Ultrastructure of wilt syndrome caused by Verticillium dahliae. V. Attempted localization of phenolic compounds in the vascular region

1978 ◽  
Vol 56 (20) ◽  
pp. 2594-2612 ◽  
Author(s):  
Jane Robb ◽  
J. D. Brisson ◽  
Lloyd Busch ◽  
B. C. Lu

Ferric chloride has been used in an attempt to detect phenolic compounds at the ultrastructure level in the petioles of chrysanthemums and sunflowers infected with Verticillium dahliae. The fungus contains two types of cytoplasmic structures which stain very densely with ferric chloride; one is similar to a multivesicular body, the other solid and apparently spherical. In treated chrysanthemums, the ferric ion accumulates mainly in vessel plugs, in laminar arrays or localized diffuse deposits in the secondary walls of vessels, in vasicentric parenchyma cells, and the protective layer of parenchyma cells immediately adjacent to the vessels. In treated sunflowers the ferric ion accumulates mainly in vessel plugs, in the pectinaceous layers of the cell wall (i.e. middle lamella and primary cell walls), and in the vasicentric parenchyma cells. Differences in the pattern of phenolic deposition in the two hosts could account wholly or in part for differences in symptom expression.

1980 ◽  
Vol 58 (21) ◽  
pp. 2269-2273 ◽  
Author(s):  
H. B. Hanten ◽  
G. E. Ahlgren ◽  
J. B. Carlson

The anatomical development of the abscission zone in grains of Zizania aquatica L. was correlated with development of the embryo. The abscission zone is well developed when the embryo sac is mature. Soon after pollination, the first anatomical evidence of abscission appears as plasmolysis of the separation layer parenchyma cells. This is followed by separation of the layers by dissolution of the middle lamella and fragmentation of cell walls. Persistence of intact vascular tissue and presence of a surrounding cone-shaped mass of lignified cells may be involved in abscission of wild rice grains.


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.


1992 ◽  
Vol 117 (1) ◽  
pp. 114-118 ◽  
Author(s):  
J.G. Luza ◽  
R. van Gorsel ◽  
V.S. Polito ◽  
A.A. Kader

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.


IAWA Journal ◽  
2016 ◽  
Vol 37 (3) ◽  
pp. 383-401 ◽  
Author(s):  
Jong Sik Kim ◽  
Geoffrey Daniel

Although there is considerable information on anatomy and gross chemistry of oak wood, little is known on the ultrastructure and chemistry at the individual cell wall level. In particular, differences in ultrastructure and chemistry within the same cell type between earlywood (EW) and latewood (LW) are poorly understood. This study investigated the ultrastructure and chemistry of (vasicentric) tracheids, vessels, (libriform) fibers and axial/ray parenchyma cells of English oak xylem (Quercus robur L.) using light-, fluorescence- and transmission electron microscopy combined with histo/cytochemistry and immunohisto/ cytochemistry. EW tracheids showed several differences from LW tracheids including thinner cell walls, wider middle lamella cell corner (MLcc) regions and lesser amounts of mannan epitopes. Fibers showed thicker cell walls and higher amounts of mannan epitopes than tracheids. EW vessels were rich in guaiacyl (G) lignin with a characteristic non-layered cell wall organization (absence of S1–3 layers), whereas LW vessels were rich in syringyl (S) lignin with a three layered cell wall structure (S1–3 layers). Formation of a highly lignified and wide protective layer (PL) inside axial/ray parenchyma cells was detected only in EW. Distribution of mannan epitopes varied greatly between cell types and between EW and LW, whereas distribution of xylan epitopes was almost identical in all cell types within a growth ring. Together, this study demonstrates that there are great variations in ultrastructure and chemistry of cell walls within a single growth ring of English oak xylem.


IAWA Journal ◽  
2014 ◽  
Vol 35 (1) ◽  
pp. 61-68
Author(s):  
Seung Gon Wi ◽  
Kwang Ho Lee ◽  
Hyeun Jong Bae ◽  
Byung Dae Park ◽  
Adya P. Singh

Lignin in the middle lamella of the secondary xylem of angiosperms appears to be inhomogeneously distributed, based on studies where the focus is on a close examinantion of the middle lamella region of fibre cell walls by transmission electron microscopy (TEM). This is in contrast to the secondary xylem of gymnosperms which often display a more uniform distribution of lignin in the middle lamella of secondary xylem elements. The aim of our study was to undertake TEM examination of kenaf (Hibiscus cannabinus L.), an angiosperm plant mainly cultivated for its high quality secondary phloem fibres, to investigate lignin distribution in the middle lamella of secondary vascular tissues, including secondary phloem fibres. The middle lamella displayed considerable heterogeneity in the distribution of lignin in all lignified secondary vascular tissues, including xylem and phloem fibres, vessels and axial xylem parenchyma cells. The results provided evidence of lignin inhomogeneity in the secondary phloem fibres as well as in other lignified elements of kenaf vascular tissues, extending previous observations which were confined only to fibre cells.


