Team:Bielefeld-Germany/Project/Model

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== Model of <partinfo>K389015</partinfo> ==
== Model of <partinfo>K389015</partinfo> ==
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[[Image:Bielefeld_k389015.jpg|500px|thumb|center| '''Fig. 1: Main construct of acetosyringone inducible luciferase expression system containing constitutive expression of the two component system receptor system (''virA+virG'').''']]
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[[Image:Bielefeld_k389015.jpg|500px|thumb|center| '''Fig. 1: Main construct of acetosyringone inducible luciferase expression system containing constitutive expression of the two component receptor system (''virA+virG'').''']]
== Model of <partinfo>K389016</partinfo> ==
== Model of <partinfo>K389016</partinfo> ==
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== Fitting the data ==
== Fitting the data ==
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As seen in the fig. 1 - 3 the models for the application of the used VirA/G signaling system is quite complex. Due to the fact that there were no further details to interactions between the components of this two component receptor system in the literature which are helpful for modelling the system and a determination of these parameters would be to time-consuming we decided to fit the ''vir'' promoter activity to different concentrations of the natural inducer of the VirA/G signaling system, acetosyringone.

Revision as of 19:23, 27 October 2010

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Construct Maps

Model of <partinfo>K389015</partinfo>

Fig. 1: Main construct of acetosyringone inducible luciferase expression system containing constitutive expression of the two component receptor system (virA+virG).

Model of <partinfo>K389016</partinfo>

Fig. 2: Control construct of acetosyringone inducible RFP read out system.

Model of <partinfo>K389014</partinfo>

Fig. 3: Screening construct of acetosyringone inducible kanamycin resistance read out system.

Fitting the data

As seen in the fig. 1 - 3 the models for the application of the used VirA/G signaling system is quite complex. Due to the fact that there were no further details to interactions between the components of this two component receptor system in the literature which are helpful for modelling the system and a determination of these parameters would be to time-consuming we decided to fit the vir promoter activity to different concentrations of the natural inducer of the VirA/G signaling system, acetosyringone.