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First published online November 24, 2004; 10.1104/pp.104.052324 Plant Physiology 136:4265-4274 (2004) © 2004 American Society of Plant Biologists The Role of Plastocyanin in the Adjustment of the Photosynthetic Electron Transport to the Carbon Metabolism in Tobacco1Institut für Botanik, Westfälische Wilhelms-Universität, 48 149 Munster, Germany
We investigated adaptive responses of the photosynthetic electron transport to a decline in the carbon assimilation capacity. Leaves of different ages from wild-type tobacco (Nicotiana tabacum) L. var Samsun NN and young mature leaves of tobacco transformants with impaired photoassimilate export were used. The assimilation rate decreased from 280 in young mature wild-type leaves to below 50 mmol electrons mol chlorophyll–1 s–1 in older wild-type leaves or in transformants. The electron transport capacity, measured in thylakoids isolated from the different leaves, closely matched the leaf assimilation rate. The numbers of cytochrome (cyt)-bf complexes and plastocyanin (PC) decreased with the electron transport and assimilation capacity, while the numbers of photosystem I (PSI), photosystem II, and plastoquinone remained constant. The PC to PSI ratio decreased from five in leaves with high assimilation rates, to values below one in leaves with low assimilation rates, and the PC versus flux correlation was strictly proportional. Redox kinetics of cyt-f, PC, and P700 suggest that in leaves with low electron fluxes, PC is out of the equilibrium with P700 and cyt-f and the cyt-f reoxidation rate is restricted. It is concluded that the electron flux is sensitive to variations in the number of PC, relative to PSI and cyt-bf, and PC, in concert with cyt-bf, is a key component that adjusts to control the electron transport rate. PC dependent flux control may serve to adjust the electron transport rate under conditions where the carbon assimilation is diminished and thereby protects PSI against over-reduction and reactive oxygen production.
In the light, NADPH and ATP are produced by the photosynthetic electron transport chain (ETC). These products are consumed by metabolic reactions, mainly the Calvin cycle, where the photosynthetic flux is partitioned between carbon assimilation and photorespiration. In saturating light, the overall flux depends on the Calvin cycle activity, which itself is controlled by the Rubisco activity and the carbon flux into starch or Suc synthesis. If the carbon flux in the plant is diminished by a restriction of export and consumption of carbohydrates (sink limitation), the capacity of the thylakoid-bound light reactions could exceed the demand by the Calvin cycle. The photoreactions at PSI and PSII are exergonic and virtually irreversible and potentially destructive processes. Excess electrons, deliberated at PSII from water and delivered to PSI and not used by the carbon reactions, could be transferred to alternative acceptors, among them O2 (Backhausen et al., 2000  ; Foyer and Noctor, 2000; Ort and Baker, 2002). Reduction of molecular O2 at PSI leads to the production of the superoxide radical (O2–), a strong oxidant, and other reactive oxygen species (ROS). To some extend, ROS produced in the light can be detoxified through the Mehler-Asada cycle, so that, over a certain range of physiological conditions, no oxidative damage to the photosynthetic apparatus occurs (Asada, 1999). However, at least in C3 plants, the capacity of the Mehler-Asada cycle may not exceed about 10% of the capacity of the photosynthetic electron transport (PET; Badger et al., 2000). Similarly, other potential overflow valves for excess electrons, such as the oxaloacetate/malate shuttle (Backhausen et al., 2000), are limited in their capacity. Furthermore, these overflow reactions do not consume ATP and, hence, do not serve to dissipate the proton motive force that is built up by the light-driven proton pumping across the thylakoid membrane. Thus, if the capacity of light reactions and PET exceeds that of the electron consuming reactions to a large extend, the flux of excess electrons may eventually overrun the Mehler-Asada cycle and ROS will accumulate. In the long term, free ROS will cause damage to the photosynthetic apparatus, affect numerous cellular functions, and eventually initiate leaf senescence (Desikan et al., 2001). Thus, one may expect that plants have developed mechanisms to match the capacity of the ETC to the metabolic electron demand.
