Inhibition of photosynthetic activities under slow water stress measured in vivo by the photoacoustic method

A slow water stress over several days was imposed on tobacco plants (Nicotiana tabacum L. var. Xanthi) by withholding water from the soil. Photosynthesis was measured in leaves from those water-stressed plants by the photoacoustic method. Slow drought induced marked changes in the photoacoustic signals, which were largely similar to those observed previously in leaves subjected to rapid desiccation in air (over 3–4 h), reflecting two simultaneous changes: 1) Modification of the heat and oxygen diffusion characteristics of the leaves due to changes in their anatomical structure [shown by the change in the slope of the plot of the oxygen (A_OX) to photothermal signal (A_PT) ratio vs the square root of the modulation frequency]; 2) Inhibition of gross photosynthesis measured by the extrapolation of the A_OX/A_PT ratio to zero frequency. However, in contrast to rapid water stress in detached leaves, where it was shown that mainly the oxidizing side of photosystem II (PS II) was damaged, we found a slower and more complex phenomenology having largely biphasic kinetics. During the first 6 days, there was a strong reduction in the photochemical energy storage, but the inhibition of oxygen evolution was relatively mild. The Emerson enhancement in state 1 dropped considerably, indicating lowering of the apparent absorption cross-section of PS II. Fluorescence measurements suggest that PS II reaction center itseIf may be the primary site of the damage. PS I activity, judged by cytochrome f photooxidation, remained largely intact. The subsequent days were associated with a further spectacular decrease in the oxygen evolution quantum yield with both photosystems damaged. The photochemical energy storage continued to decrease further. The Emerson enhancement ratio of the remaining activities in both State 1 and 2 showed a marked increase, indicating the reestablishment of a strong imbalance in the distribution of excitation energy within the photochemical apparatus in favor of PS II. All the photoacoustic changes observed in response to drought were completely reversible within 2–3 days upon rewatering of the soil.     

Ear of durum wheat under water stress: water relations and photosynthetic metabolism

The photosynthetic characteristics of the ear and flag leaf of well-watered (WW) and water-stressed (WS) durum wheat (Triticum turgidum L. var. durum) were studied in plants grown under greenhouse and Mediterranean field conditions. Gas exchange measurements simultaneously with modulated chlorophyll fluorescence were used to study the response of the ear and flag leaf to CO₂ and O₂ during photosynthesis. C₄ metabolism was identified by assessing the sensitivity of photosynthetic rate and electron transport to oxygen. The presence of CAM metabolism was assessed by measuring daily patterns of stomatal conductance and net CO₂ assimilation. In addition, the histological distribution of Rubisco protein in the ear parts was studied by immunocytochemical localisation. Relative water content (RWC) and osmotic adjustment (osmotic potential at full turgor) were also measured in these organs. Oxygen sensitivity of the assimilation rate and electron transport, the lack of Rubisco compartmentalisation in the mesophyll tissues and the gas-exchange pattern at night indicated that neither C₄ nor CAM metabolism occurs in the ear of WW or WS plants. Nevertheless, photosynthetic activity of the flag leaf was more affected by WS conditions than that of the ear, under both growing conditions. The lower sensitivity under water stress of the ear than of the flag leaf was linked to higher RWC and osmotic adjustment in the ear bracts and awns. We demonstrate that the better performance of the ear under water stress (compared to the flag leaf) is not related to C₄ or CAM photosynthesis. Rather, drought tolerance of the ear is explained by its higher RWC in drought. Osmotic adjustment and xeromorphic traits of ear parts may be responsible.     

Studies on the expression of marker genes in chickpea

Conditions were established for the optimum transient expression of beta-glucuronidase and neomycin phosphotransferase II genes introduced into zygotic embryos of chickpea (Cicer arietinum L. 6153 and CM72) by accelerated tungsten particles. Plasmid DNA at a concentration of 12 microgram per milligram of tungsten particles when accelerated with an inflow of helium gas at 60 kilogram per square centimeter through a distance of 24 centimeter in a chamber maintained at a negative pressure of 71.12 centimeter of mercury, resulted in optimal transient expression of the beta-glucuronidase gene in chickpea embryos. However, the expression of the marker genes was 20-40% higher under a cauliflower mosaic virus promoter in comparison to the Win6 and actin promoters. When Agrobacterium tumefaciens was used to transfer marker genes into zygotic embryos and the resultant plants were analysed for activity of the beta-glucuronidase and neomycin phosphotransferase II genes, both of these genes were expressed in tumorous tissues. When a disarmed strain of Agrobacterium was used, normal shoots were regenerated in which the lower parts showed expression of both genes at a frequency of 20%. This revised version was published online in June 2006 with corrections to the Cover Date.     

