Structure of the active site of sulfite oxidase. X-ray absorption spectroscopy of the molybdenum(IV), molybdenum(V), and molybdenum(VI) oxidation states

Biochemistry ◽  
1989 ◽  
Vol 28 (12) ◽  
pp. 5075-5080 ◽  
Author(s):  
Graham N. George ◽  
Cary A. Kipke ◽  
Roger C. Prince ◽  
Roger A. Sunde ◽  
John H. Enemark ◽  
...  

2018 ◽  
Vol 6 (4) ◽  
pp. 875-882 ◽  
Author(s):  
A. Fraile Rodríguez ◽  
C. Moya ◽  
M. Escoda-Torroella ◽  
A. Romero ◽  
A. Labarta ◽  
...  

Single-particle X-ray absorption spectroscopy reveals that the oxidation state and cation distribution of individual magnetite nanoparticles may be largely heterogeneous even when the macroscopic structural and magnetic response of the ensembles is uniform.



2014 ◽  
Vol 43 (37) ◽  
pp. 13852 ◽  
Author(s):  
Jeremy P. Krogman ◽  
James R. Gallagher ◽  
Guanghui Zhang ◽  
Adam S. Hock ◽  
Jeffrey T. Miller ◽  
...  


Biochemistry ◽  
2009 ◽  
Vol 48 (22) ◽  
pp. 5042-5049 ◽  
Author(s):  
Sven Stripp ◽  
Oliver Sanganas ◽  
Thomas Happe ◽  
Michael Haumann




Biochemistry ◽  
2003 ◽  
Vol 42 (1) ◽  
pp. 222-230 ◽  
Author(s):  
Manuel Gnida ◽  
Reinhold Ferner ◽  
Lothar Gremer ◽  
Ortwin Meyer ◽  
Wolfram Meyer-Klaucke


1997 ◽  
Vol 76 (4) ◽  
Author(s):  
C. Den Auwer ◽  
C. Madie ◽  
J. C. Berthet ◽  
M. Ephritikhine ◽  
J. J. Rehr ◽  
...  


1989 ◽  
Vol 258 (3) ◽  
pp. 733-737 ◽  
Author(s):  
J M Arber ◽  
B R Dobson ◽  
R R Eady ◽  
S S Hasnain ◽  
C D Garner ◽  
...  

Vanadium K-edge X-ray-absorption spectra were collected for samples of thionine-oxidized, super-reduced (during enzyme turnover) and dithionite-reduced VFe-protein of the vanadium nitrogenase of Azotobacter chroococcum (Acl*). Both the e.x.a.f.s and the x.a.n.e.s. (X-ray-absorption near-edge structure) are consistent with the vanadium being present as part of a VFeS cluster; the environment of the vanadium is not changed significantly in different oxidation states of the protein. The vanadium atom is bound to three oxygen (or nitrogen), three sulphur and three iron atoms at 0.215(3), 0.231(3) and 0.275(3) nm respectively.



2021 ◽  
Vol 28 (2) ◽  
pp. 455-460
Author(s):  
Suchinda Sattayaporn ◽  
Somboonsup Rodporn ◽  
Pinit Kidkhunthod ◽  
Narong Chanlek ◽  
Chutarat Yonchai ◽  
...  

A well designed compact furnace has been designed for in situ X-ray absorption spectroscopy (XAS). It enables various heat ramps from 300 K to 1473 K. The furnace consists of heaters, a quartz tube, a circulated refrigerator and a power controller. It can generate ohmic heating via an induction process with tantalum filaments. The maximum heating rate exceeds 20 K min−1. A quartz tube with gas feedthroughs allows the mixing of gases and adjustment of the flow rate. The use of this compact furnace allows in situ XAS investigations to be carried out in transmission or fluorescence modes under controlled temperature and atmosphere. Moreover, the furnace is compact, light and well compatible to XAS. The furnace was used to study cationic oxidation states in Pr6O11 and NiO compounds under elevated temperature and reduced atmosphere using the in situ X-ray absorption near-edge structure (XANES) technique at beamline 5.2 SUT-NANOTEC-SLRI of the Synchrotron Light Research Institute, Thailand. At room temperature, Pr6O11 contains a mixture of Pr3+ and Pr4+ cations, resulting in an average oxidation state of +3.67. In situ XANES spectra of Pr (L 3-edge) show that the oxidation state of Pr4+ cations was totally reduced to +3.00 at 1273 K under H2 atmosphere. Considering NiO, Ni2+ species were present under ambient conditions. At 573 K, the reduction process of Ni2+ occurred. The Ni0/Ni2+ ratio increased linearly with respect to the heating temperature. Finally, the reduction process of Ni2+ was completely finished at 770 K.



2020 ◽  
Author(s):  
Teresa Zahoransky ◽  
Christian Mikutta

<p>Being one of Earth´s most redox-active elements, manganese participates in a great variety of environmental processes and is recognized as a key player controlling carbon turnover and oxidative transformation of organic and inorganic pollutants in soils. Moreover, Mn(III), Mn(IV) or mixed-valence Mn(III/IV) oxides and (oxy)hydroxides are highly effective sorbents for metal pollutants and nutrients in soils. Chemical reactivity, mobility, and bioavailability of Mn depend crucially on its speciation (chemical form). Yet, speciation studies on soil Mn are scarce. Therefore, we employed Mn K-edge (6,539 eV) X-ray absorption spectroscopy (XAS) to determine the oxidation states and local coordination environment (<5 Å) of Mn in oxic bulk soils (Cambisols, Luvisols, Stagnosol) from various field sites in Germany. Our XAS analyses cover 23 soil L, O, A, B, and C horizons exhibiting total Mn concentrations of between 200 and 2,300 mg/kg. For comparison, we also analyze a suite of 31 Mn reference compounds, including Mn carbonate, phosphate, oxides and (oxy)hydroxides, silicates, organic Mn compounds as well as clay and hydroxide minerals with adsorbed Mn(II). X-ray absorption near-edge structure (XANES) spectra are evaluated for the oxidation states of soil Mn using linear combination fit (LCF) analysis. In addition, the average local coordination environment of Mn in the soil samples is assessed by shell-fitting of extended X-ray absorption fine structure (EXAFS) spectra. Based on our XAS results, we will test the following hypotheses: (1) Soil L/O horizons comprise predominantly organically complexed Mn(II) and Mn(III), dominated by the former Mn species; (2) soil A horizons are dominated by Mn(III/IV) in Mn(III/IV)-oxide structures owing to high microbial activity, release of Mn(II) from primary silicates and/or plant residues, and its subsequent (a)biotic oxidation and precipitation as Mn(III/IV) oxides; (3) soil B horizons of different genesis differ in their bulk Mn speciation; Bt horizons of Luvisols are dominated by Mn(II) associated with phyllosilicates, whereas the Stagnosol Bg horizon is dominated by layer-type Mn(III/IV) oxides. In summary, our study will provide first comprehensive data on bulk Mn speciation in three major European soil types. This knowledge is a prerequisite for a better understanding of the biogeochemical Mn cycle in soils.</p>



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