RÉSUMÉ
Background: Textile industry not only plays a vital role in our daily life but also a prominent factor in improving global economy. One of the environmental concern is it releases huge quantities of toxic dyes in the water leading to severe environmental pollution. Bacterial laccase and azoreductase successfully oxidize complex chemical structure of nitrogen group-containing azo dyes. Additionally, the presence of textile dye infuriates bacterial peroxidase to act as a dye degrading enzyme. Our present study deals with three textile dye degrading enzymes laccase, azoreductase, and peroxidase through analyzing their structural and functional properties using standard computational tools. Result: According to the comparative analysis of physicochemical characteristics, it was clear that laccase was mostly made up of basic amino acids whereas azoreductase and peroxidase both comprised of acidic amino acids. Higher aliphatic index ascertained the thermostability of all these three enzymes. Negative GRAVY value of the enzymes confirmed better water interaction of the enzymes. Instability index depicted that compared to laccase and preoxidase, azoreductase was more stable in nature. It was also observed that the three model proteins had more than 90% of total amino acids in the favored region of Ramachandran plot. Functional analysis revealed laccase as multicopper oxidase type enzyme and azoreductase as FMN dependent enzyme, while peroxidase consisted of α-ß barrel with additional haem group. Conclusion: Present study aims to provide knowledge on industrial dye degrading enzymes, choosing the suitable enzyme for industrial set up and to help in understanding the experimental laboratory requirements as well.
Sujet(s)
Composés azoïques/métabolisme , Myeloperoxidase/composition chimique , Laccase/composition chimique , NADH, NADPH oxidoreductases/composition chimique , Température , Composés azoïques/composition chimique , Industrie textile , Dépollution biologique de l'environnement , Simulation numérique , Stabilité enzymatique , Myeloperoxidase/métabolisme , Lactase/métabolisme , Agents colorants/métabolisme , NADH, NADPH oxidoreductases/métabolismeRÉSUMÉ
Keratinolytic microorganisms have become the subject of scientific interest due to their ability to biosynthesize specific keratinases and their prospective application in keratinic waste management. Among several bacterial classes, actinobacteria remain one of the most important sources of keratin-degrading strains, however members of the
Sujet(s)
Animaux , Kératines/métabolisme , Micrococcus luteus/enzymologie , Micrococcus luteus/métabolisme , Peptide hydrolases/métabolisme , Dépollution biologique de l'environnement , Poulets/microbiologie , Plumes/microbiologie , Micrococcus luteus/isolement et purification , NADH, NADPH oxidoreductases/métabolisme , Oxydoréduction , Volaille/microbiologie , Composés du soufre/métabolisme , Gestion des déchetsRÉSUMÉ
Endotoxic responses to bacterial lipopolysaccharide (LPS) are triggered by Toll-like receptor 4 (TLR4) and involve the production of inflammatory mediators, including interleukin-6 (IL-6), by macrophages. The detailed mechanism of IL-6 production by macrophages in response to LPS has remained unclear, however. We now show that LPS induces IL-6 synthesis in mouse peritoneal macrophages via the leukotriene B4 receptor BLT2. Our results suggest that TLR4-MyD88 signaling functions upstream of BLT2 and that the generation of reactive oxygen species (ROS) by NADPH oxidase 1 (Nox1) and consequent activation of the transcription factor nuclear factor (NF)-kappaB function downstream of BLT2 in this response. These results suggest that a TLR4-MyD88-BLT2-Nox1-ROS-NF-kappaB pathway contributes to the synthesis of IL-6 in LPS-stimulated mouse macrophages.
