Glyoxylate inhibition of ribulosebisphosphate carboxylase/oxygenase activation in intact,lysed, and reconstituted chloroplasts

At bicarbonate concentrations equivalent to air levels of CO₂, activation of ribulosebisphosphate carboxylase/oxygenase (rubisco) was inhibited by micromolar concentrations of glyoxylate in intact, lysed, and reconstituted chloroplasts and in stromal extracts. The concentration of glyoxylate required for 50% inhibition of light activation in intact chloroplasts was estimated to be 35 micromolar. No direct inhibition by glyoxylate was observed with purified rubisco or rubisco activase at micromolar concentrations. Levels of ribulose 1,5-bisphosphate and ATP increased in intact chloroplasts following glyoxylate treatment. Results from experiments with well-buffered lysed and reconstituted chloroplast systems ruled out lowering of pH as the cause of inhibition. With intact chloroplasts, micromolar glyoxylate did not prevent activation of rubisco at high (10 mM) concentrations of bicarbonate, indicating that rubisco could be spontaneously activated in the presence of glyoxylate. These results suggest the existence of a component of the in vivo rubisco activation system that is not yet identified and which is inhibited by glyoxylate.Abbreviations PEP phosphoenolpyruvate - PGA 3-phosphoglycerate - rubisco ribulosebisphosphate carboxylase/oxygenase - RuBP ribulose 1,5-bisphosphate     

Rubisco Activase Activity in Spinach Leaf Extracts

Rubisco activase is a chloroplast stromal protein that catalyzesthe activation of ribulose-1,5- bisphosphate carboxylase/oxygenase(rubisco) in vivo. Activation must occur before rubisco cancatalyze the photosynthetic assimilation of CO₂. In leaves,photosynthesis and rubisco activation increase with increasinglight intensity. Techniques are described that allow the activityof rubisco activase to be measured in extracts of spinach (Spinaceaoleracea L.) leaf tissue. In this context, rubisco activaseactivity is defined as the ability to promote activation ofthe inactive ribulose-1,5- bisphosphate-bound rubisco in anATP-dependent reaction. Determination of rubisco activase activityin extracts of dark and light treated leaf tissue revealed thatthe activation state of rubisco activase was independent oflight intensity. ¹Present address: Department of Biological Sciences, 213 Carson-TaylorHall, Louisiana Tech University, Ruston, Louisiana 71272, U.S.A.     

Influence of Temperature and O2 Concentration on Photosynthesis and Light Activation of Ribulosebisphosphate Carboxylase Oxygenase in Intact Leaves of White Clover (Trifolium repens L.)

Detached leaves of white clover (Trifolium repens L.) were keptfor 1 h under various conditions of temperature, oxygen concentrationand light intensity. Rates of photosynthesis were measured whereappropriate and then ribulosebisphosphate carboxylase oxygenase(RuBPCO) was extracted rapidly and its initial activity measuredimmediately. The extracted activity increased with increased intensity ofillumination of the leaves. Where leaves were pretreated atlow light intensity, the lower the temperature of the leavesthe higher the extracted activity of RuBPCO. At high light intensitytemperature did not affect the activity of subsequently extractedRuBPCO but the light intensity which was necessary for maximumactivity increased with temperature. Activity of RuBPCO fromleaves pretreated in the dark was least when CO₂ was low andtemperature high. Leaves, pretreated at low temperatures andhigh light intensity in 20% O₂, yielded higher activity in extractsthan leaves pretreated under similar conditions but in 2% O₂.A relatively weak temperature response of photosynthesis atlow irradiances was associated with a decrease in extractableRuBPCO activity with increasing temperature. A strong temperaturedependence of the oxygen inhibition of photosynthesis was associatedwith lower extractable RuBPCO activity in leaves pretreatedat low oxygen concentration at low temperatures. With leavesfrom plants grown at low temperatures prior to treatment ofleaves, oxygen inhibition of photosynthesis was less temperaturedependent and activity of RuBPCO in extracts was not decreasedby low O₂ at low temperatures. Differences in the activationof RuBPCO appear to influence photosynthesis and account foran absence of oxygen inhibition of photosynthesis at low temperaturesin plants grown in warm conditions. Key words: Ribulosebisphosphate carboxylase oxygenase activation, Photosynthesis, Temperature, O₂ effect, White clover     

