Difference between revisions of "Part:BBa K1632004"

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<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 DH5alpha strain.We measured the fluorescence intensity of the cells induced by arabinose. <br><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/''araC''_fimE(wild-type)(<partinfo>BBa_K1632013</partinfo>) in the E.coli DH5alpha strain.We measured the fluorescence intensity of the cells induced by arabinose. <br><br>
  
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===More information===
  
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For more information, see [[http://2015.igem.org/Team:Tokyo_Tech/Project Our work in Tokyo_Tech 2015 wiki]],  [[http://2015.igem.org/Team:Tokyo_Tech/Experiment/ssrA_tag_degradation_assay About ssrA-tag]],  [[http://2015.igem.org/Team:Tokyo_Tech/Experiment/Overview_of_fim_inversion_system About ''fim'' inversion system]]
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 00:28, 19 September 2015

fim switch[default ON](wild-type)

Fig. 1. Overview of fim inversion system

Fim switch(wild-type) is derived from wild-type sequence. Fim switch(wild-type) have sigma 70 promoter which is constitutively promoter. The promoter in the fim switch transcripts to the right. From the direction of transcription, the state is defined as [ON]. 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 [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 this promoter 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 DH5alpha strain.We measured the fluorescence intensity of the cells induced by arabinose.

More information

For more information, see http://2015.igem.org/Team:Tokyo_Tech/Project Our work in Tokyo_Tech 2015 wiki, http://2015.igem.org/Team:Tokyo_Tech/Experiment/ssrA_tag_degradation_assay About ssrA-tag, http://2015.igem.org/Team:Tokyo_Tech/Experiment/Overview_of_fim_inversion_system About ''fim'' inversion system

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
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]