Impact of Inorganic Carbon Availability on Microcystin Production by Microcystis aeruginosa PCC 7806

Batch culture experiments with the cyanobacterium Microcystis aeruginosa PCC 7806 were performed in order to test the hypothesis that microcystins (MCYSTs) are produced in response to a relative deficiency of intracellular inorganic carbon (C_i,i). In the first experiment, MCYST production was studied under increased C_i,i deficiency conditions, achieved by restricting sodium-dependent bicarbonate uptake through replacement of sodium bicarbonate in the medium with its potassium analog. The same experimental approach was used in a second experiment to compare the response of the wild-type strain M. aeruginosa PCC 7806 with its mcyB mutant, which lacks the ability to produce MCYSTs. In a third experiment, the impact of varying the C_i,i status on MCYST production was examined without suppressing the sodium-dependent bicarbonate transporter; instead, a detailed investigation of a dark-light cycle was performed. In all experiments, a relative C_i,i deficiency was indicated by an elevated variable fluorescence signal and led to enhanced phycocyanin cell quotas. Higher MCYST cell quotas (in the first and third experiments) and increased total (intracellular plus extracellular) MCYST production (in the first experiment) were detected with increased C_i,i deficiency. Furthermore, the MCYST-producing wild-type strain and its mcyB mutant showed basically the same response to restrained inorganic carbon uptake, with elevated variable fluorescence and phycocyanin cell quotas with increased C_i,i deficiency. The response of the wild type, however, was distinctly stronger and also included elevated chlorophyll a cell quotas. These differences indicate the limited ability of the mutant to adapt to low-C_i,i conditions. We concluded that MCYSTs may be involved in enhancing the efficiency of the adaptation of the photosynthetic apparatus to fluctuating inorganic carbon conditions in cyanobacterial cells.     

Limiting Factors in Photosynthesis: V. Photochemical Energy Supply Colimits Photosynthesis at Low Values of Intercellular CO(2) Concentration

Although there is now some agreement with the view that the supply of photochemical energy may influence photosynthetic rate (P) at high CO₂ pressures, it is less clear whether this limitation extends to P at low CO₂. This was investigated by measuring P per area as a function of the intercellular CO₂ concentration (C_i) at different levels of photochemical energy supply. Changes in the latter were obtained experimentally by varying the level of irradiance to normal (Fe-sufficient) leaves of Beta vulgaris L. cv F58-554H1, and by varying photosynthetic electron transport capacity using leaves from Fe-deficient and Fe-sufficient plants. P and C_i were determined for attached sugar beet leaves using open flow gas exchange. The results suggest that P/area was colimited by the supply of photochemical energy at very low as well as high values of C_i. Using the procedure developed by Perchorowicz et al. (Plant Physiol 1982 69:1165-1168), we investigated the effect of irradiance on ribulose bisphosphate carboxylase (RuBPCase) activation. The ratio of initial extractable activity to total inducible RuBPCase activity increased from 0.25 to 0.90 as leaf irradiance increased from 100 to 1500 microeinsteins photosynthetically active radiation per square meter per second. These data suggest that colimitation by photochemical energy supply at low C_i may be mediated via effects on RuBPCase activation.     

Mycorrhiza Symbiosis Increases the Surface for Sunlight Capture in Medicago truncatula for Better Photosynthetic Production

Arbuscular mycorrhizal (AM) fungi play a prominent role in plant nutrition by supplying mineral nutrients, particularly inorganic phosphate (P_i), and also constitute an important carbon sink. AM stimulates plant growth and development, but the underlying mechanisms are not well understood. In this study, Medicago truncatula plants were grown with Rhizophagus irregularis BEG141 inoculum (AM), mock inoculum (control) or with P_i fertilization. We hypothesized that AM stimulates plant growth through either modifications of leaf anatomy or photosynthetic activity per leaf area. We investigated whether these effects are shared with P_i fertilization, and also assessed the relationship between levels of AM colonization and these effects. We found that increased P_i supply by either mycorrhization or fertilization led to improved shoot growth associated with increased nitrogen uptake and carbon assimilation. Both mycorrhized and P_i-fertilized plants had more and longer branches with larger and thicker leaves than the control plants, resulting in an increased photosynthetically active area. AM-specific effects were earlier appearance of the first growth axes and increased number of chloroplasts per cell section, since they were not induced by P_i fertilization. Photosynthetic activity per leaf area remained the same regardless of type of treatment. In conclusion, the increase in growth of mycorrhized and P_i-fertilized Medicago truncatula plants is linked to an increase in the surface for sunlight capture, hence increasing their photosynthetic production, rather than to an increase in the photosynthetic activity per leaf area.     

