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Osmotic stress induces inactivation of photosynthesis in guard cell protoplasts of Vicia leaves.

Guard cell protoplasts isolated from Vicia leaves showed a strong suppression of the photosynthesis under hypotonic conditions, as reflected by changes in the chlorophyll fluorescence characteristics. The response was reversible as well. Mesophyll cell protoplasts did not show any lowering of photosynthetic activity under hypo-osmotic conditions. This result indicates that the response was guard cell specific.

Fabaceae↗

Effects of HgCl(2) on CO(2) dependence of leaf photosynthesis: evidence indicating involvement of aquaporins in CO(2) diffusion across the plasma membrane.

Experiments were conducted to examine whether mercury-sensitive aquaporins facilitate photosynthetic CO(2) diffusion across the plasma membrane of leaf mesophyll cells. Discs without abaxial epidermes from Vicia faba leaflets were treated with HgCl(2), an inhibitor of aquaporins. Hydraulic conductivity of the plasma membrane of these discs, measured as the weight loss of the discs in the 1 M sorbitol solution, was inhibited by sub-mM concentrations of HgCl(2) by 70 to 80%. Photosynthetic CO(2) fixation was also inhibited by the HgCl(2) treatment in a similar concentration range. When 0.3 mM HgCl(2) solution was fed to the V. faba leaflets with intact epidermes via the transpiration stream, the rate of photosynthesis on leaf area basis (A) measured at photosynthetically active photon flux density of 700 micromol m(-2) s(-1) and at leaf temperature of 25 degrees C, decreased by about 20 to 30% at any CO(2) concentration in the intercellular spaces (C(i)). However, when CO(2) concentration in the chloroplast stroma (C(c)) was calculated from fluorescence and gas exchange data and A was plotted against C(c), A at low C(c) concentrations did not differ before and after the treatment. The conductance for CO(2) diffusion from the intercellular spaces to the chloroplast stroma (g(i)) decreased to 40 and 30% of the control value, when the leaflets were fed with 0.3 mM and 1.2 mM HgCl(2), respectively. Similar results were obtained with leaves of Phaseolus vulgaris. Although effects of HgCl(2) were not specific, the present results showed that HgCl(2) consistently lowered g(i). It is, thus, probable that the photosynthetic CO(2) uptake across the plasma membrane of the mesophyll cells is facilitated by mercury-sensitive aquaporins.

Algorithms↗

Repair machinery of symbiotic photosynthesis as the primary target of heat stress for reef-building corals.

In a coral-algae symbiotic system, heat-dependent photoinhibition of photosystem II (PSII) leads to coral bleaching. When the reef-building coral Acropora digitifera was exposed to light, a moderate increase of temperature induced coral bleaching through photobleaching of algal pigments, but not through expulsion of symbiotic algae. Monitoring of PSII photoinhibition revealed that heat-dependent photoinhibition was ascribed to inhibition of the repair of photodamaged PSII, and heat susceptibility of the repair machinery varied among coral species. We conclude that the efficiency of the photosynthesis repair machinery determines the bleaching susceptibility of coral species under elevated seawater temperatures.

Animals↗

The ubiquitin-proteasome pathway is involved in rapid degradation of phosphoenolpyruvate carboxylase kinase for C4 photosynthesis.

In C4 photosynthesis, phosphoenolpyruvate carboxylase (PEPC) is the enzyme responsible for catalyzing the primary fixation of atmospheric CO2. The activity of PEPC is regulated diurnally by reversible phosphorylation. PEPC kinase (PEPCk), a protein kinase involved in this phosphorylation, is highly specific for PEPC and consists of only the core domain of protein kinase. Owing to its extremely low abundance in cells, analysis of its regulatory mechanism at the protein level has been difficult. Here we employed a transient expression system using maize mesophyll protoplasts. The PEPCk protein with a FLAG tag could be expressed correctly and detected with high sensitivity. Rapid degradation of PEPCk protein was confirmed and shown to be blocked by MG132, a 26S proteasome inhibitor. Furthermore, MG132 enhanced accumulation of PEPCk with increased molecular sizes at about 8 kDa intervals. Using anti-ubiquitin antibody, this increase was shown to be due to ubiquitination. This is the first report to show the involvement of the ubiquitin-proteasome pathway in PEPCk turnover. The occurrence of PEPCks with higher molecular sizes, which was noted previously with cell extracts from various plants, was also suggested to be due to ubiquitination of native PEPCk.

