Team:UCL London/From the lab/Results

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===Graphs===
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[[Image:UCL Fluorescent Bar Chart.png|700px]]  
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[[Image:UCL Fluorescent Bar Chart.png|700px]] '''''Fig.3a Relative Fluorescent (No stress) with Increasing OD'''''
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                '''''Fig.3a Relative Fluorescent (No stress) with Increasing OD'''''
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[[Image:Rpu.png|700px]]'''''Fig.3b RPU activitity of DegP and Spy promoter'''''
[[Image:Rpu.png|700px]]'''''Fig.3b RPU activitity of DegP and Spy promoter'''''

Revision as of 23:51, 21 October 2009

Contents

Copper Experiments

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Note on Copper

Copper is an essential trace metal for all living organisms. Nevertheless, free intracellular copper is very toxic and has a negative impact on most cells even at very low concentrations. Even though the system for the control of copper levels not is fully understood in E.coli two systems, CueR and CusR, have been identified as regulatory systems for copper homeostasis. According to some researchers, increased levels of extra cellular copper may have the effect of denaturing some membrane proteins. (Yamamoto and Ishihama 2005) This has however not yet been proved so there is still a risk that the CpxAR system could be activated by some additional copper mediated mechanism independent of the presence of misfolded proteins in the periplasm.

Graphs

UCL Cu op 2h.png UCL Cu op night.png CuCl2graph.png CuSO4graph.png Irongraph.png

Growth Cruves Experiments I

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Graphs

UCL Growth Curve Expt.pngFig.2a UCL TetR GC.pngFig.2b

Experiment I Conclusion

Fig.2a illustrated the growth curves of control (E.coli without any modified plasmids), RPU device ([http://partsregistry.org/Part:BBa_I20260 BBa_I20260]), degP+GFP device ([http://partsregistry.org/Part:BBa_BBa_K239015 BBa_BBa_K239015]), and spy device ([http://partsregistry.org/Part:BBa_BBa_K239009 BBa_K239009]). Fig.2b showed the growth curve of tetR+GFP device ([http://partsregistry.org/Part:BBa_K239012 BBa_K239012])


According to the data from Fig.2a, although taking in modified plasmid clearly affected the population of the bacteria, E.coli W3110 reached stationary phase after approximate 8 hours incubation. After about 2 hours of incubation, bacteria turned to start entering exponential phase (log phase). Consequently, some experiments could start at this point to investigate the cell respond at early log phase. Furthermore, the OD of cell cultures reached around 2.0 to 3.0 after 5 hours. This would give a relatively high OD for more clear and strong fluorescent measurements.

Growth Cruves Experiments II

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Graphs

UCL Fluorescent Bar Chart.png Fig.3a Relative Fluorescent (No stress) with Increasing OD Rpu.pngFig.3b RPU activitity of DegP and Spy promoter

UCL OD&F Control.png UCL OD&F RPU.png UCL OD&F degP.png UCL OD&F spy.png Fig.3cFrom left to right, the graph illustrated the OD and Relative Fluorescence VS Time of negative control (E.coli without any modified plasmids), RPU device ([http://partsregistry.org/Part:BBa_I20260 BBa_I20260]), degP+GFP device ([http://partsregistry.org/Part:BBa_BBa_K239015 BBa_BBa_K239015]), and spy device ([http://partsregistry.org/Part:BBa_BBa_K239009 BBa_K239009]). Please click on the graph to view larger image.

Results

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