Chemical and ultrastructural changes of ash wood thermally modified (TMW) using the thermo-vacuum process: II. Immunocytochemical study of the distribution of noncellulosic polysaccharides

Holzforschung ◽  
2015 ◽  
Vol 69 (5) ◽  
pp. 615-625 ◽  
Author(s):  
Jong Sik Kim ◽  
Jie Gao ◽  
Nasko Terziev ◽  
Ottaviano Allegretti ◽  
Geoffrey Daniel
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Middle Lamella ◽  
Degradation Process ◽  
Thermal Modification ◽  
Ultrastructural Changes ◽  
Immunogold Localization ◽  
Immunocytochemical Study ◽  
Rhamnogalacturonan I ◽  
Compound Middle Lamella

AbstractFollowing structural and cytochemical studies (Part I) on thermally modified ash wood (TMW) by the thermo-vacuum (Termovuoto) process, changes in the distribution of noncellulosic polysaccharides have been investigated in TMW treated for 3 h at 220°C (TMW3 h, 220°C) by means of immunogold localization methods. Pectins (homogalacturonan, rhamnogalacturonan-I) and xyloglucan were significantly degraded in compound middle lamella (CML), including the middle lamella cell corner regions (CMLcc), of all xylem cells after thermal modification. Xylan and mannan degradation were also visible in fiber cell walls. In particular, degradation of mannan was very significant and showed variation between cell wall regions even within the same cell wall. The degradation of pectins was more significant than that of hemicelluloses. In summary, results suggest that each noncellulosic polysaccharide may have a different degradation process in ash TMWs.

Ultrastructural Changes in the Cell Walls of Cambial Derivatives During Wood Formation in Indian ELM (Holoptelea Integrifolia)

IAWA Journal ◽  
2012 ◽  
Vol 33 (4) ◽  
pp. 403-416 ◽  
Author(s):  
Karumanchi S. Rao ◽  
Yoon Soo Kim ◽  
Pramod Sivan
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Middle Lamella ◽  
Ultrastructural Changes ◽  
Cell Wall Polysaccharides ◽  
Lignin Distribution ◽  
Parenchyma Cells ◽  
Ray Cells ◽  
Xylem Elements ◽  
S2 Layer

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.

Histochemical Structure and Tensile Properties of Birch Cork Cell Walls

2021 ◽  
Author(s):  
Shingo Kiyoto ◽  
Junji Sugiyama
Keyword(s):  
Cell Wall ◽  
Tensile Stress ◽  
Cell Walls ◽  
Middle Lamella ◽  
Middle Layer ◽  
Tensile Tests ◽  
Cellulose Microfibrils ◽  
Trunk Diameter ◽  
Compound Middle Lamella ◽  
Cork Cell

Abstract Tensile tests of birch cork were performed in the tangential direction. Birch cork in the wet state showed significantly higher extensibility and toughness than those in the oven-dried state. The histochemical structure of birch cork was investigated by microscopic observation and spectroscopic analysis. Birch cork cell walls showed a three-layered structure. In transmission electron micrographs, osmium tetroxide stained the outer and inner layers, whereas potassium permanganate stained the middle and inner layers. After chemical treatment to remove suberin and lignin, the outer and inner layers disappeared and Fourier-transformed infrared spectra showed the cellulose I pattern. Polarizing light micrographs indicated that molecular chains in the outer and inner layers were oriented perpendicular to suberin lamination, whereas those in the inner layer showed longitudinal orientation. These results suggested that the outer and inner layers mainly consist of suberin, whereas the middle layer and compound middle lamella consist of lignin, cellulose, and other polysaccharides. We hypothesized a hierarchical model of the birch cork cell wall. The lignified cell wall with helical arrangement of cellulose microfibrils is sandwiched between two suberized walls. Cellulose microfibrils in the middle layer act like a spring and bear tensile loads. In the wet state, water and cellulose in the compound middle lamella transfer tensile stress between cells. In the dried state, this stress-transferal system functions poorly and fewer cells bear stress. Suberin in the outer and inner layers prevents absolute drying to maintain mechanical properties of the bark and to bear tensile stress caused by trunk diameter growth.

