Influence of antichaotropic electrolytes on the ferricyanide reduction of two immobilized systems: yeast-l-lactate dehydrogenase and chloroplast membranes

Summary The interactions between chloroplast membranes or yeast-l-lactate dehydrogenase and the microenvironment within artificial proteinaceous matrix were investigated. The activities of both immobilized systems were followed by the ferricyanide reduction. The influence of high ionic strength media (0.75 M potassium and sodium citrate, 1.0 M sodium sulphate) was studied. The results show in both immobilized systems an increase of the apparent activity and a better transformation of ferricyanide in the presence of high salt concentrations. Such behaviour can be explained by the high ionic strength of the external media, diffusional constraints and ionic exchange properties of the artificial matrix. The different mobilities of the anions and cations inside the matrix are believed to account for the observed variations in initial activities and stabilities. In particular we demonstrate that citrate and sulphate facilitate the penetration of the ferricyanide to the active reaction centres of the thylakoids and protect them against photoinactivation and denaturation.     

The effects of high concentrations of salts on photosynthetic electron transport in spinach (Spinacia oleracea) chloroplasts.

1. Photosynthetic electron transport from water to lipophilic Photosystem II acceptors was stimulated 3--5-fold by high concentrations (greater than or equal to 1 M) of salts containing anions such as citrate, succinate and phosphate that are high in the Hofmeister series. 2. In trypsin-treated chloroplasts, K3Fe(CN)6 reduction insensitive to 3-(3,4-dichlorophenyl)-1,1-dimethylurea was strongly stimulated by high concentrations of potassium citrate, but there was much less stimulation of 2,6-dichloroindophenol reduction in Tris-treated chloroplasts supplied with 1,5-diphenylcarbazide as artificial donor. The results suggest that the main site of action of citrate was the O2-evolving complex of Photosystem II. 3. Photosystem I partial reactions were also stimulated by intermediate concentrations of citrate (up to 2-fold stimulation by 0.6--0.8 M-citrate), but were inhibited at the highest concentrations. The observed stimulation may have been caused by stabilizaton of plastocyanin that was complexed with the Photosystem I reaction centre, 4. At 1 M, potassium citrate protected O2 evolution against denaturation by heat or by the chaotropic agent NaNO3. 5. It is suggested that anions high in the Hofmeister series stimulated and stabilized electron transport by enhancing water structure around the protein complexes in the thylakoid membrane.     

The effects of high concentrations of salts on photosynthetic electron transport of immobilized thylakoids: Functional stability

Summary Stability studies of photosynthetic activity under continuous saturating illumination are presented. Chloroplast membranes (thylakoids) are isolated in a classical Hepes/sorbitol buffer or in high salt concentration buffers (citrate or sulphate) and then immobilized in a co-crosslinking serum albumin-glutaraldehyde matrix. The activities of these immobilized systems tested in a batch reactor are greatly increased by high concentrations of salts (223 and 277 mol ferrocyanide/mg of chlorophyll per hour for citrate; 243 and 267 mol ferrocyanide/mg of chlorophyll per hour for sulphate, compared with 141 mol ferrocyanide/mg of chlorophyll per hour for sorbitol). In continuous stirred-tank reactors, the conversion rates increase when high concentrations of salts are present in the buffer (approximately 36% for citrate and 34% for sulphate compared with 18% for sorbitol). The functional stability of these immobilized systems during continuous illuminations is higher in citrate (7.5 h) than in sulphate (5.5 h) or sorbitol (3.5 h). These experiments performed in batch or in continuous stirred-tank reactors underline the importance of salt ions in the reaction media.Abbreviations ADP Adénosine diphosphate - ATP Adénosine triphosphate - EDTA Ethylenediaminetetraacetate - Hepes 4-(2-hydroxyethyl)-1 piperazine-ethane sulphonic acid - Sorbitol thylakoids thylakoids isolated in sorbitol buffer - Citrate thylakoids thylakoids isolated in potassium citrate buffer - Sulphate thylakoids thylakoids isolated in sodium sulphate buffer - Immobilized sorbitol thylakoids thylakoids isolated in sorbital buffer and then immobilized in an albumin matrix - Immobilized citrate thylakoids thylakoids isolated in potassium citrate buffer and then immobilized in an albumin matrix - Immobilized sulphate thylakoids thylakoids isolated in sodium sulphate buffer and then immobilized in an albumin matrix - Control thylakoids thylakoids isolated in sorbitol buffer and tested in sorbitol buffer - High salt thylakoids thylakoids isolated in high salt concentration buffer and tested in this buffer     

