Preliminary trials in Artemia rearing and salt production in earthen salt ponds

The authors report on the production of Artemia obtained on a 0.5 ha pilot project with combined trials in Artemia rearing with solar salt production during the dry seasons and with production of milkfish (Chanos chanos) fingerlings and/or prawn (Penaeid sp.) juveniles during the rainy season in the Philippines

Estrategias y argumentos en el estudio descriptivo de la asociación usando microordenadores

In this work, problem solving procedures about statistical variables association using microcomputers are analysed. The effect of several didactical variables on these procedures is also studied. The studied population consisted of 18 prospective teachers who had been previously trained for 7 weeks. By studying the students' replies we determined their ideas of the scope and meaning of the term «association» and derived criteria for construction of new didactic situations

A sandwich ELISA to detect VHSV and IPNV in turbot

Abstract: The recent demonstration that reared turbot (Scophthalmus maximus L) is a natural host for salmonid rhabdoviruses has made their rapid detection relevant to these fish species. A unique protocol to select and use non-competitive monoclonal antibodies (Mabs) for two high-sensitivity sandwich ELISAs has been developed to detect both infectious pancreatic necrosis virus (IPNV) and viral haemorrhagic septicaemia virus (VHSV) in turbot kidney extracts to assess the possibility of using them in field diagnosis. For maximum sensitivity, turbot kidney extracts can be two-fold diluted with high-ionic strength buffers and assayed for the presence of the major viral proteins (VMS rhabdovirus nucleoprotein N/Nx and/or IPN birnavirus protein VP3). The use of control plates coated with irrelevant mouse antibodies (IgG1 and IgG2a) in parallel ELISAs allows for a precise estimation of possible false positives. Turbot kidney extracts with low levels of virus might now be assayed directly without using cell culture, with high precision and in a short time during the acute phase of these viral diseases in reared turbot.Acuidoro, SL; INI

Cardiac risk factors and risk scores vs cardiac computed tomography angiography: a prospective cohort study for triage of ED patients with acute chest pain.

OBJECTIVE: The objective of the study is to evaluate cardiac risk factors and risk scores for prediction of coronary artery disease (CAD) and adverse outcomes in an emergency department (ED) population judged to be at low to intermediate risk for acute coronary syndrome. METHODS: Informed consent was obtained from consecutive ED patients who presented with chest pain and were evaluated with coronary computed tomography angiography (cCTA). Cardiac risk factors, clinical presentation, electrocardiogram, and laboratory studies were recorded; the Thrombolysis in Myocardial Infarction (TIMI) and Global Registry of Acute Coronary Events (GRACE) scores were tabulated. Coronary computed tomography angiography findings were rated on a 6-level plaque burden scale and classified for significant CAD (stenosis ≥50%). Adverse cardiovascular outcomes were recorded at 30 days. RESULTS: Among 250 patients evaluated by cCTA, 143 (57%) had no CAD, 64 (26%) demonstrated minimal plaque (70% stenosis). Six patients developed adverse cardiovascular outcomes. Among traditional cardiac risk factors, only age (older) and sex (male) were significant independent predictors of CAD. Correlation with CAD was poor for the TIMI (r = 0.12) and GRACE (r = 0.09-0.23) scores. The TIMI and GRACE scores were not useful to predict adverse outcomes. Coronary computed tomography angiography identified severe CAD in all subjects with adverse outcomes. CONCLUSION: Among ED patients who present with chest pain judged to be at low to intermediate risk for acute coronary syndrome, traditional risk factors are not useful to stratify risk for CAD and adverse outcomes. Coronary computed tomography angiography is an excellent predictor of CAD and outcome

Determinación espectrofotométrica de diacetilo en mantequilla previa formación del complejo diacetil diisonicotin hidrazona-Zr(IV)

A new spectrophotometric method for determination of diacetyl has been developed. This method make use of the abili ty of diacetyl to react with isoniazid forming diacetyl diisonicotin hydrazone. This hydrazone then complexes Zr (IV) at acid pH (1,7) giving rise to a yellow and soluble chelate. The molar absorptivity is 1,7.104 l mol-1 cm-1. Themethodhas been applied tothemeasure of diacetyl in butter.Se ha desarrollado un nuevo método espectrofotométrico para la determinación de diacetilo. Se basa en la formación de diacetildiisonicotin hidrazona por reacción de diacetilo con isoniacida. La hidrazona compleja con Zr (IV) a pH ácido (1,7) formando un quelato amarillo y soluble. La absortividad molar es 1,7.104 l.mol-1 cm-1 a 410 nm. El método ha sido aplicado a la determinación de diacetilo en mantequilla

