17 research outputs found

    A Regional Red List of Montane Tree Species of the Tropical Andes: Trees at the top of the world

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    Andean montane forests are a major global conservation priority owing to their biological richness and high level of species endemism. Botanically the Andes are very rich in species but they remain relatively unstudied. In common with montane forests elsewhere in the world, Andean forests are of great value for the provision of ecosystem services relating to water supply, regulation of regional climate and the capture and storage of carbon. The forests and their component species are however under threat. This report summarises information drawn from a wide variety of sources to provide a regional Red List of trees of Andean tropical montane forests. The species evaluation process has drawn on published national red lists of threatened species, botanical literature, specimen databases, forestry information and expert knowledge. The IUCN Red List Categories and Criteria have been used for the evaluation and a component of Natalia?s PhD study has been to evaluate their use for species with limited and dispersed data. Understanding the geographical distribution of the species is very important in conservation assessment. The maps produced for this study are a valuable starting point for the Red Listing and a baseline for monitoring impacts of climate change. In this assessment 70 species are recorded as globally threatened based on the IUCN Red List of Categories and Criteria out of 127 tree species evaluated. In addition 165 national endemic trees of the region have previously been evaluated as globally threatened based on the same IUCN process. In total therefore 235 tree species are currently considered to be threatened with extinction within the Andean montane forests.Fil: Tejedor Garavito , Natalia. Bournemouth University; Reino UnidoFil: Álvarez Dávila, Esteban. Jardín Botánico de Medellín; ColombiaFil: Caro, Sandra Arango. Missouri Botanical Garden; Estados UnidosFil: Murakami, Alejandro Araujo. Museo de Historia Natural Noel Kempff Mercado; BoliviaFil: Baldeón, Severo. Universidad Nacional Mayor de San Marcos; PerúFil: Beltrán, Hamilton. Universidad Nacional Mayor de San Marcos; PerúFil: Blundo, Cecilia Mabel. Universidad Nacional de Tucumán. Facultad de Ciencias Naturales e Instituto Miguel Lillo; Argentina. Universidad Nacional de Tucumán. Facultad de Ciencias Naturales e Instituto Miguel Lillo. Laboratorio de Investigaciones Ecológicas de las Yungas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán; ArgentinaFil: Boza Espinoza, Tatiana Erika. Missouri Botanical Garden; Estados UnidosFil: Fuentes Claros, Alfredo. Herbario Nacional de Bolivia; BoliviaFil: Gaviria, Juan. Universidad de Los Andes; VenezuelaFil: Gutiérrez, Néstor. Universidad de Los Andes; VenezuelaFil: Khela, Sonia. Botanic Gardens Conservation International; Reino UnidoFil: León, Blanca. University of Texas at Austin; Estados UnidosFil: la Torre Cuadros, Maria De Los Angeles. Universidad Nacional Agraria; PerúFil: López Camacho, René. Universidad Distrital; ColombiaFil: Malizia, Lucio Ricardo. Universidad Nacional de Jujuy. Facultad de Ciencias Agrarias. Centro de Estudios Ambientales Territoriales y Sociales; ArgentinaFil: Millán, Betty. Universidad Nacional Mayor de San Marcos; PerúFil: Moraes R., Mónica. Herbario Nacional de Bolivia; BoliviaFil: Newton, Adrian C.. Bournemouth University; Reino UnidoFil: Pacheco, Silvia. Fundación Proyungas; ArgentinaFil: Reynel, Carlos. Universidad Nacional Agraria; PerúFil: Ulloa Ulloa, Carmen. Missouri Botanical Garden; Estados UnidosFil: Vacas Cruz,Omar. Pontificia Universidad Católica del Ecuador; Ecuado

    Prevalence, associated factors and outcomes of pressure injuries in adult intensive care unit patients: the DecubICUs study

