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81.
Complex formation between heavy metal ions and glutathione (GSH) is considered as the initial step in many detoxification processes in living organisms. In this study the structure and coordination between the cadmium(II) ion and GSH were investigated in aqueous solutions (pH 7.5 and 11.0) and in the solid state, using a combination of spectroscopic techniques. The similarity of the Cd K-edge and L3-edge X-ray absorption spectra of the solid compound [Cd(GS)(GSH)]ClO4·3H2O, precipitating at pH 3.0, with the previously studied cysteine compound {Cd(HCys)2·H2O}2·H3O+·ClO4 ? corresponds to Cd(S–GS)3O (dominating) and Cd(S–GS)4 four-coordination within oligomeric complexes with mean bond distances of 2.51 ± 0.02 Å for Cd–S and 2.24 ± 0.04 Å for Cd–O. For cadmium(II) solutions (C Cd(II) ~ 0.05 M) at pH 7.5 with moderate excess of GSH (C GSH/C Cd(II) = 3.0–5.0), a mix of Cd(S–GS)3O (dominating) and Cd(S–GS)4 species is consistent with the broad 113Cd NMR resonances in the range 632–658 ppm. In alkaline solutions (pH 11.0 and C GSH/C Cd(II) = 2.0 or 3.0), two distinct peaks at 322 and 674 ppm are obtained. The first peak indicates six-coordinated mononuclear and dinuclear complexes with CdS2N2(N/O)2 and CdSN3O2 coordination in fast exchange, whereas the second corresponds to Cd(S–GS)4 sites. At high ligand excess the tetrathiolate complex, Cd(S–GS)4, characterized by a sharp δ(113Cd) NMR signal at 677 ppm, predominates. The average Cd–S distance, obtained from the X-ray absorption spectra, varied within a narrow range, 2.49–2.53 Å, for all solutions (pH 7.5 and 11.0) regardless of the coordination geometry. 相似文献
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Interfacial enzymology of parvovirus phospholipases A2 总被引:1,自引:0,他引:1
Canaan S Zádori Z Ghomashchi F Bollinger J Sadilek M Moreau ME Tijssen P Gelb MH 《The Journal of biological chemistry》2004,279(15):14502-14508
The capsid of parvoviruses proteins were recently shown to contain secreted phospholipase A(2) (sPLA(2))-like activity that is required during host cell entry. Parvoviral PLA(2) domains have little sequence identity with sPLA(2)s and lack disulfide bonds. In the present study, after bacterial expression and purification, the biochemical characterizations of these first PLA(2)s identified in viruses have been investigated, and a comparison has been made with other known PLA(2)s. The specific activities of three viral PLA(2)s differed by 3 orders of magnitude, with porcine parvovirus PLA(2) displaying a specific activity similar to that of the most active sPLA(2)s (e.g. human group IIA) and the human AAV2 and B19 parvoviral enzymes displaying approximately 10(3) lower specific activities (similar to human sPLA(2) groups IIE and XIIA). These differences were not caused by weaker Ca(2+) or interfacial binding. The specific activities of the viral PLA(2)s on zwitterionic or anionic phospholipid vesicles were comparable. The viral PLA(2)s did not display a preference for unsaturated versus saturated sn-2 fatty acyl chains and hydrolyzed all major classes of glycero-phospholipids except phosphatidylinositol. Incubation of mammalian cells with porcine parvovirus PLA(2) led to the release of arachidonic acid into the culture medium. Interestingly, among nine previously known sPLA(2) inhibitors, only a subset showed inhibition of the viral PLA(2)s and with weak potency, indicating that the active sites of these new enzymes are structurally distinct from those of sPLA(2)s. Based on these distinct enzymatic and structural properties, we propose to classify the parvovirus PLA(2)s within the PLA(2) superfamily as group XIII enzymes. 相似文献
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BACKGROUNDS: Until today, human stomach is the only recognized habitat of Helicobacter pylori. However, recruitment of DNA-based methods has made possible the detection of H. pylori in water and oral cavity, thus suggesting fecal-oral and oral-oral routes for transmission of H. pylori, respectively. In this study, yeast has been proposed as a common vector for transmission of H. pylori. Thus designed primers were recruited to target 16S rDNA and cagA genes in the oral yeasts by PCR. MATERIALS AND METHODS: Eighteen yeasts were examined microscopically for the presence of bacterial-like bodies. DNAs were extracted from oral yeasts using phenol-chloroform method. Amplification conditions were optimized as 33 cycles and annealing temperatures of 63 degrees C for 16S rDNA and 51 degrees C and 52 degrees C for cagA gene which was targeted in two steps. DNAs of H. pylori and Saccharomyces cerevisiae were used as controls. Polymerase chain reaction (PCR) products of two genes from one yeast and from H. pylori were cloned in pCAP and subsequently subcloned in pSK+ and were sequenced. RESULTS: Bacterial-like bodies were observed in all oral yeasts. The amplified products of 16S rDNA from all oral yeasts were homologous in size with those of H. pylori. Fifteen out of eighteen (83%) yeasts contained cagA gene, homologous to H. pylori. CagA was not amplified from three yeasts and S. cerevisiae. Analysis of the sequenced products of 16S rDNA and cagA from one oral yeast showed 98% homology with those of H. pylori. CONCLUSIONS: The presence of H. pylori inside the yeast was indicated by light microscopy and PCR. It appears that yeasts, which are abundant in nature and thrive the mucosal surfaces of human, might serve as reservoirs and vehicles of H. pylori. 相似文献
85.
