9 results on '"Bayçu G"'
Search Results
2. Session 17 Ecophysiology
- Author
-
Aktan, N., Palavan-Ünsal, N., Andonov, A. V., Georgieva, K. M., Yordanov, I. T., Atanasiu, L., Petcu, E., Atkin, O. K., Barabás, N. K., Erdei, L., Baumann, J., Bader, K. P., Bayçu, G., Önal, M., Bock, C., Jacob, A., Mayer, A., Kirst, G. O., Borovsky, G., Voronova, L., Voinikov, V., Borowski, E., Kozlowska, L., Botos-Bálo, B., Váradi, Gy., Happ, I., Busuioc, V. M., Toma, S. I., Cabeza, C. E., Ledent, J. F., Chamont, S., Christov, C., Boshcova, M., Furnadzieva, S., Zafirova, T., Čiamporová, M., Banásová, V., Ouzounidou, G., Clement, Han, Van Hasselt, Philip R., De Gara, L., De Tullio, M. C., Paciolla, C., Stefani, A., Arrigoni, O., de Ramon, M., Reigosa, M. J., Doussi, M. A., Thanos, C. A., Fenik, S. I., Trofimyak, T. B., Blume, Ya. B., Fernandez-Pascual, M., De Lorenzo, C., De Felipe, M. R., Minchin, F. R., Gordon, A. J., Filonick, L. A., Frechilla, S., Royuela, M., Arrese-Igor, C., Aparicio-Tejo, P. M., Gabbrielli, R., Gremigni, P., Pandolfini, T., Gloser, J., Gloser, V., Goncharova, N. V., Sheverdov, V. V., Zhebrakova, I. V., Grakhov, V. P., Kozeko, V. G., Greger, M., Heyman, E., Grishko, V. N., Guglielminetti, L., Perata, P., Alpi, A., Gutterman, Yitzchak, Honour, S. J., Ihle, C., Laasch, H., Ivanova, T. I., Yudina, O. S., Kacperska, A., Kadis, C. C., Georghiou, K., Khilko, T. D., Klimov, S. V., Trunova, T. I., Kosakivska, L. V., Maidebura, E. V., Kostyuk, O. P., Mikheev, A. N., Kutlakhmedov, Yu. A., Kozlova, J. I., Reutsky, V. G., Kravetz, A. P., Pavlenco, Y. A., Kubacka, M., Kacperska, A., Kühn, F., Kuznetsov, Vladimir V., Landberg, T., Greger, M., Campos, P. S., Matos, M. C., Laureano, J. A., Ramalho, J. R., Guedes, M. E., Lidon, F. C., Laureano, J. A., Campos, P. S., Ramalho, J. R., Lidon, F. C., Guedes, M. E., Matos, M. C., Leina, G. D., Lopez-Carbonell, M., Prinsen, E., Pastor, A., Van Onckelen, H., Lösch, R., Zohlen, A., Gonzales, A., Jimenez, M. S., Morales, D., Aschan, G., Lütz, C., Kaiser, F., Masarovičová, E., Lux, A., Kobelová, G., Mattioni, C., Gabbrielli, R., Negru, P. V., Medvedeva, T. N., Tudorake, G. F., Newbery, R. M., Olah, R., Masarovičová, E., Ouzounidou, G., Čiamporová, M., Moustakas, M., Karataglis, S., Pedrol, N., Ramos, P., Reigosa, M. J., Peisker, M., Tichá, I., Václavík, J., Ostareck, D., Pfeffer, M., Peisker, M., Pons, T. L., Popović, M., Kevrešan, S., Kandrač, J., Kočiš, J., Štajner, D., Petrivić, N., Kastori, R., Popovicheva, L. A., Shevchenko, Y. B., Porankiewicz, J., Gwóźdź, E. A., Prokhnevsky, A. I., Ruchko, M. V., Sorochinsky, B. V., Sergeeva, A. Y., Kostyuk, O. P., Mikheev, A. N., Przymusiński, R., Rucińska, R., Gwóźdź, E. A., Pugnaire, F. I., Haase, P., Incoll, L. D., Clark, S. C., Pukacki, P. M., Radotić, K., Todorović, S., Zakrzewska, J., Jeremić, M., Ramos, P., Pedrol, N., Reigosa, M. J., Ruchko, M. V., Sorochinsky, B. V., Sakač, Z., Panković, D., Ćupina, T., Plesničar, M., Save, R., Biel, C., Pons, J., Massons, J., Scheuerlein, R., Treml, S., Thar, B., Tirlapur, U. K., Häder, D. -P., Schneider, J., Legocka, J., Winiarska, G., Schreiber, L., Shabala, S. N., Sheremetiev, S. N., Shtemenko, N. I., Sosak-Swiderska, B., Tyrawska, D., Mazurek, U., Stevanović, B., Šinžar, J., Glišić, O., Stroinski, A., Terbea, Maria, Micut, Gh., Titei, V., Thanos, C. A., Thibaud, M. C., Betsche, T., Tosserams, M., Visser, A. J., Groen, M. W., Kalis, G., Kwant, R., Magendans, E., Rozema, J., Tyrawska, D., Bajan, C., Popowska-Nowak, E., Grochala, K., Utrillas, M. J., Alegre, L., Van