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Leaf Cells

Glucuronomannans. Most glucuronomaimans occur as components of certain plant gums and are characterized by the presence of an 0-(P -D-glucurono-pyranosyl)-(1 2)-D-maimopyranosyl linkage ia the molecule (65). Less complex glucuronomaimans are found in the tissues of bracken Pteridium aquilinum) and in tobacco leaf cells where they may be part of the cultured cell wall (132) and exude into the medium in which the cells are grown (133). [Pg.33]

Major Features of a Higher Plant Cell A Photosynthetic Leaf Cell... [Pg.29]

Fig. 8. Activation of the PO binding with P, infestans cell walls (glucan-specific ) under pathogen inoculation and treatment with salicylic (SA) and jasmonic (JA) acids (A) Peroxidase activity in stomata guard cells and intercellular spaces of adjoining epidermal leaf cells and on the surface of mycelium contacting with the stomata (B). (1) Non-treated control (2) infection (3) treatment with SA (4) treatment with SA + infection (5) treatment with JA (6) treatment with JA + infection (7) treatment with SA + JA (8) treatment with SA + JA + infection g - gifs of P. infestans s - stomata guard cell. Specific to P, infestans cell walls, PO is highlighted. Fig. 8. Activation of the PO binding with P, infestans cell walls (glucan-specific ) under pathogen inoculation and treatment with salicylic (SA) and jasmonic (JA) acids (A) Peroxidase activity in stomata guard cells and intercellular spaces of adjoining epidermal leaf cells and on the surface of mycelium contacting with the stomata (B). (1) Non-treated control (2) infection (3) treatment with SA (4) treatment with SA + infection (5) treatment with JA (6) treatment with JA + infection (7) treatment with SA + JA (8) treatment with SA + JA + infection g - gifs of P. infestans s - stomata guard cell. Specific to P, infestans cell walls, PO is highlighted.
The diversity of responses to water stress may therefore reflect in part the diversity of signals, from turgor and water content of leaf cells, to root perception of soil water content and strength. [Pg.54]

Heilmann, B., Hartung, W. and Gimmler, H. (1980). The distribution of abscisic acid between chloroplasts juid cytoplasm of leaf cells and the permeability of the chloro-plast envelope for abscisic acid. Zeitschrift fur Pflanzenphysiologie, 97, 67-78. [Pg.90]

Tomos, A.D. (1985). The physical limitations of leaf cell expansion. In Control of Leaf Growth, ed. N.R. Baker, W.J. Davies and C. Ong, pp. 1-33. Cambridge Cambridge University Press. [Pg.92]

Boffey, S.A. and Northcote, D.H. (1975) Pectin synthesis during the wall regeneration of plasmolysed tobacco leaf cells. BiochemJ. 150 433-440. [Pg.122]

Turgor pressure of single leaf cells was measured by an improved version of the cell pressure probe according to Husken et al. (7). Mikrocapillaries were pulled on a laser heated pulling device. [Pg.668]

Fig. 1 The fluorescing images of secretory cells under luminescent microscope. A and B. Blue-fluorescing stinging and non-stinging secretory hairs of Urtica dioica, relatively on stem and leaf C and D - green-yellow-fluorescing leaf glandular trichomes of Lycopersicon esculentum and Solanum tuberosum, E. - Blue-fluorescing leaf cells of Achillea millefolium F - yellow fluoresced gland of leaf Calendula officinalis., G., H and I -secretory hairs, idioblasts and crystal on the surface on the root of Ruta graveolens, relatively. Fig. 1 The fluorescing images of secretory cells under luminescent microscope. A and B. Blue-fluorescing stinging and non-stinging secretory hairs of Urtica dioica, relatively on stem and leaf C and D - green-yellow-fluorescing leaf glandular trichomes of Lycopersicon esculentum and Solanum tuberosum, E. - Blue-fluorescing leaf cells of Achillea millefolium F - yellow fluoresced gland of leaf Calendula officinalis., G., H and I -secretory hairs, idioblasts and crystal on the surface on the root of Ruta graveolens, relatively.
SABLOWSKI, R.W.M., BAULCOME, D.C, BEVAN, M., Expression of a flower-specific Myb protein in leaf cells using a viral vector causes ectopic activation of a target promoter, Proc Natl Acad Sci USA, 1996,92, 6901-6905. [Pg.122]