Variation in the Specificity Factor of C3 Higher Plant Rubiscos Determined by the Total Consumption of Ribulose-P2

The specificity factors for ribulose 1, 5-bisphosphate carboxylase/oxygenase(rubisco) from six species of photosynthetic organisms are compared.The values were determined by measuring the oxygen uptake duringthe total consumption of ribulose-P₂ in the presence of variousconcentrations of O₂ and CO₂. The specificity factors determinedin this way were similar to values previously published; smallbut significant differences were found between the specificityfactors of rubisco from C₃ higher plant species. Key words: Specificity factor, total consumption, partitioning, carboxylase oxygenase ratios, ribulose bisphosphate carboxylase, rubisco     

Regeneration of Ribulose 1,5-bisphosphate and Ribulose 1,5-bisphosphate carboxylase/oxygenase Activity Associated with Lack of Oxygen Inhibition of Photosynthesis at Low Temperature

The nature of the lack of oxygen inhibition of C₃-photosynthesisat low temperature was investigated in white clover (Trifoliumrepens L.). Detached leaves were brought to steady-state photosynthesisin air (34 Pa p(CO²), 21 kPa p(O₂), balance N₂) at temperaturesof 20°C and 8°C, respectively. Net photosynthesis, ribulose1,5-bisphosphate (RuBP) and ATP contents, and ribulose 1,5-bisphosphatecarboxylase/oxygenase (RuBPCO) activities were followed beforeand after changing to 2·0 kPa p(O₂). At 20°C, lowering p(O₂) increased net photosynthesis by37%. This increase corresponded closely with the increase expectedfrom the effect on the kinetic properties of RuBPCO. Conversely,at 8°C net photosynthesis rapidly decreased following adecrease in p(O₂) and then increased again reaching a steady-statelevel which was only 7% higher than at 21 kPa p(O₂). The steady-staterates of RuBP and associated ATP consumption were both estimatedto have decreased. ATP and RuBP contents decreased by 18% and33% respectively, immediately after the change in p(O₂) suggestingthat RuBP regeneration was reduced at low p(O₂) due to reducedphotophosphorylation. Subsequently, RuBP content increased again.Steady-state RuBP content at 2·0 kPa p(O₂) was 24% higherthan at 21 kPa p(O₂). RuBPCO activity decreased by 22%, indicatingcontrol of steady-state RuBP consumption by RuBPCO activity. It is suggested that lack of oxygen inhibition of photosynthesisat low temperature is due to decreased photophosphorylationat low temperature and low p(O₂). This may be due to assimilateaccumulation within the chloroplasts. Decreased photophosphorylationseems to decrease RuBP synthesis and RuBPCO activity, possiblydue to an acidification of the chloroplast stroma. Key words: Oxygen inhibition, photosynthesis, ribulose bisphosphate carboxylase/oxygenase     

Effect of oxygen on photosynthesis and biosynthesis of glycolate in photoheterotrophically grown cells of Rhodospirillum rubrum

