A influência do ambiente e do espaço em comunidades de peixes estuarinos da Zona Costeira Amazônica

Um dos objetivos do estudo da ecologia de comunidades de peixes é identificar e prever padrões de estruturação dessas assembleias em função das interações bióticas e abióticas que ocorrem dentro de um ecossistema. Especificamente na Zona Costeira Amazônica, há um crescente número de estudos sendo realizados sobre a influência de fatores abióticos e da localização espaço-sazonal na estruturação de assembleias de peixes estuarinos, no entanto estas influências têm sido avaliadas separadamente tornando restrito o entendimento da dinâmica das assembleias de peixes desses ambientes. Com isso, o objetivo deste estudo é identificar o padrão de estruturação espaço-sazonal da ictiofauna na Baía de Salinas relacionando descritores de assembleias de peixes com parâmetros ambientais e espaciais. As coletas foram sazonais (chuva e estiagem de 2011) dentro da Baía de Salinópolis utilizando métodos tradicionais (malhadeiras) de coleta de peixes. Foi coletado um total de 1.293 exemplares, distribuídos em 67 espécies e 27 famílias. As espécies Cathorops spixii (n = 121) e Cathorops agassizii (n = 201) foram as mais abundantes durante a chuva e durante a estiagem, as espécies Cathorops agassizii (n = 118) e Genyatremus luteus (n = 72) foram as mais abundantes. Os resultados mostraram as assembleias de peixes entre o período de chuva e estiagem se mostraram semelhantes em termos de abundância e composição de espécies. O ambiente e a localização geográfica não influenciam a estruturação das assembleias de peixes estuarinos neotropicais, sugerindo que a estruturação da assembleia se dê de forma aleatória, seguindo o padrão de modelos nulos de distribuição.

Efeito de características ambientais no uso dos canais-de-maré por três espécies de peixes bentófagos durante o período transição-seca no estuário de Curuçá (Pará-Brasil)

O estuário de Curuçá é parte de uma Unidade de Conservação (RESEX Mãe Grande de Curuçá) desde 2002 e tem como principais cursos d’agua o Rio Curuçá e do Furo Muriá. O presente estudo objetivou analisar o efeito de características ambientais no uso dos canais-de-maré pelas espécies bentófagas Colomesus psittacus, Sciades herzbergii e Genyatremus luteus. A análise envolveu a relação de dados ambientais (salinidade, área de inundação e cobertura arbórea) com dados bióticos das três espécies estudadas (densidade, biomassa, intensidade alimentar e distribuição dos comprimentos totais). A primeira expedição ocorreu em julho de 2008 a fim de coletar a ictiofauna e a segunda em outubro de 2008 para realizar o inventário arbóreo, sendo que cada campanha teve a duração de três dias. Por todo o estuário de Curuçá, mais precisamente, ao longo do Rio Curuçá e do Furo Muriá, foram distribuídos um total de seis sítios de coleta, onde no interior de cada sítio foram amostrados dois canais-de-maré, perfazendo um total de doze canais-de-maré amostrados. As espécies C. psittacus, S. herzbergii e G. luteus estiveram entre as cinco mais abundantes e ocorreram em todos os sítios, com exceção do S. herzbergii, o qual foi capturado somente em cinco dos seis sítios. As três espécies estudadas apresentaram, entre os sítios, diferenças altamente significativas para as variações de suas médias de densidade, biomassa, índice de plenitude e comprimento total, com exceção de G. luteus que não apresentou diferenças estatísticas em suas médias de comprimento total. Todas as variações das médias das características ambientais referentes à cobertura arbórea (densidade, altura e diâmetro), assim como, a área de inundação dos canais-de-maré apresentaram significativas diferenças entre os sítios. Neste trabalho foi possível verificar: a influência do gradiente de salinidade na distribuição das espécies estudadas no interior do estuário; as relações espaciais entre a área de inundação e disponibilidade de recurso alimentar, onde os canais com maior área inundada mostraram-se mais favoráveis ao forrageio da ictiofauna bentófaga; que provavelmente, existe um melhor rendimento alimentar quando as espécies bentófagas frequentam os canais-de-maré cercados por vegetação desenvolvida.

