IGEM:UNAM Genomics Mexico/2009/Notebook/Wifi coli/2010/05/04: Difference between revisions
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We use that formula to know which is the limitant reactant and the optimum concentration. | We use that formula to know which is the limitant reactant and the optimum concentration. | ||
The next figure is to show the posible conectreations of Luciferin and Luciferase. | |||
[[Image:Model.4.May.2010.jpg]] | [[Image:Model.4.May.2010.jpg]] | ||
Revision as of 12:13, 6 May 2010
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Modeling & WetLab MeetingsModelingStoichiometry of Luciferase activity. a[Luc] + b[ Luc-ina] + c[02] + d[ATP] -> z[Luc] + y [oxyLuc-ina] + w[C02] + u[AMP] + v[PPi] We use that formula to know which is the limitant reactant and the optimum concentration. The next figure is to show the posible conectreations of Luciferin and Luciferase. To achieve a controlled model we use single copy plasmid or low copy number. LuM= Kc_cat * LUC * (Scyt/(Km+Scyt)) *RLV K_cat= [Constant of Activity] LUC= [Luciferase] Scyt = [Cytosolic Luciferase] Km= Michaelis-Menten constant. RLU= Relative Light Unit LuM= Number of moles, which react in measure, this is by colony. Whit this formula we can achieve the values for light emission and efficiency of our system. We need:
To get unidirectionality we purpose a system with optical fiber and aisled systems.Each matrax is coated by aluminium to focus photons to exit. This design is simple, we will change datails in sizes of elements and positions. Modelingblablabla Wet lab
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