By Rowan F. Sage, Russell K. Monson
Because of many matters on the topic of long term carbon dynamics, a far better knowing of the biology of C4 photosynthesis is needed via greater than the normal viewers of crop scientists, plant physiologists, and plant ecologists. This paintings synthesizes the most recent advancements in C4 biochemistry, body structure, systematics, and ecology. The booklet concludes with chapters discussing the function of C4 vegetation sooner or later improvement of the biosphere, fairly their interactive results on soil, hydrological, and atmospheric strategies.
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Additional info for C4 Plant Biology
1995). C4 photosynthesis: Effect of leaf development on the CO2 concentrating mechanism and photorespiration in maize. Plant Physiol. 107, 815-825. Day, D. , and Hatch, M. D. (1981). Transport of 3-phosphoglyceric acid, phosphoenolpyruvate and inorganic phosphate in maize mesophyll chloroplasts and the effect of 3phosphoglycerate on malate and phosphoenolpyruvate production. Arch. Biochem. Biophys. 211, 743-749. Doncaster, H. , and Leegood, R. C. (1987). Regulation of phosphoenolpyruvate carboxylase activity in maize leaves.
1884). "Physiological Plant Anatomy" (Transl. M. Drummond). Macmillan, London. Hatch, M. D. (1971a). Mechanism and function of C4 photosynthesis. In "Photosynthesis and Photorespiration" (M. D. Hatch, C. B. Osmond, and R. O. ), pp. 139-152. Wiley-Interscience, New York. Hatch, M. D. (1971b). The C4 pathway of photosynthesis: Evidence for an intermediate pool of C O 2 and the identity of the donor C 4 dicarboxylic acid. Biochem. J. 125, 425-432. Hatch, M. D. (1977). Light-dark mediated regulation of NADP malate dehydrogenase in isolated chloroplasts from Z.
As I mentioned already, by the time of the meeting held in Canberra in late 1970, there was quite strong support coming from several laboratories for the interpretations put forward at that time to account for C4 photosynthesis in NADP-ME-type grasses at least (Hatch, 1971a). I thought there was reasonably widespread acceptance of these interpretations at that time. However, in the following 3 years a number of papers appeared from one laboratory leading to claims that, in sugarcane and some other NADP-MEtype species, PEP carboxylase was largely confined to nongreen tissues, Rubisco and the PCR-cycle were located in mesophyll cells, and bundle sheath cells functioned only for synthesis and storage of starch (see Coombs and Baldry, 1972).
C4 Plant Biology by Rowan F. Sage, Russell K. Monson