Caracterização química parcial das sementes de Lecythis pisonis camb. (Sapucaia)

Estudou-se a composição química de amêndoas do fruto da sapucaia (Lecythis pisonis Camb), provenientes da Estação Experimental de Santa Rita do Passa Quatro (SP), do Instituto Florestal de São Paulo. As análises químicas foram realizadas segundo as "Normas Analíticas do Instituto Adolfo Lutz (1985). Os resultados obtidos mostraram altos teores lipídicos (63,5 g/100g), protéicos (19,9 g/l00g), vitamina C (17,1 mg/100g) e valor calórico de 684 Kcal/100g. A fração oleosa apresentou um perfil de ácido graxos e índice de iodo (113,5), equivalente ao do óleo de milho comestível, destacando-se o ácido linoléico (48,6 % p/p) considerado como ácido graxo essencial e participante nos processos de inibição de germinação de sementes. O perfil de ácidos graxos do óleo das amêndoas de sapucaia, os teores de lipídios e de proteína foram semelhantes aos das amêndoas de castanhas-do-Pará (Bertholletia excelsa), espécie da mesma família da sapucaia, cultivada na Amazônia. Para a determinação dos nutrientes, as amostras foram tratadas por via úmida (H2SO4 e H2O2), através da radiação de microondas por sistema aberto de digestão e quantificadas por Espectrometria de Emissão Atômica com Plasma de Argônio Induzido (ICP-AES). A espécie revelou teores elevados para Na (49,8 mg/g); K (46,4 mg/g); B (64,5 mg/g); Mn (91,0 ųg/g); Fe (14,2 ųg/g) e Al (4,91 ųg/g). Entretanto, o nível de Pb encontrado (0,96 ųg/g), está acima do limite máximo permitido pela legislação brasileira (0,5 ųg/g), evidenciando uma possível toxicidade da amostra e contaminação antrópica do local amostrado.

Geometría de variedades localmente homog��neas

Dado un espacio homog��neo G/K con descomposición g=k + p, de su álgebra de Lie, una estructura en p invariante por Ad k, produce una estructura en G/K tal que los elementos de G son automorfismo. Si L es un subgrupo discreto de G, la variedad L/G/K es localmente homog��nea y hereda la estructura de G/K. Los temas de investigación propuestos en geometría de variedades localmente homog��neas son: 1- Grupos de tipo H y extensiones solubles. 2- Nilvariedades homog��neas de dim 3 y 4. 3- Estructuras hipercomplejas en nilvariedades de dim 8. 4- Estructuras hermitianas en espacios simétricos. 5- Variedades compactas flat con holon Zsub2 m's Zsub2. 6- Construcción de variedades de HW generalizadas. 7- Variedades planas hiperkahlerianas.

Солнечно-суточные вариации и аномальный рост жестокой компоненты космического излучения

კოსმიური სხივების მზე-დღეღამური ვარიაციების ანალიზის საფუძველზე, რომლებიც დაკავშირებულია დედამიწის მიერ საპლანეტათშორისი მაგნიტური ველის (სმე) ნეიტრალური ფენის გადაკვეთასთან, განხილულია ანომალიური ვარიაცია ყველა სხვა მომენტებთან შედარებით, როდესაც იგი არ კვეთს ნეიტრალურ ფენას. მოცემულია მეზონური კომპონენტის ანომალური ზრდის თვისობრივი ახსნა დედამიწის ნეიტრალურ ფენაში გავლის დროს.

Солнечно-суточные вариации космических лучей (КЛ), Связанные с прохождением земли через нейтральный слой межпланетного магнитного поля (ММП)

მზე-დღეღამური ვარიაციების საშუალებით გამოვლენილია კოსმოსური სხივების ხისტი კომპონენტის ანომალური ზრდა იმ მომენტებში, როდესაც დედამიწა უახლოვდება და კვეთს საპლანეტთაშორისო მაგნიტური ველის (სმვ) ნეიტრალურ ფენას.

