Glycolate Stimulation of Oxygen Evolution During Photosynthesis

Glycolate and glyoxylate stimulated 100% to 300% the rate of oxygen evolution by Scenedesmus in the light in the absence of added carbon dioxide. This stimulation occurred either aerobically or anaerobically, and was sensitive to CMU. Aerobic dark respiration was stimulated 25% to 100% by glycolate. This phenomenon was best demonstrated with synchronized Scenedesmus at the stage of cell division. For glycolate stimulation of oxygen evolution, a dark preincubation of 1 minute or less was necessary. In comparative test with other compounds of metabolism and photosynthesis, the stimulation of oxygen evolution was greatest by glycolate and glyoxylate. In a proposed scheme glyoxylate serves as a terminal hydrogen acceptor from NADPH produced by photosynthesis, and it thereby stimulates oxygen evolution when carbon dioxide is not available. Transformation of glycolate to glyoxylate in these cells would have to occur in the absence of oxygen.     

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     

pH Dependence and Kinetics of Glycolate Uptake by Intact Pea Chloroplasts

Experiments in which [1-¹⁴C]glycolate uptake is carried out in conjunction with measurements of stromal pH indicate that only glycolic acid and not the glycolate anion is crossing the pea (Pisum sativum var. Progress No. 9, Agway) chloroplast envelope. This mechanism of glycolate transport appears to be too slow to account for observed photorespiratory carbon fluxes in C₃ plants.     

The Influence of Extremely High Concentrations of Inorganic P at Varying pH on the Growth and Photosynthesis of Unicellular Algae

An increase in the phosphate concentration due to severe pollution is without real toxic effect for the phytoplankton in eutrophic lakes, although the various species have a variable tolerance against high concentrations. Experiments on photosynthesis and growth were made with cultures of two algae, Chlorella pyrenoidosa and Nitzcshia palea, using phosphate concentrations much higher than ever found in nature. The tolerance decreases with rising pH. This seems not to be due to a higher ratio of secondary phosphate at a high pH. Nor is the rise in the osmotic pressure apparently the cause of the decrease in the growth rate at high phosphate concentrations.     

高海拔地区烟草光合作用的日变化

在高海拔地区(昆明)对5个品种(系)烟草光合作用日变化的研究结果表明,所有供试材料的净光合速率表现为不显著的"双峰型"曲线。其主要原因可能是较高的空气湿度、相对适宜的温度和强光的综合影响;一定范围内的温度和CO₂浓度变化对光合作用的日变化未能产生明显的影响。     

Kinetics of the Daily Rate of Photosynthesis at Low Temperatures for two Conifers

The daily course of photosynthesis at low temperatures in 2 coniferous species, Pinus ponderosa Laws., and Pseudotsuga menziesii (Mirb.) Franco, were studied using controlled environment facilities. After having been grown at a 23° day, and 19° night for a year, seedlings were acclimatized for 4 months to either a 3°, 7° or 11° day all under 1200 ft-c of light and followed by a 16-hour night at 3°. Measurement of photosynthesis at 1200 ft-c revealed 3 separate responses. First, the rapidity at which the plants attained their maximum photosynthesis when the lights were turned on depended upon the species, the current temperature, and the previous temperature condition to which the plants had become acclimatized. The warmer the day temperature the sooner the daily maximum was reached. Second, fluctuations in the rate of photosynthesis during the day varied with the species and the day temperature. Photosynthesis in both fir and pine kept at an 11° day and pines kept at a 7° day attained a daily peak rate followed by a decline. This decline occurred even though temperature and light were kept constant, the CO₂ level was returned to 320 ppm from 290 ppm, and the plants were kept well watered. At a 3° day neither species showed this decline. Third, a plant transferred to another temperature acquired a new stable daily photosynthetic pattern. The number of days required for stabilization depended upon the previous temperature history of the plant. The adjustment rate was faster when the temperature was raised than when it was lowered.     