At the molecular level, there exist indications for a concerted adjustment of light and carbon reactions. A decrease in the sink strength leads to accumulation of soluble sugars in the mesophyll, where they are perceived by a signaling network (sugar sensing; see Smeekens, 2000
While these studies were mainly at the level of gene expression, there is surprisingly little information about adaptive changes in the thylakoids at the level of the ETC. From studies with tobacco (Nicotiana tabacum) expressing Rubisco-antisense constructs, it was concluded that in plants with a reduced Calvin cycle activity, the electron flux through the Mehler-Asada pathway or into other alternative electron sinks was not enhanced. Instead, the PET capacity was adjusted to the assimilation rate (Ruuska et al., 2000
Here, we analyze PET and the redox components of the ETC in thylakoids from tobacco var SNN leaves with a depressed carbon assimilation capacity. In one experiment, we studied the ETC from leaves of different ages. With increasing leaf age, the level of free carbohydrates increases, while the capacities of Calvin cycle and PET decrease (Ono et al., 2001 We found that in leaves from both aging and sugar accumulating transgenic plants, the number of photosystems remained constant while the assimilation capacity decreased. Instead, the content of cyt-bf and PC decreased with photosynthetic fluxes. We demonstrate that in thylakoids isolated from leaves with depressed (sink limited) carbon assimilation, the mobile electron carrier PC is an important factor controlling the PET flux.
Assimilation Rate during Leaf Aging Assimilation and chlorophyll (chl) content were determined from leaves between the 5th and 24th leaf-generation of a wild-type plant, counted from top to bottom of the plant (Fig. 1). The plant had just started to flourish. Measurements were performed under both light- and CO2-saturated conditions (10% CO2). We have chosen these conditions as we can calculate the total assimilatory flux from oxygen evolution. Under physiological conditions, carbon assimilation may be limited by CO2 and the total photosynthetic flux is partitioned between carbon assimilation and photorespiration.
The leaves of the 5th generation were not yet fully expanded (about 15 cm long) but exhibited a maximum chl content (per leaf area) and a high assimilation rate (relative to chl). The decline in the chl content (per leaf area) from the 5th to the 12th leaf generation was due to further leaf expansion. A further decline in chl (13th–24th generation) may be related to a stepwise reduction in the number of chloroplasts as leaf aging begins. The assimilation rate had its maximum around the 10th to 12th generation (280 mmol e– mol chl–1 s–1) and then continuously declined with leaf age to 20% of its initial rate (22th–24th generation). Despite their depressed assimilation, these leaves had not yet entered the final phase of senescence, as they were still green and did not show chlorotic patches.
The electron transport capacity in thylakoids was measured in the presence of an uncoupler and with methylviologen (MV) as an electron acceptor. We selected these assay conditions, as we wanted to determine the PET capacity and exclude any mechanisms for short-term regulation of PET, such as photosynthetic control or high energy quenching. Chloroplasts were isolated from leaves of different ages as indicated by arrows in Figure 1. Under the conditions we used for the assimilation measurements (saturating CO2), the vast majority of electrons provided by the ETC may be consumed by the carbon assimilation. Thus, in a first approximation, we could calculate the electron flux during leaf assimilation and compare it to the uncoupled PET rate in thylakoids (Fig. 1, inset). The relative changes in the thylakoid PET rate exactly followed those of electron flux rates during assimilation in leaves. The absolute PET rates in thylakoids were actually slightly (15%) below the flux rates in leaves. This is perhaps due to a small fraction of damaged thylakoids in the preparations, or to the fact that the standard measuring conditions for isolated thylakoids (pH, ionic milieu) may not necessarily be optimal for the electron flux rate. The Fv/Fm ratios determined from dark-adapted leaves were comparable with those in thylakoids isolated from these leaves (measured with a PAM-101 system; data not shown), suggesting that PSII was not damaged by the isolation procedure. The results indicate that the depression in the leaf assimilation is accompanied by a decline in the PET capacity at the thylakoid level.
