O extrato metanólico da esponja Darwinella sp. coletada na costa do Rio do Janeiro, exibiu atividade leishmanicida. O extrato bruto foi particionado em três frações: fração hexânica, fração de AcOEt e fração XAD (extração da fração orgânica do extrato aquoso mediante mistura de resinas XAD-2, XAD-4 e XAD-7). Cada uma das frações foi avaliada em bioensaio atividade leishmanicida, mostrando que a fração AcOEt apresentou 100% da morte dos parasitas. A fração de AcOEt foi fracionada usando cromatografia por exclusão de tamanho (Sephadex&reg LH-20) e extrações em fase sólida (SPE) com diferentes colunas pré-empacotadas. Os compostos foram isolados e purificados por cromatografia de alta eficiência acoplada a detector ultravioleta (CLAE-UV). Sete compostos foram isolados, dos quais quatro deles foram identificados espectroscopicamente. O membranolídeo, o éster metílico da oxeatamida A, a oxeatamida H e a oxeatina são diterpenos espongianos que possuem um esqueleto aplysulfurano nitrogenado, excetuando o membranolídeo. Tanto o éster metílico da oxeatamida A quanto a oxeatamida H, pertencem a uma série de compostos denominados de oxeatamidas. O membranolídeo, o éster metílico A e a oxeatina foram avaliados em teste de atividade antiparasitária contra Leishmania infantum, porém nenhum deles apresentou atividade leishmanicida. / The sponge Darwinella sp. was collected in Rio de Janeiro’s coast and its methanolic extract showed leishmanicidal activity. The crude extract was partitioned in three fractions: hexane, AcOEt and XAD fractions. This last one was obtained by resin adsorption (mixture of XAD-2, XAD-4 and XAD-7 resins) of organic constituents from the aqueous fraction and subsequent recovery by extraction from the resins mixture. All of three fractions were also tested in leishmanicidal bioassay. The AcOEt fraction promoted 100% of parasite death. This fraction was separated into less complex fractions by size exclusion chromatography (Sephadex&reg LH-20) and solid phase extractions (SPE). The compounds were isolated and purified by high-performance liquid chromatography (HPLC) combined with on-line UV detector. Seven substances were isolated, which four of them were spectroscopically identified. The membranolide, the oxeatamide A methyl ester, the oxeatamide H and the oxeatin are spongian diterpenes with nitrogenous aplysulphurane skeleton, except for the membranolide. The oxeatamides are a series of nitrogenous aplysulphurane metabolites that includes the oxeatamide A methyl ester and the oxeatamide H. All of these compounds, except the oxeatamide H, were evaluated for antiprotozoal activity against Leishmania infantum. None of these compounds displayed leishmanicidal activity.

Australia's marine environment covers extended areas, from the warm northern tropical, to the sub tropical central water, the cool temperate water of the south and the cold sub-Antarctic and Antarctic water. Australia has rich area of coral reefs. The marine biodiversity in Australia is enormous. Despite incredible biodiversity, Australian research in the marine anticancer drug discoveries is low in comparison with other countries. In this research we investigated a collection of marine sponges as a source for new anticancer leads. This thesis comprises six chapters. Chapter 1 covers the importance of natural products as a source of new drugs, and an introduction to cancer as a disease, chemotherapy in cancer treatments, and the natural products as a source for anticancer drugs. Also, the basic anticancer drug development process is highlighted. Finally, a thorough review of anticancer alkaloids isolated from marine sponges is presented. Chapter 2 presents the chemical investigation into a southern Australian marine sponge Stelletta sp., which led to the isolation and structure elucidation of bistellettazines A-C the first reported examples of terpenyl-pyrrolizidines conjugate, and bistellettazole A, a unique cyclic terpenyl-imidazole conjugate. Bistellettazines A-C and bistellettazole A feature unprecedented carbon skeletons that are proposed to share a common convergent biosynthetic origin, arising via the biogenic equivalent of a Diels-Alder addition between two hypothetical polyenyl norsesquiterpene precursors. The cytotoxic activity (in vitro) for these new alkaloids is also discussed. Chapter 3 discusses the isolation and structure elucidation of four new discorhabdins analogues namely, dihydrodiscorhabdin A, debromodiscorhabdin A, discorhabdin X and dihydrodiscorhabdin L. In addition, the known compounds discorhabdin A and discorhabdin D, were isolated from two southern Australian marine sponge specimens of the genera Higginsia and Spongosorites. The cytotoxic activity (in vitro) for these new alkaloids was also discussed. Chapter 4 discloses chemical investigation into two southern Australian marine sponge specimens of the genera Clathria and Ptilocaulis. Four new mirabilin analogues (mirabilins H-K) were isolated and characterized along with known mirabilin C, F (for the first time as TFA salt) and mirabilin G. The cytotoxic activity (in vitro) for these new alkaloids was also discussed. Chapter 5 presents the 1H NMR data for the known compounds isolated during this study, and Chapter 6 is covering the experimental part.