Enzyme Induction↗

Temperature dependence of photosynthesis in Arabidopsis plants with modifications in Rubisco activase and membrane fluidity.

Net photosynthesis (Pn) is reversibly inhibited at moderately high temperature. To investigate this further, we examined the effects of heat stress on Arabidopsis plants in which Rubisco activase or thylakoid membrane fluidity has been modified. During heating leaves from 25 to 40 degrees C at 250 ppm CO2 and 1% O2, the wild-type (WT), plants expressing the 43 kDa isoform only (rwt43), and plants accumulating activase 40% of WT (R100) exhibited similar inhibitions in the Pn and Rubisco activation state. Despite better membrane integrity than WT, plants having less polyunsaturation of thylakoid lipids (fad7/8 double mutant) failed to maintain greater Pn than the WT. Plants expressing the 46 kDa isoform only (rwt46) exhibited the most inhibition, but plants expressing a 46 kDa isoform incapable of redox regulation (C411A) were similar to the WT. The null mutant (rca) exhibited a continuous decline in Pn. As measured by fluorescence, electron transport activity decreased concomitantly with Pn but PSII was not damaged. Following a quick recovery to 25 from 40 degrees C, whereas most lines recovered 90% Pn, the rwt46 and rca lines recovered only to 59 and <10%, respectively. As measured by NADP-malate dehydrogenase activation, after an initial increase at 30 degrees C, stromal oxidation in the WT and rwt46 plants did not increase further as Pn decreased. These results provide additional insight into the role of Rubisco activation and activase in the reversible heat inhibition of Pn.

Arabidopsis↗

Arabidopsis mutants by activation tagging in which photosynthesis genes are expressed in dedifferentiated calli.

In an effort to delineate the precise mechanisms underlying the organ-specific expression of photosynthesis genes, Arabidopsis lines homozygous for each transgene construct made with the gene for hygromycin B phosphotransferase or beta-glucuronidase (GUS) placed under control of the promoter of the nuclear gene for the small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase (RBCS-3B) were constructed. Furthermore, activation tagging with T-DNA possessing quadruply repeated enhancers derived from the cauliflower mosaic virus 35S promoter was applied to a transgenic line of Arabidopsis. Mutants resistant to hygromycin B during the growth of calli generated from non-green roots on callus-inducing medium resulted from the expression of hygromycin B phosphotransferase driven by the RBCS-3B promoter. Three mutant lines, ces101 to ces103 (callus expression of RBCS), were obtained from approximately 4,000 calli resistant to a selectable marker for transformation. The active transcription driven by the RBCS-3B promoter in all the calli of ces mutants was confirmed by expression of both the GUS reporter gene and endogenous RBCS-3B. Chlorophyll and carotenoids, as well as light-dependent O(2) evolution, have been detected in the calli of all ces mutants. The loci where T-DNA was integrated in the ces101 line were determined by thermal asymmetric interlaced (TAIL)-PCR. The introduction of a DNA fragment harboring the gene for receptor-like kinase placed under the influence of enhancers into the parental line reproduced the phenotype of ces mutants. We have thus concluded that CES101 is a receptor-like kinase. The strategy presented in this investigation may promise to select a greater number of ces mutants.

Arabidopsis↗

Is elevation of carbon dioxide concentration beneficial to seedling photosynthesis in the understory of tropical rain forests?