Chl a and b, PSII (from C550), and PSI (from P700), as well as the other redox components of the ETC, were determined in thylakoids isolated from leaves of different ages. The chl a/b ratio and the numbers of the redox components, relative to chl, were plotted against the uncoupled PET. In wild-type plants, the PET rate in thylakoids decreased from about 280 (expanded young wild-type leaves) to 40 mmol e– mol chl–1 s–1 in aging leaves (compare with data in Fig. 1). From PPA-4-80 and A-41-10 transformants, we collected relatively young leaves (5th–10th generation) from plants exhibiting different levels of the phenotype. Transformants were reduced in growth rate, plant and leaf size, and expanded leaves developed characteristic patchy chlorosis and lesions. We collected leaves just before they had developed these symptoms. The different phenotype levels indicate different levels of sugar accumulation and Calvin cycle depression (Stitt et al., 1990 Over the whole range of fluxes, the content of PQ, and of redox-active PSII and PSI centers, relative to chl, remained stable (Fig. 2). The average number of PSII centers was 2.1 mmol mol chl–1 and that of PSI centers 2.4 mmol mol chl–1 (PSII to PSI = 0.88). The chl a to b ratio exhibited some variation between leaves around an average value of 3.4, but there was no significant change in dependence of the PET, suggesting that the overall ratio between light-harvesting complexes and core antennae of PSI and PSII remained relatively constant. The average content of PQ was about 8 to 9 mmol mol chl–1. Despite some scatter, the data suggest a relatively stable PQ pool (Fig. 2).
However, cyt-bf and PC contents did vary over a wide range with flux rates (Figs. 3 and 4). The cyt-bf versus flux curves exhibits a slightly different shape for aging wild type or transformants. In the wild type (SNN), about 0.9 mmol cyt-bf mol chl–1 correlated with the highest flux rates and remained relatively constant over the flux range of 280 to 180 mmol e– mol chl–1 s–1. At lower rates, cyt-bf decreased nearly linearly with fluxes to values as low as 0.2 mmol cyt-bf mol chl–1 (Fig. 3). In transformants, the correlation was less pronounced compared to the wild type. In selected preparations, we compared the total of cyt-bf (from difference absorbance spectroscopy at selected redox potentials) with redox-active cyt-bf (from the amplitude of light-induced cyt-f redox transients in the presence of MV; data not shown). We found that the population of redox-active cyt-bf involved in PET was slightly (about 10%–15%) below the total content, suggesting that a small amount of the complexes may not actively contribute to the linear flux. However, there was no indication that the relative proportions of redox-active and -inactive cyt-bf varied over the range of fluxes.
The mobile carrier PC exhibited a nearly linear relationship with the flux rate (Fig. 4). PC varied from about 12 mmol PC mol chl–1 at high fluxes to less than 2 mmol PC mol chl–1. This corresponds to PC:PSI ratios of almost 5 at high and 0.5 at very low flux rates. At high flux rates, PC still increased with the rate, while cyt-bf seemed to approach a maximum and, hence, the PC/cyt-bf ratio increased at high flux rates (compare Figs. 3 and 4). The maximum PC to P700 ratios in young wild-type leaves are in agreement with numbers previously published for spinach (Haehnel et al., 1989 ) and barley (Burkey, 1994). The minimum values for PC contents shown here for sink-limited leaves are comparable to those published for low-light acclimated barley leaves (Burkey, 1993) and in soybean genotypes with constitutively repressed PET (Burkey et al., 1996).
Figure 5 exhibits the relationship between the maximal whole chain flux rate from H2O to the acceptor MV and the electron transport from cyt-bf, with duroquinol as an artificial donor, to MV. We isolated thylakoids from wild type and transformants as for the experiments shown in Figures 1 to 4
Redox Kinetics of Cyt-f, PC, and P700 In Figure 6, time-resolved redox kinetics of the individual reaction steps of the high potential chain in thylakoids are presented. Thylakoids were isolated from either fully expanded young or aged wild-type leaves. PET rates were 165 (young wild type) and 60 mmol e– mol chl–1 s–1 (aged wild type). The content of P700 remained constant, while PC declined from 8 in young to 1.6 mmol mol chl–1 in old wild-type leaves (80% reduction). Redox-active cyt-f decreased from 1 to 0.45 mmol mol chl–1 (about 57% reduction). Redox kinetics were measured in the presence of MV as PSI electron acceptor and with nigericine and nonactin as uncouplers.