Den Boogaard, H. A. G. M., Alewijnse, D., Veneklaas, E. J., Lambers, H., Van Der Kooij, T. A. W., De Kok, L. J., Van Der Werf, Adrie, Bouma, Tjeerd, Scheurwater, Ingeborg, Lambers, Hans, Van Hasselt, P. R., Chow, W. S., Anderson, J. M., Vidal, D., Grau, D., Sanjose, M., Fleck, I., Villar, R., Merino, J., Vincze, G. Y., Vallner, J., Balazsy, S., Balogh, A., Kiss, F., Zaric, L. J., Stefanovic, L., Kerecki, B., Radosavljevic, M., Zivalyuk, O. B., and Filonick, I. A.
- Published
- 1994
- Full Text
- View/download PDF
3. Modulation of Photosystem II Function in Celery via Foliar-Applied Salicylic Acid during Gradual Water Deficit Stress.
- Author
-
Moustakas M, Panteris E, Moustaka J, Aydın T, Bayçu G, and Sperdouli I
- Subjects
- Droughts, Water metabolism, Photosynthesis drug effects, Dehydration metabolism, Stress, Physiological, Photosystem II Protein Complex metabolism, Salicylic Acid metabolism, Plant Leaves metabolism, Plant Leaves drug effects, Chlorophyll metabolism, Apium metabolism
- Abstract
Water deficit is the major stress factor magnified by climate change that causes the most reductions in plant productivity. Knowledge of photosystem II (PSII) response mechanisms underlying crop vulnerability to drought is critical to better understanding the consequences of climate change on crop plants. Salicylic acid (SA) application under drought stress may stimulate PSII function, although the exact mechanism remains essentially unclear. To reveal the PSII response mechanism of celery plants sprayed with water (WA) or SA, we employed chlorophyll fluorescence imaging analysis at 48 h, 96 h, and 192 h after watering. The results showed that up to 96 h after watering, the stroma lamellae of SA-sprayed leaves appeared dilated, and the efficiency of PSII declined, compared to WA-sprayed plants, which displayed a better PSII function. However, 192 h after watering, the stroma lamellae of SA-sprayed leaves was restored, while SA boosted chlorophyll synthesis, and by ameliorating the osmotic potential of celery plants, it resulted in higher relative leaf water content compared to WA-sprayed plants. SA, by acting as an antioxidant under drought stress, suppressed phototoxicity, thereby offering PSII photoprotection, together with enhanced effective quantum yield of PSII photochemistry (Φ
PSII ) and decreased quantity of singlet oxygen (1 O2 ) generation compared to WA-sprayed plants. The PSII photoprotection mechanism induced by SA under drought stress was triggered by non-photochemical quenching (NPQ), which is a strategy to protect the chloroplast from photo-oxidative damage by dissipating the excess light energy as heat. This photoprotective mechanism, triggered by NPQ under drought stress, was adequate in keeping, especially in high-light conditions, an equal fraction of open PSII reaction centers (q p ) as of non-stress conditions. Thus, under water deficit stress, SA activates a regulatory network of stress and light energy partitioning signaling that can mitigate, to an extent, the water deficit stress on PSII functioning.- Published
- 2024
- Full Text
- View/download PDF
4. Mechanistic Insights on Salicylic Acid-Induced Enhancement of Photosystem II Function in Basil Plants under Non-Stress or Mild Drought Stress.