Cellular Microcystin Content in N-Limited Microcystis aeruginosa Can Be Predicted from Growth Rate

Cell quotas of microcystin (Q_MCYST; femtomoles of MCYST per cell), protein, and chlorophyll a (Chl a), cell dry weight, and cell volume were measured over a range of growth rates in N-limited chemostat cultures of the toxic cyanobacterium Microcystis aeruginosa MASH 01-A19. There was a positive linear relationship between Q_MCYST and specific growth rate (μ), from which we propose a generalized model that enables Q_MCYST at any nutrient-limited growth rate to be predicted based on a single batch culture experiment. The model predicts Q_MCYST from μ, μ_max (maximum specific growth rate), Q_MCYSTmax (maximum cell quota), and Q_MCYSTmin (minimum cell quota). Under the conditions examined in this study, we predict a Q_MCYSTmax of 0.129 fmol cell⁻¹ at μ_max and a Q_MCYSTmin of 0.050 fmol cell⁻¹ at μ = 0. Net MCYST production rate (R_MCYST) asymptotes to zero at μ = 0 and reaches a maximum of 0.155 fmol cell⁻¹ day⁻¹ at μ_max. MCYST/dry weight ratio (milligrams per gram [dry weight]) increased linearly with μ, whereas the MCYST/protein ratio reached a maximum at intermediate μ. In contrast, the MCYST/Chl a ratio remained constant. Cell volume correlated negatively with μ, leading to an increase in intracellular MCYST concentration at high μ. Taken together, our results show that fast-growing cells of N-limited M. aeruginosa are smaller, are of lower mass, and have a higher intracellular MCYST quota and concentration than slow-growing cells. The data also highlight the importance of determining cell MCYST quotas, as potentially confusing interpretations can arise from determining MCYST content as a ratio to other cell components.     

Nitrogen enhanced photosynthesis of Miscanthus by increasing stomatal conductance and phosphoenolpyruvate carboxylase concentration

Miscanthus is one of the most promising bioenergy crops with high photosynthetic nitrogen-use efficiency (PNUE). It is unclear how nitrogen (N) influences the photosynthesis in Miscanthus. Among three Miscanthus genotypes, the net photosynthetic rate (P _N) under the different light intensity and CO₂ concentration was measured at three levels of N: 0, 100, and 200 kg ha^?1. The concentrations of chlorophyll, soluble protein, phosphoenolpyruvate carboxylase (PEPC), ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) large subunit, leaf anatomy and carbon isotope discrimination (Δ) in the leaf were analyzed to probe the response of photosynthesis in Miscanthus genotypes to N levels. P _N in all genotypes rose significantly as N application increased. The initial slope of response curves of P _N to C _i was promoted by N application in all genotypes. Both stomatal conductance and C _i were increased with increased N supply, indicating that stomatal factors played an important role in increasing P _N. At a given C _i, P _N in all genotypes was enhanced by N, implying that nonstomatal factors might also play an important role in increasing P _N. Miscanthus markedly regulated N investment into PEPC rather than the Rubisco large subunit under higher N conditions. Bundle sheath leakiness of CO₂ was constant at about 0.35 for all N levels. Therefore, N enhanced the photosynthesis of Miscanthus mainly by increasing stomatal conductance and PEPC concentration.     

