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PEP + CO2 + ADP). , 1980; Chapman and Hatch, 1983), the critical question to answer was the source of the ATP. , 1993) showing that aspartate decarboxylation via oxaloacetate and PEP carboxykinase was linked with the phosphorylation-coupled respiration of malate in bundle sheath mitochondria.

J. and Lorimer, G. H. (1987). Rubisco: structure, mechanisms, and prospects for improvement. In "The Biochemistryof Plants" Vol. 10 (M. D. Hatch and N. K. ), pp. 131-218. Academic Press, New York. Berner, R. A. (1994). 3Geocarb II: A revised model of atmospheric CO2 over Phanerozoic time. Amer. J. Sci. 291, 339-376. Berner, R. , and Canfield, D. E. (1989). A new model for atmospheric oxygen over Phanerozoic time. Amer. J. Sci. 289, 333-361. 1. Why C4 Photosynthesis ? ]5 Cerling, T. , Harris, J.

Pp. 480-547. Springer-Verlag, Berlin. 16 Rowan F. Sage Owensby, C. , Ham, J. , Rice, C. , Coyne, P. I. and Auen, L. M. (1996). Ecosystem-level responses of tallgrass prairie to elevated CO2. In "Carbon Dioxide and Terrestrial Ecosystems" (G. W. Kock and H. A. ), pp. 147-162. Academic Press, San Diego. Peat, H. C. L. (1997). Dynamics of C3 and C4 Productivity in Northern Mixed Grass Prairies. M. Sc. Thesis. University of Toronto, Ontario, Canada. Pierce,J. (1988). Prospects for manipulating the substrate specificity of ribulose bisophosphate carboxylase/oxygenase.

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Cb4s plant biology by Rowan F. Sage, Russell K. Monson, Russell K. Monson


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