Difference between revisions of "Part:BBa K902041"

 
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</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 experience section of this page.</p></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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<!-- Add more about the biology of this part here

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.

Amidase pathway kilbane calgary12.jpg

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


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 670
    Illegal XhoI site found at 162
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE 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
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 406
    Illegal BsaI site found at 947