The primary step in the microbiological assessment of highly dynamic and complex food processing conditions is environmental sampling. The objectives of this study were to: (1) compare the efficacy of four sampling devices including Microbial-Vac system (MV), cellulose sponge (SP), polyester swab (SW) and composite tissue (CT), for the recovery of Listeria monocytogenes and Brochothrix thermosphacta on five surfaces and (2) to determine if there was a significant difference between the recovery of low (10 CFU/900cm2) and high (100 CFU/900cm2) L. monocytogenes inoculum levels using the sampling devices in a simulated food processing environment. Surfaces used for this study were stainless steel (SS), polyethylene cutting board (CB), polyurethane conveyor belt (PB), open hinge flat top conveyor belt (FT) and mesh conveyor belt (MB). Food contact surfaces were inoculated with L. monocytogenes to obtain a final cell population of 10 (low) or 100 (high) CFU/900 cm2. An average cell density of 10,000 CFU/25 cm2 was used for inoculating B. thermosphacta on each of the surfaces. Inoculated surfaces were dried and held for two hours at 4˚C then sampled and processed for detection. Because L. monocytogenes is a "zero tolerance" pathogen in ready-to-eat foods, the qualitative analysis included an enrichment step to detect presence/absence in the sample. In comparison, B. thermosphacta was directly plated in order to quantify the recovery capability of each device. Results indicated for recovery of 100 CFU/900 cm2 L. monocytogenes, there was no difference among devices on SS, CB or PB surfaces (p>0.05). However, a significant difference was detected at 10 CFU/900 cm2 on SS between MV and CT, 62.97 and 17.34%, respectively (p=0.0086). Results for FT indicated MV was superior over SP and SW (p=0.0004) for detection of high and low L. monocytogenes. There was no difference for the quantitative recovery of B. thermosphacta on PB and SS; however, there was a difference (p=0.0371) among devices on CB indicating MV was superior over SP and CT. The swab recovered 3.25 log CFU/25cm2 from flat top belts and was significantly lower (p=0.0259) than MV and SP devices, 4.29 and 4.12 log CFU/25cm2, respectively.

Symbiosis is commonly present in marine invertebrates. Many corals and sponges have symbiotic algae or bacteria. In the previous studies of the sponge Cinachyra australiensis, 85% of the bacteria associated with the sponge have high similarity (88.65%) with the symbiotic chemoautotrophic sulfur-oxidizing bacteria of the deep-sea hydrothermal vent mussel, Solemya reidi. This study aims to investigate the localization of the chemoautotrophic sulfur-oxidizing bacteria associated with Cinachyra australiensis. The Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase (RubisCO) large-subunit genes for autotrophic organisms were amplified by polymerase chain reaction from the sponge samples. The phylogenetic relationship of the RubisCO large subunit genes was analyzed. A total of 26 clones were selected and sequenced. They could be divided into two groups. One (9 clones) belongs to form I type IB (cynobacteria and green algae). The other (17 clones) belongs to form II type IA (chemoautotrophic symbiotic bacteria). The location of the sulfur-oxidizing chemoautotrophic bacteria was shown to be intracellular symbiosis within the mesoglial cells by fluorescence in situ hybridization.

The marine realm and, in particular, the Antarctic benthos is largely unexplored and understudied. The chemical investigation reported herein reveals not only the biodiversity, but how that biodiversity manifests remarkable chemical diversity. In our continuing study of the nudibranch Austrodoris kerguelenensis, we have isolated a diverse suite of diterpenoid glyceride esters, palmadorins D - S (2.32 - 2.47), one of which is the first reported halogenated diterpene from a dorid nudibranch. Utilizing genomic data from collaborators, we have investigated the chemical diversity from phylogenetically unique specimens collected in close proximity to one another. Chemical groupings based on comparison of LC/MS metabolite fingerprints from individual organisms correlated well to the genetic data. Our research shows that A. kerguelenensis specimens from the same phylogroups elaborate near identical metabolite profiles to each other, but distinct from other phylogroups. Dendrilla membranosa is a dominant demosponge that prior studies have shown is rarely preyed upon and deters feeding against amphipods, the principal mesograzers of the Western Antarctic Peninsula. To assess the defensive nature of the pure compounds, artificial food pellets spiked with membranolides were evaluated in a feeding assay against the omnivorous amphipod Gondogeneia antarctica whereby only artificial pellets containing membranolide exhibited significant feeding deterrence. The research reported herein demonstrates that membranolides C and D were originally misassigned. Reevaluation of new extracts evolved additional fused furan membranolides G and H, and allowed for complete characterization of the four epimers. Extraction of sponge in CD3OD resulted in incorporation of a deuterated methyl group into fragment ions as evidenced from LC/MS chromatograms. Further chemical investigation of D. membranosa without the use of methanol revealed that these non-natural products arise from aplysulphurin, a known compound originally isolated from the sponge Aplysilla sulphurea, but later isolated from D. membranosa. These studies emphasize the importance of exploring the marine realm for the presence of antiviral compounds, not only for identification of small molecules but also as a source of potent macromolecules. Subfractions from Gigartina skottsbergii possesses strong anti-influenza activity toward both the A/Wyoming/03/2003 (H3N2) and A/California/04/2009 (H1N1) virus with EC50 values in the range of 5 to 10 μg/mL. The virus-inhibitory effect was selective, dose-dependent, strain-specific and the virus induced cytopathogenic effect (CPE) was reduced at non-toxic concentrations of the extract.