Glycolate Formation and Excretion by Chlorella pyrenoidosa and Netrium digitus

Conditions are described whereby suspensions of Chlorella pyrenoidosa and Netrium digitus photosynthetically biosynthesize and excrete glycolate continuously in high yields. Aminooxyacetic acid, an inhibitor of pyridoxal phosphate-linked enzymes, increased the excretion of glycolate approximately 4-fold in 1 hour (8 millimolar) and 20-fold in 4 hours (40 millimolar) in the presence of 0.2% CO₂ in air. The amount of glycolate excreted in the presence of aminooxyacetate and an atmosphere of 0.2% CO₂ in air equaled or exceeded the amount excreted in 0.2% CO₂ in O₂ minus aminooxyacetate. CO₂ and light were required for glycolate excretion. Aminooxyacetate also stimulated photosynthetic glycolate excretion in an atmosphere of 0.2% CO₂ in nitrogen or helium, although the stimulation was not as great as when air or O₂ was present.

The excreted glycolate was converted to H₂ and CO₂ by the combined action of glycolic oxidase and the formic hydrogenlyase complex found in Escherichia coli in total conversion yields of 80%.

     

Sequence of Formation of Phosphoglycolate and Glycolate in Photosynthesizing Chlorella pyrenoidosa

In Chlorella pyrenoidosa which have been photosynthesizing in either 1.5% ¹⁴CO₂ or 0.05% ¹⁴CO₂ in air, gassing with 100% O₂ results in rapid formation of phosphoglycolate which is apparently converted to glycolate. However, only about one-third to one-half of the rate of glycolate formation can be accounted for by this route. The remaining glycolate formation may be the result of the oxidation of sugar monophosphates. The rates of formation of both glycolate and phosphoglycolate are about four times greater with algae that have been photosynthesizing in 1.5% ¹⁴CO₂ than with algae which have been photosynthesizing with air, when the algae are then gassed with 100% O₂.     

Formation of nitrosothiols from gaseous nitric oxide at pH 7.4

Nitric oxide (NO) is generated in biological systems and plays important roles as a regulatory molecule. Its ability to bind to haem iron is well known. Moreover, it may lose an electron, forming the nitrosonium ion, involved in the synthesis of S-nitrosothiols (SNOs). It has been suggested that S-nitrosohaemoglobin (-SNO Hb) and low molecular weight SNOs may act as reservoirs of NO. SNOs are formed in vitro, at strongly acidic pH values; however, the mechanism of their formation at neutral pH values is still debated. In this paper we report the anaerobic formation of SNOs (both high- and low-molecular weight) from low concentrations of NO at pH 7.4, provided Hb is also present. We propose a reaction mechanism entailing the participation of Fehaem in the formation of NO(+) and the transfer of NO(+) either to Cysbeta(93) of Hb or to glutathione; we show that this reaction also occurs in human RBCs.     

The Rate of Photosynthesis in Isolated Chloroplasts

Chloroplasts were isolated using aqueous and nonaqueous procedures.Aqueous chloroplasts lost approximately 50 per cent, of theirsoluble proteins during isolation. Nonaqueous chloroplasts retainedall their soluble enzymes, but lost their ability to performthe light reactions of photosynthesis. It was possible to reconstitutea chloroplast system of higher activity by adding soluble enzymesfrom nonaqueous chloroplasts to protein-deficient aqueous chloroplasts.The properties of the reconstituted chloroplast system wereas follows: 1. The CO₂ fixation rate of the reconstituted chloroplast system( 4 µM./. chlorophyll/hr.) was 3–4 times that ofthe aqueous chloroplasts ( I µM./. chlorophyll/hr.). Thefixation of aqueous chloroplasts isapparently limited in partby lack of soluble enzymes. 2. During light-fixation, the reconstituted chloroplast systemaccumulated PGA. This indicates that the reduction of PGA totriosephosphate is a rate-limiting step in this system. 3. It was possible to increase the CO₂ fixation to 12 µM.CO₂/mg. chlorophyll/ hr. by addition of ATP and TPNH to thesystem, but the reduction of PGA was still rate-limiting. 4. Further increase in the fixation rate was obtained by concentratingthe reaction mixture. Part of the striking differences of theCO₂-fixing capabilities of chloroplasts in vivo and in vitrois caused by dilution effects. Extrapolation of the dilutioneffect to the protein concentration which exists in chloroplastsyields a CO₂ fixation rate of approximately 30 µM./mg.chlorophyll/hr. 5. Inhibitors which are located in vivo outside the chloroplastsaffect the CO₂ fixation in vitro. 6. Under consideration of the examined factors which influencethe CO₂ fixation of isolated chloroplasts, it is possible toraise the fixation from approximately 1 per cent, to at least15 per cent, of the fixation in vivo.     

