The development of the aleurone layer in canola (Brassica napus)

1993 ◽  
Vol 71 (9) ◽  
pp. 1193-1201 ◽  
Author(s):  
Edwin P. Groot ◽  
Lawrence A. Van Caeseele
Keyword(s):  
Image Analysis ◽  
Electron Microscope ◽  
Brassica Napus ◽  
Cell Walls ◽  
Cell Layer ◽  
Aleurone Layer ◽  
Electron Microscopic ◽  
Aleurone Cells ◽  
Mature Seeds ◽  
Microscopic Techniques

The presence of the aleurone layer in developing seeds of Brassica napus becomes apparent about 22 days after pollination when examined with light and electron microscopic techniques. Prior to aleurone differentiation, the endosperm cellularizes centripetally to form characteristic columns of cells. The pigmented cell layer of the inner integument, which is present in dark-hulled seeds of Brassica, is just external to the aleurone. The first characteristic structures that become apparent inside the aleurone are spherosomes formed by the coalescence of small oil droplets. Shortly thereafter, the cell walls of the aleurone become markedly thickened relative to the surrounding cells. The aleurone cells of mature seeds contain lipid and protein reserves but lack starch. Development of the aleurone layer occurs first near the adaxial area and proceeds until the micropylar area finally differentiates. Endosperm chloroplasts have a characteristic lens shape when viewed in section with the electron microscope. They appear to congregate around a nucleus along with a small amount of cytoplasm causing an astroid-shaped aggregation of cytoplasm in the majority of endosperm cells but only transiently in the aleurone. DNA fluorometry and image analysis showed that aleurone nuclei are triploid; therefore the aleurone layer is derived from the endosperm. Key words: aleurone layer, endosperm, seed development, ploidy, anatomy, Brassica napus.

scholarly journals Ultrastructure of the Developing Aleurone Cells of Wheat Grain

1963 ◽  
Vol 16 (4) ◽  
pp. 768 ◽  
Author(s):  
MS Buttrose
Keyword(s):  
Electron Microscopy ◽  
Light Microscopy ◽  
Cell Walls ◽  
Osmium Tetroxide ◽  
Aleurone Layer ◽  
Wheat Grain ◽  
Aleurone Cells ◽  
Wheat Kernel ◽  
Large Numbers ◽  
Inner Surface

The developing aleurone layer cells of the wheat kernel have been investigated by electron microscopy and the results compared with those of light microscopy. Two weeks after flowering vacuoles appear in the cells and deposits accumulate in these until maturity when the cells are filled 'with the resulting "vacuolar units" 2-3p. in diameter, corresponding to the aleurone grains of light microscopy. The wheat aleurone grain consists of a bounding membrane (of vacuole origin) enclosing a matrix in which are embedded spherical deposits. Some of these deposits are translucent and others opaque to electrons after potassium permanganate and osmium tetroxide fixation. At all stages examined the cytoplasm of aleurone cells contained large numbers of small unidentified bodies with irregular outline and dense contents. At first they are dispersed, but towards maturity are organized as a monolayer over the surface of each aleurone grain and the inner surface of the cell walls. The apparent specificity of these structures to aleurone cells is discussed in relation to future chemical and physiological studies of the tissue.

Phytosterols in the aleurone layer of corn kernels

2000 ◽  
Vol 28 (6) ◽  
pp. 803-806 ◽  
Author(s):  
R. A. Moreau ◽  
V. Singh ◽  
A. Nuñez ◽  
K. B. Hicks
Keyword(s):  
Outer Layer ◽  
Cell Walls ◽  
Single Layer ◽  
Living Cells ◽  
Aleurone Layer ◽  
High Concentration ◽  
Aleurone Cells ◽  
Phytosterol Esters ◽  
Corn Fibre ◽  
Corn Kernels

Corn hulls are composed of two major layers: the outer layer, the pericarp, is made up of non-living cell walls, and an inner layer, the aleurone, consists of a single layer of living cells, surrounded by thick cell walls. Dissected pure pericarp and aleurone fractions were ground and extracted with hexane and the yields and compositions of the resulting oils were examined. This study revealed that the high levels of ferulate-phytosterol esters and the high concentration of sitostanol previously reported in corn-fibre oil actually originate in the aleurone cells.

