Denitrification with corncob as carbon source and biofilm carriers.

In this research the agricultural by-product corncob was investigated as a carbon source as well as a biofilm carrier to remove organic matter, expressed as chemical oxygen demand (COD) and nitrate nitrogen (nitrate-N), from wastewater in a batch laboratory reactor. The performance of a reactor with corncob as the carbon source and the biofilm carrier was compared with a control batch reactor with suspended plastic carriers and glucose as the sole carbon source. With 60 vol% of corncob carriers inside the reactor, a soluble COD/N ratio of 4.2 g COD g N(-1) was enough for total denitrification, nearly half of the control reactor (9.5 g COD g N(-1)), at 23 h reaction time. The specific denitrification rate decreased with increasing soluble COD consumption for both reactors. Nitrate and COD removal efficiencies decreased with shorter retention times, with accentuated effects in the reactor. This study suggested corncob as a feasible carbon source and that reaction time was a limiting factor with corncob used as the carbon source for denitrification.

Dendrobium officinale Flower Extraction Mitigates Alcohol-Induced Liver Injury in Mice: Role of Antisteatosis, Antioxidative, and Anti-Inflammatory.

The study aimed to evaluate the protective effect of Dendrobium officinale flower extraction (DOFE) on alcohol-induced liver injury and its probable mechanisms in mice. The chemical composition of DOFE was performed via UPLC/MS. Male Kunming mice were used to establish alcohol-induced liver injury models by oral gavage of 56% alcohol. Results showed that DOFE dramatically attenuated the increased serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), total cholesterol (TC), and triacylglycerol (TG). Meanwhile, hematoxylin and eosin and Oil Red O staining showed that DOFE attenuated degeneration, inflammatory infiltration, and lipid droplet accumulation. DOFE was also found to suppress the activity of malonaldehyde (MDA) and enhanced the level of glutathione (GSH) and the activities of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and catalase (CAT) in the liver. The protection of DOFE against oxidative stress was associated with the downregulation of hepatic cytochrome P450 2E1 (CYP2E1) and upregulation of nuclear factor erythroid 2-related factor 2 (Nrf2), heme oxygenase-1 (HO-1), and NAD(P)H quinone oxidoreductase l (NQO1). Additionally, DOFE suppressed inflammation via downregulating Toll-like receptor-4 (TLR-4) and nuclear factor kappa-B P65 (NF-κB P65). Thus, DOFE exhibited a significant protective effect against alcohol-induced liver injury through its antisteatosis, antioxidative, and anti-inflammatory effect.