Relationship between Acid Tolerance, Cytoplasmic pH, and ATP and H+-ATPase Levels in Chemostat Cultures of Lactococcus lactis

The acid tolerance response (ATR) of chemostat cultures of Lactococcus lactis subsp. cremoris NCDO 712 was dependent on the dilution rate and on the extracellular pH (pH_o). A decrease in either the dilution rate or the pH_o led to a decrease in the cytoplasmic pH (pH_i) of the cells, and similar levels of acid tolerance were observed at any specific pH_i irrespective of whether the pH_i resulted from manipulation of the growth rate, manipulation of the pH_o, or both. Acid tolerance was also induced by sudden additions of acid to chemostat cultures growing at a pH_o of 7.0, and this induction was completely inhibited by chloramphenicol. The end products of glucose fermentation depended on the growth rate and the environmental pH_o of the cultures, but neither the spectrum of end products nor the total rate of acid production correlated with a specific pH_i. The rate of ATP formation was not correlated with pH_i, but a good correlation between the cellular level of H⁺-ATPase and pH_i was observed. Moreover, an inverse correlation between the cytoplasmic levels of ATP and pH_i was established. Each pH_i below 6.6 was characterized by unique levels of ATR, H⁺-ATPase, and ATP. High levels of H⁺-ATPase also coincided with high levels of acid tolerance of cells in batch cultures induced with sublethal levels of acid. We concluded that H⁺-ATPase is one of the ATR proteins induced by acid pH_i through growth at an acid pH_o or a slow growth rate.     

Studies on carrageenans and effects of seawater phosphorus concentration on carrageenan content and growth ofAgardhiella subulata (C. Agardh) Kraft and Wynne (Rhodophyceae,Solieriaceae)

Gas liquid chromatography, chemical analyses, and infrared and¹³C-NMR spectroscopies indicated that phycocolloids extracted fromAgardhiella subulata had a dominant ι-carrageenan feature with less deviant ι-carrageenan and υ-carrageenan. The presence of methylated galactose and a small contamination by xylose were registered. Unattached plants were cultivated for 4 weeks in tanks receiving seawater enriched with 53.5 µM nitrate and 0 to 20 µM phosphate (P_i) week^?1. The growth was phosphorus (P)-limited up to a tissue P content of 0.14 ± 0.03% dry weight. Maximal specific growth rate and carrageenan content were observed with enrichments of 6 µM P_i and 3 µM P_i, respectively. Hence carrageenan production was promoted in the range of 3–6 µM P_i. Further P_i enrichment was useless. This phenomenon, observed with P nutrition, is comparable to the ‘Neish effect’ in nitrogen nutrition studies.     

Influence of phosphorus and nitrogen on photosynthetic parameters and growth in <Emphasis Type="Italic">Vicia faba</Emphasis> L.

The influence of phosphorus (P) and nitrogen (N) supply on biomass, leaf area, photon saturated photosynthetic rate (P_max), quantum yield efficiency (α), intercellular CO₂ concentration (C_i), and carboxylation efficiency (CE) was investigated in Vicia faba. The influence of P on N accumulation, biomass, and leaf area production was also investigated. An increase in P supply was consistently associated with an increase in N accumulation and N productivity in terms of biomass and leaf area production. Furthermore, P increased the photosynthetic N use efficiency (NUE) in terms of P_max and α. An increase in P supply was also associated with an increase in CE and a decrease in C_i. Under variable daily meteorological conditions specific leaf nitrogen content (N_L), specific leaf phosphorus content (P_L), specific leaf area (δ_L), root mass fraction (R_f), P_max, and α remained constant for a given N and P supply. A monotonic decline in the steady-state value of R_f occurred with increasing N supply. δ_L increased with increasing N supply or with increasing N_L. We tested also the hypothesis that P supply positively affects both N demand and photosynthetic NUE by influencing the upper limit of the asymptotic values for P_max and CE, and the lower limit for C_i in response to increasing N.     

Combined effects of light and temperature on growth, photosynthesis, and pigment content in the mat-forming cyanobacterium Geitlerinema amphibium

