The fine structure of conidial development in the genus Torula. IV. T. thermophila Cooney & Emerson

1976 ◽  
Vol 22 (8) ◽  
pp. 1102-1112 ◽  
Author(s):  
D. H. Ellis ◽  
D. A. Griffiths
Keyword(s):  
Fine Structure ◽  
Cell Walls ◽  
Secondary Wall ◽  
Wall Layer ◽  
Outer Electron ◽  
Humicola Insolens ◽  
Spore Release ◽  
Transparent Zone ◽  
Conidial Development ◽  
Dense Zone

Torula thermophila produced typical chlamydospores either as intercalary chains within prostrate hyphae or as terminal swellings on short, lateral, hyphal branches. Mature chlamydospores were spherical, dark brown, smooth-surfaced structures with thick, single-layered cell walls (= secondary wall layer) usually differentiated into an outer electron-dense zone and an inner electron-transparent zone. Disarticulation and spore release occurred after the disintegration of the original hyphal wall.The thallospores of T. thermophila arise in a manner different from the blastospores produced by other species of Torula and are structurally more closely related to the spores produced by Humicola insolens. However until further work has been completed on spore development in the Torulu-Humicola complex of fungi the name T. thermophila is retained.

The fine structure of conidial development in the genus Torula. I. T. herbarum (Pers.) Link ex S. F. Gray and T. herbarum f. quaternella Sacc.

1975 ◽  
Vol 21 (11) ◽  
pp. 1661-1675 ◽  
Author(s):  
D. H. Ellis ◽  
D. A. Griffiths
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Cell Walls ◽  
Conidiogenous Cell ◽  
Outer Electron ◽  
Transmission Electron ◽  
Conidial Development ◽  
Dense Zone ◽  
Hyaline Zone ◽  
Lateral Walls

Conidiogenesis in Torula herbarum and T. herbarum f. quaternella was observed by scanning and transmission electron microscopy. Conidia of the former were shown to be made up of three equally sized cells capped by a distinctive, and easily recognizable, conidiogenous cell. Conidiogenous cells also arose terminally on erect hyphae and on prostrate hyphae. The single-layered conidial cell walls were differentiated into an inner hyaline zone and an outer electron-dense zone formed by the deposition of melanin. Conidiogenous cells lacked melanin at the apex and, before conidiation, the lateral walls were strengthened by a further deposition of melanin. The apex bulged outwards and was modified into a new multicelled conidium bearing another apical conidiogenous cell. Continued development of new conidia resulted in an acropetal chain which became disarticulated after cytolysis within the conidiogenous cell. The relative distinctions between holoblastic and enteroblastic development are discussed and it is concluded that the conidia should be referred to as blastoconidia.

scholarly journals Involvement of CesA4, CesA7-A/B and CesA8-A/B in secondary wall formation in Populus trichocarpa wood

2019 ◽  
Vol 40 (1) ◽  
pp. 73-89 ◽  
Author(s):  
Manzar Abbas ◽  
Ilona Peszlen ◽  
Rui Shi ◽  
Hoon Kim ◽  
Rui Katahira ◽  
...  
Keyword(s):  
Solid State ◽  
Mechanical Strength ◽  
Cell Walls ◽  
Secondary Wall ◽  
Populus Trichocarpa ◽  
Wood Formation ◽  
Fiber Cell ◽  
Modulus Of Rupture ◽  
Cellulose Content ◽  
Wall Formation

Abstract Cellulose synthase A genes (CesAs) are responsible for cellulose biosynthesis in plant cell walls. In this study, functions of secondary wall cellulose synthases PtrCesA4, PtrCesA7-A/B and PtrCesA8-A/B were characterized during wood formation in Populus trichocarpa (Torr. & Gray). CesA RNAi knockdown transgenic plants exhibited stunted growth, narrow leaves, early necrosis, reduced stature, collapsed vessels, thinner fiber cell walls and extended fiber lumen diameters. In the RNAi knockdown transgenics, stems exhibited reduced mechanical strength, with reduced modulus of rupture (MOR) and modulus of elasticity (MOE). The reduced mechanical strength may be due to thinner fiber cell walls. Vessels in the xylem of the transgenics were collapsed, indicating that water transport in xylem may be affected and thus causing early necrosis in leaves. A dramatic decrease in cellulose content was observed in the RNAi knockdown transgenics. Compared with wildtype, the cellulose content was significantly decreased in the PtrCesA4, PtrCesA7 and PtrCesA8 RNAi knockdown transgenics. As a result, lignin and xylem contents were proportionally increased. The wood composition changes were confirmed by solid-state NMR, two-dimensional solution-state NMR and sum-frequency-generation vibration (SFG) analyses. Both solid-state nuclear magnetic resonance (NMR) and SFG analyses demonstrated that knockdown of PtrCesAs did not affect cellulose crystallinity index. Our results provided the evidence for the involvement of PtrCesA4, PtrCesA7-A/B and PtrCesA8-A/B in secondary cell wall formation in wood and demonstrated the pleiotropic effects of their perturbations on wood formation.

