forward: ATATGAATTCATATTCTAGATGAGTGCAGGCGTGATAACCGGCGTATT
           -Forward: ATAT'''GAATTC'''ATAT'''TCTAGA'''TGAGTGCAGGCGTGATAACCGGCGTATT
         
                        ''EcoRI''      ''XbaI''
 
           -Reverse: CTCTCTGCAGCTCTACTAGTTTATTCATCAAGTTTATCCAGCGCCAGAT
           -Reverse: CTCTCTGCAGCTCTACTAGTTTATTCATCAAGTTTATCCAGCGCCAGAT



Revision as of 07:27, 4 September 2008

KdpF-C Biobrick

Gene Selection

  • Kdp is a well documented P-Type K+ ATPase found naturally in E.coli, used to actively pump ions into the cell.
  • It consists of a 6-gene operon: F,A,B,C,D,E Where F-C are the functional membrane protein subunits, and D-E comprises a bacterial 2-component regulatory system.

  • Literature shows that Kdp acts as a high-affinity transport system, and works most effectively at low external potassium concentrations, where a change in ion flux would be most likely to produce a measurable voltage difference.
  • The D-E 2-component system consists of a membrane protein turgidity sensor and a transcription factor. It controls Kdp operon expression in vivo, by reducing gene expression when turgor is high.
  • Since we wish to over-express Kdp, we decided not to include the regulatory system in our biobrick. (Osmotic buffering would be used instead.)

Amplification from E.coli MG1655

  • This was performed via PCR amplification of the genome template using the following primers:
         -Forward: ATATGAATTCATATTCTAGATGAGTGCAGGCGTGATAACCGGCGTATT 
                       EcoRI      XbaI
         -Reverse: CTCTCTGCAGCTCTACTAGTTTATTCATCAAGTTTATCCAGCGCCAGAT
  • Primer overhangs incorporated the biobrick prefix and suffix into the section, restriction sites shown in bold .
  • The result of this PCR is shown below:

Integration into Vector

Promoter+RBS Biobrick

Promoter and RBS Selection

Amplification from E.coli MG1655

Integration into Vector

GluR0 Biobrick

Gene Selection

DNA Synthesis