دورية أكاديمية
Photosynthetic plasticity aggravates the susceptibility of magnesium-deficient leaf to high light in rapeseed plants: the importance of Rubisco and mesophyll conductance.
العنوان: | Photosynthetic plasticity aggravates the susceptibility of magnesium-deficient leaf to high light in rapeseed plants: the importance of Rubisco and mesophyll conductance. |
---|---|
المؤلفون: | Ye X; Microelement Research Center, Huazhong Agricultural University, Wuhan, 430070, China.; Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Wuhan, 430070, China., Gao Z; Microelement Research Center, Huazhong Agricultural University, Wuhan, 430070, China.; Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Wuhan, 430070, China., Xu K; Microelement Research Center, Huazhong Agricultural University, Wuhan, 430070, China.; Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Wuhan, 430070, China., Li B; Microelement Research Center, Huazhong Agricultural University, Wuhan, 430070, China.; Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Wuhan, 430070, China., Ren T; Microelement Research Center, Huazhong Agricultural University, Wuhan, 430070, China.; Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Wuhan, 430070, China., Li X; Microelement Research Center, Huazhong Agricultural University, Wuhan, 430070, China.; Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Wuhan, 430070, China., Cong R; Microelement Research Center, Huazhong Agricultural University, Wuhan, 430070, China.; Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Wuhan, 430070, China., Lu Z; Microelement Research Center, Huazhong Agricultural University, Wuhan, 430070, China.; Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Wuhan, 430070, China., Cakmak I; Faculty of Engineering and Natural Sciences, Sabanci University, Istanbul, 34956, Turkey., Lu J; Microelement Research Center, Huazhong Agricultural University, Wuhan, 430070, China.; Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Wuhan, 430070, China. |
المصدر: | The Plant journal : for cell and molecular biology [Plant J] 2024 Jan; Vol. 117 (2), pp. 483-497. Date of Electronic Publication: 2023 Oct 30. |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: Blackwell Scientific Publishers and BIOS Scientific Publishers in association with the Society for Experimental Biology Country of Publication: England NLM ID: 9207397 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-313X (Electronic) Linking ISSN: 09607412 NLM ISO Abbreviation: Plant J Subsets: MEDLINE |
أسماء مطبوعة: | Original Publication: Oxford : Blackwell Scientific Publishers and BIOS Scientific Publishers in association with the Society for Experimental Biology, c1991- |
مواضيع طبية MeSH: | Brassica napus*/metabolism , Anemia, Hypochromic*, Ribulose-Bisphosphate Carboxylase/metabolism ; Magnesium ; Carbon Dioxide ; Photosynthesis/physiology ; Plant Leaves/metabolism |
مستخلص: | Plants grown under low magnesium (Mg) soils are highly susceptible to encountering light intensities that exceed the capacity of photosynthesis (A), leading to a depression of photosynthetic efficiency and eventually to photooxidation (i.e., leaf chlorosis). Yet, it remains unclear which processes play a key role in limiting the photosynthetic energy utilization of Mg-deficient leaves, and whether the plasticity of A in acclimation to irradiance could have cross-talk with Mg, hence accelerating or mitigating the photodamage. We investigated the light acclimation responses of rapeseed (Brassica napus) grown under low- and adequate-Mg conditions. Magnesium deficiency considerably decreased rapeseed growth and leaf A, to a greater extent under high than under low light, which is associated with higher level of superoxide anion radical and more severe leaf chlorosis. This difference was mainly attributable to a greater depression in dark reaction under high light, with a higher Rubisco fallover and a more limited mesophyll conductance to CO (© 2023 Society for Experimental Biology and John Wiley & Sons Ltd.) |
