Difference between revisions of "Part:BBa K1741003"
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===Design=== | ===Design=== | ||
− | + | MelR transcription factor translated from becterial chromosome is sufficient to activate the melibiose MelAB promoter copied from ''E. coli'' K12 chromosome (upon addition of melibiose to M9 minimal medium or to a rich medium 2xLB [0,4%]). Shortened MelWT with removed PstI site is also induced. In both media induction is much weaker than that of arabinose or rhamnose induced promoters. | |
Legend: | Legend: | ||
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− | The sfGFP fluorescence [RFU] was measured using Tecan | + | The sfGFP fluorescence [RFU] was measured using Tecan fluorometer. |
We also checked the tightness of our promoters. | We also checked the tightness of our promoters. |
Latest revision as of 09:00, 27 September 2015
sfGFP under melibiose promoter
Design
MelR transcription factor translated from becterial chromosome is sufficient to activate the melibiose MelAB promoter copied from E. coli K12 chromosome (upon addition of melibiose to M9 minimal medium or to a rich medium 2xLB [0,4%]). Shortened MelWT with removed PstI site is also induced. In both media induction is much weaker than that of arabinose or rhamnose induced promoters.
Legend:
MelS [BBa_K1741004]
MelWT [BBa_K1741003]
Results
Legend:
MelS [BBa_K1741004]
MelWT [BBa_K1741003]
The sfGFP fluorescence [RFU] was measured using Tecan fluorometer.
We also checked the tightness of our promoters.
All of our promoters are induced only by their respective sugars with a small exception of xylose promoters being slightly induced by arabinose and arabinose promoters being slightly induced by xylose. All of our promoters are repressed by glucose.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 154
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 206