Monitoring of methanogen density using near-infrared spectroscopy

In order to improve anaerobic digester productivity, raising the microbial mass in the reactor and the prediction of changes in the biomass is required. In this study the possibilities for using near-infrared spectroscopy (NIR) to monitor methanogen density in a biogas process was examined. Methane production from H₂ and CO₂ was carried out with acclimated-methanogens with fed-batch substrate gas (H₂/CO₂, 80:20 v/v) at pH 7 and 37°C. The cells of the methanogens were washed and dried, and then original NIR spectra for predicting methanogen density were recorded. The specified absorption spectra were collected and examined. As a result, absorption spectrum peaks were found to be predominantly based on alpha proteins and lipids mainly from the cytoplasm and cell membranes of the methanogens. Furthermore, NIR was used to monitor the methane fermentation system using acetic acid as substrate. The responses from NIR analysis were correlated to methanogen density of fermentation broth by partial least-squares regressions. The correlation coefficient (R), model standard error of calibration (SEC) and standard error of prediction (SEP) of the test calibration for methanogen density were 0.99, 0.14 gl⁻¹ and 0.55 gl⁻¹, respectively. For volatile fatty acids (acetic acid) R, SEC and SEP were 0.99, 0.36 gl⁻¹ and 0.63 gl⁻¹, respectively. The results indicated that within the range of the density of methanogens and the concentration of acetic acid used in this study, it was possible to monitor the important variables of methanogen density and acetate concentration simultaneously in pure substrate-fed anaerobic digesters.     

Preparation and characterization of porous granular ceramic containing dispersed aluminum and iron oxides as adsorbents for fluoride removal from aqueous solution

Porous granular ceramic adsorbents containing dispersed aluminum and iron oxides were synthesized by impregnating with salt solutions followed by precipitation at 600°C. In the present work detailed studies were carried out to investigate the effect of contact time, adsorbent dose, initial solution pH and co-existing anions. Characterization studies on the adsorbent by SEM, XRD, EDS, and BET analysis were carried out to clarify the adsorption mechanism. The adsorbents were sphere in shape, 2-3mm in particle size, highly porous and showed specific surface area of 50.69 sq m/g. The fluoride adsorption capacity of prepared adsorbent was 1.79 mg/g, and the maximum fluoride removal was obtained at pH 6. Both the Langmuir and Freundlich isotherm models were found to represent the measured adsorption data well. The experimental data were well explained with pseudo-second-order kinetic model. Results from this study demonstrated potential utility of Al/Fe dispersed in porous granular ceramics that could be developed into a viable technology for fluoride removal from aqueous solution.     

Nitrate removal from groundwater by cooperating heterotrophic with autotrophic denitrification in a biofilm-electrode reactor

An intensified biofilm-electrode reactor (IBER) combining heterotrophic and autotrophic denitrification was developed for treatment of nitrate contaminated groundwater. The reactor was evaluated with synthetic groundwater (NO₃⁻-N50 mg L⁻¹) under different hydraulic retention times (HRTs), carbon to nitrogen ratios (C/N) and electric currents (I). The experimental results demonstrate that high nitrate and nitrite removal efficiency (100%) were achieved at C/N = 1, HRT = 8 h, and I = 10 mA. C/N ratios were reduced from 1 to 0.5 and the applied electric current was changed from 10 to 100 mA, showing that the optimum running condition was C/N = 0.75 and I = 40 mA, under which over 97% of NO₃⁻-N was removed and organic carbon (methanol) was completely consumed in treated water. Simultaneously, the denitrification mechanism in this system was analyzed through pH variation in effluent. The CO₂ produced from the anode acted as a good pH buffer, automatically controlling pH in the reaction zone. The intensified biofilm-electrode reactor developed in the study was effective for the treatment of groundwater polluted by nitrate.     

