Difference between revisions of "Part:BBa K1819008"

Revision as of 21:15, 18 September 2015

Promoter test circuit to analyze the kill switch efficiency

BBa_K1819008 construction indicates lactose promoter (pLac) efficiency to control a TetR promoter inhibited by TetR protein. This circuit was used to verify a kill switch mechanism (See more details in Brasil-USP team wiki)

In the absence of pLac inductor (Lactose or IPTG), RFP will be constitutively expressed under TetR promoter control. If inducer is added, TetR promoter is repressed and, consequently, RFP expression ceases and GFP expression starts.

Characterization

DH5-alpha

    We first started with DH5α. For protocols, we refer to our Protocols section. We evaluated the fluorescence per cell by measuring Optical Density (OD) of our colonies and their fluorescences. We show in figures 1 and 2 our results.

Figure 1 - Optical Density (OD) measurements over time, showing that all colonies were in their log phase.

Figure 2 - Fluorescence per cell for each promoter, normalized by the fluorescence with no induction. In the x-axis, the higher the concentration label, the higher the concentration, with zero means no induction at all. Only Rhamnose showed some actual induction. All errors may be considered about 0.05 a.u.

    Except for Rhamose, fluorescence was very weak and basically at the level of our negative control (E. Coli without plasmid), confirmed by a Mann-Whitney U test. Rhamnose showed some level of activity which would be considered weak, compared to, for instance, our Interlab Results. Finally, no considerable changes were detected in the RFP measures. Since there results are not good indicatives, we performed this experiment three different times (to reduce possible experimental artifacts with assembling or other steps in our protocol). Yet we have always observed the same behavior consistently.

BL21 DE3

Sequence and Features