Geitlerinema amphibium (BA-13), mat-forming cyanobacterium from the southern Baltic Sea, was grown at three irradiances [5, 65, and 125 μmol(photon) m^?2 s^?1] and three temperatures (15, 22.5, and 30°C). To determine the effect of the investigated factors and their interaction on culture concentration, pigment content, and photosynthetic parameters of cyanobacterium, factorial experiments and two-way analysis of variance (ANOVA) were carried out. Both chlorophyll (Chl) a and phycobilins (PB) were influenced by the irradiance and temperature, but stronger effect was noted in the case of the former one. Chl a and PB concentration per 100 μm of filament dropped above 4-fold with the increasing irradiance. The ratios between individual carotenoids [β-carotene, zeaxanthin, and myxoxanthophyll (Myx)] and Chl a increased significantly with an increase in the irradiance. The greatest fluctuations were observed in the ratio of Myx to Chl a (above 10-fold). Thus, Myx was suggested as the main photoprotective carotenoid in G. amphibium. Based on photosynthetic light response (PI) curves, two mechanisms of photoacclimation in G. amphibium were recognized: a change of photosynthetic units (PSU) number and a change of PSU size. These two mechanisms constituted the base of significant changes in photosynthetic rate and its parameters, such as the compensation point (P _C), the initial slope of photosynthetic curve (α), saturation irradiance (E _K), maximal photosynthetic rate (P _max), and dark respiration rate (R _D). The greatest changes were observed in P _C values (about 15-fold within the range of the factors tested). Studied parameters showed a wide range of changes, which might indicate G. amphibium ability to acclimatize well to irradiance and temperature, and indirectly might explain the successful growth of cyanobacterium in dynamically changing environmental conditions.     

Steady-state and dynamic photosynthetic performance and nitrogen partitioning in the shade-demanding plant Panax notoginseng under different levels of growth irradiance

In this study, we examined steady-state and dynamic photosynthetic performance and leaf nitrogen (N) partitioning in the typical shade-demanding herb Panax notoginseng grown along a light gradient. Gas exchange on a leaf area basis was significantly reduced under low irradiance, with gas exchange on a leaf mass basis reaching a maximum value and then decreasing along the light gradient. Specific leaf area significantly increased with decreasing irradiance levels (P < 0.001), whereas carboxylation efficiency was decreased (P < 0.001). In addition, decreasing growth irradiance levels led to declines in maximum carboxylation rate (V _cmax) and maximum electron transport rate (J _max), although V _cmax/mass and J _max/mass were relatively less affected than V _cmax/area and J _max/area. Slow photosynthetic response to simulated sunflecks was observed under low levels of growth irradiance, with stomatal limitations only detected in leaves grown under low-light conditions. Chlorophyll content increased significantly with decreasing irradiance levels. N content on a leaf mass basis apparently increased, while N content on a leaf area basis markedly decreased. The fraction of leaf N allocated to light-harvesting components increased significantly with decreasing growth irradiance levels, whereas the fraction allocated to carboxylation and bioenergetics was significantly reduced. As an adaptation strategy to growth irradiance, we conclude that adjustments in specific leaf area may be more important than changes in leaf physiology and biochemistry in typical shade-demanding species such as P. notoginseng.     

PHOSPHORUS AND THE GROWTH OF JUVENILE MACROCYSTIS PYRIFERA (PHAEOPHYTA) SPOROPHYTES1

The effect of phosphate (P_i) supply on growth rate and tissue phosphorus content of juvenile Macrocystis pyrifera (L.) C. Ag. sporophytes was examined. Sporophytes were batch cultured in aquaria with flowing recirculated seawater enriched by 30 μM nitrate. Each aquarium was supplemented with a different seawater P_i concentration, 0, 0.3, 1, 2, 3, and 6 μM. Sporophyte mean specific growth rates declined with time in all cultures presumably due to the normal developmental decrease in the proportion of meristematic tissue of each plant. Growth rate declines were more pronounced in cultures that were nutrient limited. Sporophyte growth was P-limited after two-week exposure to P_i less than 1 μM, corresponding to a tissue P concentration of less than 0.20% dry weight. Plants cultured at 6 μM P_i contained tissue P levels of 0.53% dry weight after three weeks. Luxury consumption and storage of P occurred.     