In vivo and in sacco digestibility and rumen microbial degradation of cell walls of soyabean and rape integuments and of dehydrated beet pulp in sheep, observed by scanning electron microscopy

1990 ◽  
Vol 115 (3) ◽  
pp. 429-435 ◽  
Author(s):  
E. Grenet ◽  
P. Barry
Keyword(s):  
Microbial Degradation ◽  
Cell Walls ◽  
Cell Layer ◽  
Aleurone Layer ◽  
Palisade Layer ◽  
Cell Layers ◽  
Beet Pulp ◽  
A Cell ◽  
In Sacco

SUMMARYThe in vivo digestibility of soyabean integuments, rape integuments and dehydrated beet pulp was determined in sheep in the Centre de Recherches de Clermont-Ferrand-Theix, in 1985. Organic matter digestibility was 83·5, 59·6 and 85·0%, respectively, for the three feeds. The nylon bag method was used to determine the disappearance of dry matter (DM) in the rumen. After 72 h, 89 and 96% DM had disappeared for soyabean integuments and beet pulp, respectively, but only 61% for rape integuments. The DM disappearance rate was slowest (P < 0·05) for soyabean integuments. Microscopic examination showed that the different layers of the soyabean integument could be ranked in increasing order of resistance to microbial degradation as follows: parenchyma, aleurone layer, column cell layer, palisade layer and epidermis. The hilum area was the most resistant and the only one lignified. The cell layers of the rape integument could be ranked in increasing order of resistance as follows: epidermis, aleurone layer and palisade layer. The last was highly lignified and not degradable. Degradation of beet pulp was fast, occurring first in the parenchyma. The vessels resisted degradation but were only a small part of the feed. This study shows why beet pulp has a low fill value and allows high intake. The soyabean integument is very digestible and is degraded slowly, whereas almost half of the rape integument is made up of a cell layer that is not degradable.

Peroxiredoxin antioxidants in seed physiology

1999 ◽  
Vol 9 (4) ◽  
pp. 285-295 ◽  
Author(s):  
R. B. Aalen
Keyword(s):  
Late Embryogenesis Abundant ◽  
Aleurone Layer ◽  
Oxygen Species ◽  
Transcript Levels ◽  
Aleurone Cells ◽  
Seed Desiccation ◽  
Seed Physiology ◽  
Late Embryogenesis ◽  
High Concentrations ◽  
Mature Seeds

AbstractPeroxiredoxins are thiol–requiring antioxidants found in organisms ranging from bacteria to humans. They can be divided into two subgroups with either one or two conserved cysteine residues. In plants, 1–Cys peroxiredoxins have been identified in a number of grasses and cereals, and in the dicotyledonous speciesArabidopsis thaliana. In contrast to other antioxidants, the 1–Cys peroxiredoxin genes are expressed solely in seeds, and only in the parts of the seeds surviving desiccation, i.e. the embryo and the aleurone layer. The expression pattern is characteristic of late embryogenesis–abundant genes. The PER1 protein of barley is present in high concentrations in the nucleus at the onset of desiccation. 1–Cys genes are expressed in a dormancy–related manner in mature seeds, in that transcript levels are high in imbibed dormant seeds, but disappear upon germination of their non–dormant counterparts. 1–Cys transcript levels can be up–regulated by ABA and osmotic stresses and suppressed by gibberellic acid. Two hypotheses have been put forward on the function of 1–Cys peroxiredoxins in seed physiology. First, these proteins might protect macromolecules of embryo and aleurone cells against damaging reactive oxygen species during seed desiccation and early imbibition. And second, seed peroxiredoxins might play a role in the maintenance of dormancy. These hypotheses are discussed, taking into account present knowledge of the biochemistry and molecular biology of peroxiredoxins.

A Reproducible Selective Stain for Cardiac Sarcoplasmic Reticulum

1974 ◽  
Vol 32 ◽  
pp. 214-215
Author(s):  
R. A. Waugh ◽  
J. R. Sommer
Keyword(s):  
Complex System ◽  
Electron Microscope ◽  
Sarcoplasmic Reticulum ◽  
Transmission Electron Microscope ◽  
Electron Microscopic ◽  
Cardiac Sarcoplasmic Reticulum ◽  
Transmission Electron

Cardiac sarcoplasmic reticulum (SR) is a complex system of intracellular tubules that, due to their small size and juxtaposition to such electron-dense structures as mitochondria and myofibrils, are often inconspicuous in conventionally prepared electron microscopic material. This study reports a method with which the SR is selectively “stained” which facilitates visualizationwith the transmission electron microscope.

Observation of biological macromolecules using various electron microscopic methods

1978 ◽  
Vol 36 (2) ◽  
pp. 170-171
Author(s):  
Mitsuo Ohtsuki ◽  
Michael Sogard
Keyword(s):  
Electron Microscope ◽  
Phase Contrast ◽  
Image Interpretation ◽  
Density Lipoprotein ◽  
Biological Macromolecules ◽  
Contrast Effects ◽  
Biological Structure ◽  
Electron Microscopic ◽  
Structural Investigations ◽  
Staining Techniques

Structural investigations of biological macromolecules commonly employ CTEM with negative staining techniques. Difficulties in valid image interpretation arise, however, due to problems such as variability in thickness and degree of penetration of the staining agent, noise from the supporting film, and artifacts from defocus phase contrast effects. In order to determine the effects of these variables on biological structure, as seen by the electron microscope, negative stained macromolecules of high density lipoprotein-3 (HDL3) from human serum were analyzed with both CTEM and STEM, and results were then compared with CTEM micrographs of freeze-etched HDL3. In addition, we altered the structure of this molecule by digesting away its phospholipid component with phospholipase A2 and look for consistent changes in structure.

