Extracellular phosphatase activity of freshwater phytoplankton exposed to different in situ phosphorus concentrations

2005 ◽  
Vol 56 (4) ◽  
pp. 417 ◽  
Author(s):  
A. Ŝtrojsová ◽  
J. Vrba ◽  
J. Nedoma ◽  
K. Ŝimek
Keyword(s):  
Enzyme Activity ◽  
Phosphatase Activity ◽  
Microcystis Aeruginosa ◽  
Image Cytometry ◽  
Phosphorus Concentration ◽  
Phytoplankton Species ◽  
Freshwater Phytoplankton ◽  
Fragilaria Crotonensis ◽  
Species Specific

Extracellular phosphatase production and biomass change were investigated in phytoplankton species transplanted from the phosphorus-limited dam area of a eutrophic reservoir and exposed to the phosphorus-sufficient inflow part and vice versa. Extracellular phosphatase activity was studied using the enzyme-labelled fluorescence (ELF) technique, allowing for direct microscopic detection of enzyme activity and, moreover, its quantification using image cytometry. Several phytoplankton species (e.g. Anabaena planctonica, Microcystis aeruginosa, Fragilaria crotonensis, Ankyra ancora and Planktosphaeria gelatinosa) regulated phosphatase activity according to external phosphorus concentration. On the contrary, picocyanobacteria and several green algae (Coelastrum microporum, Crucigeniella sp., Pediastrum tetras, and Staurastrum planctonicum) did not produce extracellular phosphatases at all. The species-specific extracellular phosphatase activity of F. crotonensis, A. ancora, and P. gelatinosa ranged between 0.02 and 3.5 fmol μm−2 h−1.

The species-specific effects of sublethal concentrations of cadmium on freshwater phytoplankton communities in a Canadian Shield lake

1985 ◽  
Vol 63 (11) ◽  
pp. 1997-2003 ◽  
Author(s):  
Danny C. Reinke ◽  
Frank DeNoyelles Jr.
Keyword(s):  
Cadmium Concentration ◽  
Continuous Cultures ◽  
Experimental Lakes Area ◽  
Batch Cultures ◽  
Freshwater Phytoplankton ◽  
Specific Effects ◽  
Cell Counts ◽  
Phytoplankton Communities ◽  
Species Specific

The species-specific responses of natural phytoplankton communities to low cadmium concentrations were measured in Lake 239 (Experimental Lakes Area, northwestern Ontario). Both in situ and laboratory 5-L continuous-flow cultures, and 5-L and 100-mL cultures were used. Asterionella formosa, Dinobryon sertularia, and Dinobryon bavaricum showed dramatic negative sensitivity to low cadmium concentrations (5–100 μg/L), while Rhabdoderma gorskii and Elakatothrix sp. consistently increased in numbers at the same cadmium concentrations. In all experiments, some species exhibited no apparent effect to cadmium addition as measured by cell counts. The "bottle effect" of each technique was evaluated by comparing the community similarity valves of the control cultures to the lake samples and showed the in situ continuous cultures to be most similar to the lake followed by the laboratory continuous cultures, the in situ 5-L batch cultures, the 5-L laboratory cultures, and the 100-mL batch cultures. Replicate cadmium cultures, all techniques, were more similar to each other than the lake samples. The similarity of the cadmium cultures to the lake sample or control cultures decreased with increased cadmium concentration and incubation time.

Species-diagnostic and species-specific DNA sequences evenly distributed throughout pine and spruce chromosomes

Genome ◽  
2010 ◽  
Vol 53 (10) ◽  
pp. 769-777 ◽  
Author(s):  
Melanie Mehes-Smith ◽  
Paul Michael ◽  
Kabwe Nkongolo
Keyword(s):  
Dna Sequences ◽  
Random Amplified Polymorphic Dna ◽  
Inter Simple Sequence Repeat ◽  
Issr Markers ◽  
Pinus Monticola ◽  
The Family ◽  
Species Specific ◽  
Rapd And Issr ◽  
Specific Sequences

Genome organization in the family Pinaceae is complex and largely unknown. The main purpose of the present study was to develop and physically map species-diagnostic and species-specific molecular markers in pine and spruce. Five RAPD (random amplified polymorphic DNA) and one ISSR (inter-simple sequence repeat) species-diagnostic or species-specific markers for Picea mariana , Picea rubens , Pinus strobus , or Pinus monticola were identified, cloned, and sequenced. In situ hybridization of these sequences to spruce and pine chromosomes showed the sequences to be present in high copy number and evenly distributed throughout the genome. The analysis of centromeric and telomeric regions revealed the absence of significant clustering of species-diagnostic and species-specific sequences in all the chromosomes of the four species studied. Both RAPD and ISSR markers showed similar patterns.

scholarly journals Retention of relict satellite DNA sequences in Anemone (Ranunculaceae)

2013 ◽  
Vol 72 (1) ◽  
pp. 1-133 ◽  
Author(s):  
Višnja Besendorfer ◽  
Jelena Mlinarec
Keyword(s):  
Dna Sequences ◽  
Southern Hybridization ◽  
Repeat Unit ◽  
Similar Species ◽  
Genomic Component ◽  
Library Hypothesis ◽  
Species Specific ◽  
Eukaryotic Organisms ◽  
Fish Signal

