Composite

Part:BBa_K2275010

Designed by: I-Tai Shih   Group: iGEM17_NCKU_Tainan   (2017-10-14)
Revision as of 15:27, 27 October 2017 by TedShihncku (Talk | contribs)


PIacI-B0034-K2275004 (glnA-gudB)

We combined the gudB and glnA gene into pSB1C3 backbone. By SDS-PAGE method, we test the expression of both proteins as well. The gel image shows below, where "WC" indicates whole cell, "S" for supernatant, "P" for pellet, and "C" indicates the control of sample without plasmid.

SDS-PAGE result of GlnA and GudB.png

We can see that the glnA and gudB both expressed in E. coli at the same time. Next, we want to test if the Biobrick can function to convert ammonium to glutamine, so we add different ammonium concentration and use kit to detect the glutamine concentration.

Functional test of glnA-gudB.png

The figure above is the functional test result. When merely adding ammonium, the concentration of glutamine is very low. However, if both harboring the plasmid and adding ammonium, the concentration if glutamine is higher.The second and third bar can show the ability of converting ammonium to glutamine. Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 675
    Illegal BamHI site found at 1309
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 322
    Illegal NgoMIV site found at 1088
    Illegal NgoMIV site found at 2454
    Illegal AgeI site found at 578
    Illegal AgeI site found at 2891
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 1481


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