Anodic Stripping Voltammetric Determination of Lead (II) and Cadmium (II) by Using a Carbon Nanotubes Paste Electrode Modified with Ion Exchange Synthetic Resin

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Anticholinesterasic, Nematostatic and Anthelmintic Activities of Pyridinic and Pyrazinic Compounds

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Alkyl Hydroxybenzoic Acid Derivatives that Inhibit HIV-1 Protease Dimerization

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Alterações em algumas propriedades de um latossolo degradado com uso de lodo de esgoto e resíduos orgânicos

A recuperação de áreas muito impactadas, como as oriundas da construção de hidrelétricas, é um processo lento e, usualmente, requer a adição de resíduos orgânicos, como fonte de matéria orgânica, e de nutrientes, como condicionador das propriedades do solo. O objetivo deste trabalho foi verificar o efeito da adição de lodo de esgoto e resíduos orgânicos (maravalha e torta de filtro de cana-de-açúcar) sobre o crescimento de duas espécies arbóreas de Cerrado na recuperação de um subsolo de uma área degradada pela construção da Usina Hidrelétrica de Ilha Solteira, localizada em Selvíria - MS. O experimento foi conduzido em casa de vegetação em delineamento experimental inteiramente casualizado, com oito tratamentos, seis repetições e uma planta por repetição, para cada planta-teste. Cada repetição (saco plástico) teve 3,3 L e as proporções em volume da mistura de cada resíduo foram de: 30 % de lodo de esgoto, 20 % de torta de filtro e 10 % de maravalha de madeira. Foram mensuradas a fertilidade, a micorrização, a atividade microbiana (C-CO2 liberado) do subsolo, a massa do sistema radicular e parte aérea e a altura de plantas de duas espécies nativas do Cerrado [monjoleiro (Acacia polyphylla DC.) e jatobá-do-Cerrado (Hymenaea stigonocarpa Mart)]. Os tratamentos com lodo de esgoto proporcionaram maior atividade microbiana no substrato e maior crescimento para as duas espécies arbóreas. A presença do lodo de esgoto promoveu melhora na fertilidade do subsolo, com aumento dos teores de matéria orgânica, P, K, Ca e Mg. A matéria orgânica e o P tiveram seus teores elevados nos tratamentos com mistura de lodo de esgoto e demais resíduos. Os resultados permitem concluir que as misturas contendo lodo associado a resíduos promoveram melhores incrementos na qualidade do subsolo, com perspectivas de sua recuperação.

Regeneração natural em remanescentes florestais e áreas reflorestadas da várzea do rio Mogi-Guaçu, Luiz Antônio - SP

O trabalho objetivou descrever e avaliar a estrutura da regeneração de espécies arbóreas em dois remanescentes naturais e em três áreas reflorestadas com espécies nativas e em um povoamento de Eucalyptus robusta, situados em área de várzea do rio Mogi-Guaçu, Luiz Antônio, SP (21º31'S e 47º55'W). Foram amostradas 40 subparcelas de 2 m² em cada remanescente natural e sub-bosque de eucalipto e 60 subparcelas de 3,5 m² em cada área reflorestada. Foram amostrados todos os indivíduos arbóreos de regeneração com altura > a 10 cm e diâmetro do caule até a altura do peito (DAP) < 5,0 cm e analisados separadamente, em quatro classes de altura, a diversidade florística, a regeneração natural (Rn%), o valor de importância (VI) e a similaridade da regeneração com indivíduos de DAP > 5 cm. Foram identificados 1.990 indivíduos, pertencentes a 24 famílias, 46 gêneros e 51 espécies. Cabralea canjerana, Psidium cattleyanum, Nectandra megapotamica, Acacia polyphylla e Syzygium cumini estavam entre as espécies mais representadas nas quatro categorias de tamanho. O reflorestamento com espécies nativas em áreas degradadas da várzea do rio Mogi-Guaçu promoveu a regeneração natural com biodiversidade superior aos remanescentes naturais de florestas ciliares sob efeito de borda e contribuiu para com o processo de restauração de ecossistemas florestais. O povoamento de Eucalyptus robusta com cerca de 20 anos de idade favoreceu a regeneração de espécies climácicas e secundárias.

Produção de mudas de essências florestais em diferentes substratos e acompanhamento do desenvolvimento em campo

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Crystal structure of myotoxin-II: A myotoxic phospholipase A2 - Homologue from Bothrops moojeni venom.

The crystal structure of Myotoxin-II (MjTX-II), a Lys49 PLA(2)-homologue from Bothrops moojeni venom has been determined and refined at 2.0 Angstrom to a crystallographic residual of 19.7% (R-free = 28.1%). MjTX-II is a dimer in the crystal, with the monomers in the asymmetric unit related by a two-fold symmetry axis running through the dimer interface. The dimers of MjTX-II and the Lys49 PLA(2) from B. asper venom are similar, however the relative orientations of the monomers suggests a flexible dimer interface, which serves as a hinge between the two molecules.

THE SPECIES OF SESBANIA SCOP (LEGUMINOSAE) IN BRAZIL

The species of Sesbania Scopoli (Leguminosae) occurring in Brazil are presented with keys for their identification, synonyms, descriptions and distribution. The study, based on herbarium specimens of national and foreign institutions, comes from a taxonomic revision of the genus for the New World. The species are S. sesban (L.) Merrill, S. emerus (Aubl.) Urban, S. exasperata H.B.K., S. oligosperma Taub., S. bispinosa (Jacq.) W.F. Wight, S. punicea (Cav.) Bentham, S. virgata (Cav.) and S. grandiflora (L.) Pers.

