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Research Article

Effects of cadmium and zinc ions on purified lamb kidney cortex glucose-6-phosphate dehydrogenase activity

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Pages 225-230 | Received 25 Jul 2005, Accepted 24 Oct 2005, Published online: 04 Oct 2008

Figures & data

Figure 1 Inhibition of lamb kidney cortex glucose-6-phosphate dehydrogenase by zinc. The velocities were determined in 100 mM Tris/HCl buffer pH 8.0.

Figure 1 Inhibition of lamb kidney cortex glucose-6-phosphate dehydrogenase by zinc. The velocities were determined in 100 mM Tris/HCl buffer pH 8.0.

Figure 2 Lineweaver-Burk double reciprocal plot of initial velocity against G-6-P as varied substrate and Zn 2+(1.0–2.0 mM) as inhibitor at different fixed NADP+(0.1 mM).

Figure 2 Lineweaver-Burk double reciprocal plot of initial velocity against G-6-P as varied substrate and Zn 2+(1.0–2.0 mM) as inhibitor at different fixed NADP+(0.1 mM).

Figure 3 Lineweaver-Burk double reciprocal plot of initial velocity against NADP+ as varied substrate and Zn2+(1.0–2.0 mM) as inhibitor at different fixed G-6-P (0.4 mM) concentrations. The velocities were determined in 100 mM Tris/HCl buffer pH 8.0.

Figure 3 Lineweaver-Burk double reciprocal plot of initial velocity against NADP+ as varied substrate and Zn2+(1.0–2.0 mM) as inhibitor at different fixed G-6-P (0.4 mM) concentrations. The velocities were determined in 100 mM Tris/HCl buffer pH 8.0.

Figure 4 Inhibition of lamb kidney cortex glucose-6-phosphate dehydrogenase by cadmium. The velocities were determined in 100 mM Tris/HCl buffer pH 8.0.

Figure 4 Inhibition of lamb kidney cortex glucose-6-phosphate dehydrogenase by cadmium. The velocities were determined in 100 mM Tris/HCl buffer pH 8.0.

Figure 5 Lineweaver-Burk double reciprocal plot of initial velocity against G-6-P as varied substrate and Cd 2+(1.5–3.0 mM) as inhibitor at different fixed NADP+(0.1 mM) concentrations. The velocities were determined in 100 mM Tris/HCl buffer pH 8.0.

Figure 5 Lineweaver-Burk double reciprocal plot of initial velocity against G-6-P as varied substrate and Cd 2+(1.5–3.0 mM) as inhibitor at different fixed NADP+(0.1 mM) concentrations. The velocities were determined in 100 mM Tris/HCl buffer pH 8.0.

Figure 6 Lineweaver-Burk double reciprocal plot of initial velocity against NADP+ as varied substrate and Cd 2+(1.5–3.0 mM) as inhibitor at different fixed G-6-P (0.4 mM) concentrations. The velocities were determined in 100 mM Tris/HCl buffer pH 8.0.

Figure 6 Lineweaver-Burk double reciprocal plot of initial velocity against NADP+ as varied substrate and Cd 2+(1.5–3.0 mM) as inhibitor at different fixed G-6-P (0.4 mM) concentrations. The velocities were determined in 100 mM Tris/HCl buffer pH 8.0.

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