RESUMEN
Seasonal dynamics and the distribution of dinophysistoxin-3 (DTX-3) in organs of mussel Crenomytilus grayanus, collected in 2013 in Peter the Great Bay, Sea of Japan, were determined. Active toxin forms (OA, DTX-1/2) concentrated in digestive glands (60-80%), whereas non-active 7-O-acyl derivatives (DTX-3) were more abundant in edible soft tissues (more than 80%). Possible mechanism of fast removing of DTX-3 from the digestive gland and accumulation of DTX-3 in the soft tissues is supposed.
Asunto(s)
Toxinas Marinas/farmacocinética , Mytilidae/química , Piranos/farmacocinética , Mariscos/análisis , Animales , Cromatografía Líquida de Alta Presión , Japón , Ácido Ocadaico/análogos & derivados , Distribución TisularRESUMEN
Several unusual overlong-chain unsaturated aldehydes (22:1, 22:2, 23:1, 24:1, 24:2, and 25:2) were found in total lipids of the endemic sponge Lubomirskia baicalensis from Baikal Lake. Tetracos-17-enal was identified as the major aldehyde of the mixture using GC-MS and 1H and 13C NMR spectroscopy. A procedure for the isolation of total overlong-chain aldehydes was suggested. We think that the overlong-chain aldehydes defend the sponge from fouling and predators. The English version of the paper: Russian Journal of Bioorganic Chemistry, 2005, vol. 31, no. 6; see also http://www.maik.ru.
Asunto(s)
Aldehídos/química , Lípidos/química , Poríferos/química , Aldehídos/aislamiento & purificación , Animales , Agua Dulce , SiberiaRESUMEN
The fatty acid (FA) composition of total lipids isolated from the marine sponge Halichondria panicea inhabiting Peter the Great Bay of Sea of Japan was studied. GC and GC-MS techniques helped identify 63 FAs, with the main attention being paid to FAs with 14-22 carbon atoms. 4, 8, 12-Trimethyl-13:0 FA was for the first time identified as the main saturated FA along with the branched FAs br-25:1, br-27:1, and br-27:2. The contents of arachidonic, eicosapentaenoic, docosapentaenoic, and the major demospongic acids [26:3(5, 9, 19), 26:3(5, 9, 17), 27:3(5, 9, 20), and 28:3(5, 9, 21)] considerably differed from those previously found for H. panicea, which may be due to seasonal changes in the species composition of organisms consumed by the sponge.
Asunto(s)
Ácidos Grasos/análisis , Poríferos/química , Animales , Ácido Araquidónico/análisis , Ácido Araquidónico/química , Ácidos Grasos/química , Ácidos Grasos Insaturados/análisis , Ácidos Grasos Insaturados/química , Cromatografía de Gases y Espectrometría de Masas/métodos , Japón , Lípidos/química , Océanos y Mares , Estaciones del AñoRESUMEN
The influence of solar irradiance and seasons on prostaglandin (PG) and arachidonic acid (AA) content in the marine red alga Gracilaria verrucosa (Huds.) Papenf. (unattached form) was investigated. PGA(2), PGE(2), PGF(2), and 15-keto-PGE(2) were isolated from the alga, quantitatively analyzed as 4-methyl-7-methoxycoumarin esters by high-performance liquid chromatography, and their chemical structures were confirmed by 1H NMR. In June-September, the PG content in the alga was relatively stable (420 microg/g of dry wt. of PGE(2)+PGF(2); 40 microg/g of PGA(2)) and it increased 1.5 times in October. The highest level of PGs was detected in November (2500 microg/g of PGE(2)+PGF(2); 74 microg/g of PGA(2)) when water temperature was fairly low (5-10 degrees C). Algae grown for five months at 50% of incident photosynthetic active radiation (PAR(0)) contained two times less PGE(2) and PGF(2) than algae grown under natural conditions, but the amount of these PG in algae grown at 5% of PAR(0) was close to the normal level. On the contrary, when algae were grown at 5% of PAR(0) the content of PGA(2) increased up to 4 times compared to algae cultivated at 100% PAR(0). In June-November, the amount of AA in total algal lipids slightly varied from 48.9 to 56.7% and did not virtually depend on the light intensity. The probable reasons of the PG content variation in response to environmental factors are discussed.
