Gemini spectra of 12000K white dwarf stars

We report signal-to-noise ratio SNR ~ 100 optical spectra for four DA white dwarf stars acquired with the GMOS spectrograph of the 8m Gemini north telescope. These stars have 18<g<19 and are around Teff ~ 12000 K, were the hydrogen lines are close to maximum. Our purpose is to test if the effective temperatures and surface gravities derived from the relatively low signal-to-noise ratio ( ~ 21) optical spectra acquired by the Sloan Digital Sky Survey through model atmosphere fitting are trustworthy. Our spectra range from 3800A to 6000A, therefore including H beta to H9. The H8 line was only marginally present in the SDSS spectra, but is crucial to determine the gravity. When we compare the values published by Kleinman et al. (2004) and Eisenstein et al. (2006) with our line-profile (LPT) fits, the average differences are: Delta Teff ~ 320 K, systematically lower in SDSS, and Delta log g ~ 0.24 dex, systematically larger in SDSS. The correlation between gravity and effective temperature can only be broken at wavelengths bluer than 3800 A. The uncertainties in Teff are 60% larger, and in log g larger by a factor of 4, than the Kleinman et al. (2004) and Eisenstein et al. (2006) internal uncertainties.Comment: 11 pages and 8 figure

Being a temporary agency worker: A motivation profile analysis

info:eu-repo/semantics/draf

Escherichia coli expression, refolding and characterization of human laforin

Laforin is a unique human dual-specificity phosphatase as it contains an amino terminal carbohydrate binding module (CBM). Laforin gene mutations lead to Lafora disease, a progressive myoclonus epilepsy with an early fatal issue. Previous attempts to produce recombinant laforin faced various difficulties, namely the appearance of protein inclusion bodies, the contamination with bacterial proteins and a high tendency of the protein to aggregate, despite the use of fusion tags to improve solubility and ease the purification process. In this work, we have expressed human laforin in Escherichia coli in the form of inclusion bodies devoid of any fusion tags. After a rapid dilution refolding step, the protein was purified by two chromatographic steps, yielding 5–7 mg of purified protein per liter of bacterial culture. The purified protein was shown to have the kinetic characteristics of a dual-specificity phosphatase, and a functional carbohydrate binding module. With this protocol, we were able for the first time, to produce and purify laforin without fusion tags in the amounts traditionally needed for the crystallographic structural studies paving the way to the understanding of the molecular mechanisms of laforin activity and to the development of novel therapies for Lafora disease.Fundação para a Ciência e a Tecnologia (FCT) – Programa Operacional “Ciência, Tecnologia, Inovação” (POCTI

Expression of the functional carbohydrate-binding module (CBM) of human laforin

Laforin is a human protein associated with the glycogen metabolism, composed of two structurally and functionally independent domains: a phosphatase catalytic domain and a substrate-binding module with glycogen and starch affinity. The main goal of this work is the development of a methodology for the expression of the so far poorly characterized carbohydrate-binding module (CBM) of laforin, allowing its study and development of biomedical applications. The laforin’s CBM sequence was originally cloned by PCR from a human muscle cDNA library. The recombinant protein, containing laforin’s CBM fused to an Arg-Gly-Asp sequence (RGD), was cloned and expressed using vector pET29a and recovered as inclusion bodies (IBs). Refolding of the IBs allowed the purification of soluble, dimeric and functional protein, according to adsorption assays using starch and glycogen. Several other experimental approaches, using both bacteria and yeast, were unsuccessfully tested, pointing towards the difficulties in producing the heterologous protein. Indeed, this is the first work reporting the production of the functional CBM from human laforin.Fundação para a Ciência e a Tecnologia (FCT, Portugal)

Development of pH-sensitive magnetoliposomes containing shape anisotropic magnetic nanoparticles for applications in dual cancer therapy

In this work, anisotropic magnetic nanoparticles of mixed calcium/magnesium ferrite were synthesized and characterized. These nanoparticles were encapsulated in pH-sensitive liposomes loaded with doxorubicin, and the resulting nanosystems were characterized by DLS. Fluorescence emission assays were performed to elucidate the structural characterization and study the release profile of doxorubicin at different pH values and promising results were obtained for application in combined cancer therapy.FCT under Strategic funding of CF-UM-UP (UIDB/04650/2020)

Carbon footprint of apple and pear : orchards, storage and distribution

Apple and pear represent 51% of fresh fruit orchards in Portugal. This paper presents a life-cycle (LC) greenhouse gas (GHG) assessment (so-called carbon footprint) of 3 apple and 1 pear Portuguese production systems. An LC model and inventory were implemented, encompassing the farm stage (cultivation of fruit trees in orchards), storage and distribution (transport to retail). The functional unit considered in this study was 1 kg of distributed fruit (at retail). Four different LC inventories for orchards were implemented based on data collected from three farms. Inventory data from two storage companies were also gathered. The main results show that the GHG emissions of apple and pear ranged between 192 and 229 gCO2eq kgfruit-1. The GHG emissions (direct and indirect) from the cultivation phase ranged from 36% to 60% of total emissions. Fruit storage, which lasted for as much as 8-10 months, was also responsible for significant emissions due to high energy requirements

Analytical method for the determination of strychnine in tissues by gas chromatography/mass spectrometry: two case reports

This paper describes an analytical method for strychnine determination in biological samples by gas chromatography/mass spectrometry and their application in the investigation of two cases involving strychnine ingestion: A fatal case and a clinical one. The strychnine is isolated from biological samples using a liquid-liquid extraction procedure. The clean-up procedure is performed using an acid solution. Papaverine is used as internal standard in the quantification of strychnine. In the analysed specimens, the limits of quantification were 0.1 [mu]g/ml or 0.1 [mu]g/g. The recovery rate ranged from 75.0% to 98.7% and the coefficients of variation ranged from 4.8% to 10.5%.http://www.sciencedirect.com/science/article/B6T6W-408KCFB-8/1/f8bbeefad9e20909aef50467f67a2e8