Difference between revisions of "Part:BBa K3505006"
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Tyrosinase catalyzes the conversion of L-Tyrosine to L-Dopa and L-Dopa quinone. These derivatives can be detected electochemically, producing peak currents.[1] | Tyrosinase catalyzes the conversion of L-Tyrosine to L-Dopa and L-Dopa quinone. These derivatives can be detected electochemically, producing peak currents.[1] | ||
| + | |||
| + | [[File:T--Thessaly--ai.png|700px|thumb|none|<i><b>Fig.1:</b>Level 0 part Signal Peptide- Tyrosinase- AIDA</i>]] | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
| Line 12: | Line 14: | ||
*The passeger of AIDA which is the part that is on the exterior side. | *The passeger of AIDA which is the part that is on the exterior side. | ||
| − | We placed as passenger the Tyr1 gene coding to Rhizobium etli tyrosinase Because is the smallest of all tyrosinases (34kDa) and lack cysteines[3] compared to the melA tyrosinase BBa_K193600 used in iGEM before. | + | We placed as passenger the Tyr1 gene coding to Rhizobium etli tyrosinase Because is the smallest of all tyrosinases (34kDa) and lack cysteines[3] compared to the melA tyrosinase <bbpart>BBa_K193600</bbpart> used in iGEM before. |
===Design Notes=== | ===Design Notes=== | ||
The coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. | The coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. | ||
| − | The sequence is present in pUPD2 <bbpart>BBa_K3505007</bbpart>as Level 0 and has overhangs compatible for | + | The sequence is present in pUPD2 <bbpart>BBa_K3505007</bbpart>as Level 0 and has overhangs compatible for GoldenBraid cloning. |
The CDS has position B3-B5. | The CDS has position B3-B5. | ||
| − | [[File:T--Thessaly--GB-AATG-GCTT.jpeg|700px|thumb|none|<i><b>Fig.2:</b>The overhangs of this part in the | + | [[File:T--Thessaly--GB-AATG-GCTT.jpeg|700px|thumb|none|<i><b>Fig.2:</b>The overhangs of this part in the GoldenBraid Grammar</i>]] |
===Experimental Use and Experince=== | ===Experimental Use and Experince=== | ||
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===Source=== | ===Source=== | ||
| + | Synthesized by IDT | ||
*Tyr1 from <i>Rhizobium etli</i> in the supplementary of [3] | *Tyr1 from <i>Rhizobium etli</i> in the supplementary of [3] | ||
Latest revision as of 00:04, 28 October 2020
Tyr1-AIDAc Tyrosinase fused to membrane protein AIDAc. GB compatible B3-B5
Tyrosinase catalyzes the conversion of L-Tyrosine to L-Dopa and L-Dopa quinone. These derivatives can be detected electochemically, producing peak currents.[1]
Usage and Biology
AIDA is native E.coli outer membrane protein. AIDA's CDS constists of 3 parts: [2]
- A Signal Peptide that is cleaved in order the rest of the protein to be transported to the outer membrane.
- The AIDAc is the autotransporter with the transmembrane part.
- The passeger of AIDA which is the part that is on the exterior side.
We placed as passenger the Tyr1 gene coding to Rhizobium etli tyrosinase Because is the smallest of all tyrosinases (34kDa) and lack cysteines[3] compared to the melA tyrosinase BBa_K193600 used in iGEM before.
Design Notes
The coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is present in pUPD2 BBa_K3505007as Level 0 and has overhangs compatible for GoldenBraid cloning. The CDS has position B3-B5.
Experimental Use and Experince
This part is used in BBa_K3505035
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal XbaI site found at 1043
Illegal PstI site found at 1487
Illegal PstI site found at 2073 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal PstI site found at 1487
Illegal PstI site found at 2073
Illegal NotI site found at 1211 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal BglII site found at 471
Illegal BamHI site found at 454
Illegal BamHI site found at 2337 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal XbaI site found at 1043
Illegal PstI site found at 1487
Illegal PstI site found at 2073 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal XbaI site found at 1043
Illegal PstI site found at 1487
Illegal PstI site found at 2073
Illegal AgeI site found at 533 - 1000COMPATIBLE WITH RFC[1000]
Source
Synthesized by IDT
- Tyr1 from Rhizobium etli in the supplementary of [3]
- AIDA from E.coli in the supplementary of [2]
References
- [1] Eric VanArsdale, David Hörnström, Gustav Sjöberg, Ida Järbur, Juliana Pitzer, Gregory F. Payne, Antonius J. A. van Maris, and William E. Bentley. A Coculture Based Tyrosine-Tyrosinase Electrochemical Gene Circuit for Connecting Cellular Communication with Electronic Networks.ACS Synthetic Biology 2020 9 (5), 1117-1128
DOI: 10.1021/acssynbio.9b00469
- [2] Gustavsson, M., Hörnström, D., Lundh, S. et al. Biocatalysis on the surface of Escherichia coli: melanin pigmentation of the cell exterior. Sci Rep 6, 36117 (2016). https://doi.org/10.1038/srep36117
- [3] David Hörnström, Gen Larsson, Antonius J.A. van Maris, Martin Gustavsson, Molecular optimization of autotransporter-based tyrosinase surface display, Biochimica et Biophysica Acta (BBA) - Biomembranes , Volume 1861, Issue 2, 2019, Pages 486-494, https://doi.org/10.1016/j.bbamem.2018.11.012.