Sujet(s)
Animaux , Souris , Lignée cellulaire , Interleukine-6/biosynthèse , Leucotriène B4/métabolisme , Ligands , Lipopolysaccharides/immunologie , Macrophages/immunologie , Macrophages péritonéaux/immunologie , Facteur de différenciation myéloïde-88/métabolisme , NADH, NADPH oxidoreductases/métabolisme , Facteur de transcription NF-kappa B/métabolisme , Espèces réactives de l'oxygène/métabolisme , Récepteurs aux leucotriènes B4/métabolisme , Transduction du signalRÉSUMÉ
Introdução: A hipertensão arterial tem alta prevalência em renais crônicos, sendo a hipervolemia um de seus fatores causais. Objetivo: Avaliar a influência da redução da volemia no controle pressórico e em parâmetros ecocardiográficos de pacientes renais crônicos em diálise peritoneal contínua. Métodos: Doze renais crônicos sem sinais clínicos de hipervolemia foram submetidos à intensificação da diálise com o objetivo de reduzir o peso corporal em 5%. A volemia foi avaliada pela bioimpedância elétrica e pela ultrassonografia de veia cava inferior (VCI). Os voluntários foram submetidos à monitorização ambulatorial da pressão arterial e a exame ecocardiográfico no período basal e após 5 semanas de intervenção. Resultados: Após a intensificação da ultrafiltração, houve redução significativa do peso corporal, da água extracelular e do diâmetro inspiratório da VCI, enquanto o índice de colapsamento da VCI não alterou de modo significativo. A despeito da redução do número de anti-hipertensivos, a pressão sistólica do período de sono reduziu de 138,4 ± 18,6 para 126,7 ± 18,0 mmHg, o descenso pressórico do sono aumentou e o diâmetro sistólico final do ventrículo esquerdo reduziu significantemente. Conclusão: A redução da volemia de pacientes em diálise peritoneal, clinicamente euvolêmicos, se associou a melhor controle pressórico e à diminuição do diâmetro sistólico final do ventrículo esquerdo. .
Introduction: Hypertension is highly prevalent in patients with chronic kidney disease and hypervolemia is one of the principal causes. Objective: To evaluate the influence of the reduction of volemia on blood pressure as well as on echocardiographic parameters in patients on continuous ambulatory peritoneal dialysis. Methods: Twelve patients with no clinical evidence of hypervolemia were submitted to an increase in the rate of the dialysis with the purpose of reducing body weight by 5%. The volemia was evaluated by electrical bioimpedance and by ultrasound of the inferior cava vena (ICV). Blood pressure was measured by ambulatory blood pressure monitoring and cardiac function was evaluated by echocardiography both at baseline and 5 weeks after the intervention period. Results: After the increase in the ultrafiltration, body weight, extracellular water and the inspiratory diameter of the ICV decreased significantly in parallel with a non-significant increase in the collapsing ICV index. Despite the reduction of anti-hypertensive drugs, systolic blood pressure during the sleep period decreased from 138.4 ± 18.6 to 126.7 ± 18.0 mmHg, the nocturnal blood pressure drop increased and the final systolic left ventricular diameter decreased significantly. Conclusion: Reduction of the volemia of patients on peritoneal dialysis, with no signs of hypervolemia, was associated with a better blood pressure control and with a decrease of the final systolic left ventricular diameter. .
Sujet(s)
Animaux , Bovins , NADH, NADPH oxidoreductases/composition chimique , NADH, NADPH oxidoreductases/métabolisme , Ubiquinones/métabolisme , Sites de fixation , Complexe I de la chaîne respiratoire , Antienzymes/pharmacologie , Techniques in vitro , Cinétique , Myocarde/enzymologie , NADH, NADPH oxidoreductases/antagonistes et inhibiteurs , Résonance magnétique nucléaire biomoléculaire , Roténone/pharmacologieRÉSUMÉ
The ascorbate-glutathione (ASC-GSH) cycle has an important role in defensive processes against oxidative damage generated by drought stress. In this study, the changes that take place in apoplastic and symplastic ASC-GSH cycle enzymes of the leaf and petiole were investigated under drought stress causing leaf rolling in Ctenanthe setosa (Rose.) Eichler (Marantaceae). Apoplastic and symplastic extractions of leaf and petiole were performed at different visual leaf rolling scores from 1 to 4 (1 is unrolled, 4 is tightly rolled and the others are intermediate forms). Glutathione reductase (GR), a key enzyme in the GSH regeneration cycle, and ascorbate (ASC) were present in apoplastic spaces of the leaf and petiole, whereas dehydroascorbate reductase (DHAR), which uses glutathione as reductant, monodehydroascorbate reductase (MDHAR), which uses NAD(P)H as reductant, and glutathione were absent. GR, DHAR and MDHAR activities increased in the symplastic and apoplastic areas of the leaf. Apoplastic and symplastic ASC and dehydroascorbate (DHA), the oxidized form of ascorbate, rose at all scores except score 4 of symplastic ASC in the leaf. On the other hand, while reduced glutathione (GSH) content was enhanced, oxidized glutathione (GSSG) content decreased in the leaf during rolling. As for the petiole, GR activity increased in the apoplastic area but decreased in the symplastic area. DHAR and MDHAR activities increased throughout all scores, but decreased to the score 1 level at score 4. The ASC content of the apoplast increased during leaf rolling. Conversely, symplastic ASC content increased at score 2, however decreased at the later scores. While the apoplastic DHA content declined, symplastic DHA rose at score 2, but later was down to the level of score 1. While GSH content enhanced during leaf rolling, GSSG content did not change except at score 2. As well, there were good correlations between leaf rolling and ASC-GSH cycle enzyme activities ...
