Difference between revisions of "Part:BBa K3600004"
(→Usage and Biology) |
|||
Line 3: | Line 3: | ||
<partinfo>BBa_K3600004 short</partinfo> | <partinfo>BBa_K3600004 short</partinfo> | ||
− | + | GLR1 promoter part plasmid was made in order to create a part plasmid which contains the GLR1 promoter and compatible with the Yeast Toolkit in the mean time. | |
+ | |||
+ | At first, a gBlocks consisting of the 500bp promoter region, that was retrieved from the yeast genome database, was added linking sequences to both ends. These linkers contained a BsaI and a BsmBI cutting site each to make Golden Gate assembly possible. Then, the ...was inserted into the part plasmid entry vector (pYTK001) to create GLR1 part plasmid through a BsmBI assembly. | ||
+ | |||
===Usage and Biology=== | ===Usage and Biology=== |
Revision as of 15:33, 27 October 2020
GLR1 promoter part plasmid
GLR1 promoter part plasmid was made in order to create a part plasmid which contains the GLR1 promoter and compatible with the Yeast Toolkit in the mean time.
At first, a gBlocks consisting of the 500bp promoter region, that was retrieved from the yeast genome database, was added linking sequences to both ends. These linkers contained a BsaI and a BsmBI cutting site each to make Golden Gate assembly possible. Then, the ...was inserted into the part plasmid entry vector (pYTK001) to create GLR1 part plasmid through a BsmBI assembly.
Usage and Biology
- activator: Yap1p
- The GLR1 gene encodes glutathione reductase, which catalyses the reduction of the oxidized form of glutathione (GSSG) to Glutathione (GSH).1
- The promoter GLR1 has been chosen in order to express fluorescent protein [ref] when the S.cervisiae is exposed to oxidative stress.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 778
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 778
- 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 778
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 624
Illegal BsaI.rc site found at 1145