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.

Freeze-Fracture Replication in the Ultrastructure of Blue-Green Algae

1967 ◽  
Vol 25 ◽  
pp. 74-75
Author(s):  
L. V. Leak
Keyword(s):  
Cell Wall ◽  
Electron Microscope ◽  
Green Algae ◽  
Three Dimensional ◽  
Freeze Fracture ◽  
Electron Microscopic ◽  
Photosynthetic Membranes ◽  
Blue Green Algae ◽  
Cell Biol ◽  
Cellular Components

Electron microscopic observations of freeze-fracture replicas of Anabaena cells obtained by the procedures described by Bullivant and Ames (J. Cell Biol., 1966) indicate that the frozen cells are fractured in many different planes. This fracturing or cleaving along various planes allows one to gain a three dimensional relation of the cellular components as a result of such a manipulation. When replicas that are obtained by the freeze-fracture method are observed in the electron microscope, cross fractures of the cell wall and membranes that comprise the photosynthetic lamellae are apparent as demonstrated in Figures 1 & 2.A large portion of the Anabaena cell is composed of undulating layers of cytoplasm that are bounded by unit membranes that comprise the photosynthetic membranes. The adjoining layers of cytoplasm are closely apposed to each other to form the photosynthetic lamellae. Occassionally the adjacent layers of cytoplasm are separated by an interspace that may vary in widths of up to several 100 mu to form intralamellar vesicles.

A scanning electron microscopic study on dissolving process of cholesterol gallstones by chenodeoxycholic acid (CDCA)

1978 ◽  
Vol 36 (2) ◽  
pp. 522-523
Author(s):  
T. Kanetaka ◽  
M. Cho ◽  
S. Kawamura ◽  
T. Sado ◽  
K. Hara
Keyword(s):  
Electron Microscope ◽  
Chenodeoxycholic Acid ◽  
Outer Surface ◽  
Electron Microscopic ◽  
Cholesterol Gallstones ◽  
The Core ◽  
Scanning Electron Microscopic Study ◽  
Scanning Electron Microscopic ◽  
Acceleration Voltage ◽  
Scanning Electron

The authors have investigated the dissolution process of human cholesterol gallstones using a scanning electron microscope(SEM). This study was carried out by comparing control gallstones incubated in beagle bile with gallstones obtained from patients who were treated with chenodeoxycholic acid(CDCA).The cholesterol gallstones for this study were obtained from 14 patients. Three control patients were treated without CDCA and eleven patients were treated with CDCA 300-600 mg/day for periods ranging from four to twenty five months. It was confirmed through chemical analysis that these gallstones contained more than 80% cholesterol in both the outer surface and the core.The specimen were obtained from the outer surface and the core of the gallstones. Each specimen was attached to alminum sheet and coated with carbon to 100Å thickness. The SEM observation was made by Hitachi S-550 with 20 kV acceleration voltage and with 60-20, 000X magnification.

Further Observations on the Virus of Epizootic Diarrhea of Infant Mice. An Electron Microscopic Study

1967 ◽  
Vol 25 ◽  
pp. 110-111
Author(s):  
W. G. Banfield ◽  
G. Kasnic ◽  
J. H. Blackwell
Keyword(s):  
Electron Microscope ◽  
Infected Cell ◽  
Microscopic Study ◽  
Intestinal Epithelium ◽  
Ultrastructural Study ◽  
Osmium Tetroxide ◽  
Lead Citrate ◽  
Electron Microscopic ◽  
Virus Particles ◽  
Infected Cells

An ultrastructural study of the intestinal epithelium of mice infected with the agent of epizootic diarrhea of infant mice (EDIM virus) was first performed by Adams and Kraft. We have extended their observations and have found developmental forms of the virus and associated structures not reported by them.Three-day-old NLM strain mice were infected with EDIM virus and killed 48 to 168 hours later. Specimens of bowel were fixed in glutaraldehyde, post fixed in osmium tetroxide and embedded in epon. Sections were stained with uranyl magnesium acetate followed by lead citrate and examined in an updated RCA EMU-3F electron microscope.The cells containing virus particles (infected) are at the tips of the villi and occur throughout the intestine from duodenum through colon. All developmental forms of the virus are present from 48 to 168 hours after infection. Figure 1 is of cells without virus particles and figure 2 is of an infected cell. The nucleus and cytoplasm of the infected cells appear clearer than the cells without virus particles.

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