- Author
-
Sperdouli I, Panteris E, Moustaka J, Aydın T, Bayçu G, and Moustakas M
- Subjects
- Chlorophyll metabolism, Photosynthesis drug effects, Thylakoids metabolism, Thylakoids drug effects, Light, Photosystem II Protein Complex metabolism, Salicylic Acid pharmacology, Salicylic Acid metabolism, Ocimum basilicum metabolism, Ocimum basilicum drug effects, Droughts, Plant Leaves metabolism, Plant Leaves drug effects, Stress, Physiological
- Abstract
Photosystem II (PSII) functions were investigated in basil ( Ocimum basilicum L.) plants sprayed with 1 mM salicylic acid (SA) under non-stress (NS) or mild drought-stress (MiDS) conditions. Under MiDS, SA-sprayed leaves retained significantly higher (+36%) chlorophyll content compared to NS, SA-sprayed leaves. PSII efficiency in SA-sprayed leaves under NS conditions, evaluated at both low light (LL, 200 μmol photons m
-2 s-1 ) and high light (HL, 900 μmol photons m-2 s-1 ), increased significantly with a parallel significant decrease in the excitation pressure at PSII (1- qL ) and the excess excitation energy (EXC). This enhancement of PSII efficiency under NS conditions was induced by the mechanism of non-photochemical quenching (NPQ) that reduced singlet oxygen (1 O2 ) production, as indicated by the reduced quantum yield of non-regulated energy loss in PSII (ΦNO ). Under MiDS, the thylakoid structure of water-sprayed leaves appeared slightly dilated, and the efficiency of PSII declined, compared to NS conditions. In contrast, the thylakoid structure of SA-sprayed leaves did not change under MiDS, while PSII functionality was retained, similar to NS plants at HL. This was due to the photoprotective heat dissipation by NPQ, which was sufficient to retain the same percentage of open PSII reaction centers (q p ), as in NS conditions and HL. We suggest that the redox status of the plastoquinone pool (q p ) under MiDS and HL initiated the acclimation response to MiDS in SA-sprayed leaves, which retained the same electron transport rate (ETR) with control plants. Foliar spray of SA could be considered as a method to improve PSII efficiency in basil plants under NS conditions, at both LL and HL, while under MiDS and HL conditions, basil plants could retain PSII efficiency similar to control plants.- Published
- 2024
- Full Text
- View/download PDF
5. Arbuscular Mycorrhizal Symbiosis Enhances Photosynthesis in the Medicinal Herb Salvia fruticosa by Improving Photosystem II Photochemistry.
- Author
-
Moustakas M, Bayçu G, Sperdouli I, Eroğlu H, and Eleftheriou EP
- Abstract
We investigated the influence of Salvia fruticosa colonization by the arbuscular mycorrhizal fungi (AMF) Rhizophagus irregularis on photosynthetic function by using chlorophyll fluorescence imaging analysis to evaluate the light energy use in photosystem II (PSII) of inoculated and non-inoculated plants. We observed that inoculated plants used significantly higher absorbed energy in photochemistry (Φ
PSII ) than non-inoculated and exhibited significant lower excess excitation energy (EXC). However, the increased ΦPSII in inoculated plants did not result in a reduced non-regulated energy loss in PSII (ΦNO ), suggesting the same singlet oxygen (1 O2 ) formation between inoculated and non-inoculated plants. The increased ΦPSII in inoculated plants was due to an increased efficiency of open PSII centers to utilize the absorbed light (F v '/F m ') due to a decreased non-photochemical quenching (NPQ) since there was no difference in the fraction of open reaction centers (qp ). The decreased NPQ in inoculated plants resulted in an increased electron-transport rate (ETR) compared to non-inoculated. Yet, inoculated plants exhibited a higher efficiency of the water-splitting complex on the donor side of PSII as revealed by the increased F v /F o ratio. A spatial heterogeneity between the leaf tip and the leaf base for the parameters ΦPSII and ΦNPQ was observed in both inoculated and non-inoculated plants, reflecting different developmental zones. Overall, our findings suggest that the increased ETR of inoculated S. fruticosa contributes to increased photosynthetic performance, providing growth advantages to inoculated plants by increasing their aboveground biomass, mainly by increasing leaf biomass.- Published
- 2020
- Full Text
- View/download PDF
6. Spatiotemporal heterogeneity of photosystem II function during acclimation to zinc exposure and mineral nutrition changes in the hyperaccumulator Noccaea caerulescens.
