Molecular Identification of Four Genetically Modified Maize (Bt11, Bt176, Mon810 and T25) by Duplex Quantitative Real-Time PCR

In response to the increasing number of genetically modified (GM) events released on the market, control laboratories explore various strategies to simplify and reduce the number of tests needed to characterise the content in genetically modified organism (GMO) of a given sample. Lastly, multiplexing is considered as one of the possible ways to decrease the time and cost of analysis. Here, we report the development of four duplex polymerase chain reaction (PCR) tests for the identification and the quantification of four maize transformation events from which commercial lines have been authorised in Europe namely, Bt11 and Bt176 (Syngenta, DE, USA), Mon810 MaisGard? (Monsanto, MO, USA) and T25 Liberty Link? (Bayer CropScience, Monheim, Germany). The duplex PCR tests combine a maize-specific PCR test hybridising in the Adh1 locus with an event-specific detection system designed on a junction fragment for each of these four GM maize. Real-time PCR tests, suitable to comply with the European regulation, were designed by using Taqman® chemistry.     

MtBE biodegradation in a gravity flow, high-biomass retaining bioreactor

The aerobic biodegradation of methyl tert-butyl ether (MtBE), a widely used fuel oxygenate, was investigated using a pilot-scale biomass-retaining bioreactor called a Biomass Concentrator Reactor (BCR). The reactor was operated for a year at a flow rate of 2500 L/d on Cincinnati dechlorinated tap water and an influent MtBE concentration of 5 mg/L. Treatment efficiency of MtBE in the reactor during stable operations exceeded 99.9%. The upper 95% confidence levels of effluent MtBE concentrations and its degradation byproduct tert-butyl alcohol (TBA) were 2.9 and 0.9 microg/L, respectively, during these stable conditions. In addition, the effluent was found to be of better quality than the influent tap water as reflected by dissolved organic carbon analysis. Microbial community DNA profiling was carried out using denaturing gradient gel electrophoresis (DGGE) of polymerase chain reaction amplified 16s rDNA. The BCR was found to be inhabited by a wide spectrum of bacterial species, most notably microorganisms related to the genera Hydrogenophaga, Methylobacterium, Sphingomonas, and Pseudomonas. These organisms were previously reported to be associated with MtBE degradation. With the contamination of groundwater by MtBE being a wide-ranging problem throughout the United States, it is essential to develop a technology capable of effectively remediating such aquifers in order to protect public health and the environment. The BCR's simple operation and low maintenance requirements may render it an economically attractive approach to remediating groundwater contaminated with MtBE.     

Flexible large area polymer solar cells based on poly(3-hexylthiophene)/fullerene

Photovoltaic devices based on regioregular poly(3-hexylthiophene) (P3HT) and ([6,6]-phenyl-C61-butyric acid methyl ester) (PCBM) were fabricated and characterized using 5×5 cm ITO polyester foils with an active cell area of 0.5×0.5 cm². The HOMO/LUMO of P3HT and PCBM were estimated from cyclic voltammetry data. The complete quenching of photoluminescence of P3HT after mixing with PCBM indicates an effective charge transfer from P3HT to PCBM. The absorption spectrum of a blend (1:3 wt%) of both components shows that there is no ground state doping. Following device parameters without any special postproduction treatment were determined: V_OC=600 mV, I_SC=6.61 mA/cm², FF=0.39 and η_AM1.5 (P_IN:100 mW/cm²)=1.54%.     

Ultra-shallow raised p+−n junctions formed by diffusion from selectively depositedIn-situ doped Si0.7Ge0.3

In this paper, a novel raised p⁺−n junction formation technique is presented. The technique makes use ofin- situ doped, selectively deposited Si_0.7Ge_0.3 as a solid diffusion source. In this study, the films were deposited in a tungsten halogen lamp heated cold-walled rapid thermal processor using SiCl₂H₂, GeH₄, and B₂H₆. The microstructure of the Si_0.7Ge_0.3 layer resembles that of a heavily defected epitaxial layer with a high density of misfit dislocations, micro-twins, and stacking faults. Conventional furnace annealing or rapid thermal annealing were used to drive the boron from thein- situ doped Si_0.7Ge_0.3 source into silicon to form ultra-shallow p⁺−n junctions. Segregation at the Si_0.7Ge_0.3/Si interface was observed resulting in an approximately 3:1 boron concentration discontinuity at the interface. Junction profiles as shallow as a few hundred angstroms were formed at a background concentration of 10¹⁷ cm⁻³.     

TRANSIENT VARIATIONS OF THERMAL STRESSES AND THE RESULTING RESIDUAL STRESSES WITHIN A THIN PLATE DURING WELDING PROCESSES

Variations of thermal and residual stresses are investigated inside a thin mild steel plate during welding processes. The temperature distribution is determined analytically using Green's functions. Transient thermal stresses developed within the plate are computed numerically. The resulting residual stresses, which remain after cooling of the plate, are found based on a method presented originally by Tall (L. Tall, Welding Journal, vol. 43, pp. 10–23, 1964). It is found that welding speed and heat source intensity are the main factors that affect the residual stress formation in the plate.     