Nutrição mineral do cajueiro (Anacardium occidentale L.): III - absorção de nutrientes - nota prévia

Na presente nota prévia os autores apresentam os primeiros dados acerca da extração e exportação de nutrientes através do cajueiro a partir de 1 a 14 anos de idade. As plantas foram colhidas de uma plantação localizada no Município de Terezinha, BA, situadas em um latossolo de baixa fertilidade, exceto em K. As plantas foram pesadas e analisadas para N, P, K, Ca, Mg, S, B, Cu, Fe, Mn e Zn. Constataram os autores que o cajueiro cresce continuamente até aos 14 anos. Uma árvore aos 10 anos de idade contém: N- 1,5 kg; P- 0,2 kg; K- 1,1 kg; Ca-0,2 kg;Mg-0,3 kg; S- 0,1 kg; B- 4,0 g;Cu-1,4 g;Fe- 2,0 g;Mn- 7,8 g;Zn- 2,6 g. Aquilataram os autores que a exportação de nutrientes através de 1 kg de frutos é a seguinte: N- 13,9 g; P- 1,3 g; K- 6,2 g; Ca- 0,3 g; Mg- 1,3 g; S- 0,5 g; B-18,5 mg; Cu-16,2 mg; Fe- 36,9 mg; Mn-13,2 mg. Finalmente observaram que a concentração de N, Mg, S, Cu, Fe e Zn não varia nas folhas em função da idade da planta; sendo que a concentração em P, K, Ca, B e Mn varia com a idade da planta.

Nutrição mineral do mamoeiro(Carica papaya L.): IV - desenvolvimento dos frutos e exportação de nutrientes através da colheita

Os propósitos deste trabalho foram: avaliar o desenvolvimento do fruto do mamoeiro (Carica papaya L.), determinar as variações das concentrações dos nutrientes durante seu crescimento e calcular as quantidades de nutrientes exportados pela colheita dos frutos. Dentre os resultados obtidos constatou-se que, as quantidades de nutrientes exportadas através da colheita, por tonelada de frutos foram: N-1.770g- P - 220 g; K-2.120 g; Ca-350 g; Mg - 180 g; S-200g: B-989 mg; Cu-130 mg; Fe-3.364 mg; Mn -1.847 mg; Mo-8 mg e Zn-1.385 mg.

Nutrição mineral de hortaliças: LXXV. absorção de nutrientes pela cultura de almeirão

De uma plantação de almeirão (Chicorium intybus c.v. Folha Larga) foram coletadas 30 plantas com 4 repetições aos 25, 35, 45 e 55 dias após a emerg��ncia. O material coletado foi dividido em folhas e raízes e analisados por N, P, K, Ca, Mg, S, B, Cu, Fe, Mn, Zn, pelos métodos convencionais de laboratório. O elemento extraído em maior quantidade foi o nitrog��nio, seguido de potássio, cálcio, fósforo, magnésio e enxofre. Dentre os micronutrientes o elemento extraído em maiores quantidades foi o ferro, seguido do manganês, zinco, boro e finalmente pelo cobre. Estabelece-se o nível crítico para os nutrientes os seguintes valores: 4,39% N, 0,47% P, 2,93 K, 1,00 % Ca, 0,35% Mg, 0,20% S, 59 ppm B, 15 ppm Cu, 2,926 ppm Fe, 117 ppm Mn e 80 ppm Zn. A extração total por folhas e raízes foi de 5.000 plantas/100 m² e de 92,3 g N, 13,3 g P, 83,2 g K, 28,8 g Ca, 8,6 g Mg, 5,45 g S, 154 mg B, 38 mg Cu, 7,979 mg Fe, 301 mg Mn e 214 mg Zn.

Proteomic and Metabolomic Analyses of Mitochondrial Complex I-deficient Mouse Model Generated by Spontaneous B2 Short Interspersed Nuclear Element (SINE) Insertion into NADH Dehydrogenase (Ubiquinone) Fe-S Protein 4 (Ndufs4) Gene.

