Modeling Tetrachloroethylene Decomposition in Photosonolysis Reactor

A mathematical model was developed for the decomposition of halogenated compounds in water and applied for tetrachloroethylene (PCE) in a flow-through photosonolysis reactor. To develop the model, a series of differential equations were formulated based on the principles of conservation of mass and mass action for hypothetical parent and daughter species, which were then solved analytically. The model sensitivity analysis was performed to determine if the model gives intuitive results. In support of the modeling effort, experiments were conducted. In a flow-through bench-scale reactor, simulated groundwater contaminated with PCE was irradiated with ultraviolet light and ultrasound concurrently in the presence of titanium dioxide (TiO2). The model was calibrated against the concentrations of PCE, trichloroethylene, methylene chloride, and chloride ion, obtained from the experiments. The proposition for the rate constants is based on fitting the model result to the experimental data. The model was further verified by comparing the model results against a different set of experimental data. The model results against available data indicated good agreement within experimental variations. The modeling suggests that PCE is more susceptible to the C-C double bond cleavage than the C-Cl bond cleavage. The results also support the assumptions that chlorinated methane compounds can be degraded at higher rates than chlorinated ethylene and that the values of the degradation rate constants increase with a decreasing number of chlorine atoms attached to the hydrocarbon compound.     

Identification of Tumor Suppressive Genes Regulated by miR-31-5p and miR-31-3p in Head and Neck Squamous Cell Carcinoma

We identified the microRNA (miRNA) expression signature of head and neck squamous cell carcinoma (HNSCC) tissues by RNA sequencing, in which 168 miRNAs were significantly upregulated, including both strands of the miR-31 duplex (miR-31-5p and miR-31-3p). The aims of this study were to identify networks of tumor suppressor genes regulated by miR-31-5p and miR-31-3p in HNSCC cells. Our functional assays showed that inhibition of miR-31-5p and miR-31-3p attenuated cancer cell malignant phenotypes (cell proliferation, migration, and invasion), suggesting that they had oncogenic potential in HNSCC cells. Our in silico analysis revealed 146 genes regulated by miR-31 in HNSCC cells. Among these targets, the low expression of seven genes (miR-31-5p targets: CACNB2 and IL34; miR-31-3p targets: CGNL1, CNTN3, GAS7, HOPX, and PBX1) was closely associated with poor prognosis in HNSCC. According to multivariate Cox regression analyses, the expression levels of five of those genes (CACNB2: p = 0.0189; IL34: p = 0.0425; CGNL1: p = 0.0014; CNTN3: p = 0.0304; and GAS7: p = 0.0412) were independent prognostic factors in patients with HNSCC. Our miRNA signature and miRNA-based approach will provide new insights into the molecular pathogenesis of HNSCC.     

Conventional detection of 2,4-dinitrophenol using quartz crystal microbalance

We present conventional detection of 2,4-dinitrophenol (DNP) for using the competitive reaction between DNP and DNP-conjugated albumin onto DNP antibody immobilized quartz crystal microbalance (QCM). This QCM method allows detection of DNP concentration in the range of 0.01 to 100 ng/ml; linear correlation obtains DNP concentration from 1 to 100 ng/ml.     

Effects of Samarium Oxide Addition on the Phase Composition, Microstructure, and Electrical Resistivity of Aluminum Nitride Ceramics

The phase composition, microstructure, and electrical resistivity of hot-pressed AlN ceramics with 0–4.8 wt% Sm₂O₃ additive were investigated. The phase composition was approximately consistent with that estimated from the Sm₂O₃–Al₂O₃ phase diagram using the amount of added Sm₂O₃ and oxygen content of the AlN raw material. When sintered at more than 1800°C, the AlN ceramics with 1.0–2.9 wt% Sm₂O₃ additive contained an Sm-β-alumina phase wetting the grain boundaries, and their electrical resistivity considerably decreased to 10¹⁰–10¹²Ω·cm. This resistivity decrease was caused by the continuity of the Sm-β-alumina phase with a resistivity lower than that of bulk AlN.     

