NiFe Hydrogenase

Figure 1. Hydrogen oxidation and reduction {{{2}}}

[NiFe] hydrogenase is a type of hydrogenase, which is an oxidative enzyme that reversibly activates molecular hydrogen in prokaryotes and some eukaryotes. The catalytic site on the enzyme provides simple hydrogen-metabolizing microorganisms a redox mechanism by which to store and utilize energy via the reaction shown in Figure 1. This is particularly essential for the anaerobic, sulfate-reducing bacteria of the genus Desulfovibrio. The practical application of this enzyme is a renewable, more environmentally friendly energy source.

Structure

File:Desulfovibrio vulgaris Miyazaki F.jpg

Figure 2. The structure of D. vulgaris Miyazaki F consisted of two subunits: the large subunit (blue) and the small subunit(magenta). The Figure was prepared using Jmol and the coordinates from 1H2A.pdb.

The structure of [NiFe] hydrogenase was obtained from x-ray crystallography studies of five different sulfate-reducing bacteria: D. vulgaris Miyazaki F, D. gigas, D. frutosovorans, D. desulfuricans and Desulfomicrobium baculatum. The [NiFe] hydrogenase isolated from D. vulgaris Miyazaki F is shown in Figure 2. The larger subunit is in blue, has a molecular mass of 62.5 kDa, and houses the Ni-Fe active site. The smaller subunit is in magenta, has a molecular mass of 28.8 kDa, and contains the Fe-S clusters (see Iron-sulfur cluster).

File:Nickel Iron Hydrogenase Active Site.png

Figure 2. The active site of [NiFe] hydrogenase in the oxidized form. L refers to non-protein ligand (2 C≡O and 1 ⁻C≡N). X can be an oxide, sulfur, hydroperoxide, or a hydroxide.

From the infrared spectra and X-ray crystallography studies, the [NiFe] hydrogenase active site was found to be (S-Cys)₄Ni(μ-X)Fe(CO)(CN)₂, in which the generic ligand X is either an oxide, sulfur, hydroperoxide, or a hydroxide found in an oxidized state only (Figure 3). While the nickel atom participates in redox reactions, the iron atom is consistently in a Fe(II) coordination state. The exact geometry of the three non-protein ligands (denoted as L) coordinating to the Fe metal ion is not known; however, they were identified as one carbon monoxide (C≡O) molecule and two cyanide (⁻C≡N) molecules.

Fe-S clusters

Almost all hydrogenases contain at least one iron-sulfur cluster (Fe-S cluster). As previously mentioned, these Fe-S clusters connect the nickel active site of the enzyme to the surface of the protein because they serve as an electron transport chain from the Ni-Fe redox site to the electron acceptor cytochrome c₃ (see Cytochrome c family). These electrons are produced from the heterolytic cleavage of the hydrogen molecule at the Ni-Fe active site. Crystal structures of the hydrogenase show a Fe₃S₄ in the center of the chain, and a Fe₄S₄ cluster at the molecular surface. The distance between the internal Fe₄S₄ cluster and the active site is approximately 12 Å (Figure 4).

The [NiFe] and [NiFeSe] hydrogenases have remarkably similar structures, leading to the suggestion that one sulfur on a Fe-S cluster was replaced by a selenium atom, but these hydrogenases differ in catalytic reactivity and sensitivity to enzyme inhibitors.

File:NiFe hydrogenase active site.jpg

Figure 4. Illustration of [NiFe] hydrogenase enzyme with three Fe-S clusters in the small subunit with Mg²⁺ and Ni-Fe dimetal active site in the large subunit. Figure was prepared using Jmol and the coordinates from 1H2A.pdb. Mg ion = neon green; Ni ion = dark green; Fe ion = orange; sulfur = yellow; oxygen = red; carbon = dark gray

Mg metal ion and the proton pathways

[NiFe] hydrogenase has a Mg²⁺ cation bonded in the C-terminus region of the larger subunit. This cation is bonded to three water molecules and three amino acids, and it stabilizes this solvent-free region. At approximately 13 Å away from the [NiFe] moiety, this cation connects the active site to a hydrogen bonding network and serves as a proton (H⁺) transfer pathway.

