RESUMO
A comparative study on the behavior in the air-water interface of ß-lactoglobulin, α-lactoalbumin, glycinin and ß-conglycinin was performed. The behavior at the interface was evaluated by equilibrium surface tension and surface rheological properties of adsorbed films. There were significant differences (α ≤ 0.05) in the values of the constants of adsorption to the interface of the four proteins. The glycinin had the slowest rate of adsorption, due to its low average hydrophobicity, low molecular flexibility and large molecular size. Smaller proteins like ß-lactoglobulin and α-lactoalbumin tended to greater equilibrium pressure values than the larger proteins because of its higher rate of adsorption to the interface. The foam capacity of proteins showed a positive correlation with the average hydrophobicity; the maximal retained liquid volume or the initial rate of passage of liquid to foam were significantly lower (α ≤ 0.05) when protein was glycinin. The dilatational modulus of glycinin was the lowest, which implies lowest resistance to disruption of the film. Glycinin protein has lower proportion of gravitational drainage and higher disproportionation having perhaps a less resistant film. In conclusion, ß-conglycinin and whey proteins showed a similar behavior, so ß-conglycinin might be the best soybean protein to replace milk proteins in food formulations.
Assuntos
Ar , Interações Hidrofóbicas e Hidrofílicas , Proteínas/química , Reologia , Propriedades de Superfície , Água/químicaRESUMO
The wax hydrocarbon fractions of native Butia and Syagrus species collected from Palms in different regions of the of Rio Grande do Sul state (Brazil) and in Rocha (Uruguay) were analyzed to evaluate their potential as chemotaxonomic markers. The wax was extracted with chloroform and the resulting wax was fractionated by preparative TLC. The hydrocarbon fractions were analyzed by GC-MS. Statistical analyses were completed with the Statistica 5.0 program. The total crude wax yields averaged 0.31% w.w-1 dried leaves for Butia samples and 0.28% for Syagrus samples. The linear hydrocarbons represented on average 15% of the total waxes in the case of Butia samples and 13.7% in Syagrus samples. Hentriacontane and triacontane were the main components of all samples. The comparison of the means showed significant differences among Butia and Syagrus samples, and amongst Butia samples collected in different localities. In the case of the Syagrus collections no consistent groupings could be made. In the case of Butia samples the formation of three groupings could be observed, which were consistent with the species described for their geographical distribution. These results are discussed in the paper.
Assuntos
Arecaceae/química , Arecaceae/classificação , Hidrocarbonetos/análise , Ceras/análise , Arecaceae/ultraestrutura , Biomarcadores/análise , Cromatografia Gasosa-Espectrometria de Massas , Microscopia Eletrônica de VarreduraRESUMO
The wax hydrocarbon fractions of native Butia and Syagrus species collected from Palms in different regions of the of Rio Grande do Sul state (Brazil) and in Rocha (Uruguay) were analyzed to evaluate their potential as chemotaxonomic markers. The wax was extracted with chloroform and the resulting wax was fractionated by preparative TLC. The hydrocarbon fractions were analyzed by GC-MS. Statistical analyses were completed with the Statistica 5.0 program. The total crude wax yields averaged 0.31% w.w1 dried leaves for Butia samples and 0.28% for Syagrus samples. The linear hydrocarbons represented on average 15% of the total waxes in the case of Butia samples and 13.7% in Syagrus samples. Hentriacontane and triacontane were the main components of all samples. The comparison of the means showed significant differences among Butia and Syagrus samples, and amongst Butia samples collected in different localities. In the case of the Syagrus collections no consistent groupings could be made. In the case of Butia samples the formation of three groupings could be observed, which were consistent with the species described for their geographical distribution. These results are discussed in the paper.
Frações de hidrocarbonetos das ceras de espécies nativas de Butia e Syagrus coletadas de palmeiras em diferentes regiões do Rio Grande do Sul (Brasil) e em Rocha (Uruguai) foram analisadas para avaliar o seu potencial como marcadores quiomiotaxonômicos. As ceras foram extraídas com clorofórmio e fracionadas por TLC preparativo. As frações de hidrocarbonetos foram analisadas por CG-EM. As análises estatísticas foram realizadas com auxílio do programa Statistica 5.0. O rendimento total de cera das folhas secas foi de 0,31% g.g1 para as amostras de Butia e de 0,28% para Syagrus. Os hidrocarbonetos lineares representaram em média 15 e 13% do total das ceras para Butia e Syagrus, respectivamente. Hentriacontano e triacontano foram os compostos majoritários em todas as amostras. A comparação de médias mostrou diferenças significativas entre as amostras de Butia e Syagrus e entre as amostras de Butia coletadas em diferentes localidades. As amostras de Syagrus não formaram agrupamentos relacionados com os locais de coleta. Já no caso de Butia, três agrupamentos puderam ser observados e são consistentes com a distribuição geográfica desta espécie. Estes resultados são discutidos no trabalho.
Assuntos
Arecaceae/química , Arecaceae/classificação , Hidrocarbonetos/análise , Ceras/análise , Arecaceae/ultraestrutura , Biomarcadores/análise , Cromatografia Gasosa-Espectrometria de Massas , Microscopia Eletrônica de VarreduraRESUMO
The wax hydrocarbon fractions of native Butia and Syagrus species collected from Palms in different regions of the of Rio Grande do Sul state (Brazil) and in Rocha (Uruguay) were analyzed to evaluate their potential as chemotaxonomic markers. The wax was extracted with chloroform and the resulting wax was fractionated by preparative TLC. The hydrocarbon fractions were analyzed by GC-MS. Statistical analyses were completed with the Statistica 5.0 program. The total crude wax yields averaged 0.31% w.w-1 dried leaves for Butia samples and 0.28% for Syagrus samples. The linear hydrocarbons represented on average 15% of the total waxes in the case of Butia samples and 13.7% in Syagrus samples. Hentriacontane and triacontane were the main components of all samples. The comparison of the means showed significant differences among Butia and Syagrus samples, and amongst Butia samples collected in different localities. In the case of the Syagrus collections no consistent groupings could be made. In the case of Butia samples the formation of three groupings could be observed, which were consistent with the species described for their geographical distribution. These results are discussed in the paper.