Photosynthetic CO₂ fixation was studied using cells of Rhodospirillumrubrum grown heterotrophically on malate or butyrate. Ratesof CO₂ fixation were higher in the malategrown cells than inthe butyrate-grown bacteria but ribulosebisphosphate (RUP₂)carboxylase/oxygenase activities were higher in the extractsprepared from the butyrate-grown bacteria. The photosyntheticCO₂ fixation in the butyrate-grown R. rubrum cells was inhibitedby KCN, and the inhibitory effect of O₂ on CO₂ fixation wasreversed when cells were returned to an N₂ atmosphere. In themalate-grown cells, photosynthetic CO₂ fixation was insensitiveto KCN and the inhibitory effect exerted by O₂ was practicallyirreversible. ¹⁴CO₂ was not incorporated into glycolate by either malate-or butyrate-grown cells in an N₂ atmosphere, but small amountsof labeled glycolate were found in malate- and butyrate-growncells in air or 100% O₂. Glycolate excreted by these cells in100% O₂ was measured colorimetrically and its identity establishedby mass spectrometry. When the O₂ atmosphere was labeled with¹⁸O₂, only one of the carboxyl oxygens of the excreted glycolatewas labeled, and the enrichment of ¹⁸O in this carboxyl oxygenrelative to the ¹⁸O₂ provided was greater than 80%. These studiesshow that significant glycolate production by R. rubrum onlyoccurs in the presence of O₂ and that in both malateand butyrate-growncells, the glycolate so formed is presumably produced via RuP₂oxygenase. ¹ Paper No. 46 in the series "Structure and Function of ChloroplastProteins", and research supported in part by research grantsfrom the Japanese Ministry of Education (No. 211113), the TorayScience Foundation (Tokyo), and the Nissan Science Foundation(Tokyo). (Received August 19, 1978; )     

A CO2 Concentrating System in Leaves of Higher C3-Plants Predicted by a Model Based on RuBP Carboxylase/Oxygenase Kinetics and 14CO2/12CO2 Exchange

Mächler, F., Lehnherr, B., Schnyder, H. and Nösberger,J. 1985. A CO₂ concentrating system in leaves of higher C₃-plantspredicted by a model based on RuBP carboxylase/oxygenase kineticsand ¹⁴CO₂/¹²CO₂ exchange.–J. exp. Bot. 36: 1542–1550. A model is presented which compares the ratio of the two activitiesof the enzyme nbulose bisphosphate carboxylase/oxygenase asdetermined in vitro with the ratio of photosynthesis to photorespirationin leaves as determined from differential ¹⁴CO₂/¹²CO₂ uptakeor from CO₂ compensation concentration. Discrepancies betweenmeasurements made in vitro and in vivo are attributed to theeffect of a CO₂ concentrating system in the leaf cells. Interferencefrom dark respiration is discussed. A CO₂ concentrating systemis postulated which is efficient mainly at low temperature andlow CO₂ concentration. Key words: —Photosynthesis, photorespiration, ribulose bisphosphate carboxylase/oxygenase     

Influence of Temperature on the Ratio of Ribulose Bisphosphate Carboxylase to Oxygenase Activities and on the Ratio of Photosynthesis to Photorespiration of Leaves

Lehnherr, B., Mächler, F. and Nösberger, J. 1985.Influence of temperature on the ratio of ribulose bisphosphatecarboxylase to oxygenase activities and on the ratio of photosynthesisto photorespiration of leaves.—J. exp. Bot. 36: 1117–1125. Rates of net and gross photosynthesis of intact white cloverleaves were measured by infrared gas analysis and by short termuptake of ¹⁴CO₂ respectively. Ribulose bisphosphate carboxylaseoxygenase (RuBPCO) was purified from young leaves and kineticproperties investigated in combined and separate assays. Theratio of carboxylase to oxygenase activities was compared withthe ratio of photosynthesis to photorespiration at various temperaturesand CO₂ concentrations. The ratio of photosynthesis to photorespiration at 30 Pa p(CO₂)was consistent with the ratio of carboxylase activity to oxygenaseactivity when each was measured above 20 °C. However, theratio of photosynthesis to photorespiration increased with decreasingtemperature, whereas the ratio of carboxylase to oxygenase activitywas independent of temperature. This resulted in a disagreementbetween the measurements on the purified enzyme and intact leafat low temperature. No disagreement between enzyme and leafat low temperature occurred, when the ratio of photosynthesisto photorespiration was determined at increased CO₂ concentrations. The results suggest an effect of low temperature and low CO₂concentration on the ratio of photosynthesis to photorespirationindependent of the enzyme. Key words: Ribulose bisphosphate carboxylase oxygenase, photorespiration, temperature     

Photosynthetic efficiency of Panicum hians and Panicum milioides in relation to C3 and C4 plants

