| Name | Type | Description | Design | Length(bp) | Experiment |
|---|---|---|---|---|---|
| BBa_K1632000 | Regulatory | fim switch[default ON](Tokyo_Tech/J23119) | Riku Shinohara | 382 | Work |
| BBa_K1632001 | Regulatory | fim switch[default ON](Tokyo_Tech/J23119) | Riku Shinohara | 382 | Work |
| BBa_K1632004 | Regulatory | fim switch[default OFF](wild-type) | Riku Shinohara | 382 | Work |
| BBa_K1632005 | Regulatory | fim switch[default OFF](wild-type) | Riku Shinohara | 382 | Work |
| BBa_K1632006 | Regulatory | fim switch[default ON](Tokyo_Tech/B0010) | Riku Shinohara | 597 | Work |
| BBa_K1632010 | Coding | fimB(wild-type) | Riku Shinohara | 603 | Work |
| BBa_K1632011 | Coding | fimE(wild-type) | Riku Shinohara | 597 | Work |
Team:Tokyo Tech/Basic Part
Basic Parts
Tokyo Tech 2015 iGEM Team Basic Parts
1. fim switch (Tokyo_Tech): BBa_K1632000, BBa_K1632001, BBa_K1632006
- BBa_K1632000
fim switch[default ON](Tokyo_Tech/J23119) - BBa_K1632001
fim switch[default OFF](Tokyo_Tech/J23119) - BBa_K1632006
fim switch[default ON](Tokyo_Tech/B0010)
We designed another fim switch with a standardized interchangeable promotor, fim switch (Tokyo_Tech). A difference between the wild type fim switch and the fim switch (Tokyo_Tech) is that we replaced the sigma 70 promoter to the J23119 promotor" (BBa_J23119). We also inserted two restriction enzyme sites in both the front (SalI and BamHI) and the back (BglII and MluI) of the promotor. By inserting the restriction enzymes, our fim switch (Tokyo_Tech) turned into a fim switch with a standardized interchangeable promotor (Fig.5-1-1-1). There is an example. BBa_K1632006 is made by removing the J23119 promotor (BBa_J23119) and inserted Plac promotor (BBa_B0010) .
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Fig.5-3-1-1. Design of Fim Switch (Tokyo_Tech) |
2. fim switch (wild-type): BBa_K1632004, BBa_K1632005
- BBa_K1632004
fim switch[default ON](wild-type) - BBa_K1632005
fim switch[default OFF](wild-type)
We are the first team in iGEM to successfully construct both the fim switch default state ON and the fim switch default state OFF and assay them. These fim switch is derived from a wild type and the gene sequence is the same as that of a wild type E.coli. The fim switch is inverted by the Fim recombinase. Therefore, we can regulate the expression of the gene downstream of the fim switch by adding the Fim recombinase. From the flow cytometers assay, they work ideally.
 |
Fig.5-1-2-1. The result of our assay used BBa_K1632007,BBa_K1632008 and BBa_K1632013 with flow cytometers |
3. fimB (wild-type): BBa_K1632010
- BBa_K1632010
fimB(wild-type)
FimB (BBa_K1632010) is a Fim recombinase. This is derived from the wild type MG1655. FimB invert the fim switch from the ON state to the OFF state and from the OFF state to the ON state (Fig.5-1-3-1.).
From our experimental results, we confirmed that the FimB protein inverts the fim switch in the ON-to-OFF direction and in the OFF-to-ON direction with approximately equal probability and works ideally (Fig.5-1-3-2.). The expression of FimB is controlled by arabinose in BBa_K1632012.
 |
Fig.5-1-3-1. fim switch is inverted by two recombinases, FimB and FimE. These proteins have distinct activities. The FimB protein inverts fim switch in the ON-to-OFF and the OFF-to-ON direction with approximately equal probability |
 |
Fig.5-1-3-2. The result of our assay used BBa_K1632007, BBa_K1632008 and BBa_K1632012 with flow cytometers. |
4. fimE (wild-type): BBa_K1632011
FimE(wild-type)
FimE(wild-type)(BBa_K1632011) is Fim recombinases. This Fim recombinase is derived from the wild type MG1655. FimE invert the fim switch (wild-type) from the ON state to the OFF state. The expression of this Fim recombinase is controlled by arabinose in BBa_K1632013. From our experimental results (Fig. 5-1-2-1.), they work ideally.