Determinación espectrofotométrica de diacetilo en mantequilla previa formación del complejo diacetil diisonicotin hidrazona-Zr(IV)

Se ha desarrollado un nuevo método espectrofotométrico para la determinación de diacetilo. Se basa en la formación de diacetildiisonicotin hidrazona por reacción de diacetilo con isoniacida. La hidrazona compleja con Zr (IV) a pH ácido (1,7) formando un quelato amarillo y soluble. La absortividad molar es 1,7.1041.mol·1 cm·1 a 410 nm. El método ha sido aplicado a la determinación de diacetilo en mantequilla.A new spectrophotometric method for determination of diacetyl has been developed. This method make use of the abili ty of diacety 1 to react with isoniazid forming diacetyl diisonicotin hydrazone. This hydrazone then complexes Zr (IV) at acid pH ( 1, 7) giving rise to a yellow and soluble chelate. The molar absorptivity is 1, 7.1041 mol·1 cm·l. Themethodhas been applied tothemeasure of diacetyl in butter

The UlaG protein family defines novel structural and functional motifs grafted on an ancient RNase fold

Background: Bacterial populations are highly successful at colonizing new habitats and adapting to changing environmental conditions, partly due to their capacity to evolve novel virulence and metabolic pathways in response to stress conditions and to shuffle them by horizontal gene transfer (HGT). A common theme in the evolution of new functions consists of gene duplication followed by functional divergence. UlaG, a unique manganese-dependent metallo-b-lactamase (MBL) enzyme involved in L-ascorbate metabolism by commensal and symbiotic enterobacteria, provides a model for the study of the emergence of new catalytic activities from the modification of an ancient fold. Furthermore, UlaG is the founding member of the so-called UlaG-like (UlaGL) protein family, a recently established and poorly characterized family comprising divalent (and perhaps trivalent)metal-binding MBLs that catalyze transformations on phosphorylated sugars and nucleotides. Results: Here we combined protein structure-guided and sequence-only molecular phylogenetic analyses to dissect the molecular evolution of UlaG and to study its phylogenomic distribution, its relatedness with present-day UlaGL protein sequences and functional conservation. Phylogenetic analyses indicate that UlaGL sequences are present in Bacteria and Archaea, with bona fide orthologs found mainly in mammalian and plant-associated Gramnegative and Gram-positive bacteria. The incongruence between the UlaGL tree and known species trees indicates exchange by HGT and suggests that the UlaGL-encoding genes provided a growth advantage under changing conditions. Our search for more distantly related protein sequences aided by structural homology has uncovered that UlaGL sequences have a common evolutionary origin with present-day RNA processing and metabolizing MBL enzymes widespread in Bacteria, Archaea, and Eukarya. This observation suggests an ancient origin for the UlaGL family within the broader trunk of the MBL superfamily by duplication, neofunctionalization and fixation. Conclusions: Our results suggest that the forerunner of UlaG was present as an RNA metabolizing enzyme in the last common ancestor, and that the modern descendants of that ancestral gene have a wide phylogenetic distribution and functional roles. We propose that the UlaGL family evolved new metabolic roles among bacterial and possibly archeal phyla in the setting of a close association with metazoans, such as in the mammalian gastrointestinal tract or in animal and plant pathogens, as well as in environmental settings. Accordingly, the major evolutionary forces shaping the UlaGL family include vertical inheritance and lineage-specific duplication and acquisition of novel metabolic functions, followed by HGT and numerous lineage-specific gene loss events

Nucleases of Metallo-Beta-Lactamase and Protein Phosphatase Families in DNA Repair

24 páginas, 5 figuras, 3 tablas -- PAGS nros. 211-234, Capítulo 11DNA repair is fundamental to all cell types to maintain genomic stability. A collection of cutting-edge reviews, DNA Repair - On the pathways to fixing DNA damage and errors covers major aspects of the DNA repair processes in a large variety of organisms, emphasizing foremost developments, questions to be solved and new directions in this rapidly evolving area of modern biology. Written by researchers at the vanguard of the DNA repair field, the chapters highlight the importance of the DNA repair mechanisms and their linkage to DNA replication, cell-cycle progression and DNA recombination. Major topics include: base excision repair, nucleotide excision repair, mismatch repair, double-strand break repair, with focus on specific inhibitors and key players of DNA repair such as nucleases, ubiquitin-proteasome enzymes, poly ADP-ribose polymerase and factors relevant for DNA repair in mitochondria and embryonic stem cells. This book is a journey into the cosmos of DNA repair and its frontiersThe authors will like to acknowledge financial support from grants PET2008_0101 and BFU2010-22260-C02-02 from the Spanish Ministry of Science and Innovation (MICINN) to MCV. FJF and MLE were supported by the MICINN grant PET2008-0101 and a fellowship (ME-517217) from the Spanish Ministry of Education, respectivelyPeer reviewe