Cavity Length Independent Continuous Repetition Rate Tuning of a Self-Seeded Gain-Switched Fabry–PÉrot Laser

We propose a novel method that allows continuous repetition rate tuning of a self-seeded gain-switched Fabry-Perot laser without the need for change in cavity length. This is achieved by employing a linearly chirped fiber Bragg grating with a large dispersion parameter. The dispersed pulses overlap to produce a continuous-wave-like feedback into the gain-switched laser cavity. By using the proposed experimental setup, we demonstrate pulses portraying sidemode suppression ratios of at least 30 dB and widths of about 30 ps over the entire repetition rate tuning range of 2.5-10 GHz.     

Next‐Generation Activated Carbon Supercapacitors: A Simple Step in Electrode Processing Leads to Remarkable Gains in Energy Density

The global supercapacitor market has been growing rapidly during the past decade. Today, virtually all commercial devices use activated carbon. In this work, it is shown that laser treatment of activated carbon electrodes results in the formation of microchannels that can connect the internal pores of activated carbon with the surrounding electrolyte. These microchannels serve as electrolyte reservoirs that in turn shorten the ion diffusion distance and enable better interaction between the electrode surfaces and electrolyte ions. The capacitance can be further increased through fast and reversible redox reactions on the electrode surface using a redox‐active electrolyte, enabling the operation of a symmetric device at 2.0 V, much higher than the thermodynamic decompostion voltage of water. This simple approach can alleviate the low energy density of supercapacitors which has limited the widespread use of this technology. This work represents a clear advancement in the processing of activated carbon electrodes toward the next‐generation of low‐cost supercapacitors.     

Swallowing performance in patients with vocal fold motion impairment

Twenty-seven patients with vocal fold motion impairment underwent detailed pharyngoesophagel manometry with a strain gauge assembly linked to a computer recorder. Nine were known to have lesions of the central vagal trunk or nucleus, 9 had recurrent laryngeal nerve (RLN) palsy, and the remainder were idiopathic. The site of the lesion was a more important determinant of subjective swallowing performance than the position of the involved cord at laryngoscopy. Patients with central lesions had lower tonic and contraction upper esophageal sphincter (UES) pressures than 25 age-matched controls, suggesting that high cervical branches of the lower cranial nerves are important in UES excitatory innervation. RLN palsy patients showed significantly increased pharyngeal contraction amplitude and reduced pharyngoesophageal wave durations. The results suggest that the dysphagia associated with vocal fold motion impairment is not simply due to the disruption of laryngeal deglutitive kinetics, but to independent effects on pharyngeal function.     

Distribution of fibroblast growth factor (FGF)-2 and FGF receptor-1 messenger RNA expression and protein presence in the mid-trimester human fetus

Fibroblast growth factors (FGF) are known to have key roles in embryonic growth and morphogenesis, but their presence and contributions to fetal development are unclear. In particular, little information exists as to the relevance of FGF and their specific receptors to human fetal development. We studied the anatomical distribution of messenger RNA encoding FGF-2 and one of its high affinity receptors, FGFR1, using in situ hybridization in a variety of human fetal tissues in early second trimester. Corresponding protein distributions were determined by immunohistochemistry. Both FGF-2 and FGFR1 mRNA and proteins were found to be present in every organ and tissue examined, but with defined cellular localizations. In skeletal muscle, both FGF-2 and FGFR1 mRNA and peptides were present in differentiated fibers, and both co-localized to proliferating chondrocytes of the epiphyseal growth plate. FGF-2 and FGFR1 mRNA and peptides were also present within cardiac or gastrointestinal smooth muscle. Within the gastrointestinal tract FGF-2 mRNA and peptide were located in the submucosal tissue, whereas FGFR1 was expressed within the overlying mucosa. Similarly, in skin, FGF-2 was expressed within the dermis whereas FGFR1 mRNA and peptide were most apparent in the stratum germinativum of the epidermis. In kidney and lung, FGFR1 mRNA was located in the tubular and alveolar epithelia respectively, whereas FGF-2 was expressed in both epithelial and mesenchymal cell populations. Both growth factor and receptor were widespread in both neuroblasts and glioblasts in the cerebral cortex of the brain. Immunoreactivity for FGF-2 and FGFR1 was seen in all vascular endothelial cells of major vessels and capillaries. Within the skin, kidney, lung, and intestine FGF-2 immunoreactivity was found in basement membranes underlying epithelia, and was associated with the extracellular matrix and plasma membranes of many cell types. The results show that FGF-2 and one of its receptors are widely expressed anatomically in the mid-trimester human fetus.