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. 2010 Jun 22;2010:719856. doi: 10.1155/2010/719856

Figure 2.

Figure 2

Disulfide reductase activities and specificity of mTGR. Enzyme activities were carried out at 25°C as described under Materials and Methods. (a) Saturation kinetics with different disulfides. Initial velocity data were fitted to a hyperbolic saturation kinetic function with the aid of Sigma plot. The scale of the lower abscissa represent concentration of either GSSG or DTNB, while the upper-abscissa scale corresponds to Trx concentration. (▲) GSSG reductase activity; (Inline graphic) Trx reductase activity with T. crassiceps Trx; (Δ) Trx reductase activity with DTNB. (b) Specificity of mTGR toward exogenous Trx. The reductase activity of mTGR was assayed in the presence of a variety of prokaryotic and eukaryotic Trx. A final concentration of 50 μM of the corresponding Trx was used. Abbreviations are as follows. Tc, Taenia crassiceps Trx; Pf: Plasmodium falciparum Trx; Hs, Homo sapiens Trx; Ec: Escherichia coli Trx; S, Spirulina sp Trx.