Figure 3.
Figure 3. Steady-state kinetics of recombinant wild-type and mutant P5′N-1 as a function of CMP. (A) Steady-state kinetics of recombinant wild-type and mutant P5′N-1 using CMP as substrate. (B) Semilog plot of the data in panel A to highlight the difference of Km of mutants with respect to the wild-type enzyme. v/Vmax represents the ratio of the initial (v) to the maximal (Vmax) rate of enzyme reaction. Enzyme activity was assayed at 37°C, pH 7.5, as described in “Materials and methods.” • indicates wild type; □, D87V; ▴, L131P; ♦, N179S; ▿, G230R. The solid line differentiates the wild-type from mutants (dashed lines).

Steady-state kinetics of recombinant wild-type and mutant P5N-1 as a function of CMP. (A) Steady-state kinetics of recombinant wild-type and mutant P5′N-1 using CMP as substrate. (B) Semilog plot of the data in panel A to highlight the difference of Km of mutants with respect to the wild-type enzyme. v/Vmax represents the ratio of the initial (v) to the maximal (Vmax) rate of enzyme reaction. Enzyme activity was assayed at 37°C, pH 7.5, as described in “Materials and methods.” • indicates wild type; □, D87V; ▴, L131P; ♦, N179S; ▿, G230R. The solid line differentiates the wild-type from mutants (dashed lines).

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