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  • 1
    ISSN: 1615-6102
    Keywords: Callose ; Cell wall ; Gasteria ; Melanin ; Phytomelan layer ; Seed coat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary In this study we document the development of the phytomelan layer in the outer epidermis of the outer integument ofGasteria verrucosa. Phytomelan has been described as a black, melanin-like substance which is chemically very inert. Using histochemical techniques we show that phytomelan development in the cell wall can be divided into three stages. The first stage is deposition of a callosic layer against the tangential wall, with simultaneous thickening of the adjacent parts of the radial walls. The second stage is the conversion of this callosic wall, which we call a tertiary wall, into a noncallosic inner and outer layer. The inner layer stains predominantly for cellulose and a little for pectin. The outer layer is of unknown composition, since it did not react with the stains that were used. In the third stage the outer tertiary layer becomes black, the phytomelan. The callosic wall deposited in the first developmental stage seems to function as a carbohydrate source and as a mould for the tertiary cell wall. The conversion of the callose in the second stage might be the result of penetration of substances which react with callose. All the components for phytomelan seem to be present in the outer layer before the conversion. Phenolics might be involved in this second conversion.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1615-6102
    Keywords: Carbohydrate ; Gasteria verrucosa ; Invertase activity ; Ovule ; Seed development ; Sucrose synthase activity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The development ofGasteria verrucosa ovules and seeds seems to follow a pattern of growth in which the majority of carbohydrates is first used in the sporophytic tissue (nucellus, integuments, and arillus) around the gametophyte-derived cells. After fertilization the carbohydrates are used for further development of the arillus and seed coat. During the next stage carbohydrates are directed to develop the endosperm, followed by carbohydrate investment in the developing embryo and in storage products. This utilization pattern is deducted from a localization study on sucrose synthase and invertase. These two enzymes break down imported sucrose and are in that perspective used as markers for carbohydrate transport since diffusion is expected to be induced towards cells and tissues with high sucrose-hydrolyzing activities.
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  • 3
    ISSN: 1615-6102
    Keywords: Floral binding protein ; Flower development ; Immunocytochemistry ; MADS-box genes ; Ovule ; Transcription factors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary DuringPetunia hybrida seed development, the MADS-box genes encoding the floral binding proteins (FBP) 7 and 11 are expressed in the seed coat and not in the endosperm or embryo. These proteins are thought to function as transcription factors and are essential for ovule formation inPetunia spp. Immunocytochemical methods were used to analyze the distribution of FBP7 and FBP11 after fertilization in wild type and ectopic and cosuppression mutants. During the first nine days of seed development the protein was found in the nuclei of seed coat cells, of both wild-type plants and plants which ectopically expressedFBP11. The signal for FBP7 and -11 proteins diminished during seed development, was first lost in the outer epidermis of the seed coat, then in the endothelium, and finally, at 9 days after pollination (DAP), the protein could not be detected anymore in the parenchyma cells of the seed coat. Although the distribution patterns in wild-type andFBP11 ectopically expressing plants are similar, the latter exhibited higher protein levels. A mild-cosuppression mutant ofFBP7 andFBP11, having only a total of 5%FBP7 and -11 mRNA, showed hardly any FBP7 and -11 proteins. The lack of FBP7 and -11 caused endosperm degeneration in the mutant at a moment when the protein had already decreased to an undetectable level in the wild type and ectopic expression mutant (i.e., at 13 DAP). It is suggested that till about 9 DAP a minimal amount of FBP7 and -11 is needed for the normal functioning of the seed coat during later stages, i.e., for transfer of nutrients to endosperm and embryo. Besides the immunocytochemical data on theFBP7 andFBP11 MADS-box gene products, the morphological analysis of wild type and mutants contributes details on early seed development inPetunia hybrida.
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