Metallo-inhibition of Mnx, a bacterial manganese multicopper oxidase complex.

The manganese oxidase complex, Mnx, from Bacillus sp. PL-12 contains a multicopper oxidase (MCO) and oxidizes dissolved Mn(II) to form insoluble manganese oxide (MnO) mineral. Previous kinetic and spectroscopic analyses have shown that the enzyme's mechanism proceeds through an activation step that facilitates formation of a series of binuclear Mn complexes in the oxidation states II, III, and IV on the path to MnO formation.

Investigation of the physical, optical, and chemical properties of phase segregated AlCoOx thin films from a novel hexol-type cluster.

The use of a novel inorganic nanoscale cluster (Al[(μ-OH)Co(NH)](NO)) was investigated for its utility as a precursor for AlCoOx films. Mixed-metal aluminum and cobalt oxide thin films were solution deposited from the novel cluster solution via the spin-coating method on Si (100) and quartz substrates. The films were annealed at increasing temperatures up to 800 °C, and characterization of these films via TEM and XRD confirms binary CoO crystalline phase present in an amorphous AlO network.

The Surface Chemistry of Metal Oxide Clusters: From Metal-Organic Frameworks to Minerals.

Many metal-organic frameworks (MOFs) incorporate nodes that are small metal oxide clusters. Some of these MOFs are stable at high temperatures, offering good prospects as catalysts-prospects that focus attention on their defect sites and reactivities-all part of a broader subject: the surface chemistry of metal oxide clusters, illustrated here for MOF nodes and for polyoxocations and polyoxoanions. Ligands on MOF defect sites form during synthesis and are central to the understanding and control of MOF reactivity.

Dynamics of Cation-Induced Conformational Changes in Nanometer-Sized Uranyl Peroxide Clusters.

Conformational changes of the pyrophosphate (Pp)-functionalized uranyl peroxide nanocluster [(UO)(O)(PO)] ({UPp}), dissolved as a Li/Na salt, can be induced by the titration of alkali cations into solution. The most symmetric conformer of the molecule has idealized octahedral () molecular symmetry. One-dimensional P NMR experiments provide direct evidence that both K and Rb ions trigger an -to- conformational change within {UPp}.

Mn(III) species formed by the multi-copper oxidase MnxG investigated by electron paramagnetic resonance spectroscopy.

The multi-copper oxidase (MCO) MnxG from marine Bacillus bacteria plays an essential role in geochemical cycling of manganese by oxidizing Mn(aq) to form manganese oxide minerals at rates that are three to five orders of magnitude faster than abiotic rates. The MCO MnxG protein is isolated as part of a multi-protein complex, denoted as Mnx, which includes one MnxG unit and a hexamer of MnxEF subunit. During the oxidation of Mn(aq) catalyzed by the Mnx protein complex, an enzyme-bound Mn(III) species was trapped recently in the presence of pyrophosphate (PP) and analyzed using parallel-mode electron paramagnetic resonance (EPR) spectroscopy.

Rates of Ligand Exchange around the Bis-Oxalato Complex [NpO (C O ) ] Measured by Using Multinuclear NMR Spectroscopy under Neutral to Semi-Alkaline Conditions.

The kinetics of ligand exchange between the free oxalate ion, C O , and the bis-oxalato Np complex, [NpO (C O ) ] , in aqueous solution are reported by using C and O NMR spectroscopy methods. Rates of exchange were measured in the pH regime of 6.5-9.

Synthesis, characterization and properties of a glycol-coordinated ε-Keggin-type Al chloride.

Herein we present the first example of a glycol-coordinated ε-Keggin Al13 chloride (gl-ε-Al13), which is the first chelated version since discovery of Al13 in 1960. The molecular structure consists of [AlO4Al12(OH)12(OC2H4OH)12]Cl7·H2O units with chelating mono-anionic ethylene glycol units replacing one bridging and one terminal oxygen site.

The Propensity of Uranium-Peroxide Systems to Preserve Nanosized Assemblies.

Understanding the stability fields and decomposition products of various metal- and actinide-oxide nanoclusters is essential for their development into useful materials for industrial processes. Herein, we explore the spontaneous transformation of the sulfate-centered, phosphate functionalized uranyl peroxide nanocluster {UP} to {U} under aqueous ambient conditions using time-resolved small-angle X-ray scattering, Raman, and P NMR spectroscopy. We show that the unusual μ-η:η bridging mode of peroxide between uranyl ions observed in {UP} may lead to its rapid breakdown in solution as evidenced by liberation of phosphate groups that were originally present as an integral part of its cage structure.

