Table 5.
EPR Parameters for Model Compounds vs Nitrile Hydratase
g values | |||
---|---|---|---|
[FeIII(DITpy)2]+ (1)a | 2.16 | 2.10 | 2.02 |
[FeIII(DITIm)2]+ (2)a | 2.19 | 2.15 | 2.01 |
[FeIII(ADIT)2]+ (3)b | 2.19 | 2.13 | 2.01 |
[FeIII(AMIT)2]+ (4)b | 2.20 | 2.16 | 2.00 |
[FeIII(PyAS)2]+c | 2.17 | 2.11 | 2.01 |
[FeIII(PyMS)2]+c | 2.13 | 2.09 | 2.03 |
[FeIII(PyPepS)2]+d | 2.22 | 2.14 | 1.98 |
NHase enzyme + N3−e,g | 2.23 | 2.14 | 1.99 |
NHase enzyme (pH = 9)e,f,h | 2.20 | 2.12 | 1.99 |
NHase enzyme (pH = 7.3)e,f,h | 2.27 | 2.14 | 1.97 |
NHase enzyme + (CH3)2CHCN (pH = 7.2)e,g | 2.21 | 2.12 | 1.98 |
This work.
Shoner, S. C.; Barnhart, D.; Kovacs, J. A. Inorg. Chem. 1995, 34, 4517–4518.
Noveron, J. C.; Herradora, R.; Olmstead, M. M.; Mascharak, P., K. Inorg. Chim. Acta. 1999, 285, 269–276.
Noveron, J. C.; Olmstead, M. M.; Mascharak, P. K. Inorg. Chem. 1998, 37, 1138–1139.
These spectra were recorded in the presence of a butyrate buffer, which was added in order to stabilize the samples. Butyrate appears to act as an inhibitor.
The reported g-values are those of a “butyrate-inhibited” form of the enzyme.
Sugiura, Y.; Kuwahara, J.; Nagasawa, T.; Yamada, H. J. Am. Chem. Soc. 1987, 109, 5848- 5850.
Brennan, B. A.; Cummings, J. G.; Chase, D. B.; Turner, I. M., Jr.; Nelson, M. J. Biochemistry 1996, 35, 10068–10077.