Made available in DSpace on 2015-03-26T13:37:43Z (GMT). No. of bitstreams: 1 texto completo.pdf: 2701343 bytes, checksum: b9c5cc5b07f66e4816776e04f12b0511 (MD5) Previous issue date: 2010-08-27 / Conselho Nacional de Desenvolvimento Científico e Tecnológico / Considering the importance of Meloidogyne enterolobii (= M. mayaguensis) to the culture of guava and the potential of Essential Oil of Mustard (EOM) on nematode control, was aimed to evaluate the efficiency of EOM on control of these nematodes in the field, on a orchard of plants uprooted and cut off at 0.3 m from soil level or in intact plants in production. An orchard of guava trees naturally infested with M. enterolobii, in Viçosa, MG, was selected. EOM was applied on soil at 100 μg/mL, by strips of cardboard in the rhizosphere of intact plants, or by irrigating the cultivation area with EOM diluted in water after the plants have been cut off or uprooted. Samples were collected over 140 days after the product application and evaluated on the number of J2 in soil and number of galls and eggs in roots of tomato plants in the bioassay. The J2 population in soil underwent rapid reduction, regardless of treatment, and was configured as an unreliable variable. By the bioassay, was obtained a reduction of 71%, 81% and 99% for number of galls and 60%, 80% and 83% for number of eggs at 45, 75 and 140 days after application, respectively, for plots treated with EOM, in uprooted or cutted plants. The terbuphos only reduced the number of galls during 45 days. The biological evaluation at 140 days revealed a general trend of population reduction, considering the number of galls and eggs. In intact plants, there was no control of nematodes, as the average variations of J2, galls and eggs did not differ significantly between treatments. In conclusion, the EOM was effective in controlling M. enterolobii at the field in the absence of the host. / Considerando a importância de Meloidogyne enterolobii (= M. mayaguensis) para a cultura da goiabeira e o potencial do óleo essencial de mostarda (OEM) no controle de nematoides, objetivou-se avaliar a eficiência do OEM no controle do nematoide no campo, em pomares de plantas arrancadas, recepadas ou em produção. Selecionou-se um pomar de goiabeiras naturalmente infestado por M. enterolobii, em Viçosa, MG. O OEM foi aplicado no solo a 100 μg/mL, por meio de tiras de papelão na rizosfera de plantas intactas ou irrigando a área de cultivo com OEM diluído em água, após as plantas serem recepadas ou arrancadas. Em amostras coletadas ao longo de 140 dias após aplicação do produto, avaliou-se o número de J2 no solo e número de galhas e ovos em raízes de tomateiros, no teste biológico. Como a população de J2 no solo sofreu rápida redução, independente do tratamento, ela foi considerada uma variável pouco confiável para a avaliação. Pelo teste biológico, obteve-se uma redução de 71%, 81% e 99% para número de galhas e 60%, 80% e 83% para número de ovos aos 45, 75 e 140 dias após a aplicação, respectivamente, para as parcelas tratadas com OEM, em plantas arrancadas ou recepadas. O terbufós reduziu apenas o número de galhas aos 45 dias, o qual voltou a aumentar posteriormente. Aos 140 dias, houve tendência generalizada de redução da população, considerando-se o número de galhas e ovos. Nas plantas intactas não houve controle do nematoide, pois as médias das variações de J2, galhas e ovos não diferiram significativamente entre os tratamentos. Em conclusão, o OEM foi eficiente em controlar M. enterolobii no campo na ausência do hospedeiro.

