Part:BBa_K316005:Experience

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Applications of BBa_K316003

• The enzymatic reaction catalysed by C2,3O is an ideal output signal for our engineered bacterial detector and it can also serve as a very useful reporter gene.
• Catechol, the substrate of C2,3O, is colourless. However within seconds of its addition, the colonies/liquid cultures of XylE-expressing cells become yellow, indicating production of a product which absorbs light in the visible spectrum

User Reviews

UNIQ74c380787f9480aa-partinfo-00000000-QINU

••••• Imperial College iGEM 2010
Characterization in r.p.u. of Pveg promoter Our experiment was performed on 96-well plates comparing four different populations of Catechol(2,3)dioxygenase expessing E.coli cells. These four different populations (initial O.D. 0.5) were: 1) XylE under the influence of J23101 promoter in pSB1C3 vector, 2) ) XylE under the influence of J23101 promoter in 3K3 vector, 3) XylE under the influence of pVeg promoter in pSB1C3 vector and 4) ) XylE under the influence of pVeg promoter in 3K3 vector. All 4 populations were grown under same condition and tested for the expression of catechol dioxygenase enzyme by addition 0.25mM catechol substrate. Reaction was monitored using spectrophotomer and the production of colored product was recorded. Production of HMS colored product is directly proportional to total enzyme presence. Since total enzyme presence depends on the strength of the promoter, this provides a means for quantification of the strength of promoters in relative promoter units. The results showed that pVeg promoter in pSB1C3 vector, a high copy plasmid, has an 1.62 r.p.u value and in 3K3 vector, a low copy plasmid an 0.79 r.p.u. value. These values were derived by dividing signal from the production of HMS by the pVeg promoter population of cells by signal from the standard promoter J23101 (r.p.u value of 1).Figure below: Absorbtion spectrum assay Spectra of cultures of cells expressing the XylE and cells negative for the XylE gene. Note the broad peak in the spectra of Xyle transformed cells, which is centered around 380nm. The spectra showed that in XylE transformed cells, a broad peak appears at about 380nm. The absorbance at this particular wavelength is by the product of the C2,3O reaction which is called 2-hydroxymuconic semialdehyde and is what causes the yellow output.
2-hydroxymuconate semialdehyde production rate Graph shows production of HMS (yellow product) over time after catechol addition at time 0 minutes. Different curves represent different catechol concentration added to the cell cultures. Data that delineate the course of the reaction in terms of yellow product production over time at various catechol concentrations. The results of one of these assays is presented in the figure below. In order to extract data that will allow characterization of the kinetic parameters of catechol dioxygenase enzyme our lab team proposes purification of the protein from cell lysate, several fold dilution, and in vitro characterization.
Cytotoxicity of Catechol Growth with Catechol (LB) The addition of catechol had distinctive effects on the XylE expressing cells growing in LB medium. While at 0% catechol growth-behavior did not show a significant change (dark blue), even the lowest concentration of 0.25% catechol appeared to drastically reduce cell-survival (red). In contrast, CMR-control cells did not change their growing behavior in the presence of catechol. From this we conclude that in LB medium, the breakdown product of catechol, 2-hydroxymuconic semialdehyde, has a lethal effect on E. coli.
O.D. at 600 over 3h for XylE-transformed Top10 cells in presence of different catechol concentrations, growing in LB medium. O.D. at 600 over 3h for CMR-transformed Top10 cells in presence of different catechol concentrations, growing in LB medium.
(M9) Cells growing in M9 medium appeared more resistant to the effects of catechol. With absorbance at 380 nm increased significantly in well containing XylE expressing cells, indicating strong turnover of Catechol by C2,3O (4), Catechol showed strong influence on growing behavior in generalizable fashion: increasing concentrations of catechol progressively inhibited cell population growth. However, the overall effect of the breakdown product HMS appeared less severe than compared with the LB – XylE samples.
O.D. at 600 over 3h for XylE-transformed Top10 cells in presence of different catechol concentrations, growing in M9 medium. O.D. at 600 over 3h for CMR-transformed Top10 cells in presence of different catechol concentrations, growing in M9 medium.
C23O kinetics The Michaelis-Menten curve was delineated by non-linear regression analysis using GraFit software tool. The calculated Km is 0.71mM catechol (with a Vmax of 3.37 in O.D. arbitrary units for this dilution of cell lysate).
Sequencing results from Imperial College London iGEM 2011 The Imperial college 2011 iGEM team had intended to use this part in order to construct BBa_K515100 through CPEC assembly. Before assembly we discovered that there is a one base pair mutation in the promoter. We named the new promoter Pveg2. For more information on this new part visit: BBa_K515010.

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