Paris/ConstructionProcess
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| - | + | == Overview == | |
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The aim of the Molecular biology work was to construct the backbone for SMB genomic cassette: | The aim of the Molecular biology work was to construct the backbone for SMB genomic cassette: | ||
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| - | == | + | == Constructs == |
| + | === Upstream construct === | ||
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| - | == | + | === Downstream construct === |
| - | === Intermediate construct === | + | ==== Intermediate construct ==== |
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| - | === Backward construct with DapA E.Coli === | + | ==== Backward construct with DapA E.Coli ==== |
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| - | === Backward construct with DapA Subtilis === | + | ==== Backward construct with DapA Subtilis ==== |
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| - | == | + | === Recombinaison rate measurement === |
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Revision as of 08:11, 23 October 2007
Contents |
Overview
The aim of the Molecular biology work was to construct the backbone for SMB genomic cassette:
In order to construct this genomic cassette, we have considered 2 solutions:
- 1. Either the construct is cloned on a plasmid. Then inserted in the genome strain of a dapA-, ftsK-(ts) E.coli strain. This was the initial strategy we adopted then subsequently abandoned (see here why LIEN).
- 2. Or the cassette is sequentially assembled, in the genome, around the essential gene selected (ftsK in our case).
We have chosen the second strategy. The different steps of this process are as follow:
2 plasmid born constructs were constructed. These are termed the UP “upstream construct” & the DP “downstream construct”:
Upstream construct:
Downstream construct:
As their names indicate, these constructs are to be inserted upstream and downstream of ftsK in the genome. We chose to insert these constructs using a strategy described by Wanner et al.
We have yet to insert the constructs in the genome. This will be done sequentially:
Constructs
Upstream construct
Downstream construct
Intermediate construct
Backward construct with DapA E.Coli
Backward construct with DapA Subtilis
Recombinaison rate measurement