夏季自然高温对桉树光合速率和暗呼吸速率的影响

在湖南夏季的自然高温下,所测7种桉树的日平均净光合速率在12.56～27.85 mg*dm-2*h-1之间,日平均暗呼吸速率在6.06～22.39 mg*dm-2*h-1之间。高温对桉树净光合速率的影响依品种而异。樟脑桉和蓝桉的净光合速率最高峰值出现在35 ℃的气温下,而邓恩桉的净光合速率却受35 ℃气温的显著抑制。桉树暗呼吸速率并不随气温的升高而增大。     

夏季自然高温对桉树光合速率和暗呼吸速率的影响

在湖南夏季的自然高温下,所测7种桉树的日平均净光合速率在12.56～27.85mg·dm     

Glycolate Excretion and the Oxygen to Carbon Dioxide Net Exchange Ratio during Photosynthesis in Chlamydomonas reinhardtii

Chlamydomonas reinhardtii cells were grown in high (5% v/v) or low (0.03% v/v) CO₂ concentration in air. O₂ evolution, HCO₃⁻ assimilation, and glycolate excretion were measured in response to O₂ and CO₂ concentration. Both low- and high-CO₂-grown cells excrete glycolate. In low-CO₂-grown cells, however, glycolate excretion is observed only at much lower CO₂ concentrations in the medium, as compared with high-CO₂-adapted cells. It is postulated that the activity of the CO₂-concentrating mechanism in low-CO₂-grown cells is responsible for the different dependence of glycolate excretion on external CO₂ concentration in low- versus high-CO₂-adapted cells.     

Resistance of Spirulina platensis to Ammonia at High pH Values

Spirulina platensis is an alkalophilic cyanobacterium, exhibitingoptimal growth at pH 9.0 to 10.0. It grows well at pH 11.5 butnot at pH 7.0. Unlike many other photosynthetic microorganisms,it is capable of utilizing ammonia³ even at high pH values,and is resistant to the ammonia-mediated uncoupling of photosynthesis.The entry of ammonia into the cells is pH-dependent, and islimited by a relatively high average internal pH. This highpH value appears to be maintained predominantly by a high intrathylakoidpH. (Received November 20, 1990; Accepted July 3, 1991)     

Enhanced Incorporation of Tritium into Glycolate during Photosynthesis by Tobacco Leaf Tissue in the Presence of Tritiated Water

Tobacco (Nicotiana tabacum var. Havana Seed) leaf discs were allowed to photosynthesize for 3 to 20 minutes in the presence of ¹⁴CO₂ and ³H₂O. Several metabolites of the Calvin cycle and photorespiratory pathway were isolated and purified and the ³H:¹⁴C values measured. Glycolate had a 5- to 10-fold higher ³H:¹⁴C than the Calvin cycle intermediate 3-phosphoglyceric acid, or its end product sucrose. The glycolate oxidase inhibitor α-hydroxy-2-pyridinemethanesulfonic acid caused glycolate to accumulate in the tissue and lowered the ³H:¹⁴C in glycolate to a value similar to that in 3-phosphoglyceric acid. Phosphoglycolate, a possible precursor of glycolate arising from the Calvin cycle, exhibited a ³H:¹⁴C value similar to 3-phosphoglyceric acid under all conditions. The finding of a ³H enrichment in glycolate suggests that another source of glycolate, possibly the reduction of glyoxylate, exists in leaf tissue. Analyses of incorporation of ³H into the pro-2R and pro-2S hydrogens of glycolate, in the presence and absence of α-hydroxy-2-pyridinemethanesulfonic acid, suggest an alternative source of glycolate. Biochemical mechanisms to account for ³H enrichment into glycolate are evaluated.     

