Difference between revisions of "Part:BBa K3866010"
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<partinfo>BBa_K3866010 short</partinfo> | <partinfo>BBa_K3866010 short</partinfo> | ||
− | + | Tyrosinase fused to AIDA autotranporter<bbpart>BBa_K3505006</bbpart> for outer membrane exxpression[2]. Uder control of constitutive Anderson promoter<bbpart>BBa_K3505012</bbpart>. | |
+ | |||
+ | [[File:T--Thessaly--tyr.png|600px|thumb|none|<i><b>Fig.1:</b>The Tyrosine Tyrosinase Reporter Module </i>]] | ||
+ | |||
− | |||
===Usage and Biology=== | ===Usage and Biology=== | ||
+ | This Transcripion Unit is an electrochemical reporter module [1]. L-Tyrosine is converted to L-Dopa and L-Dopa quinone which is electrochemical detectable. This electochemical signal has the advantage of high quality and easy digitalization. The only advamtage is that is not well characterized. | ||
− | + | ===Verification of the cloning=== | |
− | + | ||
− | + | ||
+ | [[File:T--Thessaly--tyr11.png|600px|thumb|none|<i><b>Fig.2:</b>pAndersonJ23115:RBS-tyrosinase:AIDA-terminator Digested with BamHI. Expected bands 2847, 1883, 520, 353 </i>]] | ||
+ | |||
+ | |||
+ | ===Experimental Use and Experince=== | ||
+ | The Tyrosinase assay from the literature [1] is the addition of 1 g/L of L-Tyrosine into liquid cultures and incubation for 6 hours at 30 celcius. | ||
+ | <p>Measurements are the average of 9 total replicates (3 biological replicates and 3 technical replicates per biological replicate). Error bars represent standard deviation of biological replicates | ||
+ | |||
+ | [[File:T--Thessaly--ty.png|600px|thumb|none|<i><b>Fig.3:</b> The Tyrosinase asssay checking the activity of the Tyrosinase </i>]] | ||
+ | <b>The constitutive Promoter led to toxicity so we plan next year to add an inducble one </b> | ||
+ | |||
+ | [[File:T--Thessaly--tyg.png|600px|thumb|none|<i><b>Fig.4:</b> The Bacterial Growth after 6 hours incubation at 30 celcius Bacteria with Tyrosinase assay Buffer </i>]] | ||
+ | |||
+ | ===Sequence and Features=== | ||
+ | <partinfo>BBa_K3866010 SequenceAndFeatures</partinfo> | ||
− | + | ===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.<em>ACS Synthetic Biology</em> 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.<em> Sci Rep </em> 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, <em>Biochimica et Biophysica Acta (BBA) - Biomembranes</em> , Volume 1861, Issue 2, 2019, Pages 486-494, https://doi.org/10.1016/j.bbamem.2018.11.012. |
Revision as of 11:26, 27 September 2021
ParaBAD-tyrosinase:AIDA-terminator
Tyrosinase fused to AIDA autotranporterBBa_K3505006 for outer membrane exxpression[2]. Uder control of constitutive Anderson promoterBBa_K3505012.
Usage and Biology
This Transcripion Unit is an electrochemical reporter module [1]. L-Tyrosine is converted to L-Dopa and L-Dopa quinone which is electrochemical detectable. This electochemical signal has the advantage of high quality and easy digitalization. The only advamtage is that is not well characterized.
Verification of the cloning
Experimental Use and Experince
The Tyrosinase assay from the literature [1] is the addition of 1 g/L of L-Tyrosine into liquid cultures and incubation for 6 hours at 30 celcius.
Measurements are the average of 9 total replicates (3 biological replicates and 3 technical replicates per biological replicate). Error bars represent standard deviation of biological replicates
The constitutive Promoter led to toxicity so we plan next year to add an inducble one
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1852
Illegal EcoRI site found at 2548
Illegal XbaI site found at 1456
Illegal PstI site found at 1900
Illegal PstI site found at 2486 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1852
Illegal EcoRI site found at 2548
Illegal PstI site found at 1900
Illegal PstI site found at 2486
Illegal NotI site found at 1624 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1852
Illegal EcoRI site found at 2548
Illegal BglII site found at 884
Illegal BamHI site found at 867
Illegal BamHI site found at 2750 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1852
Illegal EcoRI site found at 2548
Illegal XbaI site found at 1456
Illegal PstI site found at 1900
Illegal PstI site found at 2486 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1852
Illegal EcoRI site found at 2548
Illegal XbaI site found at 1456
Illegal PstI site found at 1900
Illegal PstI site found at 2486
Illegal AgeI site found at 946 - 1000COMPATIBLE WITH RFC[1000]
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.