320 research outputs found
Otvaranje zvukovnih arhiva Europe: projekt Europeana Sounds
Europeana Sounds is a project co-funded by the European Commission within the ICT Policy Support Programme as part of the Competitiveness and Innovation Framework Programme. The project aimed to enhance the total amount of the sound contents available through Europeana. Currently, more than 600,000 audio items and more than 300,000 audio-related contents have been aggregated thanks to the activities carried out by Europeana Sounds. The project has achieved other important objectives such as the enrichment of the metadata related to the digital objects, the realization of a set of Policy Recommendations, the launch of the first thematic channel of Europeana entirely devoted to the music named Europeana Music and a Radio that makes 200,000 music tracks available online. Europeana Sounds will continue to pursuit its objectives through the Task force established within the International Association of Sound and Audiovisual Archives (IASA).Slogan projekta Europeana Sounds kaže Ā»Zvukovno nasljeÄe Europe pod vaÅ”im prstima Ā« i to je, u suÅ”tini, glavni cilj Projekta. Ovaj Älanak daje pregled Europeana Sounds projekta koji je zapoÄet u veljaÄi 2014, a zavrÅ”en u sijeÄnju 2017. godine. Projekt Äini dostupnim sadržaje sakupljene putem Europeane koja nudi pristup do viÅ”e od 53,870.000 izvora, ukljuÄujuÄi knjige, videosnimke, slike, zvukove, umjetniÄka djela i joÅ” mnogo viÅ”e iz europskog kulturnog nasljeÄa. U prvome dijelu Älanka objaÅ”njavaju se ciljevi Europeana Sounds, a to su: poveÄati ukupnu koliÄinu zvuÄnih izvora koji su dostupni putem portala Europeana, obogatiti metapodatke vezane uz te izvore, kreirati specifiÄan kanal posveÄen zvukovima i ostalim srodnim sadržajima, istražiti u svrhu rjeÅ”avanja ograniÄenja domene vezane uz zvukovno nasljeÄe, potaknuti kreativno koriÅ”tenje navedenih resursa te kreirati mrežu interesenata i struÄnjaka na polju zvuka. Unutar projekta formirano je nekoliko grupa koje su provele radnje vezane uz konaÄne ciljeve projekta: od sakupljanja sadržaja do tehniÄke infrastrukture koja omoguÄava objavljivanje na Europeani, od obogaÄivanja metapodataka vezanih za izvore i crowdsourcinga do pitanja autorskih prava, od realizacije tematskog kanala do složenih aktivnosti voÄenja projekta. Za vrijeme projekta svi postignuti ciljevi promovirani su kroz Å”irok spektar aktivnosti, ukljuÄujuÄi dva meÄunarodna skupa, sudjelovanjem na dogaÄanjima, dinamiÄnim blogom s viÅ”e objava koje su vezane za zvukovno nasljeÄe te stranicama na druÅ”tvenim mrežama. ZakljuÄno, trud uložen u pokretanje tematskoga kanala posveÄenoga glazbi. Projekt, koji je u rasponu od tri godine ostvario razne ciljeve, nastavit Äe svoje aktivnosti zahvaljujuÄi radnoj skupini formiranoj unutar International
Association of Sound and Audiovisual Archives (IASA)
Bootstrapping the Chiral Anomaly at Large
The bootstrap approach (demanding consistency conditions to scattering
amplitudes) has shown to be quite powerful to tightly constrain gauge theories
at large . We extend previous analysis to scattering amplitudes involving
pions and external gauge bosons. These amplitudes allow us to access the chiral
anomaly and connect low-energy physical quantities to UV properties of the
theory. In particular, we are able to obtain an analytic bound on the chiral
anomaly coefficient as a function of the pion dipole polarizabilities. This
bound can be useful for holographic models whose dual UV completions are not
known, and provide a consistency condition to lattice simulations.Comment: 20 pages, 1 figure. v2: bound on the anomaly generalised and typos
correcte
IMAPlate Based Miniature, High Sensitive, Rapid Screening Method for Detecting Bioengineered, Secreted Lipase Activities in Yeast Expression Systems
A spectrophotometric assay based on a miniaturized 96-well plate device (IMAPlate) enables a rapid and simple screening of bioengineered recombinant lipases expressed and secreted by Saccharomyces cerevisiae. Starting from a colony, the test delivers a quantitative estimation
of enzymatic activity titer in 24 h or less with manual high throughput performances
Building response to tunnelling