Panicum hians and Panicum milioides were found to have characteristicsintermediate to those of C₃ and C₄ species with respect to CO₂compensation point, percentage inhibition of photosynthesisby O₂ at various O₂/CO₂ solubility ratios, and water use efficiency.C₄ species have a higher carboxylation efficiency than eitherthe intermediate or C₃ species. During photosynthesis, evenunder 2.5% O₂, C₄ species have a higher affinity for intercellularCO₂ (Km 1.6 µM) apparently due to the initial carboxylationthrough PEP carboxylase. Under low O₂ the intermediate and C₃species had a similar affinity for intercellular CO₂ duringphotosynthesis (Km 5–7 µM) consistent with carboxylationof atmospheric CO₂ through RuDP carboxylase. There were considerablevariation in photosynthesis/unit leaf area at saturating CO₂levels in the species examined which in part is due to differencesin RuDP carboxylase /unit leaf area. The highest rates of photosynthesis/unitleaf area under CO₂-saturating conditions were with the C₃ specieswhich had a correspondingly high level of RuDP carboxylase/unitleaf area. Possibilities for the greater efficiency of P. hiansand P. milioides in comparison to C₃ species in utilizing lowlevels of CO₂ in the presence of atmospheric O₂ are discussed. ¹ This research was supported by the College of Agriculturaland Life Sciences, University of Wisconsin, Madison; and theUniversity of Wisconsin Research Committee with funds from theWisconsin Alumni Research Foundation. (Received June 25, 1977; )     

Limitation to Photosynthesis in Water-stressed Leaves: Stomata vs. Metabolism and the Role of ATP

Decreasing relative water content (RWC) of leaves progressivelydecreases stomatal conductance (g_s), slowing CO₂ assimilation(A) which eventually stops, after which CO₂ is evolved. In somestudies, photosynthetic potential (A_pot), measured under saturatingCO₂, is unaffected by a small loss of RWC but becomes progressivelymore inhibited, and less stimulated by elevated CO₂, below athreshold RWC (Type 1 response). In other studies, A_pot andthe stimulation of A by elevated CO₂ decreases progressivelyas RWC falls (Type 2 response). Decreased A_pot is caused byimpaired metabolism. Consequently, as RWC declines, the relativelimitation of A by g_s decreases, and metabolic limitation increases.Causes of decreased A_pot are considered. Limitation of ribulosebisphosphate (RuBP) synthesis is the likely cause of decreasedA_pot at low RWC, not inhibition or loss of photosynthetic carbonreduction cycle enzymes, including RuBP carboxylase/oxygenase(Rubisco). Limitation of RuBP synthesis is probably caused byinhibition of ATP synthesis, due to progressive inactivationor loss of Coupling Factor resulting from increasing ionic (Mg²⁺)concentration, not to reduced capacity for electron or protontransport, or inadequate trans-thylakoid proton gradient (pH).Inhibition of A_pot by accumulation of assimilates or inadequateinorganic phosphate is not considered significant. DecreasedATP content and imbalance with reductant status affect cellmetabolism substantially: possible consequences are discussedwith reference to accumulation of amino acids and alterationsin protein complement under water stress.     

CO2-Fixation, Glycolate Formation, and Enzyme Activities of Photorespiration and Photosynthesis during Greening and Senescence of Sunflower Cotyledons

Time-courses of ¹⁴CO₂-fixation and of enzyme activities involvedin photorespiration and photosynthesis were determined duringthe life span of cotyledons from sunflower seedlings (Helianthusannuus L.). Glycolate formation in vivo was estimated from theresults of combined labelling and inhibitor experiments. NADPH-glyceraldehyde-3-phosphatedehydrogenase, NADPH-glyoxylate reductase and chlorophyll werewell correlated with the time-course of ¹⁴CO₂-fixation (photosynthesis).There was, however, a considerable discrepancy between the developmentalsequence of photosynthesis and that of both ribulose-l,5-bisphosphatecarboxylase and glycolate oxidase. Furthermore, time-coursesof glycolate oxidase activity in vitro and of glycolate formationin vivo differed significantly. Therefore, the use of glycolateoxidase as a marker for the activity of photorespiration ingreening sunflower cotyledons may be questionable. Results from¹⁴CO₂-labelling experiments with cotyledons treated with theglycolate oxidase inhibitor 2-hydroxy butynoic acid suggestthat glycolate formation relative to CO₂-fixation is reducedin senescent cotyledons. Key words: Development, glycolate oxidase, photorespiration, ribulose-l,5-bisphosphate carboxylase, oxygenase     