Eukaryotic cells generate energy in the form of ATP, through a network of mitochondrial complexes and electron carriers known as the oxidative phosphorylation system. In mammals, mitochondrial complex I (CI) is the largest component of this system, comprising 45 different subunits encoded by mitochondrial and nuclear DNA. Humans diagnosed with mutations in the gene NDUFS4, encoding a nuclear DNA-encoded subunit of CI (NADH dehydrogenase ubiquinone Fe-S protein 4), typically suffer from Leigh syndrome, a neurodegenerative disease with onset in infancy or early childhood. Mitochondria from NDUFS4 patients usually lack detectable NDUFS4 protein and show a CI stability/assembly defect. Here, we describe a recessive mouse phenotype caused by the insertion of a transposable element into Ndufs4, identified by a novel combined linkage and expression analysis. Designated Ndufs4(fky), the mutation leads to aberrant transcript splicing and absence of NDUFS4 protein in all tissues tested of homozygous mice. Physical and behavioral symptoms displayed by Ndufs4(fky/fky) mice include temporary fur loss, growth retardation, unsteady gait, and abnormal body posture when suspended by the tail. Analysis of CI in Ndufs4(fky/fky) mice using blue native PAGE revealed the presence of a faster migrating crippled complex. This crippled CI was shown to lack subunits of the "N assembly module", which contains the NADH binding site, but contained two assembly factors not present in intact CI. Metabolomic analysis of the blood by tandem mass spectrometry showed increased hydroxyacylcarnitine species, implying that the CI defect leads to an imbalanced NADH/NAD(+) ratio that inhibits mitochondrial fatty acid β-oxidation.

The significance of variation in the susceptibility of Schistosoma mansoni to the antischistosomal drug oxamniquine

Clinical and laboratory evidence is reviewed which shows that there is a great deal of variation in the susceptibility of Schistosoma mansoni to oxamniquine. This variation occurs both among endemic regions and within endemic regions in Brazil and Kenya. It is genetically controlled. It is suggested that the parasite possesses a large capacity for developing resistance to the drug and that resistance will develop where sufficient drug pressure is maintained.

Testosterone Restoration by Enclomiphene Citrate in Men with Secondary Hypogonadism: a pharmacodynamic and Pharmacokinetic study.

OBJECTIVES: To determine the pharmacodynamic (PD) profile of serum total testosterone levels (TT) and luteinizing hormone (LH) in men with secondary hypogonadism following initial and chronic daily oral doses of enclomiphene citrate in comparison to transdermal testosterone. To determine the effects of daily oral doses of enclomiphene citrate (Androxal®) in comparison to transdermal testosterone on other hormones and markers in men with secondary hypogonadism. PATIENTS AND METHODS: This was a randomized, single blind, two-center phase II study to evaluate three different doses of enclomiphene citrate (6.25mg, 12.5mg and 25 mg Androxal®), versus AndroGel®, a transdermal testosterone, on 24-hour LH and TT in otherwise normal healthy men with secondary hypogonadism. Forty-eight men were enrolled in the trial (ITT Population), but 4 men had T levels &gt;350 ng/dL at baseline. Forty-four men completed the study per protocol (PP population). All subjects enrolled in this trial had serum TT in the low range (<350 ng/dL) and had low to normal LH (<12 IU/L) on at least two occasions. TT and LH levels were assessed each hour for 24 hours to examine the effects at each of three treatment doses of enclomiphene versus a standard dose (5 grams) of transdermal testosterone (AndroGel). In the initial profile TT and LH were determined in a naïve population following a single initial oral or transdermal treatment (Day 1). This was contrasted to that seen after six weeks of continuous daily oral or transdermal treatment (Day 42). The pharmacokinetics of enclomiphene was performed in a select subpopulation. Serum samples were obtained over the course of the study to determine levels of various hormones and lipids. RESULTS: After six weeks of continuous use, the mean ± SD concentration of TT at Day 42 C0hrTT, was 604 ± 160 ng/dL for men taking the highest of dose of enclomiphene citrate (enclomiphene, 25 mg daily) and 500 ± 278 ng in those men treated with transdermal testosterone. These values were higher than Day 1 values but not different from each other (p = 0.23, T-test). All three doses of enclomiphene increased C0hrTT, CavgTT, CmaxTT, CminTT and CrangeTT. Transdermal testosterone also raised TT, albeit with more variability, and with suppressed LH levels. The patterns of TT over 24 hour period following six weeks of dosing could be fit to a non-linear function with morning elevations, mid-day troughs, and rising night-time levels. Enclomiphene and transdermal testosterone increased levels of TT within two weeks, but they had opposite effects on FSH and LH Treatment with enclomiphene did not significantly affect levels of TSH, ACTH, cortisol, lipids, or bone markers. Both transdermal testosterone and enclomiphene citrate decreased IGF-1 levels (p<0.05) but suppression was greater in the enclomiphene citrate groups. CONCLUSIONS: Enclomiphene citrate increased serum LH and TT; however, there was not a temporal association between the peak drug levels and the Cmax levels LH or TT. Enclomiphene citrate consistently increased serum TT into the normal range and increased LH and FSH above the normal range. The effects on LH and TT persisted for at least one week after stopping treatment.

