Ultrastructural Changes in Poplar Cell Wall during Steam Explosion Treatment

Holzforschung ◽  
1991 ◽  
Vol 45 (3) ◽  
pp. 175-179 ◽  
Author(s):  
G. Michalowicz ◽  
B. Toussaint ◽  
M.R. Vignon
Author(s):  
R.H.M. Cross ◽  
C.E.J. Botha ◽  
A.K. Cowan ◽  
B.J. Hartley

Senescence is an ordered degenerative process leading to death of individual cells, organs and organisms. The detection of a conditional lethal mutant (achloroplastic) of Hordeum vulgare has enabled us to investigate ultrastructural changes occurring in leaf tissue during foliar senescence.Examination of the tonoplast structure in six and 14 day-old mutant tissue revealed a progressive degeneration and disappearance of the membrane, apparently starting by day six in the vicinity of the mitochondria associated with the degenerating proplastid (Fig. 1.) where neither of the plastid membrane leaflets is evident (arrows, Fig. 1.). At this stage there was evidence that the mitochondrial membranes were undergoing retrogressive changes, coupled with disorganization of cristae (Fig. 2.). Proplastids (P) lack definitive prolamellar bodies. The cytoplasmic matrix is largely agranular, with few endoplasmic reticulum (ER) cisternae or polyribosomal aggregates. Interestingly, large numbers of actively-budding dictysomes, associated with pinocytotic vesicles, were observed in close proximity to the plasmalemma of mesophyll cells (Fig. 3.). By day 14 however, mesophyll cells showed almost complete breakdown of subcellular organelle structure (Fig. 4.), and further evidence for the breakdown of the tonoplast. The final stage of senescence is characterized by the solubilization of the cell wall due to expression and activity of polygalacturonase and/or cellulose. The presence of dictyosomes with associated pinocytotic vesicles formed from the mature face, in close proximity to both the plasmalemma and the cell wall, would appear to support the model proposed by Christopherson for the secretion of cellulase. This pathway of synthesis is typical for secretory glycoproteins.


Author(s):  
Roncaglia Bianca ◽  
Papini Alessio ◽  
Chini Zittelli Graziella ◽  
Rodolfi Liliana ◽  
Mario R. Tredici

AbstractNannochloropsis oceanica F&M-M24 is able to increase its lipid content during nitrogen starvation to more than 50% of the total biomass. We investigated the ultrastructural changes and the variation in the content of main cell biomolecules that accompany the final phase of lipid accumulation. Nitrogen starvation induced a first phase of thylakoid disruption followed by chloroplast macroautophagy and formation of lipid droplets. During this phase, the total amount of proteins decreased by one-third, while carbohydrates decreased by 12–13%, suggesting that lipid droplets were formed by remodelling of chloroplast membranes and synthesis of fatty acids from carbohydrates and amino acids. The change in mitochondrial ultrastructure suggests also that these organelles were involved in the process. The cell wall increased its thickness and changed its structure during starvation, indicating that a disruption process could be partially affected by the increase in wall thickness for biomolecules recovery from starved cells. The wall thickness in strain F&M-M24 was much lower than that observed in other strains of N. oceanica, showing a possible advantage of this strain for the purpose of biomolecules extraction. The modifications following starvation were interpreted as a response to reduction of availability of a key nutrient (nitrogen). The result is a prolonged survival in quiescence until an improvement of the environmental conditions (nutrient availability) allows the rebuilding of the photosynthetic apparatus and the full recovery of cell functions.


2001 ◽  
Vol 91 (2) ◽  
pp. 165-172 ◽  
Author(s):  
Ki Woo Kim ◽  
Eun Woo Park ◽  
Young Ho Kim ◽  
Kyung-Ku Ahn ◽  
Pan Gi Kim ◽  
...  