After complete oxidation of the high potential chain by a saturating 100-ms light pulse, the dark relaxation kinetics of cyt-f, PC, and P700 were followed. The noncorrected P700 redox kinetics exhibited a slowly relaxing component (half-time [t1/2] > 250 ms, about 15% of total P700). As no such slow signals were observed in leaves (data not shown), we relate this slow phase to a small fraction of damaged thylakoids (see also discussion in Kirchhoff et al., 2004 ). Therefore, we subtracted the slow phases from the reduction kinetics, so that only cyt-f, PC, and P700 involved in fast PET were considered for the further analysis. In the figure, all signals were normalized by setting the oxidized state at the end of the light pulse to one, and the reduced state (established after 500 ms) to zero. Recordings were displayed from the end of the light pulse (time zero). The half-time of the slightly sigmoid P700+ reduction kinetics increased from about 6 in thylakoids from young to 16 ms in thylakoids from old wild-type leaves, which reflects the observed decline in PET capacity (see above). In high-flux thylakoids, PC and cyt-f relaxed with halftimes of 20 and about 30 ms, respectively. In low-flux thylakoids, cyt-f relaxation exhibited a slight lag phase but, overall, was relatively little affected (t1/2 about 45 ms). A drastic change, however, was seen in the PC kinetics. Relaxation (t1/2 about 65 ms) was now slower than that of cyt-f. PC became even slightly oxidized in the dark before its reduction started with a 25-ms lag phase, in which almost all P700+ had already been reduced. Obviously, about 10% of PC had not been oxidized during the pulse.
These results suggest that in thylakoids from aged wild-type leaves, the reoxidation of cyt-f is slowed down and the equilibration of PC and cyt-f is disturbed, compared to the situation in high flux thylakoids. This becomes more obvious in the equilibration plots displayed in Figure 7. Normalized values for oxidized PC from redox kinetics are plotted against those of cyt-f. From the resulting curves, apparent equilibrium constants (Kapp) for the redox couple PC/cyt-f could be deviated (for details, see Kirchhoff et al., 2004
PSII Activity and Whole Chain Electron Transport In Figure 8, the light saturated PSII capacity was plotted against the whole chain flux. As expected, the reduction rate of the PSII acceptor by far exceeded that of the whole chain electron flux. Wild-type values scattered between 600 and 350 mmol e– mol chl–1 s–1, but did not show any significant correlation between PSII activity and whole chain flux. In transformants, however, the PSII activity showed a tendency to decline with the whole chain flux. In plants exhibiting a relatively strong phenotype, the PSII activity could be as low as 150 mmol e– mol chl–1 s–1. On the other hand, Figure 2 shows that the number of PSII centers, derived from the amplitude of the C550 signal, remained fairly constant. Obviously, in transformants, a large fraction of PSII could exist in an inactive state. The PSII activity assay with 2,5-dimethyl-1,4-benzoquinone (DMBQ) as an acceptor requires intact water splitting and primary electron-accepting PQ of PSII (QA)-acceptor sites. The C550 signal, however, reflects the very primary charge separation (QA reduction) occurring within the reaction center and does not require a functioning donor- and acceptor-site. Hence, the discrepancy between stable PSII contents, derived from the C550 signals, and the partially diminished DMBQ photoreduction may point to an impaired PSII donor- or acceptor-site in the transformants, possibly by photoinhibitory processes. This conclusion is further supported by the observation that the Fv/Fm ratios of both dark-adapted leaves and isolated thylakoids decreased from about 0.8 in wild type with high photosynthesis to about 0.6 in transformants with reduced PET capacity (data not shown).
Assimilation Capacity and PC Content in Leaves In Figure 9, the PC to PSI (P700) ratio was plotted against leaf photosynthesis from O2 evolution with saturating CO2 as an acceptor. The PC and P700 transients were recorded in leaf discs and corrected for the related absorption coefficients. Over the whole range of fluxes, the PC/P700 versus flux correlation was linear, in agreement with the result shown for thylakoids in Figure 4. The P700 content remained constant in all leaves (from P700 signals normalized to chl contents). When the PC to P700 ratio, determined in leaves, was multiplied with the average P700 content determined after thylakoid solubilization (Fig. 2), absolute PC contents of about 1 to 10 mmol mol chl–1 resulted, which is comparable to the absolute contents determined in thylakoids. Therefore, our method for PC quantification is also valid in planta.
