Difference between revisions of "Part:BBa K1497002:Design"

 
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__NOTOC__
 
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<partinfo>BBa_K1497002 short</partinfo>
 
<partinfo>BBa_K1497002 short</partinfo>
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===Design Notes===
 
===Design Notes===
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<html>For improving the enzyme the iGEM team TU Darmstadt 2014 decided to remove the tail and to construct their pelargonidin operon with this engineered ANS (eANS). The laboratory results cover the previous modeling results. The engineered ANS exhibited better yields than the original one when used in an operon producing pelargonidin (<a href="/Part:BBa_K1497015">BBa_K1497015</a>). </html>
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Gene was E. coli optimated synthezied by Eurofins.
 
Gene was E. coli optimated synthezied by Eurofins.
  

Revision as of 19:57, 17 October 2014

B0034-eANS (engineered anthocyanidin synthase with strong RBS)


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

For improving the enzyme the iGEM team TU Darmstadt 2014 decided to remove the tail and to construct their pelargonidin operon with this engineered ANS (eANS). The laboratory results cover the previous modeling results. The engineered ANS exhibited better yields than the original one when used in an operon producing pelargonidin (BBa_K1497015).


Gene was E. coli optimated synthezied by Eurofins.


Source

Fragia anassana

References