RESUMO
RESUMO: Avaliou-se a degradação anaeróbia do alquilbenzeno linear sulfonato (LAS) e seus homólogos em experimento em escala de laboratório. Foi usado lodo disperso para minimizar o efeito da adsorção. Em primeiro lugar, determinaram-se a maior concentração de LAS (substrato) e a menor concentração de etanol (cossubstrato) que manteriam os micro-organismos ativos, resultando em 25 e 200 mg.L-1, nessa ordem. Posteriormente, o experimento (90 dias) foi realizado em um reator somente com etanol (controle) e outro (reator teste, triplicata) com ambos os substratos nas concentrações anteriores. Os micro-organismos apresentaram crescimento exponencial em 48 h para os 2 reatores; não ocorreu toxicidade pelo LAS no reator teste durante esse período inicial, quando o etanol foi todo consumido. Após então, houve decréscimo de micro-organismos, indicando possível toxicidade por LAS ou intermediários. Observou-se também a diminuição ou ausência da produção de ácidos graxos voláteis e de metano. Portanto, com lodo disperso, a maior parcela da remoção foi por conta da biodegradação, porém, com formação de intermediários que não o acetato nem o metano, apontando a inibição à acidogênese e à metanogênese. Ao final, a remoção do LAS foi de 35% por biodegradação e apenas 0,35% por adsorção ao lodo. A ordem preferencial de biodegradação para os homólogos foi de C13 para C12, C11 e C10, com percentual de degradação em relação à massa inicial de 49, 31, 24 e 17%, respectivamente. A mesma ordem deu-se para a adsorção, da maior para a menor cadeia alquílica, sendo a remoção por adsorção de 0,85; 0,32; 0,13 e 0,01%, respectivamente.
ABSTRACT: The anaerobic degradation of linear alquibenzene sulfonate (LAS) and its homologues was evaluated in batch experiment. Dispersed sludge was used to minimize the effect of adsorption. Initially, the highest concentration of LAS (substrate) and the lowest concentration of ethanol (co-substrate) were determined to maintain the microorganisms active; the results were 25 and 200 mg.L-1, respectively. Afterwards, a 90-day period experiment was conducted with one reactor with only the addition of ethanol (control) and the other (test reactor in triplicate) with both substrates and the previous concentrations found. The microorganisms showed exponential growth in the first 48 h for both reactors; LAS toxicity has not occurred in the test reactor during the first 4 days, during which ethanol was consumed. After that, the microorganisms decreased, indicating possible toxicity due to LAS or intermediates; a decrease or absence of volatile organic acids and methane production was also observed. Therefore, with dispersed sludge the largest removal was due to biodegradation, but with formation of intermediates other than acetate or methane, indicating inhibition of acidogenesis and methanogenesis. At the end, the removal was 35% by biodegradation and only 0.35% by adsorption to the biomass. The preferential order of the biodegradation for the homologues was from C13 to C12, C11 and C10; and the removal in relation to the initial mass of each was 49, 31, 24 and 17%, respectively. The same order occurred to adsorption, from the higher to the lower alkyl chain, with removal of 0.86, 0.32, 0.13 and 0.01%, respectively.
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Snake venom metalloproteinases (SVMPs) play key biological roles in prey immobilization and digestion. The majority of these activities depend on the hydrolysis of relevant protein substrates in the tissues. Hereby, we describe several isoforms and a cDNA clone sequence, corresponding to PII SVMP homologues from the venom of the Central American pit viper Bothriechis lateralis, which have modifications in the residues of the canonical sequence of the zinc-binding motif HEXXHXXGXXH. As a consequence, the proteolytic activity of the isolated proteins was undetectable when tested on azocasein and gelatin. These PII isoforms comprise metalloproteinase and disintegrin domains in the mature protein, thus belonging to the subclass PIIb of SVMPs. PII SVMP homologues were devoid of hemorrhagic and in vitro coagulant activities, effects attributed to the enzymatic activity of SVMPs, but induced a mild edema. One of the isoforms presents the characteristic RGD sequence in the disintegrin domain and inhibits ADP- and collagen-induced platelet aggregation. Catalytically-inactive SVMP homologues may have been hitherto missed in the characterization of snake venoms. The presence of such enzymatically-inactive homologues in snake venoms and their possible toxic and adaptive roles deserve further investigation.
