51 resultados para Malpighia
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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Os teores de micronutrientes nas folhas necessários para obter boa produtividade e qualidade de frutos de aceroleira (Malpighia emarginata DC.) e sua variação sazonal são pouco conhecidas. Para melhor entendimento da dinâmica de absorção de nutrientes e o desenvolvimento dessa frutífera avaliaram-se teores foliares de Cu, Fe, Mn e Zn, em seis progênies de aceroleira no período de dezembro de 1999 a outubro de 2000. O estudo foi conduzido na Empresa Brasileira de Pesquisa Agropecuária (EMBRAPA) Agroindústria Tropical, em Pacajus, e envolveu 6 progênies (P52, P66, P78, P91, P93 e P97) e 6 épocas de amostragem das folhas (dezembro, fevereiro, abril, junho, agosto e outubro de 2000). A variação sazonal foi confirmada para os teores de Cu, Fe, Mn e Zn nas folhas, enquanto o Zn não sofreu alteração significativa nas progênies consideradas pela pesquisa. Os teores de Cu foram superiores em fevereiro, e os de Fe e Mn em agosto. As progênies apresentaram habilidade diferenciada na manutenção das concentrações de Cu, Mn e Zn nas folhas. A melhor época para amostragem de folhas e diagnóstico do estado nutricional foi em outubro, início do florescimento das aceroleiras, quando os teores de Cu, Fe, Mn e Zn devem ser superiores a 3, 125, 80 e 15 mg/kg.
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Knowing that maternal diabetes is related to hyperglycemia and fetal hyperinsulinemia, which affect the lipid metabolism, the aim of this study was to evaluate the effects of Malpighia emarginata (acerola) juice on the glycemic and lipid profile of offspring of diabetic and nondiabetic Wistar rats. The adult offspring of non-diabetic dams and of dams with severe streptozotocin-induced diabetes were divided into groups: G1, offspring (of control dams) treated with water, G2, offspring (of diabetic dams) treated with water, G3, male offspring (of control dams) treated with acerola juice, and G4, male offspring (of diabetic dams) treated with acerola juice. The offspring of diabetic dams treated with acerola juice showed significantly decreased levels of glucose, cholesterol, triglycerides, and increased HDL-c. The use of acerola juice is a potential strategy to aid in the prevention of DM and dyslipidemia and its complications or to act as an auxiliary in the treatment of these diseases.
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Com o objetivo de avaliar o uso do ácido giberélico (GA3) e da benzilaminopurina (BAP) na conservação de acerolas (Malpighia glabra L.) colhidas no estádio verde e armazenadas sob refrigeração, acerolas foram submetidas aos seguintes tratamentos, sob imersão por 30 minutos: controle (água), 50 mg L-1 e 100 mg L-1 de GA3, 50 mg L-1 e 100 mg L-1 de BAP. Após os tratamentos, os frutos foram deixados para secar ao ar em local fresco e, então, embalados em bandejas de isopor cobertas com filme de polietileno e armazenados em câmara B.O.D a 8±1ºC, por 14 dias. As avaliações foram realizadas em intervalos de 4 dias. Os frutos amostrados foram submetidos a avaliações de coloração, teor de sólidos solúveis, acidez titulável e teor de ácido ascórbico. A análise dos resultados mostrou que a aplicação dos reguladores não teve efeito no aumento da conservação refrigerada de acerolas e que somente a refrigeração foi suficiente para conservá-las durante 14 dias.
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INTRODUÇÃO: Este estudo investigou o tempo necessário de suplementação com vitamina C, para a normalização dos níveis séricos em idosos com deficiência dessa vitamina e comparar o efeito da vitamina natural do suco de acerola (Malpighia glabra L.) com o da vitamina na forma de fármaco. MÉTODOS: Foram estudados 37 idosos institucionalizados do município de João Pessoa, Paraíba, Brasil, divididos em 3 grupos: Grupo I - controle, Grupo II - suplementação com o suco de acerola e Grupo III - suplementação com fármaco. A metodologia empregada consistiu na dosagem sérica de ácido ascórbico e na verificação do consumo alimentar por inquérito dietético. Constatou-se um aumento significativo (p<0,05) nas médias dos níveis séricos de ácido ascórbico, após 10 dias (1,27±0,41mg/dL), 20 (1,69±0,45mg/dL) e 30 dias (1,55±0,42mg/dL) de suplementação aos valores iniciais (0,38±0,28mg/dL). No 10º dia de suplementação, os idosos suplementados com suco de acerola apresentaram níveis significativamente mais elevados (1,41±0,43mg/dL) do que aqueles que foram suplementados com comprimidos (1,03±0,25mg/dL). CONCLUSÃO: Considerando-se que, no 20º dia, o efeito da suplementação foi satisfatório para a normalização dos níveis séricos daqueles indivíduos, esse tempo poderia ser utilizado para idosos em geral e, em especial, para aqueles que vivem em instituições destinadas a idosos carentes, sendo o suco de acerola um suplemento indicado por ser um produto natural e de fácil aquisição.
