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Due to its characteristic of high biomass yield potential, there is considerable interest in cultivating Phalaris arundinacea L. cv. 'chuancaoyin No.3' (reed canary grass) on the Qinghai-Tibet Plateau where there is an abundance of alpine steppe meadow and a potential large market for animal husbandry. In this study, we 1) investigate whether reed canary grass exhibits superior productive capacity to Elymus nutans 'Aba' (E. nutans), ordinary common pasture, during the long warm days of summer at high-altitude; and 2) compare the cold tolerance between reed canary grass and E. nutans, including photosynthesis, photo-inhibition, and photo-protection. The results suggest that reed canary grass exhibits higher photosynthetic capacity compared to E. nutans at latitudes of the cool temperate zone. Meanwhile, cold-induced photo-inhibition and photo-damage at high altitudes in reed canary grass were due to both stomatal and non-stomatal limitation, and the enhancement in photo-respiration, thermal dissipation, and Mehler reaction are important processes to minimize the negative effects of high elevation and a cold environment., (Copyright © 2017 The Authors. Published by Elsevier GmbH.. All rights reserved.)

This study investigated the feasibility of using photosynthetic bacteria (PSB) to produce biomass and carotenoid while treating wastewater. The effects of light intensity on the biomass, carotenoid and bacteriochlorophyll accumulation in together with pollutant removal were studied. Results showed that it was feasible to use PSB to treat wastewater as well as to produce biomass or carotenoid. 2000 lux was an optimal intensity for biomass production and COD removal, and the corresponding values were 2645 mg/L and 94.7%. 8000 lux was an optimal light intensity for carotenoid production (1.455 mg/L). Mechanism analysis displayed that the greater the bacteriochlorophyll and carotenoid were secreted, the lower the light conversion efficiency turned out to be. The highest light conversion efficiency was achieved at 500 lux; the ATP production, biomass production, and COD removal were the highest at 2000 lux, but the bacteriochlorophyll and carotenoid content were the lowest at 2000 lux., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

The recent advances in plant biology have significantly improved our understanding of reactive oxygen species (ROS) as signaling molecules in the redox regulation of complex cellular processes. In plants, free radicals and non-radicals are prevalent intra- and inter-cellular ROS, catalyzing complex metabolic processes such as photosynthesis. Photosynthesis homeostasis is maintained by thiol-based systems and antioxidative enzymes, which belong to some of the evolutionarily conserved protein families. The molecular and biological functions of redox regulation in photosynthesis are usually to balance the electron transport chain, photosystem II, photosystem I, mesophyll and bundle sheath signaling, and photo-protection regulating plant growth and productivity. Here, we review the recent progress of ROS signaling in photosynthesis. We present a comprehensive comparative bioinformatic analysis of redox regulation in evolutionary distinct photosynthetic cells. Gene expression, phylogenies, sequence alignments, and 3D protein structures in representative algal and plant species revealed conserved key features including functional domains catalyzing oxidation and reduction reactions. We then discuss the antioxidant-related ROS signaling and important pathways for achieving homeostasis of photosynthesis. Finally, we highlight the importance of plant responses to stress cues and genetic manipulation of disturbed redox status for balanced and enhanced photosynthetic efficiency and plant productivity. [ABSTRACT FROM AUTHOR]

Abstract Background As yields of major crops such as wheat (T. aestivum) have begun to plateau in recent years, there is growing pressure to efficiently phenotype large populations for traits associated with genetic advancement in yield. Photosynthesis encompasses a range of steady state and dynamic traits that are key targets for raising Radiation Use Efficiency (RUE), biomass production and grain yield in crops. Traditional methodologies to assess the full range of responses of photosynthesis, such a leaf gas exchange, are slow and limited to one leaf (or part of a leaf) per instrument. Due to constraints imposed by time, equipment and plant size, photosynthetic data is often collected at one or two phenological stages and in response to limited environmental conditions. Results Here we describe a high throughput procedure utilising chlorophyll fluorescence imaging to phenotype dynamic photosynthesis and photoprotection in excised leaves under controlled gaseous conditions. When measured throughout the day, no significant differences (P > 0.081) were observed between the responses of excised and intact leaves. Using excised leaves, the response of three cultivars of T. aestivum to a user—defined dynamic lighting regime was examined. Cultivar specific differences were observed for maximum PSII efficiency (F v′/F m′—P 130 μmol m−2 s−1 photosynthetic photon flux density (PPFD). Conclusions Here we demonstrate the development of a high-throughput (> 500 samples day−1) method for phenotyping photosynthetic and photo-protective parameters in a dynamic light environment. The technique exploits chlorophyll fluorescence imaging in a specifically designed chamber, enabling controlled gaseous environment around leaf sections. In addition, we have demonstrated that leaf sections do not different from intact plant material even > 3 h after sampling, thus enabling transportation of material of interest from the field to this laboratory based platform. The methodologies described here allow rapid, custom screening of field material for variation in photosynthetic processes.

