Glutathione Reductase (GR) plays a key role in the maintenance of GSH homeostasis, variations in its activity may indicate damage from environmental contaminants. Experimental planning is a strategy to reduces time and cost in enzymatic assays. In this work, DCCR experimental planning was used to standardize and to validate the measure of GR in Aegla singularis bioindicator. Samples of A. singularis were collected in three watersheds with different percentages of naturalness and land uses. At all, were selected 7 streams, in which collections were performed at one upstream (most preserved) and one downstream (less preserved) point. Effects of temperature, reading time, substrate (GSSG) and protein concentration in GR reaction medium were evaluated, being that the two latter variables were optimized by DCCR. GR was not affected by temperature (15 to 30 °C) or reading time (6 and 10 minutes). Increased concentrations of proteins from biological extract had negative correlation with GR, whereas higher concentrations of GSSG resulted in higher GR activity. Environmental validation showed that GR in Aeglawas influenced primarily by the watershed of origin. DCCR planning was efficient to optimizing the use of GR as a biomarker of environmental quality.

Foram estudados os efeitos da razão molar aromático/cloreto de alquila, adição de base, solvente e agente alquilante, na alquilação do etilbenzeno catalisada pela zeólita FeY. Ficou caracterizada a alquilação ocorrendo no interior dos poros da zeólita, uma vez que ela é pouco afetada pela razão molar dos reagentes. A adição de bases e solventes oxigenados, capazes de complexar com o sítio ativo, inibe a reação. Foi proposto um mecanismo envolvendo transferência de um elétron entre as espécies de ferro ativas e o cloreto de alquila, para explicar os resultados.

The effect of aromatic/alkylchloride molar ratio, base addition, solvent and alkylating agent on the ethylbenzene alkylation over FeY zeolite was investigated. It was shown that alkylation occurs inside the pores and it is little affected by the reactants molar ratio. On the other hand, addition of bases or oxygenated compounds, capable of complexing with the active site, blocks the reaction. A mechanism involving single electron transfer between the active iron species and the alkylchloride was propose to account for the results.