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  • 1
    ISSN: 1432-2048
    Keywords: Key words: Cold-induced gene expression ; Elongation ; Invertase ; Sucrose synthase ; Tonoplast intrinsic protein ; Tulipa
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. Many bulbous plants need a low-temperature treatment for flowering. Cold, for example, affects the elongation of the stalk, thereby influencing the quality of the cut flower. How the elongation of the stalk is promoted by cold and which physiological and biochemical mechanisms are involved have remained obscure. As invertase has been shown to be involved in the cold-induced elongation of the flower stalks of tulips (Lambrechts et al., 1994, Plant Physiol 104: 515–520), we further characterized this enzyme by cloning the cDNA and analysing its expression in various tissues of the tulip (Tulipa gesneriana L. cv. Apeldoorn) stalk. In addition, the role of sucrose synthase was investigated. Since turgor pressure is an important force driving cell elongation, the role of a water-channel protein (γTIP) was studied in relation to these two enzymes. The mRNA level of the invertase found was substantially up-regulated as a result of cold treatment. Analysis of the amino acid sequence of this invertase revealed the presence of a vacuolar targeting signal. Two different forms of sucrose synthase were found, the expression of one of them appeared to be restricted to the vascular tissue while the other form was present in the surrounding tissue. Both sucrose synthases were present in the stalk during the entire period of bulb storage and after planting, but their activities declined during stalk elongation. The expression of the γTIP gene was restricted mainly to the vascular tissue and its expression profile was identical to that of invertase. Simultaneous expression of invertase and γTIP possibly leads to an increase in osmotic potential and vacuolar water uptake, thus providing a driving force for stretching the stalk cells.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2048
    Keywords: Key words: Cell lineage ; Floral development ; Iris (floral development) ; Meristem (floral ; inflorescence) ; Plasmodesma (distribution) ; Symplasm (mapping)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. The transition from vegetative to reproductive development involves extensive revisions of cellular collaboration at the apical meristem and results in the production of novel appendages. In Dutch Iris (Iris xiphium) the transition from vegetative apical meristem to inflorescence meristem was morphologically signalled by the appearance of a `spathe leaf '. After enlargement of the inflorescence meristem, a second spathe leaf and a double floral meristem were formed. The then undulated surface corresponded to general topological changes and a beginning of altered cell division patterns. Throughout, all cells produced in the meristem remained in contact via plasmodesmata (Pd), thus maintaining the symplasmic unity of the meristem. Since the symplasm harbours part of the signal network that coordinates the activities of the meristem cells, we investigated if alterations in Pd numbers could underlie meristem transitions. Prior to Pd counting, potentially important borders inside the meristem, representing primary and secondary cell contacts, were identified by the construction of a symplasmetric map. During the transition, significant alterations did take place at some of the borders defined by the map. Within the second tunica layer (L2), and between the L2 and adjacent cells, Pd numbers were strongly reduced. Within the first tunica layer (L1) and within the corpus they remained the same. The reduction was 25% between L2-cells, and between L2- and L1-cells; it was 40% between the L2 and the outer corpus layer. The reductions appeared to be due to a lowered production of primary and secondary Pd by L2-cells towards each other and towards adjacent cells. As a result of this the integration of all L2-cells and, as a consequence, of the L1 as a whole in the symplasmic network of the meristem was reduced. The implied gain in autonomy of the individual L2-cells and of the L1-layer may reflect their new functions in the floral meristem.
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  • 3
    Publication Date: 1997-09-26
    Print ISSN: 0032-0935
    Electronic ISSN: 1432-2048
    Topics: Biology
    Published by Springer
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  • 4
    Publication Date: 1999-09-09
    Print ISSN: 0032-0935
    Electronic ISSN: 1432-2048
    Topics: Biology
    Published by Springer
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