Tunable Biogenic Manganese Oxides.

Influence of the conditions for aerobic oxidation of Mn2+(aq) catalysed by the MnxEFG protein complex on the morphology, structure and reactivity of the resulting biogenic manganese oxides (MnO ) is explored. Physical characterisation of MnO includes scanning and transmission electron microscopy, and X-ray photoelectron and K-edge Mn, Fe X-ray absorption spectroscopy. This characterisation reveals that the MnO materials share the structural features of birnessite, yet differ in the degree of structural disorder.

Mn(II) Oxidation by the Multicopper Oxidase Complex Mnx: A Coordinated Two-Stage Mn(II)/(III) and Mn(III)/(IV) Mechanism.

The bacterial manganese oxidase MnxG of the Mnx protein complex is unique among multicopper oxidases (MCOs) in carrying out a two-electron metal oxidation, converting Mn(II) to MnO nanoparticles. The reaction occurs in two stages: Mn(II) → Mn(III) and Mn(III) → MnO. In a companion study , we show that the electron transfer from Mn(II) to the low-potential type 1 Cu of MnxG requires an activation step, likely forming a hydroxide bridge at a dinuclear Mn(II) site.

Mn(II) Oxidation by the Multicopper Oxidase Complex Mnx: A Binuclear Activation Mechanism.

The bacterial protein complex Mnx contains a multicopper oxidase (MCO) MnxG that, unusually, catalyzes the two-electron oxidation of Mn(II) to MnO biomineral, via a Mn(III) intermediate. Although Mn(III)/Mn(II) and Mn(IV)/Mn(III) reduction potentials are expected to be high, we find a low reduction potential, 0.38 V (vs Normal Hydrogen Electrode, pH 7.

Copper Binding Sites in the Manganese-Oxidizing Mnx Protein Complex Investigated by Electron Paramagnetic Resonance Spectroscopy.

Manganese-oxide minerals (MnO) are widely distributed over the Earth's surface, and their geochemical cycling is globally important. A multicopper oxidase (MCO) MnxG protein from marine Bacillus bacteria plays an essential role in producing MnO minerals by oxidizing Mn(aq) at rates that are 3 to 5 orders of magnitude faster than abiotic rates. The MnxG protein is isolated as part of a multiprotein complex denoted as "Mnx" that includes accessory protein subunits MnxE and MnxF, with an estimated stoichiometry of MnxEFG and corresponding molecular weight of ≈211 kDa.

Stable Heterometallic Cluster Ions based on Werner's Hexol.

Large aqueous ions are interesting because they are useful in materials science (for example to generate thin films) but also because they serve as molecular models for the oxide-aqueous mineral interface where spectroscopy is difficult. Here we show that new clusters of the type M[(μ-OH) Co(NH ) ] (NO ) (M=Al, Ga) can be synthesized using Werner's century-old cluster as a substitutable framework. We substituted Group 13 metals into the hexol Co[(μ-OH) Co(NH ) ] ion to make diamagnetic heterometallic ions.

Synthesis of an Aluminum Hydroxide Octamer through a Simple Dissolution Method.

Multimeric oxo-hydroxo Al clusters function as models for common mineral structures and reactions. Cluster research, however, is often slowed by a lack of methods to prepare clusters in pure form and in large amounts. Herein, we report a facile synthesis of the little known cluster Al (OH) (H O) (SO ) (Al ) through a simple dissolution method.

Hierarchy of Pyrophosphate-Functionalized Uranyl Peroxide Nanocluster Synthesis.

Herein, we report a new salt of a pyrophosphate-functionalized uranyl peroxide nanocluster {UPp} (1) exhibiting O molecular symmetry both in the solid and solution. Study of the system yielding 1 across a wide range of pH by single-crystal X-ray diffraction, small-angle X-ray scattering, and a combination of traditional P and diffusion-ordered spectroscopy (DOSY) NMR affords unprecedented insight into the amphoteric chemistry of this uranyl peroxide system. Key results include formation of a rare binary {U}·{UPp} (3) system observed under alkaline conditions, and evidence of acid-promoted decomposition of {UPp} (1) followed by spatial rearrangement and condensation of {U} building blocks into the {UPp} (2) cluster.

Pressure Dependence of Carbonate Exchange with [NpO(CO)] in Aqueous Solutions.

