The fine structure of some strains of Humicola Traaen

1974 ◽  
Vol 20 (2) ◽  
pp. 237-239 ◽  
Author(s):  
M. de Bertoldi ◽  
F. Mariotti ◽  
C. Filippi
Keyword(s):  
Cell Wall ◽  
Fine Structure ◽  
Cell Surface ◽  
Outer Wall ◽  
Wall Layer ◽  
The Other ◽  
Electron Microscopic ◽  
Thin Sections ◽  
Different Types ◽  
Microscopic Studies

The fine structure of three unclassified strains of Humicola and of H. grisea has been investigated. The hyphae of all the strains show septa with Woronin bodies of the ascomycetous type. The cytoplasm contains many nuclei per cell, mitochondria, ribosomes, and endoplasmic vesicles, all typical of fungal cells. Electron-microscopic studies of thin sections of mature aleuriospores reveal a thick multilayered cell wall and an accumulation, inside the spore, of β-hydroxybutyrate granules. Aleuriospores exhibit different types of cell surface; the outer wall layer of two strains is smooth, while the outer layer of the other strains is rough because of the presence of melanizing bodies on the cell wall matrix. The fine structure of phialospores and microconidia is also described. Differences in the fine structure among the strains studied are reported.

The fine structure and development of chlamydospores of Fusarium oxysporum

1972 ◽  
Vol 18 (7) ◽  
pp. 997-1002 ◽  
Author(s):  
I. L. Stevenson ◽  
S. A. W. E. Becker
Keyword(s):  
Endoplasmic Reticulum ◽  
Cell Wall ◽  
Fine Structure ◽  
Electron Microscope ◽  
Cell Surface ◽  
Outer Layer ◽  
Outer Wall ◽  
Wall Layer ◽  
Thin Sections ◽  
Hyphal Wall

Methods have been developed for the rapid, reproducible induction of high-density populations of F. oxysporum chlamydospores. On transferring washed pregerminated conidia to a simple two-salts medium, chlamydospore morphogenesis was evident by 12 h and masses of mature spores could be harvested at the end of 4 days. Electron-microscope studies of thin sections of mature chlamydospores reveal a thick triple-layered cell wall. The cytoplasm contains, in addition to large lipid deposits, a nucleus, mitochondria, and endoplasmic reticulum all typical of fungal cells. Chlamydospores of F. oxysporum exhibit two distinct types of cell surface in thin section. The outer wall layer of two of the isolates studied was smooth-surfaced while the outer layer of the two other isolates was distinctly fibrillose. Some evidence is presented suggesting that the fibrillose material arises through the partial breakdown of the original hyphal wall.

Ultracytochemical Localization of Acid Phosphatase in Humicola lutea Conidia and Mycelia

2007 ◽  
Vol 62 (1-2) ◽  
pp. 65-69
Author(s):  
Dimitrina Spasova ◽  
Penka Aleksieva ◽  
Lilyana Nacheva ◽  
Spasimira Radoevska
Keyword(s):  
Cell Wall ◽  
Acid Phosphatase ◽  
Enzymatic Degradation ◽  
Outer Wall ◽  
Wall Layer ◽  
Outer Side ◽  
Electron Microscopic ◽  
Exterior Surface ◽  
The Relationship ◽  
Humicola Lutea

Electron microscopic cytochemical procedures were used to determine the cellular location of acid phosphatase in the fungus Humicola lutea grown in casein-containing medium lacking in mineral orthophosphates. In our investigations acid phosphatase in nongerminating conidia was localized on the outer side of the cell wall, in the cell wall, and on the exterior surface of the plasma membrane. The reaction product of acid phosphatase in germinating conidia was seen in the outer wall layer while in young mycelium on the cell surface and in the exocellular space. The relationship between phosphatase activities localized in the cell wall and their role in the enzymatic degradation of the phosphoprotein casein providing available phosphates for cell growth is discussed.

scholarly journals Acidification of the cytosol inhibits endocytosis from coated pits.