Sujet(s)
Acide ascorbique/métabolisme , Glutathion/métabolisme , Marantaceae/enzymologie , Feuilles de plante/enzymologie , Rosa/enzymologie , Sécheresses , Glutathione reductase/métabolisme , NADH, NADPH oxidoreductases/métabolisme , Oxidoreductases/métabolisme , Stress physiologiqueRÉSUMÉ
Glutathione is the major intracellular antioxidant thiol protecting mammalian cells against oxidative stress induced by oxygen- and nitrogen-derived reactive species. In trypanosomes and leishmanias, trypanothione plays a central role in parasite protection against mammalian host defence systems by recycling trypanothione disulphide by the enzyme trypanothione reductase. Although Kinetoplastida parasites lack glutathione reductase, they maintain significant levels of glutathione. The aim of this study was to use Leishmania donovani trypanothione reductase gene mutant clones and different Leishmania species to examine the role of these two individual thiol systems in the protection mechanism against S-nitroso-N-acetyl-D,L-penicillamine (SNAP), a nitrogen-derived reactive species donor. We found that the resistance to SNAP of different species of Leishmania was inversely correlated with their glutathione concentration but not with their total low-molecular weight thiol content (about 0.18 nmol/10(7) parasites, regardless Leishmania species). The glutathione concentration in L. amazonensis, L. donovani, L. major, and L. braziliensis were 0.12, 0.10, 0.08, and 0.04 nmol/10(7) parasites, respectively. L. amazonensis, that have a higher level of glutathione, were less susceptible to SNAP (30 and 100 µM). The IC50 values of SNAP determined to L. amazonensis, L. donovani, L. major, and L. braziliensis were 207.8, 188.5, 160.9, and 83 µM, respectively. We also observed that L. donovani mutants carrying only one trypanothione reductase allele had a decreased capacity to survive (40 percent) in the presence of SNAP (30-150 µM). In conclusion, the present data suggest that both antioxidant systems, glutathione and trypanothione/trypanothione reductase, participate in protection of Leishmania against the toxic effect of nitrogen-derived reactive species.
Sujet(s)
Animaux , Glutathion/métabolisme , Leishmania/effets des médicaments et des substances chimiques , NADH, NADPH oxidoreductases/métabolisme , Pénicillamine/analogues et dérivés , Fluorescéines , Leishmania/enzymologie , Masse moléculaire , NADH, NADPH oxidoreductases/génétique , Ouabaïne/analogues et dérivés , Pénicillamine/toxicité , Spécificité d'espèceRÉSUMÉ
Lactococcus lactis, the most extensively characterized lactic acid bacterium, is a mesophilic- and microaerophilic-fermenting microorganism widely used for the production of fermented food products. During industrial processes, L. lactis is often exposed to multiple environmental stresses (low and high temperature, low pH, high osmotic pressure, nutrient starvation and oxidation) that can cause loss or reduction of bacterial viability, reproducibility, as well as organoleptic and/or fermentative qualities. Among these stress factors, oxidation can be considered one of the most deleterious to the cell, causing cellular damage at both molecular and metabolic levels. During the last two decades, considerable efforts have been made to improve our knowledge of oxidative stress in L. lactis. Many genes involved with both oxidative stress resistance and control mechanisms have been identified; functionally they seem to overlap. The finding of new genes, and a better understanding of the molecular mechanisms of stress resistance in L. lactis and other lactic acid bacterium, will lead to the construction and isolation of stress-resistant strains. Such strains could be exploited for both traditional and probiotic uses
Sujet(s)
Stress oxydatif/physiologie , Lactococcus lactis/métabolisme , Complexes multienzymatiques/métabolisme , Stress oxydatif/génétique , Gènes bactériens/génétique , Lactococcus lactis/génétique , NADH, NADPH oxidoreductases/métabolisme , Peroxidases/métabolisme , Rec A Recombinases/métabolisme , Survie cellulaire/génétique , Superoxide dismutase/métabolismeRÉSUMÉ