Pathway for ATP synthesis by sarcoplasmic reticulum ATPase

Millisecond mixing and quenching experiments were performed in order to study the rate of phosphorylation by P_i of the Ca²⁺-dependent ATPase of sarcoplasmic reticulum vesicles. A rapid phosphoenzyme formation was observed when the vesicles were preincubated in the absence of Ca²⁺ prior to the addition of P_i and Mg²⁺ to the medium, the half-time being in the range of 6 to 10 ms. A lag phase and a 5- to 10-fold slower rate of phosphoenzyme formation were observed when the enzyme was preincubated with Ca²⁺ prior to the addition to the reaction mixture of P_i, Mg²⁺, and an excess of ethylene glycol bis(β-aminoethyl ether)N,N′-tetraacetic acid. The rate of phosphoenzyme hydrolysis was measured either by the addition of Ca²⁺ or, in the absence of Ca²⁺, by tracing the hydrolysis of radioactive phosphoenzyme upon the addition of nonradioactive P_i. In the presence of Ca²⁺, the rate of phosphoenzyme hydrolysis was found to be one order of magnitude slower than the rate of hydrolysis measured in the absence of Ca²⁺. Different rates of phosphoenzyme formation and cleavage were found depending on whether sarcoplasmic reticulum vesicles or purified Ca²⁺-dependent ATPase were used. A transient phosphorylation by P_i was observed when the enzyme was preincubated in the absence of Ca²⁺ and then added to a medium containing P_i, Mg²⁺, and excess of Ca²⁺. The enzyme was phosphorylated during the initial 100 ms, the phosphoenzyme formed being slowly hydrolyzed in the subsequent incubation intervals. In these conditions ATP synthesis was observed if ADP was added to the mixture 100 ms after starting the reaction. No transient phosphorylation by P_i was observed when the enzyme was preincubated with Ca²⁺. Synthesis of a small but significant amount of ATP was observed when the enzyme was preincubated in the absence of Ca²⁺ and then added to a medium containing P_i, ADP, Mg²⁺, and 20 mm CaCl₂. This was not observed when the enzyme was preincubated in the presence of Ca²⁺.     

Regulation of Pi,uptake by Acer pseudoplatanus cells

In view of the importance of P_i in the control of cell metabolism, it was of interest to study the mechanism and regulation of P_i uptake by Acer pseudoplatanus cells grown as cell suspensions. At low external P_i concentrations up to 10 mm, sycamore cells incorporate phosphate against a concentration gradient, by a process which is energy dependent. Under these conditions the intracellular P_i concentration is maintained constant (2–3 mm). On the contrary at high external P_i concentrations, higher than that which counterpoises the cytoplasmic P_i concentration (approximately 10 mm), P_i enters the cell by slow diffusion and the intracellular P_i concentration increases continuously as the extracellular P_i concentration increases from 15 to 50 mm. When sycamore cells are transferred to a phosphate-deficient medium, growth slows down considerably and ceases after 4–5 days. During this time, intracellular P_i concentration falls from 3 to 0.1 mm and phosphate esters from 8 to 2 mm. Phosphate starvation stimulates the uptake indicating that phosphate uptake depends on the intracellular phosphate and/or cytoplasmic ester-P pool. P_i uptake by P_i-starved cells is strongly dependent on the pH of the medium.     

Effects of nitrogen source and irradiance on <Emphasis Type="Italic">Porphyridium cruentum</Emphasis>

We determined the effects of two nitrogen sources (ammonium and nitrate) and two irradiance levels (50 and 200 μmol photons m^?2 s^?1) on the growth rate, cell size, proximate composition, pigment content, and photosynthesis of the unicellular red alga, Porphyridium cruentum. Irradiance significantly affects growth rate, as well as carbohydrate, protein, and phycoerythrin content. Nitrogen form significantly affects cell size, total dry weight, organic dry weight, ash content, carotene content, phycocyanin content, allophycocyanin content, maximum relative electron transport rate (rETRm), and photosynthetic efficiency (α). However, the irradiance and nitrogen source had significantly interaction with the content of lipids and chlorophyll a content, relative electron transport rate (rETR), and irradiance of saturation (I_k). These findings demonstrate that irradiance and nitrogen source influence the metabolism of P. cruentum and that the combination of these two variables induces the production of chemical products for biotechnological, aquaculture, and nutraceutical industry.     

Regulation of Growth at Steady-state Nitrogen Nutrition in Lettuce (Lactuca sativa L.): Interactive Effects of Nitrogen and Irradiance