References: | Alric, J. & Johnson, X. (2017) Alternative electron transport pathways in photosynthesis: a confluence of regulation. Current Opinion in Plant Biology, 37, 78-86. Arnon, D.I. (1949) Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiology, 24, 1-15. Bailey-Serres, J., Parker, J.E., Ainsworth, E.A., Oldroyd, G.E.D. & Schroeder, J.I. (2019) Genetic strategies for improving crop yields. Nature, 575, 109-118. Buckley, T.N. & Diaz-Espejo, A. (2015) Partitioning changes in photosynthetic rate into contributions from different variables. Plant, Cell & Environment, 38, 1200-1211. Cakmak, I. & Kirkby, E.A. (2008) Role of magnesium in carbon partitioning and alleviating photooxidative damage. Physiologia Plantarum, 133, 692-704. Cakmak, I. & Marschner, H. (1992) Magnesium deficiency and high light intensity enhance activities of superoxide dismutase, ascorbate peroxidase, and glutathione reductase in bean leaves. Plant Physiology, 98, 1222-1227. Cakmak, I. & Yazi̇ci̇, A.M. (2010) Magnesium - a forgotten element in agricultural production. Better Crops, 94, 23-25. Carmo-Silva, A.E. & Salvucci, M.E. (2011) The activity of Rubisco's molecular chaperone, Rubisco activase, in leaf extracts. Photosynthesis Research, 108, 143-155. Carmo-Silva, E., Scales, J.C., Madgwick, P.J. & Parry, M.A. (2015) Optimizing Rubisco and its regulation for greater resource use efficiency. Plant, Cell & Environment, 38, 1817-1832. Carriquí, M., Nadal, M. & Flexas, J. (2021) Acclimation of mesophyll conductance and anatomy to light during leaf aging in Arabidopsis thaliana. Physiologia Plantarum, 172, 1894-1907. Chen, X.H., Wang, Z., Muneer, M.A., Ma, C.C., He, D.D., White, P.J. et al. (2022) Short planks in the crop nutrient barrel theory of China are changing: evidence from 15 crops in 13 provinces. Food and Energy Security, 12, e389. Cousins, A.B., Mullendore, D.L. & Sonawane, B.V. (2020) Recent developments in mesophyll conductance in C3, C4 and CAM plants. The Plant Journal, 101, 816-830. D'Alessandro, S., Beaugelin, I. & Havaux, M. (2020) Tanned or sunburned: how excessive light triggers plant cell death. Molecular Plant, 13, 1545-1555. Earles, J.M., Buckley, T.N., Brodersen, C.R., Busch, F.A., Cano, F.J., Choat, B. et al. (2019) Embracing 3D complexity in leaf carbon-water exchange. Trends in Plant Science, 24, 15-24. Elstner, E.F. & Heupel, A. (1976) Inhibition of nitrite formation from hydroxylammoniumchloride: a simple assay for superoxide dismutase. Analytical Biochemistry, 70, 616-620. Evans, J.R. (2021) Mesophyll conductance: walls, membranes and spatial complexity. New Phytologist, 229, 1864-1876. Evans, J.R. & Poorter, H. (2001) Photosynthetic acclimation of plants to growth irradiance: the relative importance of specific leaf area and nitrogen partitioning in maximizing carbon gain. Plant, Cell & Environment, 24, 755-767. Farhat, N., Ivanov, A.G., Krol, M., Rabhi, M., Smaoui, A., Abdelly, C. et al. (2015) Preferential damaging effects of limited magnesium bioavailability on photosystem I in Sulla carnosa plants. Planta, 241, 1189-1206. Farquhar, G.D., von Caemmerer, S. & Berry, J.A. (1980) A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta, 149, 78-90. Foyer, C.H. & Hanke, G. (2022) Abiotic stress and adaptation of electron transport: regulation of the production and processing of ROS signals in chloroplasts. In: Ruban, A., Foyer, C.H. & Murchie, E.H. (Eds.) Photosynthesis in action. New York: Academic Press, pp. 85-102. Gao, J., Wang, F., Sun, J., Tian, Z., Hu, H., Jiang, S. et al. (2018) Enhanced Rubisco activation associated with maintenance of electron transport alleviates inhibition of photosynthesis under low nitrogen conditions in