313 resultados para Electrophoresis, Agar Gel
Resumo:
Polyacrylamide gel electrophoresis, SDS-PAGE system, was adjusted to detect the presence of additional whey in dairy beverages distributed in a Brazilian Government School Meals Program. Aqueous solutions of samples in 8 M urea were submitted to a polyacrylamide gel gradient (10% to 18%). Gel scans from electrophoresis patterns of previously adulterated milk samples showed that caseins peak areas decreased while peak areas of beta -lactoglobulin plus alpha -lactalbumin increased as the percentage of raw milk powder replaced by whey powder increased. The relative densitometer areas of caseins or beta -lactoglobulin plus alpha -lactalbumin plotted against the percentage of whey added to the raw milk showed a linear correlation coefficient square higher than 0.97. The caseins plot was used to determine the percentage of additional whey in 116 dairy beverages, chocolate or coffee flavor. Considering that the lowest relative caseins concentration found in commercial milk powder samples by the present method was 72%, the dairy beverages containing caseins percentages equal to or higher than this value were considered free of additional whey. Based on this criterion, about 49% of the coffee-flavor dairy beverages and 29% of the chocolate-flavor beverages, among all the samples analyzed were adulterated with whey protein to reach the total protein contents specified on their labels. The present method showed a sensitivity of 5% to additional whey.
Resumo:
Testou-se a utilização do CO2 supercrítico na extração seletiva de compostos oxigenados (linalol e acetato de linalila) contidos no óleo essencial de bergamota (Citrus bergamia Risso), var. bergamia, adsorvido em sílica gel contendo baixo teor de limoneno e bergapteno. A densidade do dióxido de carbono e a temperatura de extração foram otimizadas, e os extratos obtidos foram analisados por cromatografia. Nas condições estudadas, observou-se uma redução de 72% no teor de limoneno e 92,5% para o bergapteno, sendo extraídos 52% de linalol e 69,4% de acetato de linalila.
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O presente trabalho tem como objetivo determinar a influência das interações das gomas xantana e guar com o amido de milho de alto teor de amilose na textura de gel durante o armazenamento. Foram utilizadas amostras de amido milho Hylon VII® (71% de amilose, National Starch, goma guar (Higum 55I®, Rhodia) e goma xantana (Rhodigel 200®, Rhodia). Foram utilizadas diferentes concentrações das gomas guar e xantana, que variaram de 0 a 1%, de acordo com o delineamento experimental central composto rotacional. Em cada tratamento foram utilizadas 50g de amido com alto teor de amilose (Hylon VII), adicionadas das gomas. Estas amostras foram diluídas em água destilada e submetidas à agitação mecânica até completa dissolução. As soluções foram aquecidas até 95°C por 5 minutos para formação dos géis, os quais foram acondicionados em recipientes plásticos de 50mL e mantidos em temperatura de 5-10°C até 120h. Nos tempos T1 (24h), T2 (48h), T3 (72h), T4 (96h) e T5 (120h) de armazenamento foram feitas medidas da força máxima do gel de amilose em texturômetro (Stable Micro-System, Modelo TAX-T2). No período inicial, de 24 horas, a goma guar não apresentou influência positiva na redução da força do gel, sendo que a aplicação de goma xantana entre 0,7 e 1,0% apresentou os menores valores de força do gel de amilose. Após 120h de armazenamento, a força do gel de amilose diminuiu com a adição de 0,5-1,0% de goma xantana e 0-0,15% de goma guar.
Resumo:
Este trabalho objetivou a otimização da imobilização das enzimas amilases extraídas do malte do milho, usando alginato de sódio. A concentração do malte no extrato, a porcentagem de alginato de sódio e o pH foram usados como fatores que influenciam na imobilização das enzimas. Os resultados mostraram que as melhores condições de imobilização foram obtidas quando se usou as soluções de malte de milho em duas faixas de concentrações, uma entre 3,75 a 5 g.L-1 e outra entre 15 a 16,25 g.L-1, em pH entre 4,83 a 6,6 e 4% (m/v) de alginato de sódio, condições nas quais se conseguiu imobilizar 100% das enzimas com baixa perda de atividade. Este trabalho mostrou como se obter amilases de malte de milho imobilizadas por oclusão em alginato de sódio e que podem ser usadas em processos industriais de hidrólise de amido.
