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| - | {{:Team:BCCS-Bristol/Header}}
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| - | {{:Team:BCCS-Bristol/NotebookHeader}}
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| - | ===Week 11===
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| - | ====Alternative Assembly Constructs====
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| - | *Last week's experiment was repeated with ARabinose induction occuring overnight. Again the FhuA-GFP construct seemed not to be growing.
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| - | *Cell concentration assays revealed that the fusion construct was inhibiting E.coli growth. The only GFP control seemed to be growing normally. (see results here)
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| - | *To test the inhibition fresh transformants of :
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| - | 1) AraC-RBS-OsmE
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| - | 2) AraC-RBS-FhuA
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| - | 3) AraC-RBS-FhuA-GFP
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| - | 4) AraC-RBS-GFP-Terminator
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| - | were set up. 3 colonies of each were picked and grown overnight. The next day 20ml cultures were set-up for each colony and growth was tested with A600 O.D. every half an hour (pre and post arabinose induction).
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| - | * Results indicate that construct 1 and 3 lyse the cells.
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| - | ==== Bioscaffold Tests =====
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| - | * To test for successful mutation 3 colonies of each mutated construct (BpuEI site mutated out) were miniprepped and tested with BpuEI. Unfortunately the enzyme was not working.
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| - | * To test the Bioscaffold the mutated construct of AraC-RBS-FhuA-Bioscaffold-GFP was transferred to the pSB2k3 backbone that is compatible with the Bioscaffold specific enzymes. (enzymes used by the bioscaffold A2(BseRI and BpuEI) do not appear in this backbone.
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| - | * As a back-up plan, if the mutation was unsuccessful the C-terminal region of GFP will be cut out in order to assess Bioscaffold efficiency.
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Latest revision as of 23:49, 20 October 2009
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