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Schwefellost (SM) ist ein verbotener chemischer Kampfstoff. Nach Aufnahme über die Haut führt SM zu einer Reihe von Symptomen. Auf der molekularen Ebene beruht die Toxizität von SM auf der Reaktion mit DNA und Proteinen. Diese kovalenten Addukte eignen sich zum forensischen Nachweis und können über Flüssigkeitschromatographie gekoppelte Massenspektrometrie (LC-MS) detektiert werden. Ein Hauptziel war es in vitro zu untersuchen ob chemisches Scavenging von N-Acetylcystein (NAC) und Glutathion (GSH) Einfluss in der Behandlung von SM-Vergiftungen hat. Es konnte geklärt werden, dass NAC und GSH a) die Alkylierung von Cys34 in humanen Serum Albumin (HSA) durch SM nicht unterbinden kann und b) den Abbau von SM in gepufferter Lösung nicht beschleunigt. Somit ist Scavenging von SM durch NAC und GSH vernachlässigbar. Trotzdem konnte die Stabilität und die Zuverlässigkeit des Testsystems gezeigt werden. Das zweite Hauptziel war es neue peptidische Biomarker für den Nachweis von SM-Vergiftungen zu finden. Es wurde eine Methode entwickelt, um SM-alkylierte Aminosäurereste in HSA zu finden. Somit konnten 42 SM-alkylierte Peptide gefunden werden. Insgesamt wurden 27 Alkylierungsstellen identifiziert, von denen 24 noch nicht in der Literatur beschrieben wurden. Die vielversprechendste der neue Alkylierungsstellen war das Met329 in HSA. Durch Proteolyse mittels Pepsin wurde das LGM(-HETE)F Tetrapeptid freigeschnitten. Probenvorbereitung und LC-MS Bedingungen wurden optimiert. Allerdings gelang der Nachweis von LGM(-HETE)F in Patientenplasma nicht, was möglicherweise an einer geringeren Stabilität der SM-Alkylierung von Met329 lag. Trotzdem kann sich LGM(-HETE)F als Kurzzeitmarker eignen. Der beobachtete Transfer der HETE-Modifikation vom Met329 zu Glu und Cys Seitenketten stellt einen neuen Einblick in den molekularen Wirkmechanismus von SM dar. Basierend auf diesen Erkenntnissen konnte in Nachfolgestudien die Hemmung von Enzymen durch Alkylierung von Met durch SM gezeigt werden. / Sulfur mustard (SM) is a banned chemical warfare agent. After incorporation, SM may cause tremendous symptoms. On the molecular level, SM reacts with DNA and proteins. These covalent adducts may be useful for forensic or analytical purposes. After adducting SM, proteins can be proteolyzed forming peptides with a SM-modified amino acid residue. These peptide biomarkers can be detected using liquid chromatography-mass spectrometry (LC-MS). One major aim was to develop an in vitro assay to clarify the impact of chemical scavenging of N-acetylcysteine (NAC) and glutathione (GSH) in the treatment of SM. It was found that NAC and GSH had no relevant influence on a) the extent of alkylation of Cys34 in human serum albumin (HSA) and b) the degradation velocity of SM in buffered solution. Accordingly, it was concluded that chemical scavenging of SM by NAC or GSH is negligible. Nevertheless, the robustness and reliability of the developed in vitro assay was shown. The second major aim was to identify novel peptide biomarkers of SM poisoning. An untargeted method to identify SM-alkylated amino acid residues in HSA was developed. Application of this method revealed 42 SM-modified peptides alkylated at 27 different positions. 24 of these positions were not described in the literature so far. A highly interesting target, Met329 in HSA, was investigated in more detail. After pepsin mediated proteolysis, the covalently modified tetrapeptide LGM( HETE)F was generated. Sample preparation and LC-MS conditions were optimized. However, when applying this novel marker to real samples, it could not be detected likely due to its limited stability. Nevertheless, LGM( HETE)F still represents a suitable short term biomarker. The observed transfer of the HETE-moiety from Met329 to Glu and Cys side chains represents a novel insight into the molecular toxicology of SM. Based on these results follow-up studies proved the enzyme inhibitory effect of SM-alkylation of Met residues in keratin kinase.

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Access to fresh water is a human right, yet more than 780 million people, especially in rural areas, rely on unimproved sources and the need for finding ways of treating water is crucial. Although the use of natural coagulant protein in drinking water treatment has been discussed for a long time, the method is still not in practice, probably due to availability of material and limited knowledge. In this study, about hundred different crude extracts made from plant materials found in Southern India were screened for coagulation activity. Extracts of three Brassica species (Mustard, Cabbage and Cauliflower) were showing activity comparable to that of Moringa oleifera and were further investigated. Their protein content and profile were compared against each other and with coagulant protein from Moringa. Mustard (large) and Moringa seed proteins were also studied for their effect against clinically isolated bacterial strains. The protein profiles of Brassica extract showed predominant bands around 9kDa and 6.5kDa by SDS-PAGE. The peptide sequence analysis of Mustard large identified the 6.5kDa protein as Moringa coagulant protein (MO2.1) and the 9kDa protein band as seed storage protein napin3. Of thirteen clinical strains analysed, Moringa and Mustard large were proven effective in either aggregation activity or growth kinetic method or both in all thirteen and nine strains respectively. To my knowledge this is the first report on the presence of coagulant protein in Brassica seeds. Owing to the promising results Brassica species could possibly be used as a substitute to Moringa coagulating agent and chemicals in drinking water treatment. / <p>QC 20121214</p>

