Table 1. Metal Content and Reactivity of Different AibH1H2 Preparationsa.
| metal/heterodimer |
|||||
|---|---|---|---|---|---|
| Fe | Mn | Ni | Zn | [d-MeSer]/[AibH1H2]b | |
| FeAibH1H2 | 2.8 ± 0.1 | 0.08 ± 0.04 | 0.03 ± 0.03 | 0c | <2d |
| LBAibH1H2 | 1.67 ± 0.07 | 1.05 ± 0.01 | 0.055 ± 0.003 | 0.131 ± 0.004 | 33 ± 1 |
| MnAibH1H2 | 0.4 ± 0.1 | 2.2 ± 0.4 | 0.03 ± 0.07 | 0 | 110 ± 30 |
| Mn*AibH1H2 | 0 | 2.4 ± 0.3 | 0 | 0 | 50 ± 10 |
| Fe*AibH1 H2 | 1.8 ± 0.2 | 0 | 0 | 0 | <2 |
| Mn/Fe Crystal | 0.0 | 1.9 | 1.3e | 0.0 | 30 |
| EPR | 0.3 | 1.5 | 0.0 | 0.1 | 73 |
Data for entries 1–5 represent the average of at least three technical replicates. Error is the standard deviation. Entries 6 and 7 represent the specific batch used for the application indicated. Error of the ICP-OES instrument is less than 0.01 ppm.
Catalytic activity assay performed with the addition of one equivalent of FeII relative to AibH1H2 (25 μM) in the reaction mixture.
Values less than the limit of detection of the ICP-OES instrument (0.01 ppm) are reported as zero.
Values less than 2 are below the minimum point on the calibration curve for GC-MS analysis of catalytic activity.
High Ni content is likely due to contamination from the Ni-NTA column during protein purification.