winter wheat seedlings. Journal of Experimental Botany, 69, 5477-5488. Geng, G.T., Cakmak, I., Ren, T., Lu, Z.F. & Lu, J.W. (2021) Effect of magnesium fertilization on seed yield, seed quality, carbon assimilation and nutrient uptake of rapeseed plants. Field Crops Research, 264, 108082. Gerbeau, P., Amodeo, G., Henzler, T., Santoni, V., Ripoche, P. & Maurel, C. (2002) The water permeability of Arabidopsis plasma membrane is regulated by divalent cations and pH. The Plant Journal, 30, 71-81. Gransee, A. & Führs, H. (2013) Magnesium mobility in soils as a challenge for soil and plant analysis, magnesium fertilization and root uptake under adverse growth conditions. Plant and Soil, 368, 5-21. Grassi, G. & Magnani, F. (2005) Stomatal, mesophyll conductance and biochemical limitations to photosynthesis as affected by drought and leaf ontogeny in ash and oak trees. Plant, Cell & Environment, 28, 834-849. Gregory, L.M., McClain, A.M., Kramer, D.M., Pardo, J.D., Smith, K.E., Tessmer, O.L. et al. (2021) The triose phosphate utilization limitation of photosynthetic rate: Out of global models but important for leaf models. Plant, Cell & Environment, 44, 3223-3226. Harley, P.C., Loreto, F., Di Marco, G. & Sharkey, T.D. (1992) Theoretical considerations when estimating the mesophyll conductance to CO2 flux by analysis of the response of photosynthesis to CO2. Plant Physiology, 98, 1429-1436. Harwood, R., Goodman, E., Gudmundsdottir, M., Huynh, M., Musulin, Q., Song, M. et al. (2020) Cell and chloroplast anatomical features are poorly estimated from 2D cross-sections. New Phytologist, 225, 2567-2578. Hashida, S., Miyagi, A., Nishiyama, M., Yoshida, K., Hisabori, T. & Kawai-Yamada, M. (2018) Ferredoxin/thioredoxin system plays an important role in the chloroplastic NADP status of Arabidopsis. The Plant Journal, 95, 947-960. Hauer-Jákli, M. & Tränkner, M. (2019) Critical leaf magnesium thresholds and the impact of magnesium on plant growth and photo-oxidative defense: a systematic review and meta-analysis on 70 years of research. Frontiers in Plant Science, 10, 766. Hawkesford, M.J., Cakmak, I., Coskun, D., De Kok, L.J., Lambers, H., Schjoerring, J.K. et al. (2023) Functions of macronutrients. In: Rengel, Z., Cakmak, I. & White, P.J. (Eds.) Marschner's mineral nutrition of Plants, 4th edition. San Diego: Academic Press, pp. 201-281. Hazra, S., Henderson, J.N., Liles, K., Hilton, M.T. & Wachter, R.M. (2015) Regulation of ribulose-1,5-bisphosphate carboxylase/oxygenase (rubisco) activase: product inhibition, cooperativity, and magnesium activation. Journal of Biological Chemistry, 290, 24222-24236. Hermans, C., Johnson, G.N., Strasser, R.J. & Verbruggen, N. (2004) Physiological characterisation of magnesium deficiency in sugar beet: acclimation to low magnesium differentially affects photosystems I and II. Planta, 220, 344-355. Hermans, C. & Verbruggen, N. (2005) Physiological characterization of Mg deficiency in Arabidopsis thaliana. Journal of Experimental Botany, 56, 2153-2161. Hu, W.S., Lu, Z.F., Meng, F.J., Li, X.K., Cong, R.H., Ren, T. et al. (2020) The reduction in leaf area precedes that in photosynthesis under potassium deficiency: the importance of leaf anatomy. New Phytologist, 227, 1749-1763. Jamali Jaghdani, S., Jahns, P. & Tränkner, M. (2021a) The impact of magnesium deficiency on photosynthesis and photoprotection in Spinacia oleracea. Plant Stress, 2, 100040. Jamali Jaghdani, S., Jahns, P. & Tränkner, M. (2021b) Mg deficiency induces photo-oxidative stress primarily by limiting CO2 assimilation and not by limiting photosynthetic light utilization. Plant Science, 302, 110751. Jensen, R.G. (2000) Activation of rubisco regulates photosynthesis at high temperature and CO2. Proceedings of the National Academy of Sciences of the United States of America, 97, 12937-12938. Kim, K. & Portis, A.R. (2006) Kinetic analysis of the slow inactivation of Rubisco during catalysis: effects of temperature, O2 and Mg2+. Photosynthesis Research, 87, 195-204. Knauer, J., Cuntz, M., Evans, J.R., Niinemets, Ü., Tosens, T., Veromann-Jürgenson, L.