Difference between revisions of "Part:BBa K2683019"
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<partinfo>BBa_K2683019 short</partinfo> | <partinfo>BBa_K2683019 short</partinfo> | ||
− | + | Lysine tRNA synthetase is a protein responsible for attaching lysine onto its tRNA to form an aminoacyl-tRNA [1]. This part is codon optimized for use in <i> Escherichia coli </i>, contains a N-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 in 2017 (http://2017.igem.org/Team:Lethbridge). | |
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+ | This part was improved by LEthbridge iGEM 2018 by placing the part in the pSB1C3 plasmid. | ||
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+ | https://static.igem.org/mediawiki/2018/f/f5/T--Lethbridge--LysRSOE.PNG | ||
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+ | Figure 1- Overexpression of LysRS protein run on a 12% SDS-PAGE gel. Samples were taken at point of induction and in 1 hour increments after. The induced samples can be seen at about the 60kDa mark. | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Latest revision as of 03:28, 17 October 2018
Lysine tRNA Synthetase (LysRS) in pSB1C3
Lysine tRNA synthetase is a protein responsible for attaching lysine onto its tRNA to form an aminoacyl-tRNA [1]. This part is codon optimized for use in Escherichia coli , contains a N-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 in 2017 (http://2017.igem.org/Team:Lethbridge).
This part was improved by LEthbridge iGEM 2018 by placing the part in the pSB1C3 plasmid.
Figure 1- Overexpression of LysRS protein run on a 12% SDS-PAGE gel. Samples were taken at point of induction and in 1 hour increments after. The induced samples can be seen at about the 60kDa mark.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1459
Illegal NgoMIV site found at 1531 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 733