The morphological and physiological adaptation of Lactuca sativaL. (‘Vegas’) to different irradiance levels andrates of nitrogen supply was analysed in such a way that effectsof irradiance were clearly distinguished from the effects ofnitrogen. Lettuce was grown in a glasshouse in aerated nutrientsolutions containing all necessary nutrients except nitrogen.Nitrogen was supplied in excess and at limiting rates in relationto plant growth to provide steady state nutrition. Shading theplants created the low irradiance level. The effects of nitrogensupply and irradiance on growth showed a marked interaction.Dry matter production decreased strongly with decreasing nitrogensupply at high irradiance, but decreased only slightly at lowirradiance. Nitrogen had no effect on radiation use efficiencyexcept for the lowest nitrogen treatment at high irradiance.The effect of nitrogen on growth was mainly mediated by itseffect on leaf area development and hence on light interception.Decreases in leaf area were due to decreases in specific leafarea and dry matter partitioning towards the leaves, while thedecrease in specific leaf area was the result of an increasein leaf dry matter percentage at low nitrogen supply. Dry matterand nitrogen partitioning, and nitrate concentration were closelyrelated to plant nitrogen concentration. Irradiance did notaffect these relationships. Irradiance influenced partitioningonly indirectly by affecting plant nitrogen concentration. Thedemand for organic nitrogen per unit leaf area was lower atlower irradiance. Organic nitrogen per unit leaf area appearedto be adjusted to the irradiance level, independently of thenitrogen supply, suggesting priority of nitrogen usage in photosynthesis.Copyright 2000 Annals of Botany Company Lactuca sativa L., lettuce, growth, irradiance, leaf area, nitrogen, radiation use efficiency, partitioning     

Effect of climatic gradients on the photosynthetic responses of four Phragmites australis populations

Four populations of Phragmites australis collected from geographically distinct areas in Europe were propagated in outdoor experimental plots at four sites with dissimilar climate (Denmark, The Netherlands, Spain and Czech Republic). During the second growing season the photosynthetic characteristics of Phragmites leaves were evaluated under controlled conditions for each site, each population, and their interaction, and related to tissue nutrient and pigment content. The light-saturated rate of photosynthesis (P_max), dark respiration rate (R_d), light compensation point (I_c), and apparent quantum efficiency (φ_i) were significantly affected by growth site, whereas differences between populations were less pronounced. Plants grown in the more northerly climates appeared to be more photosynthetically limited through lower P_max values and lower φ_i levels, reflecting phenotypic acclimation to the lower summer temperatures and irradiance levels at the northern growth sites. The higher P_max levels in the southern climate were correlated with higher nutrient levels in the tissue of leaves. The study shows that the four genetically distinct populations of P. australis exhibited high phenotypic plasticity in photosynthetic response to climatic change. The degree of photosynthetic plasticity within P. australis genotypes is large, and generally larger than the genetically determined differences between European populations. The results are discussed in relation to the prospected global climate change.     

The Influence of Temperature on Meloidogyne incognita on Soybean

The effects of temperature and initial inoculum density of Meloidogyne incognita on soybean growth and nematode reproduction were investigated in greenhouse temperature tanks and in controlled-growth chambers. The interactions of initial inoculum density (P_i) and soil temperature in effects on shoot growth were adequately described by multiple-regression models. At the highest temperatures (30 or 32/28 C), moderate to high inoculum killed many plants. A P_i of 27,000 eggs/15-cm-diam pot retarded shoot growth at 26 C. Only the greatest P_i (81,000 eggs/15-cm pot) suppressed shoot growth at 18, 22, or 20/16 C. Inoculation with 3,000 or 9,000 eggs/plant resulted in heavier root systems at all temperatures except 30 C. At that temperature, 9,000 eggs suppressed root growth. At 18 and 26 C, a Pi of 81,000 eggs was required to retard root growth. Nematode reproduction was related directly to temperature and P_i except at a density of 81,000 eggs/15-cm pot.     

Whole-tissue determination of the rate coefficients of photoinactivation and repair of photosystem II in cotton leaf discs based on flash-induced P700 redox kinetics

Using radioactively labelled amino acids to investigate repair of photoinactivated photosystem II (PS II) gives only a relative rate of repair, while using chlorophyll fluorescence parameters yields a repair rate coefficient for an undefined, variable location within the leaf tissue. Here, we report on a whole-tissue determination of the rate coefficient of photoinactivation k _i , and that of repair k _r in cotton leaf discs. The method assays functional PS II via a P700 kinetics area associated with PS I, as induced by a single-turnover, saturating flash superimposed on continuous background far-red light. The P700 kinetics area, directly proportional to the oxygen yield per single-turnover, saturating flash, was used to obtain both k _i and k _r . The value of k _i , directly proportional to irradiance, was slightly higher when CO₂ diffusion into the abaxial surface (richer in stomata) was blocked by contact with water. The value of k _r , sizable in darkness, changed in the light depending on which surface was blocked by contact with water. When the abaxial surface was blocked, k _r first peaked at moderate irradiance and then decreased at high irradiance. When the adaxial surface was blocked, k _r first increased at low irradiance, then plateaued, before increasing markedly at high irradiance. At the highest irradiance, k _r differed by an order of magnitude between the two orientations, attributable to different extents of oxidative stress affecting repair (Nishiyama et al., EMBO J 20: 5587–5594, 2001). The method is a whole-tissue, convenient determination of the rate coefficient of photoinactivation k _i and that of repair k _r .     

