Enantioselective Manganese-Porphyrin-Catalyzed Epoxidation and C–H Hydroxylation with Hydrogen Peroxide in Water/Methanol Solutions

2012 ◽  
Vol 51 (10) ◽  
pp. 5850-5856 ◽  
Author(s):  
Hassan Srour ◽  
Paul Le Maux ◽  
Gerard Simonneaux
Keyword(s):  
Hydrogen Peroxide ◽  
Manganese Porphyrin ◽  
Methanol Solutions

scholarly journals Biomimetic oxidation of carbamazepine with hydrogen peroxide catalyzed by a manganese porphyrin

Química Nova ◽  
2012 ◽  
Vol 35 (7) ◽  
pp. 1477-1481 ◽  
Author(s):  
Cláudia M. B. Neves ◽  
Mário M. Q. Simões ◽  
Fernando M. J. Domingues ◽  
M. Graça P. M. S. Neves ◽  
José A. S. Cavaleiro
Keyword(s):  
Hydrogen Peroxide ◽  
Manganese Porphyrin ◽  
Biomimetic Oxidation

Hydrogen peroxide as oxidant in bio-mimetic catalysis by manganese porphyrin: Theoretical DFT studies

2013 ◽  
Vol 91 (7) ◽  
pp. 642-647 ◽  
Author(s):  
Agnieszka Drzewiecka-Matuszek ◽  
Dorota Rutkowska-Zbik ◽  
Malgorzata Witko
Keyword(s):  
Hydrogen Peroxide ◽  
Density Functional ◽  
Active Oxygen Species ◽  
Dft Method ◽  
Manganese Porphyrin ◽  
Functional Theory ◽  
Interatomic Distances ◽  
The Density Functional Theory ◽  
Spin Populations ◽  
Spin Densities

The aim of this study is to elucidate the geometry and electronic structure of various adducts that may be formed between manganese(III) (Mn(III)) porphyrin and hydrogen peroxide. Hydrogen peroxide may interact with Mn(III) porphyrin either as H2O2 or, after dissociation, as OOH–. In the former, it may decompose into two hydroxo groups, which acquire OH– character or an oxo group (=O) and a water molecule. Therefore, the following systems are considered: MnP(H2O2)+, MnP(H2O2)(OH), MnP(OH)3, [Formula: see text], MnPO+, MnPO(OH), MnP(OOH), MnP(OOH)(OH)–, and the possible transformations between them are taken into account. The reported studies are performed within the Density Functional Theory (DFT) method with the GGA-BP functional. The geometry and electronic structures of the structures found along the studied reaction pathways are discussed in terms of interatomic distances, valence angles, Mulliken charges, and spin densities. It was found that different active oxygen species may be formed in the reaction between Mn(III) porphyrin and hydrogen peroxide. As manganese is a transition metal, numerous possible spin states for each of the studied structures are found, where the relative energies of different multiplicities depend strongly on the ligands present in the complex. In view of the catalytic properties, all oxygen-containing ligands are negatively charged, which results in their behaviour as nucleophiles towards hydrocarbons. Finally, the analysis of charge and spin populations on different parts of the studied systems indicate the porphyrin ligand as active in charge transfer processes.

Peroxidase Localization in Hartmanella Trophozoites

1971 ◽  
Vol 29 ◽  
pp. 346-347 ◽  
Author(s):  
George E. Childs ◽  
Joseph H. Miller
Keyword(s):  
Hydrogen Peroxide ◽  
Ultrastructural Localization ◽  
Pathogenic Strain ◽  
Oxidative Enzymes ◽  
Differential Centrifugation ◽  
Electron Microscopic ◽  
Microscopic Studies ◽  
The Subject ◽  
Axenic Cultures

Biochemical and differential centrifugation studies have demonstrated that the oxidative enzymes of Acanthamoeba sp. are localized in mitochondria and peroxisomes (microbodies). Although hartmanellid amoebae have been the subject of several electron microscopic studies, peroxisomes have not been described from these organisms or other protozoa. Cytochemical tests employing diaminobenzidine-tetra HCl (DAB) and hydrogen peroxide were used for the ultrastructural localization of peroxidases of trophozoites of Hartmanella sp. (A-l, Culbertson), a pathogenic strain grown in axenic cultures of trypticase soy broth.

