Difference between revisions of "Part:BBa K1024005"

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<partinfo>BBa_K1024005 short</partinfo>
 
<partinfo>BBa_K1024005 short</partinfo>
  
<img height="auto" src="https://static.igem.org/mediawiki/2013/c/c7/Tsinghua_BBa_K1024000.png" width="100%"/>
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<b>Part Name:</b> BBa_K1024005
 
<b>Part Name:</b> BBa_K1024005
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<b>Design:</b> The part was the reporter of the pathogen detector. Tet operator and CYC1 TATA region was followed by ADE2 gene. In the yeast S. cerevisiae the ade2, and/or the ade1, mutation in the adenine biosynthetic pathway leads to the accumulation of a cell-limited red pigment. Mated with sensor yeast (BBa_K1024004) which is induced by AHL, the ADE2 gene will be activated and rescuing the ADE2 knockout yeast by making it white.
 
<b>Design:</b> The part was the reporter of the pathogen detector. Tet operator and CYC1 TATA region was followed by ADE2 gene. In the yeast S. cerevisiae the ade2, and/or the ade1, mutation in the adenine biosynthetic pathway leads to the accumulation of a cell-limited red pigment. Mated with sensor yeast (BBa_K1024004) which is induced by AHL, the ADE2 gene will be activated and rescuing the ADE2 knockout yeast by making it white.
 
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https://static.igem.org/mediawiki/igem.org/a/a5/Tsinghua-BB-005.png
  
  

Revision as of 16:29, 27 September 2013

Report yeast (inducible ADE2)


Part Name: BBa_K1024005

Short Description: Report yeast (inducible ADE2)

Part Type: Signaling

Design: The part was the reporter of the pathogen detector. Tet operator and CYC1 TATA region was followed by ADE2 gene. In the yeast S. cerevisiae the ade2, and/or the ade1, mutation in the adenine biosynthetic pathway leads to the accumulation of a cell-limited red pigment. Mated with sensor yeast (BBa_K1024004) which is induced by AHL, the ADE2 gene will be activated and rescuing the ADE2 knockout yeast by making it white.

Tsinghua-BB-005.png


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 1053
    Illegal BamHI site found at 456
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]