Shikimate kinase: A potential target for development of novel antitubercular agents

Tuberculosis (TB) remains the leading cause of mortality due to a bacterial pathogen, Mycobacterium tuberculosis. However, no new classes of drugs for TB have been developed in the past 30 years. Therefore there is an urgent need to develop faster acting and effective new antitubercular agents, preferably belonging to new structural classes, to better combat TB, including MDR-TB, to shorten the duration of current treatment to improve patient compliance, and to provide effective treatment of latent tuberculosis infection. The enzymes in the shikimate pathway are potential targets for development of a new generation of antitubercular drugs. The shikimate pathway has been shown by disruption of aroK gene to be essential for the Mycobacterium tuberculosis. The shikimate kinase (SK) catalyses the phosphorylation of the 3-hydroxyl group of shikimic acid (shikimate) using ATP as a co-substrate. SK belongs to family of nucleoside monophosphate (NMP) kinases. The enzyme is an alpha/beta protein consisting of a central sheet of five parallel beta-strands flanked by alpha-helices. The shikimate kinases are composed of three domains: Core domain, Lid domain and Shikimate-binding domain. The Lid and Shikimate-binding domains are responsible for large conformational changes during catalysis. More recently, the precise interactions between SK and substrate have been elucidated, showing the binding of shikimate with three charged residues conserved among the SK sequences. The elucidation of interactions between MtSK and their substrates is crucial for the development of a new generation of drugs against tuberculosis through rational drug design.

Combinatorial synthesis and directed evolution applied to the production of alpha-helix forming antimicrobial peptides analogues

Antimicrobial peptides (AMPs) are effector molecules of innate immune systems found in different groups of organisms, including microorganisms, plants, insects, amphibians and humans. These peptides exhibit several structural motifs but the most abundant AMPs assume an amphipathic alpha-helical structure. The alpha-helix forming antimicrobial peptides are excellent candidates for protein engineering leading to an optimization of their biological activity and target specificity. Nowadays several approaches are available and this review deals with the use of combinatorial synthesis and directed evolution in order to provide a high-throughput source of antimicrobial peptides analogues with enhanced lytic activity and specificity.

New anti-Alzheimer drugs from biodiversity: the role of the natural acetylcholinesterase inhibitors

Alzheimer's disease (AD) is a progressive neurodegenerative pathology with severe economic and social impact. There is currently no cure, although cholinesterase inhibitors provide effective temporary relief of symptoms in some patients. Nowadays, drug research and development are based on the cholinergic hypothesis that supports the cognition improvement by regulation of the synthesis and release of acetylcholine in the brain. There are only four commercial medicines approved for treatment of AD, and natural products have played an important alternative role in the research for new acetylcholinesterase inhibitors, as exemplified through the discovery of galantamine. This profile conducts us to give in this paper an overview relating the several classes of natural products with anti-cholinesterasic activity as potential templates to the design of new selective and powerful anti-Alzheimer drugs.

Structural Basis for Interaction of Inhibitors with Cyclin-Dependent Kinase 2

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Synthetic and natural polycations for gene therapy: State of the art and new perspectives

Currently, the major drawback of gene therapy is the gene transfection rate. The two main types of vectors that. are used in gene therapy are based on viral or non-viral gene delivery systems. There are several non-viral systems that can be used to transfer foreign genetic material into the human body. In order to do so, the DNA to be transferred must escape the processes that affect the disposition of macromolecules. These processes include the interaction with blood components, vascular endothelial cells and uptake by the reticuloendothelial system. Furthermore, the degradation of therapeutic DNA by serum nucleases is also a potential obstacle for functional delivery to the target cell. Cationic polymers have a great potential for DNA complexation and may be useful as non-viral vectors for gene therapy applications. The objective of this review was to address the state of the art in gene therapy using synthetic and natural polycations and the latest strategies to improve the efficiency of gene transfer into the cell.

Crystallization of the secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus 39E.

The secondary alcohol dehydrogenase from the thermophile Thermoanaerobacter ethanolicus 39E has been crystallized at 40 degrees C by vapour difussion using polyethelene glycol as a precipitant. The orthorhombic crystals belong to the space group P 2(1)2(1)2 with cell constants of a=170.0 Angstrom, b=125.7 Angstrom and c=80.5 Angstrom. A native X-ray diffraction data set has been collected to 2.7 Angstrom resolution.

Purine nucleoside phosphorylase: A potential target for the development of drugs to treat T-cell- and apicomplexan parasite-mediated diseases

Purine nucleoside phosphorylase (PNP) catalyzes the reversible phosphorolysis of nucleosides and deoxynucleosides, generating ribose 1-phosphate and the purine base, which is an important step of purine catabolism pathway. The lack of such an activity in humans, owing to a genetic disorder, causes T-cell impairment, and thus drugs that inhibit human PNP activity have the potential of being utilized as modulators of the immunological system to treat leukemia, autoimmune diseases, and rejection in organ transplantation. Besides, the purine salvage pathway is the only possible way for apicomplexan parasites to obtain the building blocks for RNA and DNA synthesis, which makes PNP from these parasites an attractive target for drug development against diseases such as malaria. Hence, a number of research groups have made efforts to elucidate the mechanism of action of PNP based on structural and kinetic studies. It is conceivable that the mechanism may be different for PNPs from diverse sources, and influenced by the oligomeric state of the enzyme in solution. Furthermore, distinct transition state structures can make possible the rational design of specific inhibitors for human and apicomplexan enzymes. Here, we review the current status of these research efforts to elucidate the mechanism of PNP-catalyzed chemical reaction, focusing on the mammalian and Plamodium falciparum enzymes, targets for drug development against, respectively, T-Cell and Apicomplexan parasites-mediated diseases.