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. Author manuscript; available in PMC: 2015 Jun 30.
Published in final edited form as: Inorg Chem. 2001 Mar 26;40(7):1646–1653. doi: 10.1021/ic001271d

Table 3.

Comparison of Electronic Spectral Data for Nitrile Hydratase Enzyme vs Model Compounds

λmax (ε)

MeCN H2O
[FeIII(DITpy)2]+ (1)a 784 (1300) 732 (1400)
[FeIII(DITIm)2]+ (2)a 802 (1300) 740 (1200)
[FeIII(ADIT)2]+ (3)b 718 (1400) 693 (1400)
[FeIII(AMIT)2]+ (4)b,g 696 (1100)
inactive enzyme (pH = 9)c,d 690 (~1200)
active enzyme (pH = 7.3)c,d 710 (~1200)
active enzyme (butyrate-free)e 676 (NR)h
enzyme + CH3CH2CNf 690 (~4200)
a

This work.

b

Shoner, S. C.; Barnhart, D.; Kovacs, J. A. Inorg. Chem. 1995, 34, 4517–4518.

c

These spectra were recorded in the presence of a butyrate buffer.

d

Brennan, B. A.; Cummings, J. G.; Chase, D. B.; Turner, I. M., Jr.; Nelson, M. J. Biochemistry 1996, 35, 10068–10077.

e

Honda, J.; Kandori, H.; Okada, T.; Nagamune, T.; Shichida, Y.; Sasabe, H.; Endo, I. Biochemistry, 1994, 33, 3577–3583.

f

Sugiura, Y.; Kuwahara, J.; Nagasawa, T.; Yamada, H. J. Am. Chem. Soc. 1987, 109, 5848–5850.

g

Aqueous solution values not reported for complex 4 due to rapid decomposition in water.

h

NR = not reported.