256 research outputs found

    Reactividad de 2-acetilhidrazonometil-1-arilimidazol frente a agentes reductores

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    Catalytic hydrogenation of compounds 1 led mainly to the products resulting of the hydrogenolysis of the bond C=N, while the hydrazides 2 were obtained in small yields using Pd(C) as catalyst. Reduction of la with AlLiH4 yielded the hydrazide 2a for the Z stereoisomer and the products 4a and 5a for the E stereoisomer by hydrogenolysis.La hidrogenación catalítica de los compuestos 1 origina mayoritariamente el producto resultante de la hidrogenolisis del enlace C=N y sólo se obtienen bajos rendimientos de las hidracidas 2 al utilizar Pd(C) como catalizador. La reducción con AlLiH4 de la rinde, para el estereoisómero Z, la hidracida 2a; mientras que el estereoisómero E conduce por hidrogenolisis a los compuestos 4a y 5a

    Reactivity of 2-acetylhydrazonemethyl-l -arylimidazole with reducing agents

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    La hidrogenación catalítica de los compuestos 1 origina mayoritariamente el producto resultante de la hidrogenolisis del enlace C=N y sólo se obtienen bajos rendimientos de las hidracidas 2 al utilizar Pd(C) como catalizador. La reducción con AILiH4 de la rinde, para el estereoisómero Z, la hidracida 2a; mientras que el estereoisómero E conduce por hidrogenolisis a los compuestos 4a y 5a.Catalytic hydrogenation of compounds 1 led mainly to the products resulting of the hydrogenolysis of the bond C=N, while the hydrazides 2 were obtained in small yields using Pd(C) as catalyst. Reduction of la with AILiH. yielded the hydrazide 2a for the Z stereoisomer and the products 4a and 5a for the E stereoisomer by hydrogenolysis

    Cumarinas en especies del género seseli (fam. umbelliferae)

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    A survey of the coumarins from species of the genus Seseli (Fam. Umbelliferae) is reported.Se presenta una revisión de cumarinas en especies del género Seseli (Fam. Umbelliferae)

    Conjugative DNA Transfer From E. coli to Transformation-Resistant Lactobacilli

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    Lactic acid bacteria (LAB) belonging to the genus classically known as Lactobacillus, recently split into 25 different genera, include many relevant species for the food industry. The well-known properties of lactobacilli as probiotics make them an attractive model also for vaccines and therapeutic proteins delivery in humans. However, scarce tools are available to accomplish genetic modification of these organisms, and most are only suitable for laboratory strains. Here, we test bacterial conjugation as a new tool to introduce genetic modifications into many biotechnologically relevant laboratory and wild type lactobacilli. Using mobilizable shuttle plasmids from a donor Escherichia coli carrying either RP4 or R388 conjugative systems, we were able to get transconjugants to all tested Lactocaseibacillus casei strains, including many natural isolates, and to several other genera, including Lentilactobacillus parabuchneri, for which no transformation protocol has been reported. Transconjugants were confirmed by the presence of the oriT and 16S rRNA gene sequencing. Serendipitously, we also found transconjugants into researcher-contaminant Staphylococcus epidermidis. Conjugative DNA transfer from E. coli to S. aureus was previously described, but at very low frequencies. We have purified this recipient strain and used it in standard conjugation assays, confirming that both R388 and RP4 conjugative systems mediate mobilization of plasmids into S. epidermidis. This protocol could be assayed to introduce DNA into other Gram-positive microorganisms which are resistant to transformation.FUNDING: Work in ML lab was supported by the grant BIO2017-87190-R from the Spanish Ministry of Science and Innovation. Work in MÁ lab was funded by the Spanish State Research Agency (AEI) and the European Regional Development Fund (FEDER) (AGL2016-78708-R, AEI/FEDER, EU). DG-H was a recipient of a predoctoral appointment from the University of Cantabria. RM-C received an ErasmusC traineeship grant

    Caregivers' Malaria Knowledge, Beliefs and Attitudes, and Related Factors in the Bata District, Equatorial Guinea

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    OBJECTIVES: Adequate community knowledge about malaria is crucial in order to improve prevention by reducing exposure to the disease. Malaria is a major cause of morbidity and mortality among children of less than five years of age in Equatorial Guinea. However, information concerning the accuracy of community knowledge is insufficient. This study aimed at assessing the depth of caregivers' knowledge of malaria, their beliefs and attitudes about this disease, and their socioeconomic determinants in the Bata district of Equatorial Guinea. METHODOLOGY: A cross-sectional study was conducted in the district of Bata, involving 440 houses selected from 18 rural villages and 26 urban neighbourhoods. A combined "Malaria Knowledge Score" was generated based on caregivers' knowledge about transmission, symptoms, prevention, the treatment of children, and best place to seek treatment. Multivariate logistic regressions analyses were performed to assess those factors that are associated with knowledge about malaria. RESULTS: A total of 428 caregivers were interviewed; 255 (59.6%) and 173 (40.4%) lived in urban and rural areas respectively. Significant differences between rural and urban households were observed in caregivers' malaria knowledges and beliefs. Almost 42% of urban and 65% of rural caregivers were unaware as to how malaria is transmitted (OR = 2.69; 95% CI: 1.78-4.05). Together with rurality, the factors most significantly associated with the Malaria Knowledge were the level of education of the caregiver and the socioeconomic status of the household. CONCLUSIONS: Improvements in educational programs are needed to empower the most vulnerable households such that they can pro-actively implement malaria control measures. This could be achieved by a comprehensive communication strategy aimed at changing individual and community behaviours, and delivered by suitably trained community health workers and indoor residual spraying personnel.This study was funded by the Agencia Española de Cooperación Internacional (AECID), TREG1415/11, http://www.aecid.es/ES; and the Tropical Diseases Research Network (RICET), RD12/0018/0001, http://www.ricet.es/. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.S