Protoplasts isolated from Cuscuta reflexa exhibited a higher rate of exogenous NADH oxidation as compared to NADPH in the dark. NAD(P)H oxidation was monitored by measuring the rate of oxygen consumption and this oxidase system was sensitive to blue light. Both NADH oxidase and its blue light sensitivity were inhibited by -SH group reacting agents. The corresponding changes occurring in H+-extrusion activity and intracellular ATP levels were also monitored. Stimulation of NADH oxidation under blue light corresponded to increased rate of H+-extrusion and intracellular ATP level, the converse was also true under NADH oxidase inhibitory conditions. These observations suggested a close functional association between blue light-sensitive plasma membrane bound redox activity and H+-ATPase in this tissue. Further, concanavalin A binding of protoplasts resulted in a loss in NADH oxidase activity and its blue light sensitivity suggesting apoplastic location and glycoprotein nature of the blue light sensitive NADH oxidase system in Cuscuta.
Sujet(s)
Membrane cellulaire/enzymologie , Cuscuta/enzymologie , Lumière , Complexes multienzymatiques/métabolisme , NAD/métabolisme , NADH, NADPH oxidoreductases/métabolisme , OxydoréductionRÉSUMÉ
Azo reductase activity of microbial population of stomach, small intestine, caecum and large intestine of different animals was investigated. There was low activity in stomach flora of wistar rat and 3 strains of mice. Flora of proximal portion of small intestine in different species revealed that carnivorous animals exhibited maximum activity followed by grazing animals. Maximum activity in middle portion of small intestine was noted in dog (98.2%), while minimum was observed in guinea pig (23.3%). Majority of test animals revealed maximum floral azo reductase activity (58-98%) in caecum. Activity in proximal portion of large intestine was highest in dog while pigeon and guinea pig had least activity (23.3-27.1%). Appreciable microbial activity in distal end of large intestine was noted in sheep and goat. In all the 15 animal species investigated caecum showed maximum activity followed by pre and post caecal segments while stomach possessed the least. The results suggest that inter-species differences exist in microbial reductive activity which may be due to variation in composition and distribution of GI tract microflora and thus can influence toxicological implication of various dyes.
Sujet(s)
Animaux , Bactéries anaérobies/enzymologie , Système digestif/microbiologie , Chiens , Cochons d'Inde , Mâle , Souris , NADH, NADPH oxidoreductases/métabolisme , Rats , Spécificité d'espèceRÉSUMÉ
Para estudiar el posible rol de la agregación de polimorfonucleares neutrófilos (PMNs) en el Lupus Eritematoso Sistémico (LES), se investigó la actividad agregante de neutrófilos (AAN) de sueros de 32 pacientes lúpicos. En 24 pacientes con LES en actividad se detectaron AAN con un valor medio significativamente mayor que el de los 8 restantes, no activos, y los controles. Particularmente, en 4 pacientes con compromiso del sistema nervioso central la característica fue el hallazgo de altos niveles de AAN. Esto sugiere que la formación intravascular de leucoagregados puede contribuir a la morbidad del LES. Los PMNs normales aumentan la producción de anión superóxido O2- cuando son estimulados con sueros lúpicos. Los PMNs de pacientes lúpicos muestran un aumento del 100% en la producción de 02- in vitro al ser estimulados con su propio suero. Cuando el estímulo es N formil metionil leucil fenilalanina FMLP los PMNs lúpicos producen 5 veces más superóxido que los normales. Factores séricos y celulares contribuyen a un aumento en la producción de O2- por PMNs lúpicos proporcionando las condiciones requeridas para el daño inmune tisular