Difference between revisions of "Part:BBa K606027:Experience"

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__NOTOC__
 
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This experience page is provided so that any user may enter their experience using this part.<BR>Please enter
 
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how you used this part and how it worked out.
 
  
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===Applications of BBa_K606027===
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==Characterization: Biobricked YFP:TetR==
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===User Reviews===
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'''Parts construction''':<br>
 
'''Parts construction''':<br>
 
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<html>
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Origins of TetO Array are from pDAG479 of D. Lane (Toulouse 2 University).
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Origins of YFP:TetR are from pFX234 of D. Lane (Toulouse 2 University).
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<center><img src="https://static.igem.org/mediawiki/2011/a/a0/TetOarray2.jpg">
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<center><img src="https://static.igem.org/mediawiki/2011/c/cb/YFPtetR10.jpg">
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<p>Cloning plan of TetO array construction</center></p>  
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<p>Cloning plan of YFP:TetR construction</center></p>  
 
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<br><br>We characterize it with arabinose-induced YFP:TetR Wild Type from pFX234 plasmid of F-X Barre and D. Lane (Kinetics of plasmid segregation, Molecular Microbiology, 2004).<br><br>
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<br><br>We characterize it with TetO Array from pDAG479 plasmid of F-X Barre and D. Lane (Kinetics of plasmid segregation, Molecular Microbiology, 2004).<br><br>
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'''Microscopy of double transformated pFX234 / Biobricked TetO Array <i>E. Coli</i>''':<br>
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In order to do this characterization, we took pictures of different plasmids containing only TetO array (K606026); TetR + YFP (pFX234); TetO + TetR + YFP (K606026 and pFX234). In each case we made a control by non inducing the promoter with arabinose. Cells were grown at 37°C and induced at least 45min.
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'''Microscopy of double transformed pDAG470 / Biobricked YFP:TetR in <i>E. Coli</i>:'''
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<p>To characterize this part properly, we took pictures of different strains containing YFP:TetR alone and both TetO array (from pDAG479, D.Lane) and expression YFP:TetR system (BBa_K606027).</p>
  
 
<center>
 
<center>
 
{| border="1" class="wikitable" style="text-align: center;" align="center"
 
{| border="1" class="wikitable" style="text-align: center;" align="center"
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|+ tetO array : 37°C
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|+ Biobricked YFP:TetR only
 
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|[[Image:teto_minus_trans.jpg|350px|thumb|center|tetO / TetO array induced without arabinose on E. Coli .]]
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|[[Image:yfptetrbb_trans.jpg|350px|thumb|center|Biobricked expression YFP:tetR system in E. coli.]]
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|[[Image:teto_minus_Fluo20.jpg|350px|thumb|center|tetO / TetO array induced without arabinose on E. Coli .]]
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|[[Image:yfptetrbb_Fluo2.jpg|350px|thumb|center|Biobricked expression YFP:tetR system in E. coli.]]
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|-
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|[[Image:teto_Arab_trans.jpg|350px|thumb|center|tetO / TetO array induced with 0,2% arabinose on E. Coli .]]
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|[[Image:teto_arab_Fluo20.jpg|350px|thumb|center|tetO / TetO array induced with 0,2% arabinose on E. Coli .]]
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{| border="1" class="wikitable" style="text-align: center;"
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{| border="1" class="wikitable" style="text-align: center;" align="center"
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|+TetR:YFP : 37°C
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|+ Biobricked YFP:TetR and TetO Array
 
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|[[Image:yfp_tetr_minus_trans.jpg|350px|thumb|center|tetR:YFP / TetR-YFP induced without arabinose on E. Coli .]]
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|[[Image:yfptetrbb_teto_trans.jpg|350px|thumb|center|Biobricked expression YFP:tetR system and TetO Array from D. Lane in E. coli.]]
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|[[Image:yfp_tetr_minus_fluo20.jpg|350px|thumb|center|tetR:YFP / TetR-YFP induced without arabinose on E. Coli .]]
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|[[Image:yfptetrbb_teto__Fluo2.jpg|350px|thumb|center|Biobricked expression YFP:tetR system and TetO Array from D. Lane in E. coli.]]
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|[[Image:yfp_tetr_Arab_trans.jpg|350px|thumb|center|tetR:YFP / TetR-YFP induced with 0,2% arabinose on E. Coli .]]
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|[[Image:yfp_tetr_Arab_fluo20.jpg|350px|thumb|center|tetR:YFP / TetR-YFP induced with 0,2% arabinose on E. Coli .]]
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</center>
 
</center>
  
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The pictures of TetO show no YFP activity, which is normal because there is no YFP sequence in these plasmids.<br>
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The TetR-YFP construct which (emitter part) occasionally shows gross aggregated YFP. <br>
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The TetR-YFP construct which constitutes the transmitter part, occasionally shows gross aggregated YFP. This is not what we expected at first, but that does not prevent us to characterize the full construct.<br>
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After observing the cells carrying both the TetO and YFP:TetR constructs, we can obviously distinguish glowing dots in some cells. They reflect the behavior we expected.
  
  
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More information on : iGEM Paris Bettencourt 2011 wiki [http://2011.igem.org/Team:Paris_Bettencourt/Experiments/YFP_TetR_diffusion]
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More information on : TetO Array characterization (<partinfo>BBa_K606026</partinfo>) and iGEM Paris Bettencourt 2011 wiki [http://2011.igem.org/Team:Paris_Bettencourt/Experiments/YFP_TetR_diffusion]
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===User Reviews===
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Enter the review inofrmation here.
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Latest revision as of 16:27, 24 October 2011


Characterization: Biobricked YFP:TetR

Parts construction:
Origins of YFP:TetR are from pFX234 of D. Lane (Toulouse 2 University).

Cloning plan of YFP:TetR construction



We characterize it with TetO Array from pDAG479 plasmid of F-X Barre and D. Lane (Kinetics of plasmid segregation, Molecular Microbiology, 2004).

Microscopy of double transformed pDAG470 / Biobricked YFP:TetR in E. Coli:

To characterize this part properly, we took pictures of different strains containing YFP:TetR alone and both TetO array (from pDAG479, D.Lane) and expression YFP:TetR system (BBa_K606027).

Biobricked YFP:TetR only
Biobricked expression YFP:tetR system in E. coli.
Biobricked expression YFP:tetR system in E. coli.
Biobricked YFP:TetR and TetO Array
Biobricked expression YFP:tetR system and TetO Array from D. Lane in E. coli.
Biobricked expression YFP:tetR system and TetO Array from D. Lane in E. coli.

The TetR-YFP construct which (emitter part) occasionally shows gross aggregated YFP.
After observing the cells carrying both the TetO and YFP:TetR constructs, we can obviously distinguish glowing dots in some cells. They reflect the behavior we expected.


More information on : TetO Array characterization (BBa_K606026) and iGEM Paris Bettencourt 2011 wiki [http://2011.igem.org/Team:Paris_Bettencourt/Experiments/YFP_TetR_diffusion]

User Reviews

UNIQd5a0073182e3e0bc-partinfo-00000002-QINU UNIQd5a0073182e3e0bc-partinfo-00000003-QINU