Difference between revisions of "Part:BBa K2683021"
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<partinfo>BBa_K2683021 short</partinfo> | <partinfo>BBa_K2683021 short</partinfo> | ||
− | Serine tRNA synthetase is a protein responsible for attaching serine onto its tRNA to form an aminoacyl-tRNA. The part is codon optimized for use in <i> Escherichia coli </i>, contains a C-terminal hexahistidine tag with a serine glycine linker and has a T7 Promoter, medium strength RBS and double terminator. These designs were originally done by the Lethbridge iGEM team 2017 (http://2017.igem.org/Team:Lethbridge). The part was characterized in the pUC57 plasmid | + | Serine tRNA synthetase is a protein responsible for attaching serine onto its tRNA to form an aminoacyl-tRNA [1]. The part is codon optimized for use in <i> Escherichia coli </i>, contains a C-terminal hexahistidine tag with a serine glycine linker and has a T7 Promoter, medium strength RBS and double terminator. These designs were originally done by the Lethbridge iGEM team 2017 (http://2017.igem.org/Team:Lethbridge). The part was characterized in the pUC57 plasmid |
(https://parts.igem.org/Part:BBa_K2443017). | (https://parts.igem.org/Part:BBa_K2443017). | ||
Revision as of 00:08, 12 October 2018
Serine tRNA Synthetase (SerRS) in pSB1C3
Serine tRNA synthetase is a protein responsible for attaching serine onto its tRNA to form an aminoacyl-tRNA [1]. The part is codon optimized for use in Escherichia coli , contains a C-terminal hexahistidine tag with a serine glycine linker and has a T7 Promoter, medium strength RBS and double terminator. These designs were originally done by the Lethbridge iGEM team 2017 (http://2017.igem.org/Team:Lethbridge). The part was characterized in the pUC57 plasmid (https://parts.igem.org/Part:BBa_K2443017).
The part was improved by placing it within the pSB1C3 plasmid.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 172