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1.
Sci Total Environ ; 762: 143134, 2021 Mar 25.
Artigo em Inglês | MEDLINE | ID: mdl-33148447

RESUMO

Massive strandings of the pelagic brown algae Sargassum have occurred in the Caribbean, and to a lesser extent, in western Africa, almost every year since 2011. These events have major environmental, health, and economic impacts in the affected countries. Once on the shore, Sargassum is mechanically harvested and disposed of in landfills. Existing commercial applications of other brown algae indicate that the pelagic Sargassum could constitute a valuable feedstock for potential valorisation. However, limited data on the composition of this Sargassum biomass was available to inform on possible application through pyrolysis or enzymatic fractionation of this feedstock. To fill this gap, we conducted a detailed comparative biochemical and elemental analysis of three pelagic Sargassum morphotypes identified so far as forming Atlantic blooms: Sargassum natans I (SnI), S. fluitans III (Sf), and S. natans VIII (SnVIII). Our results showed that SnVIII accumulated a lower quantity of metals and metalloids compared to SnI and Sf, but it contained higher amounts of phenolics and non-cellulosic polysaccharides. SnVIII also had more of the carbon storage compound mannitol. No differences in the content and composition of the cell wall polysaccharide alginate were identified among the three morphotypes. In addition, enzymatic saccharification of SnI produced more sugars compared to SnVIII and Sf. Due to high content of arsenic, the use of pelagic Sargassum is not recommended for nutritional purposes. In addition, low yields of alginate extracted from this biomass, compared with brown algae used for industrial production, limit its use as viable source of commercial alginates. Further work is needed to establish routes for future valorisation of pelagic Sargassum biomass.


Assuntos
Sargassum , Alga Marinha , África Ocidental , Biomassa , Região do Caribe , Índias Ocidentais
2.
Chem Biodivers ; 10(6): 1055-60, 2013 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-23776020

RESUMO

Cut specimens of the common reef sponge of the Verongid family, Aplysina fistularis, were retained in flow-through seawater tanks over a six-week period to assess the metabolite profile of the sponge when subjected to stress, compare the profile with the source material, and assess the preliminary feasibility of the protocol for sponge culture. The living specimens were harvested, extracted with MeOH/CH2Cl2 1:1, and subjected to column chromatography to identify metabolites. The brominated isoxazoline compounds, aerothionin (1) and 11-oxoaerothionin (2), along with aeroplysinin 2 (3) and 2-(3,5-dibromo-4-hydroxyphenol)acetamide (4), were detected in the cuttings from the tank-maintained sponge. An examination of the metabolite profile of the sponge from the natural habitat showed that the compounds 1 and 2 were present. The identities of all the compounds were ascertained by analysis of the mass-spectral data and NMR spectra (¹H, ¹³C, HMBC, and HSQC) of the compounds, which were compared with reported data. The survival rate was 44% with limited necrosis or exposed skeletal tissue being observed in eight of the 18 cuttings, suggesting that protocol modifications would be required for culturing the sponge.


Assuntos
Poríferos/metabolismo , Alcaloides/química , Alcaloides/isolamento & purificação , Animais , Halogenação , Jamaica , Oxazóis/química , Oxazóis/isolamento & purificação , Poríferos/química , Compostos de Espiro/química , Compostos de Espiro/isolamento & purificação
3.
Chem Biodivers ; 7(8): 1904-10, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20730956

RESUMO

Fractionation of the MeOH/CH2Cl2 extract of the sponge Amphimedon compressa afforded the secondary metabolite amphitoxin (1), the structure of which was elucidated by interpretation of 1H- and 13C-NMR data. The crude extract and the fractions containing the metabolite 1 were assessed for ichthyotoxic and insecticidal activity towards Xiphophorus variatus (moon fish) and Cylas formicarius elegantulus (sweet potato weevil), respectively. In addition, the ability of 1 to cause mortality (toxicity and lethal effect) in the rodent Rattus norvegicus (Norway rat) was examined. Moderate insecticidal activity was observed, while the toxicity towards the moon fish was evidenced by the high mortality rates for all the fractions tested. In contrast, the rodent was not affected by the metabolite.


Assuntos
Inseticidas/farmacologia , Poríferos/química , Compostos de Piridínio/farmacologia , Gorgulhos/efeitos dos fármacos , Animais , Peixes , Inseticidas/química , Inseticidas/toxicidade , Jamaica , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Compostos de Piridínio/química , Compostos de Piridínio/toxicidade , Ratos
4.
Nat Prod Res ; 22(15): 1339-43, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-19023791

RESUMO

Investigation of the freeze-dried dichloromethane: isopropanol extract of the sponge Axinella carteri Dendy, 1889 (Demospongiae: Halichondrida: Axinellidae), collected from Derawan Island, Indonesia, has led to the isolation of a new A-nor sterol with rare D-ring unsaturation, 3beta-(hydroxymethyl)-A-nor-5alpha-cholest-14-en-16-one (1). While the efficacy of the new compound is unknown, moderate cytotoxicity was observed in the fraction from which it was purified. A more polar portion of the extract afforded the known alkaloid dibromoisophakellin (2), previously isolated from an Axinella sp. The purification of the compounds was achieved on silica gel and Sephadex LH-20 supports and the identity of the compounds was established with the aid of 1D and 2D NMR spectroscopic experiments.


Assuntos
Axinella/química , Colestenonas/química , Colestenonas/isolamento & purificação , Esteróis/química , Esteróis/isolamento & purificação , Animais , Indonésia , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular
5.
J Nat Prod ; 68(9): 1420-3, 2005 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16180828

RESUMO

The bioassay-guided fractionation of the cytotoxic crude gum obtained from the Caribbean sponge Monanchora unguifera led to the isolation and characterization of the new compounds batzelladine J (1) and crambescidic acid (2) in addition to known guanidine alkaloids ptilomycalin A (3a), ptilocaulin (4), and isoptilocaulin (5). The structures of the compounds were elucidated by interpretation of the 1D and 2D NMR experiments. The chemotaxonomic implications of these findings are discussed.


Assuntos
Antineoplásicos/isolamento & purificação , Guanidinas/isolamento & purificação , Poríferos/química , Animais , Antineoplásicos/química , Antineoplásicos/farmacologia , Ensaios de Seleção de Medicamentos Antitumorais , Guanidinas/química , Guanidinas/farmacologia , Concentração Inibidora 50 , Leucemia P388 , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular , Panamá , Células Tumorais Cultivadas
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