Goat milk production and quality on Tanzania-grass pastures, with supplementation.

It was evaluated the production and quality of milk produced by goats grazing Panicum maximum Jacq cv. Tanzania (Guineagrass) and receiving four levels of concentrate supplementation. Eight Anglo Nubian goats, aged between two and four years, 43.6 kg in average body weight and between the 2nd and 4th lactation were distributed into two 4 x 4 balanced Latin square design. The supplementation levels were: 0.0, 0.5, 1.0 and 1.5% of body weight. The concentrate was composed of corn and soybean meal. The intake of dry matter and nutrients, and the daily production of milk, 4% fat-corrected milk, fat, protein, lactose and total solids had increased (p < 0.05) with supplementation, whereas fat and total solids percentage were reduced (p < 0.05). The concentrate supplementation up to 1.5% of live weight in Tanzania-grass pasture raises the intake of dry matter and nutrients, resulting in a linear increase in milk production and of its components. [Produção e qualidade do leite de cabras em pasto cultivado de capim-Tanzânia suplementadas com concentrado]. Resumo: Avaliou-se a produção e qualidade do leite de cabras em pasto cultivado de Panicum maximum Jacq cv. Tanzânia sob níveis de suplementação com concentrado. Foram utilizadas oito cabras da raça Anglonubiana, com idade entre dois e quatro anos, peso médio de 43,6 kg, entre a 2ª e 4ª ordem de lactação, distribuídas em duplo quadrado latino balanceado 4 x 4. Os níveis de suplementação avaliados foram: 0,0; 0,5; 1,0 e 1,5% do peso vivo. O concentrado, foi composto por grão de milho e farelo de soja. O consumo de matéria seca e de nutrientes e as produções diárias de leite, de leite corrigido a 4% de gordura, gordura, proteína, lactose e sólidos totais aumentaram com a suplementação, enquanto que os teores de gordura e sólidos totais reduziram. A suplementação com concentrado em até 1,5% do peso vivo em pasto cultivado de capim-tanzânia promove aumento no consumo de matéria seca e de nutrientes da dieta, do que resulta o aumento linear na produção de leite e de seus constituintes

Atividade antioxidante total em frutos de diferentes genótipos de umbuzeiro oriundos de Petrolina, PE.

Este trabalho teve como objetivo avaliar a atividade antioxidante total dos extratos fenólicos obtidos de frutos de 32 genótipos de umbuzeiro através de dois métodos: ABTS e Sistema l3-caroteno/ácido linoléico

Maslinic Acid, a Natural Triterpene, Induces a Death Receptor-Mediated Apoptotic Mechanism in Caco-2 p53-Deficient Colon Adenocarcinoma Cells

Maslinic acid (MA) is a natural triterpene present in high concentrations in the waxy skin of olives. We have previously reported that MA induces apoptotic cell death via the mitochondrial apoptotic pathway in HT29 colon cancer cells. Here, we show that MA induces apoptosis in Caco-2 colon cancer cells via the extrinsic apoptotic pathway in a dose-dependent manner. MA triggered a series of effects associated with apoptosis, including the cleavage of caspases -8 and -3, and increased the levels of t-Bid within a few hours of its addition to the culture medium. MA had no effect on the expression of the Bax protein, release of cytochrome-c or on the mitochondrial membrane potential. This suggests that MA triggered the extrinsic apoptotic pathway in this cell type, as opposed to the intrinsic pathway found in the HT29 colon-cancer cell line. Our results suggest that the apoptotic mechanism induced in Caco-2 may be different from that found in HT29 colon-cancer cells, and that in Caco-2 cells MA seems to work independently of p53. Natural antitumoral agents capable of activating both the extrinsic and intrinsic apoptotic pathways could be of great use in treating colon-cancer of whatever origin.This study was supported by grants Group BIO 157 from the Technology and Innovation Council of the Andalucian regional government and AGL2006-12210-C03-02/ALI, SAF2005-01627, ISCIII-RTICC (RD06/0020/0046) from the Spanish government and European Union FEDER funds

Estratégia de transferência de tecnologia e comunicação para a sustentabilidade da sojicultura brasileira.

