Inorganic Phosphate Concentration in the Stroma of Isolated Chloroplasts and Its Influence on Photosynthesis

1987 ◽  
Vol 14 (4) ◽  
pp. 451 ◽  
Author(s):  
SP Robinson ◽  
C Giersch

The concentration of inorganic orthophosphate (Pi) was determined in the stroma of isolated chloroplasts during photosynthesis under Pi-saturated and Pi-limited conditions. Pi was determined calorimetrically or by high performance liquid chromatography of extracts of chloroplasts labelled with 32Pi. When chloroplasts were illuminated in the absence of added Pi, photosynthesis soon declined due to Pi-depletion. After 5 min in the light, photosynthesis had declined to 2% of the maximum rate. At this point, stromal Pi was estimated to be 1.4 mM by the colorimetric method and 0.2 mM by 32P chromatography. Using the colorimetric method, Pi equivalent to approximately 1 mM in the stroma was found to be associated with thylakoid membranes isolated from chloroplasts, irrespective of the Pi content of the intact chloroplasts. This was considered to be a non-metabolic pool of Pi. During steady- state photosynthesis with optimal concentrations of Pi added to the reaction medium, the stromal Pi concentration was estimated to be 2.6 mM and 1.6 mM with the colorimetric and 32P methods, respectively. Measurement of stromal 32Pi in chloroplasts illuminated with varying concentrations of 32Pi in the reaction medium suggested that photosynthesis was saturated at stromal Pi concentrations above 2.0-2.5 mM. Photophosphorylation by thylakoid membranes was saturated at Pi concentrations above 1.2-1.5 mM. It is concluded that, during photosynthesis in isolated chloroplasts in the presence of an optimal supply of Pi from the reaction medium, the stromal Pi concentration is just above that required to saturate photophosphorylation. Any decrease in the supply of Pi from the medium results in a rapid decrease in stromal Pi to the point where photophosphorylation may become Pi-limited, decreasing the rate of CO2 fixation.

1978 ◽  
Vol 5 (4) ◽  
pp. 425 ◽  
Author(s):  
SP Robinson ◽  
JT Wiskich ◽  
LG Paleg

The effects of indoleactic acid (IAA) on CO2 fixation, electron transport and photophosphorylation were examined. The rate of CO2 fixation by preparations of intact chloroplasts was not significantly increased by the addition of IAA (0.2 - 5 �M). Electron transport and coupled phosphorylations were similarly unaffected when measured with ferricyanide or methyl viologen as the electron acceptor. Cyclic phosphorylntion mediated by phenazine methosulfate was also not increased by IAA. It is concluded that the hormone does not affect photosynthesis by isolated chloroplasts in short-term experiments and that the increased CO2 uptake observed with leaves following application of IAA may result from some effect of the hormone other than a direct interaction with the chloroplasts.


1969 ◽  
Vol 63 (2) ◽  
pp. 195-201 ◽  
Author(s):  
Carmen I. Asencio ◽  
Arturo Cedeño-Maldonado

Low concentrations of Cadmium inhibit the electron transport and CO2 fixation reactions of isolated chloroplasts. CO2 fixation is more sensitive to Cd than electron transport and dark pre-incubation increases the degree of toxicity to both. Carbonic anhydrase, an enzyme associated with CO2 fixation, is very sensitive to Cd either when applied directly to partially purified preparations of the enzyme or when enzyme preparations are obtained from intact chloroplasts previously exposed to Cd. Strong inhibition occurs at Cd concentrations lower than those required to inhibit any of the electron transport dependent reactions studied. These results are interpreted as evidence that carbonic anhydrase is one of the most sensitive sites of Cd action in isolated chloroplasts.


1984 ◽  
Vol 39 (6) ◽  
pp. 627-633 ◽  
Author(s):  
Ji-yu Ye ◽  
U. Heber

The effect of aureomycin on photosynthesis was investigated. This antibiotic which has been reported to stimulate photosynthesis at very low concentrations is an effective inhibitor at higher concentrations. In mesophyll protoplasts and isolated chloroplasts from spinach, 50% inhibition of CO2 reduction required about 20 μᴍ aureomycin. The reduction of 3-phosphoglycerate and of oxaloacetate by intact chloroplasts was also inhibited, but not that of nitrite and methylviologen which was actually stimulated. NADP reduction by broken chloroplasts and methylviologen- dependent photophosphorylation were also sensitive to aureomycin. The electrochromic shift at 518 nm which indicates formation of a light-dependent membrane potential was suppressed in the presence of 200 μᴍ aureomycin and the transthylakoid proton gradient was decreased. The data confirm reports that aureomycin has uncoupling properties, and they indicate that it also acts as an inhibitor of ferredoxin/NADP reductase.


1986 ◽  
Vol 32 (6) ◽  
pp. 1004-1006 ◽  
Author(s):  
D J VanderJagt ◽  
P J Garry ◽  
W C Hunt

Abstract Ascorbic acid was measured in 125 plasma samples by an automated colorimetric method involving dichlorophenolindophenol and by a "high-performance" liquid-chromatographic procedure with electrochemical detection. The two methods gave comparable results for samples with ascorbate concentrations of 1 to 20 mg/L (r = 0.97). We also measured the amount of total ascorbate (ascorbic acid + dehydroascorbic acid) in the same samples by a liquid-chromatographic procedure with precolumn derivitization of ascorbic acid. We confirmed that plasma contains little dehydroascorbic acid.