- Author
-
Moustakas M, Bayçu G, Gevrek N, Moustaka J, Csatári I, and Rognes SE
- Subjects
- Acclimatization, Chlorophyll, Hydroponics, Metals, Heavy, Minerals, Plant Leaves, Brassicaceae physiology, Photosystem II Protein Complex metabolism, Soil Pollutants toxicity, Zinc toxicity
- Abstract
We investigated changes in mineral nutrient uptake and translocation and photosystem II (PSII) functionality, in the hyperaccumulator Noccaea caerulescens after exposure to 800 μM Zn in hydroponic culture. Exposure to Zn inhibited the uptake of K, Mn, Cu, Ca, and Mg, while the uptake of Fe and Zn enhanced. Yet, Ca and Mg aboveground tissue concentrations remain unchanged while Cu increased significantly. In the present study, we provide new data on the mechanism of N. caerulescens acclimation to Zn exposure by elucidating the process of photosynthetic acclimation. A spatial heterogeneity in PSII functionality in N. caerulescens leaves exposed to Zn for 3 days was detected, while a threshold time of 4 days was needed for the activation of Zn detoxification mechanism(s) to decrease Zn toxicity and for the stomatal closure to decrease Zn supply at the severely affected leaf area. After 10-day exposure to Zn, the allocation of absorbed light energy in PSII under low light did not differ compared to control ones, while under high light, the quantum yield of non-regulated energy loss in PSII (Φ
NO ) was lower than the control, due to an efficient photoprotective mechanism. The chlorophyll fluorescence images of non-photochemical quenching (NPQ) and photochemical quenching (qp ) clearly showed spatial and temporal heterogeneity in N. caerulescens exposure to Zn and provided further information on the particular leaf area that was most sensitive to heavy metal stress. We propose the use of chlorophyll fluorescence imaging, and in particular the redox state of the plastoquinone (PQ) pool that was found to display the highest spatiotemporal heterogeneity, as a sensitive bio-indicator to measure the environmental pressure by heavy metals on plants.- Published
- 2019
- Full Text
- View/download PDF
7. Chlorophyll Fluorescence Imaging Analysis for Elucidating the Mechanism of Photosystem II Acclimation to Cadmium Exposure in the Hyperaccumulating Plant Noccaea caerulescens .
- Author
-
Bayçu G, Moustaka J, Gevrek N, and Moustakas M
- Abstract
We provide new data on the mechanism of Noccaea caerulescens acclimation to Cd exposure by elucidating the process of photosystem II (PSII) acclimation by chlorophyll fluorescence imaging analysis. Seeds from the metallophyte N. caerulescens were grown in hydroponic culture for 12 weeks before exposure to 40 and 120 μM Cd for 3 and 4 days. At the beginning of exposure to 40 μM Cd, we observed a spatial leaf heterogeneity of decreased PSII photochemistry, that later recovered completely. This acclimation was achieved possibly through the reduced plastoquinone (PQ) pool signaling. Exposure to 120 μM Cd under the growth light did not affect PSII photochemistry, while under high light due to a photoprotective mechanism (regulated heat dissipation for protection) that down-regulated PSII quantum yield, the quantum yield of non-regulated energy loss in PSII (Φ
NO ) decreased even more than control values. Thus, N. caerulescens plants exposed to 120 μM Cd for 4 days exhibited lower reactive oxygen species (ROS) production as singlet oxygen (¹O₂). The response of N. caerulescens to Cd exposure fits the 'Threshold for Tolerance Model', with a lag time of 4 d and a threshold concentration of 40 μM Cd required for the induction of the acclimation mechanism.- Published
