Difference between revisions of "Part:BBa K1086002:Experience"

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[[File:clone2_tmao_fluo.jpg|600px|thumb|center|'''Figure 10: Fluorometric reads of cultures ''of E. coli'' XL1-Blue carrying the plasmid PSB1C3_TorCAD + RFP, after treatment with different concentrations of TMAO.''' Bacteria were treated with 0 μM, 1 μM, 10 μM, 100 μM, 1 mM, 10 mM and 100 mM. After that, fluorescence was read hourly, until 15 hours. The beginning of the fluorescence increase can be seen about seven hours after the treatment.]]
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[[File:clone2_tmao_fluo.jpg|600px|thumb|center|'''Figure 1: Fluorometric reads of cultures ''of E. coli'' XL1-Blue carrying the plasmid PSB1C3_TorCAD + RFP, after treatment with different concentrations of TMAO.''' Bacteria were treated with 0 μM, 1 μM, 10 μM, 100 μM, 1 mM, 10 mM and 100 mM. After that, fluorescence was read hourly, until 15 hours. The beginning of the fluorescence increase can be seen about seven hours after the treatment.]]
  
  

Revision as of 01:03, 29 October 2013


This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_K1086002

We have constructed the composite TorCAD+RFP to detect TMAO (trimethylamine N-oxide) in the serum of patients with cardiac risk. These patients present more TMAO than normal individuals.

TMAO enters bacterial cells and generates a cascade of signals, which ultimately activate promoter TorCAD (we have based on Ansaldi et al., 2010 to synthesize TorCAD promoter). We have added mCherry (RFP) downstream of TorCAD in order to measure the promoter’s activation by TMAO.

We made some experiments with E. coli XL1-Blue transformed with this composite to show that our construct works. We added different concentrations of TMAO and measured bacterial cultures fluorescence (excitation: 587 nm; emission: 610 nm) and absorbance (600 nm) for a certain period.


To prove that our construct works, we made some tests with transformed E. coli XL1-Blue. We added different concentrations of TMAO to bacterial cultures and measured their fluorescence and absorbance for 15 hours. The fluorescence stars to increase only 8 hours after the treatment with TMAO (Figures 10 and 11) and continue to increase until 13 hours after the treatment. We could observe fluorescence appearence only with the concentration of 100 μM of TMAO


File:Clone2 tmao fluo.jpg
Figure 1: Fluorometric reads of cultures of E. coli XL1-Blue carrying the plasmid PSB1C3_TorCAD + RFP, after treatment with different concentrations of TMAO. Bacteria were treated with 0 μM, 1 μM, 10 μM, 100 μM, 1 mM, 10 mM and 100 mM. After that, fluorescence was read hourly, until 15 hours. The beginning of the fluorescence increase can be seen about seven hours after the treatment.


Conclusion:

Our results show that the composite TorCAD+RFP generates fluorescence in the presence of TMAO.

User Reviews

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