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Oral l-citrulline (Cit) increases plasma l-arginine (Arg) concentration and the production of nitric oxide (NO). NO dilates blood vessels and potentially improves sports performance. The combination of oral Arg and Cit (Arg + Cit) immediately and synergistically increases plasma Arg and nitrite/nitrate (NOx) concentrations more than either Cit or Arg alone. This prompted us to assess the effects of oral Arg + Cit on 10-min cycling performance in a double-blind, randomized, placebo-controlled crossover trial. Twenty-four male soccer players ingested either Cit + Arg or placebo (both 1.2 g/day each) for 6 days. On day 7, they ingested Cit + Arg 1 h before performing a 10-min full-power pedaling test on a bicycle ergometer. Plasma NOx and amino acid levels were measured before and after the test, as well as the participants’ subjective perception of physical exertion. Power output was significantly greater with Cit + Arg than in the placebo group (242 ± 24 vs. 231 ± 21 W; p

Tellurium (Te) has been increasingly used as a semiconductor material in copious amounts, with a concomitant increase in its discharge from industrial effluents and mining wastewater into the environment. However, soluble Te, such as tellurate (VI) and tellurite (IV), is toxic to organisms. Thus, highly efficient technologies need to be developed for a double-benefit detoxification and recovery of soluble Te from industrial and mining wastewater. Since industrial wastewater contains high concentrations of salt, salt-tolerant microorganisms that metabolize rare metals such as Te have been the subject of focus for the effective detoxification and recovery of Te. In the present study, a total of 52 salt-tolerant tellurate-reducing microorganisms were isolated from marine environmental samples. Of these, 18 strains achieved greater than, or equal to, 50% removal of water-soluble Te from a medium containing 0.4 mM tellurate after 72 h incubation. The 18 isolated strains belonged to 13 species of the following 9 genera: Sulfitobacter, Ruegeria, Hoeflea, Alteromonas, Marinobacter, Pseudoalteromonas, Shewanella, Idiomarina, and Vibrio. No microorganism has been reported to reduce tellurate and tellurite from six of the aforementioned genera, namely, Sulfitobacter, Ruegeria, Alteromonas, Marinobacter, Idiomarina, and Vibrio. Especially, one of the isolates Sulfitobacter sp. strain TK39B, removed 82% (w/w) of soluble Te with a 4% NaCl tolerance. These results showed that salt-tolerant tellurate-reducing bacteria that can be used in the detoxification and recovery of Te are widely present in the marine environment.

Biotechnological approaches have gained significant attention as a means to recover rare earth elements from acidic mine drainage and industrial liquid wastes. We recently isolated an acidophilic fungus, Penidiella sp. strain T9, that accumulates dysprosium (Dy) from acidic model drainage during growth. To develop the potential accumulation ability of the strain T9, we elucidated the localization and the chemical structure of Dy following its biogenetic solidification by the strain T9. High-magnification scanning electron microscopic analysis showed that the strain T9 formed a precipitated Dy (T9-Dy) layer with 1.0 μm thickness over the cell surface, along with some intracellular nanometer-sized Dy particles. X-ray photoelectron spectrometry and X-ray absorption fine structure analyses showed that the chemical composition of T9-Dy over the T9 cell surface corresponded to DyPO4. The LIII-edge spectrum observed with X-ray absorption near-edge structure indicated that Dy existed as Dy3 + ions in T9-Dy. X-ray diffraction analysis did not yield a clear spectrum from T9-Dy. Therefore, we conclude that the strain T9 accumulates and incorporates Dy as an amorphous DyPO4. Further, we found that phosphoric acid was involved in the Dy accumulation by the strain T9. In order to improve Dy accumulation yield by the strain T9, we have initiated follow-on studies to optimize culture conditions using phosphoric acid.

