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  • 1980-1984  (6)
  • 1
    ISSN: 1615-6102
    Keywords: Histochemistry ; Sclerotia ; Sclerotial germination ; Sclerotinia ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Cytoplasmic reserves and extracellular substances were progressively broken down and utilized during carpogenic germination of sclerotia ofSclerotinia minor. Glycogen, wall polysaccharides and polyphosphate granules were removed first from regions of the sclerotium distant from developing apothecia, while protein bodies near the base of apothecial stipes were hydrolysed before those further away. The number of profiles of mitochondria and endoplasmic reticulum in cortical and medullary hyphae increased at the onset of germination, indicating increased metabolism in the hyphae. In contrast to developing sclerotia, simple pores with Woronin bodies were frequent in walls and septa during germination. Hyphae that appeared to converge towards the base of apothecial initials retained their cytoplasm and organelles until late in germination and hydrolysis of their reserves was delayed; these are interpreted as translocatory hyphae, although further work is required to determine their role unequivocally. When apothecia were fully developed, hyphae throughout the sclerotium were empty and the walls and extracellular matrix of cortical and medullary hyphae had almost completely broken down.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 104 (1980), S. 315-331 
    ISSN: 1615-6102
    Keywords: Fungus ; Morphogenesis ; Sclerotia ; Sclerotinia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The development and structure of sclerotia of the fungusSclerotinia minor Jagger, was studied by light, scanning and transmission electron microscopy. The sclerotia formed beneath a weft of overlying vegetative hyphae, that sometimes became enveloped as the sclerotia enlarged. Differentiation of the sclerotial hyphae into regions of rind, cortex and medulla, began only 12 to 24 hours after sclerotial initiation occurred. The cortex was the last region to become discernible. The rind cells rapidly became vacuolate, while their walls thickened and became pigmented. At maturity the rind consisted of a closely packed layer of cells around the sclerotium. The cortex was about three cells wide and was made up of pseudoparenchymatous tissue. The prosenchymatous medulla constituted the main part of the sclerotium. Cytoplasmic reserves, tentatively identified as polyphosphate granules and protein bodies, accumulated in large numbers in cortical and medullary hyphae. Extracellular material was laid down very rapidly around hyphae of the cortex and medulla, until at maturity, it almost completely filled any interhyphal spaces. The ultrastructure of young sclerotial hyphae was very similar to that of actively growing vegetative hyphae. The numbers of nuclei and profiles of mitochondria decreased at later stages of development but there was an increase in the number of profiles of endoplasmic reticulum cisternae. The cytoplasm had a granular appearance throughout differentiation. The general structure of mature sclerotia ofS. minor was similar to that reported for sclerotia of other species in the genusSclerotinia.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 104 (1980), S. 333-351 
    ISSN: 1615-6102
    Keywords: Histochemistry ; Polyphosphate ; Polysaccharide ; Protein, Sclerotia ; Sclerotinia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A detailed histochemical investigation was carried out on rind, cortical and medullary hyphae of sclerotia ofSclerotinia minor Jagger. Four developmental stages, including mature sclerotia, were studied. The walls and septa of all hyphae contained chitin and β-1,3 glucans, while those of the rind contained in addition, a melanin-like pigment. An extracellular matrix, which accumulated around cortical and medullary hyphae, consisted primarily of β-1,3 glucans, although another polysaccharide, which could not be identified by histochemical methods, was also present. Phenolic material was deposited around the extracellular matrix and in the few interhyphal spaces that remained at maturity. Glycogen was present throughout the cytoplasm of hyphae of the cortex and medulla, at all stages of their differentiation. Polyphosphate granules were laid down within small vacuoles and as sclerotia matured, became most common in the cortical region. Protein bodies developed rapidly in cortical and medullary hyphae until at maturity, they were the most obvious interhyphal feature. These bodies were either round or elongated in shape, the elongated ones often lying parallel to the long axis of the hyphae, and in close association with strands of endoplasmic reticulum. No lipid reserves were detected.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular histology 12 (1980), S. 221-234 
    ISSN: 1573-6865
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary This paper describes a simultaneous-couplng azo dye method for the measurement of estarase activity using the histochemical substrate, α-naphthyl acetate. By the choice of two diazonism salts with optimal coupling characteristics, the reaction be carried out at any pH between 3.0 and 9.5. The azo dye is maintained in solution for spectrophotometric measurements with bovine serum albumin. The simultaneous-coupling method is compared with an assay based on the direct measurement of released α-naphthol by its ultra-violet bsorbance in a pH study of hog liver esterase. There is good agreement between the data obrained by both methods.
    Type of Medium: Electronic Resource
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  • 5
    Publication Date: 1982-01-01
    Print ISSN: 0165-6147
    Electronic ISSN: 1873-3735
    Topics: Biology , Medicine
    Published by Cell Press
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  • 6
    Publication Date: 1982-01-01
    Print ISSN: 0165-6147
    Electronic ISSN: 1873-3735
    Topics: Biology , Medicine
    Published by Cell Press
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