Fluorescent proteins for in vivo imaging, where's the biliverdin?

2020 ◽  
Vol 48 (6) ◽  
pp. 2657-2667
Author(s):  
Felipe Montecinos-Franjola ◽  
John Y. Lin ◽  
Erik A. Rodriguez
Keyword(s):  
Hydrogen Peroxide ◽  
In Vivo Imaging ◽  
Near Infrared ◽  
Fluorescent Protein ◽  
Fluorescent Proteins ◽  
Fluorescent Imaging ◽  
Infrared Light ◽  
Red Fluorescent Protein ◽  
Color Palette

Noninvasive fluorescent imaging requires far-red and near-infrared fluorescent proteins for deeper imaging. Near-infrared light penetrates biological tissue with blood vessels due to low absorbance, scattering, and reflection of light and has a greater signal-to-noise due to less autofluorescence. Far-red and near-infrared fluorescent proteins absorb light >600 nm to expand the color palette for imaging multiple biosensors and noninvasive in vivo imaging. The ideal fluorescent proteins are bright, photobleach minimally, express well in the desired cells, do not oligomerize, and generate or incorporate exogenous fluorophores efficiently. Coral-derived red fluorescent proteins require oxygen for fluorophore formation and release two hydrogen peroxide molecules. New fluorescent proteins based on phytochrome and phycobiliproteins use biliverdin IXα as fluorophores, do not require oxygen for maturation to image anaerobic organisms and tumor core, and do not generate hydrogen peroxide. The small Ultra-Red Fluorescent Protein (smURFP) was evolved from a cyanobacterial phycobiliprotein to covalently attach biliverdin as an exogenous fluorophore. The small Ultra-Red Fluorescent Protein is biophysically as bright as the enhanced green fluorescent protein, is exceptionally photostable, used for biosensor development, and visible in living mice. Novel applications of smURFP include in vitro protein diagnostics with attomolar (10−18 M) sensitivity, encapsulation in viral particles, and fluorescent protein nanoparticles. However, the availability of biliverdin limits the fluorescence of biliverdin-attaching fluorescent proteins; hence, extra biliverdin is needed to enhance brightness. New methods for improved biliverdin bioavailability are necessary to develop improved bright far-red and near-infrared fluorescent proteins for noninvasive imaging in vivo.

Protective effect of chitooligosaccharides on hydrogen peroxide-induced PC-12 cells death by inhibition of oxidative damage

2010 ◽  
Vol 34 (8) ◽  
pp. S27-S27
Author(s):  
Xueling Dai ◽  
Ping Chang ◽  
Ke Xu ◽  
Changjun Lin ◽  
Hanchang Huang ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Oxidative Damage ◽  
Protective Effect ◽  
Pc 12 Cells ◽  
Cells Death

Signal-regulated oxidation of proteins via MICAL

2020 ◽  
Vol 48 (2) ◽  
pp. 613-620
Author(s):  
Clara Ortegón Salas ◽  
Katharina Schneider ◽  
Christopher Horst Lillig ◽  
Manuela Gellert
Keyword(s):  
Signal Transduction ◽  
Hydrogen Peroxide ◽  
Cell Death ◽  
Redox Regulation ◽  
Signal Transduction Pathways ◽  
Cellular Functions ◽  
Intracellular Signals ◽  
Amino Acid Side Chains ◽  
Specific Receptors ◽  
Sulfur Containing

Processing of and responding to various signals is an essential cellular function that influences survival, homeostasis, development, and cell death. Extra- or intracellular signals are perceived via specific receptors and transduced in a particular signalling pathway that results in a precise response. Reversible post-translational redox modifications of cysteinyl and methionyl residues have been characterised in countless signal transduction pathways. Due to the low reactivity of most sulfur-containing amino acid side chains with hydrogen peroxide, for instance, and also to ensure specificity, redox signalling requires catalysis, just like phosphorylation signalling requires kinases and phosphatases. While reducing enzymes of both cysteinyl- and methionyl-derivates have been characterised in great detail before, the discovery and characterisation of MICAL proteins evinced the first examples of specific oxidases in signal transduction. This article provides an overview of the functions of MICAL proteins in the redox regulation of cellular functions.

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