Asunto(s)
Prostaglandinas/metabolismo , Rhodophyta/metabolismo , Estaciones del Año , Luz Solar , Cromatografía Líquida de Alta Presión , Resonancia Magnética Nuclear BiomolecularRESUMEN
A practical synthesis of cis-monoepoxides from free arachidonic 20:4 (n-6), eicosapentaenoic 20:5 (n-3) and docosahexaenoic 22:6 (n-3) acids, their cytochrome P-450 epoxygenase metabolites, is described. The free polyunsaturated fatty acids (PUFA) were oxidized each by 1.25 eq. m-chloroperbenzoic acid in ethanol to give a mixture of PUFAs' mono-epoxy derivatives (45%) which was separated by HPLC and the individual isomers were characterised by mass spectrometry. All regioisomers of the free PUFAs' cis-monoepoxides were thus obtained.
Asunto(s)
Ácido Araquidónico/química , Ácidos Docosahexaenoicos/química , Ácido Eicosapentaenoico/química , Compuestos Epoxi/síntesis química , Cromatografía Líquida de Alta Presión , Espectrometría de MasasRESUMEN
It has already been shown that influenza virus binds unspecifically to liposomes containing ganglioside GM1 wheras with gangliosides GD1b and GT1b binding occurs in a specific and saturable manner [Slepushkin et al. (1986) Biol. Membr. 3, 229-235]. In the present study the mode of interaction between influenza virus and various gangliosides or phospholipid liposomes containing cholesterol and gangliosides has been investigated. The influence of exogenous gangliosides on the structure of the viral envelope was studied using fluorescent and photoactivatable phospholipids incorporated into the viral membrane. With both types of probes maximal effects of gangliosides were caused by GT1b. Addition of that ganglioside resulted in a marked decrease in the fluorescence polarization (P) of fluorescent labeled virus as well as in substantial changes in the binding of photoactivatable analogues of sphingomyelin and phosphatidylcholine to virus proteins, mainly hemagglutinin. The effects of GT1b and GD1b on P value were comparable, whereas gangliosides with other oligosaccharide chains caused much smaller changes in P. Furthermore GT1b but not GM1 influenced phospholipid-hemagglutinin cross-linking. Interaction of the virus with large unilamellar liposomes was monitored by two fluorescence assays based on resonance-energy transfer from the tryptophans and tyrosines of viral proteins to vesicles labeled with a triacylglycerol (anthrylvinyldioleoylglycerol) or from these labeled vesicles to virions labeled with a perylenoyl derivative of galactosylcerebroside (PGalSph). A third fluorescence assay was based on relief of self-quenching in PGalSph-labeled virions, upon low-pH-induced virus-liposome fusion. With all three fusion assays the changes of fluorescence caused by GT1b were more pronounced than those induced by GM1. On the other hand, virus-induced release of [14C]glucose from multilamellar liposomes was enhanced by GM1 but not by GT1b or GD1b. It is concluded that the interaction of GT1b or GD1b with virus hemagglutinin induces a rearrangement of the viral lipids rendering lipid bilayer areas of the viral envelope significantly fluid, which in turn promotes fusion of the virus with target membranes. Probably virus-liposome fusion and virus-induced liposome leakage are brought about by different mechanisms depending on specific or unspecific binding of the virions to the target.
Asunto(s)
Gangliósidos/metabolismo , Liposomas/metabolismo , Orthomyxoviridae/metabolismo , Sitios de Unión , Transferencia de Energía , Gangliósido G(M1)/metabolismo , Pruebas de Hemaglutinación , Concentración de Iones de Hidrógeno , Espectrometría de FluorescenciaRESUMEN
The synthesis of fluorescently labelled PAF-acether, 1-alkyl-2-acetyl-sn-glycero-3-phospho-[N-(9-anthrylmethyl)-N, N-dimethylethanolamine] with the label in the choline moiety is described, plasmalogen lysophosphatidylcholine of bovine heart being used as starting material.
Asunto(s)
Colorantes Fluorescentes , Factor de Activación Plaquetaria , Fenómenos Químicos , Química , Plasmalógenos , Espectrometría de FluorescenciaRESUMEN
Synthesis of fluorescently labeled cerebrosides--N-[12-(9-anthryl)-11-trans-dodecenoyl]-1 beta-O-galactosylsphingosine and its 9-(3-perylenoyl)nonanoyl analog is described. Both probes are easily inserted in phosphatidylcholine vesicles.