Difference between revisions of "Part:BBa K902041"
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− | AmdA coding sequence downstream of a strong TetR repressible promoter (R0040) and a ribosome binding site ( | + | <html><p><i>AmdA</i> coding sequence (<a href="https://parts.igem.org/Part:BBa_K902035">K902035</a>) downstream of a strong TetR repressible promoter (<a href="https://parts.igem.org/Part:BBa_R0040">R0040</a>) and a ribosome binding site (<a href="https://parts.igem.org/Part:BBa_B0034">B0034</a>). AmdA is an amidase enzyme from <i>Rhodococcus erythropolis</i> that can remove amine and amide groups from carbon rings. It can potentially replace the function of the genes responsible for the lower half of the carbazole degradation pathway by cleaving the second C-N bond after the carA enzyme has converted carbazole into 2'-aminobiphenyl-2,3-diol.</p> |
− | </html> | + | </html>[[Image:amidase pathway kilbane calgary12.jpg|center]]<html> |
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+ | <p>It can also remove the nitrogen from amides and replace it with a hydroxyl group, creating a carboxylic acid. This part's function was characterized using benzamide as a model compound as detailed in the <a href=" https://parts.igem.org/Part:BBa_K902041:Experience">experience</a> section of this page.</p></html> | ||
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Latest revision as of 03:01, 27 October 2012
Constitutive AmdA Generator
AmdA coding sequence (K902035) downstream of a strong TetR repressible promoter (R0040) and a ribosome binding site (B0034). AmdA is an amidase enzyme from Rhodococcus erythropolis that can remove amine and amide groups from carbon rings. It can potentially replace the function of the genes responsible for the lower half of the carbazole degradation pathway by cleaving the second C-N bond after the carA enzyme has converted carbazole into 2'-aminobiphenyl-2,3-diol.
It can also remove the nitrogen from amides and replace it with a hydroxyl group, creating a carboxylic acid. This part's function was characterized using benzamide as a model compound as detailed in the experience section of this page.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 670
Illegal XhoI site found at 162 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 170
Illegal NgoMIV site found at 1375
Illegal NgoMIV site found at 1481
Illegal AgeI site found at 548
Illegal AgeI site found at 732 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 406
Illegal BsaI site found at 947