Inactive Fluorescently Labeled Xylanase as a Novel Probe for Microscopic Analysis of Arabinoxylan Containing Cereal Cell Walls

2011 ◽  
Vol 59 (12) ◽  
pp. 6369-6375 ◽  
Author(s):  
Emmie Dornez ◽  
Sven Cuyvers ◽  
Ulla Holopainen ◽  
Emilia Nordlund ◽  
Kaisa Poutanen ◽  
...  
Keyword(s):  
Cell Walls ◽  
Microscopic Analysis

UV-microscopic analysis of acetylated spruce and birch cell walls

Holzforschung ◽  
2004 ◽  
Vol 58 (5) ◽  
pp. 483-488 ◽  
Author(s):  
Christian Hansmann ◽  
Manfred Schwanninger ◽  
Barbara Stefke ◽  
Barbara Hinterstoisser ◽  
Wolfgang Gindl
Keyword(s):  
Cell Walls ◽  
Middle Lamella ◽  
Microscopic Analysis ◽  
Weight Percent ◽  
Cellular Level ◽  
Uv Spectrum ◽  
Spectral Shifts ◽  
Microscopy Analysis ◽  
Absorbance Peak ◽  
Absorbance Spectra

Abstract Spruce and birch earlywood was acetylated to different weight percent gains using three different acetylation procedures. The absorbance spectra of secondary cell wall and compound cell corner middle lamella were determined by means of UV microscopy. Analysis of the spectra showed that the characteristic lignin absorbance peak in the UV spectrum of wood around 280 nm shifted to shorter wavelengths in acetylated samples. A distinct relationship between achieved weight percent gains after acetylation and observed spectral shifts could be established revealing a certain potential to measure acetylation on a cellular level by means of UV microscopy.

Reduced pectin content of cell walls prevents stress-induced root cell elongation in Arabidopsis

2020 ◽  
Author(s):  
Xiaohui Liu ◽  
Huiying Cui ◽  
Bochao Zhang ◽  
Min Song ◽  
Shaolin Chen ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Elongation ◽  
Cell Walls ◽  
Microscopic Analysis ◽  
Root Cell ◽  
Cellulose Microfibrils ◽  
Composition Analysis ◽  
Cellulose Content ◽  
Cell Extension ◽  
Mechanistic Basis

Abstract The primary cell walls of plants provide mechanical strength while maintaining the flexibility needed for cell extension growth. Cell extension involves loosening the bonds between cellulose microfibrils, hemicelluloses and pectins. Pectins have been implicated in this process, but it remains unclear if this depends on the abundance of certain pectins, their modifications, and/or structure. Here, cell wall-related mutants of the model plant Arabidopsis were characterized by biochemical and immunohistochemical methods and Fourier-transform infrared microspectroscopy. Mutants with reduced pectin or hemicellulose content showed no root cell elongation in response to simulated drought stress, in contrast to wild-type plants or mutants with reduced cellulose content. While no association was found between the degrees of pectin methylesterification and cell elongation, cell wall composition analysis suggested an important role of the pectin rhamnogalacturonan II (RGII), which was corroborated in experiments with the RGII-modifying chemical 2β-deoxy-Kdo. The results were complemented by expression analysis of cell wall synthesis genes and microscopic analysis of cell wall porosity. It is concluded that a certain amount of pectin is necessary for stress-induced root cell elongation, and hypotheses regarding the mechanistic basis of this result are formulated.

scholarly journals Strategies to Optimize Microalgae Conversion to Biogas: Co-Digestion, Pretreatment and Hydraulic Retention Time

Molecules ◽  
2018 ◽  
Vol 23 (9) ◽  
pp. 2096 ◽  
Author(s):  
Maria Solé-Bundó ◽  
Humbert Salvadó ◽  
Fabiana Passos ◽  
Marianna Garfí ◽  
Ivet Ferrer
Keyword(s):  
Retention Time ◽  
Cell Walls ◽  
Hydraulic Retention Time ◽  
Microscopic Analysis ◽  
Fold Increase ◽  
Resistant Cell ◽  
Methane Yield ◽  
Thermal Pretreatment ◽  
Primary Sludge ◽  
Yield Increase

