scholarly journals SCALE FORMATION IN CHRYSOPHYCEAN ALGAE

1970 ◽  
Vol 45 (2) ◽  
pp. 246-271 ◽  
Author(s):  
R. Malcolm Brown ◽  
Werner W. Franke ◽  
Hans Kleinig ◽  
Heinz Falk ◽  
Peter Sitte

The cell wall of the marine chrysophycean alga Pleurochrysis scherfellii is composed of distinct wall fragments embedded in a gelatinous mass. The latter is a polysaccharide of pectic character which is rich in galactose and ribose. These wall fragments are identified as scales. They have been isolated and purified from the vegetative mother cell walls after zoospore formation. Their ultrastructure is described in an electron microscope study combining sectioning, freeze-etch, and negative staining techniques. The scales consist of a layer of concentrically arranged microfibrils (ribbons with cross-sections of 12 to 25 x 25 to 40 A) and underlying radial fibrils of similar dimensions. Such a network-plate is densely coated with particles which are assumed to be identical to the pectic component. The microfibrils are resistant to strong alkaline treatment and have been identified as cellulose by different methods, including sugar analysis after total hydrolysis, proton resonance spectroscopical examination (NMR spectroscopy) of the benzoylated product, and diverse histochemical tests. The formation and secretion of the scales can be followed along the maturing Golgi cisternae starting from a pronounced dilated "polymerization center" as a completely intracisternal process which ends in the exocytotic extrusion of the scales. The scales reveal the very same ultrastructure within the Golgi cisternae as they do in the cell wall. The present finding represents the first evidence on cellulose formation by the Golgi apparatus and is discussed in relation to a basic scheme for cellulose synthesis in plant cells in general.

1975 ◽  
Vol 53 (16) ◽  
pp. 1698-1711 ◽  
Author(s):  
R. L. Peterson ◽  
M. S. Firminger ◽  
L. A. Dobrindt

A β-1,3-glucan which has characteristics of callose was identified as a component of the cell wall in stomatal guard cells in three species of the fern, Ophioglossum. This identification was made by the fluorochrome properties of callose when stained with aqueous solutions of aniline blue. Controls involved both the effect of solutions of different pH on autofluorescence of guard cell walls and the extraction of leaf tissues with β-1,3-glucanases before staining with aniline blue. An electron-translucent region between the plasmalemma and the cell wall proper was observed with the electron microscope and corresponded in position with the areas that fluoresced after aniline blue staining.Other components of the guard cell wall identified included cellulose, which was identified by staining techniques, polarization microscopy, and electron microscopy; and a phenolic substance identified by a number of staining reactions. The cell wall failed to stain with a number of reagents for the identification of lignin.


2021 ◽  
Author(s):  
Jiawei Zhu ◽  
Wenting Ren ◽  
Fei Guo ◽  
Hankun Wang ◽  
Yan Yu

Abstract The mechanical and physical properties of lignocellulosic materials are closely related to the orientation and interaction of the polymers within cell walls. In this work, Imaging Polarized FTIR, combined with directional chemical removal, was applied to characterize the spatial orientation and interaction of cell wall polymers in bamboo fibers and parenchyma cells from two bamboo species. The results demonstrate the cellulose in bamboo fibers is nearly axially oriented whereas it is almost transversely arranged in parenchyma cells. Xylan and lignin are both preferentially oriented alongside cellulose, but with less orientation degre in the parenchyma cells. After lignin removal, the average orientation of xylan and cellulose is little affected, suggesting a strong interaction between cellulose and xylan. Meanwhile, the alkaline treatment significantly weakens the orientation of lignin in both fibers and parenchyma cells, and more significant for the latter, indicating the easy-degradable nature of lignin in parenchyma cells. And, it seemed the lignin and xylan in fibers were more difficult to be removed as compared to parenchyma cells, supporting the assumption that stronger interaction exists between lignin and xylan in the fibers. In a word, it was believed parenchyma cells are more suitable for biorefinery owing to its less ordered and relatively loose molecular assembly, as compared to fibers.


