In order to help the iGEM team Bordeaux, we had to read the paper <b>« Dynamics of plasmid transfer on surfaces »</b> <ref name="Dynamic">[http://www.microbiologyresearch.org/docserver/fulltext/micro/136/6/mic-136-6-1001.pdf?expires=1476877711&id=id&accname=guest&checksum=2F0A0D5E398EA4193E7D9B5926D0CCE5 Lone Simonse Department of Zoology, University of Massachusetts, Amherst, MA 01003, USA .]</ref> and collect and organize some data about their experiments on plasmids transfer. Thanks to this, the iGEM team Bordeaux can compare those results to their own computaionnal results.

In order to help the iGEM team Bordeaux, we had to read the paper <b>« Dynamics of plasmid transfer on surfaces »</b> <ref name="Dynamic">[http://www.microbiologyresearch.org/docserver/fulltext/micro/136/6/mic-136-6-1001.pdf?expires=1476877711&id=id&accname=guest&checksum=2F0A0D5E398EA4193E7D9B5926D0CCE5 Lone Simonse Department of Zoology, University of Massachusetts, Amherst, MA 01003, USA .]</ref> and collect and organize some data about their experiments on plasmids transfer. Thanks to this, the iGEM team Bordeaux can compare those results to their own computaionnal results.

Using a surface slide system (SSS) the dynamics of the plasmid R1 and its permanently derepressed mutant Rldvdl9 in surface cultures of Escherichia coli K12 was examined.

Using a surface slide system (SSS) the dynamics of the plasmid R1 and its permanently derepressed mutant Rldvdl9 in surface cultures of Escherichia coli K12 was examined.

The experiments were carried on E.coli K12 strain J53 hosting the plasmid R1 or it's premanently repressed mutant R1drd19. those two strains were used as donor cells. The recipient used is E.coli CH50.

The experiments were carried on E.coli K12 strain J53 hosting the plasmid R1 or it's premanently repressed mutant R1drd19. those two strains were used as donor cells. The recipient used is E.coli CH50.

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