Difference between revisions of "Part:BBa K1813032"
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− | A construct used to achieve the bacterial expression of HUMCYPDB1 (<html><b><a href="https://parts.igem.org/Part:BBa_K1813005">BBa_K1813005</b></a></html> and the <i> A. gambiae </i> NADPH p450 reductase simultaneously (<html><b><a href="https://parts.igem.org/Part: | + | A construct used to achieve the bacterial expression of HUMCYPDB1 (<html><b><a href="https://parts.igem.org/Part:BBa_K1813005">BBa_K1813005</b></a></html>) and the <i> A. gambiae </i> NADPH p450 reductase simultaneously (<html><b><a href="https://parts.igem.org/Part:BBa_K1813010">BBa_K1813010</b></a></html>) under regulative authority of the LacI repressor. <br> |
Revision as of 08:29, 18 September 2015
LacIR, AgCPR and CYP2D6 Regulon
A construct used to achieve the bacterial expression of HUMCYPDB1 (BBa_K1813005) and the A. gambiae NADPH p450 reductase simultaneously (BBa_K1813010) under regulative authority of the LacI repressor.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 105
Illegal BglII site found at 1737 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 2327
- 1000COMPATIBLE WITH RFC[1000]
Background
Repressed by the presence of the LacI regulatory element, this construct does not allow significant expression of either gene without induction by the presence of Isopropyl β-D-1-thiogalactopyranoside in a bacterial host. In doing so, the cytochrome p450 enzyme receives a steady supply of electrons from the reductase, critical for p450 mediated catalysis, once the construct is expressed.