-L. et al. (2022) Contrasting anatomical and biochemical controls on mesophyll conductance across plant functional types. New Phytologist, 236, 357-368. Koch, M., Busse, M., Naumann, M., Jákli, B., Smit, I., Cakmak, I. et al. (2019) Differential effects of varied potassium and magnesium nutrition on production and partitioning of photoassimilates in potato plants. Physiologia Plantarum, 166, 921-935. Kourghi, M., Nourmohammadi, S., Pei, J.V., Qiu, J., McGaughey, S., Tyerman, S.D. et al. (2017) Divalent cations regulate the ion conductance properties of diverse classes of aquaporins. International Journal of Molecular Sciences, 18, 2323. Kramer, D.M., Johnson, G., Kiirats, O. & Edwards, G.E. (2004) New fluorescence parameters for the determination of QA redox state and excitation energy fluxes. Photosynthesis Research, 79, 209-218. Laing, W., Greer, D., Sun, O., Beets, P., Lowe, A. & Payn, T. (2000) Physiological impacts of Mg deficiency in Pinus radiata: growth and photosynthesis. New Phytologist, 146, 47-57. Li, C.P., Qi, Y.P., Zhang, J., Yang, L.T., Wang, D.H., Ye, X. et al. (2017) Magnesium-deficiency-induced alterations of gas exchange, major metabolites and key enzymes differ among roots, and lower and upper leaves of Citrus sinensis seedlings. Tree Physiology, 37, 1564-1581. Li, J., Yokosho, K., Liu, S., Cao, H.R., Yamaji, N., Zhu, X.G. et al. (2020) Diel magnesium fluctuations in chloroplasts contribute to photosynthesis in rice. Nature Plants, 6, 848-859. Lorimer, G.H., Badger, M.R. & Andrews, T.J. (1976) The activation of ribulose-1,5-bisphosphate carboxylase by carbon dioxide and magnesium ions. Equilibria, kinetics, a suggested mechanism, and physiological implications. Biochemistry, 15, 529-536. Lu, Z.F., Hu, W.S., Ye, X.L., Lu, J.W., Gu, H.H., Li, X.K. et al. (2022) Potassium regulates diel leaf growth of Brassica napus by coordinating the rhythmic carbon supply and water balance. Journal of Experimental Botany, 73, 3686-3698. Lu, Z.F., Lu, J.W., Pan, Y.H., Lu, P.P., Li, X.K., Cong, R.H. et al. (2016) Anatomical variation of mesophyll conductance under potassium deficiency has a vital role in determining leaf photosynthesis. Plant Cell & Environment, 39, 2428-2439. Lu, Z.F., Ren, T., Li, J., Hu, W.S., Zhang, J.L., Yan, J.Y. et al. (2020) Nutrition-mediated cell and tissue-level anatomy triggers the covariation of leaf photosynthesis and leaf mass per area. Journal of Experimental Botany, 71, 6524-6537. Lu, Z.F., Ren, T. & Lu, J.W. (2021) Soil available magnesium status and effects of magnesium application on rapeseed yield in main producing area of China. Journal of Huazhong Agricultural University, 40, 17-23. Makino, A., Mae, T. & Ohira, K. (1986) Colorimetric measurement of protein stained with coomassie brilliant blue R on sodium dodecyl sulfate-polyacrylamide gel electrophoresis by eluting with formamide. Agricultural and Biological Chemistry, 50, 1911-1912. Marschner, H. & Cakmak, I. (1989) High light intensity enhances chlorosis and necrosis in leaves of zinc, potassium, and magnesium deficient bean (Phaseolus vulgaris) plants. Journal of Plant Physiology, 134, 308-315. Maxwell, K. & Johnson, G.N. (2000) Chlorophyll fluorescence-a practical guide. Journal of Experimental Botany, 51, 659-668. Mengutay, M., Ceylan, Y., Kutman, U.B. & Cakmak, I. (2013) Adequate magnesium nutrition mitigates adverse effects of heat stress on maize and wheat. Plant and Soil, 368, 57-72. Navarro, J., Powers, J.M., Paul, A. & Campbell, D.R. (2022) Phenotypic plasticity and selection on leaf traits in response to snowmelt timing and summer precipitation. New Phytologist, 234, 