Cuttings of the southeast Asian tropical rain forest tree species, Pongamia pinnata (L.) Pierre were raised in growth chambers providing a photosynthetic photon flux density (PPFD) of 60 micromol m(-2) s(-1) with either a low or a high red:far-red light ratio (LR and HR, repectively). The chambers were supplied with air containing CO(2) at a concentration of either 400 (LR4 and HR4, respectively) or 800 micromol mol(-1) (HR8 and LR8, respectively). After 4 months, leaf morphology and photosynthetic characteristics were determined. Relative to HR4, the LR4 treatment increased leaf area and total chlorophyll concentration (Chl) by 24 and 25%, respectively, but reduced leaf mass per unit area (LMA) by 19%. Elevated [CO(2)] significantly increased leaf area and LMA but did not affect Chl of LR or HR plants. Leaf nitrogen concentration was unaffected by the red:far-red light ratio but decreased significantly in seedlings in the elevated [CO(2)] treatment. Photosynthesis measured in situ under the growth conditions of ambient light and [CO(2)] (A(amb)) was 30% lower on an area basis and 14% lower on a mass basis in LR4 plants than in HR4 plants. Elevated [CO(2)] reduced the activity of ribulose-1,5-bisphosphate carboxylase/oxygenase and thus decreased light-saturated photosynthetic rate in both HR and LR plants. Elevated [CO(2)] increased mean leaf area and decreased respiration rates in both LR and HR plants. The LR8 plants had significantly higher A(amb) than LR4 plants, but similar A(amb) to HR8 plants.

Carbon Dioxide↗

Effects of soil temperature on parameters of a coupled photosynthesis-stomatal conductance model.

To examine the effects of soil temperature on a coupled photosynthesis-stomatal conductance model, seedlings of trembling aspen (Populus tremuloides Michx.), jack pine (Pinus banksiana Lamb.), black spruce (Picea Mariana (Mill.) B.S.P.) and white spruce (Picea glauca (Moench) Voss) were exposed to soil temperatures ranging from 5 to 35 degrees C for 4 months. Light and CO(2) response curves of foliar gas exchange were measured for model parameterization. The effects of soil temperature on four key model parameters, V(cmax) (maximum rate of carboxylation), J(max) (maximum rate of electron transport), alpha (energy conversion efficiency or quantum efficiency of electron transport) and R(d) (daytime dark respiration), were modeled using two third-order polynomial equations and a modified Arrhenius equation. In all species, V(cmax) and J(max) increased with soil temperature up to an optimum, and then decreased with further increases in soil temperature. In the conifers, alpha showed a similar response to soil temperature as V(cmax) and J(max), but soil temperature had no significant effect on alpha in aspen. Soil temperature had no significant effect on R(d) in any species. The three equations described the relationships between soil temperature and the model parameters reasonably well, but performed best for V(cmax) and worst for alpha. No significant relationships were identified between soil temperature and the parameters of the stomatal conductance model.

Carbon Dioxide↗

Photosynthesis and respiration of black spruce at three organizational scales: shoot, branch and canopy.

To gain insight into the function of photosynthesis and respiration as processes operating within a global ecosystem, we measured gas exchange of mature black spruce (Picea mariana (Mill.) B.S.P.) trees at three organizational scales: individual shoots, whole branches and a forest canopy. A biochemical model was fitted to these data, and physiological parameters were extracted. Pronounced seasonal variation in the estimated model parameters was found at all three organizational scales, highlighting the need to make physiological measurements throughout the year. For example, it took over 100 days for physiological activity to increase from zero during the springtime thaw to its yearly maximum. Good agreement was found between parameter values estimated for the different organizational scales, suggesting that, in the case of aerodynamically rough, largely mono-specific forest canopies, physiological parameters can be estimated from eddy covariance flux measurements. The small differences between photosynthetic parameters estimated at the different scales suggest that the overall spatial organization of photosynthetic capacity is nearly optimized for carbon uptake at each scale.

Carbon Dioxide↗

Annual pattern of photosynthesis in Scots pine in the boreal zone.

To detect seasonal changes in photosynthetic rate in the field, a set of 18,000 photosynthetic measurements made between April and October on three shoots of Scots pine growing near the northern timberline was studied. The measurements were analyzed in the framework of an optimal stomatal control model of photosynthesis, in which irradiance (photosynthetically active radiation, I), air humidity and ambient temperature are driving variables. All driving variables were monitored concomitantly with gas exchange measurements throughout the growing season. The model has nine parameters, of which six were assumed to be constant over the growing season and were fixed based on previous information. The three variable parameters were the initial slope (alpha) and saturation value (gamma) of the light-response curve of carboxylation efficiency in the intercellular cavity, and the cost of transpiration (lambda), in carbon units, regulating the degree of stomatal opening. These parameters could not be estimated independently, nor could their values be satisfactorily found by standard nonlinear regression techniques. A Monte Carlo based simulation procedure was devised to analyze the best-fit parameters and their mutual correlations near the minimum of the residual sum of squares. This was accomplished by replacing the saturation value of the light-response curve with a linearity parameter that determined the shape of the curve. In the best fit solutions, only alpha and lambda varied from day to day, whereas the shape of the curve was constant (i.e., gamma was proportional to alpha). Both alpha and lambda showed consistent patterns from spring to autumn, but the seasonal variation was considerably greater for alpha than for lambda. The optimal stomatal control model with the seven fixed and two daily parameter values gave a good overall fit for photosynthetic rate over the season (PEV > 95%).