Apple fruit tissues infected with Botryosphaeria dothidea were examined by transmission electron microscopy using susceptible cv. Fuji and resistant cv. Jonathan. Immature (green) and mature (red) fruits of cv. Fuji with restricted or expanding lesions were also examined to reveal subcellular characteristics related with latent and restricted disease development. In infected susceptible mature fruits, cytoplasmic degeneration and organelle disruption commonly occurred, accompanying cell wall dissolution around invading hyphae. Cell wall dissolution around invading hyphae in subepidermis was rare in immature, red halo-symptomed cv. Fuji and resistant cv. Jonathan fruits. In infected immature fruits of cv. Fuji, presumably at the latent state of disease development, cellular degeneration was less severe, and invading hyphae contained prominent microbody-lipid globule complexes or the deposition of thin electron-dense outer layer around cell wall of intercellular hyphae. Both mature fruits with red halos and resistant apple fruits formed cell wall protuberances at the outside of cell walls. In addition, electron-dense extramural layers were formed in the resistant apple fruits. Aberrant hyphal structures such as intrahyphal hyphae were found only in resistant fruit tissues, indicating the physiologically altered fungal growth. These ultrastructural changes of host tissues and fungal hyphae may reflect the pathogenesis of apple white rot under varying conditions of apple fruits.


2005 ◽  
Vol 17 (4) ◽  
pp. 409-416 ◽  
Author(s):  
L. Angiolella ◽  
B. Maras ◽  
A.R. Stringaro ◽  
G. Arancia ◽  
F. Mondello ◽  
...  

IAWA Journal ◽  
2012 ◽  
Vol 33 (4) ◽  
pp. 403-416 ◽  
Author(s):  
Karumanchi S. Rao ◽  
Yoon Soo Kim ◽  
Pramod Sivan

Sequential changes occurring in cell walls during expansion, secondary wall (SW) deposition and lignification have been studied in the differentiating xylem elements of Holoptelea integrifolia using transmission electron microscopy. The PATAg staining revealed that loosening of the cell wall starts at the cell corner middle lamella (CCML) and spreads to radial and tangential walls in the zone of cell expansion (EZ). Lignification started at the CCML region between vessels and associated parenchyma during the final stages of S2 layer formation. The S2 layer in the vessel appeared as two sublayers,an inner one and outer one.The contact ray cells showed SW deposition soon after axial paratracheal parenchyma had completed it, whereas noncontact ray cells underwent SW deposition and lignification following apotracheal parenchyma cells. The paratracheal and apotracheal parenchyma cells differed noticeably in terms of proportion of SW layers and lignin distribution pattern. Fibres were found to be the last xylem elements to complete SW deposition and lignification with differential polymerization of cell wall polysaccharides. It appears that the SW deposition started much earlier in the middle region of the fibres while their tips were still undergoing elongation. In homogeneous lignin distribution was noticed in the CCML region of fibres.


Hydrobiologia ◽  
1990 ◽  
Vol 204-205 (1) ◽  
pp. 597-601 ◽  
Author(s):  
L. Talarico ◽  
G. Guida ◽  
E. Murano ◽  
A. M. Piacquadio
Keyword(s):  

1968 ◽  
Vol 171 (1023) ◽  
pp. 249-259 ◽  

During the life cycle of the unicellular alga Cyanidium caldarium the surfaces of the plasmalemma and the adjacent cell wall develop a number of differentiated structures which can be demonstrated with the freeze-etching technique. While cell division takes place, the plasma membrane is undifferentiated and covered with randomly distributed 55 and 80 Å particles as well as small holes from torn out particles that can be found adhering to the adjacent cell wall. The 80 Å particles possess a substructure and sometimes 40 Å fibrils can be seen leading from these particles into the cell wall. Just after cell division, shallow depressions showing a hexagonal surface pattern with a spacing of 105 Å and arrays of approximately hexagonally packed 55 Å particles are formed on the plasmalemma. The corresponding structures found on the cell wall are particle-studded humps, which fit into the shallow depressions, and faintly striated regions, which match the 55 Å particle arrays. During the next stage of development, the hexagonally patterned shallow depressions on the plasma membrane are transformed into regularly striated 300 to 350 Å wide and approximately 250 Å deep folds, while the arrays of 55 Å particles increase in size. On the adjacent cell wall we can follow the development of the particle-studded humps into ridges covered with 70 Å particles. The plasmalemma of old mature cells is characterized by long striated folds that replace nearly all network structured depressions, and a few small arrays of 55 Å particles. Long ridges covered with particles are the corresponding dominant feature on the inside of the cell wall. Prior to cell division, the striated folds and the other differentiations of the plasmalemma are broken down and eventually disappear so that the cell has again an undifferentiated ‘embryonic’ plasma membrane for cell division. Simultaneously the differentiated structures on the cell wall disappear. All the described particles and units forming plasma membrane differentiations seem to be confined to the surface layer of the plasmalemma. The outlined development cycle of the plasmalemma of Cyanidium shows that biological membranes have the potential to differentiate in time and space.


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