Wild mustard (Brassica spp.) is used as an edible wild leafy vegetable by indigenous people in South Africa. The potential of wild leafy vegetables in agriculture is not well understood, because there is generally no agronomic research on their production practices. The objective of this study was to examine the performance of three wild mustard species (herein referred to as I, K and M) over four cropping seasons in an intercropping system with green beans (Phaseolus vulgaris L. cv. Imbali). The crops were grown with and without organic fertiliser under dryland conditions at two sites (The University of KwaZulu-Natal Research Farm, Ukulinga and in a rural area of Umbumbulu, KwaZulu-Natal within the farmers' locality) during autumn, winter, spring and summer of 2004 to 2005. Plant development (leaf number, plant height and fresh biomass) during the first six weeks after sowing and seed yield were used to determine agronomic performance of each species. Nutrient status of the rhizosphere soil was determined at 42 days after sowing for each species to determine what effect growing the species would have on mineral availability. Wild mustard production significantly (P < 0.01) performed better at Ukulinga than Umbumbulu. Polyculture was beneficial for wild mustard leaf accumulation and green bean production as determined by land equivalent ratios greater than one for all species combinations, regardless of fertiliser application. Cool environmental conditions occurring in autumn and spring were more favourable (P < 0.05) for wild mustard and green bean biomass accumulation than summer and winter conditions. However, wild mustard seed yield was highest in winter compared with autumn and spring, and there was no measurable seed production in summer. Soil analysis results at 42 days after sowing showed an increase in P, K, Cu and Mg in the rhizosphere of wild mustard without organic fertiliser. Polyculture improved Zn, Cu, Mn and K in wild mustard leaf tissue. It is concluded that wild mustard can be grown as a leafy vegetable throughout the year, but it requires cool environmental conditions to enhance seed yield. Species M significantly yielded better biomass and seeds than species I and K during all the seasons. However, species K performed the least in all aspects. / Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg, 2005.

In this work, the [3,3] sigmatropic rearrangement of different substituted propargyl thiocyanates and double [3,3] sigmatropic rearrangement of enynyl isothiocyanates either by flash vacuum pyrolysis or by thermolysis in solution are studied. Additionally, the intramolecular reactions of the resulting allenyl isothiocyanates are studied, and the reaction mechanisms for the generation of the final products, such as [1,5] sigmatropic migrations or electrocyclic ring closures, are explained. These highly reactive allenyl isothiocyanates are used as appropriate electrophilic precursors for the preparation of novel examples of thiazoles substituted at C-2 position using different types of nucleophiles. For the formation of these substituted thiazoles, the necessary nucleophilicity as well as the regioselectivity, the stereoselectivity, and the reaction mechanisms are investigated. / In der vorliegenden Arbeit sind die [3,3]-sigmatrope Umlagerung von verschiedenen Propargylthiocyanaten und die doppelte [3,3]-sigmatrope Umlagerung von Eninylisothiocyanaten entweder durch Blitzvakuumthermolyse oder Thermolyse in Lösung untersucht worden. Zusätzlich wurden die intramolekularen Reaktionen der resultierten Allenylisothiocyanate studiert. Außerdem sind die Reaktionsmechanismen zur Bildung der Thermolyseprodukte wie z.B. die [1,5]-sigmatropen Umlagerungen und die elektrocyclischen Ringschlüsse erklärt. Die hochreaktiven Allenylisothiocyanate sind als geeignet elektrophile Vorläufer zur Synthese von neuen Thiazolen verwendbar, die an der C-2 Position substituiert sind. Dabei kommen verschiedene Nucleophile zum Ansatz. Für die Bildung dieser substituierten Thiazole sind die Regioselektivität, Stereoselektivität, Reaktionsmechanismen und der Bereich der einsetzbaren Nucleophile untersucht worden.

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