Models, Biological↗

Response of photosynthesis in second-generation Pinus radiata trees to long-term exposure to elevated carbon dioxide partial pressure.

Second-generation Pinus radiata D. Don trees, propagated from cuttings of 4-year-old trees previously grown at ambient (36 Pa) and elevated (65 Pa) CO2 partial pressure (Ca) were grown under the same conditions in open-top chambers for a further year. As cuttings of the original trees, these second-generation trees were physiologically the same age as the first-generation trees with the only difference between the two being size. This allowed us to test the effects of tree size independently of age or duration of exposure. Total non-structural carbohydrate concentration, area-based nitrogen concentration, leaf mass per unit area and chlorophyll concentration measured in three foliage age cohorts were unaffected by either age or Ca. There were no signs of photosynthetic down-regulation in trees grown at elevated Ca. When measured at the growth Ca, photosynthetic rate in young needles during summer, autumn and spring was 34, 43 and 38% higher, respectively, in trees grown at elevated Ca than in trees grown at ambient Ca. In older needles, the corresponding photosythetic rate increases were 26, 47 and 49%. Water-use efficiency, determined by stable carbon isotope analysis, was 49% higher in foliage in the elevated Ca treatment than in foliage in the ambient Ca treatment. This increase was entirely due to photosynthetic enhancement, because stomatal conductance did not differ between treatments. We conclude that down-regulation of photosynthesis at elevated Ca is related to tree size rather than tree age or duration of exposure, and that enhanced photosynthetic rates can be maintained while sink strength is high enough to use the excess photosynthates.elevated CO2, needle age, photosynthetic down-regulation, photosynthetic enhancement, sink strength, water-use efficiency.

Carbon Dioxide↗

Integrating within-crown variation in net photosynthesis in loblolly and slash pine families.

We examined photosynthetic characteristics of two fast- and two slow-growing half-sib families of both loblolly pine (Pinus taeda L.) and slash pine (Pinus elliottii var. elliottii Engelm.) on two sites in northern Florida to: (1) quantify variation in light-saturated net photosynthesis (Amax) associated with vertical crown position and foliage age; (2) quantify the amount and distribution of leaf area by foliage age class; and (3) determine whether photosynthetic indices, ranging from leaf-level through whole-crown Amax, were related to growth differences among species and families. In both species, leaf-level Amax was higher in more recently formed foliage both within the same year (where Amax in the third flush averaged 10 to 30% higher than Amax in the first flush) and between years (where Amax in current-year foliage averaged 20 to 40% higher than Amax in 1-year-old foliage). When expressed on a leaf area basis, Amax of current-year foliage was higher in slash pine than in loblolly pine, but Amax expressed on a mass basis did not differ between species. Loblolly pine had higher whole-tree leaf area than slash pine, whereas whole-tree Amax did not differ between species. When the mean values for fast-growing families were compared with the mean values for slow-growing families, there were no differences in leaf-level characteristics, whereas at the whole-tree level, fast-growing families had higher leaf area and whole-tree Amax than slow-growing families in both species. When comparisons were made among the individual fast- and slow-growing families, however, results were more variable. In both species, stem volume growth was strongly correlated with whole-tree Amax, with most of the strength of the correlation deriving from the relationship between volume growth and tree leaf area.

Genetic Variation↗

Seasonal changes in photosynthesis and photoprotection in a Quercus ilex subsp. ballota woodland located in its upper altitudinal extreme in the Iberian Peninsula.