Ciclo de vida e estrutura de uma assembléia de peixes teleósteos em um manguezal da Raposa, Maranhão, Brasil

Pós-graduação em Ciências Biológicas (Zoologia) - IBRC

DETERMINACIÓN DE MEDIOS DE CULTIVO Y PH PARA LA MASIFICACIÓN in vitro DE CEPAS DE Suillus luteus Aubl. ASOCIADAS A Pinus radiata D. Don Y Scleroderma citrinum Pers. ASOCIADAS A Eucalyptus globulus Labill. DE LA REGIÓN DEL BIOBÍO, CHILE

El uso de agentes biológicos en la producción en vivero ha aflorado como un elemento que permite no sólo mejorar la calidad morfológica y fisiológica de las plantas, sino que también posibilitar un mayor éxito en el ámbito silvicultural de una plantación. Estos agentes biológicos requieren de un ambiente óptimo para crecer, asociarse y reproducirse. El objetivo de este estudio fue determinar la dependencia del pH y el medio de cultivo en el crecimiento in vitro de distintas cepas de Suillus luteus y Scleroderma citrinum asociadas a Pinus radiata y Eucalyptus globulus, respectivamente. El estudio se realizó en condiciones controladas de temperatura y humedad, disponiendo los inóculos en placas Petri con diferentes medios cultivo, evaluando parámetros de crecimiento y biomasa a los 38 días para S. luteus y 105 días para S. citrinum. Los resultados indican que tanto el medio de cultivo, el pH del medio, así como las cepas de cada especie estudiada, son determinantes en las respuestas de crecimiento de los hongos ectomicorrícicos in vitro evaluados. Las cepas de S. luteus se desarrollaron adecuadamente en un medio de cultivo con abundancia de nutrientes (BAF, MMN) como en baja presencia de ellos (EMA), y con pH más bien ácido (4,8 y 5,8). Por otro lado, las cepas de S. citrinum presentaron, para los mismos ambientes, un desarrollo inferior y lento, no obstante, la cepa Sc8 se reprodujo de forma óptima y rápida bajo un medio de cultivo BAF y con un pH moderadamente ácido de 5,8.

Untersuchung der Strukturdynamik arbeitender F1-ATPase und ATP-Synthase aus Micrococcus luteus in Einzelschußexperimenten mit Synchrotronstrahlung

ZusammenfassungDie ATP-Synthase koppelt im Energiestoffwechsel der Zellen den Protonentransport über die biologische Membran mit der Synthese des energiespeichernden Moleküls ATP aus ADP und Phosphat. ATP-Synthasen bestehen aus 2 Subkomplexen, wobei der katalytische F1-Teil von der membranständigen Domäne abgelöst werden kann und nur zur ATP-Hydrolyse fähig ist. Der hochkooperative Reaktionsmechanismus der dreizentrigen ATP-Synthasen ist weitgehend unklar.Im Rahmen dieser Arbeit wurde der ATP-Synthasekomplex und ihr wasserlösliches katalytisches F1-Fragment aus Micrococcus luteus in präparativem Maßstab mittels chromatographischer Trennmethoden isoliert. Die Überprüfung der Funktionalität beider Enzyme erfolgte mit enzymatischen Methoden. Durch zeitaufgelöste Röntgenkleinwinkelstreuung wurde die Strukturdynamik der arbeitenden ATP-Synthase und ihres F1-Fragmentes aus Micrococcus luteus im Laufe des ATP-Hydrolysezyklus untersucht. Diese Methode diente zum Nachweis weiträumiger Konformationsänderungen innerhalb der arbeitenden Enzyme unter nativen physiologischen Bedingungen. Die zeitaufgelösten Streuexperimente fanden an der ESRF (Europäische Synchrotronstrahlungsquelle) in Grenoble (F) statt. Dort wurden für beide Enzyme im Laufe des ATP-Hydrolysezykus molekulare Bewegungen nachgewiesen. Als Referenz zu den zeitaufgelösten Messungen dienten statische Messungen zur Strukturuntersuchung der Proteine am schwächeren DESY. Anhand dieser Strukturdaten wurden Molekülmodelle der F1-ATPase und ATP-Synthase aus Micrococcus luteus konstruiert. Das Molekülmodell der F1-ATPase war die Grundlage zur Modellierung einzelner Teilschritte des ATP-Hydrolysezyklus bei 20°C. Die experimentellen Daten wurden mit einer Kippbewegung der membranseitigen Domäne der katalytischen b-Untereinheiten der F1-ATPase während des ATP-Hydrolysezyklus interpretiert.

Einige Bemerkungen über Nigritella angustifolia Rich. und Mimulus luteus L.

Nägele, Pfr.