The recent advances in plant biology have significantly improved our understanding of reactive oxygen species (ROS) as signaling molecules in the redox regulation of complex cellular processes. In plants, free radicals and non-radicals are prevalent intra- and inter-cellular ROS, catalyzing complex metabolic processes such as photosynthesis. Photosynthesis homeostasis is maintained by thiol-based systems and antioxidative enzymes, which belong to some of the evolutionarily conserved protein families. The molecular and biological functions of redox regulation in photosynthesis are usually to balance the electron transport chain, photosystem II, photosystem I, mesophyll and bundle sheath signaling, and photo-protection regulating plant growth and productivity. Here, we review the recent progress of ROS signaling in photosynthesis. We present a comprehensive comparative bioinformatic analysis of redox regulation in evolutionary distinct photosynthetic cells. Gene expression, phylogenies, sequence alignments, and 3D protein structures in representative algal and plant species revealed conserved key features including functional domains catalyzing oxidation and reduction reactions. We then discuss the antioxidant-related ROS signaling and important pathways for achieving homeostasis of photosynthesis. Finally, we highlight the importance of plant responses to stress cues and genetic manipulation of disturbed redox status for balanced and enhanced photosynthetic efficiency and plant productivity.

To more thoroughly characterize the mechanism regulating the conversion of red maple tree ( Acer rubrum L. ‘Brandywine’) foliar coloration in autumn, we analyzed the leaf coloration process using the Lab color space scale, and compared the anthocyanin concentrations, photosynthetic pigment contents, soluble sugar contents, and the phenylalanine ammonia lyase and polyphenol oxidase activities between control and band-treated red maple seedlings. We observed that stem banding enhanced the development of leaves exhibiting brilliant red coloration in the upper treated branches, and weakened the brightness of yellow leaves. Additionally, studies also revealed that leaf anthocyanin contents increased significantly. Moreover, carotenoid contents and polyphenol oxidase activity decreased considerably by banding. In contrast, the chlorophyll pigment, phenylalanine ammonia lyase activity and soluble sugar contents were only minimally affected by the long-term banding of trees. Our results indicate that the Lab color model is appropriate for quantifying leaf coloration changes, and for revealing the relationship between leaf coloration and internal physiological changes. Changes to leaf coloration are a consequence of the actions of photosynthetic pigments and anthocyanins. Our results also demonstrate that anthocyanin accumulation influences the underlying biochemical mechanism. The successful manipulation of leaf coloration changes highlights the significance of anthocyanins in this process, and is consistent with the possibility that anthocyanin accumulation influences the underlying biochemical activities. [ABSTRACT FROM AUTHOR]

Abstract: Some solar-powered sea slugs are capable of incorporating chloroplasts directly in their cell cytosol sustaining photosynthesis for significant time periods. This phenomenon is known as kleptoplasty. Kleptoplastids show high functionality levels but little is known about their photo-regulatory mechanisms. The main objective was to investigate the functionality of the xanthophyll cycle using the sacoglossan Elysia timida that acquires kleptoplasts from Acetabularia acetabulum. Xanthophyll cycle functionality was tested using a combination of PAM fluorescence and HPLC pigment analysis. Rapid light curves (RLC) and steady state light curves were carried out in both organisms. E. timida RLC showed a rETR inflexion point after 700μmolE−1 m−2 s−1 that was not visible on A. acetabulum. This was attributed to the fact that the animal closed the parapodia in high light intensities, thus shading the kleptoplasts leading to higher PSII quantum efficiencies. This behaviour also resulted in Ek values being significantly higher in E. timida (ANOVA, F(1, 27) =7.49, p<0.05). The xanthophyll cycle was shown to be functional with kleptoplasts xanthophyll ratio, i.e. zea/(vio+ant+zea) increasing with exposure to higher light intensities (F(1, 23) =122.83, p<0.01) and showing a strong linear relationship with non-photochemical quenching measurements. The present study showed that E. timida was capable of combining a behavioural photo-regulation mechanism (opening/closing the parapodia) with a functional physiological photo-regulation mechanism (xanthophyll cycle) increasing their photo-regulation capacity, keeping their maximum photosynthetic capacity for longer periods than their food source. [ABSTRACT FROM AUTHOR]