Quercus ilex L. subsp. ballota (Desf.) Samp., a Mediterranean evergreen species growing in a continental Mediterranean climate, did not experience water stress and showed greater sensitivity to winter stress than to summer stress over a 12-month period. Net CO2 assimilation rates and photosystem II (PSII) efficiency decreased markedly during the cold months and recovered completely in spring. Lutein, neoxanthin and beta-carotene to chlorophyll (Chl) molar ratios all showed the same trend throughout the year, increasing from September to March. This increase was a result of increases in carotenoid concentrations, because Chl concentration per unit leaf area remained stable, and was higher at the end than at the beginning of the first growing season. Lutein-epoxide was a minor component of the total lutein pool. Thermal energy dissipation and non-photochemical quenching (NPQ) were associated with the de-epoxidated forms of the xanthophyll cycle pigments in the warm months. Photosynthetic rates decreased slightly at midday in summer. These changes were accompanied by decreases in maximum potential PSII efficiency (which recovered during the night), actual and intrinsic PSII efficiencies, photochemical quenching and increases in NPQ. Overall, our data indicate down-regulation of photosynthesis during the summer. The diurnal de-epoxidation of violaxanthin to antheraxanthin and zeaxanthin occurred throughout the year, except in January. Antioxidant enzymatic activity increased in the winter months, especially during the coldest months, highlighting its key role in photoprotection against photo-oxidation. Structural and functional modifications protected PSII from permanent damage and allowed 1-year-old leaves to photosynthesize at high rates when temperatures increased in spring.

Altitude↗

Fruit load and branch ring-barking affect carbon allocation and photosynthesis of leaf and fruit of Coffea arabica in the field.

Increasing fruit load (from no berries present to 25, 50 and 100% of the initial fruit load) significantly decreased branch growth on 5-year-old coffee (Coffea arabica L.) trees of the dwarf cultivar 'Costa Rica 95', during their third production cycle. Ring-barking the branches further reduced their growth. Berry dry mass at harvest was significantly reduced by increasing fruit load. Dry matter allocation to berries was four times that allocated to branch growth during the cycle. Branch dieback and berry drop were significantly higher at greater fruit loads. This illustrates the importance of berry sink strength and indicates that there is competition for carbohydrates between berries and shoots and also among berries. Leaf net photosynthesis (P(n)) increased with increasing fruit load. Furthermore, leaves of non-isolated branches bearing full fruit load achieved three times higher P(n) than leaves of isolated (ring-barked) branches without berries, indicating strong relief of leaf P(n) inhibition by carbohydrate demand from berries and other parts of the coffee tree when excess photoassimilates could be exported. Leaf P(n) was significantly higher in the morning than later during the day. This reduction in leaf P(n) is generally attributed to stomatal closure in response to high irradiance, temperature and vapor pressure deficit in the middle of the day; however, it could also be a feedback effect of reserves accumulating during the morning when climatic conditions for leaf P(n) were optimal, because increased leaf mass ratio was observed in leaves of ring-barked branches with low or no fruit loads. Rates of CO(2) emission by berries decreased and calculated photosynthetic rates of berries increased with increasing photosynthetic photon flux (PPF) especially at low PPFs (0 to 100 micromol m(-2) s(-1)). The photosynthetic contribution of berries at the bean-filling stage was estimated to be about 30% of their daily respiration costs and 12% of their total carbon requirements at PPF values commonly experienced in the field (200 to 500 micromol m(-2) s(-1)).

Carbohydrate Metabolism↗

Photoinhibition of photosynthesis in needles of two cypress (Cupressus sempervirens) clones.

Photoinhibition of photosynthesis and photosynthetic recovery were studied in detached needles of cypress (Cupressus sempervirens L.) Clones 52 and 30 under controlled conditions of high irradiation (about 1900 micromol m(-2) s(-1) for 60 min; HL treatment), followed by 60 min in darkness. The degree of photoinhibition was determined based on the ratio of variable to maximum chlorophyll fluorescence (Fv/Fm), which is a measure of the potential efficiency of photosystem II (PSII), and on electron transport measurements. The Fv/Fm ratio declined in needles of both clones in response to the HL treatment. Minimal fluorescence (Fo) increased in HL-treated needles of both clones. The HL treatment decreased rates of whole-chain and PSII activity of isolated thylakoids more in Clone 52 than in Clone 30. In needles of both clones, PSI activity was less sensitive to photoinhibition than PSII activity. In the subsequent 60-min dark incubation, fast recovery was observed in needles of both clones, with PSII efficiencies reaching similar values to those in non-photoinhibited needles. The artificial exogenous electron donors diphenyl carbazide (DPC), hydroxylamine (NH2OH) and manganese chloride (MnCl2) failed to restore the HL-induced loss of PSII activity in needles of Clone 30, whereas DPC and NH2OH significantly restored PSII activity in photoinhibited needles of Clone 52. Quantification of the PSII reaction center protein D1 and the 33-kDa protein of the water-splitting complex following HL treatment of needles revealed pronounced differences between Clone 52 and Clone 30. The large decrease in PSII activity in HL-treated needles was caused by the marked loss of D1 protein and 33-kDa protein in Clone 30 and Clone 52, respectively.