1987 ◽  
Vol 105 (2) ◽  
pp. 679-689 ◽  
Author(s):  
K Sandvig ◽  
S Olsnes ◽  
O W Petersen ◽  
B van Deurs
Keyword(s):  
Cell Surface ◽  
Lucifer Yellow ◽  
Fluid Phase ◽  
Endocytic Pathway ◽  
Electron Microscopic ◽  
Coated Pits ◽  
Internal Ph ◽  
Microscopic Studies ◽  
Epidermal Growth ◽  
In Cells

Acidification of the cytosol of a number of different cell lines strongly reduced the endocytic uptake of transferrin and epidermal growth factor. The number of transferrin binding sites at the cell surface was increased in acidified cells. Electron microscopic studies showed that the number of coated pits at the cell surface was not reduced in cells with acidified cytosol. Experiments with transferrin-horseradish peroxidase conjugates and a monoclonal anti-transferrin receptor antibody demonstrated that transferrin receptors were present in approximately 75% of the coated pits both in control cells and in cells with acidified cytosol. The data therefore indicate that the reason for the reduced endocytic uptake of transferrin at internal pH less than 6.5 is an inhibition of the pinching off of coated vesicles. In contrast, acidification of the cytosol had only little effect on the uptake of ricin and the fluid phase marker lucifer yellow. Ricin endocytosed by cells with acidified cytosol exhibited full toxic effect on the cells. Although the pathway of this uptake in acidified cells remains uncertain, some coated pits may still be involved. However, the data are also consistent with the possibility that an alternative endocytic pathway involving smooth (uncoated) pits exists.

Electron microscopic studies on the formation of vesicular bodies during cell wall degradation and regeneration in yeast

1977 ◽  
Vol 17 (4) ◽  
pp. 293-297
Author(s):  
V. V. Dmitriev ◽  
A. B. Tsiomenko ◽  
E. N. Ratner ◽  
V. K. Akimenko ◽  
B. A. Fikhte
Keyword(s):  
Cell Wall ◽  
Cell Wall Degradation ◽  
Electron Microscopic ◽  
Microscopic Studies

scholarly journals Further Observations on the Fine Structure of Chrysochromulina Ericina Parke & Manton

1961 ◽  
Vol 41 (1) ◽  
pp. 145-155 ◽  
Author(s):  
I. Manton ◽  
G. F. Leedale
Keyword(s):  
Electron Microscopy ◽  
Fine Structure ◽  
Cell Surface ◽  
Light Microscopy ◽  
Flat Plate ◽  
Outer Layer ◽  
Living Cells ◽  
Layered Plates ◽  
Thin Sections ◽  
Micro Anatomy

C. ericina Parke & Manton has been re-investigated to add salient features of micro-anatomy from the electron microscopy of thin sections and also to add photographs of living cells taken with anoptral contrast light microscopy.The most important new observations concern the scales which are shown to be essentially two-layered plates in which the layers in the very large spined scales have become separated except at their edges, with the outer layer greatly hypertrophied to produce a hollow spine with a flared base closed at the bottom by a flat plate. The patterns of external marking on the two layers are very similar in both plate-scales and spines in this species and the orientation of both with respect to the cell surface has been demonstrated by a section of the scales in situ.

Fine structure of Wolffia arrhiza

1973 ◽  
Vol 51 (9) ◽  
pp. 1619-1622 ◽  
Author(s):  
J. L. Anderson ◽  
W. W. Thomson ◽  
J. A. Swader
Keyword(s):  
Fine Structure ◽  
Cell Division ◽  
Vegetative Reproduction ◽  
Guard Cells ◽  
Epidermal Cells ◽  
Electron Microscopic ◽  
Meristematic Cells ◽  
Wolffia Arrhiza ◽  
Microscopic Studies

Light and electron microscopic studies of Wolffia arrhiza L. frond development during vegetative reproduction showed that the fronds were composed entirely of chlorenchymous cells. Chloroplasts in the epidermal cells other than the guard cells were unique in that they contained no starch. Cell division occurred only at the proximal end of daughter fronds early in their development. Meristematic cells contained chloroplasts with clearly defined grana. Proplastids, commonly observed in meristematic cells of apical regions of other plants, were absent in the cells of these plants.