p-nitroacetophenoxime N-methylcarbamate,a new electron acceptor in isolated thylakoids

p-Nitroacetophenoxime N-methylcarbamate (MCPNA) is a rather potent inhibitor of the electron transfer in spinach class A chloroplasts. In isolated thylakoids, MCPNA is an electron acceptor at the level of photosystem I (PS I). It inhibits O₂ evolution in the presence of NADP and ferredoxin but not the reduction of ferricyanide. MCPNA is active as an acceptor between 3 μM and 100 μM. At concentrations higher than 300 μM, inhibition of photosystem II (PS II) occurs. MCPNA has no uncoupling effect on photophosphorylation. Reduction of MCPNA by thylakoids in the presence of light is in accordance with the E′_o of this compound (??0.57 V) and is followed by an electron transfer to O₂. This reaction probably explains the inhibitory effect of MCPNA on class A chloroplasts.     

Alkaloids as inhibitors of photophosphorylation in spinach chloroplasts

A group of 12 alkaloids were tested as inhibitors of photophosphorylation in spinach chloroplasts. Ajmaline, a dihydroindole alkaloid, was found to be the strongest inhibitor of both cyclic and non-cyclic photophosphorylation. Low concentrations of ajmaline also inhibited the dark and light ATPases, and the coupled electron flow from water to ferricyanide, measured either as ferrocyanide formed or as oxygen evolved, but not the uncoupled electron transport or the pH rise of illuminated unbuffered suspensions of chloroplasts. Higher concentrations of ajmaline stimulated, instead of inhibiting, photosynthetic electron transport or oxygen evolution and decreased the pH rise, thus behaving as an uncoupler, such as ammonia.Photophosphorylation was partially inhibited by 100 μM dihydrosanguinarine, 100 μM dihydrochelerythrine (benzophenanthridine alkaloids); 500 μM O,O'-dimethylmagnoflorine, 500 μM N-methylcorydine (aporphine alkaloids) and 1 mM julocrotine. They also inhibited coupled oxygen evolution and only partially (dihydrosanguinarine and dihydrochelerythrine) or not at all (the other alkaloids) uncoupled oxygen evolution.Spegazzinine (dihydroindole alkaloid), magnoflorine, N-methylisocorydine, coryneine (aporphine alkaloids), candicine and ribalinium chloride were without effect on photophosphorylation at 500 μM.     

The role of photophosphorylation in SO2 and SO 3 2- inhibition of photosynthesis in isolated chloroplasts

Sulphur dioxide inhibits noncyclic photophosphorylation in isolated envelope-free chloroplasts. This inhibition was shown to be reversible and competitive with phosphate, with an inhibitor constant of K_i=0.8mM. The same inhibition characteristics were observed when phosphoglycerate (PGA)- or ribulose-1,5-bisphosphate (RuBP)-dependent oxygen evolution was examined in a reconstituted chloroplast system in the presence of SO ₃ ^2- . Using an ATP-regenerating system (phosphocreatine-creatine kinase), it was demonstrated that the inhibition of PGA-dependent oxygen evolution is solely the result of inhibited photophosphorylation. It is concluded that at low SO₂ and SO ₃ ^2- concentrations the inhibition of photophosphorylation is responsible for the inhibition of photosynthetic oxygen evolution.Abbreviations Chl chlorophyll - PGA D-3-phosphoglyceric acid trisodium salt - Pi inorganic phosphate - RuBP D-ribulose-1,5-bisphosphoric acid tetrasodium salt     

Influence of immobilization procedure and salt environment on functional stability of chloroplast membranes: experimental data and numerical analysis

The interactions between chloroplast membranes and their microenvironment within artificial matrices (albumin-glutaraldehyde matrix, polyurethane foam) where investigated. Particularly, the influence of a high-ionic-strength medium (0.75 M potassium citrate) on the stability of the photosynthetic ferricyanide reduction by immobilized thylakoids has been studied. A method of data analysis based on a nonlinear identification method combined with the numerical integration of the equation of the transient state of the continuous stirred tank reactor (CSTR) is proposed to estimate the actual degradation of the photosynthetic electron transfer. A statistical analysis achieved on the parameter values has allowed a quantitative assessment of the global behavior of immobilized chloroplast membranes. From the mathernatical analysis of the experimental data, we demonstrate that citrate used in the reaction media prevents the photoinactivation of the electron transfer chain whatever the nature of the matrix or the type of the reactor. The use of an albumin-glutaraldehyde matrix or an open reactor during experiments also has allowed a better stabilization of the photosystems under operational conditions.     

