Difference between revisions of "Part:BBa J100126:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | We had to shorten the pMekA promotor sequence form the front and back by more than 30 nucleotides. This may cause the promoter to lose its normal function. | + | We had to shorten the pMekA promotor sequence form the front and back by more than 30 nucleotides. This may cause the promoter to lose its normal function. pMekA is repressed by glucose. The glucose concentration required to repress the promoter is 0.2%. |
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===Source=== | ===Source=== |
Latest revision as of 13:59, 12 September 2013
pMekA mutated, repressed by glucose
Assembly Compatibility:
- 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
We had to shorten the pMekA promotor sequence form the front and back by more than 30 nucleotides. This may cause the promoter to lose its normal function. pMekA is repressed by glucose. The glucose concentration required to repress the promoter is 0.2%.
Source
http://link.springer.com/content/pdf/10.1007%2Fs00253-013-5030-7.pdf