Figure 1
Figure 1. The sigmoidal “apparent zero order” behavior of the nitrite reaction with deoxyhemoglobin. Deoxyhemoglobin (50 μM) reaction with nitrite (10 mM) at pH 7.4 and 37°C. (A) Time-resolved absorption spectra were deconvoluted to determine the percentage of each species as a function of time. Deoxyhemoglobin is observed to form equal amounts of methemoglobin and iron-nitrosyl-hemoglobin. Deviation from first-order behavior is evident in the curve for decay of deoxyhemoglobin, having a sigmoidal shape. In experiments with excess nitrite, the spectrum of nitrite bound to methemoglobin (nitrite-methemoglobin) should be included. (B) The instantaneous rate of the reaction shown in panel A where the negative of the slope of the decay curve for deoxyhemoglobin is plotted as a function of time. The figure is reproduced from Grubina et al15 with permission.

The sigmoidal “apparent zero order” behavior of the nitrite reaction with deoxyhemoglobin. Deoxyhemoglobin (50 μM) reaction with nitrite (10 mM) at pH 7.4 and 37°C. (A) Time-resolved absorption spectra were deconvoluted to determine the percentage of each species as a function of time. Deoxyhemoglobin is observed to form equal amounts of methemoglobin and iron-nitrosyl-hemoglobin. Deviation from first-order behavior is evident in the curve for decay of deoxyhemoglobin, having a sigmoidal shape. In experiments with excess nitrite, the spectrum of nitrite bound to methemoglobin (nitrite-methemoglobin) should be included. (B) The instantaneous rate of the reaction shown in panel A where the negative of the slope of the decay curve for deoxyhemoglobin is plotted as a function of time. The figure is reproduced from Grubina et al15  with permission.

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