scholarly journals THE CYTOPLASMIC FINE STRUCTURE OF THE DIATOM, NITZSCHIA PALEA

1963 ◽  
Vol 18 (2) ◽  
pp. 429-440 ◽  
Author(s):  
Ryan W. Drum
Keyword(s):  
Cell Wall ◽  
Fine Structure ◽  
Electron Microscope ◽  
Hydrofluoric Acid ◽  
Oil Bodies ◽  
Oil Droplets ◽  
Pennate Diatom ◽  
Thin Sections ◽  
Nitzschia Palea ◽  
Peripheral Cytoplasm

The cytoplasmic fine structure of the motile, pennate diatom, Nitzschia palea was studied in thin sections viewed in the electron microscope. The cells were fixed in OsO4, embedded in methacrylate, and immersed in 10 per cent hydrofluoric acid (HF) for 36 to 40 hours to remove the siliceous cell wall prior to sectioning. The HF treatment did not cause any obvious cytoplasmic damage. The dictyosome complex is perinuclear, and located only in the central cytoplasm. Mitochondria are sparse in the central cytoplasm, but abundant in the peripheral cytoplasm, and fill many of the transvacuolar cytoplasmic strands. Characteristic, amorphous oil bodies fill certain cytoplasmic strands and probably are not leucosin. The pyrenoid appears to be membrane limited, and oil droplets are found adjacent to the pyrenoid. The pyrenoid of another diatom, Cymbella affinis, is also membrane-limited. The membrane limiting the pyrenoid may be a composite of the terminal portions of chloroplast discs, facilitating rapid movement of photosynthate into the pyrenoid matrix, where the characteristic oil droplets may be formed. Carinal fibrils are found singly in each carinal pore, and may be involved in the locomotion of Nitzschia palea.

Method for electron microscopic studies of circulating human leukocytes and observations on their fine structure

1967 ◽  
Vol 20 (5-6) ◽  
pp. 366-382 ◽  
Author(s):  
Itaru Watanabe ◽  
Sheila Donahue ◽  
Norma Hoggatt
Keyword(s):  
Fine Structure ◽  
Electron Microscopic ◽  
Human Leukocytes ◽  
Microscopic Studies

Fine structure during ontogeny of xylem transfer cells in the rhizome of Hieracium floribundum

1975 ◽  
Vol 53 (5) ◽  
pp. 432-438 ◽  
Author(s):  
Edward C. Yeung ◽  
R. L. Peterson
Keyword(s):  
Cell Wall ◽  
Fine Structure ◽  
Wall Layer ◽  
Transfer Cells ◽  
Cellulose Microfibrils ◽  
Tracheary Elements ◽  
Large Vacuole ◽  
Wall Ingrowths ◽  
Cytological Changes ◽  
Thickened Wall

A number of cytological changes occur in rhizome transfer cells with age, the most striking being the appearance of microbodies each with a crystalline nucleoid and the presence of unusual plastids. Plastids in older transfer cells develop one or more electron-translucent regions and lack a defined thylakoid system. The number and size of vacuoles increases until ultimately one large vacuole is formed in old transfer cells. Accompanying these cytological changes in the cytoplasm the wall ingrowths change from being highly involuted and reaching a considerable distance into the cytoplasm of the cell to becoming thicker and less numerous, and finally form a rather uniformly thickened wall layer. The orientation of microfibrils in the thickened cell wall, resulting from the joining of the original wall projections adjacent to the tracheary elements, is random, while the wall thickenings away from the tracheary elements have more orderly arrangements of cellulose microfibrils.

scholarly journals Electron Microscopic Studies of Surface Fine Structure of Papers

1970 ◽  
Vol 24 (10) ◽  
pp. 528-536
Author(s):  
Tadahira Hamada
Keyword(s):  
Fine Structure ◽  
Electron Microscopic ◽  
Microscopic Studies
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