Residual Amount (residual + amount)

Distribution by Scientific Domains


Selected Abstracts


Biogenesis of the yeast frataxin homolog Yfh1p

FEBS JOURNAL, Issue 11 2000
Tim44-dependent transfer to mtHsp70 facilitates folding of newly imported proteins in mitochondria
Tim44 is an essential component of the mitochondrial inner membrane protein import machinery. In this study we asked if Tim44 is of relevance in intramitochondrial protein folding. We investigated the role of Tim44 in the biogenesis of the authentic mitochondrial protein Yfh1p, the yeast homolog of mammalian frataxin, which was recently implicated in Friedreich ataxia. After inactivation of Tim44, binding of mitochondrial heat shock protein (mtHsp)70 to translocating Yfh1p and subsequent folding to the native state was nearly completely blocked. Residual amounts of imported Yfh1p showed an increased tendency to aggregate. To further characterize the functions of Tim44 in the matrix, we imported dihydrofolate reductase (DHFR) as a model protein. Depletion of Tim44 allowed import of DHFR, although folding of the newly imported DHFR was delayed. Moreover, the depletion of Tim44 caused a strongly reduced binding of mtHsp70 and Mge1 to the translocating polypeptide. Subsequent dissociation of mtHsp70 from imported DHFR was delayed, indicating that mtHsp70,substrate complexes formed independently of Tim44 differ from the complexes that form under the control of Tim44. We conclude that Tim44 not only plays a role in protein translocation but also in the pathways of mitochondrial protein folding. [source]


Effects of different rates and timing of application of nitrogen as slurry and mineral fertilizer on yield of herbage and nitrate-leaching potential of a maize/Italian ryegrass cropping system in north-west Portugal

GRASS & FORAGE SCIENCE, Issue 1 2009
H. Trindade
Abstract Efficient use of cattle-slurry to avoid nitrogen (N) leaching and other losses is important in designing intensive dairy systems to minimize pollution of air and water. The response in dry-matter (DM) yield of herbage and nitrate-leaching potential to different rates and timing of application of N as cattle slurry and/or mineral fertilizer in a double-cropping system producing maize (Zea mays L.) silage and Italian ryegrass (Lolium multiflorum Lam.) was investigated in north-west Portugal. Nine treatments with different rates and combinations of cattle slurry, and with or without mineral-N fertilizer, applied at sowing and as a top-dressing to both crops, were tested and measurements were made of DM yield of herbage, N concentration of herbage, uptake of N by herbage and amounts of residual soil nitrate-N to a depth of 1 m, in a 3-year experiment. Regression analysis showed that the application of 150 and 100 kg of available N ha,1 to maize and Italian ryegrass, respectively, resulted in 0·95 of maximum DM yields of herbage and 0·90 of maximum N uptake by herbage. Residual amounts of nitrate-N in soil after maize ranged from 48 to 278 kg N ha,1 with an exponential increase in response to the amount of N applied; there were higher values of nitrate-leaching potential when mineral-N fertilizer was applied. The results suggest that it is possible in highly productive maize/Italian ryegrass systems to obtain high DM yields of herbage for maize silage and Italian ryegrass herbage with minimal leaching losses by using slurry exclusively at annual rates of up to 250 kg available N ha,1 (equivalent to 480 kg total N ha,1) in three applications. [source]


The amount of newly formed bone in sinus grafting procedures depends on tissue depth as well as the type and residual amount of the grafted material

JOURNAL OF CLINICAL PERIODONTOLOGY, Issue 2 2005
Zvi Artzi
Abstract Objectives: Bone replacement substitutes are almost unavoidable in augmentation procedures such as sinus grafting. The objective of the present study was to evaluate the osteoconductive capability of two different scaffold fillers in inducing newly formed bone in this procedure. Material and Methods: Sinus floor augmentation and implant placement were carried out bilaterally in 12 patients. Bovine bone mineral (BBM) was grafted on one side and , -tricalcium phosphate (, -TCP) on the contralateral side. Both were mixed (1:1 ratio) with autogenous cortical bone chips harvested from the mandible by a scraper. Hard tissue specimen cores were retrieved from the augmented sites (at the previous window area) at 12 months. Decalcified sections were stained with haematoxylin,eosin and the fraction area of new bone and filler particles was measured. In addition to the effect of the filler on new bone formation, the latter was tested to determine whether it correlated with the tissue depth and residual amount of the grafted material. Results: Bone area fraction increased significantly from peripheral to deeper areas at both grafted sites in all cores: from 26.0% to 37.7% at the , -TCP sites and from 33.5% to 53.7% at the BBM-grafted sites. At each depth the amount of new bone in BBM sites was significantly greater than that in TCP sites. However, the average area fraction of grafted material particles was similar in both fillers and all depth levels (, -TCP=27.9,23.2% and BBM=29.2,22.6%, NS). A significant negative correlation was found between bone area fraction and particle area fraction at the middle (p=0.009) and deep (p=0.014) depths in the , -TCP sites, but not at the BBM sites. Conclusion: At 12 months post-augmentation, the two examined bone fillers, , -TCP and BBM, promoted new bone formation in sinus grafting but the amount of newly formed bone was significantly greater in BBM-grafted sites. However, both exhibited similar residual grafted material area fraction at this healing period. This could imply that BBM possesses better osteoconductive properties. [source]