    Inhibidores selectivos de la monoamino oxidasa. 1. Hidracinas de formilimidazoles 1-sustitudos

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    A series of hydrazinomethylimidazole 1-sustituted was prepared and evaluated for their monoamine oxidase (MAO) inhibitory activity. In vitro testing revealed that the 1-arylimidazole derivatives were selectively inhibitors of MAO A at low concentrations.Se ha preparado una serie de hidracinometilimidazoles 1-sustituidos y estudiado su actividad IMAO. Los ensayos in vitro revelan que los 1-arilimidazoles son inhibidores selectivos de la MAO A a bajas concentraciones

    Sampling design variance estimation of small area estimators in the Spanish Labour Force Survey

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    The main goal of this paper is to investigate how to estimate sampling design variances of modelbased and model-assisted small area estimators in a complex survey sampling setup. For this purpose the Spanish Labour Force Survey is considered. Sample and aggregated data are taken from the Canary Islands in the second trimester of 2003 in order to obtain some small area estimators of ILO unemployment totals. Several problems arising from the application of standard small area estimation procedures to the survey are described. It is shown that standard variance estimators based on explicit formulas are not applicable in the strict sense, since the assumptions under which they are derived do not hold. In addition two resampling techniques, bootstrap and jackknife, are considered. These methods treat all the considered estimators in the same manner and therefore they can be used as performance measures to compare them. From the analysis of the obtained results, some recommendations are given

    Estudio de carcinoma medular de tiroides a partir de un caso índice

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    El carcinoma de tiroides es un tumor infrecuente; constituye menos del 1% de las neoplasias malignas en la población general y el 0, 5%-3% en la edad pediátrica. Existen cuatro tipos: papilar (80%-90% de los casos), folicular (5%-10%), medular (5%) y anaplásico (2%-3%). En el tipo medular, el 80% son esporádicos, y un 20% se asocia a un síndrome hereditario que se divide, fundamentalmente, en tres grupos: neoplasia endócrina múltiple 1, neoplasia endócrina múltiple 2 y carcinoma medular de tiroides familiar. Las formas hereditarias se producen por una mutación en el protooncogén RET, localizado en el brazo largo del cromosoma 10. Se presenta un caso de carcinoma medular de tiroides detectado a raíz de un estudio genético familiar con el propósito de resaltar la importancia del diagnóstico precoz y la intervención de equipos multidisciplinares expertos en esta patología para su manejo y seguimiento. Thyroid cancer is an uncommon type of cancer, accounting less than 1% of all cancers in adults, and 0.5-3% of all cancers in children. There are four different types: papillary carcinoma (80-90% of cases), follicular (5-10%), medullary (5%) and anaplastic cell (2-3%). Eighty per cent of cases of medullary thyroid cancer are sporadic, but 20% are associated with an inherited syndrome that is divided into three groups: multiple endocrine neoplasia type 1, multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma. The inherited forms are caused by a disruption in the RET oncogene, which is located in the long arm of chromosome 10. A hereditary case of medullary thyroid carcinoma is presented. It was detected because of a familial genetic study. The purpose of the paper is emphasize the importance of the early diagnosis and the intervention of multidisciplinary teams of experts

    Dynamic Dystroglycan Complexes Mediate Cell Entry of Lassa Virus.

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    Recognition of functional receptors by viruses is a key determinant for their host range, tissue tropism, and disease potential. The highly pathogenic Lassa virus (LASV) currently represents one of the most important emerging pathogens. The major cellular receptor for LASV in human cells is the ubiquitously expressed and evolutionary highly conserved extracellular matrix receptor dystroglycan (DG). In the host, DG interacts with many cellular proteins in a tissue-specific manner. The resulting distinct supramolecular complexes likely represent the functional units for viral entry, and preexisting protein-protein interactions may critically influence DG's function in productive viral entry. Using an unbiased shotgun proteomic approach, we define the largely unknown molecular composition of DG complexes present in highly susceptible epithelial cells that represent important targets for LASV during viral transmission. We further show that the specific composition of cellular DG complexes can affect DG's function in receptor-mediated endocytosis of the virus. Under steady-state conditions, epithelial DG complexes underwent rapid turnover via an endocytic pathway that shared some characteristics with DG-mediated LASV entry. However, compared to steady-state uptake of DG, LASV entry via DG occurred faster and critically depended on additional signaling by receptor tyrosine kinases and the downstream effector p21-activating kinase. In sum, we show that the specific molecular composition of DG complexes in susceptible cells is a determinant for productive virus entry and that the pathogen can manipulate the existing DG-linked endocytic pathway. This highlights another level of complexity of virus-receptor interaction and provides possible cellular targets for therapeutic antiviral intervention.IMPORTANCE Recognition of cellular receptors allows emerging viruses to break species barriers and is an important determinant for their disease potential. Many virus receptors have complex tissue-specific interactomes, and preexisting protein-protein interactions may influence their function. Combining shotgun proteomics with a biochemical approach, we characterize the molecular composition of the functional receptor complexes used by the highly pathogenic Lassa virus (LASV) to invade susceptible human cells. We show that the specific composition of the receptor complexes affects productive entry of the virus, providing proof-of-concept. In uninfected cells, these functional receptor complexes undergo dynamic turnover involving an endocytic pathway that shares some characteristics with viral entry. However, steady-state receptor uptake and virus endocytosis critically differ in kinetics and underlying signaling, indicating that the pathogen can manipulate the receptor complex according to its needs. Our study highlights a remarkable complexity of LASV-receptor interaction and identifies possible targets for therapeutic antiviral intervention
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