Beitrag zur kenntniss der in den samen von lupinus luteus entha...

Thesis (doctoral)--

Constituintes químicos e atividade antimicrobiana dos extratos de Dilodendron bipinnatum (sapindaceae)

The phytochemical investigation of ethanolic extracts from leaves, branches and stems of D. bipinnatum afforded the steroids β-sitosterol, stigmasterol, campesterol, sitostenone and sitosterol-3-O-β-D-glycopyranoside, along with two cycloartane triterpenes: cycloeucalenol and 24-methylenecycloartenol. The antimicrobial activity of the extracts was evaluated against Staphylococcus aureus (ATCC 25923), Escherichia coli (ATCC 25922), Bacillus subtilis (ATCC 6623), Pseudomonas aeruginosa (ATCC 15442), Micrococcus luteus (ATCC 9341) and Candida albicans (ATCC 10231). The extracts of the leaves and branches showed moderate activity against Candida albicans. The extract of the branches was active against Micrococcus luteus. This is the first report on the phytochemical study of D. bipinnatum.

Filmes ultrafinos de ésteres de celulose: preparo, caracterização e imobilização de proteínas

In this study cellulose acetate butyrate (CAB) and carboxymehtylcellulose acetate butyrate (CMCAB) films adsorbed onto silicon wafers were characterized by means of ellipsometry, atomic force microscopy (AFM), sum frequency generation spectroscopy (SFG) and contact angle measurements. The adsorption behavior of lysozyme (LIS) or bovine serum albumin (BSA) onto CAB and CMCAB films was investigated. The amounts of adsorbed LIS or BSA onto CMCAB films were more pronounced than those onto CAB films due to the presence of carboxymethyl group in the CMCAB structure. Besides, the adsorption of BSA molecules on CMCAB films was more favored than that of LIS molecules. Antimicrobial effect of LIS bound to CAB or CMCAB layers was evaluated using Micrococcus luteus as substrate.

Effects of stingless bee and honey bee propolis on four species of bacteria

We examined the antibacterial activities of several types of propolis, including Africanized honey bee green propolis and propolis produced by meliponini bees. The antibacterial activity of green propolis against Micrococcus luteus and Staphylococcus aureus was superior to that of Melipona quadrifasciata and Scaptotrigona sp propolis. Only two samples of propolis (green propolis and Scaptotrigona sp propolis) were efficient against Escherichia coli. Melipona quadrifasciata propolis was better than green propolis and Scaptotrigona sp propolis against Pseudomonas aeruginosa. We concluded that these resins have potential for human and veterinary medicine.

Suramin inhibits macrophage activation by human group IIA phospholipase A(2), but does not affect bactericidal activity of the enzyme

Suramin is a polysulphonated napthylurea antiprotozoal and anthelminitic drug, which also presents inhibitory activity against a broad range of enzymes. Here we evaluate the effect of suramin on the hydrolytic and biological activities of secreted human group IIA phospholipase A(2) (hsPLA(2)GIIA). The hsPLA(2)GIIA was expressed in E. coli, and refolded from inclusion bodies. The hydrolytic activity of the recombinant enzyme was measured using mixed dioleoylphosphatidylcholine/dioleoylphosphatidylglycerol (DOPC/DOPG) liposomes. The activation of macrophage cell line RAW 264.7 by hsPLA(2) GIIA was monitored by NO release, and bactericidal activity against Micrococcus luteus was evaluated by colony counting and by flow cytometry using the fluorescent probe Sytox Green. The hydrolytic activity of the hsPLA(2) GIIA was inhibited by a concentration of 100 nM suramin and the activation of macrophages by hsPLA(2) GIIA was abolished at protein/suramin molar ratios where the hydrolytic activity of the enzyme was inhibited. In contrast, both the bactericidal activity of hsPLA(2) GIIA against Micrococcus luteus and permeabilization of the bacterial inner membrane were unaffected by suramin concentrations up to 50 mu M. These results demonstrate that suramin selectively inhibits the activity of the hsPLA(2) GIIA against macrophages, whilst leaving the anti-bacterial function unchanged.