The Rate of Apparent Photosynthesis of Whole Sugarcane Plants

The rates of apparent photosynthesis of whole sugarcane plantswhich do not suffer from water stress are linearly related tothe rates of solar radiation on a horizontal surface up to intensitiesof at least 840 Wm^–2. This holds good over a wide rangeof leaf areas from 200 dm² for young plants to 700 dm² for olderplants, and for temperatures in the range 14–35 °C. The amount of CO₂ assimilated per unit area of ground coveredby the leaves, at any intensity of insolation up to 840 Wm^–2,is approximately constant for plants between 3 and 18 monthsold. Thus the assimilation of CO₂ by a crop of sugarcane is linearlyrelated to the intensity of the insolation and the area of groundcovered by green leaves. Very young plants (3 months old) consisting mainly of numerousyoung leaves have apparent photosynthetic rates per unit leafarea which are some 1.5 times those of older plants (7 to 8or 17 to 18 months old) which carry fewer but proportionatelymore mature leaves. Water stress, caused either by under- or over-watering, reducesapparent photosynthetic rates below normal levels. The extentand duration of the reduction depends on the degree of stress. The onset of and recovery from such stresses are illustrated.     

Photosynthesis and Formation of Fats in a Diatom

A study has been made, using C¹⁴ as a tracer, of the variationswhich occur according to the physiological condition of thecells in the distribution of carbon fixed, both in the lightand in the dark, by the diatom Navicula pelliculosa (Bréb.)Hilse during periods of 30 to 300 seconds. Fixation into thefollowing cell fractions was determined: (A) material solublein 80 per cent. ethanol but insoluble in benzene, (B) materialsoluble both in 80 per cent. ethanol and in benzene, and (C)material insoluble in 80 per cent. ethanol. Carbon fixed inphotosynthesis was incorporated, rapidly and in amounts representingup to 70 per cent. of the total fixation, into fractions B andC, as well as into fraction A. Considerable variation was foundin the proportions of carbon entering the three fractions inthe light; in actively growing cells the proportion enteringfraction C preponderated over that in B, corresponding to thesynthesis of protein, whereas in nitrogen-deficient cells fixationin B was the greater, corresponding to the synthesis of fat.These patterns changed only slowly, over periods of days, followingthe transfer of cells to altered conditions of nitrate supply.However, when ammonium nitrogen was supplied to nitrogen-deficientcells a marked change in distribution of carbon fixed occurredwithin 5 minutes, fixation in fraction B falling to a low valueand that in A rising correspondingly. In cells subjected toprolonged nitrogen-deficiency, fixation in fraction B fell toa relatively low value but the proportion which this fractionformed of the total dry matter in the cells rose as a resultof an increased rate of loss from the cells of constituentsother than lipides. The distribution of carbon fixed was alsodependent on light intensity. Fixation in fractions B and Crose relatively to that in A as light intensity was increasedup to 100 foot-candles but fell again at the highest intensityused, 2,000 foot-candles. These results are discussed with particularreference to the relationship between fat accumulation and photosynthesisin algae.     

pH Dependence of Photosynthesis and Photorespiration in Soybean Leaf Cells

The effect of pH on the kinetics of photosynthesis, O(2) inhibition of photosynthesis, and photorespiration was examined with mesophyll cells isolated from soybean (Glycine max [L.] Merr.) leaves. At constant, subsaturating bicarbonate concentration (0.5 mm), O(2) inhibition of photosynthesis increased with increasing pH because high pH shifts the CO(2)-bicarbonate equilibrium toward bicarbonate, thereby reducing the CO(2) concentration. At constant, substrating CO(2) concentrations, cell photorespiration decreased with increasing pH. This was indicated by decreases in the CO(2) compensation concentration, O(2) inhibition of photosynthesis, and glycine synthesis. Km(CO(2)) values for isolated cell photosynthesis and in vitro ribulose-1, 5-diphosphate carboxylase activity decreased with increasing pH, while the Ki(O(2)) for both systems was similar at all pH values. The responses to pH of the corresponding kinetic constants of cell photosynthesis and in vitro RuDP carboxylase with respect to CO(2) and O(2) were identical. This provides additional evidence that the relative rates of photosynthesis and photorespiration in C(3) plants are determined by the kinetic properties of RuDP carboxylase.