Verification analysis of thermoluminescent albedo neutron dosimetry at MOX fuel facilities

Radiation workers engaging in the fabrication of MOX fuels at the Japan Atomic Energy Agency-Nuclear Fuel Cycle Engineering Laboratories are exposed to neutrons. Accordingly, thermoluminescent albedo dosemeters (TLADs) are used for individual neutron dosimetry. Because dose estimation using TLADs is susceptible to variation of the neutron energy spectrum, the authors have provided TLADs incorporating solid-state nuclear tracks detectors (SSNTDs) to selected workers who are routinely exposed to neutrons and have continued analysis of the relationship between the SSNTD and the TLAD (T/R(f)) over the past 6 y from 2004 to 2009. Consequently, the T/R(f) value in each year was less than the data during 1991-1993, although the neutron spectra had not changed since then. This decrease of the T/R(f) implies that the ratio of operation time nearby gloveboxes and the total work time has decreased.     

A new microbial method for more efficient production of Nalpha-benzyloxycarbonyl-L-aminoadipate delta-semialdehyde and Nalpha-benzyloxycarbonyl-D-aminoadipate delta-semialdehyde

A new biochemical method for more efficient production of Nalpha-benzyloxycarbonyl-L-aminoadipate delta-semialdehyde (Nalpha-Z-L-AASA) and Nalpha-Z-D-AASA was developed with cells of Rhodococcus sp. AIU Z-35-1. Using the cells harvested after 1 d of cultivation, more than 95 mM Nalpha-Z-L-AASA was produced from 100 mM Nalpha-Z-L-lysine by incubating at pH 5.0 for 1 d at 30 degrees C or by incubating at pH 7.0 for 2 d at 10 degrees C. A similar conversion yield of Nalpha-Z-D-AASA was also obtained under the same conditions. These reaction times required were 1/4 and 1/2 of the respective ones by the method with amine oxidase, and the yields of Nalpha-Z-L-AASA and Nalpha-Z-D-AASA were 2 times higher than the respective ones by the method with amine oxidase. In addition, this method had the advantages of not requiring purification of enzyme and addition of catalase. Thus, the microbial method proposed here was superior to the chemical and other biochemical methods in simplicity, reaction rate, and yield.     

Inhibitory Action of Antidepressants on Mouse Betaine/GABA Transporter (BGT1) Heterologously Expressed in Cell Cultures

Betaine/γ-aminobutyric acid (GABA) transporter (BGT1, SLC6A12) is a member of the Na(+)- and Cl(-)-dependent neurotransmitter transporter gene family with a homology to the GABA transporters (GATs), GAT1 (SLC6A1), GAT2 (SLC6A13) and GAT3 (SLC6A11) (HUGO nomenclature). Since antidepressants have been reported to inhibit GABA uptake, we examined those effects on mouse BGT1 (mBGT1) in comparison with other mouse GAT (mGAT) subtypes in the heterologously expressed cell cultures. All antidepressants tested here inhibited the [(3)H]GABA uptake through mBGT1 and mGATs in a rank order of potency with mBGT1 > mGAT1-3. Kinetic analyses for maprotilline, mianserine and trimipramine revealed that they inhibited mBGT1 and mGAT1 noncompetitively, except that mianserine competitively inhibited mBGT1. These results provided a clue to investigate the structure-function relationship of mBGT1 using antidepressants as a tool, leading to the identification of potential candidates for selective and specific inhibitors of mBGT1.     

Sorption kinetics of heavy oil into porous carbons

Sorption kinetics of heavy oil into porous carbons was evaluated by a concept of liquid sorption coefficient obtained from the weight increase of heavy oil with sorption time, which was measured by a wicking test. Exfoliated graphite, carbonized fir fibers and carbon fiber felts were used as porous materials. It was found that the liquid sorption coefficient of fibrous carbons was twice larger than that of exfoliated graphite. Such a difference in the liquid sorption coefficient between the exfoliated graphite and two fibrous carbons was caused by a difference in effective sorption porosity and tortuosity between them. For the exfoliated graphite and carbonized fir fibers, the liquid sorption coefficient and the effective sorption porosity were strongly dependent on their density. The maximum values of both liquid sorption coefficient and effective sorption porosity of the exfoliated graphite were shown at the bulk density around 16 kg/m³. The liquid sorption coefficient of the carbonized fir fibers increased with increasing the density in the range from 6 to 30 kg/m³. When the carbonized fir fibers were densified above 30 kg/m³, the sorption rate was saturated. On the other hand, the sorption kinetics into the carbon fiber felt was almost independent of the bulk density, because the density of the carbon fiber felt is not effective for the pore structure. The effect of bulk density on the sorption kinetics could be supported from an analysis of pore structure of the porous carbons with different densities, which was measured by mercury porosimeter.     