The gas-access channel

Studies in which xenon was bound to the hydrogenase suggest a hydrophobic gas channel through which H₂, CO, and O₂ gases could reach the deeply buried active site within the enzyme. Crystal structure revealed several small channels at the surface, which combined into one larger channel that reached the [Ni-Fe] active site.

Since hydrogenases are well-known to be oxygen sensitive, the diffusion of gas to the active site depends on the size and environment of the gas-access channel, the reaction of molecular oxygen (O₂) at the active site, and the recovery of the active site after oxidation.

Mechanism

The exact reaction mechanism of [NiFe] hydrogenases has been a matter of great debate. In 2009, a mechanism was proposed by Higuchi and coworkers based on X-ray crystallography and spectroscopic data of Desulfovibrio vulgaris Miyazaki F. During the catalytic process, the Fe metal ion in the active site does not change its oxidation state while the Ni metal ion participates in redox chemistry. There are two main groups of redox states that [NiFe] hydrogenases pass through during catalysis 1) Inactive redox states and 2) Active redox states (Figure 5).

File:Redox states of NiFe hydrogenase.png

Figure 5. Different redox states of [NiFe] hydrogenase's metal active site. The redox states in the red are the inactive redox states. The redox states in the green are the active redox states. (Adapted from Ref.11).

Inactive Redox States

Ni-A (the “unready” state) and Ni-B (the “ready” state) are the most oxidized forms of the [NiFe] metal center and are activated via one-electron reduction with proton transfer. The rate of reductive activation of Ni-A to Ni-SU can take hours while the rate of reductive activation of Ni-B to Ni-SIr happens in seconds. The reason for this disparity in activation kinetics between Ni-A and Ni-B was proposed to be a result of the difference in bridging ligands between the two different redox states. At the Ni-SIr state, a water molecule was released to form the Ni-SIa state, the first catalytic redox active state of [NiFe] hydrogenases.

Active Redox States

The 3 most important catalytic redox active states of [NiFe] hydrogenases are Ni-SIa, Ni-C and Ni-R (which have three different variations:). The light-sensitive Ni-C state can be obtained via one electron reduction of Ni-SIa. The electron paramagnetic resonance spectroscopic studies of the Ni-C state, which contained a Ni³⁺ with S=1/2 (see Spin-1/2) and a hydride bridging the two metals Ni and Fe, showed that the heterolytic cleavage of H₂ takes place in the [NiFe] hydrogenase active site.

The CO-inhibited states

Ni-SIa state can be inhibited by CO, which binds directly to Ni metal ion in a bent conformation to form Ni-SCO (see below). Since Ni-C is light sensitive, upon illumination at 100K results in Ni-L redox state. In the presence of CO, Ni-L forms Ni-CO state.

File:NiFe-CO inhibited.jpg

Figure 6. Illustration of the [NiFe] hydrogenase active site inhibited by CO. Top-down view (left). Side view (center). Chemdraw depiction of the inhibited active site (right). The figure was prepared with Jmol and coordinates from 1UBK.pdb. Ni ion = green; Fe ion = orange; sulfur = yellow; oxygen = red; carbon = dark gray; nitrogen = blue.

Application

Since [NiFe] hydrogenase is a member of the hydrogenase family, these enzymes can catalyze both the consumption and production of hydrogen. By studying [NiFe] hydrogenase, scientists can optimize a condition in which the protein will only produce hydrogen. Additionally, small enzyme mimic of [NiFe] hydrogenase can also be synthesized to act as hydrogen gas generator.

See also

• Hydrogenase
• Fe-Ni Clusters
• Bioinorganic