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    Funder: European Society of Intensive Care Medicine; doi: http://dx.doi.org/10.13039/501100013347Funder: Flemish Society for Critical Care NursesAbstract: Purpose: Intensive care unit (ICU) patients are particularly susceptible to developing pressure injuries. Epidemiologic data is however unavailable. We aimed to provide an international picture of the extent of pressure injuries and factors associated with ICU-acquired pressure injuries in adult ICU patients. Methods: International 1-day point-prevalence study; follow-up for outcome assessment until hospital discharge (maximum 12 weeks). Factors associated with ICU-acquired pressure injury and hospital mortality were assessed by generalised linear mixed-effects regression analysis. Results: Data from 13,254 patients in 1117 ICUs (90 countries) revealed 6747 pressure injuries; 3997 (59.2%) were ICU-acquired. Overall prevalence was 26.6% (95% confidence interval [CI] 25.9–27.3). ICU-acquired prevalence was 16.2% (95% CI 15.6–16.8). Sacrum (37%) and heels (19.5%) were most affected. Factors independently associated with ICU-acquired pressure injuries were older age, male sex, being underweight, emergency surgery, higher Simplified Acute Physiology Score II, Braden score 3 days, comorbidities (chronic obstructive pulmonary disease, immunodeficiency), organ support (renal replacement, mechanical ventilation on ICU admission), and being in a low or lower-middle income-economy. Gradually increasing associations with mortality were identified for increasing severity of pressure injury: stage I (odds ratio [OR] 1.5; 95% CI 1.2–1.8), stage II (OR 1.6; 95% CI 1.4–1.9), and stage III or worse (OR 2.8; 95% CI 2.3–3.3). Conclusion: Pressure injuries are common in adult ICU patients. ICU-acquired pressure injuries are associated with mainly intrinsic factors and mortality. Optimal care standards, increased awareness, appropriate resource allocation, and further research into optimal prevention are pivotal to tackle this important patient safety threat

    Phthalimides as Exceptionally Efficient Single Electron Transfer Acceptors in Reductive Coupling Reactions Promoted by Samarium Diiodide

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    4 páginas, 3 figuras, 1 esquema, 1 tabla.-- Supporting Information Available: Experimental procedures, spectroscopic data for the coupling products, crystallographic data of 2, 4c, and 8 (minor diastereoisomer), and energies and Cartesian coordinates for new compounds in Table 1. This material is available free of charge via the Internet at http://pubs.acs.org.Experimental and theoretical evidence shows that phthalimides are highly efficient single electron transfer acceptors in reactions promoted by samarium diiodide, affording ketyl radical anion intermediates, which participate in high-yielding inter- and intramolecular reductive coupling processes with different radicophiles including imides, oxime ethers, nitrones, and Michael acceptors.We thank MEC for financial support (projects BQU2003-03550-C03-02 and CTQ2006-15515- C02-02/BQU) and for a predoctoral fellowship to T.V.Peer reviewe

    Estudio sobre reconocimiento de aminoglicósidos por ARN y enzimas de resistencia

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    Tesis doctoral inédita leída en la Universidad Autónoma de Madrid, Facultad de Ciencias, Departamento de Química Orgánica. Fecha de lectura: 17-07-200

    1-Silyl-2,6-diketones: Versatile Intermediates for the Divergent Synthesis of Five- and Six-Membered Carbocycles under Radical and Anionic Conditions

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    4 páginas, 5 esquemas, 1 tabla.-- Supporting Information Available: Complete experimental procedures and characterization data for compounds 2-13. This material is available free of charge via the Internet at http://pubs.acs.org.1-Silyl-2,6-diketones, readily prepared by addition of (silylmethyl)metal reagents to 1,5-lactols followed by oxidation of the resultant diols, can be efficiently transformed into 3-hydroxycyclohexanones, cyclohex-2-enones, or 1-(silylmethyl)cyclopentane-1,2-diols under nucleophilic, basic, or single electron-transfer reduction conditions, respectively. The latter cyclitols can be further transformed into 2-methylenecyclopentanols or 1-(hydroxymethyl)cyclopentane-1,2-diols by Peterson elimination or Tamao−Fleming oxidation, respectively.Financial support from the Ministry of Science and Technology of Spain (project BQU2000- 1501-C02-01), Fundación Ramón Areces, and Comunidad de Madrid (predoctoral fellowships to A.G and E.S., respectively) are gratefully acknowledged.Peer reviewe

    NMR-based analysis of aminoglycoside recognition by the resistance enzyme ANT(4´): the pattern of OH/NH3(+) substitution determines the preferred antibiotic binding mode and is critical for drug inactivation

