RESUMEN
The freshwater cyanobacteria, Microcystis aeruginosa (M. aeruginosa), is well known to produce microcystins (MCs) and induce the formation of harmful algal blooms (HABs) in aquatic environments, but the effects that urea fertilizer has on cyanobacterial growth and toxin production from a molecular biology perspective remain poorly understood. We evaluated changes in the growth and toxicity of M. aeruginosa cultured under different conditions of nitrogen (N) starvation (NN), low nitrogen (LN), and high nitrogen (HN). Cell density and chlorophyll-a concentrations decreased in cyanobacteria exposed to N starvation and increased following the addition of urea, whereas MCs content increased to a peak and then decreased after urea addition. Transcriptomic analysis confirmed that most genes encoding MCs and genes involved in N metabolic pathways were upregulated under N starvation and LN conditions, whereas these genes were downregulated under HN conditions. Our results offer important insights into the exploring N in controlling the formation of HABs and toxin production based on both physiological and molecular response.
Asunto(s)
Microcistinas/biosíntesis , Microcystis/crecimiento & desarrollo , Nitrógeno/metabolismo , Transcriptoma/efectos de los fármacos , Urea/farmacología , Clorofila A/metabolismo , Perfilación de la Expresión Génica , Floraciones de Algas Nocivas , Microcistinas/genética , Microcystis/efectos de los fármacos , Microcystis/metabolismo , Modelos Teóricos , Urea/metabolismoRESUMEN
Harmful algal blooms in source water are a worldwide issue for drinking water production and safety. UV/H2O2, a pre-oxidation process, was firstly applied to enhance Fe(II) coagulation for the removal of Microcystis aeruginosa [M. aeruginosa, 2.0 (±0.5) × 106 cell/mL] in bench scale. It significantly improved both algae cells removal and algal organic matter (AOM) control, compared with UV irradiation alone (254 nm UVC, 5.4 mJ/cm2). About 94.7% of algae cells were removed after 5 min UV/H2O2 pre-treatment with H2O2 dose 375 µmol/L, FeSO4 coagulation (dose 125 µmol/L). It was also certified that low residue Fe level and AOM control was simultaneously achieved due to low dose of Fe(II) to settle down the cells as well as the AOM. The result of L9(3)4 orthogonal experiment demonstrated that H2O2 and FeSO4 dose was significantly influenced the algae removal. UV/H2O2 induced an increase of intracellular reactive oxidant species (ROS) and a decrease in zeta potential, which might contribute to the algae removal. The total microcystins (MCs) concentration was 1.5 µg/L after UV/H2O2 pre-oxidation, however, it could be removed simultaneously with the algae cells and AOM. This study suggested a novel application of UV/H2O2-Fe(II) process to promote algae removal and simultaneously control AOM release in source waters, which is a green and promising technology without secondary pollution.
Asunto(s)
Compuestos Ferrosos/química , Peróxido de Hidrógeno/química , Microcystis , Rayos Ultravioleta , Purificación del Agua/métodos , Microcistinas/análisis , Oxidación-Reducción , Contaminantes del Agua/análisisRESUMEN
Oxidative stress is considered to be a major contributor to age-related hearing loss (ARHL). Here, we investigated whether pomegranate peel extract (PPE) protected against hearing loss by decreased oxidative stress in the cochlea of D-galactose-induced accelerated aging mice. The aging mice exhibited an increase in hearing threshold shifts and hair cells loss, which were improved in the PPE-treated aging mice. The aging mice also exhibited an increase in 4-hydroxynonenal, the expression of protein phosphatase 1 nuclear targeting subunit (PNUTS), p53 and caspase-3, and a decrease in protein phosphatase 1 (PP1) and MDM2 in the cochlea. PPE treatment reversed the changes in aforementioned molecules. Our results suggested that PPE can protect against ARHL, the underlying mechanisms may involve in the inhibition of oxidative damage of cochlea, possibly by regulating PNUTS/PP1 pathway. The results from the present study provide a new therapeutic strategy to use PPE for prevention of ARHL.
Asunto(s)
Cóclea/metabolismo , Proteínas de Unión al ADN/metabolismo , Pérdida Auditiva/etiología , Pérdida Auditiva/prevención & control , Lythraceae/química , Proteínas Nucleares/metabolismo , Estrés Oxidativo/efectos de los fármacos , Extractos Vegetales/farmacología , Proteína Fosfatasa 1/metabolismo , Proteínas de Unión al ARN/metabolismo , Envejecimiento/genética , Envejecimiento/metabolismo , Envejecimiento/fisiología , Aldehídos/metabolismo , Animales , Galactosa/toxicidad , Ratones Endogámicos BALB C , Fitoterapia , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/uso terapéutico , Transducción de Señal/efectos de los fármacosRESUMEN
Microcystins, a toxin produced by Microcystis aeruginosa have become a global environmental issue in recent years. As a consequence of eutrophication, microcystins have become widely disseminated in drinking water sources, seriously impairing drinking water quality. This review focuses on the relationship between microcystins synthesis and physical, chemical, and biological environmental factors that are significant in controlling their production. Light intensity and temperature are the more important physical factors, and in many cases, an optimum level for these two factors has been observed. Nitrogen and phosphorus are the key chemical factors causing frequent occurrence of harmful algal blooms and microcystins production. The absorption of nutrients and metabolic activities of algae are affected by different concentrations and forms of nitrogen and phosphorus, leading to variations in microcystins production Metal ions and emerging pollutants are other significant chemical factors, whose comprehensive impact is still being studied. Algae can also interact with biological agents like predators and competitors in aquatic environments, and such interactions are suggested to promote MCs production and release. This review further highlights areas that require further research in order to gain a better understanding of microcystins production. It provides a theoretical basis for the control of microcystins production and releasing into aquatic environments.