224 research outputs found

    Solvent Effect on Electrochemical CO<sub>2</sub> Reduction Reaction on Nanostructured Copper Electrodes

    Get PDF
    The electrochemical reduction of CO2 (CO2RR) is a sustainable alternative for producing fuels and chemicals, although the production of highly desired hydrocarbons is still a challenge due to the higher overpotential requirement in combination with the competitive hydrogen evolution reaction (HER). Tailoring the electrolyte composition is a possible strategy to favor the CO2RR over the HER. In this work we studied the solvent effect on the CO2RR on a nanostructured Cu electrode in acetonitrile solvent with different amounts of water. Similar to what has been observed for aqueous media, our online gas chromatography results showed that CO2RR in acetonitrile solvent is also structure-dependent, since nanocube-covered copper (CuNC) was the only surface (in comparison to polycrystalline Cu) capable of producing a detectable amount of ethylene (10% FE), provided there is enough water present in the electrolyte (&gt;500 mM). In situ Fourier Transform Infrared (FTIR) spectroscopy showed that in acetonitrile solvent the presence of CO2 strongly inhibits HER by driving away water from the interface. CO is by far the main product of CO2RR in acetonitrile (&gt;85% Faradaic efficiency), but adsorbed CO is not detected. This suggests that in acetonitrile media CO adsorption is inhibited compared to aqueous media. Remarkably, the addition of water to acetonitrile has little quantitative and almost no qualitative effect on the activity and selectivity of the CO2RR. This indicates that water is not strongly involved in the rate-determining step of the CO2RR in acetonitrile. Only at the highest water concentrations and at the CuNC surface, the CO coverage becomes high enough that a small amount of C2+ product is formed

    Modelos acoplados do IPCC-AR4 e o gradiente meridional de temperatua da superficie do mar no atlântico tropical : relaçoes com a precipitaçao no norte do nordeste do Brasil

    Get PDF
    Este artigo mostra como três modelos acoplados do Intergovernmental on Panel Climate Change - (IPCC-AR4), o FGOALS1. 0G &#8211; LASG do Institute of Atmospheric Physics of China, o GISSER da National Aeronautics Space Admnistration (NASA) e o GFDL_CM2 da National Oceanic and Atmospheric Administration (NOAA), simularam a variabilidade do gradiente meridional de Temperatura da Superfície do Mar (TSM), entre os meses de fevereiro a maio, no Atlântico Tropical (1901-1999). A precipitação durante a estação chuvosa (fevereiro a maio) no setor norte do Nordeste do Brasil (NEB) foi também analisada pelos três modelos e comparada com as observações. Os modelos GISSER e FGOALS1.0G mostraram melhor desempenho na simulação do sinal do gradiente meridional de TSM no Atlântico Tropical para o período de 1901 a 1999. Destaca-se que os modelos apresentaram um melhor desempenho na simulação da tendência decadal, conseguindo explicar entre 50% a 80% da variabilidade do gradiente, com a TSM do setor sul sendo mais bem simulada

    Expanded Bed Adsorption Of Bromelain (e.c. 3.4.22.33) From Ananas Comosus Crude Extract

