Protective effect of ions against cell death induced by acid stress in Saccharomyces

Saccharomyces boulardii is a probiotic used to prevent or treat antibiotic-induced gastrointestinal disorders and acute enteritis. For probiotics to be effective they must first be able to survive the harsh gastrointestinal environment. In this work, we show that S. boulardii displayed the greatest tolerance to simulated gastric environments compared with several Saccharomyces cerevisiae strains tested. Under these conditions, a pH 2.0 was the main factor responsible for decreased cell viability. Importantly, the addition of low concentrations of sodium chloride (NaCl) protected cells in acidic conditions more effectively than other salts. In the absence of S. boulardii mutants, the protective effects of Na 1 in yeast viability in acidic conditions was tested using S. cerevisiae Na 1 -ATPases (ena1-4), Na 1 /H 1 antiporter (nha1D) and Na 1 /H 1 antiporter prevacuolar (nhx1D) null mutants, respectively. Moreover, we provide evidence suggesting that this protection is determined by the plasma membrane potential, once altered by low pH and low NaCl concentrations. Additionally, the absence or low expression/activity of Ena proteins seems to be closely related to the basal membrane potential of the cells

Euterpe edulis

We investigated the effects of E. edulis bioproducts (lyophilized pulp [LEE], defatted lyophilized pulp [LDEE], and oil [EO]) on nonalcoholic fatty liver disease (NAFLD) induced by a high-fat diet (HFD) in rats. All products were chemically analyzed. In vivo, 42 rats were equally randomized into seven groups receiving standard diet, HFD alone or combined with EO, LEE, or LDEE. After NAFLD induction, LEE, LDEE, or EO was added to the animals’ diet for 4 weeks. LEE was rich in polyunsaturated fatty acids. From LEE degreasing, LDEE presented higher levels of anthocyanins and antioxidant capacity in vitro. Dietary intake of LEE and especially LDEE, but not EO, attenuated diet-induced NAFLD, reducing inflammatory infiltrate, steatosis, and lipid peroxidation in liver tissue. Although both E. edulis bioproducts were not hepatotoxic, only LDEE presented sufficient benefits to treat NAFLD in rats, possibly by its low lipid content and high amount of phenols and anthocyanins

Characterization and expression of two genes encoding P-type ATPases in Blastocladiella emersonii

A TPases do tipo P são proteínas integrais de membrana que usam a energia química contida na molécula de ATP para o transporte de cátions através de membranas. O nosso trabalho apresenta a clonagem e o sequenciamento de um gene (BePAT2) e a caracterização da expressão de dois genes (BePAT1 e BePAT2) codificando isoformas de uma ATPase do tipo P no fungo aquático Blastocladiella emersonii. As proteínas codificadas por estes genes, surpreendentemente se mostraram mais similares às Na+/K+ e H+/K+-ATPases de eucariotos superiores do que a outras ATPases de fungos. Experimentos de \"Northern blot\", imunoprecipitação e \"Western blot\" demonstraram que as ATPases (BePAT1 e BePAT2) são diferencialmente expressas durante o desenvolvimento de B. emersonii. Os resultados obtidos mostraram que o aumento da transcrição dos genes refletiu em um aumento da síntese e do acúmulo das ATPases, sugerindo um controle pré-traducional da expressão de BePAT1/2. Estudos de formação de fosfoenzima na presença de diferentes íons e inibidores, utilizando as enzimas imunopurificadas, sugerem que as proteínas codificadas por estes genes tenham uma atividade semelhante às Na+/K+-ATPases. Os nossos resultados de expressão e atividade mostram pela primeira vez, evidências da funcionalidade de genes codificando uma proteína similar às Na+/K+-ATPases em um eucarioto inferior.P- type A TPases are integral membrane proteins which use the energy stored in the A TP molecule to drive the transport of cations through biological membranes. In this work we report the cloning and sequencing of the BePAT2 gene and the characterization and expression of two genes (BePAT1 and BePAT2) encoding isoforms of a P-Type ATPase in the aquatic fungus Blastocladiella emersonii. Surprisingly the putative BePAT1 and BePAT2 proteins are more similar to Na+/K+and H+/K+-ATPases from animal cells than to other P-type ATPases from fungi. Northern blot, immunoprecipitation and Western blot experiments demonstrated that these ATPases (BePAT1 and BePAT2) are developmentally regulated in B. emersonii. The results showed that the increase in the BePAT1/2 transcription reflects in an increase in the synthesis and accumulation of the proteins, suggesting a transcriptional control of the BePAT1/2 expression. Studies of phosphoenzyme formation using the immunopurified enzymes in the presence of different ions and inhibitors suggested a Na/K-ATPase like activity. Our results demonstrate for the first time biochemical evidences of functionality of genes encoding a Na+ /K+-ATPase like protein in an eucaryotic microorganism