Catechols stimulate ferricyanide reduction in chloroplast photosystem II.

In isolated chloroplasts (Spinacia olearacea), where electron transport to Photosystem I is blocked by the plastoquinone antagonist, dibromothymoquinone, lipophilic catechols in concentrations of 50--150 microM stimulate ferricyanide reduction in Photosystem II and associated O2 evolution. Non-permeating catechols, such as Tiron, are unable to stimulate this reaction. Those quinones, such as 2,5-dimethylbenzoquinone, which act as class III electron acceptors, do not lead to stimulation of ferricyanide reduction in Photosystem II or stimulation fo associatied O2 evolution, when electron transport to Photosystem I is blocked by dibromoquinone. Stimulation of ferricyanide reduction is not observed in Tris-treated chloroplasts, implying that electron donation to Photosystem II by catechols is not responsible for the stimulation. Various mechanisms for this stimulation in class II chloroplasts are discussed.     

Sodium chloride stimulated respiration of Anacystis nidulans.

With certain salts a stimulation of respiration of the blue-green alga Anacystis nidulans was found in the dark. The stimulation was observed only at high concentrations (10(-2)M--10(-1)M). NaCl or LiCl are the most effective salts and on addition the increase of the respiration is about 2.5fold. Li is assumed to function as a substitute for Na. Potassium salts, except KCl, are ineffective. The order for the effectiveness is: NaCl greater than NaNO3, Na2SO4 greater than KCl greater than KNO3, K2SO4 (=zero). Accordingly, the cation Na+, and to a less degree the anion Cl- are responsible for the stimulatory effect. K, which is ineffective, is passively accumulated by Anacystis according to the membrane potential. Na is actively extruded. At 0.1 M external NaCl, the passive influx of Na is high, but even then it is balanced by an active efflux. This increases the energy consumption of the cells and leads to a stimulated respiration. With DCCD (N,N'-dicyclohexylcarbodiimide) or NEM (N-ethylmaleimide), the Na efflux is inhibited, simultaneously the stimulation of respiration is abolished and the passive influx of Na becomes detectable. At 0.1 M NaCl, the passive influx of Na measured in presence of DCCD is 5 x 10(-6) moles Na/min and ml packed cells. In absence of DCCD on addition of 0.1 M NaCl the extra oxygen consumption is 2 x 10(-6) moles O2/min and ml cells. This may prove that the stimulation of respiration is mainly caused by the active Na extrusion.     

Effect of potassium salts and distillery effluent on carbon mineralization in soil

Distillery effluent, a rich source of potassium, is used for irrigation at many places in the world. A laboratory experiment was conducted to study the influence of potassium salts present in post-methanation distillery effluent (PME) along with two other salts, KCl and K2SO4, on mineralization of carbon in soil. PME oxidized with H2O2, raw PME, KCl and K2SO4 solutions containing K equivalent to 10%, 20%, 40% and 100% of K present in PME were added to the soil separately, maintaining four replications for each treatment and control. Addition of salts up to a certain concentration stimulated C mineralization but a decline was noticed at higher concentrations. All the levels of salts caused higher CO2 evolution than the control suggesting that the presence of K salts enhanced the microbial activity resulting in increased CO2 evolution. The influence of K2SO4 was significantly higher than KCl in stimulating C mineralization in soil. Oxidized effluent had a higher stimulating effect than inorganic salts, showing the influence of other salts accompanying K in the PME. Raw PME, which contained excess organic C, increased CO2 evolution even at the highest salt level (100% PME) signifying the effect of added C on alleviating the salt stress on microbial activity.     

