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  • 1
    ISSN: 1615-6102
    Keywords: Sieve-element plastids ; Wound phloem ; Regeneration ; Sieve-tube starch ; Coleus ; Pisum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary In experimentally-induced wound phloem, sieve-element plastids express their genetically determined type in depositing amylopectinrich sieve-tube starch (Coleus, S-type) and polygonal protein crystals (Pisum, P-type). Sieve-element plastids budd off from preexisting amyloplasts, pass through a short amoeboid state and develop into spherical plastids with translucent matrix. During early phases of differentiation wound sieve-elements contain two populations of plastids: typical sieve-element plastids and residual parenchyma plastids with large amylose-rich starch grains. The retardation in the break down of the latter is discussed. Sieve-tube and amyloplast starches are likewise digested by α-1,4- and α-1,6-bond cleaving glucosidases.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 130 (1986), S. 12-26 
    ISSN: 1615-6102
    Keywords: Phloem initiation ; Phloem regeneration ; Pisum ; Sieve element, sequential differentiation ; Wound-sieve elements
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 48 hours after interrupting the root stele ofPisum, wound phloem initiated (proximally or distally to the wound) to reconnect the vascular stumps was found to contain some nucleate wound-sieve elements. At the elongating end of an incomplete wound-sieve tube these elements exhibit a sequence of ultrastructural changes as known from protophloem-sieve tubes. Elongation occurs by the addition of newly divided (wound-) sieve-element/companion-cell complexes. In order to dedifferentiate and assume a new specialization formerly quiescent stelar or cortical cells require at least one (mostly more) preliminary division. Companion cells are consequently obligatory sister cells to wound-sieve elements. By reconstruction using serial sections it could be shown that wound-sieve tubes elongate bidirectionally, starting in an early activated procambial cell of the stele. The elongation is directed by the existence of plasmodesmata, preferably when lying in primary pit fields, and by the plane of preceding divisions. Thus, the developing wound-sieve tube can deviate from the damaged bundle and radiate into the cortex as soon as the plane of the preceding divisions is favourable. In the opposite direction, elongating wound-sieve tubes run parallel to pre-existing phloem traces, thus broading their base at the bundle for the deviating part of the wound-sieve tube. Frequently an individual wound-sieve tube is supplemented at the bundle by a further wound-sieve tube which is partly running parallel to it. Both sieve tubes are interlinked with sieve plates by three-poled sieve elements. Ultrastructurally, the developmental changes of nucleate wound-sieve elements follow the known pattern. In spite of its contrasting origin and odd shape a mature wound-sieve element eventually has the same contents as regular sieve elements: sieve-element plastids, mitochondria, stacked ER and small amounts of P-protein within an electronlucent cytoplasm.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 130 (1986), S. 27-40 
    ISSN: 1615-6102
    Keywords: Phloem contact ; Phloem regeneration ; Pisum ; Sieve pores ; Wound phloem
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Following severance of the root stele mature bundle-sieve tubes show a rapid wound response, plugging their sieve pores and depositing callose. Close to the blocked sieve tubes the predetermined but still immature bundle sieve tubes differentiate and consist of mature sieve elements 48 hours after wounding. Within a serially sectioned area the existence of lateral sieve pores connecting blocked bundle-sieve tubes with those which matured after wounding could be proved. Wound-sieve tubes are initiated close to the latter, linked to them by lateral sieve pores. The wound-sieve tubes elongate bidirectionally, parallel to the interrupted phloem trace, until a first (towards the cortex) deviating member is established on one end and, on the other, the length of the common course with the bundle is sufficient for assimilate transfer. Presumably, both initiation and elongation of wound-sieve tubes are guided by preexisting plasmodesmata, which later give rise to sieve pores. Eventually the deviating wound-sieve tubes are in close plasmatic contact with those bundle-sieve tubes which mature after wounding and hence, indirectly, with blocked sieve tubes. One precondition to the restitution of translocation within blocked bundle-sieve tubes is a secondary opening of the plugged sieve pores. The reversibility of callose deposition and the structure of functional pores are discussed. The model of sequential differentiation for channelling auxin in undifferentiated tissue (Sachs 1975) is compared with the sequential differentiation of wound-sieve tubes.
    Type of Medium: Electronic Resource
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