This study aims at optimizing the anaerobic digestion (AD) of biomass in microalgal-based wastewater treatment systems. It comprises the co-digestion of microalgae with primary sludge, the thermal pretreatment (75 °C for 10 h) of microalgae and the role of the hydraulic retention time (HRT) in anaerobic digesters. Initially, a batch test comparing different microalgae (untreated and pretreated) and primary sludge proportions showed how the co-digestion improved the AD kinetics. The highest methane yield was observed by adding 75% of primary sludge to pretreated microalgae (339 mL CH4/g VS). This condition was then investigated in mesophilic lab-scale reactors. The average methane yield was 0.46 L CH4/g VS, which represented a 2.9-fold increase compared to pretreated microalgae mono-digestion. Conversely, microalgae showed a low methane yield despite the thermal pretreatment (0.16 L CH4/g VS). Indeed, microscopic analysis confirmed the presence of microalgae species with resistant cell walls (i.e., Stigioclonium sp. and diatoms). In order to improve their anaerobic biodegradability, the HRT was increased from 20 to 30 days, which led to a 50% methane yield increase. Overall, microalgae AD was substantially improved by the co-digestion with primary sludge, even without pretreatment, and increasing the HRT enhanced the AD of microalgae with resistant cell walls.

scholarly journals Basidiomycetes Biodiversity in the Area of Impact of Emissions of the Volgograd Aluminum Plant

2021 ◽  
pp. 14-18
Author(s):  
Helen Oganesyan ◽  
◽  
Nadezhda Kuragina ◽  
Keyword(s):  
Cell Walls ◽  
Microscopic Analysis ◽  
Field Research ◽  
Toxic Substances ◽  
Fruiting Bodies ◽  
Aluminum Plant ◽  
Binocular Microscope ◽  
Standard Set ◽  
Harmful Substances ◽  
The City

There are a large number of operating plants, combines and factories on the territory of Volgograd. Daily they emit tons of pollutants into the atmosphere, such as sulfur dioxide, carbon monoxide, fluoride compounds, nitrogen oxides, inorganic dust, etc. All of them are absorbed by the environment, including mushrooms. It is known that fruiting bodies of fungi accumulate heavy metals from the environment well and are excellent bioindicators. The study of the accumulation of toxic substances in the basidiomes of macromycetes in Volgograd has not previously been carried out. The purpose of our study was to assess the contamination of mushroom fruiting bodies in the sanitary protection zone of the plant by the bioindication method. We used standard methods of field research, microscopic analysis of samples using a Mikmed-5 binocular microscope, a Levenhuk C 510 NG camera and a standard set of reagents (5 % alkali solution and Meltzer’s reagent for determining the reaction of cell walls to iodine) and the bioindication method with the use of the lower crustaceans Daphnia as a test object. During mycological studies performed in fall-2019 in the study area, 14 species of fungi were identified. As a result of the bioindication research, a macromycete that accumulates harmful substances to a greater extent – Tricholoma equestre (L.) P. Kumm was identified. This species is considered tasty by the inhabitants of the city. The study proves that picking and eating mushrooms from the territory of sanitary protection factories, in particular the Aluminum Plant, is unsafe.

