Endosperm Morphology and Protein Body Formation in Developing Wheat Grain

1981 ◽  
Vol 8 (1) ◽  
pp. 5 ◽  
Author(s):  
WP Campbell ◽  
JW Lee ◽  
TP O'brien ◽  
MG Smart

The development of wheat grain from intact plants and from detached ears growing in culture has been studied by light and electron microscopy. Provided the sucrose concentration was at a level sufficient to maintain a normal rate of starch synthesis, the endosperm morphology of grain from cultured ears was essentially identical to that of endosperm from intact plants. If, however, sucrose concentration in the culture medium was very low (0.25%), some morphological abnormalities occurred in the endosperm near the crease and adjacent to the seed coat. The synthesis of storage protein in the endosperm is believed to occur largely on polyribosomes attached to endoplasmic reticulum even at the earliest stages of development. Protein bodies are always surrounded by a single membrane, the origin of which may vary. Some protein bodies arise by distention of the endoplasmic reticulum and clearly the membrane here represents the sac into which the protein is discharged after synthesis. In other cases the bounding membrane may be that of a true vacuole or it may be dictyosomal in origin. The methods by which it is suggested that protein bodies are formed in wheat endosperm have parallels in other seeds, although there are some significant differences.

2012 ◽  
Vol 24 (8) ◽  
pp. 3447-3462 ◽  
Author(s):  
Guifeng Wang ◽  
Fang Wang ◽  
Gang Wang ◽  
Fei Wang ◽  
Xiaowei Zhang ◽  
...  

2007 ◽  
Vol 19 (8) ◽  
pp. 2569-2582 ◽  
Author(s):  
David R. Holding ◽  
Marisa S. Otegui ◽  
Bailin Li ◽  
Robert B. Meeley ◽  
Thao Dam ◽  
...  

1979 ◽  
Vol 6 (1) ◽  
pp. 81 ◽  
Author(s):  
S Craig ◽  
DJ Goodchild ◽  
AR Hardham

Structural changes in pea cotyledons during development were studied using light and electron microscopy. Changes in the vacuolar system and cytoplasm of cotyledon parenchyma cells, during the period of storage protein deposition, are reported. Eight days after flowering, the parenchyma cells each contain one or two large vacuoles that are replaced by progressively smaller vacuoles during the next 10 days of development. Stainable material that can be histochemically identified as protein appears on the inner surface of the vacuole tonoplast 8 days after flowering. These vacuoles become smaller and more frequent during development and the amount of proteinaceous material within each vacuole increases until, at days 16-20 after flowering, they become densely packed with protein and are described as protein bodies. At day 8, the vacuole(s) have an average diameter of 39 �m, an average volume of 41 000 �m� , representing 75 % of the cell volume, and a surface area of 5500 �m�. By day 20, the average protein body diameter has fallen to 1 �m. There are, however, approx. 175 000 such protein bodies per cell, occupying 91 500 �m� or approx. 20 % of the cell volume, and whose total surface area is 550 000 �m�. The surface to volume ratlo of the vacuole/protein bodies Increases 55 times between days 8 and 20. Apart from this increase in surface area available for possible entry of protein, no mechanism for such entry can be suggested from our nlicrographs.


1990 ◽  
Vol 68 (8) ◽  
pp. 1747-1755 ◽  
Author(s):  
John S. Greenwood ◽  
Cobi Demmers ◽  
Suzanne Wetzel

The inner bark tissues of temperate hardwoods often act in the temporary storage of reduced nitrogen as protein during the overwintering period. Electron microscopic studies reported here demonstrate the analogy between the protein-storage vacuoles of the inner bark tissues and protein bodies in seeds. Development of these organelles parallels that of protein body formation seen in many dicotyledonous seeds. Coincident with the synthesis and sequestering of specific proteins, the large central vacuoles of the phloem parenchyma cells are slowly replaced over a 3- to 4-week period with numerous smaller protein-storage vacuoles (protein bodies). These arise via the subdivision of the larger vacuole and subsequent filling of the smaller vacuoles with protein. During this process there is a proliferation of both free ribosomes and rough endoplasmic reticulum in the ground cytoplasm. Stacks of rough endoplasmic reticulum are present in the peripheral cytoplasm and surround the smaller vacuoles as proteinaceous material is deposited. Golgi complexes, although not numerous, are present in the ground cytoplasm during the filling of the protein storage vacuoles. Key words: protein-storage vacuoles, protein body development, Salix microstachya, hardening, nitrogen storage, dormancy onset.


2016 ◽  
Vol 14 (9) ◽  
pp. 1876-1882 ◽  
Author(s):  
Katie L. Moore ◽  
Paola Tosi ◽  
Richard Palmer ◽  
Malcolm J. Hawkesford ◽  
Chris R.M Grovenor ◽  
...  

2002 ◽  
Vol 14 (3) ◽  
pp. 655-672 ◽  
Author(s):  
Cheol Soo Kim ◽  
Young-min Woo ◽  
Amy M. Clore ◽  
Ronald J. Burnett ◽  
Newton P. Carneiro ◽  
...  

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