Difference between revisions of "Part:BBa I719005"
Line 37: | Line 37: | ||
Summary: We adapted the part to be able to assemble transcriptional units with the Golden Gate assembly method | Summary: We adapted the part to be able to assemble transcriptional units with the Golden Gate assembly method | ||
<br> | <br> | ||
− | |||
===Contribution=== | ===Contribution=== | ||
Group: Valencia_UPV iGEM 2018 | Group: Valencia_UPV iGEM 2018 | ||
Line 46: | Line 45: | ||
<br> | <br> | ||
Documentation: | Documentation: | ||
− | + | In order to create our complete [http://2018.igem.org/Team:Valencia_UPV/Part_Collection part collection] of parts compatible with the Golden Gate assembly method, we made the part [https://parts.igem.org/Part:BBa_K2656000 BBa_K2656000] which is this part adapted to the Golden Gate technology. |
Revision as of 07:47, 17 October 2018
T7 Promoter
Constitutive promoter derived from the T7 bacteriophage. Allows high expression of proteins only when the T7 polymerase is present. This part is identical to the part BBa_R0085 which currently hasn't been built.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Characterization in vitro
This part has been characterized for temperature sensitivity in the Cell-Free Chassis by iGEM Imperial 2007. For more detail, please check the testing [http://2007.igem.org/Imperial/Wet_Lab/Protocols/Prot1.9 protocols]and [http://2007.igem.org/Imperial/Wet_Lab/Results/Res1.9 results].
Parameter | Value and Description |
---|---|
Optimum temperature | The T7 promoter has a highest output at 25°C, with a one-fold increase in GFP molecules synthesized compared to 37°C. The T7 promoter also has a minimal amount of output at 4°C. |
Expression Life-span | The rate of GFP synthesis by the T7 promoter reaches a peak at around 30-60 minutes. |
Peak Expression | The production of GFP decreases to minimal levels after 2 hours and tends towards nil after 4 hours. |
Team Warsaw 2010's measurement
Absolute promoter strength: 41,8pg RNA/minute/ug substrate DNA. It equals 8,92 microPoPSContribution
Group: Valencia_UPV iGEM 2018
Author: Adrián Requena Gutiérrez, Carolina Ropero
Summary: We adapted the part to be able to assemble transcriptional units with the Golden Gate assembly method
Contribution
Group: Valencia_UPV iGEM 2018
Author: Adrián Requena Gutiérrez, Carolina Ropero
Summary: We adapted the part to be able to assemble transcriptional units with the Golden Gate assembly method
Documentation:
In order to create our complete [http://2018.igem.org/Team:Valencia_UPV/Part_Collection part collection] of parts compatible with the Golden Gate assembly method, we made the part BBa_K2656000 which is this part adapted to the Golden Gate technology.