Difference between revisions of "Part:BBa K1632002"

Line 7: Line 7:
 
[[Image:Tokyo Tech fim switch Tokyo Tech design.png|thumb|center|600px|Fig. 1.  ''fim'' switch(Tokyo_Tech/J23119) design (Up:on state  Down:off state)]]<br>
 
[[Image:Tokyo Tech fim switch Tokyo Tech design.png|thumb|center|600px|Fig. 1.  ''fim'' switch(Tokyo_Tech/J23119) design (Up:on state  Down:off state)]]<br>
  
<span style="margin-left: 10px;">From our results of our assay, the inversion of ''fim'' switch(Tokyo_Tech/J23119) by FimB/FimE was not confirmed correctly. The FimB protein inverts ''fim'' switch from [ON] state to [OFF] state and  [OFF] state to [ON] state correctly (Fig.2.). However the FimE protein didn’t invert ''fim'' switch predominantly from [ON] state to [OFF] state. In the assay, the FimE protein inverts ''fim'' switch from [ON] state to [OFF] state and the [OFF] state to [ON] state. In other words, the FimE protein works as the FimB protein.
+
<span style="margin-left: 10px;">From our results of our assay, the inversion of ''fim'' switch(Tokyo_Tech/J23119) by FimB/FimE was not confirmed correctly. The FimB protein inverts ''fim'' switch from [ON] state to [OFF] state and  [OFF] state to [ON] state correctly (Fig.2.). However the FimE protein didn’t invert ''fim'' switch predominantly from [ON] state to [OFF] state. In the assay, the FimE protein inverts ''fim'' switch from [ON] state to [OFF] state and the [OFF] state to [ON] state (Fig.3.). In other words, the FimE protein works as the FimB protein.
  
 
[[Image:Tokyo_Tech_fim_switch_TT_FimB_assay_Results.png |thumb|center|700px|<b>Fig. 2. </b>The histograms of the samples with FimB measured by flow cytometer]]<br>
 
[[Image:Tokyo_Tech_fim_switch_TT_FimB_assay_Results.png |thumb|center|700px|<b>Fig. 2. </b>The histograms of the samples with FimB measured by flow cytometer]]<br>

Revision as of 23:44, 18 September 2015

fim switch[default ON](Tokyo_Tech/J23119)_rbs_gfp

The fim switch is the promoter containing repeated DNA sequence which is inverted by the Fim recombinase. Therefore, we can control the expression of the gene downstream of the fim switch by adding the Fim recombinase.
We designed this fim switch which has a J23119 promoter(BBa_J23119). Also between the promoter and the inverting site, there are two restriction enzyme sites in each front (SalIand BamHI) and back (BglII and MluI)(Fig. 1. fim switch (Tokyo_Tech/J23119) design). So the promoter can easily be interchanged. Except for insertion of restriction enzyme sites, basically, the design of fim switch(Tokyo_Tech) is similar with fim switch(wild-type).

Fig. 1. fim switch(Tokyo_Tech/J23119) design (Up:on state Down:off state)

From our results of our assay, the inversion of fim switch(Tokyo_Tech/J23119) by FimB/FimE was not confirmed correctly. The FimB protein inverts fim switch from [ON] state to [OFF] state and [OFF] state to [ON] state correctly (Fig.2.). However the FimE protein didn’t invert fim switch predominantly from [ON] state to [OFF] state. In the assay, the FimE protein inverts fim switch from [ON] state to [OFF] state and the [OFF] state to [ON] state (Fig.3.). In other words, the FimE protein works as the FimB protein.

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

Fig. 3. The histograms of the samples with FimE measured by flow cytometer

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
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 345
    Illegal NheI site found at 368
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 374
    Illegal BamHI site found at 333
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1102