Difference between revisions of "Part:BBa K2255004"

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This part enable us to produce in high quantities proteins in ''Xylella fastidiosa''. It was engineered for the phage-like particle design of our project. Check out our [http://2017.igem.org/Team:Aix-Marseille/M13_Design design page] for more informations.
 
This part enable us to produce in high quantities proteins in ''Xylella fastidiosa''. It was engineered for the phage-like particle design of our project. Check out our [http://2017.igem.org/Team:Aix-Marseille/M13_Design design page] for more informations.
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To evaluate the activity of the promoter and RBS, [https://parts.igem.org/Part:BBa_K1321337 sfGFP] protein was expressed in ''Escherichia coli'' DH5α bacteria and it fluorescence properties was studied. We compared our promoter and RBS to a well studied biobrick [https://parts.igem.org/Part:BBa_K608002 BBa_K608002] which is an ''E. coli'' strong promoter and RBS.
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We used [http://2017.igem.org/Competition/InterLab_Study/Plate_Reader InterLab protocol] and [https://parts.igem.org/Part:BBa_R0040 negative control] to test the fluorescence properties of these promoters and RBS.
  
 
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Revision as of 22:49, 14 October 2017


Xylella fastidiosa constitutive promoter + strong RBS

This sequence is a strong constitutive promoter with a strong RBS designed for Xylella fastidiosa.

It is the upstream sequence of a putative highly transcribed gene from Xylella fastidiosa 9a5c, found by analyzing the Best Bidirectional Hits (BBH) between Escherichia coli str. K-12 substr. MG1655 genes and Xylella fastidiosa 9a5c.

Usage and Biology

This part enable us to produce in high quantities proteins in Xylella fastidiosa. It was engineered for the phage-like particle design of our project. Check out our [http://2017.igem.org/Team:Aix-Marseille/M13_Design design page] for more informations.

To evaluate the activity of the promoter and RBS, sfGFP protein was expressed in Escherichia coli DH5α bacteria and it fluorescence properties was studied. We compared our promoter and RBS to a well studied biobrick BBa_K608002 which is an E. coli strong promoter and RBS.

We used [http://2017.igem.org/Competition/InterLab_Study/Plate_Reader InterLab protocol] and negative control to test the fluorescence properties of these promoters and RBS.

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]