Reporter
NG3

Part:BBa_K2623023

Designed by: Jiyang Zheng   Group: iGEM18_XMU-China   (2018-10-02)
Revision as of 13:36, 11 October 2018 by Hanyulong (Talk | contribs) (Other information)


Bacterial outer membrane protein A (OmpA) fused with SpyTag and GFP at its N-termini

SUMMARY

It’s another form of the BBa_K2623021 designed to target our archaeal ribosomal protein protein L7Ae and then siRNA into outer-membrane vesicles (OMVs). The only difference is that we inserted SpyTag to C-termini of OmpA protein(instead of the N-termi in BBa_K2623021). As mentioned in BBa_K2623021, SpyTag was constructed in order to anchore L7Ae to outer membrane through the bioconjugation of the SpyTag/SpyCatcher system. Through the fluorescence intensity of GFP, we can compare and evaluate expression efficiency of SpyTag between the BBa_K2623021 and this part. Then the better one would be uesd to construct our final gene circuit.

Other information

You can click the website (http://2018.igem.org/Team:XMU-China/Results) to see the results of comparison of two reporters (BBa_K2623021 and BBa_K2623023)<a href="http://2013.igem.org/Team:TU-Munich/Results/Software">documentation</a> Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 65
  • 1000
    COMPATIBLE WITH RFC[1000]


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