Effect of vermicompost fertilizer on photosynthetic characteristics of chickpea (Cicer arietinum L.) under drought stress

Water availability is an important factor for plant growth in arid environments. In recent decades, vermicompost (VC) fertilizer has been used in agriculture as a safe and effective fertilizer with high water-holding capacity. The aim of the present study was to characterize effects of VC fertilizer on photosynthetic activity of chickpea (Cicer arietinum L. cv. Karaj) under drought conditions at three different growth stages. Tests were carried out with four volumetric ratios of VC to soil, i.e., 0:100, 10:90, 20:80, and 30:70, and three levels of drought stress, i.e., no stress (NS), moderate drought (MS), and severe drought (SS) (100, 75, and 25% of field capacity, respectively). Evaluations were performed at the seedling, flowering, and podding stage. We found that the VC treatment under NS conditions significantly increased total chlorophyll content [Chl (a+b)], intercellular CO₂ concentration (C_i), net photosynthetic rate (P_N), transpiration rate (E), and maximal quantum yield of PSII photochemistry (F_v/F_m) at all three stages. The VC addition of 10 and 20% significantly enhanced the Chl content and F_v/F_m under MS and F_v/F_m, C_i, and P_N under SS at the flowering stage. In conclusion, our results proved a positive effect of the VC fertilizer on photosynthesis of chickpea under NS conditions, but it was not found under MS and SS.     

水分胁迫对短枝型果树光合作用的非气孔限制

水分胁迫使叶片相对含水量降低,气孔阻力增大.水分胁迫光合速率的下降除受气孔因素影响之外,随着胁迫时间的延长和胁迫程度的加剧,水分胁迫导致O-·2累积,H2O2含量增加,从而引发膜脂过氧化,造成膜渗漏,质膜相对膜透性增大,膜脂过氧化产物MDA含量升高,由膜系统破坏而诱发的非气孔因素成为光合速率下降的主要原因.     

Photosystem II: The machinery of photosynthetic water splitting

This review summarizes our current state of knowledge on the structural organization and functional pattern of photosynthetic water splitting in the multimeric Photosystem II (PS II) complex, which acts as a light-driven water: plastoquinone-oxidoreductase. The overall process comprises three types of reaction sequences: (1) photon absorption and excited singlet state trapping by charge separation leading to the ion radical pair [Formula: see text] formation, (2) oxidative water splitting into four protons and molecular dioxygen at the water oxidizing complex (WOC) with P680+* as driving force and tyrosine Y(Z) as intermediary redox carrier, and (3) reduction of plastoquinone to plastoquinol at the special Q(B) binding site with Q(A)-* acting as reductant. Based on recent progress in structure analysis and using new theoretical approaches the mechanism of reaction sequence (1) is discussed with special emphasis on the excited energy transfer pathways and the sequence of charge transfer steps: [Formula: see text] where (1)(RC-PC)* denotes the excited singlet state (1)P680* of the reaction centre pigment complex. The structure of the catalytic Mn(4)O(X)Ca cluster of the WOC and the four step reaction sequence leading to oxidative water splitting are described and problems arising for the electronic configuration, in particular for the nature of redox state S(3), are discussed. The unravelling of the mode of O-O bond formation is of key relevance for understanding the mechanism of the process. This problem is not yet solved. A multistate model is proposed for S(3) and the functional role of proton shifts and hydrogen bond network(s) is emphasized. Analogously, the structure of the Q(B) site for PQ reduction to PQH(2) and the energetic and kinetics of the two step redox reaction sequence are described. Furthermore, the relevance of the protein dynamics and the role of water molecules for its flexibility are briefly outlined. We end this review by presenting future perspectives on the water oxidation process.     

