Difference between revisions of "Part:BBa K2739001:Design"
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===Source=== | ===Source=== | ||
− | This part is | + | |
− | The | + | This part is consisted PhaR's native promoter. This part was designed to allow the investigation of phaR relation with phasin, and PHA production through PHA operon with and without phasin. |
+ | |||
+ | The promoter used in this part is native to phaR and R.eutropha. Sequence of this native promoter could be found in iGEM registry, as a basic parts (BBa_K108014) and being not available. The source of these sequences were recorded as 1. Regulation of phasin expression and polyhydroxyalkanoate (PHA) granule formation in Ralstonia eutropha H16. Microbiology. 2002, 148:2413–2426. and 2. NCBI (with no further information), having no mentioned if the sequence was codon optimised. | ||
+ | |||
+ | We access the online NCBI data and found out the current available the functional promoter is being 134bp shorter. Therefore we have used the new phaR and promoter sequence as our new template. Due to the excessive GC in the sequence, we have it codon optimised to E.coli and generated the part through the IDT company service. | ||
===References=== | ===References=== |
Revision as of 22:38, 14 October 2018
The promoter (ProR) + RBS for the phasin autoregulation system (PhaR)
- 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
The ProR promoter is native to R.eutropha.
Source
This part is consisted PhaR's native promoter. This part was designed to allow the investigation of phaR relation with phasin, and PHA production through PHA operon with and without phasin.
The promoter used in this part is native to phaR and R.eutropha. Sequence of this native promoter could be found in iGEM registry, as a basic parts (BBa_K108014) and being not available. The source of these sequences were recorded as 1. Regulation of phasin expression and polyhydroxyalkanoate (PHA) granule formation in Ralstonia eutropha H16. Microbiology. 2002, 148:2413–2426. and 2. NCBI (with no further information), having no mentioned if the sequence was codon optimised.
We access the online NCBI data and found out the current available the functional promoter is being 134bp shorter. Therefore we have used the new phaR and promoter sequence as our new template. Due to the excessive GC in the sequence, we have it codon optimised to E.coli and generated the part through the IDT company service.