2,086 research outputs found

    The synthesis of phenyl carbamate (from urea, phenol, and a Lewis acid)

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    The synthesis of phenyl carbamate from urea, phenol, and Lewis acid was attempted with varied results being observed. The proposed reaction mechanism involves and Acyl-2 type reaction with a nucleophilic attack on urea by phenol. The Lewis acid is present to add carbocation character to the urea and to further complex with by-products, thus driving the reaction to completion. The solvents utilized were isopropyl alcohol, dichloromethane, and tetrahydrofuran. The reaction parameters were varied in an effort to successfully run a reaction mechanism. Phenyl carbamate was not isolated and what was observed of the reactions did not appear to follow the proposed mechanism. A white crystalline product was isolated and found to have both amide and aromatic character, but its identity remains unknown

    ALS Resistant Smooth Pigweed in Western Kentucky

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    Pigweeds The pigweed, or Amaranthus, family contains some of the most commonly occurring weeds of midwest agriculture. Species from this family that occur in Kentucky include smooth pigweed (Amaranthus hybridus, most common), tumble pigweed, prostrate pigweed, spiny amaranth,Palmer amaranth,common waterhemp, and tall waterhemp. Research has shown that some pigweed species respond differently to various herbicides, therefore, proper identification is necessary to achieve acceptable control. Pigweed identification in early stages of seedling growth can be difficult because the distinguishing physical characteristics do not appear until plants are mature or have produced seed. Also, some pigweed species may cross-pollinate to produce hybrid plants that exhibit characteristics of both parents

    Metabolomic profiling of macrophages determines the discrete metabolomic signature and metabolomic interactome triggered by polarising immune stimuli

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    Priming and activating immune stimuli have profound effects on macrophages, however, studies generally evaluate stimuli in isolation rather than in combination. In this study we have investigated the effects of pro-inflammatory and anti-inflammatory stimuli either alone or in combination on macrophage metabolism. These stimuli include host factors such as IFNÎł and ovalbumin-immunoglobulin immune complexes, or pathogen factors such as LPS. Untargeted LC-MS based metabolomics provided an in-depth profile of the macrophage metabolome, and revealed specific changes in metabolite abundance upon either individual stimuli or combined stimuli. Here, by factoring in an interaction term in the linear model, we define the metabolome interactome. This approach allowed us to determine whether stimuli interact in a synergistic or antagonistic manner. In conclusion this study demonstrates a robust approach to interrogate immune-metabolism, especially systems that model host-pathogen interactions

    A DNA Damage-Induced, SOS-Independent Checkpoint Regulates Cell Division in Caulobacter crescentus

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    Cells must coordinate DNA replication with cell division, especially during episodes of DNA damage. The paradigm for cell division control following DNA damage in bacteria involves the SOS response where cleavage of the transcriptional repressor LexA induces a division inhibitor. However, in Caulobacter crescentus, cells lacking the primary SOS-regulated inhibitor, sidA, can often still delay division post-damage. Here we identify didA, a second cell division inhibitor that is induced by DNA damage, but in an SOS-independent manner. Together, DidA and SidA inhibit division, such that cells lacking both inhibitors divide prematurely following DNA damage, with lethal consequences. We show that DidA does not disrupt assembly of the division machinery and instead binds the essential division protein FtsN to block cytokinesis. Intriguingly, mutations in FtsW and FtsI, which drive the synthesis of septal cell wall material, can suppress the activity of both SidA and DidA, likely by causing the FtsW/I/N complex to hyperactively initiate cell division. Finally, we identify a transcription factor, DriD, that drives the SOS-independent transcription of didA following DNA damage.National Institutes of Health (U.S.) (Grant R01GM082899)National Science Foundation (U.S.). Graduate Research Fellowship Progra

    Green fluorescent diamidines as diagnostic probes for trypanosomes

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    LED fluorescence microscopy offers potential benefits to the diagnosis of human African trypanosomiasis, as well as to other aspects of diseases management, such as detection of drug resistant strains. To advance such approaches reliable and specific fluorescent markers to stain parasites in human fluids are needed. Here we report a series of novel green fluorescent diamidines and their suitability as probes to stain trypanosomes

    Drug resistance and treatment failure in leishmaniasis: A 21st century challenge

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    Reevaluation of treatment guidelines for Old and New World leishmaniasis is urgently needed on a global basis because treatment failure is an increasing problem. Drug resistance is a fundamental determinant of treatment failure, although other factors also contribute to this phenomenon, including the global HIV/AIDS epidemic with its accompanying impact on the immune system. Pentavalent antimonials have been used successfully worldwide for the treatment of leishmaniasis since the first half of the 20th century, but the last 10 to 20 years have witnessed an increase in clinical resistance, e.g., in North Bihar in India. In this review, we discuss the meaning of “resistance” related to leishmaniasis and discuss its molecular epidemiology, particularly for Leishmania donovani that causes visceral leishmaniasis. We also discuss how resistance can affect drug combination therapies. Molecular mechanisms known to contribute to resistance to antimonials, amphotericin B, and miltefosine are also outlined
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