Silicification of wood-cell walls

1994 ◽  
Vol 52 ◽  
pp. 428-429
Author(s):  
S. E. Keckler ◽  
D. M. Dabbs ◽  
N. Yao ◽  
I. A. Aksay
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Cell Walls ◽  
Lignin Content ◽  
Resin Composite ◽  
Middle Lamella ◽  
Cellulose Fibers ◽  
Complex Structures ◽  
Rich Region ◽  
Inorganic Precursors

Cellular organic structures such as wood can be used as scaffolds for the synthesis of complex structures of organic/ceramic nanocomposites. The wood cell is a fiber-reinforced resin composite of cellulose fibers in a lignin matrix. A single cell wall, containing several layers of different fiber orientations and lignin content, is separated from its neighboring wall by the middle lamella, a lignin-rich region. In order to achieve total mineralization, deposition on and in the cell wall must be achieved. Geological fossilization of wood occurs as permineralization (filling the void spaces with mineral) and petrifaction (mineralizing the cell wall as the organic component decays) through infiltration of wood with inorganics after growth. Conversely, living plants can incorporate inorganics into their cells and in some cases into the cell walls during growth. In a recent study, we mimicked geological fossilization by infiltrating inorganic precursors into wood cells in order to enhance the properties of wood. In the current work, we use electron microscopy to examine the structure of silica formed in the cell walls after infiltration of tetraethoxysilane (TEOS).

scholarly journals Domain-specific and cell type-specific localization of two types of cell wall matrix polysaccharides in the clover root tip.

1992 ◽  
Vol 118 (2) ◽  
pp. 467-479 ◽  
Author(s):  
M A Lynch ◽  
L A Staehelin
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Cellular Differentiation ◽  
Cortical Cell ◽  
Middle Lamella ◽  
Root Cap ◽  
Root Tip ◽  
Cortical Cells ◽  
Peripheral Cell ◽  
Clover Root

Using immunocytochemical techniques and antibodies that specifically recognize xyloglucan (anti-XG), polygalacturonic acid/rhamnogalacturonan I (anti-PGA/RG-I), and methylesterified pectins (JIM 7), we have shown that these polysaccharides are differentially synthesized and localized during cell development and differentiation in the clover root tip. In cortical cells XG epitopes are present at a threefold greater density in the newly formed cross walls than in the older longitudinal walls, and PGA/RG-I epitopes are detected solely in the expanded middle lamella of cortical cell corners, even after pretreatment of sections with pectinmethylesterase to uncover masked epitopes. These results suggest that in cortical cells XG and PGA/RG-I are differentially localized not only to particular wall domains, but also to particular cell walls. In contrast to their nonoverlapping distribution in cortical cells, XG epitopes and PGA/RG-I epitopes largely colocalize in the epidermal cell walls. The results also demonstrate that the middle lamella of the longitudinal walls shared by epidermal cells and by epidermal and cortical cells constitutes a barrier to the diffusion of cell wall and mucilage molecules. Synthesis of XG and PGA/RG-I epitope-containing polysaccharides also varies during cellular differentiation in the root cap. The differentiation of gravitropic columella cells into mucilage-secreting peripheral cells is marked by a dramatic increase in the synthesis and secretion of molecules containing XG and PGA/RG-I epitopes. In contrast, JIM 7 epitopes are present at abundant levels in columella cell walls, but are not detectable in peripheral cell walls or in secreted mucilage. There were also changes in the cisternal labeling of the Golgi stacks during cellular differentiation in the root tip. Whereas PGA/RG-I epitopes are detected primarily in cis- and medial Golgi cisternae in cortical cells (Moore, P. J., K. M. M. Swords, M. A. Lynch, and L. A. Staehelin. 1991. J. Cell Biol. 112:589-602), they are localized predominantly in the trans-Golgi cisternae and the trans-Golgi network in epidermal and peripheral root cap cells. These observations suggest that during cellular differentiation the plant Golgi apparatus can be both structurally and functionally reorganized.

Ultrastructure des parois de cerises Bigarreau Burlat de textures différentes au cours de la maturation

1996 ◽  
Vol 74 (12) ◽  
pp. 1974-1981 ◽  
Author(s):  
C. Batisse ◽  
P. J. Coulomb ◽  
C. Coulomb ◽  
M. Buret
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Middle Lamella ◽  
Primary Cell ◽  
Wall Material ◽  
Cell Wall Degradation ◽  
Composition And Structure ◽  
Cell Wall Texture ◽  
Synthesis And Degradation ◽  
Soft Fruits