Proton motive force (pmf) across thylakoid membranes is not only for harnessing solar energy for photosynthetic CO2 fixation, but also for triggering feedback regulation of photosystem II antenna. The mechanisms for balancing these two roles of the proton circuit under the long-term environmental stress, such as prolonged drought, have been poorly understood. In this study, we report on the response of wild watermelon thylakoid ‘proton circuit’ to drought stress using both in vivo spectroscopy and molecular analyses of the representative photosynthetic components. Although drought stress led to enhanced proton flux via a ∼34% increase in cyclic electron flow around photosystem I (PS I), an observed ∼fivefold decrease in proton conductivity, gH+, across thylakoid membranes suggested that decreased ATP synthase activity was the major factor for sustaining elevated qE. Western blotting analyses revealed that ATP synthase content decreased significantly, suggesting that quantitative control of the complex plays a pivotal role in down-regulation of gH+. The expression level of cytochrome b6 f complex – another key control point in photosynthesis – also declined, probably to prevent excess-reduction of PS I electron acceptors. We conclude that plant acclimation to long-term environmental stress involves global changes in the photosynthetic proton circuit, in which ATP synthase represents the key control point for regulating the relationship between electron transfer and pmf. [ABSTRACT FROM AUTHOR]

The review deals with thermal dissipation of absorbed excitation energy within pigment-protein complexes of thylakoid membranes in higher plants. We focus on the de-excitation regulatory processes within photosystem 2 (PS2) that can be monitored as non-photochemical quenching of chlorophyll (Chl) a fluorescence consisting of three components known as energy-dependent quenching (qE), state-transition quenching (qT), and photoinhibitory quenching (qI). We summarize the role of thylakoid lumen pH, xanthophylls, and PS2 proteins in qE mechanism. Further, both the similarity between qE and qI and specific features of qI are described. The other routes of thermal energy dissipation are also mentioned, that is dissipation within photosystem 1 and dissipation through the triplet Chl pathway. The significance of the individual de-excitation processes in protection against photo-oxidative damage to the photosynthetic apparatus under excess photon supply is stretched. [ABSTRACT FROM AUTHOR]

Background: As yields of major crops such as wheat (T. aestivum) have begun to plateau in recent years, there is growing pressure to efficiently phenotype large populations for traits associated with genetic advancement in yield. Photosynthesis encompasses a range of steady state and dynamic traits that are key targets for raising Radiation Use Efficiency (RUE), biomass production and grain yield in crops. Traditional methodologies to assess the full range of responses of photosynthesis, such a leaf gas exchange, are slow and limited to one leaf (or part of a leaf) per instrument. Due to constraints imposed by time, equipment and plant size, photosynthetic data is often collected at one or two phenological stages and in response to limited environmental conditions. Results: Here we describe a high throughput procedure utilising chlorophyll fluorescence imaging to phenotype dynamic photosynthesis and photoprotection in excised leaves under controlled gaseous conditions. When measured throughout the day, no significant differences (P > 0.081) were observed between the responses of excised and intact leaves. Using excised leaves, the response of three cultivars of T. aestivum to a user—defined dynamic lighting regime was examined. Cultivar specific differences were observed for maximum PSII efficiency (Fv′/Fm′—P < 0.01) and PSII operating efficiency (Fq′/Fm′—P = 0.04) under both low and high light. In addition, the rate of induction and relaxation of non-photochemical quenching (NPQ) was also cultivar specific. A specialised imaging chamber was designed and built in-house to maintain gaseous conditions around excised leaf sections. The purpose of this is to manipulate electron sinks such as photorespiration. The stability of carbon dioxide (CO2) and oxygen (O2) was monitored inside the chambers and found to be within ± 4.5% and ± 1% of the mean respectively. To test the chamber, T. aestivum 'Pavon76' leaf sections were measured under at 20 and 200 mmol mol−1 O2 and ambient [CO2] during a light response curve. The Fv′/Fm′was significantly higher (P < 0.05) under low [O2] for the majority of light intensities while values of NPQ and the proportion of open PSII reaction centers (qP) were significantly lower under > 130 μmol m−2 s−1 photosynthetic photon flux density (PPFD). Conclusions: Here we demonstrate the development of a high-throughput (> 500 samples day−1) method for phenotyping photosynthetic and photo-protective parameters in a dynamic light environment. The technique exploits chlorophyll fluorescence imaging in a specifically designed chamber, enabling controlled gaseous environment around leaf sections. In addition, we have demonstrated that leaf sections do not different from intact plant material even > 3 h after sampling, thus enabling transportation of material of interest from the field to this laboratory based platform. The methodologies described here allow rapid, custom screening of field material for variation in photosynthetic processes. [ABSTRACT FROM AUTHOR]