Difference between revisions of "Part:BBa K415000"

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The fluorescence of mCherry was then quantified using FACs(Fluorescence-activated cell sorting) running two samples: -AHL and +AHL. Negative control of plasmid pRCV3(Plux-GFP) was used to ensure adequate concentrations of AHL induction. The addition of AHL tests whether or not the circuit will respond without LuxR. The fluorescence of mCherry was measured in arbitrary units.  
+
The fluorescence of mCherry was then quantified using FACs(Fluorescence-activated cell sorting) running two samples: -AHL and +AHL. Plasmid pRCV3(Plux-GFP) was used as control to ensure adequate concentrations of AHL induction. The addition of AHL tests whether or not the circuit will respond without LuxR. The fluorescence of mCherry was measured in arbitrary units.  
  
 
Figure 3
 
Figure 3

Revision as of 04:15, 26 October 2010

pLux/cI-OR : RBS-mCherry : Term


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


BBa_K415000 represents an AND-Gate promoter controlling the expression of expressing mCherry. The promoter requires two inputs: an environment free of cI and secondly, quorum sensing, in the form of LuxR-homoserine-lactone for triggering the pLux promoter. The part was constructed via the insertion of BBa_J06702 into a BBa_R0065 backbone(pSB1A2). The following 1% agarose gel, prepared from powder and 1% TAE and stained with SYBR® Safe DNA gel stain, presents confirmation of said construction. The part was run along the standard of Hyperladder 1.

Figure 1

K415000 gel.jpg


The following is a plasmid map of the part in the pSB1A2 backbone:

Figure 2

K415000 geneious.jpg


The fluorescence of mCherry was then quantified using FACs(Fluorescence-activated cell sorting) running two samples: -AHL and +AHL. Plasmid pRCV3(Plux-GFP) was used as control to ensure adequate concentrations of AHL induction. The addition of AHL tests whether or not the circuit will respond without LuxR. The fluorescence of mCherry was measured in arbitrary units.

Figure 3

K415000.jpg


It is clear that the circuit does not respond to the addition of AHL. The following are FACs sheets:

Figure 4: -AHL

K415000Basal.jpg


Figure 5: +AHL

K415000+AHL facs.jpg



Source

https://parts.igem.org/wiki/index.php?title=Part:BBa_R0065

https://parts.igem.org/wiki/index.php?title=Part:BBa_J06702

References