Reporter

Part:BBa_K649104

Designed by: Hiroki Yoshise   Group: iGEM11_Tokyo_Tech   (2011-09-26)

PlsrA-RBS-gfp

We characterized BBa_K649104 and BBa_K117002 in E.coli lsrR(-).

Fluorescence intensity of BBa_K649104 was much higher than that of promoterless-gfp(negative control).
Strain used in this assay lacks lsrR.
This work is done by Takuya Tsubaki.


We measured the transcriptional activity of our lsrA promoter(BBa_K649100) by introducing a gfp gene downstream of the promoter. Its fluorescence intensity was much higher than that of promoterless-gfp(negative control), showing that our new lsrA promoter works. Moreover,fluorescence intensity of lsrA promoter-gfp((BBa_K117002)-gfp) was almost the same as a promoterless-gfp(negative control), showing that lsrA promoter(BBa_K117002) does not work properly.


We improved previous lsrA promoter(BBa_K117002).our assay of BBa_K117002


For more information, see our work in Tokyo_Tech 2011 wiki.


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
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 770


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