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The content of ascorbic acid was assayed in acerolas harvested in three phases of maturation: green-yellow fruits (I); light red (II) and wine-coloured (III). Phase I and Phase II fruit were packed in aluminium sheets and stoppered flasks and stored in freezer (-10o.C) and in refrigerator (8o.C). Samples of 8 fruits from each experimental condiction were analysed for ascorbic acid determination by 2-chlorophenol indophenol discolouration method. The averages of 1.393,5 mg./100g. for Phase I sample, 1024,9 for Phase II and 756,5 for Phase III fruits, showed a statistically significative linear decreasing of the ascorbic acid content related with the maturation extent Phase I samples stored in freezing showed statitically significative decreasing of that vitamin at 408 hours of storage in both: aluminium sheet and stoppered flask package; in chilling temperature there was significative reduction of ascorbic acid content after 240 and 312 hours, respectively, for fruits packed in aluminium sheet and stopped flasks. Phase Il samples showed significative lost at 72 hours of storage when maintained in freezing temperature either, in aluminium sheet or in stoppered flasks: When stored in chilling temperature showed progressive lost of ascorbic acid in all measuring periods in every package. After 144 hours suffered deterioration suggested by colour changes.
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The aim of this work was to develop an efficient reactor for the production of low methoxyl pectin, using pectinmethylesterase (PME, EC 3.1.1.11) from acerola immobilized on silica. The immobilized enzyme was used in up to 50 successive bioconversion runs at 50 degrees C with an efficiency loss of less than 20%. The fixed-bed reactor (6.0 x 1.5 cm) was prepared using PME immobilized in glutaraldehyde-activated silica operated at 50 degrees C with an optimum flow rate of 10 mL h(-1). The bioconversion yield was shown to strongly depend on the nature of the enzymatic preparation. An efficiency of 44% was achieved when concentrated PME was used, compared with only 30% with purified PME, both after an 8-h run. The process described could provide the basis for the development of a commercial-scale process. (c) 2006 Society of Chemical Industry.
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The total and partially purified enzyme pectinmethylesterase from acerola fruit was covalently immobilized on porous silica particles. These efficiency values were 114% for the total PME and 351% for the partially purified PME. In both forms the immobilization resulted in compounds with high thermal stability.
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A partially purified extract of pectinmethylesterase (PME) from acerola fruit was immobilized on various supports: glass, celite, chrysotile, agarose, concanavalin A Sepharose 4B, egg shell, polyacrylamide and gelatin. In addition, reticulation with glutaraldehyde was assessed, as well as the use of gelatin in the presence of celite, glass and silica. The highest immobilization yields were obtained when the pectinmethylesterase was immobilized in concanavalin A Sepharose 4B (81.7%) and in gelatin-water (78.0%). (C) 2004 Society of Chemical Industry.
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The enzyme pectin methylesterase (PME) is present in acerola fruit and was partially purified by gel filtration on Sephadex G-100. The results of gel filtration showed different PME isoforms. The total PME (precipitated by 70% salt saturation) and one of these isoforms (fraction from Sephadex G-100 elution) that showed a molecular mass of 15.5 +/- 1.0 kDa were studied. The optimum pH values of both forms were 9.0. The total and the partially purified PME showed that PME specific activity increases with temperature, the total acerola PME retained 13.5% of its specific activity after 90 min of incubation at 98 degreesC. The partially purified acerola (PME isoform) showed 125.5% of its specific activity after 90 min of incubation at 98 degreesC. The K-m values of the total PME and the partially purified PME isoform were 0.081 and 0.12 mg/mL, respectively. The V-max values of the total PME and the partially purified PME were 2.92 and 6.21 mumol/min/mL/mg of protein, respectively.
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The composition of substrates with different sources of organic matter is considered as a key factor to obtain seedlings of good quality. Then, this study aimed to evaluate the best source and the best quantity of organic matter that should be used in order to produce barbados cherry (Malpighia emarginata DC.) seedlings of good quality. A factorial arrangement of four (20: 80, 40: 60, 60:40 and 80:20% of organic matter: earth) by four (earthworm compost, burnt rice husk, powdered coconut husk and carnauba straw) levels was used and it was designed in randomized blocks with four replicates. The nitrogen, phosphorus, potassium and calcium content of the leaves and stems were quantified in the dry tissue. The results showed that the proportion 80% of earthworm compost: 20% of earth allowed good development of the plants and sufficient accumulation of N, P, K and Ca. Burnt rice husk, powdered coconut husk and carnauba straw have not generated seedlings of good quality.
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The enzyme pectinmethylesterase (PME) from acerola was extracted and purified by gel anion-exchange chromatography (Q Sepharose) and filtration on Sephadex G-100. The results showed two different PME isoforms (PME1 and PME2), with molecular masses of 25.10 and 5.20 kDa, respectively. PMEI specific activity increased by 9.63% after 60 min incubation at 98 degrees C, while PME2 retained 66% of its specific activity under the same conditions. The K-m values of PMEI, PME2 and concentrated PME were 0.94, 0.08 and 0.08mg mL(-1), respectively. The V-max value of PMEI, PME2 and concentrated were 204.08, 2, 158.73 and 2.92 mu mol min(-1) mg(-1) protein, respectively. (c) 2007 Society of Chemical Industry.
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Pós-graduação em Alimentos e Nutrição - FCFAR
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)