Latent structure of the alexithymia construct: A taxometric investigation.

Despite a wealth of research on the validity of alexithymia and its association with a number of common medical and psychiatric disorders, the fundamental question of whether alexithymia is best conceptualized as a dimensional or categorical construct remains unresolved. In the current investigation, taxometric analysis is used to examine the nature of the latent structure of alexithymia. Several nonredundant taxometric procedures were performed with item sets from the 20-item Toronto Alexithymia Scale (R. M. Bagby, J. D. A. Parker, & G. J. Taylor, 1994) as indicators. These procedures were applied separately in large community (n = 1,933) and undergraduate (n = 1,948) samples and in a smaller sample of psychiatric outpatients (n = 302). The results across various taxometric procedures and the different samples provide strong support that alexithymia is a dimensional construct. Some theoretical implications of these findings for research on the alexithymia construct are discussed. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Arginine of Chlamydomonas reinhardtii [Fe–Fe] hydrogenase HydA1 plays a crucial role in electron transfer to its catalytic center

[Fe–Fe] hydrogenases, with hydrogen evolution activities outperforming [Ni–Fe] hydrogenases by 3–4 orders of magnitude, are still the most promising enzyme class for hydrogen production purposes. For Chlamydomonas reinhardtii [Fe–Fe] hydrogenase HydA1 the question of catalytic activity and electron transport is of main importance. Here we report the characterization of two mutant forms of C. reinhardtii HydA1. An aspartic acid in place of arginine¹⁷¹ leads to a six-fold increase of the catalytic activity in comparison to the wild type protein during methyl viologen-dependent hydrogen production. Tryptophan in position 171 does not result in any change in methyl viologen-induced activity. At the same time these mutations lead to a strong decrease in ferredoxin-dependent hydrogen production while the catalytic center of mutant forms stays intact. The localization of this amino acid (arginine¹⁷¹) in the environment of CrHydA1 H-cluster indicates that the limitation of the catalytic activity of this hydrogenase is due to the electron transfer step to the catalytic center where the reduction of protons takes place.     

Antimicrobial properties and thermal stability of polycarbonate modified with 1‐alkyl‐3‐methylimidazolium tetrafluoroborate ionic liquids

Four water immiscible ionic liquids (ILs): 1‐hexyl‐3‐methylimidazolium tetrafluoroborate, 1‐heptyl‐3‐methylimidazolium tetrafluoroborate, 1‐octyl‐3‐methylimidazolium tetrafluoroborate and 1‐dodecyl‐3‐methylimidazolium tetrafluoroborate have been synthesized. Polycarbonate (PC) films containing ILs were prepared by solvent casting from methylene chloride solutions. Scanning electron microscopy measurements showed the high homogeneity of PC/IL films with the IL content up to 4 wt %. The tendency to IL aggregation was observed for polymeric films with higher IL content (5%). PC/IL composites were found to have the reduced thermal decomposition temperature under both an air and a nitrogen atmosphere in comparison with the neat PC. The effect of IL content on the antimicrobial activity of PC films against Escherichia coli bacteria was studied. Pronounced antimicrobial efficacy was revealed for PC/IL films for all studied ILs starting from 3 wt % of IL. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40050.     

Nanoscale graphite-supported Pt catalysts for oxygen reduction reactions in fuel cells

The nanoscale graphite particles were prepared and the Pt catalysts supported on such graphites were developed for oxygen reduction in the polymer electrolyte membrane fuel cells. Catalytic activity and carbon corrosion of the developed catalysts were evaluated using rotating disc electrode techniques and results were compared with those of a state-of-the-art commercial E-TEK Pt catalyst supported on carbon black Vulcan XC72. The results showed that the particle distribution and the structure of the developed Pt nanoparticles supported on the nanoscale graphite were similar to those of the commercial catalyst. The accelerated degradation testing results showed that the electrochemical active surface area losses after 1500 cycles were 46.92% and 62.2% for the developed catalyst and the commercial catalyst, respectively, while mass activity losses were 45.3% and 84.2%, respectively. The temperature-programmed oxidation results suggest that the developed catalysts had better corrosion resistance than the commercial catalyst. The developed Pt catalysts had similar catalytic performance to the commercial catalyst; however, the developed catalysts had much better corrosion resistance than the commercial catalyst. Overall, nanoscale graphite can be a promising electrocatalyst support to replace the currently used Vulcan XC72 carbon black.     

Facile synthesis of Ag/Zn1-xCuxO nanoparticle compound photocatalyst for high-efficiency photocatalytic degradation: Insights into the synergies and antagonisms between Cu and Ag

By carefully balancing synergies and antagonisms that arise from incorporating Cu and Ag within a single ZnO-based catalytic platform, the photocatalytic activity of Ag/ZnO based on three-dimensional modified ceramic structures can be further significantly enhanced. The performance of Ag/ZnO heterostructure (Z0) was significantly improved by only 0.2 mol% Cu incorporation (Z0.2) and the first-order degradation kinetics constants (K) of Z0.2 were 2 and 1.5 times higher than that of Z0 under simulated sunlight and UV light. The synergies between Cu dopants and metallic Ag were mainly the significantly enhanced visible light absorption capacity and the prolonged photo-excited charge lifetime. However, with the excessive introduction of Cu precursors, the surface Cu²⁺ was found to inhibit the interfacial charge transfer between Ag and ZnO NPs under UV and visible light irradiation, but the transformation from Cu²⁺ to Cu⁺ was also presumed to be a driving factor for the improvement of photocatalytic efficiency. These interactions may provide a useful pathway for enhancing photocatalytic efficiency of low-cost ZnO-based catalytic platforms.     

