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Figure 2 | Journal of Biological Engineering

Figure 2

From: Rational design of modular circuits for gene transcription: A test of the bottom-up approach

Figure 2

Fluorescence levels. The normalized fluorescence, equation 2, in arbitrary units, is shown for cells transformed with: Reporter plasmid without the operator sequence (n = 6); Reporter plasmids with the O1 (n = 5), O2 (n = 8), and Os (n = 10) operator sequence; Repressor plasmids with any of the three operator sequences and Reporter plasmid lacking the lactose operator sequence (n = 10); O2O2 induced with 1 mM IPTG (n = 13); O1O1 induced with 1 mM (n = 9) and 2 mM (n = 5) IPTG; OsOs induced with 1 mM (n = 4) and 8 mM (n = 3) IPTG. In absence of Repressor plasmids, the normalized fluorescence is the same if the Reporter plasmid does not include the operator sequence, or if it includes any of the three operator sequences tested. Co-transformation with a Repressor plasmid and a Reporter plasmid without the operator site causes a decrease in the maximum fluorescence, even if no LacI activity is exerted. The same fluorescence was observed in the O2O2 gene circuit at saturating concentrations of IPTG. On the other hand, the maximum fluorescence in the O1O1 and OsOs gene circuits is statistically different from the maximum value.

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