    Get PDF
    This work focuses on the adsorption of Bromelain in expanded bed conditions, such as the adsorption kinetics parameters. The adsorption kinetics parameters showed that after 40 minutes equilibrium was achieved and maximum adsorption capacity was 6.11 U per resin mL. However, the maximum adsorption capacity was only determined by measuring the adsorption isotherm. Only by the Langmuir model the maximum adsorption capacity, Qm, and dissociation constant, kd, values could be estimated as 9.18 U/mL and 0.591, respectively, at 25°C and 0.1 mol/L phosphate buffer pH 7.5. A column made of glass with an inner diameter of 1 cm was used for the expanded bed adsorption (EBA). The residence time was reduced 10 fold by increasing the expansion degree 2.5 times; nonetheless, the plate number (N) value was reduced only 2 fold. After adsorption, the bromelain was eluted in packed bed mode, with a downward flow. The purification factor was about 13 fold and the total protein was reduced 4 fold. EBA showed to be feasible for purification of bromelain.261149157Amersham Pharmacia Biotech. EBA Handbook: Principles and Methods. Uppsala, ISBN 91-630-5519-8 (1997)Anspach, F.B., Curbelo, D., Hartman, R., Garke, G., Deckwer, W.D., Expanded-bed chromatography in primary protein purification (1999) J. Chromatogr. A, 865, p. 129Bruce, L.J., Chase, H.A., Hydrodynamics and adsorption behaviour within an expanded bed adsorption column studied using in-bed sampling (2001) Chem. Eng. Sci, 56, p. 3149Camprubi, S., Bruguera, M., Canalias, F., Purification of recombinant histidine-tag streptolysin O using immobilized metal affinity expanded bed adsorption (IMA-EBA). International (2006) J. Biol. Macromolecules, 38, pp. 134-139Chang, Y.K., McCreath, G.E., Chase, H.A., (1994) Advances in Bioprocess Engineering, p. 519. , Galindo, E, Ramirez, O.T, Eds, Kluwer Academics Publisher: Netherlands, pChase, H.A., Purification of proteins by adsorption chromatography in expanded beds (1994) Trends Biotechnol, 12, p. 296Dainiak, M.B., Galaev, I.Y., Matiasson, B., Direct capture of product from fermentation broth using a cell-repelling ion exchanger (2002) J. Chromatogr. A, 942, pp. 123-131Deutscher, M.P., Guide to protein purification (1990) Method. Enzymol, p. 182Fernandez-Lahore, H.M., Lin, D.-Q., Hubbuch, J.J., Kula, M.R., Thommes, J., The use of ionselective electrodes for evaluating residence time distributions in expanded bed adsorption systems (2001) Biotechnol. Progr, 17, pp. 1128-1136Gaspani, L., Limiroli, E., Ferrario, P., Bianchi, M., In vivo and in vitro effects of bromelain on PGE(2) and SP concentrations in the inflammatory exudate in rats (2002) Pharmacology, 65, pp. 83-86Haq, S.K., Rasheedi, S., Khan, R.H., Characterization of a partially folded intermediate of stem bromelain at low pH (2002) Eur. J. Biochem, 269, pp. 47-52Harrach, T., Eckert, K., Maurer, H.R., Machleidt, I., Machleidt, W., Nuck, R., Isolation and characterization of two forms of an acidic bromelain stem proteinase (1998) J. Protein Chem, 17, pp. 351-361Hatano, K., Sawano, Y., Tanokura, M., Structure-function relationship of bromelain isoinhibitors from pineapple stem (2002) Biol. Chem, 383, pp. 1151-1156Hatano, K., Tanokura, M., Takahashi, K., The amino acid sequences of isoforms of the bromelain inhibitor from pineapple stem (1998) J. Biochem, 124, pp. 457-461Hjorth, R., Expanded bed adsorption in industrial bioprocessing: Recent developments (1997) Trends Biotechnol, 15, p. 230Hochstrasser, D.F., Patchornik, A., Merril, C.R., Development of Polyacrylamide gels that improve the separation of proteins and their detection by silver staining (1998) Analyt. Biochem, 173, pp. 412-423Hochstrasser, D.F., Merril, C.R., Catalysts' for Polyacrylamide gel polymerization and detection of proteins by silver staining (1998) Appl. Theor. Electrophoresis, 1, pp. 35-40Hebbar, H.U., Sumana, B., Raghavarao, K.S.M.S., Use of reverse micellar systems for the extraction and purification of bromelain term from pineapple wastes (2008) Bioresource Technology, 99, pp. 4896-4902Khan, R.H., Rasheedi, S., Haq, S.K., Effect of pH, temperature and alcohols on the stability of glycosylated and deglycosylated stem bromelain (2003) J. Biosci, 28, pp. 709-714Kim, M. H., Kim, H. K., Lee, J. K., Park, S. Y., Oh, T. K., Thermostable lipase of Bacillus stearothermophilus, high level production, purification and calciumdependent thermostability. Korea Res. Inst. Biosci. Biotechnol. 