The fate of acetyl groups and sugar components during the digestion of grass cell walls in sheep

1977 ◽  
Vol 89 (2) ◽  
pp. 327-340 ◽  
Author(s):  
E. Jane Morris ◽  
J. S. D. Bacon
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Lignin Content ◽  
Sodium Ethoxide ◽  
Mesophyll Cell ◽  
Cell Types ◽  
Gas Liquid Chromatography ◽  
Cell Wall Preparation ◽  
The Relationship ◽  
Isolated Cell

SummaryThe digestibilities of grass cell wall constituents determined in a digestion trial were compared with those obtained by suspending various isolated cell wall preparations in nylon bags in the rumen of a sheep. Particular attention was paid to acetyl groups and to individual sugars, which were determined in both cases by gas liquid chromatography.For dried grass and hay in the digestion trial the cell wall constituents showed digestibilities decreasing in the following order: arabinose, galactose, glucose, xylose, acetyl, lignin.For a leaf cell wall preparation derived from all cell types except mesophyll, the nylon bag technique allowed the same order of digestibilities; rhamnose and uronic acids were also measured and found to be rapidly digested. Mesophyll cell walls placed in nylon bags were more readily digested than non-mesophyll. All the sugars, and also acetyl groups, were digested to the same extent.In a grass cell wall preparation isolated from sheep faeces, tested similarly, xylose and glucose were digested to the same extent, but acetyl groups were less digested.Removal of acetyl groups, using sodium ethoxide, which left the sugar composition and lignin content unchanged, increased the digestibility particularly of the cell walls from faeces.The results are discussed with reference to the relationship between cell wall composition and digestibility.

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 STUDIES ON BACTERIOPHAGES OF HEMOLYTIC STREPTOCOCCI

1957 ◽  
Vol 106 (3) ◽  
pp. 365-384 ◽  
Author(s):  
Richard M. Krause
Keyword(s):  
Cell Wall ◽  
Hyaluronic Acid ◽  
Cell Walls ◽  
Receptor Site ◽  
Surface Proteins ◽  
Phage Antibody ◽  
Group A ◽  
Phage Receptor ◽  
Hyaluronic Acid Capsule ◽  
Isolated Cell

The host ranges of bacteriophages for group A, types 1, 6, 12, and 25 and group C streptococci have been determined. The findings indicate that the susceptibility to these phages is primarily a group-specific phenomenon, although it is modified by several factors such as the hyaluronic acid capsule, lysogeny, and possibly the presence of surface proteins. Phage antibody studies indicate that while the group A phages are antigenically related, they are distinct from the group C phage. This is in agreement with the observation that group A phages are not specific for their homologous streptococcal types. The purified group C carbohydrate inactivates group C phage but not the group A phages, thus suggesting that the carbohydrate, a component of the cell wall, may serve as the phage receptor site. It has not been possible to inactivate the group A phages with group A carbohydrate. Phage lysis of groups A and C streptococci is accompanied by fragmentation of the cell wall since the C carbohydrate has been identified serologically and chemically in the supernate of centrifuged lysates. The immediate lysis of groups A and C hemolytic streptococci and their isolated cell walls by an accesory heat-labile lytic factor in fresh group C lysates is also described.

scholarly journals Ionic Relations of Cells of Ohara Australis I. Ion Exchange in the Cell Wall

1959 ◽  
Vol 12 (4) ◽  
pp. 395 ◽  
Author(s):  
J Dainty ◽  
AB Hope
Keyword(s):  
Cell Wall ◽  
Ion Exchange ◽  
Free Space ◽  
Cell Walls ◽  
Plant Cells ◽  
External Solution ◽  
Exchangeable Cations ◽  
Intact Cells ◽  
Donnan Free Space ◽  
Isolated Cell

Measurements of ion exchange were made between isolated cell walls of Ohara australis and an external solution. Comparison between intact cells and cell walls showed that nearly all the easily exchangeable cations are located in the cell wall. The wall is hown to consist of "water free space" (W.F.S.) and "Donnan free space" (D.F.S.); the concentration of in diffusible anions in the D.F.S. is about O� 6 equivjl. This finding is contrary to past suggestions that the D.F.S. is in the cytoplasm of plant cells.

