Difference between revisions of "Part:BBa M36533"
 
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<partinfo>BBa_M36533 short</partinfo>
 
<partinfo>BBa_M36533 short</partinfo>
  
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This part was made in order to reduce arsenate to arsenite and increase arsenite resistance in ''S. cerevisiae.''
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This part was made in order to increase arsenate uptake by ''S. cerevisiae.''
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Construct uses DNA 2.0 plasmid backbone (pD1207) with GAL1 inducible (galactose-inducible/glucose-repressible) promoter, high copy number ORI, and ampicillin and histidine selectable markers in E. coli and yeast, respectively. A self-cleaving 2A peptide sequence was inserted between ACR2 and ACR1 genes to allow for both genes to be transcribed.
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Construct uses DNA 2.0 plasmid backbone (pD1201) with GAL1 inducible (galactose-inducible/glucose-repressible) promoter, high copy number ORI, and ampicillin and leucine as selectable markers in E. coli and yeast, respectively.
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 06:49, 8 December 2015

Arsenate Bioremediation Actuator Plasmid Containing PHO84 Gene

This part was made in order to increase arsenate uptake by S. cerevisiae.

Construct uses DNA 2.0 plasmid backbone (pD1201) with GAL1 inducible (galactose-inducible/glucose-repressible) promoter, high copy number ORI, and ampicillin and leucine as selectable markers in E. coli and yeast, respectively.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 1647
    Illegal PstI site found at 1002
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 1002
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 1438
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 1647
    Illegal PstI site found at 1002
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 1647
    Illegal PstI site found at 1002
  • 1000
    COMPATIBLE WITH RFC[1000]