64:280-286 (2000)Kordel, M., Hofmann, B., Schomburg, D., Schimid, R.D., Extracelluar lipase of Pseudomonas sp. strain ATCC 21808: Purification, characterization, crystallization and preliminary X-ray diffraction data (1991) J. Bacteriol, 173, pp. 4836-4841Kunitz, M., Crystalline soybean trypsin inhibitor: II general properties (1974) J. Gen. Physiol, 30, pp. 291-310Lali, A.M., Khare, A.S., Joshi, J.B., Behaviour of solid particles in viscous non-newtonian solutions: Settling velocity, wall effects and bed expansion in solid-liquid fluidized beds (1989) Powder Tech, 57, pp. 39-50Maurer, H.R., Bromelain: Biochemistry, pharmacology and medical use (2001) Cell. Mol. Life Sci, 58, pp. 1234-1245Mullick, A., Flickinger, M.C., Expanded bed adsorption of human serum albumin from very dense saccharomyces cerevesiae suspensions on fluoride-modified zirconia (1999) Biotechnol. Bioeng, 65, pp. 282-290Murachi, T., Bromelain enzymes (1976) Methods Enzymol, 45, pp. 475-485Ota, S., Horie, K., Hagino, F., Hashimoto, C., Date, H., Fractionation and some properties of the proteolytically active components of bromelains in the stem and the fruit of the pineapple plant (1972) J. Biochem, 71, pp. 817-830Rasheedi, S., Haq, S.K., Khan, R.H., Guanidine hydrochloride denaturation of glycosylated and deglycosylated stem bromelain (2003) Biochemistry, 68, pp. 1097-1100Roy, I., Pai, A., Lali, A., Gupta, M.N., Comparison of batch, packed bed and expanded bed purification of A. niger cellulose beads (1999) Bioseparation, 8, pp. 317-326Santos, E.S., Guirardello, R., Franco, T.T., Distributor Effect on Expanded Bed Adsorption (2000) International Conference IEX 2000 (Ion Exchange at the Millennium), , Cambridge/UKSantos, E.S., Guirardello, R., Franco, T.T., Preparative chromatography of xylanase using expanded bed adsorption (2002) J. Chrom. A, 944, pp. 217-224Silveira, E., (2007) Purificação e caracterização de bromelina a partir do extrato bruto de Ananas comosus por adsorção em leito expandido, , Dissertação de Mestrado. Faculdade de Engenharia Química: UnicampSilverstein, R.M., Kezdy, F.J., Characterization of the pineapple stem proteases (bromelain) (1975) Arch. Biochem.Biophys, 167, pp. 678-686Suh, H.J., Lee, H., Cho, H.Y., Yang, H.C., Purification and characterization of bromelain isolated from pineapple (1992) Han'guk Nonghwa Hakhoechi, 35, pp. 300-307Takahashi, N., Yasuda, Y., Goto, K., Miyake, T., Murachi, T., Multiple molecular forms of stem bromelain. Isolation and characterization of two closely related components, SB1 and SB2 (1973) J. Biochem, 74, pp. 355-373Tan, Y.P., Ling, T.C., Tan, W.S., Yusoff, K., Tey, B.T., Purification of recombinant nucleocapsid protein of Newcastle disease virus from unclarifled feedstock using expanded bed adsorption chromatography (2006) Prot. Expr. Purif, 46, pp. 114-121Thömmes, J., Fluidized bed adsorption as a primary recovery step in protein purification (1997) Adv. Biochem. Eng, 58, p. 185Toledo, A.L., Severo, J.J.B., Souza, R.R., Campos, E.S., Santana, J.C.C., Tambourgi, E.B., Purification by expanded bed adsorption and characterization of an a-amylase FORILASE NTL®from A. niger (2006) J. Chrom. B, 846, pp. 51-56Trinh, L., Phue, J.-N., Jaluria, P., Tsai, C.W., Narum, D.L., Shiloach, J., Screen-less expanded bed column: New approach for the recovery and purification of a malaria transmission blocking vaccine candidate from Pichia pastoris (2006) Biotechnol. Lett, 28, pp. 951-958Walter, H. E., Proteinases: methods with hemoglobin, casein, and azocoll as substrates. Pp. 270-277 in Methods of Enzymatic Analysis, 5, H.U. Bergmeyer, ed. Verlag Chemie, Weinheim, Germany (1984)Wang, S.-L., Peng, J.-H., Liang, T.-W., Liu, K.-C., Purification and characterization of a chitosanase from Serratia marcescens TKU011 (2008) Carbohydrate Research, 343, pp. 1316-1323Wharton, C.W., The structure and mechanism of stem bromelain. Evaluation of the homogeneity of purified stem bromelain, determination of the molecular weight and kinetic analysis of the bromelain-catalysed hydrolysis of N-benzyloxycarbonyl-L-phenylalanyl-L-serine methyl ester (1974) Biochem. J, 143, pp. 575-586Wheelwright, S.M., (1994) Protein purification: Design and scale up of downstream processing, , Munich: Hanser PublishersYamamoto, S., Okamoto, A., Walter, P., Effects of adsorbent properties on zone spreading in expanded bed chromatography (2001) Bioseparation, 1, pp. 1-10Yun, J.X., Yao, S.-J., Lin, D.-Q., Lu, M.-H., Zhao, W.-T., Modeling axial distributions of adsorbent particle size and local voidage in expanded bed (2004) Chem. Eng. Sci, 59, p. 449Yun, X.L., Lin, D.-Q., Lu, M.-H., Zhong, L.-N., Yao, S.-L., Measurement and modeling of axial distribution of adsorbent particles in expanded bed: Taking into account the particle density difference (2004) Chem. Eng. Sci, 59, p. 587