Effect of High Cation Concentrations on Photosystem II Activities

The effects of wide concentration ranges of NaCl, KCl, and MgCl₂ on ferricyanide reduction and the fluorescence induction curve of isolated spinach (Spinacia oleracea) chloroplasts were investigated. Concentrations of the monovalent salts above 100 mm and MgCl₂ above 25 mm produced a decrease in the rate of ferricyanide reduction by thylakoids uncoupled with 2.5 mm NH₄Cl which cannot be attributed to changes in the primary photochemical capacity of photosystem II. Salt-induced decreases in the effective concentration of the secondary electron acceptor of photosystem II, plastoquinone, reduce the capacity for secondary photochemistry of photosystem II and this could contribute to the reduction in ferricyanide reduction by uncoupled thylakoids at high salinities. The rate of ferricyanide reduction by coupled thylakoids is little affected by salinity changes, indicating that the rate-limiting phosphorylation mechanism in electron flow from water to ferricyanide in coupled thylakoids is salt-tolerant, whereas the rate-limiting reaction in uncoupled ferricyanide reduction is considerably affected by salinity changes. Salt-induced changes in the fluorescence induction curve are interpreted in terms of changes in the rate constants for excitation decay by radiationless transitions, exciton transfer from photosystem II chlorophylls to other associated chlorophyll species, and photochemistry.     

Freezing the effect of eutectic crystallization on biological membranes

Thylakoids from isolated spinach chloroplasts were frozen in the presence of various concentrations of inorganic and organic salts, amino acids and sugars and the kinetics of inactivation of cyclic photophosphorylation with phenazine methosulfate and of electron transport reactions were measured as a function of temperature.During freezing of membranes in the presence of neutral nontoxic compounds membrane damage did not occur until the eutectic temperature was reached. Then photophosphorylation became rapidly inactivated. With weakly membrane-toxic compounds there was a slow inactivation during freezing followed by rapid inactivation at the eutectic temperature. Freezing in the presence of strongly membrane-toxic compounds led to inactivation of photophosphorylation before the eutectic temperature was reached. The temperature at which eutectic crystallization occurred was dependent on the nature of the solutes present. The ratio between solute and membranes was also important: the lower the initial concentration of solutes added to membrane suspensions the lower the temperature at which eutectic solidification occurred. Some compounds such as mannitol crystallized gradually during the decrease in temperature; in this case inactivation of photophosphorylation took place parallel to the crystallization process.In contrast to photophosphorylation, electron transport reactions were not decreased during eutectic freezing in the presence of neutral membrane-protective compounds. Rather a stimulation of electron transport was observed. However, in the presence of inorganic salts or of sodium succinate, electron transport reactions were also inactivated in addition to photophosphorylation during eutectic solidification. This inactivation seems to be a salt effect and may not directly be related to the crystallization process. Various soluble enzymes and the Ca²⁺-dependent ATPase of thylakoids were not affected by eutectic crystallization.The results demonstrate that eutectic crystallization which may take place during freezing is a factor in membrane damage and has to be considered as a possible cause of membrane alterations in in vitro studies on freezing resistance.     

Freezing of isolated thylakoid membranes in complex media: I. The effect of potassium and sodium chloride,nitrate, and sulfate

Thylakoid membranes isolated from spinach leaves (Spinacia oleracea L. cv. Monatol) were subjected to a freeze-thaw cycle in the presence of a buffered medium containing sorbitol as a cryoprotectant and various combinations of potassium and sodium chloride, nitrate, and sulfate. Above a certain total salt concentration, an increase in the concentration of a single electrolyte, or of potassium plus sodium salts with identical anions, always led to a decrease in photophosphorylation activity. A similar effect was obtained with combinations of nitrate plus chloride with identical cations and of KNO₃ plus NaCl. By contrast, in the presence of suitable combinations of NaNO₃ plus KCl, NaNO₃ plus sulfates, and chlorides plus sulfates, inactivation of photophosphorylation was diminished, sometimes dramatically, at initial molarities of nitrate or chloride which alone caused partial or complete membrane damage. When NaNO₃, KCl, and potassium or sodium sulfate were simultaneously present during freezing, thylakoids were affected very little over a wide range of concentration. Diminution or prevention of inactivation of photophosphorylation by suitable combinations of two or more cryotoxic inorganic salts can be explained by postulating that the different solutes act on different sites and that each reduces the concentration of the others by colligative action, together with specific effects of the various electrolytes on individual membrane sites.     

