Difference between revisions of "Part:BBa K1632007"
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<span style="margin-left: 10px;">We constructed ''fim'' switch[default ON](wild-type)_rbs_gfp(<partinfo>BBa_K1632007</partinfo>) to characterize the function of this part, by inserting ''fim'' switch[default ON](wild-type)(<partinfo>BBa_K1632004</partinfo>) upstream of a GFP coding sequence. <br> | <span style="margin-left: 10px;">We constructed ''fim'' switch[default ON](wild-type)_rbs_gfp(<partinfo>BBa_K1632007</partinfo>) to characterize the function of this part, by inserting ''fim'' switch[default ON](wild-type)(<partinfo>BBa_K1632004</partinfo>) upstream of a GFP coding sequence. <br> | ||
− | <span style="margin-left: 10px;">In the fimB dependent ''fim'' switch state assay, we transformed ''fim'' switch[default ON](wild-type)_rbs_gfp and PBAD/ | + | <span style="margin-left: 10px;">In the fimB dependent ''fim'' switch state assay, we transformed ''fim'' switch[default ON](wild-type)_rbs_gfp and PBAD/''araC''_''fimB''(<partinfo>BBa_K1632012</partinfo>) in the E.coli DH5alpha strain. We measured the fluorescence intensity of the cells induced by arabinose. <br> |
− | <span style="margin-left: 10px;">Similary,in the fimE dependent ''fim'' switch state assay, we transformed ''fim'' switch[default ON](wild-type)_rbs_gfp and PBAD/ | + | <span style="margin-left: 10px;">Similary,in the fimE dependent ''fim'' switch state assay, we transformed ''fim'' switch[default ON](wild-type)_rbs_gfp and PBAD/''araC''_''fimE''(wild-type)(<partinfo>BBa_K1632013</partinfo>) in the E.coli DH5alfpha strain. We measured the fluorescence intensity of the cells induced by arabinose. <br><br> |
For more information, see [http://2015.igem.org/Team:Tokyo_Tech/Project our work in Tokyo_Tech 2015 wiki]. | For more information, see [http://2015.igem.org/Team:Tokyo_Tech/Project our work in Tokyo_Tech 2015 wiki]. |
Revision as of 22:07, 18 September 2015
fim switch[default ON](wild-type)_rbs_gfp
Fim switch(wild-type) is derived from wild-type sequence. Fim switch(wild-type) have sigma 70 promoter which is constitutive promoter. The promoter in the fim switch transcripts to the right. From the direction of transcription, the state is defined as [ON] state. On the other hand, fim switch[default OFF](wild-type) (BBa_K1632005) transcripts to the left.
Fim switch is inverted by two recombinase, FimB and FimE. The FimB protein inverts fim switch from [ON] state to [OFF] state and from [OFF] state to [ON] state with approximately equal efficiencies. On the other hand, the FimE protein inverts fim switch predominantly from [ON] state to [OFF] state.
We constructed fim switch[default ON](wild-type)_rbs_gfp(BBa_K1632007) to characterize the function of this part, by inserting fim switch[default ON](wild-type)(BBa_K1632004) upstream of a GFP coding sequence.
In the fimB dependent fim switch state assay, we transformed fim switch[default ON](wild-type)_rbs_gfp and PBAD/araC_fimB(BBa_K1632012) in the E.coli DH5alpha strain. We measured the fluorescence intensity of the cells induced by arabinose.
Similary,in the fimE dependent fim switch state assay, we transformed fim switch[default ON](wild-type)_rbs_gfp and PBAD/araC_fimE(wild-type)(BBa_K1632013) in the E.coli DH5alfpha strain. We measured the fluorescence intensity of the cells induced by arabinose.
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]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1052