Difference between revisions of "Part:BBa K1632011"

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[[Image:Tokyo_Tech_arabinosefimEsummary.png |thumb|center|900px|<b>Fig. 1. </b>New plasmids we constructed to confirm the function of BBa_K1632013 plasmid for Decision making coli.]]<br>
 
[[Image:Tokyo_Tech_arabinosefimEsummary.png |thumb|center|900px|<b>Fig. 1. </b>New plasmids we constructed to confirm the function of BBa_K1632013 plasmid for Decision making coli.]]<br>
  
<span style="margin-left: 10px;">The <i>fim</i> switch is inverted by FimE.The FimE protein inverts the ''fim'' switch predominantly in the ON-to-OFF direction.<br>
+
<span style="margin-left: 10px;">The <i>fim</i> switch is inverted by FimE.The FimE protein inverts the ''fim'' switch predominantly in [ON] state to [OFF] state.<br>
  
  
<span style="margin-left: 10px;">In order to assay the function of our FimE, we added a GFP coding sequence on the downstream of the <i>fim</i> switch.The <i>fim</i> switch[default ON](wild-type)_gfp (BBa_K1632007) emitts fluorescence when expressed, while the <i>fim</i> switch [default OFF](wild-type)_gfp(BBa_K1632008) does not emit florescence when expressed. We also added PBAD/''araC'' on the upstream of fimE.PBAD/''araC''_fimE (BBa_K1632013) can induce the expression of FimE in the presence of arabinose. We co-transformed a <i>fim</i> switch_gfp and a PBAD/''araC''_fim recombinase in the E. coli DH5alpha strain. We measured the fluorescence intensity of the cells induced by different concentraions of arabinose.<br>
+
<span style="margin-left: 10px;">In order to assay the function of our FimE, we added a GFP coding sequence on the downstream of the <i>fim</i> switch(wild-type).The <i>fim</i> switch[default ON](wild-type)_gfp (BBa_K1632007) emitts fluorescence when expressed, while the <i>fim</i> switch [default OFF](wild-type)_gfp(BBa_K1632008) does not emit florescence when expressed. We also added PBAD/''araC'' on the upstream of fimE.PBAD/''araC''_fimE (BBa_K1632013) can induce the expression of FimE(wild-type) in the presence of arabinose. We co-transformed a <i>fim</i> switch(wild-type)_gfp and a PBAD/''araC''_fim recombinase in the E. coli DH5alpha strain. We measured the fluorescence intensity of the cells induced by different concentraions of arabinose.<br>
  
 
[[Image:Tokyo_Tech_FimE_assay_Results.png |thumb|center|700px|<b>Fig. 2. </b>The histograms of the samples measured by flow cytometer]]<br>
 
[[Image:Tokyo_Tech_FimE_assay_Results.png |thumb|center|700px|<b>Fig. 2. </b>The histograms of the samples measured by flow cytometer]]<br>
  
<span style="margin-left: 10px;">From the experimental results,our fimE inverted the <i>fim</i> switch[default ON](wild-type) from ON-to-OFF but did not invert the <i>fim</i> switch[default OFF](wild-type) from the OFF state, depending on the concentration of arabinose.<br><br><br>
+
<span style="margin-left: 10px;">From the experimental results,our fimE inverted the <i>fim</i> switch[default ON](wild-type) from [ON] state to [OFF] state but did not invert the <i>fim</i> switch[default OFF](wild-type) from [OFF] state, dependent on the concentration of arabinose.<br><br><br>
  
 
For more information, see [http://2015.igem.org/Team:Tokyo_Tech/Project our work in Tokyo_Tech 2015 wiki]. <br><br><br>
 
For more information, see [http://2015.igem.org/Team:Tokyo_Tech/Project our work in Tokyo_Tech 2015 wiki]. <br><br><br>

Revision as of 15:45, 18 September 2015

fimE (wild-type)

Fig. 1. New plasmids we constructed to confirm the function of BBa_K1632013 plasmid for Decision making coli.

The fim switch is inverted by FimE.The FimE protein inverts the fim switch predominantly in [ON] state to [OFF] state.


In order to assay the function of our FimE, we added a GFP coding sequence on the downstream of the fim switch(wild-type).The fim switch[default ON](wild-type)_gfp (BBa_K1632007) emitts fluorescence when expressed, while the fim switch [default OFF](wild-type)_gfp(BBa_K1632008) does not emit florescence when expressed. We also added PBAD/araC on the upstream of fimE.PBAD/araC_fimE (BBa_K1632013) can induce the expression of FimE(wild-type) in the presence of arabinose. We co-transformed a fim switch(wild-type)_gfp and a PBAD/araC_fim recombinase in the E. coli DH5alpha strain. We measured the fluorescence intensity of the cells induced by different concentraions of arabinose.

Fig. 2. The histograms of the samples measured by flow cytometer

From the experimental results,our fimE inverted the fim switch[default ON](wild-type) from [ON] state to [OFF] state but did not invert the fim switch[default OFF](wild-type) from [OFF] state, dependent on the concentration of arabinose.


For more information, see [http://2015.igem.org/Team:Tokyo_Tech/Project our work in Tokyo_Tech 2015 wiki].



Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 22
  • 1000
    COMPATIBLE WITH RFC[1000]