Photosynthetic Electron Transport Adjusts to the Assimilation Capacity
In aging leaves, sugar export gradually decreases and soluble sugars increase (Ono et al., 2001
PET flux rates were analyzed in the uncoupled state, which is a nonphysiological situation. With regard to the in vivo situation, the uncoupled rate may reflect, in a first approximation, the potential capacity of PET under conditions where ATP and NADPH are rapidly consumed by metabolic processes. We are aware that in the plant, the actual PET rate could be significantly below its capacity and may be adjusted by a number of regulatory feed-back processes, such as photosynthetic control during the induction phase of photosynthesis (for review, see Kramer et al., 1999 Over the whole range of assimilation capacity, the number of PSI and PSII (relative to chl a and b) remained constant (Figs. 2 and 9). This demonstrates that in low assimilation leaves a large potential overcapacity of photoreactions could exist. On the other hand, the depression in the carbon flux capacity is accompanied by a depression in the ETC such that the whole chain electron flux from water to PSI closely matches the assimilation capacity (Fig. 1, inset). Obviously, there is no substantial overflow of electrons through alternative pathways such as the Mehler-Asada cycle or the oxaloacetate/malate shuttle. Certainly, these pathways do play an important role in detoxification and fine adjustment of the chloroplast redox poise, but at least in the leaves used in this study, these reactions may not act as overflow valves to drain large fluxes of excess electrons, when the assimilation capacity is reduced compared to the initial high assimilation state in expanded young leaves.
Evidently, the high potential chain from cyt-bf to PSI, via the mobile redox-protein PC, exerts control to the whole chain flux (see Fig. 5). This raises the question about the factors controlling the flux. While PSI remains stable, both cyt-bf and PC decrease with flux, suggesting that these two components could be involved in the flux control. Decrease in cyt-bf with PET capacity is not a surprising result. There are numerous studies suggesting that PQ-reoxidation by the cyt-bf is the slowest step in PET and, hence, cyt-bf should be an important factor controlling the PET during various physiological conditions (e.g. Holloway et al., 1983
On the other hand, the strictly linear correlation of PC over a wide range of fluxes shown in this study (Figs. 4 and 9) is striking. As we obtain the numbers for PC from light-induced redox kinetics in the presence of MV, all PC included in the analysis should participate in the linear flux. The ratio of PC:PSI decreases from 4 to 5 in leaves with high assimilation rates to values below 1 in leaves, whose assimilation is depressed. Although a general correlation between PC content and PET has already been reported for barley (Burkey, 1994
The strict PC versus flux correlation shown in this study per se is not a sufficient criterion for a PC flux control. If the PC reaction would be very fast, relative to whole chain flux, the correlation could be a coincidence and meaningless with regard to flux control. The PC versus flux correlation would represent PC flux control only under the condition that the PC redox cycle is slow, relative to PET. Only in this case, the electron flux rate would be sensitive to the number of PC located in the thylakoid lumen. Electron transfers within the PC-PSI and PC-cyt-bf complexes are 10 to 100 times faster than quinole oxidation and, thus, cannot limit the flux (Drepper et al., 1996
A second limiting factor could be protruding proteins in the luminal diffusion space (Haehnel, 1984