Maleimides stimulate oxygen reduction in illuminated thylakoids

N-ethylmaleimide (NEM) and N,N'-(1,4-phenylene)dimaleimide (PDM) were discovered to stimulate light-induced oxygen uptake in isolated thylakoids, and PDM provided the same stimulation at one order less concentrations. Oxygen uptake rate increased promptly after NEM or PDM addition to thylakoids. The inhibitors of photosynthetic electron transport as well as catalase decreased this rate close to zero, whereas ascorbate increased it almost three-fold. Dithiothreitol suppressed oxygen uptake stimulated by NEM. NEM stimulated light-induced reduction of cytochrome c, and this stimulation was suppressed by superoxide dismutase. It was concluded that NEM and PDM being reduced can effectively reduce molecules O(2) producing superoxide radicals.     

Inhibition and uncoupling of photophosphorylation in isolated chloroplasts by organotin, organomercury and diphenyleneiodonium compounds

1. Trialkyltin, triphenyltin and diphenyleneiodonium compounds inhibited ADP-stimulated O(2) evolution by isolated pea chloroplasts in the presence of phosphate or arsenate. Tributyltin and triphenyltin were the most effective inhibitors, which suggests a highly hydrophobic site of action. Phenylmercuric acetate was a poor inhibitor of photophosphorylation, which suggests that thiol groups are not involved. 2. Triethyltin was a potent uncoupler of photophosphorylation by isolated chloroplasts in media containing Cl(-), but had little uncoupling activity when Cl(-) was replaced by NO(3) (-) or SO(4) (2-), which are inactive in the anion-hydroxide exchange. It is suggested that uncoupling by triethyltin is a result of the Cl(-)-OH(-) exchange together with a natural uniport of Cl(-). Tributyltin, triphenyltin and phenylmercuric acetate had low uncoupling activity, probably because in these compounds the uncoupling activity is partially masked by inhibitory effects. 3. At high concentrations the organotin compounds caused inhibition of electron transport uncoupled by carbonyl cyanide m-chlorophenylhydrazone or NH(4)Cl. At these high concentrations the organotin compounds may be producing a detergent-like disorganization of the membrane structure. In contrast, diphenyleneiodonium sulphate inhibited uncoupled electron transport at low concentrations; however, this inhibition is less than the inhibition of photophosphorylation, which suggests that the compound also inhibits the phosphorylation reactions as well as electron transport. 4. The effects of these compounds on basal electron transport were complex and depended on the pH of the reaction media. However, they can be explained on the basis of three actions: inhibition of the phosphorylation reactions, uncoupling and direct inhibition of electron transport. 5. The inhibition of cyclic photophosphorylation in the presence of phenazine methosulphate by diphenyleneiodonium sulphate shows that it inhibits in the region of photosystem 1.     

Spin label motion in the internal aqueous compartment of spinach thylakoids.

We have measured the motion of the spin label TEMPAMINE (2,2,6,6-tetramethyl piperidine-N-oxyl-4-amine) in the internal aqueous compartment of spinach thylakoids by using potassium ferricyanide (80 mm) to remove TEMPAMINE signals eminating from the external aqueous regions. We found (1): that ferricyanide does not inhibit phosphorylation or electron transport at the concentrations required for TEMPAMINE broadening, but TEMPAMINE acts as a potent uncoupler of electron transport; (2) that TEMPAMINE does not bind detectably to the thylakoid membrane or thylakoid components during the time course of a typical electron spin resonance experiment, but that some binding does occur over a 48-h period to intact thylakoids; (3) that tightly packed intact thylakoids or thylakoids which have been disrupted in a 20% Triton X-100 do not hinder the motion of TEMPAMINE by more than a factor of 1.9; (4) that TEMPAMINE in the presence of 80 mm potassium ferricyanide gives rise to a signal characteristic of TEMPAMINE tumbling isotropically in an aqueous environment with a bulk viscosity of about 10 cP; and (5) that, although ferricyanide leaks slowly into the thylakoid interior, it does not alter the measurement of TEMPAMINE rotation. We conclude that the thylakoid interior is more viscous than bulk water. This may have functional significance regarding transport of electrons from Photosystem II and I to the ATP synthetase.     

The relationship between the S system of blood groups and potassium levels in red blood cells of cattle

Red cell potassium concentrations were determined in 5 breeds of cattle. Most cattle had red cells with less than 50 mmol K/litre and although a few Hereford and Friesian cows had levels approaching 70 mmol K/litre, it was only in the Jersey breed that values above this were found. Attempts were made to correlate potassium levels with serological specificity using cattle S system and sheep M system blood typing reagents. Red cells negative for cattle factors S, H', and S were never positive for sheep L; cells positive for H' were usually positive for M, and those positive for S were always positive for L. No obvious relationship was found between potassium levels and serological type, although some consistent trends were noted in Friesians and Herefords. Limited family data indicated that a major difference in potassium levels of red cells in cattle may be controlled by two codomi-nant alleles.     

