Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros

Base de dados
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
Res Microbiol ; 146(5): 371-83, 1995 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-8525054

RESUMO

Cloning and characterization of the gor gene of the lactic acid bacterium Streptococcus thermophilus, encoding glutathione reductase, are described in this paper. This enzyme is a part of the enzymatic defences against oxidative stress in eukaryotic cells and in Gram-negative bacteria, but was never found in Gram-positive bacteria before this study. The amino acid sequence shares extensive similarities with glutathione reductases from other organisms, e.g. 62% amino acid identity with Escherichia coli protein. Northern blot analysis and glutathione reductase enzyme assays gave evidence that the gene is expressed in aerobically growing cells.


Assuntos
DNA Bacteriano/química , Genes Bacterianos/genética , Glutationa Redutase/genética , Streptococcus/genética , Sequência de Bases , Northern Blotting , Clonagem Molecular , DNA Bacteriano/genética , Eletroforese em Gel de Poliacrilamida , Glutationa Redutase/farmacocinética , Técnicas In Vitro , Dados de Sequência Molecular , Reação em Cadeia da Polimerase , Mapeamento por Restrição , Streptococcus/enzimologia , Streptococcus/crescimento & desenvolvimento
2.
Free Radic Biol Med ; 65: 1385-1397, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-24120751

RESUMO

Glutathione reductase (GR) catalyzes the reduction of oxidized glutathione (GSSG) to reduced glutathione (GSH) using NADPH as the reducing cofactor, and thereby maintains a constant GSH level in the system. GSH scavenges superoxide (O2(*-)) and hydroxyl radicals (OH) nonenzymatically or by serving as an electron donor to several enzymes involved in reactive oxygen species (ROS) detoxification. In either case, GSH oxidizes to GSSG and is subsequently regenerated by the catalytic action of GR. Although the GR kinetic mechanism has been extensively studied under various experimental conditions with variable substrates and products, the catalytic mechanism has not been studied in terms of a mechanistic model that accounts for the effects of the substrates and products on the reaction kinetics. The aim of this study is therefore to develop a comprehensive mathematical model for the catalytic mechanism of GR. We use available experimental data on GR kinetics from various species/sources to develop the mathematical model and estimate the associated model parameters. The model simulations are consistent with the experimental observation that GR operates via both ping-pong and sequential branching mechanisms based on relevant concentrations of its reaction substrate GSSG. Furthermore, we show the observed pH-dependent substrate inhibition of GR activity by GSSG and bimodal behavior of GR activity with pH. The model presents a unique opportunity to understand the effects of products on the kinetics of GR. The model simulations show that under physiological conditions, where both substrates and products are present, the flux distribution depends on the concentrations of both GSSG and NADP(+), with ping-pong flux operating at low levels and sequential flux dominating at higher levels. The kinetic model of GR may serve as a key module for the development of integrated models for ROS-scavenging systems to understand protection of cells under normal and oxidative stress conditions.


Assuntos
Dissulfeto de Glutationa/metabolismo , Glutationa Redutase/farmacocinética , Radical Hidroxila/química , NADP/química , Superóxidos/química , Animais , Catálise , Bovinos , Dissulfeto de Glutationa/química , Humanos , Modelos Teóricos , NADP/metabolismo , Oxirredução , Estresse Oxidativo/efeitos dos fármacos
3.
Ecotoxicol Environ Saf ; 38(2): 122-31, 1997 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-9417853

RESUMO

The aim of this study was to evaluate the usefulness of antioxidant parameters in the freshwater bivalve, Unio tumidus, as biomarkers of exposure to pollutants and to study their potential interest in predicting toxicity. Selenium-dependent glutathione peroxidase (Se-GPx), non-selenium-dependent glutathione peroxidase (non-Se-GPx), glutathione reductase (GRd), catalase, and superoxide dismutase (SOD) activities; reduced (GSH) and oxidized (GSSG) glutathione levels; and lipid peroxidation were measured in the gills and digestive glands of Unio. Control mussels were encaged and transplanted for 15 and 30 days to sites where the contamination of sediments was analyzed, along a river receiving domestic and industrial sources of pollution. After 15 days of exposure, all antioxidant parameters of the bivalves transferred to the most polluted sites had strongly decreased compared with control values. This was particularly true for Se-GPx and GRd activities, which were inhibited by 60 and 80% in the two tissues, and for GSH levels (80% reduction in the gills and 60% in digestive glands). These decreases were associated in the gills with lipid peroxidation (measured by malondialdehyde content) and with a high level of contamination of sediments by polycyclic aromatic hydrocarbons and polychlorinated biphenyls. In the mussels exposed at the least polluted sites, the same parameters decreased in the gills, but to a lesser extent: 50% for Se-GPx and 32% for GRd activities, and 45% for GSH levels. The gills appeared more sensitive than the digestive glands. After 30 days of exposure, while Se-GPx, GRd, and GSH remained reduced, a significant induction of non-Se-GPx and catalase activities was recorded in the gills, which reflected an adaptation of the transplanted species to their unsafe environment. All the results indicated that antioxidant defense components, namely, Se-GPx, GRd, and GSH, are sensitive parameters that could be useful biomarkers for the evaluation of contaminated aquatic ecosystems. The relationship between the degree of deficiency of antioxidant defenses and lipid peroxidation suggests that these parameters could also be biomarkers for toxicity.


Assuntos
Poluentes Ambientais/análise , Glutationa Peroxidase/análise , Glutationa Redutase/análise , Glutationa/análise , Peroxidação de Lipídeos , Moluscos/química , Animais , Antioxidantes/análise , Antioxidantes/farmacocinética , Biomarcadores , Monitoramento Ambiental/métodos , Previsões , Glutationa/farmacocinética , Glutationa Peroxidase/farmacocinética , Glutationa Redutase/farmacocinética , Distribuição Tecidual , Testes de Toxicidade , Poluição da Água
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA