Difference between revisions of "Part:BBa K2683021"

Line 3: Line 3:
 
<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:
  • 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
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 172