A randomized double‑blind placebo‑controlled clinical study was conducted to evaluate the chondroprotective action of glucosamine on healthy subjects (soccer players) without joint disorders. Collegiate soccer players (n=43) without joint disorders were randomly assigned to receive a glucosamine (2 g/day)‑containing supplement (n=22, glucosamine group) or a placebo (n=21, placebo group) for 16 weeks, and cartilage metabolism was evaluated by analyzing markers for type II collagen degradation urine C‑terminal telopeptide‑II (CTX‑II) and serum collagen type II cleavage (C2C) and synthesis urine C-terminal type II procollagen peptide (CPII). In the initial analysis of all subjects, urine CTX‑II level substantially decreased in the glucosamine group, but not in the placebo group after the intervention for 16 weeks (P=0.05). Moreover, CTX‑II level in the glucosamine group was also significantly lower than that in the placebo group at week 16 during the intervention. In the second analysis, to make the effect of the test supplement more clear, 41 subjects with less variation of exercise loading were evaluated. The results revealed that urine CTX‑II level significantly decreased in the glucosamine group (n=21), but not in the placebo group (n=20) after the intervention (P

With an aim to develop a highly efficient method for the recovery of rare earth elements (REEs) by using microorganisms, we attempted to isolate dysprosium (Dy)-accumulating microorganisms that grow under acidic conditions from environmental samples containing high concentrations of heavy metals. One acidophilic strain, T9, which was isolated from an abandoned mine, decreased the concentration of Dy in medium that contained 100 mg/liter Dy to 53 mg/liter Dy after 3 days of cultivation at pH 2.5. The Dy content in the cell pellet of the T9 strain was 910 μg/mg of dry cells. The T9 strain also accumulated other REEs. Based on the results of 28S-D1/D2 rRNA gene sequencing and morphological characterization, we designated this fungal strain Penidiella sp. T9. Bioaccumulation of Dy was observed on the cell surface of the T9 strain by elemental mapping using scanning electron microscopy-energy dispersive X-ray spectroscopy. Our results indicate that Penidiella sp. T9 has the potential to recover REEs such as Dy from mine drainage and industrial liquid waste under acidic conditions.

Biomineralization approaches have gained significant attention as a means to recover rare earth elements from acidic mine drainage and industrial liquid wastes. We isolated an acidophilic fungus, Penidiella sp. strain T9, that accumulates dysprosium (Dy) from acidic model drainage during growth. To develop the application of biomineralization by the strain T9, we elucidated the localization and the chemical structure of biomineralized Dy and performed to establish the labo-scale bioprocess for selective recovery of Dy. High-magnification scanning electron microscopic analysis showed that the strain T9 formed a mineralized Dy (T9-Dy) layer with 1.0 μm thickness over the cell surface, along with some intracellular nano-micro meter-sized Dy particles. X-ray photoelectron spectrometry and X-ray absorption fine structure analyses showed that the chemical composition of T9-Dy corresponded to DyPO4. X-ray diffraction analysis did not yield any spectrum from T9-Dy. Therefore, we concluded that the strain T9 accumulates and mineralizes Dy as an amorphous DyPO4. Dysprosium desorption rate from T9-Dy was 100% using 0.3 M hydrochloric acid. Furthermore, after desorption process, the strain T9 grows again in the new medium and retains the Dy accumulation ability. Thus, the strain T9 has a potential as a bioaccumulator for Dy recovery from acidic drainage through biomineralization.

Background: Jellyfish stings cause painful, papular-urticarial eruptions due to the immediate allergic, acute toxic and persistent inflammatory responses. In spite of many marine accidents and their economic impact, modes of first-aid treatment remain conventional and specific allergen and medical treatment are not yet available. The purpose of this study was to define the specific allergen of the box jellyfish Chironex yamaguchii and to study the precise mechanism of the resulting dermatitis. Methods: We comprehensively studied the immunoglobulin-binding molecules from the box jellyfish C. yamaguchii with a purification procedure and Western blotting, using sera from 1 patient and from several controls. Results: From the nematocyst wall and spine, we detected IgG-binding acidic glycoprotein (of 66 and 30 kDa) as determined by Western blot and ion-exchange chromatography. In addition, the 66-kDa protein was found to be an asparagine residue-coupled N-linked glycoprotein and the epitope resided in the protein fraction. We found that CqTX-A, the major toxic protein of the nematocyst, is also a heat-stable IgE-binding allergen. This was confirmed as a 45-kDa protein by Western blot from both nematocyst extracts and purified CqTX-A. Conclusions: The detection of these proteins may, in part, explain the combined immediate allergic-toxic and persistent allergic responses. Hopefully, our findings will lead to the development of specific venom immunotherapy for marine professional workers and tourists for jellyfish-sting dermatitis and anaphylaxis.