Effect of Oxygen and Carbon Dioxide on Photorespiratory Flux Determined from Glycine Accumulation in a Mutant of Arabidopsis thaliana

Exposure to atmospheric conditions which promote photorespirationstrongly inhibits photosynthesis in a mutant of Arabidopsislacking mitochondrial serine transhydroxymethylase activity,and glycine accumulates as a stable end-product of photorespiratorycarbon and nitrogen flow. By providing exogenous serine andammonia to leaves of the mutant, wild-type photosynthesis ratescan be temporarily maintained in the absence of photorespiratoryCO₂ evolution. In these circumstances, the rate of glycine accumulationprovides a direct measure of photorespiratory flux which isnot complicated by the efflux and refixation of photorespiredCO₂, the dilution of radioactive label by endogenous metabolicpools, or non-specific effects of metabolic inhibitors. At thestandard atmospheric concentration of CO₂, the rate of glycineaccumulation in the mutant was proportional to the oxygen concentration,amounting to 53% of the rate of gross CO₂-fixation at 21% O₂.At normal levels of O₂, glycine accumulation was maximal atabout 475 µl CO₂1^–1 and was reduced at higher orlower CO₂ concentrations, being almost abolished at 3000µ1CO₂1^–1. These observations are discussed in the contextof a model of photorespiration based on the properties of ribulose1, 5-bisphosphate carboxylase/oxygenase, and in relation tothe results of previous attempts to measure photorespiration.Preliminary evidence from ¹⁴CO₂-labelling experiments whichsuggests a non-photorespiratory pathway of serine synthesisis also presented. Key words: Arabidopsis mutant, Photorespiration, Serine transhydroxymethylase     

Effect of Oxygen on Photosynthetic 14CO2 Fixation in Chroomonas sp. (Cryptophyta) III: Effect of Oxygen on Photosynthetic Carbon Metabolism

Photosynthetic carbon metabolism was studied with Chroomonassp. cells in which the rate of photosynthesis was inhibitedunder both an anaerobic condition and high concentrations ofoxygen. The time course of ¹⁴C-incorporation into photosyntheticproducts showed that 3-phosphoglycerate was the initial productof photosynthetic CO₂ fixation in Chroomonas sp. cells. During5-min photosynthesis, a considerable amount of ¹⁴C was incorporatedinto the insoluble fraction (mostly cryptomonad starch), andoxygen predominantly affected ¹⁴C-incorporation into this fraction.Although ¹⁴C-incorporation into intermediates of the photorespiratorypathway increased with increasing O₂ concentration, the amountswere much less than expected from the degree of oxygen inhibition.It is noteworthy that ¹⁴C-dihydroxyacetone phosphate accumulatedduring photosynthesis only under the anaerobic condition, whereasthe levels of the other phosphate esters were scarcely affectedby the oxygen concentration. Ribulose-1,5-bisphosphate carboxylase from Chroomonas sp. wascompetitively inhibited by oxygen, and its K_m(CO₂) value wassimilar to those of terrestrial C₃ plant enzymes. (Received November 19, 1984; Accepted May 20, 1985)     

Photosynthetic and Photorespiratory Enzymes in Widely Divergent Plant Species with Special Reference to the Moss Ceratodon purpureus: Properties of Ribulose Bisphosphate Carboxylase/ Oxygenase, Phosphoenolpyruvate Carboxylase and Glycolate Oxidase

