Changes in homocysteine and non-mercaptoalbumin levels after acute exercise: a crossover study.

BACKGROUND: Acute exercise is one factor that increases blood homocysteine levels, and elevated homocysteine levels cause oxidative stress. Albumin, which is abundant in blood, is an antioxidant, and the redox state of albumin is used as an index of oxidative stress in blood. This study aimed to assess the effect of acute exercise on plasma homocysteine levels and the blood non-mercaptoalbumin/mercaptoalbumin ratio as an oxidative stress marker. METHODS: This study used a crossover design with exercise and control conditions. Under exercise conditions, a bicycle ergometer was used to perform 40 min of transient constant-load exercise at 65% heart rate reserve. Under control conditions, participants rested for 40 min. Blood was collected before, 30 min after, and 90 min after exercise, and at the same time points under control conditions. Samples were analyzed for the homocysteine concentration and non-mercaptoalbumin/mercaptoalbumin ratio. RESULTS: The results revealed that a 65% heart rate reserve and 40 min of acute exercise increased plasma homocysteine concentration and non-mercaptoalbumin ratio. In the intra-condition comparison, the plasma Hcy concentration was significantly increased at Post 30 min (+ 0.83 ± 0.70 µmol/L, P = 0.003) compared with that at Pre in the exercise condition. Furthermore, 90 min after exercise, the blood non-mercaptoalbumin ratio was significantly increased (+ 0.35 ± 0.71%, P = 0.030) compared to Pre. CONCLUSION: These results indicate that the plasma Hcy concentration first increased, and then the non-mercaptoalbumin/mercaptoalbumin ratio increased as the elevated state was maintained. This study revealed that 65% heart rate reserve, 40 min of acute exercise increased plasma Hcy concentration and non-mercaptoalbumin ratio.

High-flux operation of MBRs with ceramic flat-sheet membranes made possible by intensive membrane cleaning: Tests with real domestic wastewater under low-temperature conditions.

This study investigated the efficiency of intensive membrane cleaning for membrane bioreactors (MBRs) using a combination of mechanical scouring with granules and chemically enhanced backwashing (CEB). The implementation of such intensive cleaning was possible with ceramic flat-sheet membranes. Experiments were carried out using bench-scale MBRs at an existing wastewater treatment plant. First, CEB with NaClO was investigated in terms of the CEB frequency, duration, and concentration of the chemical reagent. CEB carried out for 60 min every 6 h, with 50 ppm of NaClO, was found to be effective, and it enabled an MBR to operate at 50 LMH, two to three times higher than the flux of full-scale MBRs. However, these CEB conditions were insufficient when the temperature was low (i.e. in winter), when an adhesive gel layer formed on the membrane surface. Its high resistance to cleaning might be explained by the increased levels of soluble microbial products and/or the presence of algal cells. Alkaline-assisted CEB, with NaClO (pH 12) and an increase in the volume of granules in the membrane tank, solved this problem. With the modified cleaning method, the fouling could be almost perfectly controlled at low-temperature conditions, such as 13 °C. MBRs may be regarded as fouling-free MBRs when the proposed cleaning method is used with ceramic flat-sheet membranes. Most real-world MBR operations operate with lower fluxes than the flux examined in this study, and at higher temperatures.

OsCERK1 plays a crucial role in the lipopolysaccharide-induced immune response of rice.

Plant cell surface receptor-like kinases (RLKs) mediate the signals from microbe-associated molecular patterns (MAMPs) that induce immune responses. Lipopolysaccharide (LPS), the major constituent of the outer membrane of gram-negative bacteria, is a common MAMP perceived by animals and plants; however, the plant receptors/co-receptors are unknown except for LORE, a bulb-type lectin S-domain RLK (B-lectin SD1-RLK) in Arabidopsis. OsCERK1 is a multifunctional RLK in rice that contains lysin motifs (LysMs) and is essential for the perception of chitin, a fungal MAMP, and peptidoglycan, a bacterial MAMP. Here, we analyzed the relevance of OsCERK1 to LPS perception in rice. Using OsCERK1-knockout mutants (oscerk1), we evaluated hydrogen peroxide (H2 O2 ) production and gene expression after LPS treatment. We also examined the LPS response in knockout mutants for the B-lectin SD1-RLK genes in rice and for all LysM-protein genes in Arabidopsis. Compared with wild-type rice cells, LPS responses in oscerk1 cells were mostly diminished. By contrast, rice lines mutated in either of three B-lectin SD1-RLK genes and Arabidopsis lines mutated in the LysM-protein genes responded normally to LPS. From these results, we conclude that OsCERK1 is an LPS receptor/co-receptor and that the LPS perception systems of rice and Arabidopsis are significantly different.