Difference between revisions of "Part:BBa K799009"
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− | + | YMR251W-A promoter is expected to drive gene expression in Saccharomyces cerevisiae in the presence of ethanol. | |
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+ | We tested this by expressing GFP under the control of YMR251W-A promoter in the presence of multiple different concentrations of ethanol. We found an induction of GFP. | ||
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− | === | + | ===Characterization=== |
− | [[]] | + | [[Image:ProA5 fluoro.png]] |
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+ | This is fluorescence data for the expression of GFP under the control of YMR251W-A, our ethanol induced promoter. Fluorescence can be seen soon after ethanol induction. Furthermore, the fluorescence plateaus but remains significant till our last time point of 230 minutes. | ||
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+ | ===Plasmid Map=== | ||
+ | [[Image:YMR251W-A plasmid.png]] | ||
===Sequencing=== | ===Sequencing=== |
Latest revision as of 04:15, 3 October 2012
Ethanol/Stress Inducible YMR251W-A Promoter
YMR251W-A promoter is expected to drive gene expression in Saccharomyces cerevisiae in the presence of ethanol.
We tested this by expressing GFP under the control of YMR251W-A promoter in the presence of multiple different concentrations of ethanol. We found an induction of GFP.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 120
Illegal PstI site found at 277 - 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 169
Illegal NheI site found at 355
Illegal PstI site found at 277 - 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 120
Illegal PstI site found at 277 - 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 120
Illegal PstI site found at 277 - 1000COMPATIBLE WITH RFC[1000]
Characterization
This is fluorescence data for the expression of GFP under the control of YMR251W-A, our ethanol induced promoter. Fluorescence can be seen soon after ethanol induction. Furthermore, the fluorescence plateaus but remains significant till our last time point of 230 minutes.
Plasmid Map
Sequencing
This is the sequencing result for YMR251W-A. As can be seen, it is a perfect match to the genomic DNA promoter.