Characterization and expression of two genes encoding P-type ATPases in Blastocladiella emersonii

A TPases do tipo P são proteínas integrais de membrana que usam a energia química contida na molécula de ATP para o transporte de cátions através de membranas. O nosso trabalho apresenta a clonagem e o sequenciamento de um gene (BePAT2) e a caracterização da expressão de dois genes (BePAT1 e BePAT2) codificando isoformas de uma ATPase do tipo P no fungo aquático Blastocladiella emersonii. As proteínas codificadas por estes genes, surpreendentemente se mostraram mais similares às Na+/K+ e H+/K+-ATPases de eucariotos superiores do que a outras ATPases de fungos. Experimentos de \"Northern blot\", imunoprecipitação e \"Western blot\" demonstraram que as ATPases (BePAT1 e BePAT2) são diferencialmente expressas durante o desenvolvimento de B. emersonii. Os resultados obtidos mostraram que o aumento da transcrição dos genes refletiu em um aumento da síntese e do acúmulo das ATPases, sugerindo um controle pré-traducional da expressão de BePAT1/2. Estudos de formação de fosfoenzima na presença de diferentes íons e inibidores, utilizando as enzimas imunopurificadas, sugerem que as proteínas codificadas por estes genes tenham uma atividade semelhante às Na+/K+-ATPases. Os nossos resultados de expressão e atividade mostram pela primeira vez, evidências da funcionalidade de genes codificando uma proteína similar às Na+/K+-ATPases em um eucarioto inferior.P- type A TPases are integral membrane proteins which use the energy stored in the A TP molecule to drive the transport of cations through biological membranes. In this work we report the cloning and sequencing of the BePAT2 gene and the characterization and expression of two genes (BePAT1 and BePAT2) encoding isoforms of a P-Type ATPase in the aquatic fungus Blastocladiella emersonii. Surprisingly the putative BePAT1 and BePAT2 proteins are more similar to Na+/K+and H+/K+-ATPases from animal cells than to other P-type ATPases from fungi. Northern blot, immunoprecipitation and Western blot experiments demonstrated that these ATPases (BePAT1 and BePAT2) are developmentally regulated in B. emersonii. The results showed that the increase in the BePAT1/2 transcription reflects in an increase in the synthesis and accumulation of the proteins, suggesting a transcriptional control of the BePAT1/2 expression. Studies of phosphoenzyme formation using the immunopurified enzymes in the presence of different ions and inhibitors suggested a Na/K-ATPase like activity. Our results demonstrate for the first time biochemical evidences of functionality of genes encoding a Na+ /K+-ATPase like protein in an eucaryotic microorganism

Expression of genes encoding cytosolic and endoplasmic reticulum HSP90 proteins in the aquatic fungus Blastocladiella emersonii

HSP90 proteins are important molecular chaperones involved in multiple cellular processes. This work reports the characterization of cDNAs encoding two distinct HSP90 proteins (named HSP90A and HSP90B) from the chytridiomycete Blastocladiella emersonii. Deduced amino acid sequences of HSP90A and HSP90B exhibit signatures of the cytosolic and endoplasmic reticulum (ER) HSP90 proteins, respectively. A genomic clone encoding HSP90A was also characterized indicating the presence of a single intron of 184 bp interrupting the coding region, located near the amino-terminus of the protein. Expression of both HSP90A and HSP90B genes increases significantly during heat shock at 38 degrees C, with highest induction ratios observed in cells stressed during germination of the fungus. Changes in the amount of HSP90A transcript were also evaluated during B. emersonii life cycle at physiological temperature (27 degrees C), and its levels were found to increase both during germination and sporulation of the fungus. HSP90A protein levels were analyzed during B. emersonii life cycle and significant changes were observed only during sporulation. Furthermore, during heat stress a large increase in the amount of HSP90A protein was observed. Induction of HSP90A and HSP90B genes during heat stress indicates the importance of both genes in the response to high temperature in B. emersonii. (C) 2008 Elsevier B.V. All rights reserved

Colleters in Bathysa cuspidata (Rubiaceae): Development, ultrastructure and chemical composition of the secretion