CHEMICAL CHARACTERIZATION AND EVALUATION OF ANTIBACTERIAL, ANTIFUNGAL, ANTIMYCOBACTERIAL, AND CYTOTOXIC ACTIVITIES OF Talinum paniculatum

SUMMARY In this study, the bioactivity of Talinum paniculatum was evaluated, a plant widely used in folk medicine. The extract from the T. paniculatum leaves (LE) was obtained by percolation with ethanol-water and then subjecting it to liquid-liquid partitions, yielding hexane (HX), ethyl acetate (EtOAc), butanol (BuOH), and aqueous (Aq) fractions. Screening for antimicrobial activity of the LE and its fractions was evaluated in vitro through broth microdilution method, against thirteen pathogenic and non-pathogenic microorganisms, and the antimycobacterial activity was performed through agar diffusion assay. The cytotoxic concentrations (CC90) for LE, HX, and EtOAc were obtained on BHK-21 cells by using MTT reduction assay. The LE showed activity against Serratia marcescens and Staphylococcus aureus, with Minimum Inhibitory Concentration (MIC) values of 250 and 500 µg/mL, respectively. Furthermore, HX demonstrated outstanding activity against Micrococcus luteus and Candida albicans with a MIC of 31.2 µg/mL in both cases. The MIC for EtOAc also was 31.2 µg/mL against Escherichia coli. Conversely, BuOH and Aq were inactive against all tested microorganisms and LE proved inactive against Mycobacterium tuberculosisand Mycobacterium bovisas well. Campesterol, stigmasterol, and sitosterol were the proposed structures as main compounds present in the EF and HX/EtOAc fractions, evidenced by mass spectrometry. Therefore, LE, HX, and EtOAc from T. paniculatumshowed potential as possible sources of antimicrobial compounds, mainly HX, for presenting low toxicity on BHK-21 cells with excellent Selectivity Index (SI = CC90/MIC) of 17.72 against C. albicans.

Morphological aspects of cell reabsorption in laying queens and workers of Apis mellifera (Hymenoptera, Apidae)

The occurrence of cell reabsorption in the ovaries of queens in several rates of laying eggs, artificially impeded of laying, and in nurse workers, of Apis mellifera (Linnaeus, 1758), was studied with light (LM) and transmission electron microscopy (TEM). Two types of structures were described and named by analogy with vertebrates ovarian structures, as corpus luteus, when resulting from the reabsorption of the follicular cells after ovulation, and corpus atresicus when resulting from total follicular reabsorption at any oocyte developmental stage. These structures have the same morphological characteristics and physiological signification in both castes. The corpus luteus occurrence indicates ovulation and its number is correspondent to the queen's rates of oviposition. The presence of this structure in nurse workers ovarioles shows that this caste may lay eggs. The incidence of corpus atresicus in queens decay with the increasing of the oviposition indicating that the inhibition of the normal sequence of oocyte maturation in the ovaries is deleterious. Both, corpus luteus and corpus atresicus incidence may be influenced by environmental factors.

Quatro especies nuevas de nematodos del sur del Perú y redescripción de Hedruris Orestiae Moniez, 1889

En el estudio helmintológico de anfibios del género Telmatobius Wiegmann, 1834, y del pez Orestias luteus Valenciennes, 1839, de las zonas de Arequipa, Puno y del Lago Titicaca, se han encontrado nematodes de los géneros Hedruris Nitzsch, 1821 y Falcaustra Lane, 1915. Se redescribe Hedruris orestiae Moniez, 1889 y se describen cuatro especies nuevas: Hedruris moniezi sp. n., Falcaustra condorcanquii sp. n., Falcaustra pumacahuai sp. n. y Falcaustra tiahuanaquensis sp. n.

Detection of extracellular proteases from microorganisms on agar plates

We present herein an improved assay for detecting the presence of extracellular proteases from microorganisms on agar plates. Using different substrates (gelatin, BSA, hemoglobin) incorporated into the agar and varying the culture medium composition, we were able to detect proteolytic activities from Pseudomonas aeruginosa, Micrococcus luteus and Serratia marcescens as well as the influence that these components displayed in the expression of these enzymes. For all microorganisms tested we found that in agar-BHI or yeast extract medium containing gelatin the sensitivity of proteinase detection was considerably greater than in BSA-agar or hemoglobin-agar. However, when BSA or hemoglobin were added to the culture medium, there was an increase in growth along with a marked reduction in the amount of proteinase production. In the case of M. luteus the incorporation of glycerol in BHI or yeast extract gelatin-agar induced protease liberation. Our results indicate that the technique described here is of value for detecting extracellular proteases directly in the culture medium, by means of a qualitative assay, simple, inexpensive, straight forward method to assess the presence of the proteolytic activity of a given microorganism colony with great freedom in substrate selection.