The genome of Laccaria bicolor provides insights into mycorrhizal symbiosis

Mycorrhizal symbioses--the union of roots and soil fungi--are universal in terrestrial ecosystems and may have been fundamental to land colonization by plants. Boreal, temperate and montane forests all depend on ectomycorrhizae. Identification of the primary factors that regulate symbiotic development and metabolic activity will therefore open the door to understanding the role of ectomycorrhizae in plant development and physiology, allowing the full ecological significance of this symbiosis to be explored. Here we report the genome sequence of the ectomycorrhizal basidiomycete Laccaria bicolor (Fig. 1) and highlight gene sets involved in rhizosphere colonization and symbiosis. This 65-megabase genome assembly contains approximately 20,000 predicted protein-encoding genes and a very large number of transposons and repeated sequences. We detected unexpected genomic features, most notably a battery of effector-type small secreted proteins (SSPs) with unknown function, several of which are only expressed in symbiotic tissues. The most highly expressed SSP accumulates in the proliferating hyphae colonizing the host root. The ectomycorrhizae-specific SSPs probably have a decisive role in the establishment of the symbiosis. The unexpected observation that the genome of L. bicolor lacks carbohydrate-active enzymes involved in degradation of plant cell walls, but maintains the ability to degrade non-plant cell wall polysaccharides, reveals the dual saprotrophic and biotrophic lifestyle of the mycorrhizal fungus that enables it to grow within both soil and living plant roots. The predicted gene inventory of the L. bicolor genome, therefore, points to previously unknown mechanisms of symbiosis operating in biotrophic mycorrhizal fungi. The availability of this genome provides an unparalleled opportunity to develop a deeper understanding of the processes by which symbionts interact with plants within their ecosystem to perform vital functions in the carbon and nitrogen cycles that are fundamental to sustainable plant productivity.

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.

We report the generation and analysis of functional data from multiple, diverse experiments performed on a targeted 1% of the human genome as part of the pilot phase of the ENCODE Project. These data have been further integrated and augmented by a number of evolutionary and computational analyses. Together, our results advance the collective knowledge about human genome function in several major areas. First, our studies provide convincing evidence that the genome is pervasively transcribed, such that the majority of its bases can be found in primary transcripts, including non-protein-coding transcripts, and those that extensively overlap one another. Second, systematic examination of transcriptional regulation has yielded new understanding about transcription start sites, including their relationship to specific regulatory sequences and features of chromatin accessibility and histone modification. Third, a more sophisticated view of chromatin structure has emerged, including its inter-relationship with DNA replication and transcriptional regulation. Finally, integration of these new sources of information, in particular with respect to mammalian evolution based on inter- and intra-species sequence comparisons, has yielded new mechanistic and evolutionary insights concerning the functional landscape of the human genome. Together, these studies are defining a path for pursuit of a more comprehensive characterization of human genome function.