The changes in texture of fruits during ripening are linked to cell wall degradation involving synthesis and degradation of polymers. An increase in pectin solubility leads to cell sliding and an elastic aspect of tissues. The biochemical cell wall process differs between soft and crisp fruits originating from a same cultivar but cultivated under different agroclimatic conditions. Although the proportions of cell wall material are similar, the composition and structure of the two cell walls are very different at maturity. A solubilization of the middle lamella and a restructuration of the primary cell walls arising from the cells separation is observed in crisp fruits. In contrast, the middle lamella of the soft fruits is better preserved and the primary cell walls are thin and show degradation bags delimited by residual membrane formations. In addition, the macroendocytosis process by endosome individualization is more important in soft fruits. In conclusion, the fruit texture depends on the extent of the links between cell wall polymers. Keywords: cherry, cell wall, texture, ultrastructural study.

Microdistribution of copper in copper-ethanolamine (Cu-EA) treated southern yellow pine (Pinus spp.) related to density distribution

Holzforschung ◽  
2005 ◽  
Vol 59 (1) ◽  
pp. 82-89 ◽  
Author(s):  
Jinzhen Cao ◽  
D. Pascal Kamdem
Keyword(s):  
Cell Wall ◽  
Density Distribution ◽  
Cell Walls ◽  
Middle Lamella ◽  
Treated Wood ◽  
Yellow Pine ◽  
Using Data ◽  
Pinus Spp ◽  
Southern Yellow Pine ◽  
The Relationship

Abstract The relationship between copper absorption and density distribution in wood cell walls was investigated in this study. The density distribution on layer level was obtained from two approaches: (1) calculation by using data obtained from literature; (2) microdistribution of carbon and oxygen atoms in the wood cell. The microdistribution of carbon and oxygen in untreated southern yellow pine (Pinus spp.) sapwood, as well as copper in cell walls of copper-ethanolamine (Cu-EA) treated wood was determined by scanning electron microscopy coupled with energy dispersive X-ray analysis (SEM-EDXA). Both approaches for density distribution led to the same result: the density was higher in the compound middle lamella and cell corners than in the secondary wall. The concentration/intensity of Cu, C and O in the cell wall follow the same trend as the density distribution; suggesting that density may play a major role in SEM-EDXA study of the distribution of metal-containing wood preservatives within the wood cell wall.

Ultrastructural Changes in the Compound Middle Lamella of Pinus thunbergii During Lignification and Lignin Removal

Holzforschung ◽  
2000 ◽  
Vol 54 (3) ◽  
pp. 234-240 ◽  
Author(s):  
Jonas Hafrén ◽  
Takeshi Fujino ◽  
Takao Itoh ◽  
Ulla Westermark ◽  
Noritsugu Terashima
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Middle Lamella ◽  
Pinus Thunbergii ◽  
Ultrastructural Changes ◽  
Woody Tissue ◽  
Compound Middle Lamella ◽  
Lignin Removal ◽  
Transmission Electron ◽  
Early Phases

SummaryThe structure of the middle lamella inPinus thunbergiihas been studied by the rapid-freeze deep-etching (RFDE) technique in combination with transmission electron microscopy (TEM). The ultrastructure of the compound middle lamella was studied in the early phases of the development of woody tissue in the cambial and differentiating xylem, before the heavy incrustation with lignin had occurred. Lignified middle lamella in the xylem was studied both directly and after delignification. It was found that the structure of the unlignified middle lamella in the cambium/developing xylem consists of a fine irregular network probably containing pectin and hemicellulose. As a result of lignin incrustation, the middle lamella becomes increasingly dense and the surface structure of the fully lignified middle lamella appeared to be compact and partly covered with globular structures. After delignification of the lignified middle lamella a thin network with a different structure was revealed. This network probably mainly consists of hemicellulose. No microfibrils of the type that occurs in the primary and secondary walls were found in the middle lamella.

scholarly journals Chilling Injury in Peaches: A Cytochemical and Ultrastructural Cell Wall Study

1992 ◽  
Vol 117 (1) ◽  
pp. 114-118 ◽  
Author(s):  
J.G. Luza ◽  
R. van Gorsel ◽  
V.S. Polito ◽  
A.A. Kader
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Prunus Persica ◽  
Periodic Acid ◽  
Chilling Injury ◽  
Middle Lamella ◽  
Wall Structure ◽  
Positive Staining ◽  
Intercellular Matrix ◽  
Parenchyma Cells

