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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Micron 25 (1994), S. 171-187 
    ISSN: 0968-4328
    Keywords: Cellulose-glucuronoxylan composites ; cell wall ; helicoidal structure ; self-assembly
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Electrical Engineering, Measurement and Control Technology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Micron 25 (1994), S. 171-187 
    ISSN: 0968-4328
    Keywords: Cellulose-glucuronoxylan composites ; cell wall ; helicoidal structure ; self-assembly
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Electrical Engineering, Measurement and Control Technology , Natural Sciences in General
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biology of the Cell 71 (1991), S. 43-55 
    ISSN: 0248-4900
    Keywords: cell wall ; cellulose ; enzyme-gold complex ; helicoidal pattern ; monoclonal antibodies ; polygalacturonans
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biology of the Cell 67 (1989), S. 209-220 
    ISSN: 0248-4900
    Keywords: cell walls ; cellulose ; fiber composite ; helicoids
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biology of the Cell 73 (1991), S. 173-178 
    ISSN: 0248-4900
    Keywords: cellulose ; liquid-crystal ; quince ; self-assembly ; xylans
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0248-4900
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Cell Biology International Reports 15 (1991), S. 611-620 
    ISSN: 0309-1651
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1615-6102
    Keywords: Erwinia chrysanthemi ; Pectate lyase ; Pectin degradation ; Plant cell wall
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Erwinia chrysanthemi is a soft-rot pathogenic enterobacterium that provokes maceration of host plant tissues by producing extracellular cell-wall-degrading enzymes, among which are pectate lyases, pectin methyl esterases, and cellulases. Cell wall degradation in leaves and petiole tissue of infectedSaintpaulia ionantha plants has been investigated in order to define the structural and temporal framework of wall deconstruction. The degradation of major cell wall components, pectins and cellulose, was studied by both classical histochemical techniques (Calcofluor and periodic acid-thiocarbohydrazide-silver proteinate staining) and immunocytochemistry (tissue printing for detection of pectate lyases; monoclonal antibodies JIM5 and JIM7 for detection of pectic substrates). The results show that the mode of progression of the bacteria within the host plant is via the intercellular spaces of the parenchyma leaf and the petiole cortex. Maceration symptoms and secretion of pectate lyases PelA, -D, and -E can be directly correlated to the spread of the bacteria. Wall degradation is very heterogeneous. Loss of reactivity with JIM5 and JIM7 was progressive and/or clearcut. The primary and middle lamella appear to be the most susceptible regions of the wall. The innermost layer of the cell wall frequently resists complete deconstruction. At the wall intersects and around intercellular spaces resistant domains and highly degraded domains occurred simultaneously. All results lead to the hypothesis that both spatial organisation of the wall and accessibility to enzymes are very highly variable according to regions. The use of mutants lacking pectate lyases PelA, -D, -E or -B, -C confirm the important role that PelA, PelD, and PelE play in the rapid degradation of pectins from the host cell walls. In contrast, PelB and PelC seem not essential for degradation of the wall, though they can be detected in leaves infected with wild-type bacteria. With Calcofluor staining, regularly localised cellulose-rich and cellulose-poor domains were observed in pectic-deprived walls.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-2048
    Keywords: Amyloid ; Cell wall breakdown ; β-Galactosidase ; Reserve mobilisation ; Seed germination ; Storage wall ; Tamarindus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The structure and breakdown of galactoxyloglucan (GXG)-rich cells was studied from cotyledons of Tamarindus indicus L. The depletion of GXG was followed at different levels: quantitative, histochemical and cytochemical. At the ultrastructural level two probes were used: one general for polysaccharides (periodic acid — thiocarbohydrazide — silver proteinate test), the other specific for the terminal galactosyl residues of GXG (β-galactosidase-gold complex). They were complemented by water-extraction of the GXG and analysis of the constituting monosaccharides by gas chromatography. Despite their collenchymateous aspect and the chemical similarity of the reserve GXG with the structural xyloglucan of growing walls, the thickened storage walls are not interpretable as being an hypertrophied primary wall. The tamarind cells produce an original type of wall construction in which GXGs are sequestered in a sort of homomolecular bulk. There is no evidence for intussusception of the molecules within a network of cellulose. The bulk of GXG is sandwiched between two thin layers: the outer is comparable to a regular primary wall, the inner behaves like a barrier during GXG withdrawal. Temporal and spatial patterns of GXG-mobilisation lead to the definition of a sequence of stages of cell activities (premobilising, mobilising, postmobilising). They are synchronized with the growth of the seedling axis, the duration and characteristics of the stages being subordinated to the location of the cells within the organ. Cell lysis is initiated in close relationship with intramural cavities. The development of digestion pockets results in a highly digested wall. The barrier prevents any engulfing of the cytoplasm in the wall clefts and creates an increasing free space. The attack front of digestion is always sharp. During all steps, the monosaccharide composition remains stable. At the end of GXG depletion, the storage wall is withdrawn and cells are rendered in a parenchyma-like state. The breakdown is not a complete wall collapse but an original controlled and limited wall-thinning. The data lead to the speculation that the hydrolytic activities result from a complementation between precursors relinquished by the cytoplasm and factors already present in the storage wall.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 126 (1985), S. 36-46 
    ISSN: 1615-6102
    Keywords: Cell wall ; Growth ; Osmotic shock ; Rhythm ; Twisted assembly
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The effect of an osmotic shock on the subsequent growth and cell wall texture was studied at 0, 1/2, 1, 2, 4 and 24 hours. Cells were taken at the beginning of their exponential growth from mung bean hypocotyl. The shock reveals the instability and the fragility of the assembly mechanisms. It induces a rupture in the texture (formation of a loose layer) or, occasionally, the apparition of a swirling pattern. After the shock, the twisting positioning can be restored. The “post-shock” deposit appears similar to the “pre-shock” deposit. The loose layer provides a visible guide-mark (time marker) within the wall. It allows one to evaluate the oscillatory period (i.e., the duration necessary for a 180° rotation of the microfibrils). This period was found to be ca. 3 hours following a lag period of ca. 1 hour. It confirms the endogenous ultradian character of the rhythm of the assembly.
    Type of Medium: Electronic Resource
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