Flux control by PC adjustment (in concert with cyt-bf) results in a donor-site control of the PSI activity. This could be a safe way to control PSI, in particular in the low-assimilation leaves where its potential photochemical capacity very much exceeds the electron demand. Donor-site control would minimize overreduction at the reducing site of PSI, which inevitably would lead to ROS production and, thus, would be potentially destructive. A mismatch due to a net shortage of electron donation to PSI reaction centers could be less damaging. P700 could accumulate in its oxidized form, P700+. This species is a rather moderate oxidant and could act as a safe quencher of excess excitation energy (Ort, 2001
PC is a small protein encoded in the nucleus where its gene is regulated by a number of physiological and metabolic signals. Regulation of petE (PC) gene expression in response to the chloroplast redox state (Sullivan and Gray, 2002
However, down-regulation of PC dependent fluxes will cause a potentially destructive overcapacity of the PSII photoreaction. Under such conditions, PQ and PSII acceptors are expected to become overreduced in high light and photoinhibition of PSII is likely to occur (Hideg et al., 2000
In this study, we demonstrate a coordinated decline in assimilation and PET capacity of leaves with reduced carbohydrate export (sink limitation) in such a way that the PET rate is well matched to the assimilation rate. Both cyt-bf and PC are adjusted to the flux in such a way that redox equilibration in the high potential chain of PC with cyt-bf is slowed down. PC, in concert with cyt-bf, is a key component that adjusts to control the PET flux. As the lateral PC diffusion in the lumen of grana stacks is relatively slow, the PET flux rate is sensitive to the number of PC, relative to cyt-bf and PSI. PC flux control may serve to adjust PET and protect PSI in high light against overreduction (and ROS production), in particular under conditions where the demand by the carbon assimilation is strongly diminished, as during sink limitation and sugar depression of photosynthesis and leaf aging. PC is the smallest redox protein in the ETC and could easily be adjusted by protein turnover control.
Plants
Wild-type tobacco (Nicotiana tabacum) L. var Samsun NN was grown in a growth chamber (14 h light, 400–600 µE m–2 s–1, 24°C day/16°C night temperature). Transgenic tobacco plants (A-41-10; Schaewen et al., 1990
Photosynthetic oxygen evolution was determined in leaf discs using a Clark-type oxygen-electrode (LD2; Hansatech Instruments, Norfolk, England). Leaf temperature was maintained at 20°C. Actinic light was applied by a tungsten halogen lamp (Schott, Mainz, Germany). To saturate the Rubisco with CO2, the leaf chamber was flushed with air containing 10% CO2 and 5% O2.
Prior to thylakoid isolation, plants were kept in the dark for 24 h to reduce the starch content. After cutting out the major veins, four to six leaves were homogenized with a Waring Blendor in an isotonic medium containing 330 mM sorbitol, 1 mM MnCl2, 5 mM MgCl2, 40 mM KCl, and 50 mM MES, pH = 6.1. The homogenate was filtered through gauze (22-µm pore size) and centrifuged at 2,000g. The pellet was suspended in hypotonic medium (osmotic shock) containing 5 mM MgCl2, 40 mm KCl, and 30 mM HEPES, pH = 7.6. After 30 s, an equal volume of hypertonic medium (5 mM MgCl2, 40 mM KCl, 700 mM sorbitol, 30 mM HEPES, pH = 7.6) was added. The suspension was centrifuged at 200g, the supernatant at 2,000g. Resuspended thylakoids were stored in a medium containing 5 mM MgCl2, 1 mM MnCl2, 40 mM KCl, 330 mM sorbitol, and 50 mM HEPES, pH = 7.8.