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Lactic acid bacteria are important in foods as potential probiotics and also due to the ability to produce antimicrobial compounds that can contribute for biopreservation. In this work, the bacteriocin produced by the food isolate Enterococcus faecium 130 was partially purified and characterized. The compound was active against Gram-positive bacteria, including Listeria monocytogenes. It was produced after 4 days of storage at a broad temperature range (4 to 37 °C); it was stable at pH ranging from 2 to 10 with no loss of activity after heating at 100 °C for 15 minutes. Bacteriocin was partially purified by the adsorption-desorption technique, and the analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) showed a molecular mass of 3.5 to 6.5 kDa. These data encourage studies on application of this bacteriocin in food systems as an additional hurdle to microbial growth.
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The aim of this study was to evaluate the influence of high hydrostatic pressure (150, 250, 350, 450, and 550 MPa), applied for 5 minutes, on antioxidant capacity, total phenolic content, color, firmness, rehydration ratio, and water holding capacity of aloe vera gel stored for 60 days at 4 °C. The analyzed properties of the pressurized gel showed significant changes after the storage period. The highest value of total phenolic content was found at 550 MPa. However, a decrease in the antioxidant capacity was observed for all pressurized gel samples when compared to the control sample (p < 0.05). The smallest changes in product color were observed at pressure levels between 150 and 250 MP. The application of high hydrostatic pressure resulted in lower gel firmness, and the lowest value was found at 150 MPa (p < 0.05). On the other hand, the untreated sample showed a greater decrease in firmness, indicating that high pressure processing preserves this property. The application of high hydrostatic pressure exhibited modifications in the food matrix, which were evaluated in terms of rehydration ratio and water holding capacity.
Resumo:
Decaffeinated coffee accounts for 10 percent of coffee sales in the world; it is preferred by consumers that do not wish or are sensitive to caffeine effects. This article presents an analytical comparison of capillary electrophoresis (CE) and high performance liquid chromatography (HPLC) methods for residual caffeine quantification in decaffeinated coffee in terms of validation parameters, costs, analysis time, composition and treatment of the residues generated, and caffeine quantification in 20 commercial samples. Both methods showed suitable validation parameters. Caffeine content did not differ statistically in the two different methods of analysis. The main advantage of the high performance liquid chromatography (HPLC) method was the 42-fold lower detection limit. Nevertheless, the capillary electrophoresis (CE) detection limit was 115-fold lower than the allowable limit by the Brazilian law. The capillary electrophoresis (CE) analyses were 30% faster, the reagent costs were 76.5-fold, and the volume of the residues generated was 33-fold lower. Therefore, the capillary electrophoresis (CE) method proved to be a valuable analytical tool for this type of analysis.
Resumo:
To investigate microbial diversity and identify spoilage bacteria in fresh pork sausages during storage, twelve industrial pork sausages of different trademarks were stored at 4 ºC for 0, 14, 28 and 42 days, 80% relative humidity and packaged in sterile plastic bags. Microbiological analysis was performed. The pH and water activity (a w) were measured. The culture-independent method performed was the Polymerase Chain Reaction - Denaturing Gradient Gel Electrophoresis (PCR-DGGE). The culture-dependent method showed that the populations of mesophilic bacteria and Lactic Acid Bacteria (LAB) increased linearly over storage time. At the end of the storage time, the average population of microorganisms was detected, in general, at the level of 5 log cfu g-1. A significant (P < 0.005) increase was observed in pH and a w values at the end of the storage time. The PCR-DGGE allowed a rapid identification of dominant communities present in sausages. PCR-DGGE discriminated 15 species and seven genera of bacteria that frequently constitute the microbiota in sausage products. The most frequent spoilage bacteria identified in the sausages were Lactobacillus sakei and Brochothrix thermosphacta. The identification of dominant communities present in fresh pork sausages can help in the choice of the most effective preservation method for extending the product shelf-life.
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There are several obstacles to the use of chymosin in cheese production. Consequently, plant proteases have been studied as possible rennet substitutes, but most of these enzymes are unsuitable for the manufacture of cheese. The aim of this study was to evaluate the potential of latex from Sideroxylon obtusifolium as a source of milk-clotting proteases and to partially characterize the enzyme. The enzyme extract showed high protease and coagulant activities, with an optimal pH of 8.0 and temperature of 55 °C. The enzyme was stable in wide ranges of temperature and pH. Its activity was not affected by any metal ions tested; but was inhibited by phenylmethanesulfonyl fluoride and pepstatin. For the coagulant activity, the optimal concentration of CaCl2 was 10 µmol L- 1. Polyacrylamide gel electrophoresis showed four bands, with molecular weights between 17 and 64 kDa. These results indicate that the enzyme can be applied to the cheese industry.
