Coding

Part:BBa_K4358001

Designed by: HUNG. CHIEN-CHUN   Group: iGEM22_NCHU_Taichung   (2022-09-14)


Xylose repressor

xylose represser

Gene expression with xylose promoter can be induced by the addition of xylose. When xylose is present, xylose will act as an inducer and bind to the xylose regulator protein to change its structure. Hence, xylR won’t bind to the operator(XylR-binding site) to inhibit the downstream gene of the xylR-binding site.

So we designed the plasmid with Pxyl, XylR and XylR-binding site. Then we transformed pqqC, pqqD and pqqE in the downstream of the xylR-binding site in addition to control the expression of pqqC, pqqD and pqqE to let more resources be used for the biosynthesis of PqqA and PqqB.


T--NCHU_Taichung--NCHU_2022_Figure_L.jpeg

Figure1. It illustrated the mechanism of how xylose regulator protein interacts with xylose promoter and inhibits downstream gene’s performance. The XylR binds to the xylose binding site until the structure changes because of xylose.


T--NCHU_Taichung--NCHU_2022_Figure_A.png

Figure 2. The 3D structure of xylose repressor


Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 870
    Illegal XbaI site found at 121
    Illegal XbaI site found at 961
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 870
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 870
    Illegal XhoI site found at 838
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 870
    Illegal XbaI site found at 121
    Illegal XbaI site found at 961
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 870
    Illegal XbaI site found at 121
    Illegal XbaI site found at 961
  • 1000
    COMPATIBLE WITH RFC[1000]


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