PET of a suspension of thylakoids was measured in a Clark-type oxygen electrode (Hansatech) at 20°C in a medium containing 5 mM MgCl2, 40 mM KCl, 330 mM sorbitol, and 30 mM HEPES, pH = 7.6. The actinic light was about 5,000 µE m–2 s–1. For whole chain electron transport, 100 µM MV, 1 mM NaN3, and 1 µM nigericin were added. For PSII activity, 2 mM DMBQ and 1 µM nigericin were added. The high-potential-chain was measured in the presence of 100 µM DCMU, 1 mM NaN3, and 1 µM nigericin with 1 mM duroquinone as donor and 100 µM MV as acceptor. The duroquinone
Both PSII (C550) and PSI (P700) were determined after solubilization of thylakoids with 0.2% (w/v) of
P700 was determined in the presence of 100 µM MV and 10 mM sodium ascorbate from light-pulse induced changes at 810 minus 860 nm using a PAM 101 photometer and an ED-P700DW emitter/detector unit (Walz, Effeltrich, Germany). The emitter/detector unit was connected by a bi-branched light guide to a reflecting (mirrored) and temperature-controlled steel chamber, as in (Kirchhoff et al., 2004
The total content of cyt-bf in a thylakoid preparation was determined by difference absorption spectra induced by step-wise addition of 1 mM ferricyanide, 10 mM sodium ascorbate, and 20 mM sodium dithionite. Signals were measured using a Hitachi U-3010 spectrophotometer (1-nm slit width, 580–520 nm). For further details, see Kirchhoff et al. (2002)
Redox kinetics of cyt-f were determined from light-pulse (100 ms, 5,000 µE m–2 s–1) induced absorption changes (547 nm, 554 nm, 568 nm) in the presence of 100 µM MV, 10 mM sodium ascorbate, 1 µM nigericine, and 0.5 µM nonactin. Signals were deconvoluted as described by Kirchhoff et al. (2004)
The number of redox-active PC relative to P700 was derived from a deconvolution of differential light-pulse-induced absorption changes at 810 nm and 810 to 860 nm. Measurements with isolated thylakoids were performed in the presence of 100 µM MV, 10 mM sodium ascorbate, 1 µM nigericine, and 0.5 µM nonactin. Ascorbate keeps the high potential chain reduced in the dark. MV is an efficient electron acceptor for PSI that keeps P700 in the light oxidized. It also should keep ferredoxin (which could contaminate the near infrared signals) redox inactive. Electrochromic signals were eliminated by nigericine plus nonactin. The mathematical deconvolution and analysis of the signals is described by Kirchhoff and his coworkers (2004) For a quantitative determination of PC relative to P700 in intact mesophyll, leaf discs were sprayed with a solution containing 10 mM MV, 1 mM DCMU, and 200 µM 2,5-dibromo-6-isopropyl-3-methyl-1,4-benzoquinone and 0.1% (v/v) Triton X-100 and then stored in a dark, moistened chamber for 45 min until measurements.
The chl-a-fluorescence induction (±DCMU) assay (Kirchhoff et al., 2000
Fluorescence induction was measured in a suspension of thylakoids (10 µg chl mL–1) with a laboratory built fluorometer in the absence or presence of 20 µM DCMU at 5°C. Excitation light was filtered through heat reflectance filters and glass filters (Schott BG18 and Corning 9782). Emission was detected with a photomultiplier protected by a Schott AL 685 filter. To minimize reoxidation of electron acceptors by oxygen, the suspension was bubbled prior to the measurements with nitrogen. The areas above the induction curves without DCMU, relative to that in presence of DCMU reflect the number of photoreduced PSII acceptors. Assuming that most electron acceptors in the high potential chain remain reduced, it may be taken, in a first approximation, as an estimate for the PQ pool. Fluorescence induction curves were analyzed according to Trissl and Lavergne (1994)
We are grateful to Prof. Dr. Uwe Sonnewald (IPK, Gatersleben, Germany) for providing the tobacco transformants and to Julia Maurer (Institut für Botanik, Münster, Germany) for help during the establishment of the PC quantification method. We thank the reviewers for their helpful comments and suggestions. Received August 24, 2004; returned for revision October 7, 2004; accepted October 7, 2004.
1 This work was supported by the Studienstiftung des Deutschen Volkes (to M.A.S.) and by the Deutsche Forschungsgemeinschaft (to H.K.).  Article, publication date, and citation information can be found at www.plantphysiol.org/cgi/doi/10.1104/pp.104.052324. * Corresponding author; e-mail schoett{at}uni-muenster.de; fax 0049–251–8323823.
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ABSTRACT
RESULTS
DMBQ; 
-dodecyl-D-maltoside, so that optical artifacts resulting from light scattering, thylakoid energetization, and cyt-bf-based redox absorbance changes were eliminated. The number of redox-active PSII centers was determined from light-induced (100-ms pulse, 5,000 µE m–2 s–1) changes in thylakoids at 540 minus 550 nm in the presence of 100 µM DCMU and 10 mM ferricyanide (C550; for details see Kirchhoff et al., 2002
= 9.6 mM–1 cm–1 for P700. 
nuclear encoded polypeptides. Aust J Plant Physiol 22: 285–297
