Difference between revisions of "Part:BBa K1741003"

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

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
INCOMPATIBLE WITH RFC[21]
Illegal BglII site found at 154
23
COMPATIBLE WITH RFC[23]
25
COMPATIBLE WITH RFC[25]
1000
INCOMPATIBLE WITH RFC[1000]
Illegal SapI.rc site found at 206

@@ Line 2: / Line 2: @@
 <partinfo>BBa_K1741003 short</partinfo>
-MelR chromosomal copy of MelR is sufficient to activate the melibiose melAB promoter copied from E. coli K12 chromosome when melibiose is added to M9 minimal medium or to a rich medium 2xLB (0,4%). In both media induction is much weaker than of arabinose or rhamnose induced promoters.
+===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 [[https://parts.igem.org/Part:BBa_K1741004 BBa_K1741004]]
+https://static.igem.org/mediawiki/parts/f/f1/UAMpoznanmelS.jpg
+MelWT [[https://parts.igem.org/Part:BBa_K1741003 BBa_K1741003]]
+https://static.igem.org/mediawiki/parts/0/02/UAMpoznanmelWT.jpg
 ===Results===
-Legend:<br>
+Legend:
-MelS [[https://parts.igem.org/Part:BBa_K1741004 Ba_K1741004]]
-<br>
-MelWT [[https://parts.igem.org/Part:BBa_K1741003 Ba_K1741003]]
+MelS [[https://parts.igem.org/Part:BBa_K1741004 BBa_K1741004]]
+MelWT [[https://parts.igem.org/Part:BBa_K1741003 BBa_K1741003]]
 https://static.igem.org/mediawiki/parts/9/97/Teamuampoznanmelibiosem9graph.png
 https://static.igem.org/mediawiki/parts/2/2c/Teamuampoznanmelibioselbgraph.png
-https://static.igem.org/mediawiki/parts/a/a2/Teamuampoznandifferentpromotersm9minimal.png
+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.
+https://static.igem.org/mediawiki/parts/4/43/Teamuampoznanpromoterscomparisongrpah.png