Azotobacter vinelandii hydrogenase

Seefeldt, E. C. and Arp, D. J. (1986) Purification to homogeneity of Azotobacter vinelandii hydrogenase A nickel and iron containing alpha beta dimmer. Biochimie, 68, 25-34. 

McTavish, H., Sayavedra-Soto, L. A., and Arp. D. 1996. Comparison of isotope exchange, H2 evolution, and H2 oxidation activities of Azotobacter vinelandii hydrogenase. Biochim. Biophys. Acta 1294, 183-190. 

McTavish, H., L.A. SayavedraSoto and D.J. Arp. (1995). Substitutions of Azotobacter vinelandii Hydrogenase Small-Subunit Cysteines by Serines Can Create Insensitivity to Inhibition by 02 and Preferentially Damages H2 Oxidation over H2 Evolutiont. J. Bacteriol. 177, 3960-3964. 

Gollin, D. J., Mortenson, L. E. and Robson, R. L. (1992) Carboxyl-terminal processing may be essential for production of active NiFe hydrogenase in Azotobacter vinelandii. FEBS Lett., 309, 371-5. 

Hyman, M. R., and Arp, D. J. (1991). Kinetic analysis of the interaction of nitric oxide with the membrane-associated, nickel and iron-sulfur-containing hydrogenase from Azotobacter vinelandii. Biochim. Biophys. Acta 1076, 165-172. 

Aerobic bacteria such as Azotobacter vinelandii, Alcaligenes eutrophus, and Nocardia opaca, and facultative anaerobes, such as Escherichia coli and various species of Rhizobium and Bradyrhizobium (the symbionts of leguminous plants), also contain hydrogenase, as do photosynthetic bacteria such as Chromatium vinosum, Rhodobacter capsulatus (formerly Rhodopseudomonas capsulata), and Anabaena variabilis (a filamentous cyanobacterium). The thermophilic hydro-... 

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