Electron microscopy of barley root infection by the fungal pathogen Bipolaris sorokiniana

1991 ◽  
Vol 69 (12) ◽  
pp. 2724-2731 ◽  
Author(s):  
H. Carlson ◽  
U. Stenram ◽  
M. Gustafsson ◽  
H.-B. Jansson
Keyword(s):  
Cell Wall ◽  
Bipolaris Sorokiniana ◽  
Root Surface ◽  
Microscopic Investigation ◽  
Electron Microscopic Investigation ◽  
Barley Root ◽  
Outer Cortex ◽  
Electron Microscopic ◽  
Helminthosporium Sativum

An electron microscopic investigation of barley roots infected in vitro by Bipolaris sorokiniana showed the existence of an extracellular sheath on germ tubes and appressoria attached to the root surface. Growth of the fungus in the epidermis and outer cortex was predominantly intracellular, whereas in the inner cortex the hyphae observed were mainly intercellular. Hyphae could not be detected in the stele 24 or 72 h after inoculation. Enzymatic activity in the apex of penetration hyphae is a possible explanation of the electron-dense areas seen in host cell walls 72 h after inoculation. Separation of plasmalemma from cell wall and degeneration of host nuclei and mitochondria were other infection-induced changes commonly seen. A host response to fungal infection involved the development of papillae between the plasma membrane and cell wall of the plant as well as around fungal hyphae. Key words: Bipolaris sorokiniana, Cochliobolus sativus, Helminthosporium sativum, Hordeum vulgare, barley, root, microscopy.

scholarly journals An Electron Microscopic Investigation of the Cell Wall Organization of Conifer Tracheids and Conifer Cambium

1950 ◽  
Vol 3 (3) ◽  
pp. 265 ◽  
Author(s):  
AJ Hodge ◽  
AB Wardrop
Keyword(s):  
Cell Wall ◽  
Microscopic Investigation ◽  
Electron Microscopic Investigation ◽  
Electron Micrograph ◽  
Electron Microscopic ◽  
X Ray ◽  
Inner Surface ◽  
Cell Wall Organization ◽  
Optical Evidence

An electron micrograph of a replica of the inner surface of the secondarycell wall of a conifer tracheid, demonstrating the almost transverse orientationof the microfibrils in this layer, is presented. This evidence provides confirmationof the type of cell wall organization of conifer tracheids proposed inother investigations on the basis of X-ray and optical evidence and of microscopicexamination. The existence of fibrils of 50-100 A in diameter has beendemonstrated in cell wall fragments obtained by the disintegration of cambiuminitials and of conifer tracheids. It is suggested that these microfibrilsmay correspond to the "micelles" or "crystalline regions" inferred from X-rayexamination.

The mechanism of surface growth involved in the differentiation of fibres and tracheids

1954 ◽  
Vol 2 (2) ◽  
pp. 165 ◽  
Author(s):  
AB Wardrop
Keyword(s):  
Cell Wall ◽  
Pinus Radiata ◽  
Microscopic Investigation ◽  
Electron Microscopic Investigation ◽  
Extension Growth ◽  
Potato Tubers ◽  
Electron Microscopic ◽  
Dimensional Changes ◽  
Storage Parenchyma ◽  
Xylem Elements

An electron microscopic investigation has been made of the differentiating xylem elements of Pinus radiata, Eucalyptus elaeophora, and Ulmus sp. In the tips of fibres and tracheids there is a tendency for the microfibrils of cellulose to be oriented in the direction of growth. It is considered that this orientation can be disturbed by subsequent dimensional changes in the cell. The thin areas of the differentiating cells which are involved in the so-called "mosaic growth" have been compared with the regions of the cell wall penetrated by plasmodesmata in the storage parenchyma of potato tubers. The suggestion is made that the thin areas are regions of the cell wall penetrated by plasmodesmata, or are developing primary pit fields. The implications of this concept, with respect to intercellular readjustment and to the differences between fibres and tracheids in extension growth, are discussed.

