Este estudo consistiu na investigação sobre a interação dos lubrificantes empregados na usinagem de metais com a matéria orgânica natural (substâncias húmicas), a sua mobilidade no solo, a degradação microbiológica e a remoção dos mesmos do solo. Realizou-se, também, um estudo sobre as mudanças nas características dos fluidos após a sua utilização. Para o processo de degradação das amostras de fluido, submetidos aos efeitos de diferentes fatores ambientais, foram utilizados quatro tratamentos : (i) microrganismos nativos, chamada amostra controle; (ii) amostra controle com matéria orgânica proveniente de turfa; (iii) amostra controle acrescida de microrganismos existentes nos efluentes de máquinas de corte; e (iv) amostra controle com adição de microrganismos de compostagem. Para a pesquisa da degradação sem o efeito dos parâmetros climáticos, foram utilizadas amostras de solo contaminadas mantendo-se em estufa, e a inoculação dos microrganismos em meios de cultura com e sem acréscimo de fonte alternativa de carbono. Como técnicas analíticas, foram utilizadas a CG-DIC e a CG-EM. Essas técnicas são indicadas tanto para estudar a composição dos fluidos quanto dos produtos de degradação microbiológica, tendo sido otimizados métodos analíticos para serem empregados no monitoramento ambiental e de estudos de degradação. As análises por IVTF e por EF também foram empregadas na identificação e quantificação dos fluidos. Observou-se uma considerável interação dos fluidos solúveis com a matéria orgânica do solo, embora tenham se apresentado com alta mobilidade para alguns constituintes, bem como um acelerado processo de degradação durante o uso. De outro modo, os fluidos insolúveis se apresentaram mais imóveis, ficando retidos na matéria orgânica do solo, entretanto, foram mais prontamente degradados no ambiente que os solúveis. A adição de matéria orgânica e de microrganismos de compostagem acelerou o processo de degradação para todos os fluidos de corte investigados. / This study is an investigation of the interaction of lubricants employed in metal machining and natural organic matter (humic substances), their mobility in soil, microbial degradation and their removal from the soil. Also, was performed study of changes in characteristic on fluids after their use. On degradation process from fluid samples, contaminated soils submitted to different environment factors, were used four treatments : (i) native microorganisms named control sample; (ii) control sample added by organic matter from peat; (iii) control sample added by microorganisms existing in flowing out from cutting machines; and (iv) control sample with addition of microorganisms from composting. For degradation research by no effect from climate parameters were used sample of contaminated soil been investigated in stove and microorganisms inoculation in culture mean with and without addition of alternative carbon source. As analytical techniques were used GC-FID and GG-MS. These techniques are both indicated for fluid composition studies and microbial degradation product. Analytic methods had been optimized to be employed on environmental monitoring and degradation studies. The FTIR and espectrofluorimetric methods were used for the fluid identification and quantification. Were observed a notable interaction between soluble fluids and soil organic matter, thought it had been verified high mobility for some compounds as well an accelerated process of degradation during their use. Otherwise, insoluble fluids were more immobile been restrained in soil organic matter, nevertheless, were readily degraded in environment than soluble ones. Organic matter and composting microorganisms\' addition accelerated the degradation process for all cutting fluids investigated.

Polychlorinated biphenyls (PCBs) are chlorinated organic compounds, which belong to persistent organic pollutants and exhibit various modes of toxic action, including mutagenicity, carcinogenicity, and endocrine disruption. PCBs were manufactured during the 20th century in many countries and extensively used due to their advantageous physicochemical properties. PCBs mostly served as insulating liquids in electrical equipment; however, they were also utilized in many open applications. Despite the worldwide ban on PCB manufacture imposed at the end of the 20th century, the contamination of the environment persists to this day as a result of their recalcitrance. Moreover, PCBs are still being inadvertently produced during many industrial activities. Because of their stability, the breakdown of PCBs in nature is extremely slow. This dissertation thesis focuses on the study of PCB biodegradation by ligninolytic fungi. This group of microorganisms belongs to the most promising, especially in regard to the degradation of organic pollutants. The biodegradation mechanism of PCBs was studied in vitro, including the identification of degradation intermediates. Laccase, an enzyme expressed by the oyster mushroom (strain Pleurotus ostreatus 3004), was able to degrade hydroxylated PCBs. In addition, chlorinated...

The purpose of this study is twofold: (1) conduct an epidemiological survey of yeasts found in clinical material; and (2) suggest an identification scheme that would identify yeasts of medical importance in the shortest possible time.

