266 research outputs found

    Catalytic and mechanistic studies into the epoxidation of styrenes using manganese complexes of structurally similar polyamine ligands

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    The synthesis and catalytic activity of manganese(ii) complexes of two polyamine ligands is reported which highlights how a small structural change in the ligand affects the overall catalytic behaviour.</p

    The use of carboxymethylcellulose for the tartaric stabilization of white wines, in comparison with other oenological additives

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    The aim of this study was to test the effectiveness of two types of carboxymethylcellulose (CMC), at different doses, for the prevention of tartaric precipitations in two white wines (Pinot Blanc and Chardonnay), in comparison with metatartaric acid and a commercial arabic gum. After the addition of the additives to the wines, the mini-contact test was carried out and the saturation temperature was determined by Ridomi’s method. The determination of the saturation temperature was then repeated on the same trials kept at -4 °C for 10 days. Both kinds of CMC caused a significant decrease in tartaric precipitations induced by the addition of potassium bitartrate (KHT) (mini-contact test), by limiting the growth of the added KHT crystals. Their effectiveness increased with the dose, following a hyperbolic trend. The stabilizing effect of the two kinds of CMC, particularly CMC2 (more viscous), was similar to the one of metatartaric acid. Their use must be considered complementary to the cold treatment (chillproofing).

    Grape by-products: extraction of polyphenolic compounds using supercritical CO2 and liquid organic solvent - a preliminary investigation.

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    This research focussed on the exploitation of grape by-products as a source of polyphenolic compounds, which are of interest to the food, pharmaceutical and cosmetic industries. In particular, two substrates were tested: Pinot Noir grape skins and grape seeds. Pinot Noir grape skins were extracted by supercritical CO2 added with ethanol as modifier at constant temperature (45 °C) and at variable pressure (200, 300, 400 or 500 bar). The supercritical extraction kinetics of polyphenolic compounds was obtained. Grape seeds were extracted by combining supercritical (at 40 °C and 500 bar and using CO2 or CO2 added with ethanol as modifier) with liquid ethanol extraction. The supercritical technique seemed not to be really effective in extracting polyphenolic compounds; it can be anyway utilized to selectively extract grape seed oil by avoiding any solvent contamination of the matrix which can be further extracted for the recovery of polyphenolic compounds by means of liquid organic solvent

    Immune Response to Cytolethal Distending Toxin of Aggregatibacter Actinomycetemcomitans in Periodontitis Patients

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    Background and Objective Cytolethal distending toxin (CDT) is a genotoxin produced by Aggregatibacter actinomycetemcomitans. In spite of its association with pathogenesis, little is known about the humoral immune response against the CDT. This study aimed to test whether subgingival colonization and humoral response to A. actinomycetemcomitans would lead to a response against CDT. Material and Methods Sera from periodontally healthy, localized and generalized aggressive periodontitis and chronic periodontitis subjects (n = 80) were assessed for immunoglobulin G titers to A. actinomycetemcomitans serotypes a/b/c and to each CDT subunit (CdtA, CdtB and CdtC) by ELISA. A. actinomycetemcomitans subgingival levels and neutralization of CDT activity were also analyzed. Results Sera from 75.0% localized and 81.8% generalized aggressive periodontitis patients reacted to A. actinomycetemcomitans. A response to serotype b was detected in localized (66.7%) and generalized aggressive periodontitis (54.5%). Reactivity to A. actinomycetemcomitans correlated with subgingival colonization (R = 0.75, p \u3c 0.05). There was no correlation between A. actinomycetemcomitans colonization or response to serotypes and the immunoglobulin G response to CDT subunits. Titers of immunoglobulin G to CdtA and CdtB did not differ among groups; however, sera of all generalized aggressive periodontitis patients reacted to CdtC. Neutralization of CDT was not correlated with levels of antibodies to CDT subunits. Conclusion Response to CdtA and CdtB did not correlate with the periodontal status of the subject in the context of an A. actinomycetemcomitans infection. However, a response to CdtC was found in sera of generalized but not of localized aggressive periodontitis subjects. Differences in response to CdtC between generalized and localized aggressive periodontitis subjects indicate that CDT could be expressed differently by the infecting strains. Alternatively, the antibody response to CdtC could require the colonization of multiple sites

    Investigation on the TransientConditions of a Rotating Biological Contactor for Bioethanol Production

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    Alcoholic fermentations of sucrose solutions were performed in a Rotating BiologicalContactor with immobilized-yeast cells, and the results collected during the transient conditions of start-up are presented and discussed. The analysis and modeling of data constitute a preliminary semi-empirical approach to the study of dynamics of such a bioprocess. The investigation has been developed on the observations of the responses to variations in the operating conditions of substrate, product, suspended- and immobilized- cell concentrations either in the fermentation broth or within a synthetic spongy matrix

    Relationships Between Subgingival Microbiota and GCF Biomarkers in Generalized Aggressive Periodontitis

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    Aim To examine relationships between subgingival biofilm composition and levels of gingival crevicular fluid (GCF) cytokines in periodontal health and generalized aggressive periodontitis (GAP). Materials and methods Periodontal parameters were measured in 25 periodontally healthy and 31 GAP subjects. Subgingival plaque and GCF samples were obtained from 14 sites from each subject. 40 subgingival taxa were quantified using checkerboard DNA-DNA hybridization and the concentrations of 8 GCF cytokines measured using Luminex. Cluster analysis was used to define sites with similar subgingival microbiotas in each clinical group. Significance of differences in clinical, microbiological and immunological parameters among clusters was determined using the Kruskal-Wallis test. Results GAP subjects had statistically significantly higher GCF levels of interleukin-1β (IL-1β) (p\u3c0.001), granulocyte-macrophage colony-stimulating factor (GM-CSF) (p\u3c0.01), and IL-1β/IL-10 ratio (p\u3c0.001) and higher proportions of Red and Orange complex species than periodontally healthy subjects. There were no statistically significant differences in the mean proportion of cytokines among clusters in the periodontally healthy subjects, while the ratio IL-1β/IL-10 (p\u3c0.05) differed significantly among clusters in the aggressive periodontitis group. Conclusions Different subgingival biofilm profiles are associated with distinct patterns of GCF cytokine expression. Aggressive periodontitis subjects were characterized by a higher IL-1β/IL-10 ratio than periodontally healthy subjects, suggesting an imbalance between pro- and anti-inflammatory cytokines in aggressive periodontitis
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