scholarly journals Cytological, Biochemical, and Transcriptomic Analyses of a Novel Yellow Leaf Variation in a Paphiopedilum (Orchidaceae) SCBG COP15

Genes ◽  
2021 ◽  
Vol 13 (1) ◽  
pp. 71
Author(s):  
Ji Li ◽  
Kunlin Wu ◽  
Lin Li ◽  
Meina Wang ◽  
Lin Fang ◽  
...  
Keyword(s):  
Molecular Mechanisms ◽  
Chloroplast Ultrastructure ◽  
Microscopic Investigation ◽  
Electron Microscopic Investigation ◽  
Color Variation ◽  
Yellow Leaf ◽  
Electron Microscopic ◽  
Chl A ◽  
Leaf Variation

The genus Paphiopedilum, belonging to the Orchidaceae, has high ornamental value. Leaf variations can considerably improve the economic and horticultural value of the orchids. In the study, a yellow leaf mutant of a Paphiopedilum hybrid named P. SCBG COP15 was identified during the in vitro plant culture process; however, little is known about their molecular mechanisms. For this, RNA-seq libraries were created and used for the transcriptomic profiling of P. SCBG COP15 and the yellow mutant. The Chl a, Chl b, and carotenoid contents in the yellow leaves decreased by approximately 75.99%, 76.92%, and 56.83%, respectively, relative to the green leaves. Decreased chloroplasts per cell and abnormal chloroplast ultrastructure were observed by electron microscopic investigation in yellowing leaves; photosynthetic characteristics and Chl fluorescence parameters were also decreased in the mutant. Altogether, 34,492 unigenes were annotated by BLASTX; 1,835 DEGs were identified, consisting of 697 upregulated and 1138 downregulated DEGs. HEMA, CRD, CAO, and CHLE, involved in Chl biosynthesis, were predicted to be key genes responsible for leaf yellow coloration. Our findings provide an essential genetic resource for understanding the molecular mechanism of leaf color variation and breeding new varieties of Paphiopedilum with increased horticultural value.

scholarly journals PROTEIN SYNTHESIS BY ISOLATED PEA NUCLEOLI

1963 ◽  
Vol 18 (1) ◽  
pp. 41-50 ◽  
Author(s):  
Max L. Birnstiel ◽  
Beal B. Hyde
Keyword(s):  
Protein Synthesis ◽  
Amino Acid Mixture ◽  
Microscopic Investigation ◽  
Electron Microscopic Investigation ◽  
Nucleolar Protein ◽  
Acid Mixture ◽  
Electron Microscopic ◽  
Submicroscopic Structure ◽  
Acid And Base

A new method is described for the preparation of active, nucleus-free nucleoli and chromatin in relatively high purity and in sufficient quantities to permit biochemical and electron microscopic investigation. This method consists of disintegrating previously isolated nuclei by grinding with glass beads in an isotonic medium thus liberating structurally intact nucleoli and chromatin threads. Nucleoli and chromatin are then purified by differential centrifugation in Ficoll solutions. A study of the chemical composition, submicroscopic structure, and biological activity of the nucleolar preparation has been made. An equivalent study of the chromatin material has also been carried out in order to assess the significance of chromosomal contamination in nucleolar protein synthesis. The isolated nucleoli rapidly incorporate leucine-C14 into acid and base stable compounds in vitro. Such incorporation lasts for 20 minutes at 37°C and is enhanced by the addition of an energy-regenerating system and a complete amino acid mixture. It is independent of the nuclear Ph 5 enzymes. The bulk of the incorporated label is recovered in the residual, ribosome-like nucleolar protein fraction and a small percentage is found in the acid-extractable basic proteins. The rate of protein synthesis by isolated nucleoli is more rapid than that occurring in the chromatin fraction. This is taken as an additional proof that the nucleolus is the principal site of protein synthesis in the interphase pea nucleus.

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