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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Planta 137 (1977), S. 85-87 
    ISSN: 1432-2048
    Keywords: Cell culture ; Daucus ; Membrane systems ; Morphometry ; Particle number ; Surface density
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Standard stereologic methods have been applied to electron micrographs of Daucus carota L. suspension culture cells. The relative frequencies of the different membrane systems within the cells have been determined and compared with published data form mature leaf cells.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2048
    Keywords: Acyl-CoA hydrolase ; Cell culture ; Daucus ; Oleosomes ; Triacylglycerol turnover
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Isolated oleosomes from Daucus carota L. cells are lipid droplets consisting mainly of triacylglycerols (〉97%) and very little protein (1–2%). The boundary between the lipid phase and the cytosol, which is visible on electron micrographs, is not built up by a true phospholipid-containing unit or half unit membrane. Enzymatic activities of lipid metabolism were not found to be associated with oleosomes with the exception of very low (contaminating) acyl-CoA:1,2-diacylglycerol acyltransferase (EC 2.3.1.20) and relatively high acyl-CoA hydrolase (EC 3.1.2.2) activities. The triacylglycerols exhibited a half life time of about 70 h, which is below the generation time of the cells (80–90 h). The fatty acid pattern of triacylglycerols was very similar to that of polar cellular membrane lipids.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 169 (1984), S. 9-20 
    ISSN: 1432-0568
    Keywords: Peroxisomes ; Marginal plates ; DAB-Cytochemistry ; Electron microscopy ; Freeze-etching
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In the canine circumanal gland, the morphological alterations of peroxisomes during differentiation and maturation of the glandular cells were studied by electron microscopy, cytochemistry and freeze-etch technique. Each of the following three cell types has its own characteristic peroxisomal population: 1) The basal cell contains only a few small peroxisomes, which appear as spherical and tubular profiles showing strong DAB reaction. In the differentiating basal cells, these are joined by a few dilated, hemispherical organelles with intensely stained small marginal plates. 2) In the intermediate cell, additional to spherical and tubular peroxisomes, numerous clongated organelles with distinct marginal plates are observed, displaying weak catalase activity. 3) In the mature cell, dumbbell-shaped peroxisomes with enlarged marginal plates predominate. Serial section analysis and freeze-etching studies reveal that these dilated particles are of erythrocyte-like shape. They exhibit very weak catalase activity or do not contain any visible DAB reaction product. In their flattened, thin central portions, the memoranes enclose the marginal plates and form straight cisternae, which are closely associated with adjacent fenestrated cisternae of ER on both sides, referred to as paramarginal cisternae. Dumbbell-shaped peroxisomes with their corresponding paramarginal cisternae form large peroxisome-ER-complexes. Furthermore, three to five dumbbell-shaped particles are often stacked in parallel. Only at their flat poles are the organelles in close contact with paramarginal cisternae. The observation of continuities, in particular between erythrocyte-like organelles and tubular peroxisomes in mature glandular cells, indicates the existence of a peroxisomal compartment composed of two segments in the mature stage. In freeze-etch replicas of mature glandular cells, only the dilated segments of the peroxisomal compartment can be easily recognized because of their unusual size and erythrocyte-like shape. Additionally, on the E-face of their central portion, a straight, square or rectangular area with a distinct crystalline pattern is seen, which corresponds to the marginal plate. These findings indicate that the circumanal gland of the dog offers unique possibility to analyze the biological properties of a well-defined peroxisomal compartment.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 120 (1979), S. 105-112 
    ISSN: 1432-072X
    Keywords: Physarum polycephalum ; Myxamoebae ; Encystment ; Differentiation ; Induction ; Mannose ; Aminopeptidases ; Acid proteases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Encystment of Physarum polycephalum myxamoebae, grown under nearly identical physiological conditions as plasmodia is induced by transfer to a salts medium containing 0.5 M mannitol or mannose. After 24 h induction approximately 50% of amoebae had differentiated to cells which were identified to be young cysts by light and electron microscopy. Several other polyols, sugars, biogenic amines, and a starvation period from 24 h to one week caused no reproducible cyst formation. In contrast to the formation of dormant forms in the plasmodial stage of the life cycle, the induction of cysts and their germination to amoebae are not inhibited neither by actinomycin C nor by cycloheximide. In addition, the isoenzyme spectra of aminopeptidases and acid proteases remain nearly identical in growing and differentiating amoebae.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-072X
    Keywords: Physarum polycephalum ; Spherulation ; Slime ; Galactan ; Sulfate ; Selenate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The myxomycetePhysarum polycephalum synthesizes copious amounts of slime when differentiating into the hard walled resting stage. The chemical composition of slime obtained after introduction of spherulation in a nutrient and a non-nutrient salt-medium has been analysed and compared. The composition of slime is almost identical after the two different induction methods. This slime could be labelled with radioactived-[U-14C]glucose,32PO4 3−,35SO4 2− and75SeO4 2−. The kinetics of slime secretion after both induction methods has been followed using different criteria. The sulfate analog75SeO4 2− seems to be incorporated into the slime, partially replacing sulfate groups of the sulfated polysaccharide. Furthermore,d-[U-14C]glucose was used to labe the spherule walls. Determination of an alkali resistent polysaccharide component serves as a new method to follow wall formation.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 260 (1990), S. 409-414 
    ISSN: 1432-0878
    Keywords: Kidney ; Peroxisomes ; Marginal plates ; Electron microscopy ; Freeze-etching ; DAB-cytochemistry ; Bovine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The ultrastructure of peroxisomes in the proximal nephron tubules of bovine kidney cortex was studied using ultrathin-sectioning, diaminobenzidine cytochemistry for the visualization of catalase, and by freeze-fracture. Peroxisomes in this nephron segment are up to 1.5 μm in diameter and exhibit a peculiar angular shape, which is probably related to the occurrence of multiple straight plate-like inclusions (marginal plates) in the matrix of peroxisomes; they lie directly underneath the peroxisomal membranes. The peroxisomal membrane in such regions follows the outline of the marginal plate. The peculiar shape of peroxisomes allows their unequivocal identification in freeze-fracture preparations. Peroxisomal membranes are recognized by their flat, often rectangular appearance. Intramembrane particles are much more numerous on P-fracture faces than on E-fracture faces. A crystalline lattice-structure with a periodicity of approximately 10 nm can be observed on the flat rectangular areas of E-fracture faces. This lattice structure is intensified after prolonged freeze-etching. Intramembranous particles seem to be superimposed over this pattern. The crystalline pattern on the E-fracture faces of peroxisomal membranes is probably not a membrane structure but it reveals the structure of the membrane-associated marginal plates. A cast of the marginal-plate surface may be generated by a collapse of the peroxisomal membrane half onto the immediately underlying matrix inclusion.
    Type of Medium: Electronic Resource
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