Raman microscopic analysis of wood after treatment with the ionic liquid, 1-ethyl-3-methylimidazolium chloride

Holzforschung ◽  
2015 ◽  
Vol 69 (3) ◽  
pp. 273-279 ◽  
Author(s):  
Toru Kanbayashi ◽  
Hisashi Miyafuji
Keyword(s):  
Molecular Structure ◽  
Cell Wall ◽  
Ionic Liquid ◽  
Raman Spectra ◽  
Cell Walls ◽  
Cryptomeria Japonica ◽  
Microscopic Analysis ◽  
Japanese Cedar ◽  
Wall Structure ◽  
Chemical Components

Abstract Japanese cedar (Cryptomeria japonica) was treated with the ionic liquid (IL) 1-ethyl-3-methylimidazolium chloride ([C2mim][Cl]), which is a solvent for cellulose, and the changes in the chemical components and their distribution in wood cell walls have been investigated by Raman microscopy. Raman spectra, recorded from various areas of the cell walls, showed that lignin in the compound middle lamellae (CML) and cell corners (CC) was resistant to the reaction with [C2mim][Cl], but its molecular structure changed partially. The reactivity of cellulose and hemicelluloses with [C2mim][Cl] was higher than that of lignin in the cell wall, and the cell wall structure was maintained even in an advanced state of the reactions. The effects of [C2mim]-[Cl] on cellulose and hemicelluloses in the cell wall were homogeneous, whereas that of lignin was inhomogeneous.

Preparatory Procedures for Electron Microscopic Analysis at the Molecular Level of Resolution

1978 ◽  
Vol 36 (3) ◽  
pp. 516-520
Author(s):  
F.J. Sjostrand
Keyword(s):  
Electron Microscope ◽  
Molecular Level ◽  
Microscopic Analysis ◽  
Resolving Power ◽  
Cellular Structures ◽  
Electron Microscopic ◽  
Systematic Analysis ◽  
Technical Developments ◽  
Thin Sectioning ◽  
Obvious Reason

In the 1940's and 1950's electron microscopy conferences were attended with everybody interested in learning about the latest technical developments for one very obvious reason. There was the electron microscope with its outstanding performance but nobody could make very much use of it because we were lacking proper techniques to prepare biological specimens. The development of the thin sectioning technique with its perfectioning in 1952 changed the situation and systematic analysis of the structure of cells could now be pursued. Since then electron microscopists have in general become satisfied with the level of resolution at which cellular structures can be analyzed when applying this technique. There has been little interest in trying to push the limit of resolution closer to that determined by the resolving power of the electron microscope.

Ectodesmata as Revealed By Freeze-Etch Preparations of Plant Epidermal Cell Walls

1973 ◽  
Vol 31 ◽  
pp. 468-469
Author(s):  
N.C. Lyon ◽  
W. C. Mueller
Keyword(s):  
Electron Microscopy ◽  
Acetic Acid ◽  
Nitric Acid ◽  
Oxalic Acid ◽  
Light Microscopy ◽  
Epidermal Cell ◽  
Cell Walls ◽  
Plant Viruses ◽  
Plant Leaves ◽  
Thin Sections

Schumacher and Halbsguth first demonstrated ectodesmata as pores or channels in the epidermal cell walls in haustoria of Cuscuta odorata L. by light microscopy in tissues fixed in a sublimate fixative (30% ethyl alcohol, 30 ml:glacial acetic acid, 10 ml: 65% nitric acid, 1 ml: 40% formaldehyde, 5 ml: oxalic acid, 2 g: mecuric chloride to saturation 2-3 g). Other workers have published electron micrographs of structures transversing the outer epidermal cell in thin sections of plant leaves that have been interpreted as ectodesmata. Such structures are evident following treatment with Hg++ or Ag+ salts and are only rarely observed by electron microscopy. If ectodesmata exist without such treatment, and are not artefacts, they would afford natural pathways of entry for applied foliar solutions and plant viruses.