1477-1490. Nicotra, A.B., Atkin, O.K., Bonser, S.P., Davidson, A.M., Finnegan, E.J., Mathesius, U. et al. (2010) Plant phenotypic plasticity in a changing climate. Trends in Plant Science, 15, 684-692. Niinemets, Ü., Keenan, T.F. & Hallik, L. (2015) A worldwide analysis of within-canopy variations in leaf structural, chemical and physiological traits across plant functional types. New Phytologist, 205, 973-993. Niinemets, Ü. & Reichstein, M. (2003) Controls on the emission of plant volatiles through stomata: differential sensitivity of emission rates to stomatal closure explained. Journal of Geophysical Research: Atmospheres, 108, 4208. Onoda, Y., Wright, I.J., Evans, J.R., Hikosaka, K., Kitajima, K., Niinemets, Ü. et al. (2017) Physiological and structural tradeoffs underlying the leaf economics spectrum. New Phytologist, 214, 1447-1463. Osnas, J.L.D., Lichstein, J.W., Reich, P.B. & Pacala, S.W. (2013) Global leaf trait relationships: mass, area, and the leaf economics spectrum. Science, 340, 741-744. Peguero-Pina, J.J., Sancho Knapik, D. & Gil, P.E. (2017) Ancient cell structural traits and photosynthesis in today's environment. Journal of Experimental Botany, 68, 1389-1392. Peng, Y.Y., Liao, L.L., Liu, S., Nie, M.M., Li, J., Zhang, L.D. et al. (2019) Magnesium deficiency triggers SGR-mediated chlorophyll degradation for magnesium remobilization. Plant Physiology, 181, 262-275. Poorter, H., Niinemets, Ü., Ntagkas, N., Siebenkäs, A., Mäenpää, M., Matsubara, S. et al. (2019) A meta-analysis of plant responses to light intensity for 70 traits ranging from molecules to whole plant performance. New Phytologist, 223, 1073-1105. Reinbothe, S., Reinbothe, C., Apel, K. & Lebedev, N. (1996) Evolution of chlorophyll biosynthesis-the challenge to survive photooxidation. Cell, 86, 703-705. Rondeau-Mouro, C., Defer, D., Leboeuf, E. & Lahaye, M. (2008) Assessment of cell wall porosity in Arabidopsis thaliana by NMR spectroscopy. International Journal of Biological Macromolecules, 42, 83-92. Sharkey, T.D., Bernacchi, C.J., Farquhar, G.D. & Singsaas, E.L. (2007) Fitting photosynthetic carbon dioxide response curves for C3 leaves. Plant, Cell & Environment, 30, 1035-1040. Sharwood, R.E., Sonawane, B.V., Ghannoum, O. & Whitney, S.M. (2016) Improved analysis of C4 and C3 photosynthesis via refined in vitro assays of their carbon fixation biochemistry. Journal of Experimental Botany, 67, 3137-3148. Shen, J., Song, L., Müller, K., Hu, Y., Song, Y., Yu, W. et al. (2016) Magnesium alleviates adverse effects of lead on growth, photosynthesis, and ultrastructural alterations of Torreya grandis seedlings. Frontiers in Plant Science, 7, 1819. Shikanai, T. & Yamamoto, H. (2017) Contribution of cyclic and pseudo-cyclic electron transport to the formation of proton motive force in chloroplasts. Molecular Plant, 10, 20-29. Stec, B. (2012) Structural mechanism of rubisco activation by carbamylation of the active site lysine. Proceedings of the National Academy of Sciences of the United States of America, 109, 18785-18790. Syvertsen, J., Lloyd, J., McConchie, C., Kriedemann, P. & Farquhar, G. (1995) On the relationship between leaf anatomy and CO2 diffusion through the mesophyll of hypostomatous leaves. Plant, Cell & Environment, 18, 149-157. Tatagiba, S.D., DaMatta, F.M. & Rodrigues, F.A. (2016) Magnesium decreases leaf scald symptoms on rice leaves and preserves their photosynthetic performance. Plant Physiology and Biochemistry, 108, 49-56. Taylor, S.H., Gonzalez-Escobar, E., Page, R., Parry, M.A.J., Long, S.P. & Carmo-Silva, E. (2022) Faster than expected Rubisco deactivation in shade reduces cowpea photosynthetic potential in variable light conditions. Nature Plants, 8, 118-124. Taylor, T.C. & Andersson, I. (1996) Structural transitions during activation and ligand binding in hexadecameric rubisco inferred from the crystal structure of the