Rintamäki, E. and Aro, E.-M. 1985. Photosynthetic and photorespiratoryenzymes in widely divergent plant species with special referenceto the moss Ceratodon purpureus: Properties of ribulose bisphosphatecarboxylase/oxygenase, phosphoenolpyruvate carboxylase and glycolateoxidase.—J. exp. Bot. 36: 1677–1684. Km(CO₂) values and maximal velocities of ribulose bisphosphatecarboxylase/oxygenase (E.C. 4.1.1.39 [EC] ) were determined for sixplant species growing in the wild, consisting of a moss, a fernand four angiosperms. The maximum velocities of the RuBP carboxylasesvaried from 0.13 to 0.;62 µmol CO₂ fixed min^–1 mg^–1soluble protein and the Km(CO₂) values from 15 to 22 mmol m^–3CO₂. The highest Km(CO₂) values found were for the moss, Ceratodonpurpureus, and the grass, Deschampsia flexuosa. These plantsalso had the highest ratios of the activities of RuBP carboxylaseto RuBP oxygenase. Glycolate oxidase (E.C. 1.1.3.1 [EC] ) activitieswere slightly lower in D.flexuosa, but not in C. purpureus,than for typical C₃ species. Phosphoenolpyruvate carboxylase(E.C. 4.1.1.31 [EC] ) was not involved in the photosynthetic carboxylationby these two plants. However, another grass, Phragmites australis,was intermediate in PEP carboxylase activity between C₃ andC₄ plants The properties of RuBP carboxylase/oxygenase are discussedin relation to the activities of PEP carboxylase and glycolateoxidase and to the internal CO₂ concentration. Key words: RuBP carboxylase, oxygenase, Km(CO₂), moss     

Model for the Relationships betweenCO2-Concentrating Mechanism, CO2 Fixation, and Glycolate Synthesis during Photosynthesis in Chlamydomonas reinhardtii

We constructed a mathematical model for simulating the relationshipsof extracellular concentration of dissolved inorganic carbon(DIC), the rates of photosynthetic CO₂ fixation and glycolatesynthesis, and the concentrations of intrachloroplast CO₂ andO₂ in Chlamydomonas reinhardtii. When we compared the photosyntheticrates of I0W-CO₂ (air)-grown C. reinhardtii measured experimentallyand the rates simulated with the incubation conditions in themodel, the model was found to function well. The calculatedrates for glycolate synthesis also matched the measured ratesbetween 80 to 200 µM extracellular DIC, found in the presenceof 1 mM aminooxyacetate. The conformity of the calculated ratesto the measured ones of the glycolate synthesis encouraged usto estimate the O₂ concentration at the active site of ribulosebisphosphate carboxylase/oxygenase; the results were 0.36 and0.40 mM at 80 and 200 µM extracellular DIC, respectively.These high concentrations of O₂ were due to stimulation of photosyntheticCO₂ fixation and further O₂ evolution by a CO₂- concentratingmechanism in the low-CO₂-grown cells. These cells were calculatedto consume 43% of ATP formed photosynthetically for CO₂ concentrationat 200 µM extracellular DIC. The model modified to simulatethese relationships in high-CO₂ (3 to 5% CO₂)-grown C. reinhardtiipredicted O₂ concentration in chloroplasts to be 0.36 mM ina 1% CO₂ atmosphere. This high concentration of O₂ caused activeglycolate synthesis at the measured rate in the high-CO₂-growncells even in the presence of 1% CO₂. The comparisons of themeasured and simulated rates of photosynthesis in low- and high-CO₂-grownC. reinhardtii indicated that no matter how the CO₂ accumulatedin the chloroplasts, it increased the O₂ concentration in theorganelles, and consequently enhanced glycolate synthesis. ¹This paper is the twenty-first in a series on glycolate metabolismin Euglena gracilis. (Received March 11, 1987; Accepted August 17, 1987)     

Photosynthesis and Light Activation of Ribulose 1,5-bisphosphate Carboxylase in the Presence of Starch