水分胁迫对牛心朴子光合生理特性影响的研究

采用PVC管种植模拟土壤干旱的方法,研究了牛心朴子(Cynanchum komarovii)在水分胁迫下光合速率(Pn)、气孔导度(Gs)、胞间CO2浓度(Ci)、叶绿素荧光的变化规律及不同生育期适应性表现。结果表明：土壤水分胁迫对牛心朴子叶片光合生理的影响与其胁迫时间及其胁迫程度都有关系,胁迫前中期Pn下降的原因主要是气孔限制,而到后期则以非气孔因素限制为主。中度土壤水分胁迫在短期内对牛心朴子叶片光合作用具有促进作用,而且有利于WUE的提高。而重度胁迫对牛心朴子Pn的影响较显著,而且非气孔因素的出现早于中度胁迫的处理。牛心朴子的光合生理对土壤水分胁迫具有一定的适应时期和适应范围。     

Inhibition of photosynthetic reactions under water stress: interaction with light level

When the shrub Nerium oleander L., growing under full natural daylight outdoors, was subjected to water stress, stomatal conductance declined, and so did non-stomatal components of photosynthesis, including the CO₂-saturated rate of CO₂ uptake by intact leaves and the activity of electron transport by chloroplasts isolated from stressed plants. This inactivation of photosynthetic activity was accompanied by changes in the fluorescence characteristics determined at 77 K (-196°C) for the upper leaf surface and from isolated chloroplasts. The maximum (F _M) and the variable (F _V) fluorescence yield at 692 nm were strongly quenched but there was little effect on the instantaneous (F _O) fluorescence. There was a concomitant quenching of the maximum and variable fluorescence at 734 nm. These results indicate an inactivation of the primary photochemistry associated with photosystem II. The lower, naturally shaded surfaces of the same leaves were much less affected than the upper surfaces and water-stress treatment of plants kept in deep shade had little or no effect on the fluorescence characteristics of either surface, or of chloroplasts isolated from the water-stressed leaves. The effects of subjecting N. oleander plants, growing in full daylight, to water stress are indistinguishable from those resulting when plants, grown under a lower light regime, are exposed to full daylight (photoinhibition). Both kinds of stress evidently cause an inactivation of the primary photochemistry associated with photosystem II. The results indicate that water stress predisposes the leaves to photoinhibition. Recovery from this inhibition, following restoration of favorable water relations, is very slow, indicating that photoinhibition is an important component of the damage to the photosynthetic system that takes place when plants are exposed to water stress in the field. The underlying causes of this water-stress-induced susceptibility to photoinhibition are unknown; stomatal closure or elevated leaf temperature cannot explain the increased susceptibility.Abbreviations and symbols Chl chlorophyll - PFD photon flux area density - PSI, PSII photosystem I, II - F _M, F _O, F _V maximum, instantaneous, variable fluorescence emission - leaf water potential C.I.W.-D.P.B. Publication No. 775     

Sequence similarity based identification of abiotic stress responsive genes in chickpea

Chickpea (Cicer arietinum L.) is an important food legume crop, particularly for the arid regions including Indian subcontinent. Considering the detrimental effect of drought, temperature and salt stress on crop yield, efforts have been initiated in the direction of developing improved varieties and designing alternate strategies to sustain chickpea production in adverse environmental conditions. Identification of genes that confer abiotic stress tolerance in plants remains a challenge in contemporary plant breeding. The present study focused on the identification of abiotic stress responsive genes in chickpea based on sequence similarity approach exploiting known abiotic stress responsive genes from model crops or other plant species. Ten abiotic stress responsive genes identified in other plants were partially amplified from eight chickpea genotypes and their presence in chickpea was confirmed after sequencing the PCR products. These genes have been functionally validated and reported to play significant role in stress response in model plants like Arabidopsis, rice and other legume crops. Chickpea EST sequences available at NCBI EST database were used for the identification of abiotic stress responsive genes. A total of 8,536 unique coding long sequences were used for identification of chickpea homologues of these abiotic stress responsive genes by sequence similarity search (BLASTN and BLASTX). These genes can be further explored towards achieving the goal of developing superior chickpea varieties providing improved yields under stress conditions using modern molecular breeding approaches.     