Of the small percentage of organisms chemically investigated over the years as potential sources of natural products, much less is known about those from the marine realm. Despite the lack of attention they have received in comparison to terrestrial organisms, marine life have recently been found to represent a valuable source for novel bioactive compounds. Cold water marine habitats are home to a plethora of organisms that have the ability to produce secondary metabolites that exhibit a great deal of diversity in both their chemical structures and biological activities. The chemical investigation of these unique and relatively unstudied ecosystems is necessary to gain insight into the dynamics between predators and prey, while also making a significant impact in the field of drug discovery. Our laboratory has focused on the chemical investigation of invertebrates from the waters of Antarctica in search of bioactive secondary metabolites that can be used for the treatment of human pathogens. This dissertation reports a small portion of the progress made in our laboratory towards the exploration of Antarctic marine invertebrates. The chemical investigation of the circumpolar colonial tunicate Synoicum adareanum and the orange, encrusting sponge Artemisina plumosa will be discussed in detail in the following chapters.

Solid-state NMR spectroscopy is used to investigate strong hydrogen bonds in a variety of solids. NMR measurements of the 2H nuclear quadrupole coupling (CQ) and nuclear magnetic shielding tensors are performed on samples of trimethylammonium chloride (TMAC), protonated 1,8-bis(dimethylamino)napthalene (DMANH+), and potassium and sodium bifluoride. 2H CPMAS is used to obtain high quality spectra while reducing experimental time. From spectral simulations, values of 127, 36, 59 and 58 kHz are determined for the 2H CQ of TMAC, DMANH+ CF3SO3-, NaHF2 and KHF2, respectively. The 2H CPMAS spectrum of TMAC shows a minor secondary component resulting from a solid phase in which the trimethylammonium cation is experiencing precessional motion. At high temperature the 2H CPMAS spectrum of DMANH+ shows unexpected spinning sideband lineshapes because of residual dipolar coupling to 14N. The experimental 2H CQ values are corroborated by ab-initio and DFT calculations; for DMAN and the bifluorides the 2H CQ values are averaged over the potential energy surface to improve the computational quality. Large values of the isotropic chemical shift (>10 ppm) are observed for all of the hydrogen-bonded deuterons. To complement the 2H NMR work, other nuclei in the compounds of interest are investigated, for TMAC these include: 35Cl, 37Cl, 1H, 14N, 15N. The 35Cl CQ shows a small, but observable deuterium/proton isotope effect. Quadrupolar and chemical shift parameters for assorted nuclei in TMAC are calculated at various N-H distances, demonstrating the strong dependence of the chlorine and hydrogen parameters on the proton position. For DMANH+ the 15N CPMAS spectrum of a static sample of DMANH+-d1 provides a value for the average dipolar 15N-D coupling constant of 870±30 Hz, corresponding to a distance of 1.29 A. Spectra of the counterions in the bifluoride salts are obtained, providing CQ values of 123 kHz and 1.141 MHz for 39K and 23Na, respectively.

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Epithelia form protective barriers and regulate molecule transport between the mesenchyme and environment. Amongst all metazoans, only sponges are said to lack 'true' epithelia however the physiology of sponge cell layers are rarely studied empirically. Aggregates and gemmules of a freshwater demosponge, Spongilla lacustris, were used to grow confluent tissue over permeable culture wells which are required for transepithelial recordings. The transepithelial potential (TEP) of S. lacustris was slightly negative (-3mV), indicating possible control of ion transport. Transepithelial resistance (TER) was recorded between 1-2 k cm2, the same order of magnitude as many vertebrate epithelia. Cultures with high resistance blocked the passage of the small tracer molecules 14C-PEG, 3H-Inulin and ruthenium red. Pinacocytes were spatially stable over time and epithelial layers were morphologically similar in freshwater and marine species. These results suggest that sponge cell layers are able to control solute and ion transport, the physiological attributes of functional epithelia. / Physiology, Cell and Development Biology