Assuntos
Metaloproteases/isolamento & purificação , Peptídeos/isolamento & purificação , Venenos de Serpentes/química , Viperidae , Adulto , Sequência de Aminoácidos , Animais , Coagulação Sanguínea/efeitos dos fármacos , Caseínas/metabolismo , Clonagem Molecular , DNA Complementar/genética , Edema , Gelatina/metabolismo , Hemorragia , Humanos , Metaloproteases/química , Metaloproteases/genética , Metaloproteases/farmacologia , Camundongos , Modelos Moleculares , Peptídeos/química , Peptídeos/genética , Peptídeos/farmacologia , Agregação Plaquetária/efeitos dos fármacos , Domínios Proteicos , Proteólise , Zinco/metabolismoRESUMO
The effect of the initial concentration of linear alkylbenzene sulfonate (LAS) on specific methanogenic activity (SMA) was investigated in this work. Six anaerobic flasks reactors with 1 L of total volume were inoculated with anaerobic sludge (2 g VSS L(-1)). The reactors were assayed for 42 days, and fed with volatile fatty acids, nutrients, and LAS. The initial LAS concentrations were 0, 10, 30, 50, 75, and 100 mg L(-1) for the treatment flasks T1 (control), T2, T3, T4, T5, and T6, respectively. When compared with T1, T2 exhibited a 30% reduction in maximum SMA and total methane production (TMP). In treatment T3 through T6, the reductions were 44-97% (T3-T6) for SMA, and 30-90% (T3-T6) for TMP. Total LAS removal increased following the increase in the initial LAS concentration (from 36% at T1 to 76% at T6), primarily due to the high degree of sludge adsorption. LAS biodegradation also occurred (32% in all treatments), although this was most likely associated with the formation of non-methane intermediates. Greater removal by adsorption was observed in long-chain homologues, when compared to short-chain homologues (C13 > C10), whereas the opposite occurred for biodegradation (C10 > C13). The C13 homologue was adsorbed to a great extent (in mass) in T4, T5 and T6, and may also have inhibited methane formation in these treatments.
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Ácidos Alcanossulfônicos/metabolismo , Reatores Biológicos , Methylococcaceae/metabolismo , Esgotos , Tensoativos/metabolismo , Águas Residuárias , Purificação da Água/métodos , Anaerobiose , Humanos , Microbiologia da ÁguaRESUMO
Alt a 1 has been recognized as the most important allergen produced by the Pleosporaceae family and is a risk factor for asthma development and/or exacerbation. The aim of this study was to develop a detection tool that is highly specific for species that produced airborne Alt a 1. Based on the highly conserved internal nucleotide region of the several Alt a 1 sequences that are available in GenBank, a pair of primers (Alta1CF/Alta1CR) was designed. A set of primers used by other authors for the production of recombinant Alt a 1 (A21F/A21R) was also tested. The molecular analyses were based on the polymerase chain reaction (PCR) amplification and sequencing of the cDNA that was obtained from thirteen common fungal species. The PCR system that utilized Alta1CF/Alta1CR was highly specific, sensitive, and was able to detect an amplicon of approximately 180 bp from Alt a 1 and Alt a 1-like encoding genes from A. alternata, A. tenuissima, A. infectoria, U. botrytis, and S. botryosum. In contrast, the A21F/A21R primers were specific for the very close taxonomically related species A. alternata and A. tenuissima. Thus, this rapid, sensitive, and specific detection tool can be used to assess Alt a 1 exposure levels and to inform the implementation of the appropriate public health measures.
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Antígenos de Fungos/genética , Fungos/genética , Técnicas de Tipagem Micológica/métodos , Reação em Cadeia da Polimerase/métodos , DNA Fúngico/análise , DNA Fúngico/genética , Monitoramento Ambiental , Fungos/classificação , Alinhamento de Sequência , Análise de Sequência de DNARESUMO
For many years, prokaryotic cells were distinguished from eukaryotic cells based on the simplicity of their cytoplasm, in which the presence of organelles and cytoskeletal structures had not been discovered. Based on current knowledge, this review describes the complex components of the prokaryotic cell cytoskeleton, including (i) tubulin homologues composed of FtsZ, BtuA, BtuB and several associated proteins, which play a fundamental role in cell division, (ii) actin-like homologues, such as MreB and Mb1, which are involved in controlling cell width and cell length, and (iii) intermediate filament homologues, including crescentin and CfpA, which localise on the concave side of a bacterium and along its inner curvature and associate with its membrane. Some prokaryotes exhibit specialised membrane-bound organelles in the cytoplasm, such as magnetosomes and acidocalcisomes, as well as protein complexes, such as carboxysomes. This review also examines recent data on the presence of nanotubes, which are structures that are well characterised in mammalian cells that allow direct contact and communication between cells.