Carbendazim alleviates effects of water stress on chickpea seedlings

Carbendazim (methyl-2-benzimidazole carbamate) promoted root growth of chickpea (Cicer arietinum L.) seedlings subjected to polyethylene glycol (PEG, osmotic potential −0.5 MPa) induced water stress. The relative water content, membrane stability index, 2,3,5-triphenyltetrazolium chloride reduction and contents of some osmolytes (proline, sucrose, glucose and fructose) enhanced significantly while the contents of lipid peroxides and hydrogen peroxide diminished effectively by addition of 0.05 % carbendazim into PEG solution. This revised version was published online in September 2005 with the corrected author information.     

Characterization of five CIPK genes expressions in maize under water stress

ABA, H₂O₂ and Ca²⁺ play critical roles as signals in the adaptive responses of plants to water and other stresses. They accumulate in plant cells under water and other stresses and induce changes in stress-related gene expressions. CIPKs, protein kinases associated with a calcineurin B-like calcium sensor, play a role in the regulation of stress gene expression in plants. However, it is still unclear whether ABA and H₂O₂ are key inducers that regulate the changes in CIPK expressions under water stress. In this study, five stress-inducible CIPKs in maize were retrieved from Database. They were designated as ZmCIPK1, 3, 8, 17 and 18, based on their homologies with known CIPK sequences. The expressions of the five ZmCIPKs in maize leaves and roots were analyzed and found to be regulated by PEG, CaCl₂, ABA and H₂O₂ to different extents. Moreover, the effect of ABA and H₂O₂ on the expressions of ZmCIPKs under water stress was in an organ-dependent manner.     

Oxidative stress inhibits the repair of photodamage to the photosynthetic machinery

Absorption of excess light energy by the photosynthetic machinery results in the generation of reactive oxygen species (ROS), such as H2O2. We investigated the effects in vivo of ROS to clarify the nature of the damage caused by such excess light energy to the photosynthetic machinery in the cyanobacterium Synechocystis sp. PCC 6803. Treatments of cyanobacterial cells that supposedly increased intracellular concentrations of ROS apparently stimulated the photodamage to photosystem II by inhibiting the repair of the damage to photosystem II and not by accelerating the photodamage directly. This conclusion was confirmed by the effects of the mutation of genes for H2O2-scavenging enzymes on the recovery of photosystem II. Pulse labeling experiments revealed that ROS inhibited the synthesis of proteins de novo. In particular, ROS inhibited synthesis of the D1 protein, a component of the reaction center of photosystem II. Northern and western blot analyses suggested that ROS might influence the outcome of photodamage primarily via inhibition of translation of the psbA gene, which encodes the precursor to D1 protein.     

水分胁迫的基因表达和信号转导(综述)

植物在水分胁迫条件下的依赖ABA和不依赖ABA的基因表达途径来调节对逆境的适应。植物通过渗透感受器感知胁迫信号,以MAPK和CDPK等途径传递信号,最终引起基因表达。     

The protective action of cytokinins on the photosynthetic machinery and productivity of plants under stress (review)

A putative way of the protective action of cytokinins on the photosynthetic processes in crops experiencing various stress factors is considered. Various cytokinins are characterized. Pathways of the multiple effects of cytokinin preparations mediating the protection of the photosynthetic machinery from stress are described. Cytokinins interact with receptor proteins, and then the signal is transduced to primary cellular targets (primary response genes). These genes, which possess receptor domains, induce synthesis of the corresponding mRNAs and photosynthesis-related proteins of chlorophyll-protein complexes, the electron-transport chain, and carbon metabolism, primarily, the key enzyme ribulose bisphosphate carboxylase/oxygenase. The protective action of cytokinins under stress conditions preserves the structure and function of the photosynthetic machinery. The application of cytokinins to improving crop yields is discussed.     

外源一氧化氮对干旱胁迫下杨树光合作用的影响

NO是生物体中一种自由基分子,其NO对树木叶片光合作用的影响研究未见报道.本文研究了外源NO对杨树叶片水分状况、光合作用和抗氧化物酶活力的调节作用.不同浓度SNP处理对杨树叶片含水量具有显著影响,杨树叶片含水率随着SNP浓度的提高而增加.当SNP浓度增加到00μmol·L^-1后各处理杨树叶片含水率变化趋于稳定.外源NO能提高水分胁迫下杨树叶片的光合、原初光能转化率Fv/Fm、Fm/Fo和Fv/Fo等的比值.其效果随水分胁迫时间的延长而降低.与此对应的是,短时间水分处理(1 h)的杨树叶片SOD和POD抗氧化物酶的活性显著高于长时间(3h)水分胁迫处理.SNP能显著提高不同干旱时间处理组的POD活性,而对SOD活性影响不明显.同时,随SNP浓度的增加,POD和SOD活性呈现先升后降的趋势.因此,干旱胁迫可引起杨树叶片光合效率降低,出现氧化伤害症状,外源NO可诱导抗氧化物酶POD和SOD活性的升高,缓解原初光能转化率Fv/Fm、Fm/Fo和Fv/Fo等值的降低,从而延缓活性氧积累,减轻水分胁迫对杨树叶片光合作用的影响.     