scholarly journals Novel tool to quantify cell wall porosity relates wall structure to cell growth and drug uptake

2019 ◽  
Vol 218 (4) ◽  
pp. 1408-1421 ◽  
Author(s):  
Xiaohui Liu ◽  
Jiazhou Li ◽  
Heyu Zhao ◽  
Boyang Liu ◽  
Thomas Günther-Pomorski ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Dynamic Structure ◽  
Cell Types ◽  
Antifungal Drugs ◽  
Drug Uptake ◽  
Wall Structure ◽  
Quenching Efficiency ◽  
Model Plant Arabidopsis Thaliana ◽  
Cell Wall Porosity

Even though cell walls have essential functions for bacteria, fungi, and plants, tools to investigate their dynamic structure in living cells have been missing. Here, it is shown that changes in the intensity of the plasma membrane dye FM4-64 in response to extracellular quenchers depend on the nano-scale porosity of cell walls. The correlation of quenching efficiency and cell wall porosity is supported by tests on various cell types, application of differently sized quenchers, and comparison of results with confocal, electron, and atomic force microscopy images. The quenching assay was used to investigate how changes in cell wall porosity affect the capability for extension growth in the model plant Arabidopsis thaliana. Results suggest that increased porosity is not a precondition but a result of cell extension, thereby providing new insight on the mechanism plant organ growth. Furthermore, it was shown that higher cell wall porosity can facilitate the action of antifungal drugs in Saccharomyces cerevisiae, presumably by facilitating uptake.

The effects of thermal treatment on the nanomechanical behavior of bamboo (Phyllostachys pubescens Mazel ex H. de Lehaie) cell walls observed by nanoindentation, XRD, and wet chemistry

Holzforschung ◽  
2017 ◽  
Vol 71 (2) ◽  
pp. 129-135 ◽  
Author(s):  
Yanjun Li ◽  
Chengjian Huang ◽  
Li Wang ◽  
Siqun Wang ◽  
Xinzhou Wang
Keyword(s):  
Cell Wall ◽  
Thermal Treatment ◽  
Cell Walls ◽  
Treatment Time ◽  
Lignin Content ◽  
Phyllostachys Pubescens ◽  
X Ray Diffraction ◽  
Wet Chemistry ◽  
X Ray ◽  
Wet Chemical

Abstract The effects of thermal treatment of bamboo at 130, 150, 170, and 190°C for 2, 4, and 6 h were investigated in terms of changes in chemical composition, cellulose crystallinity, and mechanical behavior of the cell-wall level by means of wet chemical analysis, X-ray diffraction (XRD), and nanoindentation (NI). Particularly, the reduced elastic modulus (Er), hardness (H), and creep behavior were in focus. Both the temperature and treatment time showed significant effects. Expectedly, the hemicelluloses were degraded and the relative lignin content was elevated, while the crystallinity of the cellulose moiety was increased upon thermal treatment. The Er and H data of the cell wall were increased after 6 h treatment at 190°C, from 18.4 to 22.0 GPa and from 0.45 to 0.65 GPa, respectively. The thermal treatment led to a decrease of the creep ratio (CIT) under the same conditions by ca. 28%. The indentation strain state (εi) also decreased significantly after thermal treatment during the load-holding stage.

A relationship between cell wall composition and mutant morphology in the basidiomycete Schizophyllum commune

1968 ◽  
Vol 14 (7) ◽  
pp. 809-811 ◽  
Author(s):  
Chiu-Sheng Wang ◽  
Marvin N. Schwalb ◽  
Philip G. Miles
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Single Gene ◽  
Schizophyllum Commune ◽  
Gene Mutations ◽  
Cell Wall Composition ◽  
Statistical Analyses ◽  
Morphological Mutants ◽  
Mutant Forms ◽  
Isolated Cell

Mechanically isolated cell walls of normal homokaryons and the morphological mutants thin and puff were fractionated and hydrolyzed by chemical procedures. The yields of fractionated materials and the glucose/hexosamine ratios of acid hydrolysates were determined. Results of statistical analyses of the values obtained from these determinations indicated that single-gene mutations causing the thin and puff mutant forms of this fungus produce specific differences in the composition of cell walls.