Limitation of photosynthesis and light activation of ribulose,1,5-bisphosphate carboxylase (RuBPCO) were examined in the 5thleaf of seedlings of red clover (Trifolium pratense L. cv. Renova)for 5 d following an increase in photosynthetic photon fluxdensity (PPFD) from 200 to 550µmol quanta m^–2 s^–1.Net photosynthesis and its stimulation at 2.0 kPa O₂ initialactivity of rapidly extracted RuBPCO, standard activity of RuBPCOafter incubation of the extracts in the presence of CO₂, Mg²⁺,and inorganic phosphate and contents of soluble protein, starch,soluble sugars, and various photosynthetic metabolites weredetermined. Photosynthesis decreased and starch content increased.No decrease in photosynthesis was found if, when PPFD was increased,all leaves except the investigated 5th leaf were removed, suggestingthat the decrease in photosynthesis was due to accumulated carbohydrates.The stimulation of photosynthesis at 2.0 kPa O₂ did not decreaseand the ratio of the total foliar steady-state contents of triosephosphate to 3-phosphoglycerate increased suggesting that thedecrease in photosynthesis was not due to limiting inorganicphosphate in chloroplasts. Intercellular CO₂ partial pressureand RuBP content were not decreased. Nevertheless, the ratioof photosynthesis to initial RuBPCO activity decreased, suggestingthat the catalysis per active RuBPCO site was decreased. Theincrease in PPFD in the growth cabinet and the PPFD at whichleaves were preconditioned for 1 h, affected not only initialactivity but also the standard activity of RuBPCO. The resultssuggest that a varying proportion of RuBPCO was bound to membranesand was contained in the insoluble fraction of the extracts.A comparison of photosynthesis with extracted RuBPCO activitysuggested that membrane bound RuBPCO did not contribute to photosyntheticCO₂ fixation and that the binding and release to and from membranesmodulated actual RuBPCO activity in vivo. Key words: Photosynthesis, ribulose 1,5-bisphosphate carboxylase, starch     

Response of Soybean Canopy Photosynthesis to CO2 Concentration, Light, and Temperature

Photosynthetic rates of outdoor-grown soybean (Glycine max L.Merr. cv. Bragg) canopies increased with increasing CO₂ concentrationduring growth, before and after canopy closure (complete lightinterception), when measured over a wide range of solar irradiancevalues. Total canopy leaf area was greater as the CO₂ concentrationduring growth was increased from 160 to 990 mm³ dm^–3.Photosynthetic rates of canopies grown at 330 and 660 mm³ CO₂dm^–3 were similar when measured at the same CO₂ concentrationsand high irradiance. There was no difference in ribulose bisphosphatecarboxylase/oxygenase (rubisco) activity or ribulose 1,5-bisphosphate(RuBP) concentration between plants grown at the two CO₂ concentrations.However, photosynthetic rates averaged 87% greater for the canopiesgrown and measured at 660 mm³ CO₂ dm^–3. A 10°C differencein air temperature during growth resulted in only a 4°Cleaf temperature difference, which was insufficient to changethe photosynthetic rate or rubisco activity in canopies grownand measured at either 330 or 660 mm³ CO₂ dm^–3. RuBP concentrationsdecreased as air temperature during growth was increased atboth CO₂ concentrations. These data indicate that the increasedphotosynthetic rates of soybean canopies at elevated CO₂ aredue to several factors, including: more rapid development ofthe leaf area index; a reduction in substrate CO₂ limitation;and no downward acclimation in photosynthetic capacity, as occurin some other species. Key words: CO₂ concentration, soybean, canopy photosynthesis     

Effect of CO2 Concentration During Growth on a CO2 Concentrating Mechanism in White Clover as Predicted from Differential 14CO2/12CO2Uptake

