808 research outputs found

    The Effects of Arsenical Compounds on Growth and Enzymes of Klebsiella Pneumoniae

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    For many years people have equated arsenic or compounds containing arsenic with poison. Inorganic arsenic compounds are used as chemotherapeutic agents as well as poisons. Organic arsenicals were introduced at the start of this century launching modern chemotherapy. The introduction of antibiotics in the 1940’s virtually replaced organic arsenicals in chemotherapy. Solutions of inorganic arsenic compounds are used as tonics for animals and to finish animals for show. Because arsenicals are excreted by animals in much the same structure as they are consumed and arsenite prevents both putrefaction and growth, it is possible the decomposition of animal excreta will be inhibited. The decomposition of animal wastes is of interest to the laboratory and to the nation. Thus, this study was undertaken to determine if growth could be inhibited by either the feed additive 3-nitro-40hydroxyphenylarsonic acid or 3-nitro-4 hydroxyphenlarsine oxide. Enzyme investigations were made to determine whether these two arsenicals inhibited enzymes of the tricarboxylic acid cycle

    Identification of Long stress-induced non-coding transcripts that have altered expression in cancer

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    AbstractIt has recently become clear that the transcriptional output of the human genome is far more abundant than previously anticipated, with the vast majority of transcripts not coding for protein. Utilizing whole-genome tiling arrays, we analyzed the transcription across the entire genome in both normal human bronchial epithelial cells (NHBE) and NHBE cells exposed to the tobacco carcinogen NNK. Our efforts focused on the characterization of non-coding transcripts that were greater than 300 nucleotides in length and whose expression was increased in response to NNK. We identified 12 Long Stress-Induced Non-coding Transcripts that we term LSINCTs. Northern blot analysis revealed that these transcripts were larger than predicted from the tiling array data. Quantitative real-time RT-PCR performed across a panel of normal cell lines indicates that these transcripts are more abundantly expressed in rapidly growing tissues or in tissues that are more prone to cellular stress. These transcripts that have increased expression after exposure to NNK also had increased expression in a number of lung cancer cell lines and also in many breast cancer cell lines. Collectively, our results identified a new class of long stress responsive non-coding transcripts, LSINCTs, which have increased expression in response to DNA damage induced by NNK. LSINCTs interestingly also have increased expression in a number of cancer-derived cell lines, indicating that the expression is increased in both, correlating cellular stress and cancer

    Six simple guidelines for introducing new genera of fungi

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    We formulate five guidelines for introducing new genera, plus one recommendation how to publish the results of scientific research. We recommend that reviewers and editors adhere to these guidelines. We propose that the underlying research is solid, and that the results and the final solutions are properly discussed. The six criteria are: (1) all genera that are recognized should be monophyletic; (2) the coverage of the phylogenetic tree should be wide in number of species, geographic coverage, and type species of the genera under study; (3) the branching of the phylogenetic trees has to have sufficient statistical support; (4) different options for the translation of the phylogenetic tree into a formal classification should be discussed and the final decision justified; (5) the phylogenetic evidence should be based on more than one gene; and (6) all supporting evidence and background information should be included in the publication in which the new taxa are proposed, and this publication should be peer-reviewed

    Gradient microfluidics enables rapid bacterial growth inhibition testing

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    Bacterial growth inhibition tests have become a standard measure of the adverse effects of inhibitors for a wide range of applications, such as toxicity testing in the medical and environmental sciences. However, conventional well-plate formats for these tests are laborious and provide limited information (often being restricted to an end-point assay). In this study, we have developed a microfluidic system that enables fast quantification of the effect of an inhibitor on bacteria growth and survival, within a single experiment. This format offers a unique combination of advantages, including long-term continuous flow culture, generation of concentration gradients, and single cell morphology tracking. Using Escherichia coli and the inhibitor amoxicillin as one model system, we show excellent agreement between an on-chip single cell-based assay and conventional methods to obtain quantitative measures of antibiotic inhibition (for example, minimum inhibition concentration). Furthermore, we show that our methods can provide additional information, over and above that of the standard well-plate assay, including kinetic information on growth inhibition and measurements of bacterial morphological dynamics over a wide range of inhibitor concentrations. Finally, using a second model system, we show that this chip-based systems does not require the bacteria to be labeled and is well suited for the study of naturally occurring species. We illustrate this using Nitrosomonas europaea, an environmentally important bacteria, and show that the chip system can lead to a significant reduction in the period required for growth and inhibition measurements (<4 days, compared to weeks in a culture flask)