This work deals with influence of heat processing on longevity of two selected products of the packing company Seliko trading a.s. For the research there were selected products Sterilised sauerkraut in sweet-sour pickle and Fatback spread. Evaluation has been done in laboratory premises of the packing company. There has been monitored mikrobiological stability after heat processing and sensory properties of the mentioned products always with an interval of one month. During the monitored seven months there appeared changes in taste and consistence of the products that are not defective in these products. The microbiological test taken after seven months was negative, just like at the beginning of the experiment. The result of the given findings is that the heat sterilisation was efficient and that during the storage there did not rise number of micro-organisms in the products.

This diploma thesis deals with the applicability of thermal analysis in the influence of stress factors on microorganisms. The main aim of the presented work was to design and implement a series of experiments to thest the usability of advanced methods of thermal analysis in the characterization of microorganisms. Two bacterial strains were used as model organisms: Cupriavidus necator H16 and its mutant strain Cupriavidus necator PHB-4, which differs in the ability to produce polyhydroxyalkanoates. The basic technique used thermogravimetric analysis (TGA), which was optimized and applied in the study of water transport, behavior and determination of intracellular water content with respect to the influence of the presence of intracellular PHB granules. The results of this method were subsequently supported by TEM photos.

Raman spectroscopy is a powerful tool for identification both inorganic and organic compounds including microbial biomolecules. Together with the fact, that it is considered to be the important nondestructive instrument for use on Mars within future robotic missions, it is necessary to assess its capabilities in scenarios relevant for both Martian and terrestrial conditions. In this work, the potential of Raman spectrometry was tested - including both bench-top laboratory systems as well as portable counterparts - to detect traces of life within evaporitic matrices through biomolecular identification. Due to their chemical and physical nature resulting in optical properties, pigments are important organic compounds in Raman spectroscopic analysis using visible excitation. Hence in this work we have focused on the Raman spectroscopic identification of pigments as biomarkers with relevance for investigation of life in both extreme terrestrial and potentially extraterrestrial environments. Results of methodical work are presented in Appendices I to III, dealing particularly with β-carotene as a model carotenoid pigment. The concentration limits of this biomarker in three different evaporitic matrices (halite, gypsum and epsomite) have been determined for artificially prepared powdered mixtures alone...