activated unliganded spinach enzyme. Nature Structural Biology, 3, 95-101. Terry, N. & Ulrich, A. (1974) Effects of magnesium deficiency on the photosynthesis and respiration of leaves of sugar beet. Plant Physiology, 54, 379-381. Thain, J. (1983) Curvature correction factors in the measurement of cell surface areas in plant tissues. Journal of Experimental Botany, 34, 87-94. Théroux-Rancourt, G., Earles, J.M., Gilbert, M.E., Zwieniecki, M.A., Boyce, C.K., McElrone, A.J. et al. (2017) The bias of a two-dimensional view: comparing two-dimensional and three-dimensional mesophyll surface area estimates using noninvasive imaging. New Phytologist, 215, 1609-1622. Thomas, R.L., Sheard, R.W. & Moyer, J.R. (1967) Comparison of conventional and automated procedures for nitrogen, phosphorus, and potassium analysis of plant material using a single digestion. Agronomy Journal, 59, 240-243. Tian, X.Y., He, D.D., Bai, S., Zeng, W.Z., Wang, Z., Wang, M. et al. (2021) Physiological and molecular advances in magnesium nutrition of plants. Plant and Soil, 468, 1-17. Tomás, M., Flexas, J., Copolovici, L., Galmés, J., Hallik, L., Medrano, H. et al. (2013) Importance of leaf anatomy in determining mesophyll diffusion conductance to CO2 across species: quantitative limitations and scaling up by models. Journal of Experimental Botany, 64, 2269-2281. Tränkner, M., Tavakol, E. & Jákli, B. (2018) Functioning of potassium and magnesium in photosynthesis, photosynthate translocation and photoprotection. Physiologia Plantarum, 163, 414-431. Valentini, R., Epron, D., Angelis, P., Matteucci, G. & Dreyer, E. (1995) In situ estimation of net CO2 assimilation, photosynthetic electron flow and photorespiration in Turkey oak (Q. cerris L.) leaves: diurnal cycles under different levels of water supply. Plant, Cell and Environment, 18, 631-640. Verbruggen, N. & Hermans, C. (2013) Physiological and molecular responses to magnesium nutritional imbalance in plants. Plant and Soil, 368, 87-99. Wang, Z., Hassan, M.U., Nadeem, F., Lq, W., Fs, Z. & Xx, L. (2020) Magnesium fertilization improves crop yield in most production systems: a meta-analysis. Frontiers in Plant Science, 10, 1727. Witkowski, E. & Lamont, B.B. (1991) Leaf specific mass confounds leaf density and thickness. Oecologia, 88, 486-493. Yamori, W. & Shikanai, T. (2016) Physiological functions of cyclic electron transport around photosystem I in sustaining photosynthesis and plant growth. Annual Review of Plant Biology, 67, 81-106. Yang, G.H., Yang, L.T., Jiang, H.X., Li, Y., Wang, P. & Chen, L.S. (2012) Physiological impacts of magnesium-deficiency in Citrus seedlings: photosynthesis, antioxidant system and carbohydrates. Trees, 26, 1237-1250. Yin, X.Y., Schapendonk, A.H.C.M. & Struik, P.C. (2018) Exploring the optimum nitrogen partitioning to predict the acclimation of C3 leaf photosynthesis to varying growth conditions. Journal of Experimental Botany, 70, 2435-2447. Zhang, N., Kallis, R.P., Ewy, R.G. & Portis, A.R. (2002) Light modulation of rubisco in Arabidopsis requires a capacity for redox regulation of the larger rubisco activase isoform. Proceedings of the National Academy of Sciences of the United States of America, 99, 3330-3334. |
معلومات مُعتمدة: | 2662021ZHQD002 Fundamental Research Funds for the Central Universities; IMI2018-02 International Magnesium Institute; 32272820 National Natural Science Foundation of China |
فهرسة مساهمة: | Keywords: Rubisco; high light; magnesium deficiency; mesophyll conductance; photooxidation; photosynthesis |
المشرفين على المادة: | EC 4.1.1.39 (Ribulose-Bisphosphate Carboxylase) I38ZP9992A (Magnesium) 142M471B3J (Carbon Dioxide) |
تواريخ الأحداث: | Date Created: 20231030 Date Completed: 20240130 Latest Revision: 20240130 |
رمز التحديث: | 20240130 |
DOI: | 10.1111/tpj.16504 |
PMID: | 37901950 |
قاعدة البيانات: | MEDLINE |
كن أول من يترك تعليقا!