The rates of ligand exchange into the geochemically important [NpO(CO)] aqueous complex are measured as a function of pressure in order to complement existing data on the isostructural [UO(CO)] complex. Experiments are conducted at pH conditions where the rate of exchange is independent of the proton concentration. Unexpectedly, the experiments show a distinct difference in the pressure dependencies of rates of exchange for the uranyl and neptunyl complexes.

Isomerization of Keggin Al Ions Followed by Diffusion Rates.

The solution chemistry of aluminum has long interested scientists due to its relevance to materials chemistry and geochemistry. The dynamic behavior of large aluminum-oxo-hydroxo clusters, specifically [Al O (OH) (H O) ] (Al ), is the focus of this paper. Al NMR, H NMR, and H DOSY techniques were used to follow the isomerization of the ϵ-Al in the presence of glycine and Ca at 90 °C.

Biogenic Manganese-Oxide Mineralization is Enhanced by an Oxidative Priming Mechanism for the Multi-Copper Oxidase, MnxEFG.

In a natural geochemical cycle, manganese-oxide minerals (MnO ) are principally formed through a microbial process, where a putative multicopper oxidase MnxG plays an essential role. Recent success in isolating the approximately 230 kDa, enzymatically active MnxEFG protein complex, has advanced our understanding of biogenic MnO mineralization. Here, the kinetics of MnO formation catalyzed by MnxEFG are examined using a quartz crystal microbalance (QCM), and the first electrochemical characterization of the MnxEFG complex is reported using Fourier transformed alternating current voltammetry.

Titanium-Substituted Polyoxotantalate Clusters Exhibiting Wide pH Stabilities: [Ti2 Ta8 O28 ](8-) and [Ti12 Ta6 O44 ](10.).

Two new substituted polyoxotantalate clusters, [Ti2 Ta8 O28 ](8-) and [Ti12 Ta6 O44 ](10-) , considerably expand the pH range where tantalates persist in aqueous solution. The structures of [Ti2 Ta8 O28 ](8-) and [Ti12 Ta6 O44 ](10-) are reported as tetramethylammonium salts after synthesis at hydrothermal conditions in aqueous solution. These Ti-substituted polyoxotantalate clusters have analogues among recently discovered niobates, but are slightly larger and more persistent in solution.

Characterization of decavanadate and decaniobate solutions by Raman spectroscopy.

The decaniobate ion, (Nb10 = [Nb10O28](6-)) being isoelectronic and isostructural with the decavanadate ion (V10 = [V10O28](6-)), but chemically and electrochemically more inert, has been useful in advancing the understanding of V10 toxicology and pharmacological activities. In the present study, the solution chemistry of Nb10 and V10 between pH 4 and 12 is studied by Raman spectroscopy. The Raman spectra of V10 show that this vanadate species dominates up to pH 6.

Structure and Reactivity of X-ray Amorphous Uranyl Peroxide, U2O7.

Recent accidents resulting in worker injury and radioactive contamination occurred due to pressurization of uranium yellowcake drums produced in the western U.S.A.

(2) H and (139) La NMR Spectroscopy in Aqueous Solutions at Geochemical Pressures.

Nuclear spin relaxation rates of (2) H and (139) La in LaCl3 +(2) H2 O and La(ClO4 )3 +(2) H2 O solutions were determined as a function of pressure in order to demonstrate a new NMR probe designed for solution spectroscopy at geochemical pressures. The (2) H longitudinal relaxation rates (T1 ) vary linearly to 1.6 GPa, consistent with previous work at lower pressures.

Multicopper manganese oxidase accessory proteins bind Cu and heme.

Multicopper oxidases (MCOs) catalyze the oxidation of a diverse group of metal ions and organic substrates by successive single-electron transfers to O2 via four bound Cu ions. MnxG, which catalyzes MnO2 mineralization by oxidizing both Mn(II) and Mn(III), is unique among multicopper oxidases in that it carries out two energetically distinct electron transfers and is tightly bound to accessory proteins. There are two of these, MnxE and MnxF, both approximately 12kDa.

Mn(II) Binding and Subsequent Oxidation by the Multicopper Oxidase MnxG Investigated by Electron Paramagnetic Resonance Spectroscopy.

The dynamics of manganese solid formation (as MnOx) by the multicopper oxidase (MCO)-containing Mnx protein complex were examined by electron paramagnetic resonance (EPR) spectroscopy. Continuous-wave (CW) EPR spectra of samples of Mnx, prepared in atmosphere and then reacted with Mn(II) for times ranging from 7 to 600 s, indicate rapid oxidation of the substrate manganese (with two-phase pseudo-first-order kinetics modeled using rate coefficients of: k(1obs) = 0.205 ± 0.