Pollen Tube Cell Wall Research Articles

Interaction between the pollen tube and stigmatic cell wall following pollination in Brassica oleracea

summaryElectron microscopic observations have revealed the stigmatic papilla wall of Brassica oleracea L. to be composed of several distinct layers. Measurement of the thickness of the major components of this wall has demonstrated a significant difference in cuticle thickness between the two S (incompatibility) genotypes under study. It is suggested that cuticle thickness is responsible for differences observed in the rates of pollen hydration on the stigma surface. The relevance of tins finding to the genetical control of pseudocompatibility is discussed. Unusually, the pectocellulosic component of the papillar cell wall is composed of three layers. On pollination, the outer layer detaches to permit the elongating pollen tube to pass down the papilla within the wall itself. At the base of the papilla, the tube becomes truly extracellular, growing down in the intercellular spaces between stylar parenchyma cells. Following a bud pollination, the pollen tube may even penetrate the complete cell wall and grow down the length of the cell, invested on one side by the plasma membrane and on the other by the inner face of the pectocellulosic wall. These tubes experience some difficulty in traversing the cell wall at the base of the papillar prior to entering the intercellular spaces of the style.

Ultrastructure of cell wall and plugs of tobacco pollen tubes after chemical extraction of polysaccharides

Tobacco pollen tubes grown in vitro and from pollinated tobacco styles were treated by chemical solvents to remove one or more of the following polysaccharides from the tube walls: pectin (ethylenediamine tetraacetic acid); hemicellulose (alkali); callose (alkali; potassium hypochlorite); cellulose (cuprammonium); and all polysaccharides with exception of cellulose (H2O2/glacial acetic acid). Both the inner tube wall, which we had regarded as the secondary wall, and the plugs contained, in addition to callose, microfibrils of cellulose and "non-cellulosic" microfibrils that had "pectin-like" properties. When using the expressions callosic or callose layer and callose plugs in reference to pollen tubes, one should realize that they do not imply the exclusive presence of callose in the inner tube wall layer and its localized thickenings.

Sugar composition of pollen grain and pollen tube cell walls

The sugar composition of pollen grain and pollen tube cell walls was studied for Camellia japonica, C. sasanqua, C. sinensis, Tulipa gesneriana and Lilium longiflorum. In all species, the main components of pollen grain walls were arabinose, galactose, glucose and uronic acid. On the other hand, the pollen tube walls consisted mostly of glucose. The pollen tube wall of C. japonica was fractionated into hemicellulose, α-cellulose and pectic substance fractions in yields of 61, 19 and 3 %, respectively. The hemicellulose fraction was composed essentially of glucose. The sugar composition of the pollen tube wall was not influenced by the nature of exogenously supplied sugars. Rapid growth of the pollen tube seemed to correlate with the synthesis of hemicellulosic glucan.

Isolation and characterization of secretory vesicles in germinated pollen of Lilium longiflorum

ABSTRACT Secretory vesicles containing polysaccharide were isolated from germinated pollen of Lilium longiflorum and characterized by biochemical and ultrastructural investigation. Pollen tubes exhibit a secretory pathway in which the vesicles concentrated in the tube apex are produced by the Golgi apparatus and contributed to the cell wall at the apex upon fusion of the vesicle membrane with the plasma membrane. Secretory vesicles were isolated by a method involving the size discrimination of cytoplasmic components using Millipore filters. Cells were disrupted under conditions which minimized membrane vesiculation. Identification was made by electron-microscopic comparison of the periodic acid-silver hexamine (PASH) reactivities of in situ and isolated secretory vesicles. The secretory vesicles contained polysaccharides which were high in galacturonic acid and similar in sugar composition to those of the hot-water-soluble fraction of pollen tube cell wall. A hot-water-insoluble, non-cellulosic glucan was the major component of the cell wall. Less than 7 % of the wall was cellulosic. Chitin was absent. Similarities in the ultrastructure and PASH staining of apical secretory vesicles and an amorphous component of the cell wall support a precursor-product relationship between these 2 cell components. Ultrastructural investigations revealed complexes of the endoplasmic reticulum (ER) associated with electron-translucent regions of cytoplasm, suggesting a possible function of the ER in cell wall formation. Additionally, patterns of PASH staining show that changes in polysaccharides occur in secretory vesicles after vesicles have been formed by dictyosomes. Therefore, secretory vesicles may have a role in polysaccharide synthesis as well as in membrane and product transport.