Synthesis and Characterization of Highly Dispersed Antimony-Doped Stannic Hydroxide Nanoparticles: Effects of the Azeotropic Solvents to Remove Water on the Properties and Microstructures of the Nanoparticles

JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 4 2007
Fen Yang
Highly dispersed antimony (Sb)-doped stannic hydroxide nanoparticles have been successfully prepared using the solution chemistry method. The properties and microstructures of the nanoparticles are investigated in detail by means of infrared, transmission electron microscope, X-ray diffractometer, and Brunauer-Emmett-Teller nitrogen surface area measurements. The results indicate that the properties and microstructures of the nanoparticles strongly depend on the azeotropic solvents used to remove water at the drying stage. Various azeotropic solvents are screened to investigate their effects on the size and dispersivity of dried Sb-doped stannic hydroxide. Three empirical rules are drawn for selecting an effective azeotropic solvent: (1) the solvent molecule should contain at least one atom such as oxygen as the hydrogen (H)-bond acceptor to form H bonds with the surface ,OH (acting as an H-bond donor) of polymer particle; (2) the H-bond acceptor should locate in the middle of the alkane chain rather than on the terminal so that the alkane chain can stretch out and cover more surface area, improving the dispersivity of the dried product; and (3) the solvent should have a higher boiling point (,140°C) to reduce the time of azeotropic distillation for removing water and maintain a lower residual amount of azeotropic agent. Based on the empirical rules, it is discovered that iso-amyl acetate is the most effective azeotropic solvent. [source]


Sol-Gel-Derived Silicon-Boron Oxycarbide Glasses Containing Mixed Silicon Oxycarbide (SiCxO4,x) and Boron Oxycarbide (BCyO3,y) Units

JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2001
Christel Gervais
The introduction of B atoms in SiOC glass networks has been achieved through the pyrolysis of sol-gel-derived polyborosiloxanes under an inert atmosphere. The starting gels were obtained from hydrolysis-condensation reactions of triethylborate (B(OEt)3) and an organically modified trialkoxysilane (EtSi(OEt)3). The resulting hybrid EtSiO1.5 -B2O3 gels showed a homogeneous dispersion of the B atoms in the siloxane network via ,Si,O,B, bonds. The presence of such borosiloxane bridges prevents the formation of cyclic or cage siloxane entities and leads to relatively high ceramic yields (,80%). The transformation of the polyborosiloxanes into amorphous SiBOC glasses was followed using Fourier transform infrared spectroscopy and multinuclear magic-angle spinning-nuclear magnetic resonance (MAS-NMR) (11B, 13C, and 29Si). An important change in the carbon, silicon, and boron environments occurs during pyrolysis. Interestingly, the 11B MAS-NMR spectra suggest a progressive replacement of the B,O bonds by B,C bonds, which leads to a distribution of trigonal BCxO3,x sites in the glass that was pyrolyzed at 1000°C, with a residual amount of B(OSi)3 sites. The resulting glasses can thus be described as silicon-boron oxycarbide networks that are based on SiCxO4,x and BCyO3,y mixed environments. [source]


Synthesis and Metal-Complexation Properties of a New Hydroxypyrimidinone-Functionalized Sepharose

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 3 2005
M. Alexandra Esteves
Abstract The 1-hydroxy-2-(1H)-pyrimidinone derivative 4-(3-aminopropylamino)-1-hydroxy-2-(1H)-pyrimidinone (HOPY-PrN) was synthesized and its acid-base and complexation properties towards a set of metal ions (FeIII, AlIII, and ThIV) were studied by potentiometry and spectrophotometry. The ligand was further immobilized in an epoxy-activated sepharose by chemical coupling through the aminoalkyl pendent group with the aim of improving its sequestering capacity for residual amounts of metals. The new hydroxypyrimidinone-functionalized sepharose shows a high chelating capacity for metal ions in the pH range 3,8, thus suggesting good perspectives for potential environmental applications. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005) [source]


Strategies to optimize phosphate removal from industrial anaerobic effluents by magnesium ammonium phosphate (MAP) production

JOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 1 2009
Marta Carballa
Abstract BACKGROUND: Owing to more stringent phosphate discharge requirements and the increasing prices of fertilizers, beneficial recovery and reuse of phosphate from industrial anaerobic effluents is becoming an important issue. Phosphate recovery by struvite or magnesium ammonium phosphate (MAP) permits its recycling in the fertilizer industry because struvite is a valuable slow release fertilizer. Two different approaches to MAP crystallization depending on initial levels of phosphate in the wastewaters were tested and compared. RESULTS: For low-phosphate-containing anaerobic effluents (<30 mg PO43, -P L,1), a novel approach using ureolytic induced MAP formation with MgO addition appeared to be suitable. The residual phosphate concentrations in the effluent ranged from 5 to 7 mg PO43, -P L,1 and the separated matter contained residual amounts of Mg(OH)2. High-phosphate-containing anaerobic effluents (100 to 120 mg PO43, -P L,1) were treated efficiently using air stripping combined with MgCl2 and NaOH reagents, yielding residual phosphate levels of 8 to 15 mg PO43, -P L,1 and spherical pure MAP crystals of 0.5 to 2 mm. CONCLUSION: Results show that depending on the initial phosphate concentrations in the wastewaters and the ammonium and magnesium levels, the strategy selected for struvite crystallization is a determinative factor in achieving a cost effective technology. Copyright © 2008 Society of Chemical Industry [source]