KIM, G.T., TSUKAYA, H., UCHIMIYA, H, The ROTUNDIFOLIA3 gene of Arabidopsis thaliana encodes a new member of the cytochrome P-450 family that is required for the regulated polar elongation of leaf cells, Genes Dev., 1998,12, 2381-91. [Pg.142]

Fig. 9 In vitro metabolism of pyrethroid metabolites in leaf cell suspension of cabbage (C) and tomato (T). The values in parentheses are percent of the total radioactive residues in leaf cell extract/medium after 1-day incubation, nd not detected... Fig. 9 In vitro metabolism of pyrethroid metabolites in leaf cell suspension of cabbage (C) and tomato (T). The values in parentheses are percent of the total radioactive residues in leaf cell extract/medium after 1-day incubation, nd not detected...
Fujisawa T, Matoba Y, Katagi T (2009) Application of separated leaf cell suspension to xenobiotic metabolism in plant. J Agric Food Chem 57 6982-6989... [Pg.201]

Halliwell B. Chloroplast Metabolism. The Structure and Function ofChloroplasts in Green Leaf Cells, Clarendon Press, New York, 1984. [Pg.32]

Harvey DMR, Flowers TJ, Hall JL. Localisation of chloride in leaf cells of the halophyte Suaeda maritima by silver precipitation. NewPhytol 1976 77 319-323. [Pg.289]

Until very recently, high-efficiency chloroplast transformations have been limited to Chlamydomonas and the higher plant Tobaccum. Arabidopsis chloroplasts have been successfully transformed, but none of the regenerated transformed plants were fertile. Chloroplasts from potato leaf cells and rice suspension cells have also been transformed but with poor efficiency as well, and no fertile plants were recovered (Khan et al., 1999 Hibbard et al., 1998). Therefore, a major hurdle is the development of fertile, transgenic, economically important plants. [Pg.66]

A severe mechanical wound on a single leaf of tomato plants initiates a complex series of extracellular and intracellular reactions which result in the synthesis and accumulation of two proteinase Inhibitors, Inhibitors I and II, in leaf cells (J, 2. A second wounding, within a few hours, results in a 2-3 fold Increase in the rates of accumulation initiated by the... [Pg.103]

UDP-Glucose Is the Substrate for Sucrose Synthesis in the Cytosol of Leaf Cells... [Pg.771]

For many biosynthetic reactions that liberate pyrophosphatase activity makes the process more favorable energetically, tending to make these reactions irreversible. In plants, this enzyme is present in plastids but absent from the cytosol. As a result, the cytosol of leaf cells contains a substantial concentration of PP,— enough ( 0.3 him) to make reactions such as that catalyzed by UDP-glucose pyrophosphorylase (Fig. 15-7) readily reversible. Recall from Chapter 14 (p. 527) that the cytosolic isozyme of phosphofructokinase in plants uses PPi, not ATP, as the phosphoryl donor. [Pg.772]

Role of Sedoheptulose 1,7-I5isphosphata.se What effect on the cell and the organism might result from a defect in sedoheptulose 1,7-bisphosphatase in (a) a human hepato-cyte and (b) the leaf cell of a green plant ... [Pg.785]

Much of the work on the identification of carboxylic add complexation has been pioneered by Tiffen. He was the first to positively identify an iron-citrate complex in plant xylem.22 Iron-dtrate complexes have since been identified in a number of plants. The complex formed in these plant fluids is anionic, and Tiffen has shown that a number of other metal ions (Cr, Cu, Ni, Mn and Zn) are also present as anionic complexes.23 Although the neutrality of complexes may be considered a prerequisite for metal ion penetration of membranes, this has not been demonstrated with plant roots or with leaf-cell membranes. Involvement of negatively charged dtrate complexes of Ni11 has been confirmed both for nickel uptake and for translocation in plant species.24 Trisoxalatochro-mate(III) anion has been found in the leaf tissues of a plant species.25... [Pg.962]


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