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Plant cells parenchyma

Niki T, Sakai A Ultrastructural changes related to frost hardiness in the cortical parenchyma cells from mulberry twigs. Plant Cell Physiol 1981 22 171-183. [Pg.172]

Shomer, I., Frenkel, H., and Polinger, C. (1991). The existence of a diffuse electric double layer at cellulose fibril surfaces and its role in the swelling mechanism of parenchyma plant cell walls. Carbohydr. Polym. 16 199-210. [Pg.216]

Plants are predominantly composed of parenchyma and woody tissues. Parenchyma cells dominate the green tissues in leaves and are composed of a protein-rich protoplast surrounded by a cellulose wall. Woody plant cells dominate all support (sclerenchyma) and transport (xylem and phloem) stmctures in a plant. They are composed of several layers (middle lamella, primary wall, secondary wall, and tertiary wall) with varying proportions of cellulose, hemicellulose, and lignin (Fengel and Wegener, 1984). [Pg.4116]

Air pollutants may enter plant systems by either a primary or a secondary pathway. The primary pathway is analogous to human inhalation. Figure 8-2 shows the cross section of a leaf. Both of the outer surfaces are covered by a layer of epidermal cells, which help in moisture retention. Between the epidermal layers are the mesophyll cells—the spongy and palisade parenchyma. The leaf has a vascular bundle which carries water, minerals, and carbohydrates throughout the plant. Two important features shown in Fig. 8-2 are the openings in the epidermal layers called stomates, which are controlled by guard cells which can open and close, and air spaces in the interior of the leaf. [Pg.111]

To study the transcriptional activity of pel and pern genes during pathogenesis, a culture of L37 cells harboring one of the pelA , pelB , pelC , pelD and pelE uidA fusions was inoculated into the leaf parenchyma of African violet pottexi plants. GUS activity, produced by the bacteria present in extractable fluids, was assayed at 3 hour-intervals over a 72 h period after inoculation. [Pg.877]

Fig. 4. Localization of WAP27 and WAP20 in the crude microsome fractions and the relation with marker-enzyme activities in three organelles (ER, tonoplast, and Golgi). SDS-PAGE of fractionated proteins by isopycnic linear sucrose density gradient centrifugation of microsome fraction of mulberry cortical parenchyma cells was performed using 6-pL samples in each fraction. Immunoblot analysis was performed with anti-WAP27 and anti-WAP20 antibodies. (From ref. [1], with permission from the American Society of Plant Physiologists.)... Fig. 4. Localization of WAP27 and WAP20 in the crude microsome fractions and the relation with marker-enzyme activities in three organelles (ER, tonoplast, and Golgi). SDS-PAGE of fractionated proteins by isopycnic linear sucrose density gradient centrifugation of microsome fraction of mulberry cortical parenchyma cells was performed using 6-pL samples in each fraction. Immunoblot analysis was performed with anti-WAP27 and anti-WAP20 antibodies. (From ref. [1], with permission from the American Society of Plant Physiologists.)...
Ukaji N, Kuwabara C, Takezawa D, Arakawa K, Yoshida S, Fujikawa S. Accumulation of small heat shock protein homologs in the endoplasmic reticulum of cortical parenchyma cells in mulberry in association with seasonal cold acclimation. Plant Physiol 1999 120 481-490. [Pg.172]

When the fleck is examined closely, the lesion can be associated with contiguous stomata in the upper surface. Often, the first visible symptom of ozone toxicity is the death of the palisade parenchyma cells that line the cavities directly beneath the upper stomata. In the case of beans (Phaseolus vulgaris L.) or tobacco (Nicotiana tabacum L.) and perhaps other plants, the upper stomata lie in patterns of arcs or circles, while the lower stomata are scattered randomly and regularly across the epidermis. [Pg.77]

Thimm, J. C., Burritt, D. J., Sims, I. M., Newman, R. H., Ducker, W. A., Melton, L. D. (2002). Celery (Apium graveolens) parenchyma cell walls cell walls with minimal xyloglucan. Physiol Plant., 116, 164-171. [Pg.80]

Parenchyma In higher plants, a tissue composed of living thin-walled cells which have the diameters essentially equal and remain capable of cell division after maturity. [Pg.38]

There are several kinds of plant tissues. Undifferentiated, embryonic cells found in rapidly growing regions of shoots and roots form the meristematic tissue. By differentiation, the latter yields the simple tissues, the parenchyma, collenchyma, and scleren-chyma. Parenchyma cells are among the most abundant and least specialized in plants. They give rise through further differentiation to the cambium layer, the growing layer of roots and stems. They also... [Pg.29]

Gossypol has been isolated from the roots, stems, and seeds of the cotton plant and reported as a COX inhibitor based on in vitro assay in neutrophils [165] and an inhibitor of LOX and prostaglandin synthase from rat basophilic leukemia cells [166]. Gossypol showed as a potent inhibitor of leukotrienes B4 and D4 production and also reduced PTF-induced contraction of guinea-pig lung parenchyma [167]. [Pg.697]

In the appropriate culture medium, tissue explants give rise to callus tissue. Callus tissue is comprised of large, thin-walled parenchyma cells. It is similar to the undifferentiated tissue produced by plants as a repair mechanism when they are injured. In tissue culture, dedifferentiated callus can be induced to form plantlets that grow into normal plants. The induction of callus occurs when a sterile explant is brought into contact with a nutrient medium, which contains substances that initiate cell division and support growth. An explant may be a uniform piece of tissue or tissue derived from different cell types (Yeoman, 1973). Storage parenchyma tissue from Jerusalem... [Pg.255]


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