Difference between revisions of "Part:BBa K2443019"
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<partinfo>BBa_K2443019 short</partinfo> | <partinfo>BBa_K2443019 short</partinfo> | ||
− | Tryptophan tRNA synthetase responsible for attaching Tryptophan onto its tRNA to form an aminoacyl-tRNA. Codon optimized for use in <i>Escherichia coli</i>. Contains a C-terminal hexahistidine tag with a serine glycine linker. Under the regulation of T7 Promoter, RBS and double terminator. | + | Tryptophan tRNA synthetase responsible for attaching Tryptophan onto its tRNA to form an aminoacyl-tRNA. Codon optimized for use in <i>Escherichia coli</i>. Contains a C-terminal hexahistidine tag with a serine glycine linker. Under the regulation of T7 Promoter, RBS and double terminator. The expected size of TrpRS is 39 kDa, which corresponds to the band seen in lane 5 of the overexpression gel (below). Overexpressions were performed according to the protein overexpression protocol and lab notebook on the 2017 iGEM lethbridge wiki (https://static.igem.org/mediawiki/2017/2/2c/Protein_Overexpression_.pdf and https://static.igem.org/mediawiki/2017/0/0d/October_.pdf) |
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+ | https://static.igem.org/mediawiki/parts/b/bf/Lethbridge_Oct_22_gel.png | ||
Latest revision as of 18:47, 1 November 2017
TrpRS optimized for expression in E. coli
Tryptophan tRNA synthetase responsible for attaching Tryptophan onto its tRNA to form an aminoacyl-tRNA. Codon optimized for use in Escherichia coli. Contains a C-terminal hexahistidine tag with a serine glycine linker. Under the regulation of T7 Promoter, RBS and double terminator. The expected size of TrpRS is 39 kDa, which corresponds to the band seen in lane 5 of the overexpression gel (below). Overexpressions were performed according to the protein overexpression protocol and lab notebook on the 2017 iGEM lethbridge wiki (https://static.igem.org/mediawiki/2017/2/2c/Protein_Overexpression_.pdf and https://static.igem.org/mediawiki/2017/0/0d/October_.pdf)
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 682
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]