RESUMEN
Salivary gland secretions of three species of the medicinal leech differ in the level of lysozyme peptidoglycan-lysing activity. Using the synthetic fluorogenic substrate, 4-methyl-umbelliferyl tetra N-acetyl-beta-chitotetraosid, the glycosidase activity (as one of peptidoglycan-lysing activities) of salivary gland secretion of three species of the medicinal leech was quantitatively evaluated in comparison with egg lysozyme. It is supposed, that lysozyme activity of the leech secretions is determined not only by 5 isoforms of destabilase-lysozyme, but by some other enzymes which can utilize this substrate. These may be lysozymes other than i- (invertebrate) lysozymes (such as destabilase-lysozyme, or related enzymes).
Asunto(s)
Hirudo medicinalis/enzimología , Sanguijuelas/enzimología , Muramidasa/química , Saliva/enzimología , Glándulas Salivales/enzimología , Animales , Endopeptidasas/metabolismo , Isoenzimas/química , Isoenzimas/aislamiento & purificación , Isoenzimas/metabolismo , Muramidasa/aislamiento & purificación , Peptidoglicano/química , Peptidoglicano/metabolismo , Glándulas Salivales/metabolismo , Especificidad por SustratoRESUMEN
In the Eastern Ural Radioactive Trace, concentrations of 90Sr, the main contaminant, in the upper topsoil was estimated to be 40-17000 times over the global level. The density of contamination decreased with the distance from the accident plot according to exponential law. The resulting doze loads shown an excess over the background level of about 1-3 orders of magnitude. Vegetation in the head part of the EURT is represented with synanthropic and seminatural communities undergoing different phases of degradations and recovery successions. Phytocenosis degradation is caused by the failures during the accident, subsequent reinstatement and restoration activities and also by the initial anthropogenic load. The ecological and genetic effects of permanent ionizing radiation on plants are evident from a wider spectrum of variability for all indicators of the living ability of seed posterity and their increased mutability. The effect of radioadaptation, i.e. increased the resistance to the additional irradiation, in the EURT plants was not found.
Asunto(s)
Plantas/efectos de la radiación , Liberación de Radiactividad Peligrosa , Contaminantes Radiactivos del Suelo/toxicidad , Radioisótopos de Estroncio/toxicidad , Mutación , Desarrollo de la Planta , Plantas/genética , Poaceae/genética , Poaceae/crecimiento & desarrollo , Poaceae/efectos de la radiación , Tolerancia a Radiación , Federación de Rusia , Semillas/genética , Semillas/crecimiento & desarrollo , Semillas/efectos de la radiación , Árboles/genética , Árboles/crecimiento & desarrollo , Árboles/efectos de la radiaciónRESUMEN
Lipids represent 20% of the total weight of dried pool of medicinal leech salivary gland secretion (SGS) received from about 50 individual animals. There were detected steroids, but not pospholipids in SGS lipid fraction. Immunochemiluminescent analysis identified free steroid hormones in SGS: cortisol, progesterone, testosterone, estradiol and dehydroepiandrosterone. Microchromatografic-mass-spectrometric analysis of SGS and of low-molecular weight fraction (LMW) (molecular masses ranged from 220 to 850 Da) has shown the multicomponent nature of the LMW fraction. Using standart preparations as the reference steroid hormones (cortisol, dehydroepiandrosterone, androstenedione and testosterone) and histamine and serotonine have been identified in SGS.
Asunto(s)
Hirudo medicinalis/metabolismo , Histamina/análisis , Serotonina/análisis , Esteroides/análisis , Animales , Espectrometría de Masas , Glándulas Salivales/química , Glándulas Salivales/metabolismoRESUMEN
The protein and peptide composition of medicinal leech salivary gland secretion (SGS) was analyzed in preparations obtained in July from three species--Hirudo verbana, H. medicinalis, and H. orientalis. Two-dimensional electrophoresis (molecular mass 10-150 kD and pI 3-10) revealed no distinctions in the distribution of over 100 silver-stained proteins. Differences were noted only in intensity of 10 protein spots at 30-90 kD and pI 4.7-7.5. Mass spectrometric profiling of SGS of the three leech species using the Zip-Tip/golden chip scheme and cation-exchanging chips CM-10 revealed over 50 components in SGS of each of the three leech species. It was noted that 30-40% of the individual masses of the SGS of each leech species fall within the masses present in SGS of at least one of the two other species. This rather small part of the total mass may be indicative of a high polymorphism of amino acid sequences or a high frequency of posttranslational modifications of the SGS proteins and peptides. Calculation of Jacquard's coefficient showed that H. medicinalis and H. orientalis are closest to each other in SGS composition, which is consistent with data in the literature on the phylogenetic relationship between these two species of medicinal leech. Comparison of detected molecular masses with those of six known biologically active compounds produced by medicinal leeches revealed their uneven distribution in SGS of each of the three medicinal leech species. This opens prospects for using certain species of medicinal leech for targeted therapy of various pathologies.
Asunto(s)
Hirudo medicinalis/química , Sanguijuelas/química , Péptidos/metabolismo , Proteínas/metabolismo , Glándulas Salivales/metabolismo , Animales , Electroforesis en Gel Bidimensional , Péptidos/química , Péptidos/aislamiento & purificación , Proteínas/química , Proteínas/aislamiento & purificación , Espectrometría de Masa por Láser de Matriz Asistida de Ionización DesorciónRESUMEN
A photokinetic method of detection of fluorescence resonance energy transfer (FRET) between special fluorescent labels is applied to study time-averaged spatial distribution of labeled proteins in protein assemblies. Prolonged irradiation of a sample at the absorption maximum of the energy donor label initiates FRET-sensitized fluorescence photobleaching of the energy acceptor label, which was monitored by steady-state fluorimetric measurements. Kinetics of the acceptor photobleaching and kinetics of decreasing the efficiency of FRET from donors to unbleached acceptors were determined. The FRET efficiency was found from measuring sensitization of acceptor fluorescence. Analysis of the photokinetic data permits to estimate the time-averaged distribution of acceptors on donor-acceptor distances in the range of characteristic distances of FRET. Dynamic processes influencing donor-acceptor distances can be also investigated by the method. Application of the method is demonstrated by the studies of a complex of biotinylated IgM with streptavidin and aggregates composed of concanavalin A and sodium dodecyl sulphate. A new thiadicarbocyanine dye was used as the acceptor label, R-phycoerythrin and tetramethylrhodamine isothio-cyanate were the donor labels. In the IgM-streptavidin complex, 16% of acceptors most contributed to FRET provided 90% of FRET efficiency, whereas acceptors made about the same time-averaged contribution to FRET in the concanavalin A aggregates.