Difference between revisions of "Team:NRP-UEA-Norwich/Results"
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| − | + | Cloning the FeFe and NiFe hydrogenase genes individually into iGEM BioBricks, which can then be cloned into pBAD vector using Golden Gate Cloning (GGC). | |
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Revision as of 00:56, 19 October 2016
Results
Cloning Results
Cloning the FeFe and NiFe hydrogenase genes individually into iGEM BioBricks, which can then be cloned into pBAD vector using Golden Gate Cloning (GGC).
BioBricks
In order to assess whether our BioBricks would function in our chassis organism Shewanella oneidensis MR-1 we attempted to transform and express two BioBricks into S. oneidensis MR-1; J04450 containing a gene for the red fluorescent protein (RFP) and K584001 which contains a gene for the green fluorescent protein (GFP). These BioBricks were chosen as they contain reporter genes and successfully transformed colonies could be easily identified under UV light.
Triparental conjugation and electroporation of plasmids containing 8A5 and 9A5 constructs into wild type, double knock out and FeFe knock out Shewanella oneidensis MR-1
Triparental conjugation and electroporation of plasmids containing 8A5 and 9A5 constructs into wild type, double knock out and FeFe knock out Shewanella oneidensis MR-1
Measuring the Optical Density of the Shewanella Oneidensis knockout strain (LS473) and Wildtype strain (MR-1) with a media control
Date: 18th - 19th August 2016
Aim: The aim of the experiment is to measure the optical density of both the MR-1 shewanella oneidensis strains (MR1 and LS473) when stored anaerobically and quantify the amount of hydrogen in the headspace gas using gas chromatography.
Sponsors