Structure determination of tubular crystals of membrane proteins. IV. Distortion correction and its combined application with real-space averaging and solvent flattening

A method for correction of three-dimensional distortions has been developed for helical assemblies and applied to tubular crystals of Ca2+-ATPase. This method approximates distorted helical particles with short straight segments of different orientation parameters, which are determined by fitting them to the reference data in reciprocal space. Thus, the method follows Beroukhim and Unwin [Ultramicroscopy 70 (1997) 57], but is more extended to achieve better alignment and to cope with images of poor S/N ratio. Substantial improvements were achieved by dividing the reference image into the segments of optimal lengths in exactly the same way as the test, and treating the distortions in the near and far sides of a helical particle separately. The improvement was further enhanced when combined with real-space averaging [Yonekura, Toyoshima, Ultramicroscopy 84 (2000) 15] and solvent flattening [Yonekura, Toyoshima, Ultramicroscopy 84 (2000) 29], and most pronounced when all these three were applied iteratively.     

Impact of Oncogenic Targets by Tumor-Suppressive miR-139-5p and miR-139-3p Regulation in Head and Neck Squamous Cell Carcinoma

We newly generated an RNA-sequencing-based microRNA (miRNA) expression signature of head and neck squamous cell carcinoma (HNSCC). Analysis of the signature revealed that both strands of some miRNAs, including miR-139-5p (the guide strand) and miR-139-3p (the passenger strand) of miR-139, were downregulated in HNSCC tissues. Analysis of The Cancer Genome Atlas confirmed the low expression levels of miR-139 in HNSCC. Ectopic expression of these miRNAs attenuated the characteristics of cancer cell aggressiveness (e.g., cell proliferation, migration, and invasion). Our in silico analyses revealed a total of 28 putative targets regulated by pre-miR-139 (miR-139-5p and miR-139-3p) in HNSCC cells. Of these, the GNA12 (guanine nucleotide-binding protein subunit alpha-12) and OLR1 (oxidized low-density lipoprotein receptor 1) expression levels were identified as independent factors that predicted patient survival according to multivariate Cox regression analyses (p = 0.0018 and p = 0.0104, respectively). Direct regulation of GNA12 and OLR1 by miR-139-3p in HNSCC cells was confirmed through luciferase reporter assays. Moreover, overexpression of GNA12 and OLR1 was detected in clinical specimens of HNSCC through immunostaining. The involvement of miR-139-3p (the passenger strand) in the oncogenesis of HNSCC is a new concept in cancer biology. Our miRNA-based strategy will increase knowledge on the molecular pathogenesis of HNSCC.     

Photosonolysis of TCA, TCE, and PCE in Flow-Through Reactor System

Photosonolysis of 1,1,1-trichloroethane (TCA), trichloroethylene (TCE), and tetrachloroethylene (PCE) in water was investigated using a cup-horn, flow-through reactor system. Water containing titanium dioxide was deliberately contaminated with a mixture of volatile organic compound (VOC)—TCA, TCE, and PCE—and individual VOC. These solutions were irradiated with ultraviolet light (UV) and ultrasonic waves (US), independently and concurrently (UVUS). The values of the first-order degradation rate constant and the removal efficiency for the VOC were evaluated for the UV, US, and UVUS treatments. The results showed that the concurrent use of UV and US increased the VOC degradation rate and removal efficiency beyond the additive effect of UV and US, suggesting that the UVUS effect on the decomposition of the VOC is synergistic under certain conditions. TCE and PCE were more readily degraded than TCA, suggesting that double-bond cleavage is one of the initial degradation pathways. With the reactor specifications used, the photosonolysis process can produce water meeting the drinking water standard (MCLs of 5 μg∕L) for TCE and PCE with a removal efficiency of approximately 90%.