    Fermilab E791

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    Fermilab E791, a very high statistics charm particle experiment, recently completed its data taking at Fermilab's Tagged Photon Laboratory. Over 20 billion events were recorded through a loose transverse energy trigger and written to 8mm tape in the the 1991-92 fixed target run at Fermilab. This unprecedented data sample containing charm is being analysed on many-thousand MIP RISC computing farms set up at sites in the collaboration. A glimpse of the data taking and analysis effort is presented. We also show some preliminary results for common charm decay modes. Our present analysis indicates a very rich yield of over 200K reconstructed charm decays.Comment: 4 pages, 1 figure, LaTe

    Direct measurement of the pion valence quark momentum distribution, the pion light-cone wave function squared

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    We present the first direct measurements of the pion valence quark momentum distribution which is related to the square of the pion light-cone wave function. The measurements were carried out using data on diffractive dissociation of 500 GeV/c π−\pi^- into di-jets from a platinum target at Fermilab experiment E791. The results show that the ∣qqˉ>|q\bar {q}> light-cone asymptotic wave function, which was developed using perturbative QCD methods, describes the data well for Q2∼10 (GeV/c)2Q^2 \sim 10 ~{\rm (GeV/c)^2} or more. We also measured the transverse momentum distribution of the diffractive di-jets.Comment: 13 pages, 4 figure

    Study of the Ds+→π−π+π+D^+_s \to \pi^- \pi^+ \pi^+ decay and measurement of f0f_0 masses and widths

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    From a sample of 848 ±\pm 44 Ds+→π−π+π+D_s^+ \to \pi^- \pi^+ \pi^+ decays, we find Γ(Ds+→π−π+π+)/Γ(Ds+→ϕπ+)=0.245±0.028−0.012+0.019\Gamma(D_s^+ \to \pi^- \pi^+ \pi^+) / \Gamma(D_s^+ \to \phi \pi^+) = 0.245 \pm 0.028^{+0.019}_{-0.012} . Using a Dalitz plot analysis of this three body decay, we find significant contributions from the channels ρ0(770)π+\rho^0(770)\pi^+, ρ0(1450)π+\rho^0(1450)\pi^+, f0(980)π+f_0(980)\pi^+, f2(1270)π+f_2(1270)\pi^+, and f0(1370)π+f_0(1370)\pi^+. We present also the values obtained for masses and widths of the resonances f0(980)f_0(980) and f0(1370)f_0(1370).Comment: 10 pages, 3 eps figure

    Lipase-catalysed acylation of starch and determination of the degree of substitution by methanolysis and GC

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    Background: Natural polysaccharides such as starch are becoming increasingly interesting as renewable starting materials for the synthesis of biodegradable polymers using chemical or enzymatic methods. Given the complexity of polysaccharides, the analysis of reaction products is challenging. Results: Esterification of starch with fatty acids has traditionally been monitored by saponification and back-titration, but in our experience this method is unreliable. Here we report a novel GC-based method for the fast and reliable quantitative determination of esterification. The method was used to monitor the enzymatic esterification of different starches with decanoic acid, using lipase from Thermomyces lanuginosus. The reaction showed a pronounced optimal water content of 1.25 mL per g starch, where a degree of substitution (DS) of 0.018 was obtained. Incomplete gelatinization probably accounts for lower conversion with less water. Conclusions: Lipase-catalysed esterification of starch is feasible in aqueous gel systems, but attention to analytical methods is important to obtain correct DS values
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