Resumo:
Milk is an important source of bioactive compounds. Many of these compounds are released during fermentation and refrigerated storage. The aim of this study was to determine the release of peptides by lactic acid bacteria in commercial fermented milk during refrigerated storage. The size and profile of peptides were analyzed by polyacrylamide gel electrophoresis and sizeexclusion HPLC. During electrophoresis, it was observed that the peptides were released from caseins, whereas β-lactoglobulin was the whey protein with the highest degradation. HPLC analysis confirmed the pattern of peptide formation observed in electrophoresis. Two fractions lower than 2 kDa with aromatic amino acids in their structure were separated. These results were consistent with those reported for structures of peptides with antihypertensive activity. Therefore, the presence of aromatic amino acids in the peptide fractions obtained increases the likelihood of finding peptides with such activity in refrigerated commercial fermented milk. In conclusion, during cold storage, peptides with different molecular weights are released and accumulated. This could be due to the action of proteinases and peptidases of the proteolytic system in lactic acid bacteria.
Resumo:
INTRODUÇÃO: A higienização das mãos é um importante procedimento para a prevenção de infecções relacionadas à diálise peritoneal. OBJETIVO: Comparar a eficácia de duas técnicas de higienização das mãos na redução do número de unidades formadoras de colônia em pacientes em programa de diálise peritoneal. MATERIAIS E MÉTODO: Ensaio Clínico controlado. Trinta indivíduos submetidos a três coletas da flora microbiológica das mãos, em três momentos distintos: antes e após higienização das mãos com água e sabão glicerinado; após aplicação de álcool-gel etílico glicerinado a 70%. Culturas obtidas da superfície dos dedos das mãos, diretamente em placas de Agar Sangue de Carneiro. RESULTADOS: O crescimento médio nas culturas foi 31, 30 e 12 unidades formadoras de colônia antes da higienização, após a lavagem com água e sabão glicerinado e após a fricção com álcool gel, respectivamente (p < 0, 001). Staphyloccocus epidermidis ou Estafilococo coagulase-negativo foi o germe predominante, presente em 93,7% das placas. CONCLUSÃO: A higienização com álcool gel produziu maior redução no número de unidades formadoras de colônia.
Resumo:
Dentre os processos que precedem a conservação em longo prazo, a secagem tem papel fundamental, uma vez que o conteúdo de água das sementes afeta diretamente a sua longevidade. Os objetivos desse trabalho foram pesquisar o efeito da umidificação prévia das sementes após ultrassecagem em diferentes teores de água sobre a qualidade fisiológica de sementes de girassol. Sementes com conteúdo inicial de água de 4,7% foram embebidas previamente até conteúdo de água de 10,2%, e submetidas à secagem lenta, conduzida em câmara de secagem, e à secagem rápida, em sílica gel, até conteúdos de água de 7,4; 3,2; 2,9% e 5,3; 3,2; 2,1%, respectivamente. Após a secagem rápida ou lenta, as sementes foram submetidas ou não à umidificação em caixas tipo "gerbox" até o teor de água de 15,8 a 17% e então avaliadas quanto à germinação, peso da matéria seca de raiz, parte aérea e total das plântulas e teste de condutividade elétrica. O delineamento experimental foi o inteiramente casualizado em esquema fatorial 5 (teores de água) x 2 (com e sem umidificação). Quando utilizado a secagem rápida, a germinação das sementes não é prejudicada, e a secagem lenta, até conteúdo de água de 2,9%, proporciona uma redução na germinação das sementes. Sementes de girassol podem ser desidratadas tanto em sílica gel quanto em câmara de secagem até teores de água de 3,2%, sem perda de germinação e vigor. O tratamento de umidificação após secagem propicia um melhor desenvolvimento de raiz e menores valores de condutividade elétrica nas sementes desidratadas em sílica gel e em câmara de secagem.
Resumo:
This study was done to evaluate the physiological and enzymatic alterations in papaya (Carica papaya L.) seeds during storage period. Seeds were extracted from mature fruits of Formosa group papaya hybrid Tainung 01. The sarcotesta was removed by rubbing the seeds on a wire screen under running water and then dried to the moisture content (MC) of 5, 8 or 11% The seeds were packed in multilayer paper bags, polyethylene bags, aluminum foil pouch and metallic canisters and stored for 15 months under laboratory conditions. Seeds were evaluated, at three month interval, for MC, germination, and the activity of acid phosphotase (AP) and malate dehyrogenase (MDH) was evaluated with the use of amide gel (12%) electrophoresis. The fresh seeds had post-harvest dormancy, which was broken after six month storage. Independent of the package type, the seeds could be stored for 12 months with 8 or 11% MC under ambient conditions. There was no association between seed deterioration and alterations in AP and MDH activity.