Abstract Satellite DNAis a genomic component present in virtually all eukaryotic organisms. The turnover of highly repetitive satellite DNAis an important element in genome organization and evolution in plants. Here we study the presence, physical distribution and abundance of the satellite DNAfamily AhTR1 in Anemone. Twenty-two Anemone accessions were analyzed by PCR to assess the presence of AhTR1, while fluorescence in situ hybridization and Southern hybridization were used to determine the abundance and genomic distribution of AhTR1. The AhTR1 repeat unit was PCR-amplified only in eight phylogenetically related European Anemone taxa of the Anemone section. FISH signal with AhTR1 probe was visible only in A. hortensis and A. pavonina, showing localization of AhTR1 in the regions of interstitial heterochromatin in both species. The absence of a FISH signal in the six other taxa as well as weak signal after Southern hybridization suggest that in these species AhTR1 family appears as relict sequences. Thus, the data presented here support the »library hypothesis« for AhTR1 satellite evolution in Anemone. Similar species-specific satellite DNAprofiles in A. hortensis and A. pavonina support the treatment of A. hortensis and A. pavonina as one species, i.e. A. hortensis s.l.

scholarly journals Increase in alkaline phosphatase activity in calvaria cells cultured with diphosphonates

1979 ◽  
Vol 183 (1) ◽  
pp. 73-81 ◽  
Author(s):  
R Felix ◽  
H Fleisch
Keyword(s):  
Alkaline Phosphatase ◽  
Protein Synthesis ◽  
Enzyme Activity ◽  
Phosphatase Activity ◽  
Alkaline Phosphatase Activity ◽  
Heat Inactivation ◽  
High Concentration ◽  
Control Value ◽  
Km Value ◽  
Inhibitor Of Protein Synthesis

1. Dichloromethanediphosphonate and to a lesser degree 1-hydroxyethane-1,1-diphosphonate, two compounds characterized by a P-C-P bond, increased the alkaline phosphatase activity of cultured rat calvaria cells up to 30 times in a dose-dependent fashion. 2. Both diphosphonates also slightly inhibited the protein synthesis in these cells. 3. Thymidine, an inhibitor of cell division, did not inhibit the induction of the enzyme, indicating that the increase in enzyme activity was not due to the formation of a specific population of cells with high alkaline phosphatase activity. 4. The effect on alkaline phosphatase was suppressed by the addition of cycloheximide, an inhibitor of protein synthesis. 5. After subculturing the stimulated cells in medium without diphosphonates, the enzyme activity fell almost to the control value. 6. Bovine parathyrin diminished the enzyme activity of the control cells and the cells treated with dichloromethanediphosphonate; however, at high concentration the effect of parathyrin was greater on the diphosphonate-treated cells than on the control cells. 7. The electrophoretic behaviour, heat inactivation, inhibition by bromotetramisole or by phenylalanine, and the Km value of the induced enzyme were identical with that of the control enzyme.

In Situ Localization of Enzyme Activity in Live Cells by a Molecular Probe Releasing a Precipitating Fluorochrome

2017 ◽  
Vol 129 (39) ◽  
pp. 11950-11954 ◽  
Author(s):  
Hong-Wen Liu ◽  
Ke Li ◽  
Xiao-Xiao Hu ◽  
Longmin Zhu ◽  
Qiming Rong ◽  
...  
Keyword(s):  
Enzyme Activity ◽  
Molecular Probe ◽  
Live Cells

Experimental analysis of the control of expression of the homeobox-gene Msx-1 in the developing limb and face

Development ◽  
1993 ◽  
Vol 119 (1) ◽  
pp. 41-48 ◽  
Author(s):  
J.M. Brown ◽  
S.E. Wedden ◽  
G.H. Millburn ◽  
L.G. Robson ◽  
R.E. Hill ◽  
...  
Keyword(s):  
Homeobox Gene ◽  
Host Tissue ◽  
Face To Face ◽  
Limb Mesenchyme ◽  
The Face ◽  
Mesenchyme Cells ◽  
Species Specific ◽  
Signalling Systems ◽  
Control Of Expression

Mouse mesenchyme was grafted into chick embryos to investigate the control of mesenchymal expression of Msx-1 in the developing limb and face. In situ hybridization, using species-specific probes, allows a comparison between Msx-1 expression in the graft and the host tissue. The results show that Msx-1 expression in both limb-to-limb and face-to-face grafts corresponds closely with the level of Msx-1 expression in the surrounding chick mesenchyme. Cells in grafts that end up within the host domain of Msx-1 express the gene irrespective of whether they were from normally expressing, or non-expressing, regions. Therefore Msx-1 expression in both the developing limb and the developing face appears to be position-dependent. Mesenchyme from each of the three major facial primordia behaved in the same way when grafted to the chick maxillary primordium. Reciprocal grafts between face and limb gave a different result: Msx-1 expression was activated when facial mesenchyme was grafted to the limb but not when limb mesenchyme was grafted to the face. This suggests either that there are quantitative or qualitative differences in two local signalling systems or that additional factors determine the responsiveness of the mesenchyme cells.

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