Although pharmaceutical industries have produced a number of new antibiotics in the last three decades, resistance to these drugs by infectious microorganisms has increased. For a long period of time, plants have been a valuable source of natural products for maintaining human and animal health. The use of plant compounds for pharmaceutical purposes has gradually increased worldwide. This is because there are many bioactive constituents in plants which hinder the growth or kill microbes. Plants could be considered a potential gold mine for therapeutic compounds for the development of new drugs. In this study, sixteen South African plant species were selected based on their antibacterial activity after a wide screening of leaf extracts of tree species undertaken in the Phytomedicine Programme, University of Pretoria. Literature search excluded eleven plants because of the work already performed on their antibacterial activities, while Pavetta schumaniana was found toxic and thus not included in the screening. The remaining four plants namely; Buxis natalensis, Macaranga capensis, Dracaena mannii and Garcinia livingstonei were screened for antibacterial activity by determining the minimum inhibitory concentrations (MIC) against 4 nosocomial bacterial pathogens Staphylococcus aureus, Enterococcus faecalis, Escherichia coli and Pseudomonas aeruginosa, and also by using bioautography. The extracts of Macaranga capensis, Garcinia livingstonei, Diospyros rotundifolia and Dichrostachys cinerea had good antibacterial activity with MIC values of 0.03, 0.04, 0.06 and 0.08 mg/ml against different pathogens. The average MIC values of the plant extracts against all the tested pathogens ranged from 0.23-1.77 mg/ml. S. aureus was the most susceptible bacterial pathogen with average MIC of 0.36 . The extract of Diospyros rotundifolia was the most active with an average MIC against all the organisms of 0.23 mg/ml. The extracts of Buxus natalensis, Dracaena mannii, and Pittosporum viridiflorum, Acacia sieberiana, Erythrina lattissima, Cassine papillosa and Pavetta schumanniana had lower antibacterial activity. G. livingstonei was selected for further work on the basis of its good activity. The bulk acetone extract of Garcinia livingstonei (20g) was subjected to solvent-solvent fractionation which yielded seven fractions. Only the chloroform and ethyl acetate fractions showed good bioactivity in the microdilution assay and bioautography. Column chromatography was used to isolate two bioactive biflavonoids from the ethyl acetate fraction. The structures of the two compounds were elucidated using nuclear magnetic resonance (NMR) spectroscopy, and were identified as amentoflavone (1) and 4′ monomethoxyamentoflavone (2). These two compounds have been previously isolated from plants that belong to the Clusiaceae. The two compounds were isolated in sufficient quantity with a percentage yield of 0.45% for amentoflavone and 0.55% for 4′ monomethoxyamentoflavone from 20 g crude acetone extract. The antibacterial activity was determined against four nosocomial bacterial pathogens (Escherichia coli, Staphylococcus aureus, Enterococcus faecalis and Pseudomonas aeruginosa). The MIC values ranged from 8-100 μg/ml. Except for Staphylococcus aureus which showed resistance to amentoflavone at >100 μg/ml. All the other tested organisms were sensitive to both compounds. It has long been recognized that naturally occurring substances in higher plants have antioxidant activity. Based on this, the antioxidant activities of the two isolated compounds were tested using the Trolox assay. The two flavones had good antioxidant activity. Amentoflavone had a Trolox equivalent antioxidant capacity (TEAC) of 0.9. The second compound 4′ monomethoxyamentoflavone had a TEAC value of 2.2 which is more than double the antioxidant activity of Trolox, a vitamin E analogue. To assess the safety of the two compounds on cell systems, cytotoxicity was determined using a tetrazolium based colorimetric assay (MTT assay) using Vero monkey kidney cells. The compounds indicated little to low toxicity against the cell line with cytotoxic concentration (CC50) of 386 μg/ml and >600 μg/ml for compound 1 and 2 respectively. Berberine (used as the control toxic substance) had a CC50 of 170 μg/ml. The Ames genotoxicity assay is used to assess the mutagenic potential of drugs, extracts and phytocompounds. The compounds isolated in this study were assayed for genotoxicity using the Salmonella typhimurium TA98 strain. Amentoflavone was genotoxic at the concentration of 100 μg/plate, but 4′ monomethoxyamentoflavone was inactive at the highest concentration of 400 μg/plate tested. The results of the antibacterial, antioxidant and cytotoxicity testing were encouraging and indicated the potential usefulness of Garcinia livingstonei in traditional medicine and drug discovery. However, the genotoxicity assay revealed potential mutagenic effects of amentoflavone, a compound isolated from the plant. Therefore, it is suggested that application of Garcinia livingstonei extracts in the treatment of human and animal ailments be done with caution to avoid mutagenic effects on the treated subjects. A relatively small change in the structure of the two compounds by replacing an hydroxyl group with a methoxy group had a major effect in increasing antibacterial and antioxidant activity and in decreasing cellular and genotoxicity. This illustrates the potential value of modifying a molecule before its possible therapeutic use. Copyright / Dissertation (MSc (Veterinary Science))--University of Pretoria, 2009. / Paraclinical Sciences / unrestricted

Bacterial aspartate transcarbamoylases (ATCase's) are divided into three classes that correspond to taxonomic relationships within the bacteria. The opportunistic pathogen Moraxeila catarrhalis has undergone several reclassifications based on traditional microbiological criteria. The previously uncharacterized ATCase from M. catarrhalis was purified to homogeneity and its chemical properties characterized. The ATCase from M. catarrhalis is a class C ATCase with an apparent molecular mass of 480-520 kDa. The M. catarrhalis ATCase is a dodecomer composed of six 35 kDa polypeptides and six 45 kDa polypeptides. The enzyme has an unusually high pH optimum of greater than pH 10. The enzyme exhibited hyperbolic kinetic with a Km for aspartate of 2 mM. A single, separate 78 kDa dihydroorotase from M. catarrhalis was identified and it was not associated with ATCase. These data support the reclassification of M. catarrhalis out of the Neisseriaceae family.

No description available.

This dissertation aims to explore the role of patient and family engagement in the context of two current health issues: catheter-associated urinary tract infections (CAUTI) and antibiotic resistance. Chapter One contains an introduction to patient and family engagement, CAUTI, and antibiotic resistance, followed by gaps in the science, a description of the theoretical framework, and specific aims addressed in this dissertation. Chapter Two is a systematic review of existing CAUTI prevention interventions that involve patient and family engagement. Chapter Three is a study designed to meet the learning needs of parents by developing a graphically-enhanced CAUTI-prevention educational resource using participatory design methods. Chapter Four is an environmental scan that summarizes the content and format of existing resources about antibiotic resistance and antibiotic use available from children’s hospital websites across the United States. Finally, Chapter Five contains an overall summary of the findings of this dissertation, a discussion of results within the guiding theoretical framework, practice and policy implications, and suggestions for future research.