scholarly journals Redox Properties of Wild-Type, Cys69Ala, and Cys69Ser Azotobacter Vinelandii Flavodoxin II as Measured by Cyclic Voltammetry and EPR Spectroscopy

1996 ◽  
Vol 235 (1-2) ◽  
pp. 167-172 ◽  
Author(s):  
Elles Steensma ◽  
Hendrik A. Heering ◽  
Wilfred R. Hagen ◽  
Carlo P. M. Mierlo
1993 ◽  
Vol 212 (1) ◽  
pp. 51-61 ◽  
Author(s):  
Antonio J. PIERIK ◽  
Hans WASSINK ◽  
Huub HAAKER ◽  
Wilfred R. HAGEN

1972 ◽  
Vol 27 (10) ◽  
pp. 1131-1136 ◽  
Author(s):  
P. Barz ◽  
H. P. Fritz

1,2-Dimethylhydrazine co-ordinates to numerous metal cations. The structures of the complexes of Cr, Mn, Co, Ni, Cu, Zn, Cd, Hg and Pt are discussed and the complexing abilities of the 1,2-dimethylhydrazine molecule are determined on the basis of the ligand field spectra of the nickel and the chromium derivative.The results of polarography, cyclic voltammetry and photoelectron spectroscopy yield evidence on the redox properties of the neutral molecule. By means of EPR spectroscopy the nature of the radical products obtained by irradiation of 1,2-dimethylhydrazine, especially of the radical cation, is determined.


2002 ◽  
Vol 413 (1-2) ◽  
pp. 218-223 ◽  
Author(s):  
Hellas C.M Yau ◽  
Hing Leung Chan ◽  
Sen-fang Sui ◽  
Mengsu Yang

2008 ◽  
Vol 587-588 ◽  
pp. 109-113
Author(s):  
C. Teixeira ◽  
P. Parpot ◽  
Isabel Neves ◽  
António Maurício C. Fonseca

CoPAN complex has been entrapped in the supercages of Y zeolite and the redox properties of this zeolite-encapsulated complex were investigated by cyclic voltammetry with a new method for the preparation of carbon toray-zeolite-modified electrode. Formation of the CoPAN complex was ascertained by surface analysis (SEM, XRD), chemical analysis (CA), spectroscopy methods (FTIR and UV/vis) and cyclic voltammetry in aqueous medium with zeolite-modified electrodes. The cyclic voltammetry studies obtained with a zeolite-modified electrode shows evidence for electroactivity restricted to boundary associated CoPAN complex.


2013 ◽  
Vol 68 (5-6) ◽  
pp. 458-466 ◽  
Author(s):  
Iris Klawitter ◽  
Steffen Meyer ◽  
Serhiy Demeshko ◽  
Franc Meyer

Two methylene-bridged bis(imidazolium) salts [H4L1](PF6)2 and [H4L2](PF6)2 with appended amide groups have been synthesized which, after deprotonation, may serve as potentially tetradentate ligands providing two bis(imidazole-2-ylidene) and two amide donors. Using [H4L1](PF6)2, a square-planar nickel(II) complex [NiL1] and a six-coordinate bis(ligand) iron(II) complex [Fe(HL1)2] have been isolated and structurally characterized. Their low-spin states have been confirmed spectroscopically, and their redox properties have been studied by cyclic voltammetry. Oxidations are metal-centered to give NiIII and FeIII species, respectively


2014 ◽  
Vol 67 (3) ◽  
pp. 398 ◽  
Author(s):  
Peter Comba ◽  
Hubert Wadepohl ◽  
Arkadius Waleska

The solution coordination chemistry of iron complexes with the pentadentate bispidine ligands L1, L2, and L3 (dimethyl 9-oxo-2,4-di(pyridin-2-yl)-3,7-diazabicyclo[3.3.1]nonane-1,5-dicarboxylate derivatives) was examined. While in acetonitrile, (L1,2)FeII/III species have a preference for Cl– as co-ligand. The corresponding aqua and hydroxido complexes also prevail in the presence of Cl– in aqueous solution. The observed FeII/III potentials in water (cyclic voltammetry) and potentials of (L1–3)FeIV=O (buffered and unbuffered aqueous solutions) are strikingly similar, i.e. the latter are assigned to (L1–3)FeII/III potentials, and published potentials of FeIV=O complexes with other ligands with uncharged amine-pyridine donors, obtained by cyclic voltammetry, have to be considered with caution.


1999 ◽  
Vol 181 (23) ◽  
pp. 7356-7362 ◽  
Author(s):  
Brett Brewin ◽  
Paul Woodley ◽  
Martin Drummond

ABSTRACT In Azotobacter vinelandii, nitrogen fixation is regulated at the transcriptional level by an unusual two-component system encoded by nifLA. Certain mutations innifL result in the bacterium releasing large quantities of ammonium into the medium, and earlier work suggested that this occurs by a mechanism that does not involve NifA, the activator ofnif gene transcription. We have investigated a number of possible alternative mechanisms and find no evidence for their involvement in ammonium release. Enhancement of NifA-mediated transcription, on the other hand, by either elimination ofnifL or overexpression of nifA, resulted in ammonium release, correlating with enhanced levels of nifHmRNA, raised levels of nitrogenase and acetylene-reducing activity, and increased concentrations of intracellular ammonium. Up to 35 mM ammonium can accumulate in the medium. Where measured, intracellular levels exceeded extracellular levels, indicating that rather than being actively transported, ammonium is lost from the cell passively, possibly by reversal of an NH4 + uptake system. The data also indicate that in the wild type the bulk of NifA is inactivated by NifL during steady-state growth on dinitrogen.


2015 ◽  
Vol 81 (21) ◽  
pp. 7484-7495 ◽  
Author(s):  
Pauline Woan Ying Liew ◽  
Bor Chyan Jong ◽  
Nazalan Najimudin

ABSTRACTA proteomic analysis of a soil-dwelling, plant growth-promotingAzotobacter vinelandiistrain showed the presence of a protein encoded by the hypotheticalAvin_16040gene when the bacterial cells were attached to theOryza sativaroot surface. AnAvin_16040deletion mutant demonstrated reduced cellular adherence to the root surface, surface hydrophobicity, and biofilm formation compared to those of the wild type. By atomic force microscopy (AFM) analysis of the cell surface topography, the deletion mutant displayed a cell surface architectural pattern that was different from that of the wild type.Escherichia colitransformed with the wild-typeAvin_16040gene displayed on its cell surface organized motifs which looked like the S-layer monomers ofA. vinelandii. The recombinantE. colialso demonstrated enhanced adhesion to the root surface.


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