Difference between revisions of "Part:BBa K2294007"
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The BOKU-Vienna Team 2017 submitted and characterized this part by measuring the GFP expression using flow cytometry. For detais go to the [[Part:BBa_K2294007:Experience|Experience page]]. | The BOKU-Vienna Team 2017 submitted and characterized this part by measuring the GFP expression using flow cytometry. For detais go to the [[Part:BBa_K2294007:Experience|Experience page]]. | ||
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+ | ===Reference=== | ||
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+ | Redden, H., & Alper, H. S. (2015). The development and characterization of synthetic minimal yeast promoters. Nature Communications, 6, 7810. https://doi.org/10.1038/ncomms8810 | ||
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Revision as of 09:52, 1 November 2017
Synthtic minimal Galactose induced promoter + Kozak sequence
A short synthtetic promoter which can be induced by the addition of Galactose. This promoter contains already a Kozak sequence for the expression of proteins. The promoter is only 160 bp long.
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]
Usage and Biology
This promoter is build up fully modular. The promoter starts with an GAL4 binding site derived from GAL1. After this trnaskription factor binding site a neutral spacer is placed to avoid steric hindrances between GAL4 and the TATA-box-binding- proteins of the preinitiation complex. The core element following the TATA-box contains all sequence components necessary for transcription initiation.
Promoter characterization
The BOKU-Vienna Team 2017 submitted and characterized this part by measuring the GFP expression using flow cytometry. For detais go to the Experience page.
Reference
Redden, H., & Alper, H. S. (2015). The development and characterization of synthetic minimal yeast promoters. Nature Communications, 6, 7810. https://doi.org/10.1038/ncomms8810