The Fine Structure of Fossil Plant Cell Walls

Science ◽  
1984 ◽  
Vol 225 (4662) ◽  
pp. 621-623 ◽  
Author(s):  
E. L. SMOOT ◽  
T. N. TAYLOR
Keyword(s):  
Fine Structure ◽  
Plant Cell ◽  
Cell Walls ◽  
Plant Cell Walls ◽  
Fossil Plant

Review — The Orientation of Cellulose Microfibrils in the cell walls of Tracheids in Conifers

IAWA Journal ◽  
2005 ◽  
Vol 26 (2) ◽  
pp. 161-174 ◽  
Author(s):  
Hisashi Abe ◽  
Ryo Funada
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Outer Layer ◽  
Cell Walls ◽  
Secondary Wall ◽  
Middle Layer ◽  
Cellulose Microfibrils ◽  
Conifer Species ◽  
Predominant Orientation ◽  
Scanning Electron

We examined the orientation of cellulose microfibrils (Mfs) in the cell walls of tracheids in some conifer species by field emission-scanning electron microscopy (FE-SEM) and developed a model on the basis of our observations. Mfs depositing on the primary walls in differentiating tracheids were not well-ordered. The predominant orientation of the Mfs changed from longitudinal to transverse, as the differentiation of tracheids proceeded. The first Mfs to be deposited in the outer layer of the secondary wall (S1 layer) were arranged as an S-helix. Then the orientation of Mfs changed gradually, with rotation in the clockwise direction as viewed from the lumen side of tracheids, from the outermost to the innermost S1 layer. Mfs in the middle layer of the secondary wall (S2 layer) were oriented in a steep Z-helix with a deviation of less than 15° within the layer. The orientation of Mfs in the inner layer of the secondary wall (S3 layer) changed, with rotation in a counterclockwise direction as viewed from the lumen side, from the outermost to the innermost S3 layer. The angle of orientation of Mfs that were deposited on the innermost S3 layer varied among tracheids from 40° in a Z-helix to 20° in an S-helix.

Conversaziones 1974

1975 ◽  
Vol 29 (2) ◽  
pp. 163-171
Keyword(s):  
Electron Microscopy ◽  
Fine Structure ◽  
Cell Walls ◽  
Structural Changes ◽  
Vascular Tissue ◽  
Root Systems ◽  
Plant Roots ◽  
Tracer Studies ◽  
Water Move ◽  
Intact Root

CONVERSAZIONES were held this year on 9 May and 27 June. At the first conversazione twenty-seven exhibits and two films were shown. The fine structure of plant roots in relation to transport of nutrient ions and water was demonstrated by Dr D. T. Clarkson of the A.R.C. Letcombe Laboratory, Wantage and Dr A. W. Robards of the Department of Biology, University of York. Two major pathways by which nutrients and water move radially across the cortex towards the central vascular tissue have been distinguished by the use of tracer studies of adsorption by different zones of intact root systems, microautoradiography and electron microscopy. Movement can be apoplastic through cell walls, or symplastic between cells joined by plasmodesmata. As the root ages, structural changes in the endodermis reduce movement in the former pathway but the symplast is not interrupted by the elaboration of endodermal walls because plasmodesmatal connexions remain intact. These observations help explain the contrasting extent to which different ions and water reach the shoot from young and mature parts of root systems.

Localisation structurale et ultrastructurale d'activités peroxydasiques dans les parois du mésophylle et des fibres en cours de lignification chez l'alfa (Stipa tenacissima)

1984 ◽  
Vol 62 (12) ◽  
pp. 2644-2649 ◽  
Author(s):  
M. Harche
Keyword(s):  
Peroxidase Activity ◽  
Oxidase Activity ◽  
Cell Walls ◽  
Secondary Wall ◽  
Outer Part ◽  
Potassium Cyanide ◽  
Primary Wall ◽  
Stipa Tenacissima ◽  
Parenchyma Cells

Using diaminobenzidine as substrate, peroxidase activity was localized in the walls of parenchyma cells and differentiating fibres. In mature fibres and parenchyma a slight activity could be recognized in primary walls only. In parenchyma cells, peroxidase activity was fairly inhibited with heat, potassium cyanide, and aminotriazole, which could indicate the presence of catalase within the cell walls. However, in plasmodesmatal regions peroxidases were- resistant to the above inhibitors. Syringaldazine oxidase activity was present only in the primary wall and the outer part of the secondary wall of differentiating fibres. The parallelism between lignification and peroxidase activity in the secondary walls supports the hypothesis of the involvement of these enzymes in the lignification process.

