Table 1.
t = 0 s | t = 320 ms | t = 3 s | |||
---|---|---|---|---|---|
| |||||
Prediction (At start) | Observation (Mössbauer) | Prediction (Kinetics) | Observation (Mössbauer) | Prediction (Kinetics) | Observation (Mössbauer) |
100 % Hred | 95 % diferrous | 55 % Hslred | 86 % diferrous | 50 % Hslred | 58 % diferrous |
33 % P* | 10 % P* | ||||
| |||||
3.4 % P | 3 % P | 4 % P | 7 % P | ||
3.6 % (Q + Hox) | 5 % Hox | 22 % Q | 23 % Q | ||
2 % Hox | 7 % Hox+ Hslox | ||||
6 % Hslox | |||||
| |||||
5 % unidentifieda | 5 % unidentitiedb | 5 % unidentifieda | 5 % unidentifiedb | 5 % unidentifieda |
In all samples, approximately 5 % of the Mössbauer absorption could not be positively identified as it competes with the noise. This absorption is probably associated with diferric species (not a single one). It is certainly not originating from ferrous MMOH and may derive in part from unreduced enzyme.
Assumed from the Mössbauer spectrum of the t = 0 sample.