Difference between revisions of "Part:BBa I742144"
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<partinfo>BBa_I742144 short</partinfo> | <partinfo>BBa_I742144 short</partinfo> | ||
− | This part consists of sam8, encoding tyrosine ammonia lyase (converts tyrosine to p-coumaric acid) from the bacterium ''Saccharothrix espanaensis'' DSM 44229, inserted downstream of a ''lac'' promoter with attached ''lacZ''' minigene. The purpose of this was to ensure sam8 expression on induction with IPTG and also to provide a visually selectable tag when assembling the entire pathway; by always inserting a ''lacZ | + | This part consists of sam8, encoding tyrosine ammonia lyase (converts tyrosine to p-coumaric acid) from the bacterium ''Saccharothrix espanaensis'' DSM 44229, inserted downstream of a ''lac'' promoter with attached ''lacZ''' minigene. The purpose of this was to ensure sam8 expression on induction with IPTG and also to provide a visually selectable tag when assembling the entire pathway; by always inserting a ''lacZ''-containing part into a non-''lacZ''-containing part it is easy to select the correct clones on the basis that they form blue colonies. |
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Latest revision as of 18:34, 25 October 2007
Plac+lacZ+sam8 (tyrosine ammonia lyase)
This part consists of sam8, encoding tyrosine ammonia lyase (converts tyrosine to p-coumaric acid) from the bacterium Saccharothrix espanaensis DSM 44229, inserted downstream of a lac promoter with attached lacZ' minigene. The purpose of this was to ensure sam8 expression on induction with IPTG and also to provide a visually selectable tag when assembling the entire pathway; by always inserting a lacZ-containing part into a non-lacZ-containing part it is easy to select the correct clones on the basis that they form blue colonies.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1416
Illegal BamHI site found at 1818 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1159
Illegal AgeI site found at 1106
Illegal AgeI site found at 1275 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 710
Illegal BsaI site found at 976