Selective one-electron reduction of Nitrosomonas europaea hydroxylamine oxidoreductase with nitric oxide

Inorganic Chemistry

Volumn 42, Issue 2, 2003, Pages 270-272

  Cabail, Maria Zulema ^a   Pacheco, A Andrew ^a  

^a UNIVERSITY OF WISCONSIN MILWAUKEE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; HEME; HYDROXYLAMINE; IRON DERIVATIVE; N,N' BIS(CARBOXYMETHYL) N,N' DINITROSO 1,4 PHENYLENEDIAMINE; NITRIC OXIDE; NITROUS OXIDE; OXIDOREDUCTASE; PHENYLENEDIAMINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL BINDING; ELECTRON; ENZYME ACTIVE SITE; HYDROLYSIS; NITROSOMONAS; NITROSOMONAS EUROPAEA; NONHUMAN; OXIDATION; PHOTOLYSIS; REDUCTION;

CATALYSIS; ELECTRON TRANSPORT; HEME; HYDROLYSIS; HYDROXYLAMINE; MOLECULAR STRUCTURE; NITRIC OXIDE; NITROGEN DIOXIDE; NITROSOMONAS; OXIDATION-REDUCTION; OXIDOREDUCTASES;

EID: 0037467739     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic025779n     Document Type: Article

References (34)

1. Hooper, A. B.; Nason, A. J. Biol. Chem. 1965, 240, 4044-4057.
2. Andersson, K. K.; Hooper, A. B. FEBS Lett. 1983, 164, 236-240.
3. Ferguson, S. J. Curr. Opin. Chem. Biol. 1998, 2, 182-193.
4. Hooper, A. B. In Autotrophic Bacteria; Schlegel, H. G., Bowien, B., Eds.; Science Tech Publishers: Madison-WI, 1989; pp 239-265.
5. Prince, R. C.; George, G. N. Nat. Struct. Biol. 1997, 4, 247-250.
6. Biological Nitrogen Fixation; National Academy Press: Washington, DC, 1994; pp 6-32.
7. Igarashi, N.; Moriyama, H.; Fujiwara, T.; Fukumori, Y.; Tanaka, N. Nat. Struct. Biol. 1997, 4, 276-284.
8. Arciero, D. M.; Hooper, A. B. J. Biol. Chem. 1993, 268, 14645-14654.
9. Hooper, A. B.; Terry, K. R. Biochemistry 1977, 16 (3), 455-459.
10. Hendrich, M. P.; Logan, M.; Andersson, K. K.; Arciero, D. M.; Lipscomb, J. D.; Hooper, A. B. J. Am. Chem. Soc. 1994, 116, 11961-11968.
11. Logan, M. S. P.; Balny, C.; Hooper, A. B. Biochemistry 1995, 34, 9028-9037.
12. Logan, M. S. P.; Hooper, A. B. Biochemistry 1995, 34, 9257-9264.
13. Arciero, D. M.; Balny, C.; Hooper, A. B. Biochemistry 1991, 30, 11466-11472.
14. Wehrfritz, J.-M.; Reilly, A.; Spiro, S., Richardson. FEBS Lett. 1993, 335, 246-250.
15. Moir, J. W. B.; Crossman, L. C.; Spiro, S.; Richardson, D. J. FEBS Lett. 1996, 387, 71-74.
16. Enemark, J. H.; Feltham, R. D. Coord. Chem. Rev. 1974, 13, 339-406.
17. -.
18. Hoshino, M.; Maeda, M.; Konishi, R.; Seki, H.; Ford, P. C. J. Am. Chem. Soc. 1996, 118, 5702-5707.
19. Ford, P. C.; Lorkovic, I. M. Chem. Rev. 2002, 102, 993-1017.
20. Hendrich, M. P.; Upadhyay, A. K.; Riga, J.; Arciero, D. M.; Hooper, A. B. Biochemistry 2002, 41, 4603-4611.
21. Namiki, S.; Arai, T.; Fujimori, K. J. Am. Chem. Soc. 1997, 119, 3840-3841.
22. Cabail, M. Z.; Lace, P. J.; Uselding, J.; Pacheco, A. A. J. Photochem. Photobiol., A 2002, 152, 109-121.
23. Ellis, L. M.; Lace, P. J.; Patel, N. K.; Ver Haag, M. P.; Pacheco, A. A. Manuscript in preparation.
24. -1, which is 3x the value reported in ref 10 for the molar absorptivity of the individual monomers.
25. Spectra were collected every millisecond for 30 s, using an Olis RSM-1000 rapid-scanning spectrophotometer. The data were analyzed using the Specfit 32 Global Analysis System (Version 3.0), Spectrum Software Associates, Marlborough, MA.
26. Hooper, A. B.; Maxwell, P. C.; Terry, K. R. Biochemistry 1978, 17, 2984-2989.
27. Yamanaka, T.; Shinra, M.; Takahashi, K.; Shibasaka, M. J. Biochem. 1979, 86, 1101-1108.
28. Collins, M. J.; Arciero, D. M.; Hooper, A. B. J. Biol. Chem. 1993, 268, 14655-14662.
29. Arciero, D. M.; Golombeck, A.; Hendrich, M. P.; Hooper, A. B. Biochemistry 1998, 37, 523-529.
30. The width of photoexcited solution that the spectrophotometer beam must traverse is 0.5 cm, as explained in ref 22. Therefore 0.5 cm is taken to be the solution path length in the application of Beer's law.
31. Hoshino, M.; Ozawa, K.; Seki, H.; Ford, P. C. J. Am. Chem. Soc. 1993, 115, 9568-9575.
32. Beckman, J. S. In Nitric Oxide, Principles and Actions; Lancaster, J., Ed.; Academic Press: New York, 1996; pp 1-82.
33. NO gas was Matheson CP grade 99.5%. It was manipulated using an all-glass and metal gas handling apparatus fully described in ref 22 and scrubbed using a column of NaOH pellets prior to use.
34. Hendrich M. P.; Petasis, D.; Arciero, D. M.; Hooper, A. B. J. Am. Chem. Soc. 2001, 123, 2997-3005.