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  • 1
    ISSN: 1615-6102
    Keywords: Bicarbonate transport ; Chara ; Charasome-complex ; Nitella ; Plasmalemma invaginations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Charasomes, complex membrane structures, were found along the longitudinal walls of internodal and lateral branch cells ofChara corallina andC. braunii, but not along their transverse walls or in other cell types. Charasome-complexes were larger and more numerous in the lateral branch cells than in internodal cells. InC. corallina, a dioecious species, especially large elaboration of charasome material occurs in the lateral branch cells of the female plant, sometimes reaching a cross-sectional width which is as great as that of the adjacent cell wall. Chara internodes transport hydroxyl (OH−) out of the cell and bicarbonate (HCO3 −) into the cell. Spatial distribution of charasomes along the cell was examined with respect to these transport phenomena, which occur at specific identifiable regions along the cell. Charasome-complexes were always found in regions in which HCO3 − transport occurs but were often fewer, reduced in size or absent in areas of OH− efflux.Nitella flexilis exhibited similar patterns of OH− and HCO3 − transport along the cell; however, there was a complete absence of charasomes. Ultrastructural examinations onNitella translucens indicated that charasomes were also absent in this species. The observation that charasomes are present in both transport regions ofChara but are totally lacking in the twoNitella spp. indicates that the charasome-complex is not involved in transport of either substance. Other possible functions for the charasomes, including a role in osmoregulation, are discussed. Charasome substructure is the same in bothChara species, consisting of a mass of short (50 nm average length) anastomosing tubules (30 nm average diameter) derived from the plasmalemma. The interior of the tubules is open to the cytoplasm while the area surrounding the tubules is ultimately open to the wall and thus can be considered to be wall space. Charasomes are quite variable in size and shape, but are roughly globular, with the bulk of the structure projecting into the cell cytoplasm. Tubular components of the charasome were sometimes seen to extend into the microfibrillar wall matrix. A three dimensional model of the charasome-complex presented details the great complexity of this membrane system.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 107 (1981), S. 269-284 
    ISSN: 1615-6102
    Keywords: Chara ; Charasome-complex ; Freeze-fracture ; Negative staining ; Periplasmic space ; Tannic acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Charasome structure, with special attention to the periplasmic space, is examined using various techniques. The periplasmic space appears electron lucent in sections stained with 2% aqueous uranyl acetate and lead citrate. When sections are stained with saturated methanolic uranyl acetate a densely staining central core can be seen within the periplasmic space. The region surrounding the core does not stain. If tannic acid is added to the fixative and rinse solutions during preparation of the tissue for TEM, the entire periplasmic space becomes stained. This space appears to be filled with a fine granular material. Charasomes prepared in this way appear as negatives of those stained with uranyl acetate. The periplasmic space does not contain polysaccharides of the type havingvic-glycol groups, as indicated by lack of staining by the silver methenamine technique. Severe plasmolysis of cells by treatment with 350 mM mannitol prior to fixation resulted in disruption of charasomes, but did not cause collapse of the structure. The periplasmic space of freeze-fractured charasomes contains a distinct granular material, while negatively stained isolated charasomes retain their structural configuration, even after air drying. The results give us new insight into the nature of the periplasmic space and confirm our earlier description of the charasome structure. This information is used to construct a model which attempts to explain how a structure such as the charasome can be formed along the plasmalemma of a cell having a high internal hydrostatic pressure.
    Type of Medium: Electronic Resource
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