1965 ◽  
Vol 20 (9) ◽  
pp. 890-898 ◽  
Author(s):  
W. Urbach ◽  
M. A. Hudson ◽  
W. Ullrich ◽  
K. A. Santarius ◽  
U. Heber

The distribution of phosphoglyceric acid (PGA) * between chloroplasts and cytoplasm of leaf cells during transients from dark to light and vice versa has been investigated. The data indicate that pools of PGA in the chloroplasts and cytoplasm are interchangeable and that PGA may function as a transport metabolite in actively metabolising leaf cells. These views are supported by the following results:1. In the presence of 14CO2 and light, labelled PGA rapidly appears in the cytoplasm, even though the carboxydismutase reaction, in which 14C enters into PGA, proceeds in the chloroplasts.2. After less than 1 min. illumination in the presence of 14CO2, the distribution of labelled PGA between chloroplasts and cytoplasm reaches an equilibrium, which is then maintained. The same distribution is to be found by enzymatic analyses of the total pools of PGA in chloroplasts and cytoplasm. When equilibrium is reached, the percentages of both 14C labelled and of total PGA to be found in the chloroplasts of Spinach and Elodea are approximately 75% and 35 —40% respectively.3. In both the chloroplasts and the cytoplasm, the levels of PGA first decrease after illumination to a fraction of the original dark levels and then show a concomitant slow increase. On darkening a further very rapid increase in PGA occurs in chloroplasts and cytoplasm.4. In photosynthetically active leaf material the rate of decrease in the level of cytoplasmic PGA, as observed after 12 —15 secs. illumination, is higher than the turnover rate of PGA in respiration.5. Upon illumination, aqueously isolated chloroplasts, suspended in isotonic sucrose buffer, reduce added PGA to dihydroxyacetone phosphate and other products far faster than they reduce added NADP. Whereas PGA reduction is not increased by ultrasonic disintegration of the chloroplasts, the reduction of NADP is stimulated. This indicates that whereas the movement of NADP is prevented by a permeability barrier, the transferance of PGA across the chloroplast membrane occurs easily.6. In illuminated Elodea shoots the inhibition of metabolism by cyanide after 15 secs. photosynthesis in the presence of Η14CO3⊖ leads to a rapid decrease in PGA. This applies to both the 14C labelled PGA and the total PGA to a similar extent. The decrease in PGA amounts from 70 — 85% of the original dark levels. Since the chloroplasts of Elodea contain only 35—40% of the total PGA of the cell, a fall in the level of PGA as a result of the cyanide poisoning obviously occurs not only in the chloroplasts, but also in the cytoplasm. Since cyanide effectively inhibits cytochrome oxidase, while PGA reduction in the chloroplasts is relatively resistant, the large decrease in PGA suggests that part of the cytoplasmic PGA is transferred into the chloroplasts and reduced there.


1980 ◽  
Vol 26 (7) ◽  
pp. 910-912
Author(s):  
P S Draganac ◽  
S J Steindel ◽  
W G Trawick

Abstract A "high-performance" liquid-chromatographic procedure for 5-hydroxy-3-indoleacetic acid is described and compared with a colorimetric method in which 1-nitroso-2-naphthol is used. The analyte and an internal standard, p-nitrobenzoic acid, were extracted into diethyl ether from urine at pH 4.0 (acidified with HCl) to which sodium chloride had been added, and the ether was back-extracted with acetate buffer, pH 9.2. Aliquots of this extract were injected into a reversed-phase liquid-chromatographic column and eluted with pH 3.5 acetate buffer/methanol (95/5 by vol); the effluent was monitored at 254 nm. The precision (CV) of the method was 11.8% at 1.8 mg/L, 5.5% at 92 mg/L. Analytical recovery averaged 84%. The colorimetric method gave higher values for the analyte than did the chromatographic method for all patients' urines.


1987 ◽  
Vol 33 (10) ◽  
pp. 1874-1878 ◽  
Author(s):  
A Lopez-Anaya ◽  
M Mayersohn

Abstract We describe a "high-performance" liquid-chromatographic method for separating and quantifying ascorbic acid (AA) and dehydroascorbic acid (DHA) in plasma and urine. We used a reversed-phase C18 column with an ion-pair reagent and detected the analytes by post-column reaction with 4,5-dimethyl-o-phenylenediamine to form a fluorescent derivative (measured at excitation and emission wavelengths of 365 and 440 nm, respectively). Isoascorbic acid (IA) is the internal standard. Retention times for DHA, AA, and IA are 5.6, 15.5, and 19.9 min, respectively. Between-day CVs for AA in plasma in concentrations of 8 and 20 mg/L were 9% and 7%, respectively. The limit of detection is 10 and 4 ng for AA and DHA, respectively. Results by the present method and the methoxyaniline colorimetric method for AA are comparably accurate.


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