Part:BBa_K3781006:Design
Strep-tag II + HRV 3C Motif, MocloMania B3
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This basic L0 part was de novo synthesized and thus easily codon optimized towards Leishmania tarentolae.
We generated this part by designing it in silico to carry the sequence of interest flanked by two invertedly oriented BbsI recognition sites as well as the desired B3 overhangs. After commercial synthesis, this allowed us to introduce the part into its respective L0 plasmid backbone with a simple MoClo ligation.
Source
The sequence of this part is based on a commercial, Chlamydomonas-adapted genetic part that is stored in the pCM0-096 plasmid of the Crozet MoClo Toolkit.[1] The Strep-tag II sequence itself is a synthetic peptide and doesn't have a natural genomic source. The HRV 3C motif sequence is based on the recognition sequence of a human rhinovirus protease and can thus be found in human genes, e.g. coding for transcription factors.[2]
References
- ↑ Crozet et al. (2018) Birth of a Photosynthetic Chassis: A MoClo Toolkit Enabling Synthetic Biology in the Microalga Chlamydomonas reinhardtii. ACS Synthetic Biology 7:2074–2086
- ↑ Amineva SP, Aminev AG, Palmenberg AC, Gern JE (October 2004). "Rhinovirus 3C protease precursors 3CD and 3CD' localize to the nuclei of infected cells". The Journal of General Virology. 85 (Pt 10): 2969–79. doi:10.1099/vir.0.80164-0. PMID 15448360