AbstractUnderstanding how buildings respond to tunnelling-induced ground movements is an area of great importance for urban tunnelling projects, particularly for risk management. In this paper, observations of building response to tunnelling, from both centrifuge modelling and a field study in Bologna, are used to identify mechanisms governing the soilāstructure interaction. Centrifuge modelling was carried out on an 8-m-diameter beam centrifuge at Cambridge University, with buildings being modelled as highly simplified elastic and inelastic beams of varying stiffness and geometry. The Bologna case study presents the response of two different buildings to the construction of a sprayed concrete lining (SCL) tunnel, 12m in diameter, with jet grouting and face reinforcement.In both studies, a comparison of the building settlement and horizontal displacement profiles, with the greenfield ground movements, enables the soil structure interaction to be quantified. Encouraging agreement between the modification to the greenfield settlement profile, displayed by the buildings, and estimates made from existing predictive tools is observed. Similarly, both studies indicate that the horizontal strains, induced in the buildings, are typically at least an order of magnitude smaller than the greenfield values. This is consistent with observations in the literature. The potential modification to the settlement distortions is shown to have significant implications on the estimated level of damage. Potential issues for infrastructures connected to buildings, arising from the embedment of rigid buildings into the soil, are also highlighted
Development and Characterization of an Enzymatic Method for the Rapid Determination of Gamma Hydroxybutyric Acid
Gamma hydroxybutyric acid (GHB) is a regulated therapeutic drug, which naturally occurs in mammalian brain tissues as an intermediate of the GABA (gamma aminobutyric acid) neurotransmitter metabolism. The increasing misuse of GHB as a narcotic or abusing drug in recent years calls for
the development of a simple and rapid screening method as an alternative to the currently available, technically demanding diagnostic methods. We have developed a rapid enzymatic assay based on the GHB dehydrogenase of Ralstonia eutropha. The enzyme is expressed as a recombinant protein
in Escherichia coli and characterized in terms of reaction mechanism and kinetic parameters for the catalysis of conversion of GHB into succinic semialdehyde (SSA). The concomitant NADH production enables spectrophotometric monitoring of the reaction and the quantification of GHB in
physiological fluids depending on initial velocities. We have tested a panel of twelve serum and urine samples containing GHB concentrations from 0.0 to 2.1 mmol/L. GHB dehydrogenase activity obeys a non classical bi bi ping pong mechanism exhibiting substrate inhibition by NAD+.
With an optimal NAD+ concentration of 3.7 mmol/L in the reaction, the enzyme yields a KM of 1.0 mmol/L for GHB and a Vmax of 3.37 mmol/min/mg. The assay shows a linear standard curve from 0.1 to at least 1 mmol/L of GHB. Spiking experiments result in mean recoveries
of 92% for urine and 114% for serum, respectively. The comparison to an ion chromatographic reference method exhibits a mean difference of 10% divergence from the target values in urine and 9% in serum, respectively
Antimalarials with Benzothiophene Moieties as Aminoquinoline Partners
Malaria is a severe and life-threatening disease caused by Plasmodium parasites that are spread to humans through bites of infected Anopheles mosquitoes. Here, we report on the efficacy of aminoquinolines coupled to benzothiophene and thiophene rings in inhibiting Plasmodium falciparum parasite growth. Synthesized compounds were evaluated for their antimalarial activity and toxicity, in vitro and in mice. Benzothiophenes presented in this paper showed improved activities against a chloroquine susceptible (CQS) strain, with potencies of IC50 = 6 nM, and cured 5/5 Plasmodium berghei infected mice when dosed orally at 160 mg/kg/day x 3 days. In the benzothiophene series, the examined antiplasmodials were more active against the CQS strain D6, than against strains chloroquine resistant (CQR) W2 and multidrug-resistant (MDR) TM91C235. For the thiophene series, a very interesting feature was revealed: hypersensitivity to the CQR strains, resistance index (RI) of lt 1. This is in sharp contrast to chloroquine, indicating that further development of the series would provide us with more potent antimalarials against CQR strains
Supplementary data for article : KonstantinoviÄ, J. M.; SelakoviÄ, M.; Srbljanovic, J.; Djurkovic-Djakovic, O.; BogojeviÄ, K.; Sciotti, R.; Å olaja, B. A. Antimalarials with Benzothiophene Moieties as Aminoquinoline Partners. Molecules 2017, 22 (3). https://doi.org/10.3390/molecules22030343
Supplementary material for: [https://doi.org/10.3390/molecules22030343]Related to published version: [http://cherry.chem.bg.ac.rs/handle/123456789/2441
Supplementary data for article: Opsenica, I.; Tot, M.; Gomba, L.; Nuss, J. E.; Sciotti, R. J.; Bavari, S.; Burnett, J. C.; Å olaja, B. A. 4-Amino-7-Chloroquinolines: Probing Ligand Efficiency Provides Botulinum Neurotoxin Serotype A Light Chain Inhibitors with Significant Antiprotozoal Activity. Journal of Medicinal Chemistry 2013, 56 (14), 5860ā5871. https://doi.org/10.1021/jm4006077
Supporting information for: [https://doi.org/10.1021/jm4006077]Related to published version: [http://cherry.chem.bg.ac.rs/handle/123456789/1381
- ā¦