scholarly journals THE MICROFIBRILLAR STRUCTURE OF THE CELL WALLS OF THE FILAMENTOUS FUNGUS, Allomyces

1960 ◽  
Vol 8 (1) ◽  
pp. 247-256 ◽  
Author(s):  
Jerome M. Aronson ◽  
R. D. Preston
Keyword(s):  
Cell Walls ◽  
Secondary Wall ◽  
Glacial Acetic Acid ◽  
Longitudinal Axis ◽  
Mineral Acid ◽  
Fibrillar Structure ◽  
Electron Diffraction Analysis ◽  
Hydrogen Peroxide Treatment ◽  
Longitudinal Orientation ◽  
Microfibrillar Structure

Cell walls of the fungus, Allomyces, were isolated by chemical procedures, using either potassium permanganate oxidation or glacial acetic acid-hydrogen peroxide treatment followed by dilute mineral acid. The structure of the treated walls was investigated by means of electron microscopy and electron diffraction analysis which showed that rhizoidal walls were especially suitable for observation. Chitin microfibrils exist in the extreme tips of rhizoidal walls, and tend to lie in a preferred longitudinal orientation. Older rhizoidal wall segments show a crossed fibrillar structure under a thin layer of short randomly arranged microfibrils. In the possession of systems of crossed fibrils these walls are like the cell walls of certain green algae. Walls of branch rhizoidal filaments were observed in the early stages of development, in which case the observed microfibrillar orientations are such that it is possible to envisage their origin from pre-existing fibrils that have passively reoriented. With respect to the continued growth of the filaments, however, it is difficult to explain the observed microfibrillar arrangements in terms of the "multi-net" theory. Hyphal walls usually show two layers, the outer consisting of microfibrils arranged randomly, and the inner consisting of well oriented microfibrils running parallel with the longitudinal axis of the hypha. The oriented inner layer appears to be similar in structure to the secondary wall of the Phycomyces sporangiophore.

Ultrastructural development of merosporangia in the mycoparasite Piptocephalis indica

1979 ◽  
Vol 57 (21) ◽  
pp. 2460-2465 ◽  
Author(s):  
Karen K. Baker
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Wall Layer ◽  
Outer Electron ◽  
Early Cleavage ◽  
Single Row ◽  
Transparent Wall ◽  
Cleavage Stages ◽  
Scanning Electron

Transmission and scanning electron microscopy were used to study the ultrastructural development of merosporangia of Piptocephalis indica. Merosporangial branches were initiated from heart-shaped basal-spore initials on dichotomously branched sporangiophores. After elongation, spores were cleaved out of the merosporangial protoplast by simultaneous invagination of the plasmalemma. The plasmalemmal invaginations fused at the center of the merosporangium and delimited a varying number of more or less equal-sized spores in a single row. At maturity. spores had an inner, electron-transparent wall layer and an outer, electron-opaque wall layer. Mature spores possessed scars at each end with the basal spore having scars at each point of merosporangial disarticulation. Fertile branches were highly vacuolated at the time of spore detachment. Development of merosporangiospores in P. indica is similar to that in Syncephalis sphaerica at the early cleavage stages with some differences evident at postcleavage.

CHANGES IN CELL FINE STRUCTURE OF LIMA BEAN AXES DURING EARLY GERMINATION

1966 ◽  
Vol 44 (3) ◽  
pp. 331-340 ◽  
Author(s):  
Shimon Klein ◽  
Yehuda Ben-Shaul
Keyword(s):  
Endoplasmic Reticulum ◽  
Fine Structure ◽  
Cell Walls ◽  
Lipid Droplets ◽  
Lima Bean ◽  
Amorphous Substance ◽  
Golgi Bodies ◽  
Early Germination ◽  
Almost All ◽  
Vacuolar Content

Changes in cell fine structure were studied in axes of green lima bean seeds soaked in water for 1–48 hours. At the beginning of the imbibition period the cortical and pith cells and to a smaller degree the cells of the future conductive tissues contain several vacuoles filled with an amorphous substance. Almost all of the cells contain lipid droplets arranged exclusively along cell walls. The endoplasmic reticulum appears in the form of long tubules, predominantly occupying the peripheral parts of the cell, surrounding the nucleus. A large concentration of ribosomes, mostly unattached, can be found in the cytoplasm. Similar particles make up the bulk of the nucleolus, but could not be found in plastids, which frequently contained starch, but were devoid of internal membranes. Only very few Golgi bodies occur. No changes in fine structure seem to occur during the first 4 hours of imbibition, but after 24 hours the lipid droplets and the vacuolar content have disappeared, the endoplasmic reticulum is more evenly distributed throughout the cells, and a large number of Golgi bodies can be seen.

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.

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