Tucker DE Stewart A Nallan L Bendale P Ghomashchi F Gelb MH Leslie CC 《Journal of lipid research》2005,46(10):2122-2133
Cytosolic phospholipase A(2)gamma (cPLA(2)gamma) is a member of the group IV family of intracellular phospholipase A(2) enzymes, but unlike the well-studied cPLA(2)alpha, it is constitutively bound to membrane and is calcium independent. cPLA(2)gamma contains a C-terminal CaaX sequence and is radiolabeled by mevalonic acid when expressed in cPLA(2)alpha-deficient immortalized lung fibroblasts (IMLF(-/-)). The radiolabel associated with cPLA(2)gamma was identified as the farnesyl group. The protein farnesyltransferase inhibitor BMS-214662 prevented the incorporation of [(3)H]mevalonic acid into cPLA(2)gamma and partially suppressed serum-stimulated arachidonic acid release from IMLF(-/-) and undifferentiated human skeletal muscle (SkMc) cells overexpressing cPLA(2)gamma, but not from cells overexpressing cPLA(2)alpha. However, BMS-214662 did not alter the amount of cPLA(2)gamma associated with membrane. These results were consistent in COS cells expressing the C538S cPLA(2)gamma prenylation mutant. cPLA(2)gamma also contains a classic myristoylation site and several potential palmitoylation sites and was found to be acylated with oleic and palmitic acids but not myristoylated. Immunofluorescence microscopy revealed that cPLA(2)gamma is associated with mitochondria in IMLF(-/-), SkMc cells, and COS cells. 相似文献
86.
Farideh Attar Valiollah Mozaffarian Mansour Mirtadzadini 《Nordic Journal of Botany》2016,34(2):174-177
Cousinia brevicaulis is described and illustrated as a new species from eastern Iran. This species belongs to the C. sect. Lasiandra Bunge as defined by hairy anther tube, yellow, pale yellow or rarely milky flowers, monocarpic growth form and corymbose branching of stem. It is easily distinguished from other species of the section by its very short‐stemmed habit. The new species is distributed in the same region as other species of C. sect. Lasiandra. 相似文献
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Shakeri Mahsa Zakeri Farideh Changizi Vahid Rajabpour Mohammad Reza Farshidpour Mohammad Reza 《Radiation and environmental biophysics》2019,58(2):247-255
Radiation and Environmental Biophysics - Different types of DNA damages caused by ionizing radiation may enhance the cancer risk in exposed individuals. Inherited variations in DNA repair genes... 相似文献
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Farideh Attar Atefeh Keshvari Ahmad Ghahreman Shahin Zarre Fatemeh Aghabeigi 《Flora》2007,202(2):169-175
Seed micromorphology in 22 species, capsule surface in 28 species and capsule hairs in 20 species of genus Verbascum distributed in Iran were studied using scanning electron microscopy. The seed surface is ridged or alveolate among the studied species. Depth and density of the alveoli or ridges, size of polygonal cells along with arrangement of vesicles on the walls separating the polygonal cells on the seed surface seem to be species-specific in Verbascum. The capsule surface is striate, distinctly or indistinctly, or even smooth in Verbascum. The capsules are rarely glabrous (in V. orientale and V. intricatum), densely covered by branched hairs, or loosely by glandular hairs, depending on species. From the results of this study it is obvious that no correlation exists between the studied species concerning the micromorphological aspects studied here. 相似文献
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Azadeh Azizi Bijan Ranjbar Tahereh Tohidi Moghadam Zeinab Bagheri 《Plasmonics (Norwell, Mass.)》2014,9(2):273-281
Plasmonic circular dichroism (CD) responses of hybrid nanostructures containing noble metal nanoparticles and chiral molecules have received increasing interest with various applications in nanophotonics. Chiral biomolecules show strong CD signals typically found in the ultraviolet region, whereas, in the visible range, they produce a weak signal. Strengthening the CD signal in the visible region is of high importance, which could be achieved through fabrication of novel hybrid nanostructures. Herein, gold nanoparticles (GNPs) have been assembled via DNA linker to investigate the possibility of enhancing plasmonic CD signal in the visible range. DNA-linked assemblies with pre- and postannealed conditions were characterized by ultraviolet–visible spectroscopy, dynamic light scattering (DLS), and CD spectropolarimetry. In the presence of DNA linker with sticky ends, the aggregation phenomenon was traced by red shifts of surface plasmon resonance of nanoparticles. Time-dependent hybridization of single-stranded “sticky ends” with DNA-conjugated GNPs and increased probability of hydrogen bond formation lead to enhancement of CD signals in the ultraviolet region. Complexation of biomolecule and nanoparticle assemblies induced enhanced CD signals in the visible range, which was noticed both before and after purification. DLS characterization of the assemblies also confirmed the difference in the size of aggregates, which could be controlled by the linker molecules. This investigation encourages possibility of utilizing plasmonic CD technique as a tool for tracing fabricated nanostructure assemblies with enhanced characterization possibility. 相似文献