Covalent Attachment of FeFe Hydrogenases to Carbon Electrodes for Direct Electron Transfer

Direct electron transfer between enzymes and electrodes is now commonly achieved, but obtaining protein films that are very stable may be challenging. This is particularly crucial in the case of hydrogenases, the enzymes that catalyze the biological conversion between dihydrogen and protons, because the instability of the hydrogenase films may prevent the use of these enzymes as electrocatalysts of H(2) oxidation and production in biofuel cells and photoelectrochemical cells. Here we show that two different FeFe hydrogenases (from Chamydomonas reinhardtii and Clostridium acetobutylicum) can be covalently attached to functionalized pyrolytic graphite electrodes using peptidic coupling. In both cases, a surface patch of lysine residues makes it possible to favor an orientation that is efficient for fast, direct electron transfer. High hydrogen-oxidation current densities are maintained for up to one week, the only limitation being the intrinsic stability of the enzyme. We also show that covalent attachment has no effect on the catalytic properties of the enzyme, which means that this strategy can also used be for electrochemical studies of the catalytic mechanism.     

Parental worry about indoor air quality and student symptom reporting in primary schools with or without indoor air quality problems

Poor indoor air quality (IAQ) in schools is related to increased symptom reporting in students. We investigated whether parental worry about school IAQ influences this association. Data came from survey collected from five Finnish primary schools with observed IAQ problems and five control schools. Parents (n = 1868) of primary school students reported worry about IAQ in schools and symptoms of their children. Associations between observed IAQ problems, worry, and five symptom scores (ie, respiratory, lower respiratory, eye, skin, and general symptoms) were analyzed using multivariate logistic regression and mediation analysis. Parents were on average more worried in schools with observed IAQ problems. Observed IAQ problems were strongly associated with increased worry and all symptoms under study (unadjusted ORs ranged between 1.48 [95% CI 1.48‐2.16] and 2.70 [95% CI 1.52‐5.17]). Parental worry was associated with all symptoms (unadjusted ORs ranged between 2.49 [95% CI 1.75‐3.60] and 4.92 [95% CI 2.77‐9.40]). Mediation analyses suggested that parental worry might partially explain the association between observed IAQ problems and symptom reporting (proportion mediated ranged between 67% and 84% for the different symptoms). However, prospective studies are needed to assess causal relationships between observed IAQ problems, worry, and symptom reporting in schools.     

Simulation‐Experimental Approach to Investigate the Role of Interfaces in Self‐Replenishing Composite Coatings

To investigate self‐replenishing on surface‐structured composite coatings a dual simulation‐experimental approach is employed to study the decisive role of polymer‐air and polymer‐particle interfaces. Experimentally, the composite system consists of a cross‐linked polymer network with fluorinated‐dangling chains, embedding colloidal SiO₂ nanoparticles which are incorporated in the network via covalent bonding. These particles provide the desired surface structure at the air‐interface before and after damage. Any damage replicates the rough surface, while the polymer layer on top of the particles serves as source of low surface energy groups which are able to reorient towards the new air‐interfaces. Using coarse‐grained simulations details of these self‐replenishing composite systems are revealed such as the minimum thickness of the polymer layer necessary for providing optimal self‐replenishing ability and the distribution profile of the dangling chains at the various interfaces. The principles and dual approach reported here may be applied to other self‐healing composite systems with applications in self‐cleaning, anti‐fouling or low adhesion materials.     

Thin-layer high-vacuum distillation to isolate volatile flavour compounds of cocoa powder

The volatile fraction of commercial cocoa powders was isolated using thin-layer high-vacuum distillation (TLHVD) of Soxhlet extracts. Calculated and experimental recovery of the internal standard n-undecanoic acid methylester did agree, and a good reproducibility was found for the procedure. Around 70 volatile compounds were identified and semi-quantified using internal standard-based gas chromatography (GC), coupled GC–mass spectrometry (GC–MS) and GC-olfactometry (GC-O). Dehydromevalonic acid lactone, (R)-(−)-pantolactone and two diastereomer solerols were identified for the first time after purification by micropreparative GC and re-analysis using GC–MS and chiral GC. Strong sensory contributions also came from acetic acid, 2/3-methyl butanoic acid, phenylacetaldehyde, furaneol, dihydroxymaltol, vanillin and phenylacetic acid.     

New insights into the systems for heterologous synthesis and maturation of hydrogenases,the most efficient biohydrogen producers

Biohydrogen is considered as an important key to a sustainable world power supply and is currently being seen as the versatile fuel of the future, with the potential to replace fossil fuels. The most efficient biohydrogen producers are hydrogenases. Nevertheless, due to the complex maturation processes of these enzymes, their heterologous production leaves some intriguing points not elucidated up to now. The limit of our understanding in this field makes a barrier for hydrogenases application in a variety of biotechnological processes. This review focuses on recent progresses in the development of heterologous production systems and cell-free maturation systems for the biosynthesis of active [Fe–Fe] and [Ni–Fe] hydrogenases. It also highlights some up to now un-discussed questions on the probable existence of unknown machinery able to maturate [Fe–Fe] hydrogenases or a contribution of the [Ni–Fe] hydrogenases maturases to the formation of an active H-cluster for the [Fe–Fe] hydrogenases.