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Chloroplast development

Bassi R, Dainese P (1992) In Argyroudy-Akoyonoglou J (ed) Regulation of chloroplast development, Plenium Press New York London p 511... [Pg.177]

Mego, J. L. The effect of hadacidin on chloroplast development in nondividing Euglena cells. Biochem. Biophys. Acta 79, 221 (1964). [Pg.105]

Heintze, A., Goerlach, J., Leuschner, C., Hoppe, R, Hagelstein, R, Schulze-Siebert, D. and Schultz, G. (1990) Rlastidic isoprenoid synthesis during chloroplast development change from metabolic autonomy to division-of-labor stage. Plant Physiol., 93,1121-7. [Pg.293]

Which photoreceptors are involved in light-induced chloroplast development, and how do they function ... [Pg.371]

Once metals have been transported to their target tissue, they need to be distributed within the subcellular compartments where they are required, and need to be safely stored when they are in excess. Nearly 90% of Fe in plants is located in the chloroplasts, where it is required in the electron transfer chain, and in the synthesis of chlorophylls, haem, and Fe—S clusters. Fe, Cu, and Zn are also required in chloroplasts as cofactors for superoxide dismutases to protect against damage by reactive oxygen species during chloroplast development, and Cu is also required in other enzymes including the essential Cu protein plastocyanin. Pathways of intracellular metal transport in plant cells are illustrated in Fig. 8.10. Transport into the chloroplast is best characterised for Cu,... [Pg.162]

A L uffer, Y Inoue and K Shibata (1978) Enhanced charging of thermoiuminescence A band by a combination offiash and continuous iight excitation. In G Akoyunoglou (ed) Proc Intern Sympon Chloroplast Development, pp 379-387. Elsevier... [Pg.418]

Hjy Chloroplasts contain their own DNA and the machinery for replicat-I ing and expressing it. However, chloroplasts are not autonomous they also contain many proteins encoded by nuclear DNA. How did the intriguing relation between the cell and its chloroplasts develop We now believe that, in a manner analogous to the evolution of mitochondria (p. 504), chloroplasts are the result of endosymbiotic events in which a photosynthetic... [Pg.543]

LICHTENTHALER H K, BURKHARDT G, KUHN G and PRENZEL U (1981), Light induced accumulation and stability of chlorophylls and chlorophyll-proteins during chloroplast development in radish seedlings , Z... [Pg.226]

Anandan S, Morishige DT and Thomber JP (1993) Light-induced biogenesis of light-harvesting complex I (LHC I) during chloroplast development in barley (Hordeum vulgare). Plant Physiol 101 227-236... [Pg.35]

C, H, N20 PS, Mr 416.30, isolated from liquid cultures of the plant pathogenic bacterium Pseudomonas syringae pv. tagetis. T. is phytotoxic even at a dose of 20 ng T./plant. T. induces the development of a chlorosis (bleaching) in the shoot tips. The activity is based on an impairment of chloroplast development. [Pg.630]

Impairment of Chloroplast Development and Sink Strength by Blockade of Light in... [Pg.2]

Chloroplast development bp 513-524 Elsevier Amsterdam (1981) Photosynthesis pp 717-737 Balaban Philadelphia... [Pg.618]

Okabe, K. and Schmid, G.H. (1978) in Proceedings of the Intern. Symposium on Chloroplast Development held on the Island Spetsai, Greece (Akoyunoglou,G. and Argyroudi-Akoyunoglou, J.H. eds.) pp. 501-506, Elsevier/North-Holland Biomedical Press, Amsterdam... [Pg.2285]

Chloroplast development is coupled to leaf mesophyll cell development and is controlled, in part, by light (rev. 1, 2, 3). The extent of light control over chloroplast development varies considerably between plant species and leaf type. However, a common sequence of events can be discerned in most plants which leads from undifferentiated proplastids to photosynthetically active chloroplasts (1). This sequence of events has been studied extensively in monocots such as barley because of the spatial separation of stages in chloroplast development in these plants (4-7). Barley leaf cells are produced primarily by a meristematic zone located in the leaf base. These undifferentiated dividing cells contain 10 to 15 proplastids (5, 7). Proplastids accumulate 120 to 150 copies of plastid DNA but exhibit low overall transcription activity (7). Once cells in the leaf base stop dividing they are displaced toward the leaf apex due to cell enlargement and continued formation of cells in the leaf base. During the phase of cell... [Pg.2318]

Two to 16 days of light-induced chloroplast development. LHCPII-proteins (Fig. 2) continue to accumulate up to 10-12 days of greening. In contrast, the relative amount and translatability of LHCPII-mRNA peak by two days of greening and then decline... [Pg.2442]

Mutants which identify nuclear-encoded functions essential to chloroplast development are valuable resources. Transposon mutagenesis using the Mutator system may provide access to some of the nuclear loci which are essential to chloroplast development and, in so doing, reveal patterns of interaction between the nucleus and organelle in eukaryotic systems. The work presented here lays a foundation for the isolation of nuclear loci essential to the assembly of the major components of the photosynthetic apparatus associated with the chloroplast thylakoid membrane. [Pg.2481]

Kasemir, H. and Mohr, H. (1981) In Photosynthesis V Chloroplast Development (G. Akoyunoglou ed.) Balaban Sci. Serv. Phil. Pa. [Pg.2577]


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