Team:NYMU-Taipei/Project/Promoter Strength Testing
From 2009.igem.org
Revision as of 22:42, 21 October 2009 by Blackrabbit (Talk | contribs)
- All experiments were done in E. coli DH5alpha.
- Maturation rate of GFP is 6.5mins [1]
- All our analysis was done in excel documents: File:NYMU-promotertesting.zip and done based on the paper by Leveau and Lindow [2].
Contents |
2009-08-25 Reporting Assay
Figure 1. This is the graph of our promoter strength testing. Since we did not do biological replicates, we are not able to confirm the validity of the result. |
2009-09-07 Reporting Assay
2009-09-18 Reporting Assay
2009-09-29 Reporting Assay
Figure 4. We tested new promoters and measured their strength relative to pCI. This time we did a three-fold biological replicate. The error bars are 95% confidence intervals. |
2009-10-05 Reporting Assay
2009-10-13 Reporting Assay
Conclusion
- We have tested the relative strengths of p22, pCI, pLux (basal level), pLas (basal level), pTet, pPenI, and pLac.
- We obtained relatively consistent results between the relative strengths of p22, pCI, pLux, and pLas, while obtaining not so consistent results between pTet, pPenI, and pLac.
- We think it is due to the lack of experience earlier on and confusing us which relative strengths between pTet, pPenI, and pLac were correct.
Reference
[1] Megerle JA, Fritz G, Gerland U, Jung K, Radler JO: Timing and Dynamics of Single Cell Gene Expression in the Arabinose Utilization System, Biophys J, 2008, 95(4): 2103–2115
[2] Leveau JHJ and Lindow SE, Predictive and Interpretive Simulation of Green Fluorescent Protein Expression in Reporter Bacteria, Journal of Bacteriology, 2001, 183(23): 6752-6762