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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 113 (1977), S. 73-78 
    ISSN: 1432-072X
    Keywords: Allomyces ; Cell wall carbohydrates ; Differentiation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Carbohydrate composition was determined in isolated cell walls of meiospores of Allomyces arbuscula after incubation for 15 min (encysted meiospores: cysts), 150 min (germlings: cysts + rhizoids) and 24 h (cysts + rhizoids + hyphae). The principal constituent in all cell wall samples is chitin, accounting for about 75% of the recovered carbohydrates. In addition, cell walls of all stages examined contain polysaccharides which release galactose, glucose, mannose, arabinose, xylose, fucose, and rhamnose on acid hydrolysis. While different developmental stages show minor quantitative changes in chitin, the ratio of galactose to glucose decreases sharply during differentiation of ungerminated cysts into germlings with rhizoids and hyphae. The increase in glucose is accompanied by a decrease in the amount of xylose and/or fucose and of galactose.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 109 (1976), S. 37-43 
    ISSN: 1432-072X
    Keywords: Allomyces ; Development of meiospores ; Cell wall structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Development of haploid meiospores of Allomyces arbuscula into germling cells with rhizoids and hyphae was followed during incubation in complete growth medium. The surface structure of encysted meiospores, rhizoids and hyphae before and after extraction of amorphous materials with ethanolic KOH was studied by means of carbon-platinum replicas. After 2–3 min incubation in complete medium 10% of the meiospores were surrounded by a cell wall containing microfibrils embedded in a matrix. Structure of cell walls of encysted meiospores, rhizoids, and hyphae differ from one another by the location of amorphous materials and by the arrangement of chitin microfibrils.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 98 (1974), S. 147-158 
    ISSN: 1432-072X
    Keywords: Allomyces ; Zoospores ; Cell Wall ; Wall Formation ; Lomasome ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Ultrastructural observations on encysting haploid zoospores of Allomyces arbuscula are presented with special reference to cell wall deposition. Multivesicular bodies are observed in the cytoplasm of zoospores 15 min after inoculation, lomasomes after 30 min and fine membrane profiles between the plasmalemma and the cyst wall are observed after 4 h indicating a possible system for secretion of cell wall components.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 84 (1992), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Cortical microtubules (MTs) allegedly orient nascent cellulose microfibrils (CMFs) in plant cells. The frequently observed parallelism between them, and the effect of MT-depolymerizing agents, are the bases for this hypothesis. Data have, however, accumulated about cells in which MTs and CMFs are not in parallel alignment. These data will be reviewed. MT orientation cannot be the only factor determining CMF orientation, but MTs could overrule other factors in cells where, for instance, they are more tightly attached to the plasma membrane than in other cells. MT and CMF orientations could, however, both be controlled by a third factor, and CMFs may even impose orientation on MTs.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1435-8107
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Submergence ofRumex crispus L. andR. palustris Sm. stimulates elongation of the youngest petiole. InR. palustris this response can be mimicked partially by exposure to exogenous ethylene. In both species, petiole elongation induced by ethylene and/or submergence is distributed nearly equally over the whole petiole length and is almost completely attributable to increased cell expansion. InR. acetosa L., extension of the youngest petiole is inhibited by submergence of the whole plant. The strongest growth inhibition within the youngest petiole was observed in the most distal parts and is probably the result of reduced cell expansion.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 64 (1967), S. 75-88 
    ISSN: 1615-6102
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary An investigation was conducted on the fine structure ofP. megasporum conidiospores using both chemical fixation and the freeze-etching techniques. The spore cell wall was shown to consist of several layers, one of which is chiefly fibrillar in nature. The surface of the spore appears to be covered by ordered arrays of “rodlets” which are embedded in or resting upon a thin layer of homogenous material. At higher magnification, these “rodlets” appear as linear arrays of particles approximately 50 Å in diameter. This layer may be of a cutaneous nature. In addition, the plasma membrane was shown to be covered by particles, some of which appear to migrate to the inner layer of the cell wall. Numerous invaginations of the plasma membrane were also seen.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 64 (1967), S. 439-451 
    ISSN: 1615-6102
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Penicillium megasporum conidia have spore walls consisting of several layers. There is no visible change in the outer wall layers during spore germination, but the inner layers increases in thickness on only one side of the spore, resulting in a rupture of the outer wall layers and subsequently in germ tube formation. Invaginations in the plasma membrane disappear as the germ tube forms and emerges, and the nucleus migrates into the developing germ tube. Mitochondria gather at the base of the germ tube during its formation. During germination, the amount of lipid in the spore decreases and portions migrate into the germ tube. Membrane-bound, electron dense bodies are present in resting spores. These bodies decrease in size as germination proceeds, and the cytoplasm in the developing germ tube appears much more electron dense than the cytoplasm within the spore.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 53 (1966), S. 708-708 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-2048
    Keywords: Cellulose microfibril ; Wall texture ; Cell elongation ; Microfibril reorientation ; Petunia (cell wall)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract According to Roelofsen and Houwink's (1953, Acta Bot. Neerl. 2, 218–225) multinet growth hypothesis, microfibrils originally deposited transversely in the cell wall become gradually reoriented towards more axial orientations during cell elongation. To establish the extent of reorientation, microfibrils were studied during their deposition and elongation, using stylar parenchyma and transmitting tissue cells of Petunia hybrida L. At the inner surface of very young cells, microfibrils were deposited in alternating Z- and S-helical orientations. The following sequence in deposition, from the exterior to the interior side of the wall, could be inferred: Axial: 150°–180° (Z-helical), 0°–30° (S-helical); oblique: 110°–150° (Z-helical), 30°–70° (S-helical); transverse: 90°–110° (Z-helical), 70°–90° (S-helical). With the increasing pitch, the density of the deposited microfibrils increased as well, giving rise to an alternating helical texture. During elongation, only transversely S- and Z-helically oriented microfibrils were deposited and all microfibrils underwent a certain reorientation as described in the multinet growth hypothesis. The texture resembled that of young cells and the wall maintained its thickness. The extent of passive reorientation was in agreement with the theoretical calculations made by Preston.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Planta 133 (1977), S. 303-308 
    ISSN: 1432-2048
    Keywords: β-Glucan synthetase ; Golgi vesicles ; Petunia hybrida ; Pollen tubes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract β-Glucan synthetase activity has been demonstrated in a Golgi vesicle fraction isolated from pollen tubes ofPetunia hybrida. Thisβ-glucan synthetase activity differs from that of most other higher plants in its inability to incorporate [14C]glucose from GDP-[14C]glucose. UDP-[14C]glucose, however, is an appropriate glucose donor for this enzyme. The optimum conditions for thisβ-glucan synthetase activity are: 1 mg Golgi vesicle protein/ml reaction mixture; pH=±8 and a temperature of 25°C. The newly synthesized alkali-insoluble glucan containsβ-1,3- as well as β-1,4-glucosidic linkages.
    Type of Medium: Electronic Resource
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