This paper describes the development of colleters of Bathysa cuspidata, Rubiaceae, considering anatomical, histochemical and ultrastructural aspects and going from first differentiation stages until senescence. Further, the chemical composition of the secretion is investigated. The samples were prepared according to the usual techniques for light microscopy and scanning and transmission electron microscopy. Electrophoresis and thin layer chromatography (TLC) were used to confirm the results obtained in the histochemical tests. The colleters occur at the ventral surface of the stipules which protect the leaf primordia as well as the shoot meristem. The origin of the colleters is mixed, involving protoderm and ground meristem. The Bathysa colleters are of the standard type or are bifurcated; this latter type is documented here for the first time for Rubiaceae. Colleter secretion is a mucilage rich in protein, as determined by histochemical tests and confirmed by chemical analysis. Phenolic compounds and terpenes were detected only in the colleters themselves, but not in the secretion. The epithelial cells present conspicuous nuclei and nucleoli and the cytoplasm is rich in dictyosomes, endoplasmic reticulum, mitochondria, vesicles and small vacuoles with a fibrillar content. The accumulation of phenolic compounds and terpenes, the formation of a large central vacuole, the increase of the intercellular and subcuticular spaces occupied by the secretion and, finally, the darkening and the wilting of the colleters characterize the senescence of these structures. The secretion process of the colleters of B. cuspidata suggests a process of programmed cell death

Calcium signaling and sugar-induced activation of plasma membrane H+-ATPase in Saccharomyces cerevisiae cells.

In this work, we show that glucose-induced activation of plasma membrane H+-ATPase from Saccharomyces cerevisiae is strongly dependent on calcium metabolism and that the glucose sensor Snf3p works in a parallel way with the G protein Gpa2p in the control of the pathway. The role of Snf3p is played by the Snf3p C-terminal tail, since in a strain with the deletion of the SNF3 gene, but also expressing a chimera protein formed by Hxt1p (a glucose transporter) and the Snf3p C-terminal tail, a normal glucose-activation process can be observed. We present evidences indicating that Snf3p would be the sensor for the internal signal (phosphorylated sugars) of this pathway that would connect calcium signaling and activation of the plasma membrane ATPase. We also show that Snf3p could be involved in the control of Pmc1p activity that would regulate the calcium availability in the cytosol

Evaluation of the genotoxic potential of ethanolic extracts of stem bark and leaves of Bathysa cuspidata (A.St.-Hil.) Hook

DOI: não consta, por isso foi disponibilizado o link de acesso.Bathysa cuspidata(A.St.-Hil.) Hook. is a native tree of the Brazilian Atlantic Forest biome, widely used in Brazilian herbal medicine. Despite its widespread use, there is no report as yet regarding the toxicology of this plant. In this study, the mutagenic and genotoxic effects of ethanolic extracts of B. cuspidatastem bark (SBC) and leaves (LBC) were assessed. The mutagenicity of the extracts was estimated by performing the Ames test on strains TA98 and TA100 of Salmonella typhimurium, in the absence and presence of metabolic activation. The direct action of the extracts on DNA was assessed through plasmid treatment. Phytochemical screening was conducted to compare the secondary metabolite composition of the extracts. No mutagenic activity was found in LBC when tested on strain TA98 or TA100, without or with metabolic activation. However, SBC did show mutagenic activity. Plasmid tests did not indicate genotoxic action for either SBC or LBC. Differences in the composition of secondary metabolites present in the bark and leaves, detected by phytochemical analysis, appear to be a deciding factor in differences in mutagenicity between SBC and LBC. The findings in this study suggest caution in the use of B. cuspidata bark.Bathysa cuspidata(A.St.-Hil.) Hook. é uma árvore nativa do bioma Mata Atlântica largamente utilizada na medicina popular brasileira. Apesar do amplo uso, ainda não existe relato sobre a toxicologia dos compostos obtidos dessa espécie vegetal. O presente estudo avaliou efeitos mutagênicos e genotóxicos de extratos etanólicos de B. cuspidataobtidos das cascas do caule (SBC) e das folhas (LBC). A mutagenicidade dos extratos foi avaliada utilizando o teste de Ames nas linhagens TA98 e TA100 de Salmonella typhimurium, na ausência e presença de ativação metabólica. Os efeitos dos extratos diretamente sobre o DNA foram avaliados por clivagem plasmidial. Análises fitoquímicas foram realizadas para comparar a composição de metabólitos secundários dos extratos. Não foi encontrada atividade mutagênica para LBC quando avaliados utilizando as cepas TA98 e TA100, sem ou com ativação metabólica. No entanto, SBC apresentou atividade mutagênica. Clivagem plasmidial não indicou ação genotóxica tanto para SBC quanto para LBC. Diferenças na composição dos metabólitos secundários presentes nos cascas e folhas, detectadas pelas análises fitoquímicas, devem ser determinantes para a variação do efeito mutagênico entre SBC e LBC. Os resultados sugerem cautela no emprego de cascas de B. cuspidata