Lehnherr, B. M?chler, F. and N?sberger, J. 1985. Effect of CO₂concentration during growth on a CO₂ concentrating mechanismin white clover as predicted from differential ¹⁴CO₂/¹²CO² uptake.-J. exp. Bot. 36: 1835-1841. White clover was grown at 20 and100 Pa p(CO₂). The CO₂ response of net photosynthesis and differentialuptake of ¹⁴CO₂ and ¹²CO₂ by leaves were measured at varioustemperatures and at various O₂ and CO₂ partial pressures andcompared with predictions from ribulose bisphosphate carboxylase/oxygenasekinetics. Discrepancies between the observed gas exchange characteristicsfor the leaves and those predicted from the enzyme kineticswere interpreted as being due to a CO₂ concentrating mechanism.Plants grown at 20 Pa p(CO₂) showed a higher affinity for CO₂than plants grown at 100 Pa p(CO₂) when measured at 10 ?C. Nodifference in affinity was found at 30 ?C. The postulated CO₂concentrating effect was greater in plants grown at low CO₂than in plants grown at high CO₂ concentration and occurredonly at low temperature and low CO₂ partial pressure. It issuggested that plants grown at the lower CO₂ partial pressurehave a higher affinity for CO₂ due to a more efficient CO₂ concentratingsystem than plants grown at the higher CO₂ partial pressure. Key words: Photosynthesis, CO₂, concentration, RuBP carboxylase/oxygenase     

Effects of Low Concentrations of Sulphur Dioxide on Net Photosynthesis and Dark Respiration of Vicia faba

Rates of net photosynthesis, P_N, and dark respiration of Viciafaba plants were measured in the laboratory in clean air andin air containing up to 175 parts 10^–9 (500 µg m^–3)SO₂. At all SO₂ concentrations exceeding 35 parts 10^–9,P_N was inhibited compared with clean air. At light saturation,the magnitude of inhibition depended on SO₂ concentration butat low irradiances the inhibition was independent of concentration.Dark respiration rates increased substantially, independentof concentration. When exposures continued for up to 3 days,P_N returned to clean air values about 1 h after fumigation ceased:dark respiration recovered after one photoperiod. There wereno visible injuries. Reviewing possible mechanisms responsible for the inhibitionof P_N, it is suggested that SO₂ competes with CO₂ for bindingsites in RuBP carboxylase. Analysis of resistance analoguesdemonstrates that SO₂ altered both stomatal and internal (residual)resistances. A model of crop photosynthesis shows the implications of theobserved responses for the growth of field crops in which plantsare assumed to respond like laboratory plants. Photosynthesisof the crop would be less sensitive than that of individualplants to SO₂ concentration. Daily dry matter accumulation ofhypothetical ‘polluted crops’ would be substantiallyless than clean air values but would vary relatively littlewith SO₂ concentration. It is concluded that physiological basesexist to account for observed reductions in growth of plantsat very low SO₂ concentrations, and that thresholds for plantresponses to SO₂ require reassessment.     

Effect of Methionine Sulfoximine on Photosynthetic Carbon Metabolism in Wheat Leaves

Methionine sulfoximine (MSO) greatly reduced the carbon dioxideexchange rate (CER) of detached wheat (Triticum aestivvm L.cv Roland) leaves in 21% O₂, but only slightly reduced it in2% O₂. A supply of 50 mM NH₄Cl had little effect on the CERirrespective of the O₂ concentration. A simultaneous additionof glutamine and MSO protected against the inhibition of photosynthesisto a considerable extent and caused the accumulation of moreNH₃ than did the addition of MSO alone. Fixation of ¹⁴CO₂ in wheat leaves was inhibited by MSO treatmentin 22% O₂, and there was decreased incorporation of ¹⁴G intoamino acids and sugars and increased label into acid fractions.The addition of MSO and glutamine together eliminated the effectof MSO on the photosynthetic ¹⁴CO₂ fixation pattern. NH₄Cl stimulatedthe synthesis of amino acids from ¹⁴CO₂, especially the synthesisof serine in 22% O₂. Our observations show that factors other than the uncouplingof photophosphorylation by accumulated NH₃ may be responsiblefor the early stage of photosynthesis inhibition by MSO underphotorespiratory conditions. ¹Present address: Department of Agricultural Chemistry, KyushuUniversity, Fukuoka 812 Japan. ²Also at U.S. Department of Agriculture, Agricultural ResearchService, Urbana, Illionois 61801, U.S.A. (Received September 13, 1983; Accepted February 2, 1984)