Estratégia de transferência de tecnologia e comunicação para a sustentabilidade da sojicultura brasileira, Introdução à prospecção de demandas da cadeia produtiva da soja, Estratégia de fortalecimento institucional, Planejamento estratégico de transferência de tecnologia e comunicação.bitstream/item/162787/1/DOC-392.pd

Estratégia de transferência de tecnologia e comunicação para a sustentabilidade da sojicultura brasileira.

Estratégia de transferência de tecnologia e comunicação para a sustentabilidade da sojicultura brasileira, Introdução à prospecção de demandas da cadeia produtiva da soja, Estratégia de fortalecimento institucional, Planejamento estratégico de transferência de tecnologia e comunicação.bitstream/item/162787/1/DOC-392.pd

Antioxidant compounds recovery from Juçara residue by thermal assisted extraction

This study aimed to recover bioactive compounds by solid-liquid extraction from the agro-industrial residue obtained during juçara fruits processing into pulp. A preliminary study using different solvents (methanol, ethanol and water) indicated ethanol in aqueous solution as the best solvent for antioxidants recovery. Then, a Box-Behnken design was applied considering as independent variables the solvent composition (3070% ethanol in water), temperature (3070 °C) and time (3060 min), in order to evaluate the effects of these factors on antioxidant activity in juçara extract. Results showed that the extracts with higher antioxidant activity were obtained using 30% ethanol at 70 °C for 60 min; measurements included ABTS and DPPH assays, determination of total phenolic content and total monomeric anthocyanins. Furthermore, the effect of pH in antioxidants recovery was evaluated. For this purpose, the 30% ethanol solution was acidified to pH 1 and 2 with HCl. Principal component analysis showed the formation of three distinct groups: one characterized by high bioactive compounds content (pH 1.0), another with superior antioxidant activity (pH 5.75, non-acidified), and finally the group at pH 2 presenting the worst concentrations in the evaluated responses. HPLC analysis showed the presence of cyanidin-3-O-rutinoside and cyanidin-3-O-glucoside in the extracts. Therefore, the conventional solid-liquid extraction using renewable solvent can be successfully applied to recover bioactive compounds from juçara residue, which can be used by different food industries.The authors gratefully acknowledge the institutions: Coordenação de Aperfeiçoamento Pessoal deEnsinoSuperior (CAPES), Universidade Federal do Rio de Janeiro, Embrapa Agroindústria de Alimentos and University of Minho by the financial support of the research work and Juçaí Alimentos for the juçara residue. Ricardo N. Pereira gratefully acknowledge to Portuguese Foundation for Science and Technology (FCT) the financial grant with reference SFRH/BPD/ 81887/2011.info:eu-repo/semantics/publishedVersio

Preservation and maceration of amazon açai leaflet Tissue to obtain genomic DNA.

The objective of this study was to test the efficiency of preservation and maceration methods for Euterpe precatoria leaflet tissue to obtain genomic DNA for molecular studies. The leaflets of E. precatoria were collected in an experimental field at Embrapa Acre, Brazil. The study was conducted in a completely randomized design with 10 replicates, in a 12 × 2 factorial structure, with 12 storage treatments (fresh; lyophiliser 3 days; refrigerator 3, 5, and 7 days; silica gel 7, 10, 20, and 30 days; and transport buffer 3, 5, and 7 days) and two leaf tissue maceration methods (liquid nitrogen and the TissueLyser®). Statistically significant differences in the obtained DNA concentration were found between the maceration and storage treatments. The TissueLyser® macerator produced higher DNA concentrations when compared to liquid nitrogen. For the storage treatments, five groups were formed based on DNA concentration when macerated with the TissueLyser® and two groups when macerated with liquid nitrogen. The DNA concentrations ranged from 285.00 ng/µL (7 days in transport buffer) to 702.00 ng/µL (30 days in silica gel) when the leaflets were macerated with liquid nitrogen, and from 572.73 ng/µL (30 days in silica gel) to 2,850.00 ng/µL (3 days in lyophiliser) using the TissueLyser® macerator. The DNA purity (A260/A280 nm) varied from 1.30 to 1.70 when the leaflets were macerated with liquid nitrogen and from 1.30 to 1.90 with the TissueLyser® macerator. Despite the variations in leaf tissue preservation and DNA concentration, all treatments were effective for DNA isolation and it was possible to amplify genomic regions of microsatellite markers by PCR. It was concluded that leaflets of E. precatoria stored in a lyophiliser and processed with an automatic macerator resulted in satisfactory DNA for molecular studies