- 2018
- Full Text
- View/download PDF
8. Cadmium-zinc accumulation and photosystem II responses of Noccaea caerulescens to Cd and Zn exposure.
- Author
-
Bayçu G, Gevrek-Kürüm N, Moustaka J, Csatári I, Rognes SE, and Moustakas M
- Subjects
- Copper metabolism, Hydroponics, Metals, Heavy metabolism, Norway, Photosystem II Protein Complex metabolism, Plant Leaves metabolism, Plant Roots metabolism, Thlaspi, Brassicaceae, Cadmium metabolism, Soil Pollutants metabolism, Zinc metabolism
- Abstract
A population of the metallophyte Noccaea (Thlaspi) caerulescens originating from a Zn-enriched area at Røros Copper Mine (Norway) was studied. N. caerulescens tolerance to accumulate Cd and Zn was evaluated in hydroponic experiments by chlorophyll fluorescence imaging analysis. In the field-collected N. caerulescens mother plants, Zn shoot concentrations were above Zn hyperaccumulation threshold while, in hydroponic experiments under 40-μM Cd exposure, shoot Cd concentrations were clearly above Cd hyperaccumulation threshold. Cadmium ions and, to a less extent, Zn were mainly retained in the roots. Exposure to Cd enhanced Zn translocation to the shoot, while decreased significant total Ca
2+ uptake, suggesting that Cd uptake occurs through Ca2+ transporters. Nevertheless, it increased Ca2+ translocation to the leaf, possibly for photoprotection of photosystem II (PSII). Exposure to 800 μM Zn or 40 μM Cd resulted in increased Fe3+ uptake suggesting that in N. caerulescens, Cd uptake does not take place through the pathway of Fe3+ uptake and that conditions that lead to Cd and Zn accumulation in plants may also favor Fe accumulation. Despite the significant high toxicity levels of Zn and Cd in leaves, under Zn and Cd exposure, respectively, the allocation of absorbed light energy at PSII did not differ compared to controls. The results showed that N. caerulescens keep Cd and Zn concentrations in the mesophyll cells in non-toxic forms for PSII and that the increased Ca and Fe accumulation in leaves alleviates the toxicity effects. Chlorophyll fluorescence imaging revealed that PSII of N. caerulescens resisted better the phytotoxic effects of 20 times higher Zn than Cd exposure concentration. Overall, it is concluded that the use of chlorophyll fluorescence imaging constitutes a promising basis for investigating heavy metal tolerance of plants.- Published
- 2017
- Full Text
- View/download PDF
9. Aluminum resistance in wheat involves maintenance of leaf Ca(2+) and Mg(2+) content, decreased lipid peroxidation and Al accumulation, and low photosystem II excitation pressure.
- Author
-
Moustaka J, Ouzounidou G, Bayçu G, and Moustakas M
- Subjects
- Aluminum metabolism, Plant Leaves chemistry, Plant Leaves metabolism, Triticum chemistry, Triticum metabolism, Aluminum pharmacology, Calcium metabolism, Lipid Peroxidation drug effects, Magnesium metabolism, Photosystem II Protein Complex metabolism, Plant Leaves drug effects, Triticum drug effects
- Abstract
The phytotoxic aluminum species (Al(3+)) is considered as the primary factor limiting crop productivity in over 40 % of world's arable land that is acidic. We evaluated the responses of two wheat cultivars (Triticum aestivum L.) with differential Al resistance, cv. Yecora E (Al-resistant) and cv. Dio (Al-sensitive), exposed to 0, 37, 74 and 148 μM Al for 14 days in hydroponic culture at pH 4.5. With increasing Al concentration, leaf Ca(2+) and Mg(2+) content decreased, as well as the effective quantum yield of photosystem II (PSII) photochemistry (Φ PSII ), while a gradual increase in leaf membrane lipid peroxidation, Al accumulation, photoinhibition (estimated as F v /F m ), and PSII excitation pressure (1 - q p ) occurred. However, the Al-resistant cultivar with lower Al accumulation, retained larger concentrations of Ca(2+) and Mg(2+) in the leaves and kept a larger fraction of the PSII reaction centres (RCs) in an open configuration, i.e. a higher ratio of oxidized to reduced quinone A (QA), than plants of the Al-sensitive cultivar. Four times higher Al concentration in the nutrient solution was required for Al-resistant plants (148 μM Al) than for Al-sensitive (37 μM Al), in order to establish the same closed RCs. Yet, the decline in photosynthetic efficiency in the cultivar Dio was not only due to closure of PSII RCs but also to a decrease in the quantum yield of the open RCs. We suggest that Al(3+) toxicity may be mediated by nutrient deficiency and oxidative stress, and that Al-resistance of the wheat cultivar Yecora E, may be due at least partially, from the decreased Al accumulation that resulted to decreased reactive oxygen species (ROS) formation. However, under equal internal Al accumulation (exposure Al concentration: Dio 74 μM, Yecora E 148 μM) that resulted to the same oxidative stress, the reduced PSII excitation pressure and the better PSII functioning of the Al-resistant cultivar was probably due to the larger concentrations of Ca(2+) and Mg(2+) in the leaves. We propose that the different sensitivities of wheat cultivars to Al(3+) toxicity can be correlated to differences in the redox state of QA. Thus, chlorophyll fluorescence measurements can be a promising tool for rapid screening of Al resistance in wheat cultivars.
- Published
- 2016
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.