Frações de hidrocarbonetos das ceras de espécies nativas de Butia e Syagrus coletadas de palmeiras em diferentes regiões do Rio Grande do Sul (Brasil) e em Rocha (Uruguai) foram analisadas para avaliar o seu potencial como marcadores quiomiotaxonômicos. As ceras foram extraídas com clorofórmio e fracionadas por TLC preparativo. As frações de hidrocarbonetos foram analisadas por CG-EM. As análises estatísticas foram realizadas com auxílio do programa Statistica 5.0. O rendimento total de cera das folhas secas foi de 0,31% g.g-1 para as amostras de Butia e de 0,28% para Syagrus. Os hidrocarbonetos lineares representaram em média 15 e 13% do total das ceras para Butia e Syagrus, respectivamente. Hentriacontano e triacontano foram os compostos majoritários em todas as amostras. A comparação de médias mostrou diferenças significativas entre as amostras de Butia e Syagrus e entre as amostras de Butia coletadas em diferentes localidades. As amostras de Syagrus não formaram agrupamentos relacionados com os locais de coleta. Já no caso de Butia, três agrupamentos puderam ser observados e são consistentes com a distribuição geográfica desta espécie. Estes resultados são discutidos no trabalho.
RESUMO
Investigation of the volatile fraction from the stem bark of Ocotea opifera Mart. led to the isolation and characterization of asaricin, a phenolic derivative with antifungal and insecticidal activity, as the main component, which is described for the first time for the genus Ocotea. The structure has been established by a study of its mono- and bidimensional NMR spectra and mass spectrometry.
Assuntos
Antifúngicos/isolamento & purificação , Compostos de Benzil , Dioxolanos/isolamento & purificação , Inseticidas/isolamento & purificação , Lauraceae/química , Monoterpenos , Óleos de Plantas/química , Plantas Medicinais/química , Derivados de Alilbenzenos , Antifúngicos/química , Antifúngicos/farmacologia , Bolívia , Monoterpenos Cicloexânicos , Cicloexenos , Dioxolanos/química , Dioxolanos/farmacologia , Cromatografia Gasosa-Espectrometria de Massas , Inseticidas/química , Inseticidas/farmacologia , Espectrometria de Massas , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular , Casca de Planta/química , Caules de Planta/química , Pirogalol/análogos & derivados , Estereoisomerismo , Relação Estrutura-Atividade , Temperatura , Terpenos/química , Terpenos/isolamento & purificaçãoRESUMO
A spirostanic saponin was isolated from the ethanolic extract of the aerial parts of Solanum laxum Steud. The compound, named luciamin, was characterised by NMR spectroscopy, mass spectrometry and chemical methods, as (22R, 25S)-spirost-5-en-3 beta, 15 alpha-diol 3-O-|beta-D-glucopyranosyl (1 --> 2)-beta-D-glucopyranosyl-( 1 --> 4)-[alpha-L-rhamnopyranosyl-( 1 --> 2)]-beta-D-galactopyranoside|. The compound was tested against the aphid Schizaphis graminum by incorporation in artificial diets. It showed a deterrent (toxic) activity against the insect and is the first spirostane glycoside reported to have this activity.
RESUMO
Ibicella lutea is a 'quasi-carnivorous' plant that grows wild in Uruguay where it is used in popular medicine as an antiseptic for eye and skin infections. In an earlier screening, it showed a broad antibacterial spectrum. From the chloroform extract of the plant the main antibacterial compound has now been isolated and identified by several MS and NMR methods as a new compound, 11-O-(6'-O-acetyl-beta-D-glucopyranosyl)-stearic acid.
Assuntos
Anti-Infecciosos/isolamento & purificação , Magnoliopsida/química , Anti-Infecciosos/química , Anti-Infecciosos/farmacologia , Espectroscopia de Ressonância Magnética , Estrutura MolecularRESUMO
The determination of the ratio of phospholipid/lipophilic compounds in liposomes was achieved after thin-layer chromatography (TLC) by measuring the spot intensities of dipalmitoyl phosphatidylcholine and the lipophilic compound. The liposome components under study were separated on one TLC plate, developed in two steps, and detected after charring the plate with specific visualization reagents. The method shows good reproducibility and provides a simple way to quantify the level of lipophilic compound incorporated in the liposome bilayer.
Assuntos
Cromatografia em Camada Fina/métodos , Densitometria/métodos , Lipossomos/química , Fosfolipídeos/análise , Cromatografia Gasosa , Estrutura Molecular , Fosfolipídeos/química , Reprodutibilidade dos Testes , Esteróis/análise , Esteróis/químicaRESUMO
The essential oils of the aerial parts of Achyrocline satureioides (D.C.) Lam., a regional medicinal plant, from different collection locations in the South of Brazil and Uruguay were examined by GC and GC-MS. Monoterpene and sesquiterpene hydrocarbons were the main fractions of both the oils from Brazil and Uruguay. The oxygenated monoterpenes and sequiterpenes were at much lower percentage in both samples. The Uruguayan samples have 1,8-cineole which is not present in the Brazilian samples and has not been reported in other samples from Brazil. The results indicated a high biodiversity of the native populations of A. satureioides.