Arabidopsis NPH1: a flavoprotein with the properties of a photoreceptor for phototropism.

The NPH1 gene of Arabidopsis thaliana encodes a 120-kilodalton serine-threonine protein kinase hypothesized to function as a photoreceptor for phototropism. When expressed in insect cells, the NPH1 protein is phosphorylated in response to blue light irradiation. The biochemical and photochemical properties of the photosensitive protein reflect those of the native protein in microsomal membranes. Recombinant NPH1 noncovalently binds flavin mononucleotide, a likely chromophore for light-dependent autophosphorylation. The fluorescence excitation spectrum of the recombinant protein is similar to the action spectrum for phototropism, consistent with the conclusion that NPH1 is an autophosphorylating flavoprotein photoreceptor mediating phototropic responses in higher plants.

The IC3D classification of the corneal dystrophies.

BACKGROUND: The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification. Abnormalities in different genes can cause a single phenotype, whereas different defects in a single gene can cause different phenotypes. Some disorders termed corneal dystrophies do not appear to have a genetic basis. PURPOSE: The purpose of this study was to develop a new classification system for corneal dystrophies, integrating up-to-date information on phenotypic description, pathologic examination, and genetic analysis. METHODS: The International Committee for Classification of Corneal Dystrophies (IC3D) was created to devise a current and accurate nomenclature. RESULTS: This anatomic classification continues to organize dystrophies according to the level chiefly affected. Each dystrophy has a template summarizing genetic, clinical, and pathologic information. A category number from 1 through 4 is assigned, reflecting the level of evidence supporting the existence of a given dystrophy. The most defined dystrophies belong to category 1 (a well-defined corneal dystrophy in which a gene has been mapped and identified and specific mutations are known) and the least defined belong to category 4 (a suspected dystrophy where the clinical and genetic evidence is not yet convincing). The nomenclature may be updated over time as new information regarding the dystrophies becomes available. CONCLUSIONS: The IC3D Classification of Corneal Dystrophies is a new classification system that incorporates many aspects of the traditional definitions of corneal dystrophies with new genetic, clinical, and pathologic information. Standardized templates provide key information that includes a level of evidence for there being a corneal dystrophy. The system is user-friendly and upgradeable and can be retrieved on the website www.corneasociety.org/ic3d.

Spontaneous stage differentiation of mouse-virulent Toxoplasma gondii RH parasites in skeletal muscle cells: an ultrastructural evaluation

Although the predilection for Toxoplasma gondii to form cysts in the nervous system and skeletal and heart muscles has been described for more than fifty years, skeletal muscle cells (SkMCs) have not been explored as a host cell type to study the Toxoplasma-host cell interaction and investigate the intracellular development of the parasite. Morphological aspects of the initial events in the Toxoplasma-SkMC interaction were analysed and suggest that there are different processes of protozoan adhesion and invasion and of the subsequent fate of the parasite inside the parasitophorous vacuole (PV). Using scanning electron microscopy,Toxoplasma tachyzoites from the mouse-virulent RH strain were found to be attached to SkMCs by the anterior or posterior region of the body, with or without expansion of the SkMC membrane. This suggests that different types of parasite internalization occurred. Asynchronous multiplication and differentiation of T. gondii were observed. Importantly, intracellular parasites were seen to display high amounts of amylopectin granules in their cytoplasm, indicating that tachyzoites of the RH strain were able to differentiate spontaneously into bradyzoites in SkMCs. This stage conversion occurred in approximately 3% of the PVs. This is particularly intriguing as tachyzoites of virulent Toxoplasma strains are not thought to be prone to cyst formation. We discuss whether biological differences in host cells are crucial to Toxoplasma stage conversion and suggest that important questions concerning the host cell type and its relevance in Toxoplasma differentiation are still unanswered.