Effects of light history on primary productivity in a phytoplankton community dominated by the toxic cyanobacterium Cylindrospermopsis raciborskii

1. The effects of instantaneous irradiance and short‐term light history on primary production were determined for samples from a subtropical water reservoir dominated by the toxic cyanobacterium Cylindrospermopsis raciborskii. ¹⁴C‐bicarbonate uptake incubations were conducted on water samples from the reservoir, for irradiance (photosynthetically active radiation) ranging from 0 to 1654 μmol quanta m⁻² s⁻¹. Prior to the ¹⁴C incubations, cells were pre‐treated at irradiance levels ranging from 0 to 1006 μmol quanta m⁻² s⁻¹. 2. The average irradiance experienced by cells during the 2–2.5 h pre‐treatment incubations affected the productivity–irradiance (P–I) parameters: exposure to high light in pre‐treatment conditions caused a substantial decrease in maximum rate of primary production P_max and the photoinhibition parameter β when compared to cells pre‐treated in the dark. 3. While the data collected in this study were not sufficient to develop a full dynamic model of C. raciborskii productivity, P_max and β were modelled as a function of pre‐treatment irradiance, and these models were applied to predict the rate of primary production as a function of both instantaneous and historical irradiance. The results indicated that while cells with a history of exposure to high irradiance will be the most productive in high irradiance, production rates will be highest overall for dark‐acclimated cells in moderate irradiance. 4. Our results may explain why optically‐deep mixing favours C. raciborskii. If the mixing depth z_m exceeds the euphotic depth z_eu, cells will be dark‐acclimated, which will increase their rate of production when they are circulated through the euphotic zone. These results also predict that production rates will be higher during morning hours than for the same irradiance in the afternoon, which is consistent with other phytoplankton studies. 5. Since the rate of production of C. raciborskii‐dominated systems cannot be described by a single P–I curve, accurate estimates of production rates will require measurements over the daily light cycle.     

Phosphate has dual roles in cross-bridge kinetics in rabbit psoas single myofibrils

In this study, we aimed to study the role of inorganic phosphate (P_i) in the production of oscillatory work and cross-bridge (CB) kinetics of striated muscle. We applied small-amplitude sinusoidal length oscillations to rabbit psoas single myofibrils and muscle fibers, and the resulting force responses were analyzed during maximal Ca²⁺ activation (pCa 4.65) at 15°C. Three exponential processes, A, B, and C, were identified from the tension transients, which were studied as functions of P_i concentration ([P_i]). In myofibrils, we found that process C, corresponding to phase 2 of step analysis during isometric contraction, is almost a perfect single exponential function compared with skinned fibers, which exhibit distributed rate constants, as described previously. The [P_i] dependence of the apparent rate constants 2πb and 2πc, and that of isometric tension, was studied to characterize the force generation and P_i release steps in the CB cycle, as well as the inhibitory effect of P_i. In contrast to skinned fibers, P_i does not accumulate in the core of myofibrils, allowing sinusoidal analysis to be performed nearly at [P_i] = 0. Process B disappeared as [P_i] approached 0 mM in myofibrils, indicating the significance of the role of P_i rebinding to CBs in the production of oscillatory work (process B). Our results also suggest that P_i competitively inhibits ATP binding to CBs, with an inhibitory dissociation constant of ∼2.6 mM. Finally, we found that the sinusoidal waveform of tension is mostly distorted by second harmonics and that this distortion is closely correlated with production of oscillatory work, indicating that the mechanism of generating force is intrinsically nonlinear. A nonlinear force generation mechanism suggests that the length-dependent intrinsic rate constant is asymmetric upon stretch and release and that there may be a ratchet mechanism involved in the CB cycle.