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    18 páginas, 14 figuras, 2 tablas -- PAGS nros. 5086-5103The most significant mechanism of bacterial resistance to aminoglycosides is the enzymatic inactivation of the drug. Herein, we analyze several key aspects of the aminoglycoside recognition by the resistance enzyme ANT(4′) from Staphylococcus aureus, employing NMR complemented with site-directed mutagenesis experiments and measurements of the enzymatic activity on newly synthesized kanamycin derivatives. From a methodological perspective, this analysis provides the first example reported for the use of transferred NOE (trNOE) experiments in the analysis of complex molecular recognition processes, characterized by the existence of simultaneous binding events of the ligand to different regions of a protein receptor. The obtained results show that, in favorable cases, these overlapping binding processes can be isolated employing site-directed mutagenesis and then independently analyzed. From a molecular recognition perspective, this work conclusively shows that the enzyme ANT(4′) displays a wide tolerance to conformational variations in the drug. Thus, according to the NMR data, kanamycin-A I/II linkage exhibits an unusual anti-Ψ orientation in the ternary complex, which is in qualitative agreement with the previously reported crystallographic complex. In contrast, closely related, kanamycin-B is recognized by the enzyme in the syn-type arrangement for both glycosidic bonds. This observation together with the enzymatic activity displayed by ANT(4′) against several synthetic kanamycin derivatives strongly suggests that the spatial distribution of positive charges within the aminoglycoside scaffold is the key feature that governs its preferred binding mode to the protein catalytic region and also the regioselectivity of the adenylation reaction. In contrast, the global shape of the antibiotic does not seem to be a critical factor. This feature represents a qualitative difference between the target A-site RNA and the resistance enzyme ANT(4′) as aminoglycoside receptorsFinancial support from DGES (grants CTQ2004-04494/BQU, CTQ2007-67403/BQU, and CTQ2004-03523/BQU) is acknowledged. J.R. and F.C. thank the Ministerio de Educación y Ciencia for Juan de la Cierva and Ramon y Cajal contracts, respectively. We also thank CESGA (Santiago de Compostela) for computer support. T.V. thanks CSIC for a JAE contractPeer reviewe

    NMR-based analysis of aminoglycoside recognition by the resistance enzyme ANT(4´): the pattern of OH/NH3(+) substitution determines the preferred antibiotic binding mode and is critical for drug inactivation

    No full text
    18 páginas, 14 figuras, 2 tablas -- PAGS nros. 5086-5103The most significant mechanism of bacterial resistance to aminoglycosides is the enzymatic inactivation of the drug. Herein, we analyze several key aspects of the aminoglycoside recognition by the resistance enzyme ANT(4′) from Staphylococcus aureus, employing NMR complemented with site-directed mutagenesis experiments and measurements of the enzymatic activity on newly synthesized kanamycin derivatives. From a methodological perspective, this analysis provides the first example reported for the use of transferred NOE (trNOE) experiments in the analysis of complex molecular recognition processes, characterized by the existence of simultaneous binding events of the ligand to different regions of a protein receptor. The obtained results show that, in favorable cases, these overlapping binding processes can be isolated employing site-directed mutagenesis and then independently analyzed. From a molecular recognition perspective, this work conclusively shows that the enzyme ANT(4′) displays a wide tolerance to conformational variations in the drug. Thus, according to the NMR data, kanamycin-A I/II linkage exhibits an unusual anti-Ψ orientation in the ternary complex, which is in qualitative agreement with the previously reported crystallographic complex. In contrast, closely related, kanamycin-B is recognized by the enzyme in the syn-type arrangement for both glycosidic bonds. This observation together with the enzymatic activity displayed by ANT(4′) against several synthetic kanamycin derivatives strongly suggests that the spatial distribution of positive charges within the aminoglycoside scaffold is the key feature that governs its preferred binding mode to the protein catalytic region and also the regioselectivity of the adenylation reaction. In contrast, the global shape of the antibiotic does not seem to be a critical factor. This feature represents a qualitative difference between the target A-site RNA and the resistance enzyme ANT(4′) as aminoglycoside receptorsFinancial support from DGES (grants CTQ2004-04494/BQU, CTQ2007-67403/BQU, and CTQ2004-03523/BQU) is acknowledged. J.R. and F.C. thank the Ministerio de Educación y Ciencia for Juan de la Cierva and Ramon y Cajal contracts, respectively. We also thank CESGA (Santiago de Compostela) for computer support. T.V. thanks CSIC for a JAE contractPeer reviewe
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