Difference between revisions of "Part:BBa K1632010"
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[[Image:Tokyo_Tech_fimB_summary1.png |thumb|center|900px|<b>Fig. 1. </b>New plasmids we constructed to confirm the function of BBa_K1632012 plasmid for Decision making coli.]]<br> | [[Image:Tokyo_Tech_fimB_summary1.png |thumb|center|900px|<b>Fig. 1. </b>New plasmids we constructed to confirm the function of BBa_K1632012 plasmid for Decision making coli.]]<br> | ||
− | <span style="margin-left: 10px;">The <i>fim</i> switch is inverted by FimB.The FimB protein inverts the <i>fim</i> switch in the ON | + | <span style="margin-left: 10px;">The <i>fim</i> switch is inverted by FimB.The FimB protein inverts the <i>fim</i> switch in the [ON] state to [OFF] state.<br> |
<span style="margin-left: 10px;">In order to assay the function of our FimB, 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 fimB(wild-type).PBAD/''araC''_fimB (BBa_K1632012) can induce the expression of FimB(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. | <span style="margin-left: 10px;">In order to assay the function of our FimB, 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 fimB(wild-type).PBAD/''araC''_fimB (BBa_K1632012) can induce the expression of FimB(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. |
Revision as of 16:54, 18 September 2015
fimB (wild-type)
The fim switch is inverted by FimB.The FimB protein inverts the fim switch in the [ON] state to [OFF] state.
In order to assay the function of our FimB, 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 fimB(wild-type).PBAD/araC_fimB (BBa_K1632012) can induce the expression of FimB(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.
From the experimental results, our FimB(wild-type) inverted the fim switch[default ON](wild-type) from [ON] state to[OFF] state and the fim switch[defult OFF](wild-type) from [OFF] state to [ON] state, dependent on the concentration of arabinose.
When the concentration of FimB(wild-type) increased by increasing the concentration of arabinose, we confirmed that the fluorescence intensity decreased in both [ON] to [OFF] process and [OFF] to [ON] process.
The result of the reporter cell (2) shows that when the concentration of arabinose is increased to 0〜20 microM, the fluorescence intensity increases. This shows the function of FimB(wild-type) inverting the fim switch(wild-type) from [OF] state to [ON] state. However, when the arabinose concentration is excess (5mM), the fluorescence intensity decreases (Fig. 3). According to [1], this is caused by the excess increase in the inversion rate of the fim switch(wild-type). When the inversion rate is too high, there is not enough time for transcription initiation. Consequently, the GFP expression decreases.
For more information, see [http://2015.igem.org/Team:Tokyo_Tech/Project our work in Tokyo_Tech 2015 wiki].
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]