The Advanced Implantation Detector Array (AIDA)

The Advanced Implantation Detector Array (AIDA) is a state-of-the-art detector system for the measurement of the decay properties of exotic nuclei at fragmentation/fission facilities. Built around stacks of up to eight 8cm×8cm, 128 × 128 strip (16384 pixels) or up to four 24cm×8cm, 384 × 128 strip (49152 pixels) double sided silicon strip detectors, the positions of both implanted ions and their subsequent decay products can be measured to sub-mm precision. The large number of pixels per detector provide implant-decay correlations at implantation rates ∼kHz. To process signals from the large number of strips application specific integrated circuits provide low and high gain signal processing per strip (20 GeV and 20 MeV full scale range) with a dynamic range of 1000:1, or better. A summary of the system and the analysis methodologies used are presented

Towards a comprehensive estimate of national spending on prevention

Background Comprehensive information about national spending on prevention is crucial for health policy development and evaluation. This study provides a comprehensive overview of prevention spending in the Netherlands, including those activities beyond the national health accounts. Methods National spending on health-related primary and secondary preventive activities was examined by funding source with the use of national statistics, government reports, sector reports, and data from individual health associations and corporations, public services, occupational health services, and personal prevention. Costs were broken down by diseases, age groups and gender using population-attributable risks and other key variables. Results Total expenditures on prevention were €12.5 billion or €769 per capita in the Netherlands in 2003, of which 20% was included in the national health accounts. 82% was spent on health protection, 16% on disease prevention, and 2% on health promotion activities. Most of the spending was aimed at the prevention of infectious diseases (34%) and acute physical injuries (29%). Per capita spending on prevention increased steeply by age. Conclusion Total expenditure on health-related prevention is much higher than normally reported due to the inclusion of health protection activities beyond the national health accounts. The allocative efficiency of prevention spending, particularly the high costs of health protection and the low costs of health promotion activities, should be addressed with information on their relative cost effectiveness

Contaminación de aflatoxinas en frutos secos: un problema emergente

Las aflatoxinas son micotoxinas producidas por hongos de suelo del género Aspergillus, principalmente A. flavus y A. parasiticus. Por su alta toxicidad, están reguladas en numerosos alimentos para consumo humano y animal. Ambas especies crecen sobre restos de material vegetal produciendo un gran número de conidios aerovagantes que pueden colonizar y contaminar diferentes cultivos como maíz, cacahuete, algodón y frutos secos, entre otros. La contaminación por aflatoxinas en almendro y pistachero, sus causas y control, han sido intensamente estudiados en California en los últimos 25 años. En España, la situación es menos conocida y está siendo abordada en el marco de dos proyectos de investigación entre la Universidad de Córdoba y la Universidad de California, Davis. Aquí, revisamos la importancia actual, la etiología, biología, y control de esta problemática en los frutos secos españoles

Substrate binding and catalytic mechanism of a barley b-D-glucosidase (1,4)-b-D-glucan exohydrolase

A beta-glucosidase, designated isoenzyme betaII, from germinated barley (Hordeum vulgare L.) hydrolyzes aryl-beta-glucosides and shares a high level of amino acid sequence similarity with beta-glucosidases of diverse origin. It releases glucose from the non-reducing termini of cellodextrins with catalytic efficiency factors, kcat/Km, that increase approximately 9-fold as the degree of polymerization of these substrates increases from 2 to 6. Thus, the enzyme has a specificity and action pattern characteristic of both beta-glucosidases (EC 3.2.1.21) and the polysaccharide exohydrolase, (1,4)-beta-glucan glucohydrolase (EC 3.2.1.74). At high concentrations (100 mM) of 4-nitrophenyl beta-glucoside, beta-glucosidase isoenzyme betaII catalyzes glycosyl transfer reactions, which generate 4-nitrophenyl-beta-laminaribioside, -cellobioside, and -gentiobioside. Subsite mapping with cellooligosaccharides indicates that the barley beta-glucosidase isoenzyme betaII has six substrate-binding subsites, each of which binds an individual beta-glucosyl residue. Amino acid residues Glu181 and Glu391 are identified as the probable catalytic acid and catalytic nucleophile, respectively. The enzyme is a family 1 glycoside hydrolase that is likely to adopt a (beta/alpha)8 barrel fold and in which the catalytic amino acid residues appear to be located at the bottom of a funnel-shaped pocket in the enzyme