Involvement of Thylakoid Overenergization in Tentoxin-Induced Chlorosis in Nicotiana spp

The purpose of this work was to clarify the mechanism of tentoxin-induced chlorosis in Nicotiana spp. seedlings. We found that chlorosis does not correlate with the inhibition of chloroplast ATP synthesis in vivo, since it occurs at tentoxin concentrations far higher than that required for the inhibition of photophosphorylation measured in the same seedlings. However, tentoxin-induced chlorosis does correlate with in vivo overenergization of thylakoids. We show that tentoxin induces overenergization in intact plants and isolated thylakoids, probably via multiple interactions with ATP synthase. Furthermore, gramicidin D, a protonophore that relieves overenergization, also relieves chlorosis. Two lines of evidence suggest that reactive oxygen species may be involved in the process of chlorosis: ascorbate, a quencher of oxygen radicals, significantly protects against chlorosis, whereas transgenic Nicotiana spp. mutants overexpressing chloroplast superoxide dismutase are partially resistant to tentoxin-induced chlorosis. It is proposed that chlorosis in developing seedlings results from overenergization of thylakoids, which leads to the generation of oxygen radicals.     

The photosynthetic partial reactions involved in photoelectrochemical current generation by thylakoid membranes

Summary A thylakoids containing photoelectrochemical cell was used to monitor the photocurrent under photentiostatic mode using specific electron donnors and acceptors, and inhibitors of electron transfer. It is shown that both photosystem I and II can generate a photocurrent under the appropriate conditions. The photocurrent was also monitored in the absence of oxygen evolution thus suggesting a possible application for hydrogenase catalysed hydrogen production.Abbreviations Chl chlorophyll - DCIP 2,6-dichlorophenol-indophenol - DCBQ 2,3-dichlorobenzoquinone - DCMU 3-(3,4-dichlorophenyl)-1, 1-dimethylurea - DPC p-diphenylcarbazide - FeCN potassium ferricyanide     

Effect of osmotic stress on photosynthesis studied with the isolated spinach chloroplast : generation and use of reducing power

The effect of increasing assay medium sorbitol concentration from 0.33 to 1.0 molar on the photosynthetic reactions of intact and broken spinach (Spinacia oleracea L. var. Long Standing Bloomsdale) chloroplasts was investigated by monitoring O₂ evolution supported by the addition of glyceric acid 3-phosphate (PGA), oxaloacetic acid (OAA), 2,5-dimethyl-p-benzoquinone, and 2,6-dichlorophenolindophenol or as O₂ uptake with methyl viologen as acceptor.

Uncoupled 2,6-dichlorophenolindophenol-supported whole chain electron transport (photosystems I and II) was inhibited from the 0.33 molar rate by 14% and 48.6% at 0.67 and 1.0 molar sorbitol in the intact chloroplast and by only 0.4% and 25.0% in the broken chloroplast preparation. Whole chain electron flow from water to other oxidants (OAA, methyl viologen) was also inhibited at increased osmoticum in intact preparations while electron flow from water to methyl viologen, ferricyanide, and NADP in broken preparations did not demonstrate the osmotic response. Electron transport to 2,5-dimethyl-p-benzoquinone (photosystem II) from H₂O and to methyl viologen (photosystem I) from 3,3′-diaminobenzidine were found to be unaffected by osmolarity in both intact and broken preparations.

The stress response was more pronounced (26-38%) with PGA as substrate in the presence of 0.67 molar sorbitol than the inhibition found with uncoupled and coupled linear electron flow. In addition, substrate availability and ATP generated by cyclic photophosphorylation evaluated by addition of Antimycin A were found not to be mediating the full osmotic inhibition of PGA-supported O₂ evolution. In a reconstituted (thylakoids plus stromal protein) chloroplast system to which a substrate level of PGA was added, O₂ evolution was only slightly (7.8%) inhibited by increased osmolarity (0.33-0.67 molar sorbitol) indicating that the level of osmotic inhibition above that contributed by adverse effects on electron flow can be attributed to the functioning of the photosynthetic carbon reduction cycle within the intact chloroplasts.