Difference between revisions of "Part:BBa K4368004"
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<partinfo>BBa_K4368004 short</partinfo> | <partinfo>BBa_K4368004 short</partinfo> | ||
− | ''GlgC16'' encodes for the ADP-glucose pyrophosphorylase gene of ''Escherichia coli'' ([[BBa_K118016]]). This enzyme is responsible for the synthesis of starch-like starch using glucose as a substrate. In addition, this part includes the composition used by the team, which includes a strong rbs ([https://parts.igem.org/wiki/index.php?title=Part:BBa_B0030 BBa_B0030]), a double terminator ([https://parts.igem.org/wiki/index.php?title=Part:BBa_B0015 BBa_B0015]) as well as a promoter inducible by the cI protein of the ''phage lambda'' ([https://parts.igem.org/wiki/index.php?title=Part:BBa_R1051 BBa_R1051]). | + | ''GlgC16'' encodes for the ADP-glucose pyrophosphorylase gene of ''Escherichia coli'' (<bbpart>BBa_B0010</bbpart>[[BBa_K118016]]). This enzyme is responsible for the synthesis of starch-like starch using glucose as a substrate. In addition, this part includes the composition used by the team, which includes a strong rbs ([https://parts.igem.org/wiki/index.php?title=Part:BBa_B0030 BBa_B0030]), a double terminator ([https://parts.igem.org/wiki/index.php?title=Part:BBa_B0015 BBa_B0015]) as well as a promoter inducible by the cI protein of the ''phage lambda'' ([https://parts.igem.org/wiki/index.php?title=Part:BBa_R1051 BBa_R1051]). |
The gene has been placed under the control of this promoter to build the glucose concentration-based gene regulatory circuit that integrates all our parts. | The gene has been placed under the control of this promoter to build the glucose concentration-based gene regulatory circuit that integrates all our parts. | ||
Revision as of 17:28, 4 October 2022
pcI + rbs + glgC16 + terminator
GlgC16 encodes for the ADP-glucose pyrophosphorylase gene of Escherichia coli (BBa_B0010BBa_K118016). This enzyme is responsible for the synthesis of starch-like starch using glucose as a substrate. In addition, this part includes the composition used by the team, which includes a strong rbs (BBa_B0030), a double terminator (BBa_B0015) as well as a promoter inducible by the cI protein of the phage lambda (BBa_R1051). The gene has been placed under the control of this promoter to build the glucose concentration-based gene regulatory circuit that integrates all our parts.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 272
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]