Handbook of Plant and Crop Physiology

(Steven Felgate) #1

  1. JC Jang, J Sheen. Sugar sensing in higher plants. Plant Cell 6:1665–1679, 1994.

  2. A Krapp, B Hofmann, C Schäfer, M Stitt. Regulation of the expression of rbcSand other photosynthetic genes
    by carbohydrates: A mechanism for the “sink regulation” of photosynthesis? Plant J 3:817–828, 1993.

  3. A Krapp, WP Quick, M Stitt. Ribulose-1,5-bisphosphate carboxylase-oxygenase, other photosynthetic enzymes
    and chlorophyll decrease when glucose is supplied to mature spinach leaves via transpiration stream. Planta
    186:58–69, 1991.

  4. A Krapp, M Stitt. Influence of high-carbohydrate content on the activity of plastidic and cytosolic isoenzyme
    pairs in photosynthetic tissues. Plant Cell Environ 17:861–866, 1994.

  5. J Sheen. Metabolic repression of transcription in higher plants. Plant Cell 2:1027–1038, 1989.

  6. LL Hensel, V Grbic, DA Baumgarten, AB Bleecker. Developmental and age-related processes that influence the
    longevity and senescence of photosynthetic tissues in Arabidopsis. Plant Cell 5:553–564, 1993.

  7. M Stitt, U Sonnewald. Regulation of metabolism in transgenic plants. Annu Rev Plant Physiol Plant Mol Biol
    46:341–368, 1995.

  8. AC Miller, C Schlagnhaufer, M Spalding, S Rodermel. Carbohydrate regulation of leaf development:
    Prolongation of leaf senescence in Rubisco antisense mutants of tobacco. Photosynth Res 63:1–8, 2000.

  9. A Miller, CH Tsai, D Hemphill, M Endres, S Rodermel, M Spalding. Elevated CO 2 effects during leaf
    ontogeny—a new perspective on acclimation. Plant Physiol 115:1195–1200, 1997.

  10. LD Noodén, JW Hillsberg, MJ Schneider. Induction of leaf senescence in Arabidopsis thalianaby long days
    through a light-dosage effect. Physiol Plant 96:491–495, 1996.

  11. B Veierskov. Irradiance-dependent senescence of isolated leaves. Physiol Plant 71:316–320, 1987.

  12. N Dai, A Schaffer, M Petreikov, Y Shahak, Y Giller, K Ratner, A Levine, D Granot. Overexpression of
    Arabidopsishexokinase in tomato plants inhibits growth, reduces photosynthesis, and induces rapid senescence.
    Plant Cell 11:1253–1266, 1999.

  13. CD Dickinson, T Altabella, MJ Chrispeels. Slow-growth phenotype of transgenic tomato expressing apoplastic
    invertase. Plant Physiol 95:420–425, 1991.

  14. EE Goldschmidt, SC Huber. Regulation of photosynthesis by end-product accumulation in leaves of plants
    storing starch, sucrose, and hexose sugars. Plant Physiol 99:1443–1448, 1992.

  15. PG Jones, JC Lloyd, CA Raines. Glucose feeding of intact wheat plants represses the expression of a number of
    Calvin cycle genes. Plant Cell Environ 19:231–236, 1996.

  16. A von Schaewen, M Stitt, R Schmidt, U Sonnewald, L Willmitzer. Expression of a yeast-derived invertase in
    the cell wall of tobacco and Arabidopsisplants leads to accumulation of carbohydrate and inhibition of
    photosynthesis and strongly influences growth and phenotype of transgenic tobacco plants. EMBO J
    9:3033–3044, 1990.

  17. RT Besford, LJ Ludwig, AC Withers. The greenhouse effect: Acclimation of tomato plants growing in high
    CO 2 , photosynthesis and ribulose-1,5-bisphosphate carboxylase protein. J Exp Bot 41:925–931, 1990.

  18. GY Nie, SP Long, RL Garcia, BA Kimball, RL Lamorte, PJ Pinter Jr, GW Wall, AN Webber. Effects of free-
    air CO 2 enrichment on the development of the photosynthetic apparatus in wheat, as indicated by changes in leaf
    proteins. Plant Cell Environ 18:855–864, 1995.

  19. M Pearson, GL Brooks. The influence of elevated CO 2 on growth and age-related changes in leaf gas exchange.
    J Exp Bot 46:1651–1659, 1995.

  20. JJ VanOosten, RT Besford. Some relationships between the gas exchange, biochemistry and molecular biology
    of photosynthesis during leaf development of tomato plants after transfer to different carbon dioxide concentra-
    tions. Plant Cell Environ 18:1253–1266, 1995.

  21. S Rodermel. Subunit control of Rubisco biosynthesis—a relic of an endosymbiotic past? Photosynth Res
    59:105–123, 1999.

  22. CH Tsai, A Miller, M Spalding, SR Rodermel. Source strength regulates an early phase transition of tobacco
    shoot morphogenesis. Plant Physiol 115:907–914, 1997.

  23. RJ Ellis. Protein synthesis by isolated chloroplasts. Biochim Biophys Acta 463:185–215, 1977.

  24. SR Rodermel, MS Abbott, L Bogorad. Nuclear-organelle interactions: Nuclear antisense gene inhibits ribulose
    bisphosphate carboxylase enzyme levels in transformed tobacco plants. Cell 55:673–681, 1988.

  25. S Rodermel, J Haley, CZ Jiang, CH Tsai, L Bogorad. A mechanism for intergenomic integration: Abundance of
    ribulose bisphosphate carboxylase small subunit protein influences the translation of the large subunit mRNA.
    Proc Natl Acad Sci U S A 93:3881–3885, 1996.

  26. WP Quick, U Schurr, R Scheibe, ED Schulze, SR Rodermel, L Bogorad, M Stitt. Decreased ribulose-1,5-bis-
    phosphate carboxylase-oxygenase in transgenic tobacco transformed with “antisense” rbcS. I. Impact on
    photosynthesis in ambient growth conditions. Planta 183:542–554, 1991.

  27. WP Quick, U Schurr, K Fichtner, ED Schulze, SR Rodermel, L Bogorad, M Stitt. The impact of decreased
    Rubisco on photosynthesis, growth, allocation and storage in tobacco plants which have been transformed with
    antisenserbcS. Plant J 1:51–58, 1991.

  28. M Lauerer, D Saftic, WP Quick, C Labate, K Fichtner, ED Schulze, SR Rodermel, L Bogorad, M Stitt.
    Decreased ribulose-1,5-bisphosphate carboxylase-oxygenase in transgenic tobacco transformed with “anti-
    sense”rbcS. VI. Effect on photosynthesis in plants grown at different irradiance. Planta 190:332–345,
    1993.


SOURCE STRENGTH AND LEAF DEVELOPMENT 125

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