    Resonance fluorescence from a telecom-wavelength quantum dot

    Get PDF
    © 2016 Author(s).We report on resonance fluorescence from a single quantum dot emitting at telecom wavelengths. We perform high-resolution spectroscopy and observe the Mollow triplet in the Rabi regime - a hallmark of resonance fluorescence. The measured resonance-fluorescence spectra allow us to rule out pure dephasing as a significant decoherence mechanism in these quantum dots. Combined with numerical simulations, the experimental results provide robust characterisation of charge noise in the environment of the quantum dot. Resonant control of the quantum dot opens up new possibilities for the on-demand generation of indistinguishable single photons at telecom wavelengths as well as quantum optics experiments and direct manipulation of solid-state qubits in telecom-wavelength quantum dots

    Exopolysaccharides, proteins and lipids in Pleurotus pulmonarius submerged culture using different carbon sources

    Get PDF
    AbstractFor many years mushrooms have been consumed and appreciated by their nutritional value, and medicinal properties. The traditional mushroom cultivation takes too long and the macrofungi biotechnology has not been explored in its full potential yet. The goal of this work was to observe if different carbon sources could improve the yield and diversify fungi nutrient composition in submerged culture.Pleurotus pulmonarius mycelia and exopolysacharide productions were evaluated using glucose, galactose, xylose and arabinose. The mycelia yield varied depending on the culture medium, and galactose showed to be the best carbon source to produce EPS. Samples that showed the highest protein contents were grown with xylose (19.44%) and arabinose (26.05%). Furthermore, the biomass cultivated with these carbohydrates and with galactose showed five essential amino acids. All cultured biomass showed low lipid contents (∼1%), being composed mainly of unsaturated fatty acids. All EPS fractions showed as main structures glucans and mannogalactans

    Spatial analysis of leptospirosis and toxoplasmosis seroprevalence in the canine population in an area of socioeconomic and environmental vulnerability

    Get PDF
    ABSTRACT Leptospirosis and toxoplasmosis are zoonoses of occupational character that are spread worldwide, mainly in tropical and socioeconomically vulnerable areas. Both diseases have vertebrate hosts, which spread the infectious agent to the environment and are potentially infectious to humans and can progress to fatal cases. The present study reinforces the importance of One Health for the control and prophylaxis of leptospirosis and toxoplasmosis using sentinel animals in areas of socioeconomic vulnerability based on a serological study. A total of 336 blood samples were obtained from the canine population of the urban district, which has high rates of poverty and sanitation. The results were analyzed based on seroreactivity animals and georeferencing by kernel spatial mapping. A total of 43.3% (52/120) of the animals were seroreagents for anti-Leptospira spp., with a predominance of Canicola (35/52 = 67.3%) and Pyrogenes (5/52 = 9.6%), while 52.97% (178/336) of the dogs were seroreactive for anti-Toxoplasma gondii. The presence of seroreagent dogs for both zoonosis alert to the inadequate hygienic-sanitary conditions of the studied region, and highlight the importance of a survey of the social, economic and environmental structure to identify factors related to the links in the epidemiological chain of pathogen transmission and necessary corrective actions

    Bifidobacterium animalis subsp lactis HN019 presents antimicrobial potential against periodontopathogens and modulates the immunological response of oral mucosa in periodontitis patients

    Get PDF
    Objective To evaluate the effects of Bifidobacterium animalis subsp. lactis HN019 (HN019) on clinical periodontal parameters (plaque accumulation and gingival bleeding), on immunocompetence of gingival tissues [expression of beta-defensin (BD)-3, toll-like receptor 4 (TLR4), cluster of differentiation(CD)-57 and CD-4], and on immunological properties of saliva (IgA levels) in non-surgical periodontal therapy in generalized chronic periodontitis (GCP) patients. Adhesion to buccal epithelial cells (BEC) and the antimicrobial properties of HN019 were also investigated. Materials and methods Thirty patients were recruited and monitored clinically at baseline (before scaling and root planing—SRP) and after 30 and 90 days. Patients were randomly assigned to Test (SRP+Probiotic, n = 15) or Control (SRP+Placebo, n = 15) group. Probiotic lozenges were used for 30 days. Gingival tissues and saliva were immunologically analyzed. The adhesion of HN019 with or without Porphyromonas gingivalis in BEC and its antimicrobial properties were investigated in in vitro assays. Data were statistically analyzed (p</p
    corecore