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See: Wang, J.; Mauro, J. M.; Edwards, S. L.; Oatley, S. J.; Fishel, L. A.; Ashford, V. A.; Nguyen-huu, X.; Kraut, J. Biochemistry 1990, 29, 7160-7173 and references therein.
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54
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2642679601
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-
note
-
-2) for experiments conducted with the native yeast enzyme at pH 6.1. The electroactive coverage is sensitive both to pH and to potential range, the higher switching potential necessary in these experiments giving lower coverage. Half-height widths are higher at pH 5.4 than at pH 6.1. It thus appears that the optimum pH for obtaining voltammetric signals from the enzyme is 6.1.
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-
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55
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2642702932
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note
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IV=O group from Fe(III) is limited by a slow step, assumed to be the displacement and binding of the distal water molecule (See ref 19). Similar restrictions may apply in the non-turnover transformations of CcP.
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-
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56
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2642670635
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note
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Where such cooperativity occurs and where distinctive species are generated, potentiometric titrations offer a better way to define the individual one-electron potentials (see refs 20 and 21). The advantage of voltammetry is that it is a dynamic technique, able to measure reduction potentials under catalytic conditions or where species are only generated as reactive transients.
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57
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2642640796
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note
-
By comparing our observed δ value of 74 mV with the theoretical limit for a fully cooperative two-electron process (i.e., 42 mV at 0 °C), we conclude that dispersion effects must contribute less than ca. 32 mV. This means that the active sites in the enzyme film behave as a homogeneous ensemble.
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-
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59
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2642673924
-
-
note
-
+ are transferred from the active site upon oxidation.
-
-
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60
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2642648982
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Submitted for publication
-
Detailed interpretation of catalytic wave shapes arising from enzymes adsorbed at electrodes is discussed in the following: Heering, H. A.; Hirst, J.; Armstrong, F. A. Submitted for publication.
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Heering, H.A.1
Hirst, J.2
Armstrong, F.A.3
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61
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2642643256
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note
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The complex changes in wave shape accompanying the inactivation of the WT/W51F mixed film may also be contrasted with the catalytic voltammetry of succinate dehydrogenase and fumarate reductase where progressive inactivation produces no change in wave shape. The all-or-nothing "binary" behavior is an indicator of the homogeneity of the adsorbed enzyme sample.
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