Limitation of Photosynthesis by Carbon Metabolism : I. Evidence for Excess Electron Transport Capacity in Leaves Carrying Out Photosynthesis in Saturating Light and CO(2).

It has been investigated how far electron transport or carbon metabolism limit the maximal rates of photosynthesis achieved by spinach leaves in saturating light and CO(2). Leaf discs were illuminated with high light until a steady state rate of O(2) evolution was attained, and then subjected to a 30 second interruption in low light, to generate an increased demand for the products of electron transport. Upon returning to high light there is a temporary enhancement of photosynthesis which lasts 15 to 30 seconds, and can be up to 50% above the steady state rate of O(2) evolution. This temporary enhancement is only found when saturating light intensities are used for the steady state illumination, is increased when low light rather than darkness is used during the interruption, and is maximal following a 30 to 60 seconds interruption in low light. Decreasing the temperature over the 10 to 30 degrees C range led to the transient enhancement becoming larger. The temporary enhancement is associated with an increased ATP/ADP ratio, a decreased level of 3-phosphoglycerate, and increased levels of triose phosphate and ribulose 1,5-bisphosphate. Since electron transport can occur at higher rates than in steady state conditions, and generate a higher energy status, it is concluded that leaves have a surplus electron transport capacity in saturating light and CO(2). From the alterations of metabolites, it can be calculated that the enhanced O(2) evolution must be accompanied by an increased rate of ribulose 1,5-bisphosphate regeneration and carboxylation. It is suggested that the capacity for sucrose synthesis ultimately limits the maximal rates of photosynthesis, by restricting the rate at which inorganic phosphate can be recycled to support electron transport and carbon fixation in the chloroplast.

[1]  R. Lilley,et al.  The reduction of 3-phosphoglycerate by reconstituted chloroplasts and by chloroplast extracts. , 1974, Biochimica et biophysica acta.

[2]  K. Dietz,et al.  Rate-limiting factors in leaf photosynthesis. I. Carbon fluxes in the calvin cycle , 1984 .

[3]  D. Walker,et al.  POLAROGRAPHIC MEASUREMENT OF PHOTOSYNTHETIC OXYGEN EVOLUTION BY LEAF DISCS , 1981 .

[4]  B. Buchanan Role of light in the regulation of chloroplast enzymes Annu Rev Plant Physiol 31: 341-374 , 1980 .

[5]  G. Lorimer,et al.  Interaction of sugar phosphates with the catalytic site of ribulose-1,5-bisphosphate carboxylase. , 1981, Biochemistry.

[6]  M. Stitt,et al.  Adenine nucleotide levels in the cytosol, chloroplasts, and mitochondria of wheat leaf protoplasts. , 1982, Plant physiology.

[7]  M. Stitt,et al.  On the Participation of Phosphoribulokinase in the Light Regulation of CO(2) Fixation. , 1982, Plant physiology.

[8]  S. Huber,et al.  Phosphate inhibition of spinach leaf sucrose phosphate synthase as affected by glucose-6-phosphate and phosphoglucoisomerase. , 1984, Plant physiology.

[9]  U. Heber,et al.  Changes in the intracellular levels of ATP, ADP, AMP and P1 and regulatory function of the adenylate system in leaf cells during photosynthesis. , 1965, Biochimica et biophysica acta.

[10]  M. Stitt,et al.  Control of Photosynthetic Sucrose Synthesis by Fructose 2,6-Bisphosphate : VI. Regulation of the Cytosolic Fructose 1,6-Bisphosphatase in Spinach Leaves by an Interaction between Metabolic Intermediates and Fructose 2,6-Bisphosphate. , 1985, Plant physiology.

[11]  H. Ziegler,et al.  Adenylate Levels, Energy Charge, and Phosphorylation Potential during Dark-Light and Light-Dark Transition in Chloroplasts, Mitochondria, and Cytosol of Mesophyll Protoplasts from Avena sativa L. , 1982, Plant physiology.

[12]  H. Heldt,et al.  The Chloroplast Envelope: Structure, Function, and Role in Leaf Metabolism , 1981 .