A combined study of morphology, stem anatomy and isozyme patterns was used to reveal the identity of sterile plants from two rivers on the Germany/France border. A detailed morphological examination proved that the putative hybrid is clearly intermediate between Potamogeton natans and P. nodosus. The stem anatomy had characteristics of both species. The most compelling evidence came from the isozyme analysis. The additive “hybrid” banding patterns of the six enzyme systems studied indicate inheritance from P. natans and P. nodosus. In contrast, other morphologically similar hybrids were excluded: P. ×gessnacensis (= P. natans × P. polygonifolius) by all the enzyme systems, P. ×fluitans (= P. lucens × P. natans) by AAT, EST and 6PGDH, and P. ×sparganiifolius (= P. gramineus × P. natans) by AAT and EST. All samples of P. ×schreberi are of a single multi-enzyme phenotype, suggesting that they resulted from a single hybridization event and that the present-day distribution of P. ×schreberi along the Saarland/Moselle border was achieved by means of vegetative propagation and long-distance dispersal. Neither of its parental species occur with P. ×schreberi or are present upstream, which suggests that this hybrid has persisted vegetatively for a long time in the absence of its parents. The total distribution of this hybrid is reviewed and a detailed account of the records from Germany is given. P. ×schreberi appears to be a rare hybrid. The risk of incorrect determination resulting from the identification of insufficiently developed or inadequately preserved plant material is discussed.
As compared with the swamp reed (SR) ecotype of Phragmites communis growing in the desert region of northwest China, plants of the dune reed (DR) ecotype from the same region possessed lower chlorophyll (Chl) content in leaves, and less thylakoids and grana stacks in chloroplasts. Tube gel electrophoresis without stain showed that the contents of Chl-protein (Pro) components related to photosystem 2 (PS2) were markedly lower in the DR thylakoid membranes than in the SR thylakoid membranes, while the contents of Chl-Pro components associated with PS1 were almost the same in both types. SDS-PAGE analysis indicated that the content of polypeptides of the light-harvesting Chl a/b complex of PS2 (LHC2) was lower in the DR thylakoids. Besides, the conformation of LHC2 within the DR thylakoid membranes was also altered as indicated by circular dichroism spectra. Hence in the DR, reduced energy harvesting by declining the size of LHC2 might be responsible for the down-regulated PS2 activity. Chl fluorescence parameters. Fv/Fm and quantum efficiency of PS2 (ΦPS2), were lower in the DR leaves than in the SR ones. However, non-photochemical quenching coefficient (qN) was greater in DR than that in SR, implying other energy dissipation way exists in the DR photosynthetic membranes. and X. Y. Zhu, S. M. Wang, C. L. Zhang.
The electrophoretic migration rates of several proteins of photosystem 2 particles ffom spinách were much higher iii gels containing 1 mM Ca^^ than in gels containing 1 mM ethyleneglycol-í)w(P-aminoethyl ether) N,N,N',N'-tetraacetic acid (EGTA). Incubation of gels with terbium (Tb^^) and the corresponding Tb3‘'^-fluorescence were ušed to identity the Ca^^-binding proteins on the basis of selective occupation of Ca2+-binding sites with Tb^+. The 47, 43 and particularly 33 kDa polypeptides were most probably involved in Ca2+-binding.
The distribution of differently sized HDL particles in the plasma can be assessed by measurement of the fractional rate of cholesterol esterification (FERhdl). We have characterized the isotopic assay and compared it to the enzymatic measurement of the decrease in HDL free cholesterol (mass assay). The normal values of FERhdl were established in 116 apparently healthy individuals. The isotopic assay is particularly sensitive to changes in the incubation temperature above 37 °C. The reproducibility of the assay in aliquots of plasma stored at -20 °C and -70 °C for 3 months and even up to 2 years was high. Intraindividual variability of FERhdl is low. In the subjects in whom FERhdl was measured over a 3-month and 2-5 years’ period, FERhdl showed a low variability (97.5±2.6 % and 101+6.0 % respectively in a paired t-test). Comparison of the isotopic assay and the mass assay revealed that the isotopic assay was much more reproducible. Normal values of FERhdl and the HDL subspecies distribution (using gradient gel electrophoresis) were established in 63 men and 56 women. The average values of FERhdl were significantly higher in men (16.8±4.5 %/h) than in women (10.6±3.6 %/h) and correlated well with the distribution of the HDL subspecies. FERhdl radioassay as a highly reproducible method for the assessment of HDL subspecies distribution which may be suitable for both retrospective and prospective studies of diseases of atherogenous origin.
Evidence from isozyme electrophoresis confirmed previous hypothesis on the occurrence of interspecific hybridization between Potamogeton natans L. and P. lucens L. formulated on the basis of morphology and stem anatomy. Isozyme phenotypes of the morphologically intermediate plants were compared with those obtained from the putative parents growing in the same locality. P. natans and P. lucens differed consistently in at least 12 loci and possessed different alleles at 7 loci. The hybrid had no unique alleles and exhibited an additive “hybrid” isozyme pattern for all 7 loci that could be reliably analysed and where the parents displayed different enzyme patterns. Both true parental genotypes were detected among samples of plants of P. lucens and P. natans from the same locality. The hybrid plants represent a recent F1 hybrid generation resulting from a single hybridization event. Consistent differences in enzyme activity between submerged and floating leaves of P. natans and P. ×fluitans were observed in all interpretable enzyme systems.
Prolonged agonist stimulation results in specific transfer of activated Gα subunits of Gqα/G11α family from particulate membrane fraction to soluble (cytosol) cell fraction isolated as 250 000 x g supernatant. In this study, we have used 2D electrophoresis for more defined resolution of Gα subunits of Gqα/G11α family and followed the time course of solubilization effect. The small signal of soluble G proteins was already detected in control, hormone-unexposed cells. Hormone stimulation resulted in a slow but continuous increase of both intensity and number of immunoreactive signals/spots of these G proteins (10, 30, 60, 120 and 240 min). At longer times of agonist exposure (>2 hours), a marked increase of Gqα/G11α proteins was detected. The maximal level of soluble Gqα/G11α proteins was reached after 16 hours of continuous agonist exposure. At this time interval, eight individual immunoreactive signals of Gqα/G1 α proteins could be resolved. The relative proportion among these spots was 15:42:10:11:7:7:2:5. Solubilization of this class of Gα proteins was thus observed after prolonged agonist stimulation only, induced by ultra high concentration of hormone and in cells expressing a large number of GPCRs. Our data therefore rather indicate tight/persisting binding of Gqα/G11α proteins to the membrane., D. Durchánková, J. Novotný, P. Svoboda., and Obsahuje bibliografii a bibliografické odkazy