PLANINDEX: 112-001

Contiene resúmenes bibliográficos de documentos sobre planificación y desarrollo en América Latina, recogidos y procesados en el marco del Sistema de Información para la Planificación en América Latina y el Caribe (INFOPLAN).

EIF5A dimerizes not only in vitro but also in vivo and its molecular envelope is similar to the EF-P monomer

The protein eukaryotic initiation factor 5A (eIF5A) is highly conserved among archaea and eukaryotes, but not in bacteria. Bacteria have the elongation factor P (EF-P), which is structurally and functionally related to eIF5A. eIF5A is essential for cell viability and the only protein known to contain the amino acid residue hypusine, formed by post-translational modification of a specific lysine residue. Although eIF5A was initially identified as a translation initiation factor, recent studies strongly support a function for eIF5A in the elongation step of translation. However, the mode of action of eIF5A is still unknown. Here, we analyzed the oligomeric state of yeast eIF5A. First, by using size-exclusion chromatography, we showed that this protein exists as a dimer in vitro, independent of the hypusine residue or electrostatic interactions. Protein-protein interaction assays demonstrated that eIF5A can form oligomers in vitro and in vivo, in an RNA-dependent manner, but independent of the hypusine residue or the ribosome. Finally, small-angle X-ray scattering (SAXS) experiments confirmed that eIF5A behaves as a stable dimer in solution. Moreover, the molecular envelope determined from the SAXS data shows that the eIF5A dimer is L-shaped and superimposable on the tRNAPhe tertiary structure, analogously to the EF-P monomer. © 2012 Springer-Verlag.

Isolation and characterization of SNPs within HSC70 gene in the freshwater prawn Macrobrachium amazonicum

We report the discovery of 13 synonymous single nucleotide polymorphisms (SNPs) within a fragment of HSC70 gene in Macrobrachium amazonicum. Polymorphisms were assessed using the reference sequence of the HSC70 gene in Macrobrachium rosenbergii to the primers design. The minor allele frequency ranged from 0.011 to 0.213. None of the SNPs deviated significantly from Hardy-Weinberg equilibrium. These SNPs will be useful to access the genetic variation of populations and to the study of their relations with characteristics of interest for aquaculture. Both cases, favoring the conservation of the natural stocks of Amazon river prawn. © 2013 Springer Science+Business Media Dordrecht.

Extracellular β-fructofuranosidase from Fusarium graminearum: Stability of the spray-dried enzyme in the presence of different carbohydrates

Microbial enzymes have been used for various biotechnological applications; however, enzyme stabilization remains a challenge for industries and needs to be considered. This study describes the effects of spray-drying conditions on the activity and stability of β-fructofuranosidase from Fusarium graminearum. The extracellular enzyme β-fructofuranosidase was spray dried in the presence of stabilizers, including starch (Capsul) (SC), microcrystalline cellulose (MC), trehalose (TR), lactose (LC) and β-cyclodextrin (CD). In the presence of TR (2% w/v), the enzymatic activity was fully retained. After 1 year of storage, 74% of the enzymatic activity was maintained with the CD stabilizer (10% w/v). The residual activity was maintained as high as 80% for 1 h at 70°C when MC, SC and CD (5% w/v) stabilizers were used. Spray drying with carbohydrates was effective in stabilizing the F. graminearum β-fructofuranosidase, improved enzymatic properties compared to the soluble enzyme and demonstrated a potential use in future biotechnology applications. © 2013 Informa UK Ltd. All rights reserved.

Istmo Centroamericano: estadísticas del subsector eléctrico (datos actualizados a 2003)

Incluye Bibliografía

Copenhagen +5: the Special Session on Social Development in 2000: issues of relevance to the Caribbean

Includes bibliography

Guía para orientar estudios de apoyo a la gestión del desarrollo de cuencas y microrregiones alto andinas

Incluye Bibliografía

Innovación social en salud: un aporte al avance de los Objetivos de Desarrollo del Milenio

El presente documento parte de un análisis de la situación de la salud en América Latina y el Caribe resaltando que, si bien en promedio ha mejorado, no hay duda de que existen grandes diferencias e inequidades que afectan a grupos muy amplios de la población a los que, en la práctica se les niega el acceso a servicios de salud. Con este panorama en mente se analizan en detalle experiencias innovadoras que atienden temas de salud, que se identificaron gracias al proyecto “Experiencias en innovación social en América Latina y el Caribe”, iniciativa de la CEPAL con el apoyo de la Fundación W.K. Kellogg. En particular se estudian tres programas que afectan la salud materno infantil y tres que se han dedicado a la atención de la salud de pueblo indígenas y comunidades multiculturales.

Caracterização do uso e ocupação do solo na área de influência do reservatório de Ilha Solteira

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Condições de trabalho de funcionários penitenciários de Avaré-SP e ocorrência de transtornos mentais comuns

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Associação de agentes patogênicos isolados em análise microbiológica da água, com a presença de mastite clínica ou subclínica, em propriedades leiteiras da região de Cerqueira César-SP

Pós-graduação em Medicina Veterinária - FMVZ

Análise da abordagem dos processos de dinâmica superficial em EIAs/Rimas de projetos urbanísticos no estado de São Paulo, no período de 1987 a 2007

Pós-graduação em Geociências e Meio Ambiente - IGCE

CYP21 gene mutations in Brazilian patients with 21-hydroxylase deficiency from the Amazon region

ABSTRACT: Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (P450c21, CYP21) accounts for about 95% of all CAH cases. The incidence of CYP21 gene mutations has been extensively studied in the last years, but in Brazil it has been investigated only in Southeast Brazilian patients. This study is the first report on the distribution of CYP21 mutations in patients from the Amazon region. Direct sequencing of the CYP21 gene identified at least one mutation in 96% of the studied chromosomes. The most common mutations found were IVS2-13A/C > G (36%), Q318X (12%), V281L (12%), 1760_1761insT (9%), Cluster E6 (7%), and P30L (7%). The worldwide most common mutations were identified among patients from the Amazon region at frequencies that may be expected for a population resulting from the admixture of Europeans (predominantly Portuguese), African Blacks and Amerindians, in proportions that differ from those estimated for South Brazilian populations. Interethnic mixture may explain the differences in the frequencies of some mutations between Brazilian patients from the Amazon and from the Southeast of the country. However, the differences found may also be due to variation in the number of patients with the different clinical forms of 21-hydroxylase deficiency in the studies carried out so far.

Densidade mineral óssea de adolescentes do sexo feminino e suas relaçoes com biomarcadores ósseos

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)