Close detection robotic platform for Search And Rescue missions based on Bluetooth Low Energy

Improvements in telecommunications and digitalization directly improve the efficacy of a wide variety of processes. Recently, detection systems have received considerable attention because of the importance of tracking infected people contacts during SARS-CoV-2 pandemic. Such implementations can be useful in the task of finding potential victims in the context of emergency response, especially in situations where GPS is not available or inspection by imaging is not practical. Radio signals come into play, and specifically from devices that transmit periodically and with low power consumption. With the rise of Internet of Things over the last years, the number of wearable devices that support BLE, such as smartbands, smartwatches or smartphones, has been increasing constantly, as well as the number of users that carry them. Those devices can provide considerable assistance in locating injured or unconscious people. This work presents a system for detecting victims by means of a terrestrial search and rescue (SAR) robot. A real implementation of a close detection robotic platform based on BLE for SAR interventions is laid out. To estimate the distance between a robotic agent and potential victims within an experimental area, a Log-distance path loss model is presented. The proposed scheme has been tested in realistic scenarios during SAR exercises.This work was partially funded by the Spanish project RTI2018-093421-B-I00. It has been also performed in the framework of the Horizon 2020 project LOCUS (ICT-871249) receiving funds from the European Union. This work has been also partially funded by Junta de Andalucía and ERDF projects: Consejería de Transformación Económica, Industria, Conocimiento y Universidades, Proyecto de Excelencia PENTA, P18-FR-4647; postdoctoral grant (Ref., DOC 01154, “selección de personal investigador doctor convocado mediante Resolución de 21 de mayo de 2020”, PAIDI 2020) and the I Plan Propio de Investigación, Transferencia y Divulgación Científica of the University of Málaga. The authors want to thank the collaboration of the Chair for Safety, Emergencies and Disasters of the University of Malaga, led by Prof. Jesús Miranda, as well as Javier Serón Barba for his support during the experiments. Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech

Mechanism of sulfur transfer across protein-protein interfaces: The cysteine desulfurase model system

CsdA cysteine desulfurase (the sulfur donor) and the CsdE sulfur acceptor are involved in biological sulfur trafficking and in iron-sulfur cluster assembly in the model bacterium Escherichia coli. CsdA and CsdE form a stable complex through a polar interface that includes CsdA Cys328 and CsdE Cys61, the two residues known to be involved in the sulfur transfer reaction. Although mechanisms for the transfer of a sulfur moiety across protein-protein interfaces have been proposed based on the IscS-IscU and IscS-TusA structures, the flexibility of the catalytic cysteine loops involved has precluded a high resolution view of the active-site geometry and chemical environment for sulfur transfer. Here, we have used a combination of X-ray crystallography, solution NMR and SAXS, isothermal calorimetry, and computational chemistry methods to unravel how CsdA provides a specific recognition platform for CsdE and how their complex organizes a composite functional reaction environment. The X-ray structures of persulfurated (CsdA) and persulfurated (CsdA-CsdE) complexes reveal the crucial roles of the conserved active-site cysteine loop and additional catalytic residues in supporting the transpersulfuration reaction. A mechanistic view of sulfur transfer across protein-protein interfaces that underpins the requirement for the conserved cysteine loop to provide electrostatic stabilization for the in-transfer sulfur atom emerges from the analysis of the persulfurated (CsdA-CsdE) complex structure.BFU2008-02372/BMC, CSD 2006-23, and BFU2011-22588 to M.C., CTQ2012-36253-C03-03 and CTQ2015-66223-C2 to I.T., CTQ2015-64597-C2-1-P to J.J.B., and BFU2010-22266- C02-02 and CTQ2015-66206-C2-2-R to M.C.V. Further support for this work was obtained from the Generalitat Valenciana (ACOMP/2015/239 to I.T.) and from the European Commission FP7 ComplexINC grant (contract no. 279039) to M.C.V.Peer Reviewe