2,6-Dichloroindophenol↗

Phosphorus and nitrogen limitations to photosynthesis in Rocky Mountain bristlecone pine (Pinus aristata) in Colorado.

We examined Pinus aristata Engelm. stands in four locations in Colorado: Almagre Mountain, Black Mountain, Goliath Peak and Quartzville. All stands are located at 3200-3700 m and face south-southeast. We measured maximum mass-based assimilation rates (A(max)) and nitrogen (N) and phosphorus (P) foliar concentrations on six foliar age classes, from which instantaneous photosynthetic N- and P-use efficiencies (PNUE and PPUE, respectively) and P:N ratios were estimated. Leaf mass per area (LMA) was also determined for each foliar age class from each site. Foliar age, P and N concentrations, and the P:N ratio explained the most variation in A(max) when data from all sites were combined. Leaf mass per area did not vary with foliar age class. Both P and N limit A(max), although P appears to be more limiting. The critical P:N ratio is approximately 0.12. Results for Black Mountain differed from the other sites, as A(max) was not correlated with age and was negatively correlated with LMA and P. Current findings showed no evidence of N saturation at the Front Range sites (Almagre Mountain and Goliath Peak); however, because P is a limiting nutrient, increased anthropogenic N availability at sites in the Front Range may cause adverse effects on photosynthesis, and perhaps growth, in the future.

Altitude↗

Interspecific variability of stem photosynthesis among tree species.

The photosynthetic characteristics of current-year stems of six deciduous tree species, two evergreen tree species and ginkgo (Ginkgo biloba L.) were compared. Gas exchange, chlorophyll concentration, nitrogen concentration and maximum quantum yield of PSII were measured in stems in summer and winter. A light-induced decrease in stem CO(2) efflux was observed in all species. The apparent gross photosynthetic rate in saturating light ranged from 0.72 micromol m(-2 )s(-1) (ginkgo, in winter) to 3.73 micromol m(-2) s(-1) (Alnus glutinosa (L.) Gaertn., in summer). Despite this variability, a unique correlation (slope = 0.75), based on our results and those reported in the literature, was found between gross photosynthetic rate and dark respiration rate. Mass-based gross photosynthetic rate decreased with stem mass per area and correlated to chlorophyll concentration and nitrogen concentration, both in summer and winter. The radial distribution of stem chlorophyll differed among species, but all species except ginkgo had chlorophyll as deep as the pith. In summer, the maximum quantum yield of stem PSII (estimated from the ratio of variable to maximal fluorescence; F (v)/F (m)) of all species was near the optimal value found for leaves. By contrast, the values were highly variable in winter, suggesting large differences in sensitivity to low-temperature photoinhibition. The winter values of Fv/Fm were only 31-60% of summer values for the deciduous species, whereas the evergreen conifer species maintained high F (v)/F (m) in winter. The results highlight the interspecific variability of gross photosynthesis in the stem and its correlation with structural traits like those found for leaves. The structural correlations suggest that the selection of photosynthetic traits has operated under similar constraints in stems and leaves.

Chlorophyll↗

How carotenoids protect bacterial photosynthesis.

The essential function of carotenoids in photosynthesis is to act as photoprotective agents, preventing chlorophylls and bacteriochlorophylls from sensitizing harmful photodestructive reactions in the presence of oxygen. Based upon recent structural studies on reaction centres and antenna complexes from purple photosynthetic bacteria, the detailed organization of the carotenoids is described. Then with specific reference to bacterial antenna complexes the details of the photoprotective role, triplet triplet energy transfer, are presented.

Carotenoids↗