Analyzing the performance of a cluster-based architecture for immersive visualization systems

Cluster computing has become an essential issue for designing immersive visualization systems. This paradigm employs scalable clusters of commodity computers with much lower costs than would be possible with the high-end, shared memory computers that have been traditionally used for virtual reality purposes. This change in the design of virtual reality systems has caused some development environments oriented toward shared memory computing to require modifications to their internal architectures in order to support cluster computing. This is the case of VR Juggler, which is considered one of the most important virtual reality application development frameworks based on open source code.     

Formaldehyde in human cancer cells: detection by preconcentration-chemical ionization mass spectrometry

A rapid and highly sensitive method for the detection of formaldehyde utilizing selected ion flow tube-chemical ionization mass spectrometry is reported. Formaldehyde in aqueous biological samples is preconcentrated by distillation and directly analyzed using gas-phase thermal energy proton transfer from H30+; this procedure can be performed in 30 min. The method detection limit for formaldehyde based on seven replicate measurements of reference water samples (2.5 mL) is 80 nM at the 99% confidence level. Detection is linear up to 130 microM. This technique allows the first measurement of natural formaldehyde levels in human cancer cells in vitro. Elevated levels of formaldehyde relative to the reference water are observed for doxorubicin-sensitive cells (MCF-7 breast cancer, K562 leukemia, HeLa S3 cervical cancer) with estimated intracellular formaldehyde concentrations ranging from 1.5 to 4.0 microM, whereas formaldehyde in doxorubicin-resistant MCF-7/Adr breast cancer cells is essentially at reference level. This trend is inverted for prostate cancer cells LNCaP (sensitive) and DU-145 (resistant). Correlation of natural formaldehyde level with doxorubicin cytotoxicity is a function of the expression of enzymes that neutralize oxidative stress and the drug efflux pump, P-170 glycoprotein.     

Proteins Marking the Sequence of Genotoxic Signaling from Irradiated Mesenchymal Stromal Cells to CD34+ Cells

Non-targeted effects (NTE) of ionizing radiation may initiate myeloid neoplasms (MN). Here, protein mediators (I) in irradiated human mesenchymal stromal cells (MSC) as the NTE source, (II) in MSC conditioned supernatant and (III) in human bone marrow CD34+ cells undergoing genotoxic NTE were investigated. Healthy sublethal irradiated MSC showed significantly increased levels of reactive oxygen species. These cells responded by increasing intracellular abundance of proteins involved in proteasomal degradation, protein translation, cytoskeleton dynamics, nucleocytoplasmic shuttling, and those with antioxidant activity. Among the increased proteins were THY1 and GNA11/14, which are signaling proteins with hitherto unknown functions in the radiation response and NTE. In the corresponding MSC conditioned medium, the three chaperones GRP78, CALR, and PDIA3 were increased. Together with GPI, these were the only four altered proteins, which were associated with the observed genotoxic NTE. Healthy CD34+ cells cultured in MSC conditioned medium suffered from more than a six-fold increase in γH2AX focal staining, indicative for DNA double-strand breaks, as well as numerical and structural chromosomal aberrations within three days. At this stage, five proteins were altered, among them IQGAP1, HMGB1, and PA2G4, which are involved in malign development. In summary, our data provide novel insights into three sequential steps of genotoxic signaling from irradiated MSC to CD34+ cells, implicating that induced NTE might initiate the development of MN.     

Model-based reliability analysis

Testing has typically been a key means of detecting anomalous performance and of providing a foundation for estimating reliability for weapon systems. The objective of model-based reliability analysis (MBRA) is to identify ways to capitalize on the insights gained from physical-response modeling both to supplement the information obtained from testing and to better-understand test results. Five general MBRA processes are identified which can capitalize on physical response modeling results to make both quantitative and qualitative statements about product reliability. A case study that explores 1 of these 5 processes was completed and is described in detail. It had the benefits: MBRA can be used to determine a performance baseline against which current and future test results can be compared; during the design process, MBRA can provide tradeoff studies such that development time and required test assets can be reduced; MBRA can be used to evaluate the impact of production and part changes, as well as aging degradation, if they arise during the product life cycle; and MBRA lays the foundation to evaluate anomalies that are observed in a test program. Typically it has been challenging to determine how anomalous behavior can manifest itself under different-but still valid-conditions. One can use modeling to inject hypothesized behaviors under different conditions and observe the consequences     

The lantibiotic mersacidin inhibits peptidoglycan synthesis by targeting lipid II

The lantibiotic mersacidin exerts its bactericidal action by inhibition of peptidoglycan biosynthesis. It interferes with the membrane-associated transglycosylation reaction; during this step the ultimate monomeric peptidoglycan precursor, undecaprenyl-pyrophosphoryl-MurNAc-(pentapeptide)-GlcNAc (lipid II) is converted into polymeric nascent peptidoglycan. In the present study we demonstrate that the molecular basis of this inhibition is the interaction of mersacidin with lipid II. The adsorption of [14C]mersacidin to growing cells, as well as to isolated membranes capable of in vitro peptidoglycan synthesis, was strictly dependent on the availability of lipid II, and antibiotic inhibitors of lipid II formation strongly interfered with this binding. Direct evidence for the interaction was provided by studies with isolated lipid II. [14C]mersacidin associated tightly with [14C]lipid II micelles; the complex was stable even in the presence of 1% sodium dodecyl sulfate. Furthermore, the addition of isolated lipid II to the culture broth efficiently antagonized the bactericidal activity of mersacidin. In contrast to the glycopeptide antibiotics, complex formation does not involve the C-terminal D-alanyl-D-alanine moiety of the lipid intermediate. Thus, the interaction of mersacidin with lipid II apparently occurs via a binding site which is not targeted by any antibiotic currently in use.     

The Involvement of the Psychologist's Family in the Establishment of a Public Image of the Profession.

Psychologists of late have been turning increasing attention to the problem of defining their profession (Amer. Psychologist, 1958, 13, 645-652; 1959, 14, 523-524) and outlining a public image (see record 2005-08103-001). The present writer applauds these efforts from the midst of the semantic battlefield upon which the psychologist's family finds itself when communicating with the public. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Activation of the glmS Ribozyme Confers Bacterial Growth Inhibition

The ever‐growing number of pathogenic bacteria resistant to treatment with antibiotics call for the development of novel compounds with as‐yet unexplored modes of action. Here, we demonstrate the in vivo antibacterial activity of carba‐α‐d ‐glucosamine (CGlcN). In this mode of action study, we provide evidence that CGlcN‐mediated growth inhibition is due to glmS ribozyme activation, and we demonstrate that CGlcN hijacks an endogenous activation pathway, hence utilizing a prodrug mechanism. This is the first report describing antibacterial activity mediated by activating the self‐cleaving properties of a ribozyme. Our results open the path towards a compound class with an entirely novel and distinct molecular mechanism.     

Cost Savings in the Ozone Treatment of Paper Mill Effluents Achieved By a Closed-Loop Ozone Control System

Control strategies were created to reduce the operating costs of ozone stages of effluent treatment plants in paper mills as well as to improve the quality of the effluent. Biologically treated effluents from five mills were subjected to laboratory and pilot tests. All COD target values could be reached and maintained with SAC-based control strategies. Disturbing events were compensated with a deviation of only 2% within maximum 3.1 volume exchanges, depending on the kind of event. The SAC (spectral absorption coefficient) was found to be highly suitable for controlling the ozone dosage. In a SME paper mill, 20% of the operating costs of an ozone plant can be saved. The return on investment for such a system is thus about 8 months.