Relationship of wood cell wall ultrastructure to bacterial degradation of wood

IAWA Journal ◽  
2019 ◽  
Vol 40 (4) ◽  
pp. 845-870 ◽  
Author(s):  
Adya P. Singh ◽  
Yoon Soo Kim ◽  
Ramesh R. Chavan
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Wood Cell Wall ◽  
Bacterial Degradation ◽  
Cell Wall Components ◽  
Degrading Bacteria ◽  
Wall Ultrastructure ◽  
Relationship Of ◽  
The Relationship ◽  
Wall Components

ABSTRACT This review presents information on the relationship of ultrastructure and composition of wood cell walls, in order to understand how wood degrading bacteria utilise cell wall components for their nutrition. A brief outline of the structure and composition of plant cell walls and the degradation patterns associated with bacterial degradation of wood cell walls precedes the description of the relationship of cell wall micro- and ultrastructure to bacterial degradation of the cell wall. The main topics covered are cell wall structure and composition, patterns of cell wall degradation by erosion and tunnelling bacteria, and the relationship of cell wall ultrastructure and composition to wood degradation by erosion and tunnelling bacteria. Finally, pertinent information from select recent studies employing molecular approaches to identify bacteria which can degrade lignin and other wood cell wall components is presented, and prospects for future investigations on wood degrading bacteria are explored.

Lignification of spruce tracheid secondary cell walls related to longitudinal hardness and modulus of elasticity using nano-indentation

2002 ◽  
Vol 80 (10) ◽  
pp. 1029-1033 ◽  
Author(s):  
W Gindl ◽  
H S Gupta ◽  
C Grünwald
Keyword(s):  
Cell Wall ◽  
Modulus Of Elasticity ◽  
Cell Walls ◽  
Secondary Cell Wall ◽  
Lignin Content ◽  
Wood Formation ◽  
Nano Indentation ◽  
Secondary Cell Walls ◽  
Cell Wall Development ◽  
The One

The lignin content and the mechanical properties of lignifying and fully lignified spruce tracheid secondary cell walls were determined using UV microscopy and nano-indentation, respectively. The average lignin content of developing tracheids was 0.10 g·g–1, as compared with 0.21 g·g–1 in mature tracheids. The modulus of elasticity of developing cells was on average 22% lower than the one measured in mature, fully lignified cells. For the longitudinal hardness, a larger difference of 26% was observed. As lignifying cells in the cambial zone are undergoing cell wall development, spaces in the cellulose–hemicellulose structure are filled with lignin and the density of the cell wall is believed to increase. It is therefore suggested that the observed difference in modulus of elasticity between developing and fully lignified cell walls is due to the filling of spaces with lignin and an increase of the packing density of the cell wall during lignification. Although remarkably less stiff than the composite polysaccharide structure in the secondary cell wall, lignin may be considered equally hard. Therefore, the observed increase in lignin content may contribute directly to the measured increase of hardness.Key words: secondary cell wall, hardness, lignin, modulus of elasticity, wood formation.

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.

scholarly journals STUDIES OF L FORMS AND PROTOPLASTS OF GROUP A STREPTOCOCCI

1959 ◽  
Vol 110 (6) ◽  
pp. 853-874 ◽  
Author(s):  
Earl H. Freimer ◽  
Richard M. Krause ◽  
Maclyn McCarty
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
M Protein ◽  
Group A Streptococci ◽  
Group A ◽  
Isolated Cell ◽  
Streptococcal Strain

L forms of Group A streptococci have been isolated by the use of penicillin gradient agar plates. Osmotically fragile protoplasts of Group A streptococci have been obtained by the use of Group C phage-associated lysin which lyses Group A streptococci and their isolated cell walls. Membranes surrounding these enzymatically derived protoplasts have been isolated, and chemical and immunological studies indicate that they are free of cell wall carbohydrate and M protein. The streptococcal protoplasts reproduce as colonies which are morphologically indistinguishable from streptococcal L forms. Evidence is presented to show that these two streptococcal derivatives are serologically and physiologically related to each other as well as to the parent streptococcal strain from which they were isolated.

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