Growth and differentiation of the Golgi apparatus and wall formation during carposporogenesis in the red alga, Gigartina teedii (Roth) Lamour

1981 ◽  
Vol 52 (1) ◽  
pp. 71-84
Author(s):  
I Tsekos
1974 ◽  
Vol 14 (3) ◽  
pp. 633-655
Author(s):  
EVA KONRAD HAWKINS

The fine structure of the Golgi apparatus during development of tetrasporangia of Calli-thamnion roseum is described. Dictyosomes and associated vesicles of 4 developmental stages of sporangia are examined. The wall of sporangia exhibits a heretofore unseen cuticle in red algae. Development of the spore wall and a new plasma membrane around spores occurs through fusion of adjacent Golgi vesicles along the periphery of cells. Observations are discussed in relation to wall formation and expansion of tetrads and in comparison with other work on growth and differentiation of the Golgi apparatus.


PROTOPLASMA ◽  
1974 ◽  
Vol 80 (1-3) ◽  
pp. 1-14 ◽  
Author(s):  
Eva Konrad Hawkins

1977 ◽  
Vol 58 (2) ◽  
pp. 119-133 ◽  
Author(s):  
Richard Wetherbee ◽  
John A. West
Keyword(s):  

Nature ◽  
1976 ◽  
Vol 259 (5544) ◽  
pp. 566-567 ◽  
Author(s):  
RICHARD WETHERBEE ◽  
JOHN A. WEST

1969 ◽  
Vol 41 (1) ◽  
pp. 109-123 ◽  
Author(s):  
R. M. Brown

The role of the Golgi apparatus in wall formation of vegetative cells of a marine chrysophyte, Pleurochrysis scherffelii, is described. Wall fragments are synthesized within the cisternae of the Golgi apparatus. A single Golgi apparatus is always located at the cell periphery, and the distended cisternae are oriented toward the cell surface. A highly-ordered body found near the inflated cisternae is associated with spherical, membrane-bounded bodies which may be involved in the progressive degeneration of cisternal membranes which release wall fragments. Protoplast movement has been detected by time-lapse cinephotomicrography and is correlated at the ultrastructural level with change in positions of the Golgi cisternae. Wall-synthesizing capacity is greatest during transverse wall formation. Senescent cells lack a Golgi apparatus with inflated cisternae. In addition, wall fragments are not present in the Golgi cisternae at this stage. Zoosporogenesis results in a temporary loss of the wall-forming capacity of the Golgi apparatus; this activity then resumes with the formation of a different morphological entity, the scale. Preliminary quantitative measurements of the turnover capacity of the Golgi apparatus have been made. From these data it has been determined that between 41 and 82 Golgi generations are required to synthesize the cell wall of an actively growing cell; this estimate indicates that approximately one cisterna is produced every 2 min, provided the cell generation time is 3 days. The time-lapse cinephotomicrographic data confirm that the rate of production of Golgi cisternae is at least one cisterna every 2 min.


1982 ◽  
Vol 60 (7) ◽  
pp. 1167-1176 ◽  
Author(s):  
J. C. Pargney

The use of a variety of cytochemical techniques (test of PATAg, staining with phosphotungstic acid, Swift's reaction, digestion with pectinase, extraction with EDTA and dimethyl sulfoxide (DMSO)) affords a better approach to the study of the mechanism of the growth of pollen tubes. Vesicles produced by the Golgi apparatus accumulate in the tip of the pollen tubes. Their membranes are gradually transformed and become cytochemically similar to the plasmalemma with which they fuse, participating in its renewal. Their contents contribute to the tube wall formation. The structure of the tube wall is complex and appears to be formed of a loose matrix of cellulose fibrils impregnated with pectic materials.


Author(s):  
Stylianos G. Delivopoulos

The ultrastructure of carpospore differentiation for the red alga Cryptopleura ruprechtiana is described. Carposporogenesis proceeds through three developmental stages. After cleaving from multinucleate gonimoblast initials the terminal gonimoblast cells differentiate to produce carpospores. These young carpospores possess a large nucleus and numerous proplastids with a peripheral thylakoid. During the later stages of young carpospores starch begins to polymerize. Mucilage is formed within dilating concentric membrane bodies, thus forming mucilage sacs. The latter, subsequently, release their contents initiating carpospore wall formation. Intermediate-aged carpospores have more plastids which develop their internal thylakoid system. The endoplasmic reticulum produces granular cored vesicles. Mature carpospores have numerous fully developed plastids, large floridean starch granules and fibrous vacuoles. Curved dictyosomes produce cored vesicles and adhesive vesicles. The nuclear envelope is crenulated and a two-layered wall surrounds the mature carpospore.


Author(s):  
J. Quatacker ◽  
W. De Potter

Mucopolysaccharides have been demonstrated biochemically in catecholamine-containing subcellular particles in different rat, cat and ox tissues. As catecholamine-containing granules seem to arise from the Golgi apparatus and some also from the axoplasmic reticulum we examined wether carbohydrate macromolecules could be detected in the small and large dense core vesicles and in structures related to them. To this purpose superior cervical ganglia and irises from rabbit and cat and coeliac ganglia and their axons from dog were subjected to the chromaffin reaction to show the distribution of catecholamine-containing granules. Some material was also embedded in glycolmethacrylate (GMA) and stained with phosphotungstic acid (PTA) at low pH for the detection of carbohydrate macromolecules.The chromaffin reaction in the perikarya reveals mainly large dense core vesicles, but in the axon hillock, the axons and the terminals, the small dense core vesicles are more prominent. In the axons the small granules are sometimes seen inside a reticular network (fig. 1).


Author(s):  
S.R. Allegra

The respective roles of the ribo somes, endoplasmic reticulum, Golgi apparatus and perhaps nucleus in the synthesis and maturation of melanosomes is still the subject of some controversy. While the early melanosomes (premelanosomes) have been frequently demonstrated to originate as Golgi vesicles, it is undeniable that these structures can be formed in cells in which Golgi system is not found. This report was prompted by the findings in an essentially amelanotic human cellular blue nevus (melanocytoma) of two distinct lines of melanocytes one of which was devoid of any trace of Golgi apparatus while the other had normal complement of this organelle.


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