IAWA Journal ◽  
2014 ◽  
Vol 35 (4) ◽  
pp. 395-406 ◽  
Author(s):  
Uwe Schmitt ◽  
Benjamin Lüer ◽  
Dirk Dujesiefken ◽  
Gerald Koch

Branches of Platanus × hispanica with distinct symptoms of the Massaria disease were investigated by light and transmission electron microscopy and cellular UVmicrospectrophotometry. The samples collected in the city of Mannheim, Germany, were infected in vivo with the fungus Splanchnonema platani and showed various degrees of wood decay. The investigations were focused on the decay pattern of cell walls in the different cells, i.e., fibres, vessels as well as ray and axial parenchyma cells. The following results were obtained. Hyphae of the ascomycete fungus Splanchnonema platani penetrated from cell to cell through the pits and not through the cell wall middle lamella, by the formation of thin perforation hyphae. During this process, the 1–5 μm thick hyphae became narrower without attacking the wall around the pit canal. After penetration through a pit, the hyphae again enlarged to their original diameter. This is true for all pit pairs connecting the various cell types. Late decay stages did not show a decay of cell corner regions and middle lamellae of fibres as well as vessel and parenchyma cell walls. Phenolic deposits in parenchyma cells were still present in severely attacked xylem tissue. These features point to a low lignolytic capacity of the fungus. The frequently found microscopic decay pattern with the formation of oval or spherical cavities in the S2 layer of the secondary wall with an often structurally intact S3 layer is a characteristic of softrot decay. This classification is also supported by the remaining cell corner and middle lamella regions in advanced decay stages. As a consequence of this decay type, branches fracture in a brittle mode.


IAWA Journal ◽  
2020 ◽  
Vol 41 (3) ◽  
pp. 333-355 ◽  
Author(s):  
Miroslava Mamoňová ◽  
Ladislav Reinprecht

Abstract The effect of natural and artificial weathering on the anatomy of seven tropical hardwoods: Bangkirai (Shorea obtusa Wall.), Cumaru (Dipteryx odorata (Aubl.) Wild.), Cumaru Rosa (Dipteryx magnifica (Ducke) Ducke), Ipé (Tabebuia serratifolia Nichols.), Jatobá (Hymenaea courbaril L.), Kusia (Nauclea diderrichii Merill) and Massaranduba (Manilkara bidentata A. Chev.), was studied. As a result of weathering some characteristic anatomical changes occurred: the weakening of connections between cell elements related to the degradation of the middle lamella; micro-cracks in cell walls; total degradation of parenchyma cells in xylem rays, or significant thinning of parenchyma cell walls and their extreme shrinkage; micro-cracks in the vicinity of xylem rays; significant transversal disruptions in libriform fibres; ablation of pit membranes in vessels and parenchyma cells; changes in the secondary wall of libriform fibres, for example, their defibrillation and weathering-degradation of the S1 layer; and spherical formations on the S3 layer of cell walls produced from condensing compounds of degraded lignin and hemicelluloses as well as thermo-mechanical wrinkling. The highest incidence of micro-cracks after both modes of weathering was found in the densest species; Cumaru, Ipé, and Massaranduba.


2006 ◽  
Vol 33 (3) ◽  
pp. 297 ◽  
Author(s):  
Stéphane Octave ◽  
Gabriel Roblin ◽  
Magali Vachaud ◽  
Pierrette Fleurat-Lessard

Eutypa dieback is a devastating disease of Vitis vinifera L. caused by the fungal pathogen Eutypa lata. This wood-inhabiting fungus degrades tissues in the trunk and cordons of infected vines and induces symptoms in the foliage. These symptoms have been attributed to the production of toxic metabolites by the pathogen, in particular eutypine. Recently, we have isolated polypeptide compounds secreted by the fungus in artificial culture. The aims of this study were to examine the effects induced in leaves by applying polypeptides and eutypine to detached canes and to compare this to the changes in leaf structure induced by E. lata in the vineyard. In leaves taken from vines infected with E. lata, the changes in mesophyll cells indicate that the fungus has an effect on tissue remote from the infected area. The size of mesophyll cells decreased by more than half, starch content was reduced and tannins were abundant. Plastids, mitochondria and cell walls were highly modified. In leaves taken from healthy canes treated with polypeptides of E. lata, the structure of mesophyll cells was also modified. The cell size did not change, but the tannin content increased and modifications in plastids and mitochondria were similar to those observed in leaves taken from infected vines. The major effect was the complete disorganisation of cell walls. Eutypine had less effect on organelle structure and did not modify the cell wall. In canes treated with polypeptides, vessel-associated cells (VACs) were also damaged. Abundant tannins occurred in the vacuoles of VACs and marked changes were noted in mitochondria, plastids and the protective layer, in particular in the pit at the vessel interface. In these pits, the protective layer, the primary wall and the middle lamella were all highly modified. In contrast, treatment with eutypine induced the development of a large transfer apparatus bordering the unmodified pectocellulose wall. These results illustrate that treatment with polypeptides produced by E. lata may cause changes in mesophyll cells in leaves and VACs in canes, that resemble changes observed in naturally infected vines. Comparatively, the differences with eutypine action were stressed. Both types of toxins may co-operate in vivo to produce the degeneration observed during the disease.


Author(s):  
S. E. Keckler ◽  
D. M. Dabbs ◽  
N. Yao ◽  
I. A. Aksay

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).


Crop Science ◽  
1990 ◽  
Vol 30 (2) ◽  
pp. 396 ◽  
Author(s):  
D. E. Akin ◽  
N. Ames-Gottfred ◽  
R. D. Hartley ◽  
R. G. Fulcher ◽  
L. L. Rigsby

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