An ultrastructural study of vegetative incompatibility in plants

1978 ◽  
Vol 36 (2) ◽  
pp. 436-437
Author(s):  
Randy Moore
Keyword(s):  
Ultrastructural Study ◽  
Cell Walls ◽  
Growth And Development ◽  
Solanum Pennellii ◽  
Initial Product ◽  
Basic Aspect ◽  
Tissue Interactions ◽  
Graft Interface ◽  
Antigen Antibody ◽  
Standard Fixation

Cell and tissue interactions are a basic aspect of eukaryotic growth and development. While cell-to-cell interactions involving recognition and incompatibility have been studied extensively in animals, there is no known antigen-antibody reaction in plants and the recognition mechanisms operating in plant grafts have been virtually neglected.An ultrastructural study of the Sedum telephoides/Solanum pennellii graft was undertaken to define possible mechanisms of plant graft incompatibility. Grafts were surgically dissected from greenhouse grown plants at various times over 1-4 weeks and prepared for EM employing variations in the standard fixation and embedding procedure. Stock and scion adhere within 6 days after grafting. Following progressive cell senescence in both Sedum and Solanum, the graft interface appears as a band of 8-11 crushed cells after 2 weeks (Fig. 1, I). Trapped between the buckled cell walls are densely staining cytoplasmic remnants and residual starch grains, an initial product of wound reactions in plants.

Comparison of Substructures Between Uniaxial and Biaxial Deformation in 1100-0 Aluminum

1981 ◽  
Vol 39 ◽  
pp. 52-53
Author(s):  
D. L. Rohr ◽  
S. S. Hecker
Keyword(s):  
Plastic Strain ◽  
Cell Walls ◽  
Room Temperature ◽  
Mechanical Response ◽  
Biaxial Tension ◽  
Initial Deformation ◽  
Uniaxial Deformation ◽  
Biaxial Deformation ◽  
Stress States ◽  
Comprehensive Study

As part of a comprehensive study of microstructural and mechanical response of metals to uniaxial and biaxial deformations, the development of substructure in 1100 A1 has been studied over a range of plastic strain for two stress states.Specimens of 1100 aluminum annealed at 350 C were tested in uniaxial (UT) and balanced biaxial tension (BBT) at room temperature to different strain levels. The biaxial specimens were produced by the in-plane punch stretching technique. Areas of known strain levels were prepared for TEM by lapping followed by jet electropolishing. All specimens were examined in a JEOL 200B run at 150 and 200 kV within 24 to 36 hours after testing.The development of the substructure with deformation is shown in Fig. 1 for both stress states. Initial deformation produces dislocation tangles, which form cell walls by 10% uniaxial deformation, and start to recover to form subgrains by 25%. The results of several hundred measurements of cell/subgrain sizes by a linear intercept technique are presented in Table I.

Electron Microscopic Analysis of Myonecrosis Induced by a Pure Component Isolated From Rattlesnake Venom

1976 ◽  
Vol 34 ◽  
pp. 292-293
Author(s):  
Charlotte L. Ownby ◽  
David Cameron ◽  
Anthony T. Tu
Keyword(s):  
Gel Filtration ◽  
Microscopic Analysis ◽  
The United States ◽  
Exchange Chromatography ◽  
Pure Component ◽  
Electron Microscopic Level ◽  
Electron Microscopic ◽  
Mouse Muscle ◽  
Major Health Problem ◽  
Rattlesnake Venom

In the United States the major health problem resulting from snakebite poisoning is local tissue damage, i.e. hemorrhage and myonecrosis. Since commercial antivenin does not usually prevent such damage to tissue, a more effective treatment of snakebite-induced myonecrosis is needed. To aid in the development of such a treatment the pathogenesis of myonecrosis induced by a pure component of rattlesnake venom was studied at the electron microscopic level.The pure component, a small (4,300 mol. wt.), basic (isoelectric point of 9.6) protein, was isolated from crude prairie rattlesnake (Crotalus viridis viridis) venom by gel filtration (Sephadex G-50) followed by cation exchange chromatography (Sephadex C-25), and shown to be pure by electrophoresis. Selection of the myotoxic component was based on light microscopic observations of injected mouse muscle.

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