Salt stress effects on the photosynthetic electron transport chain in two chickpea lines differing in their salt stress tolerance

The main objective of this study was to evaluate the effects of salt stress on the photosynthetic electron transport chain using two chickpea lines (Cicer arietinum L.) differing in their salt stress tolerance at the germination stage (AKN 87 and AKN 290). Two weeks after sowing, seedlings were exposed to salt stress for 2 weeks and irrigated with 200 ml of 200 mM NaCl every 2 days. The polyphasic OJIP fluorescence transient and the 820-nm transmission kinetics (photosystem I) were used to evaluate the effects of salt stress on the functionality of the photosynthetic electron transport chain. It was observed that a signature for salt stress was a combination of a higher J step (V_J), a smaller IP amplitude, and little or no effect on the primary quantum yield of PSII (φ_Po). We observed for AKN 290 a shorter leaf life cycle, which may represent a mechanism to cope with salt stress. For severely salt-stressed leaves, an inhibition of electron flow between the PQ pool and P700 was found. The data also suggest that the properties of electron flow beyond PSI are affected by salt stress.     

Evaluation of photosynthetic electron flow using simultaneous measurements of gas exchange and chlorophyll fluorescence under photorespiratory conditions

Simultaneous measurements of leaf gas exchange and chlorophyll fluorescence for Koelreuteria paniculata Laxm. at 380 ± 5.6 and 600 ± 8.5 ??mol mol^?1 were conducted, and the photosynthetic electron flow via photosystem II (PSII) to photosynthesis, photorespiration, and other electron-consuming processes were calculated. The results showed that the photosynthetic electron flow associated with carboxylation (J _c), oxygenation (J _o), and other electron-consuming processes (J _r) were 72.7, 45.7, and 29.4 ??mol(e^?) m^?2 s^?1 at 380 ??mol mol^?1, respectively; and 86.1, 35.3, and 48.2 ??mol(e^?) m^?2 s^?1 at 600 ??mol mol^?1, respectively. Our results revealed that other aspects associated with electronconsuming processes, except for photosynthesis and respiration, were neither negligible nor constant under photorespiratory conditions. Using maximum net photosynthetic rate (P _max), day respiration (R), photorespiration rate (R _l), and maximum electron flow via PSII (J _max), the use efficiency of electrons via PSII at saturation irradiance to fix CO₂ was calculated. The calculated results showed that the use efficiency of electrons via PSII to fix CO₂ at 600 ??mo^l mol^?1 was almost as effective as that at 380 ??mol mol^?1, even though more electrons passed through PSII at 600 ??mol mol^?1 than at 380 ??mol mol^?1.     

The expression profile of genes in rice roots under low phosphorus stress

Phosphorus (P) is one of the most essential macronutrients required for plant growth. Although it is abundant in soil, P is often the limiting nutrient for crop yield potential because of the low concentration of soluble P that plants can absorb directly. The gene expression profile was investigated in rice roots at 6, 24 and 72 h under low P stress and compared with a control (normal P) profile, using a DNA chip of 60000 oligos (70 mer) that represented all putative genes of the rice genome. A total of 795 differentially expressed genes were identified in response to phosphate (Pi) starvation in at least one of the treatments. Based on the analysis, we found that: (i) The genes coding for the Pi transporter, acid phosphatase and RNase were up-regulated in rice roots; (ii) the genes involved in glycolysis were first up-regulated and then down-regulated; (iii) several genes involved in N metabolism and lipid metabolism changed their expression patterns; (iv) some genes involved in cell senescence and DNA or protein degradation were up-regulated; and (v) some transmembrane transporter genes were up-regulated. The results may provide useful information in the molecular process associated with Pi deficiency and thus facilitate research in improving Pi utilization in crop species.