In vitro heat generation by ferrimagnetic maghemite microspheres for hyperthermic treatment of cancer under an alternating magnetic field

Ferrimagnetic materials can be expected to be useful as thermo seeds for hyperthermic treatment of cancer, especially where the cancer is located in deep parts of body, as they can generate heat by magnetic hysteretic loss when they are placed in an alternating magnetic field. Recently, it was reported that ferrimagnetic maghemite (γ-Fe₂O₃) microspheres 20–30 μm in diameter prepared in aqueous solution can show excellent heat generating ability. However, these microspheres have many cracks on their surfaces. In this study, the preparation conditions for the microspheres was further optimized in order to obtain crack-free ferrimagnetic microspheres, and the in vitro heat generation of the obtained microspheres was measured in an agar phantom under an alternating magnetic field. Crack-free γ-Fe₂O₃ microspheres 20–30 μm in diameter were obtained successfully. Their saturation magnetization and coercive force were 68 emu g⁻¹ and 198 Oe, respectively. Their heat generation under an alternating magnetic field of 300 Oe at 100 kHz was estimated to be 42 W g⁻¹. The microspheres showed in vitro heat generation when they were dispersed in an agar phantom and placed under an alternating magnetic field. It is believed that these microspheres may be useful for the in situ hyperthermic treatment of cancer.     

Thermochromism in an organic crystal based on the coexistence of sigma- and pi-dimers

Transition-metal complexes and organic radical molecules can be used to make electric conductors and ferromagnets, the optical properties of which can be controlled by changing temperature and are used as molecular switches and sensors. Whereas a number of organic radicals in solution show temperature-dependent optical properties, such behaviour in crystalline forms is more rare. Here, we show a fully reversible continuous thermochromism with a unique mechanism in purely organic crystals of diazaphenalenyl radical. This behaviour is based on changes in the diazaphenalenyl dimers coexisting in the crystal. From the X-ray crystal structure analyses and temperature-dependent visible spectra, we conclude the presence of a thermal equilibrium between sigma-bonded and pi-bonded dimers, which are separated by 2.62(6) kcal mol(-1). This conclusion is supported by room-temperature electron spin resonance spectra of the solid, which showed signals that are attributable to a thermally accessible triplet state of the pi-dimer structure. This proves the coexistence of two dimers of different bonding natures in the crystal, causing it to demonstrate thermometer-like behaviour.     

Cytochrome c-552 from gram-negative alkaliphilic Pseudomonas alcaliphila AL15-21T alters the redox properties at high pH

A soluble class I cytochrome c of an alkaliphile was purified and characterized, and its primary structure was determined. This is the first example of a soluble class I cytochrome c in alkaliphiles. Cells the alkaliphilic gram-negative bacterium Pseudomonas alcaliphila AL15-21(T) grown at pH 10 had a soluble cytochrome c content that was more than twofold that of strain AL15-21(T) cells grown at pH 7 under air-limited conditions. Cytochrome c-552, a soluble cytochrome c with a low molecular weight, was purified from strain AL15-21(T) cells grown at pH 10 under air-limited conditions. Cytochrome c-552 had a molecular mass of 7.5 kDa and exhibited an almost fully reduced state in the resting form, which exhibited absorption maxima at wavelengths of 552, 523 and 417 nm. In the oxidized state, it exhibited an absorption maximum at 412 nm when it was oxidized by ferricyanide, its isoelectric point (pI) was 4.3 and it contained one heme c as a prosthetic group. Cytochrome c-552 was autoreduced at pH 10, and the autoreduction was reproducible. On the other hand, the autoreduction of cytochrome c-552 was not observed at pH 7.0. When pH was increased from 7.0 to 8.3, its midpoint redox potentials (E(m) values) increased from +228 mV to +276 mV as determined by redox titrations, and from +217 mV to +275 mV as determined by cyclic voltammetric measurements. The amino acid sequence deduced by cytochrome c-552 gene analysis revealed that the sequence consists of 96 residues, including 19 residues as an amino-terminal signal peptide. A phylogenetic tree based on amino acid sequence indicated that the protein belongs to group 4, cytochrome c(5) in class I cytochrome c.