1995 ◽  
Author(s):  
Deborah Delmer ◽  
Nicholas Carpita ◽  
Abraham Marcus

Our previous work indicated that suspension-cultured plant cells show remarkable flexibility in altering cell wall structure in response either to growth on saline medium or in the presence of the cellulose synthesis inhibitor 2,-6-dichlorobenzonitrile (DCB). We have continued to analyze the structure of these modified cell walls to understand how the changes modify wall strength, porosity, and ability to expand. The major load-bearing network in the walls of DCB-adapted dicot cells that lack a substantial cellulose-xyloglucan network is comprised of Ca2+-bridged pectates; these cells also have an unusual and abundant soluble pectic fraction. By contrast, DCB-adapted barley, a graminaceous monocot achieves extra wall strength by enhanced cross-linking of its non-cellulosic polysaccharide network via phenolic residues. Our results have also shed new light on normal wall stucture: 1) the cellulose-xyloglucan network may be independent of other wall networks in dicot primary walls and accounts for about 70% of the total wall strength; 2) the pectic network in dicot walls is the primary determinant of wall porosity; 3) both wall strength and porosity in graminaceous monocot primary walls is greatly influenced by the degree of phenolic cross-linking between non-cellulosic polysaccharides; and 4) the fact that the monocot cells do not secrete excess glucuronoarabinoxylan and mixed-linked glucan in response to growth on DCB, suggests that these two non-cellulosic polymers do not normally interact with cellulose in a manner similar to xyloglucan. We also attempted to understand the factors which limit cell expansion during growth of cells in saline medium. Analyses of hydrolytic enzyme activities suggest that xyloglucan metabolism is not repressed during growth on NaCl. Unlike non-adapted cells, salt-adapted cells were found to lack pectin methyl esterase, but it is not clear how this difference could relate to alterations in wall expansibility. Salt-adaped cell walls contain reduced hyp and secrete two unique PRPP-related proteins suggesting that high NaCl inhibits the cross-linking of these proteins into the walls, a finding that might relate to their altered expansibility.


IAWA Journal ◽  
2017 ◽  
Vol 38 (2) ◽  
pp. 245-265 ◽  
Author(s):  
Barbara Ghislain ◽  
Bruno Clair

Tension wood, a tissue developed by angiosperm trees to actively recover their verticality, has long been defined by the presence of an unlignified cellulosic inner layer in the cell wall of fibres, called the G-layer. Although it was known that some species have no G-layer, the definition was appropriate since it enabled easy detection of tension wood zones using various staining techniques for either cellulose or lignin. For several years now, irrespective of its anatomical structure, tension wood has been defined by its high mechanical internal tensile stress. This definition enables screening of the diversity of cell walls in tension wood fibres. Recent results obtained in tropical species with tension wood with a delay in the lignification of the G-layer opened our eyes to the effective presence of large amounts of lignin in the G-layer of some species. This led us to review older literature mentioning the presence of lignin deposits in the G-layer and give them credit. Advances in the knowledge of tension wood fibres allow us to reconsider some previous classifications of the diversity in the organisation of the fibre walls of the tension wood.


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).


2008 ◽  
Vol 56 (3) ◽  
pp. 341-348
Author(s):  
P. Pepó ◽  
A. Kovács

Cryopreservation appears to be a suitable solution for the maintenance of potato germplasms. The protocol described in this paper can be applied for the vitrification and preservation of meristems. During histo-cytological studies it is possible to observe modifications at the cellular level and to understand the adaptive mechanism to low temperatures. Control potato meristem tissue contained a number of meristematic cells with a gradient of differentiation. After freezing there were a large number of vacuolated cells, some of which exhibited broken cell walls and plasmolysis. The thickening of the cell wall, giving them a sinuous appearance, was observed after freezing and thawing the meristems, with ruptures of the cuticle and epidermal layer.


2017 ◽  
Vol 51 ◽  
pp. 274-280
Author(s):  
A. D. Potemkin ◽  
Yu. S. Mamontov ◽  
N. S. Gamova

Study of selected specimens of Gymnomitrion collected by D. G. Long in Yunnan, China, revealed a new species, G. fissum Mamontov et Potemkin, sp. nov., with a fissured leaf surface. Comparison of SEM images of the leaf surface and leaf cross sections shows that the leaf surface of G. fissum is different from that of other known species with a superficially similar leaf surface, i. e. Mylia taylorii, M. verrucosa s. l. and Trabacellula tumidula. It has fissures around the cell lumen rather than grids and perforations. Outer cell walls of Gymnomitrion fissum are much thicker than in Mylia taylorii, M. verrucosa s. l. and Trabacellula tumidula, and their outer layers tend to be partly or completely caducous. G. fissum is related to the group of species assigned to the former genus Apomarsupella.


Plants ◽  
2021 ◽  
Vol 10 (7) ◽  
pp. 1263
Author(s):  
David Stuart Thompson ◽  
Azharul Islam

The extensibility of synthetic polymers is routinely modulated by the addition of lower molecular weight spacing molecules known as plasticizers, and there is some evidence that water may have similar effects on plant cell walls. Furthermore, it appears that changes in wall hydration could affect wall behavior to a degree that seems likely to have physiological consequences at water potentials that many plants would experience under field conditions. Osmotica large enough to be excluded from plant cell walls and bacterial cellulose composites with other cell wall polysaccharides were used to alter their water content and to demonstrate that the relationship between water potential and degree of hydration of these materials is affected by their composition. Additionally, it was found that expansins facilitate rehydration of bacterial cellulose and cellulose composites and cause swelling of plant cell wall fragments in suspension and that these responses are also affected by polysaccharide composition. Given these observations, it seems probable that plant environmental responses include measures to regulate cell wall water content or mitigate the consequences of changes in wall hydration and that it may be possible to exploit such mechanisms to improve crop resilience.


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