Fruits of mid- (`O'Henry'), late (`Airtime'), and extra-late-season (`Autumn Gem') peach [Prunus persica (L.) Batsch] cultivars were examined for changes in cell wall structure and cytochemistry that accompany the onset of mealiness and leatheriness of the mesocarp due to chilling injury. The peaches were stored at 10C for up to 18 days or at SC for up to 29 days. Plastic-embedded sections were stained by the Schiff's-periodic acid reaction, Calcofluor white MR2, and Coriphosphine to demonstrate total insoluble carbohydrates, ß-1,4 glucans, and pectins, respectively. Mealiness was characterized by separation of mesocarp parenchyma cells leading to increased intercellular spaces and accumulation of pectic substances in the intercellular matrix. Little structural change was apparent in the cellulosic component of the cell walls of these fruits. In leathery peaches, the mesocarp parenchyma cells collapsed, intercellular space continued to increase, and pectin-positive staining in the intercellular matrix increased greatly. In addition, the component of the cell walls that stained positively for ß-1,4 glucans became thickened relative to freshly harvested or mealy fruit. At the ultrastructural level, dissolution of the middle lamella, cell separation, irregular thickening of the primary wall, and plasmolysis of the mesocarp parenchyma cells were seen as internal breakdown progressed.

scholarly journals ELECTRON-OPAQUE FIBRILS AND GRANULES IN AND BETWEEN THE CELL WALLS OF HIGHER PLANTS

1972 ◽  
Vol 53 (3) ◽  
pp. 695-703 ◽  
Author(s):  
Gary G. Leppard ◽  
J. Ross Colvin
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Cultured Cells ◽  
Higher Plants ◽  
Middle Lamella ◽  
Woody Species ◽  
Morning Glory ◽  
Plant Cell Walls ◽  
Higher Plant ◽  
Cell Wall Matrix

The components of higher-plant cell walls which become electron-opaque after staining with ruthenium-osmium were studied by electron microscopy. A fibrillar material which absorbs this stain is a major wall constituent in the root epidermal cells of carrot and morning glory. In both form and size, these fibrils resemble those found on the surface of suspension-cultured cells of the same species Some cells of woody species show an irregular distribution of electron-opaque material in the cell wall matrix and middle lamella. This material, which has an amorphous appearance with many electron stains, is shown by ruthenium-osmium staining to be an aggregate of discrete granules, 150–220 A in diameter. These observations are not consistent with the concept of the cell wall matrix and middle lamella as an amorphous, uniform gel

Chemical and ultrastructural changes of ash wood thermally modified using the thermo-vacuum process: I. Histo/cytochemical studies on changes in the structure and lignin chemistry

Holzforschung ◽  
2015 ◽  
Vol 69 (5) ◽  
pp. 603-613 ◽  
Author(s):  
Jong Sik Kim ◽  
Jie Gao ◽  
Nasko Terziev ◽  
Ignazia Cuccui ◽  
Geoffrey Daniel
Keyword(s):  
Cell Walls ◽  
Lignin Content ◽  
Middle Lamella ◽  
Cell Types ◽  
Histochemical Staining ◽  
Ultrastructural Changes ◽  
Transmission Electron ◽  
Native Cell ◽  
Different Response ◽  
Light Fluorescence

Abstract Changes in structure and lignin chemistry were investigated in ash wood thermally modified (TMW) by the thermo-vacuum (Termovuoto) process for 3 h at 190–220°C by means of light, fluorescence, and transmission electron (TEM) microscopy combined with histo/cytochemistry. Variation in changes in native cell color in TMWs was positively correlated with differences in lignin content between cell types and cell wall regions in the reference wood. Histochemical staining showed increasing amounts of acidic groups in TMWs with different response to ethanol extraction between secondary cell walls and CMLcc (compound middle lamella/middle lamella cell corner) regions. Fluorescence microscopy of TMWs and references showed a difference in intensity and color emission of lignin autofluorescence, reflecting modification of lignin in TMWs. Changes in histochemistry and fluorescence were prominent at and above 200°C. With TEM, increased intensity of lignin staining and distortion of fiber S1 layers were detected in TMW treated for 3 h at 220°C (TMW3 h, 220°C). TMW3 h, 220°C differed significantly in molecular ultrastructure of fiber cell walls compared to references, such as loss of the lamellar structure and size and distribution of lignin aggregates. The modification in CMLcc structure in ash TMW3 h, 220°C is different from that of softwoods.

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