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Foliar CO2photoassimilation and chloroplast linear electron transport rates in nitrogen-sufficient and nitrogen-limited soybean plants

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Abstract

Leaflets of soybean plants which are moderately inorganic nitrogen (N)-limited exhibit either no difference in the rate of net photosynthesis or as much as a 15–23% lower net photosynthesis rate per unit area than leaflets of N-sufficient plants [Robinson JM (1996) Photosynth Res 50: 133–148; Robinson JM (1997a) Int J Plant Sci 158: 32–43]. However, mature leaflets of N-limited soybean plants have a higher CO2photoassimilation rate per unit chlorophyll than leaflets of N-sufficient soybean plants at both moderate light intensity (≈500 µmol m-2s-1) and saturating light intensity (≈1200 µmol m-2s-1) [Robinson JM (1996) Photosynth Res 50: 133–148]. This study was undertaken to determine whether chloroplast thylakoids isolated from the leaflets of nitrogen-limited soybean plants displayed similar or higher linear electron transport rates (H2O → ferredoxin → NADP) per unit chlorophyll than thylakoids isolated from leaflets of N-sufficient plants. Chlorophyll concentration in reaction mixtures containing chloroplast thylakoids prepared from leaflets of N-limited plants was manipulated so that it was similar to the chlorophyll concentration in reaction mixtures of thylakoids prepared from leaflets of N-sufficient plants. Measurements of ferredoxin dependent, NADP dependent, O2photo-evolution in thylakoid isolates were carried out in saturating light (≈1500 µmol m-2s-1) and with \(NH_4^ + \)(an uncoupler) in the chloroplast reaction mixtures. Chloroplast thylakoids isolated from N-limited soybean plant leaflets routinely had a 1.5 to 1.7 times higher rate of uncoupled, whole chain electron transport per unit chlorophyll in saturating light than did chloroplast thylakoids isolated from leaflets of N-sufficient plants. The results suggest that the photosystems and photosynthetic electron transport chain components are more active per unit Chl in leaflet chloroplast thylakoids of N-limited soybean plants than in thylakoids of N-sufficient plants.

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References

  • Bradford M (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72: 248-254

    Google Scholar 

  • Burkey KO and Wells R (1991) Response of soybean photosynthesis and chloroplast membrane function to canopy development and mutual shading. Plant Physiol 97: 245-252

    Google Scholar 

  • Champigny M-L and C Foyer 1992 Nitrate activation of cytosolic protein kinases diverts photosynthetic carbon from sucrose to amino acid biosynthesis. Basis for a New Concept. Plant Physiol 100: 7-12

    Google Scholar 

  • de Veau EJ, Robinson JM, Warmbrodt RD and van Berkum P (1990) Photosynthesis and photosynthate partitioning in N2-fixing soybeans. Plant Physiol 94: 259-267

    Google Scholar 

  • de Veau EJI, Robinson JM, Warmbrodt RD and Kremer DF (1992) Photosynthate metabolism in the source leaves of N2-fixing soybean plants. Plant Physiol 99: 1105-1117

    Google Scholar 

  • Evans JR (1983) Nitrogen and photosynthesis in the flag leaf of wheat (Triticum aestivumL.) Plant Physiol 72: 297-302

    Google Scholar 

  • Evans JR (1989) Photosynthesis and nitrogen relationships in leaves of C3plants. Oecologia 78: 9-19

    Google Scholar 

  • Evans JR and Terashima I (1987) Effects of nitrogen nutrition on electron transport components and photosynthesis in spinach. Aust J Plant Physiol 14: 59-68

    Google Scholar 

  • Evans JR and Terashima I (1988) Photosynthetic characteristics of spinach leaves grown with different nitrogen treatments. Plant Cell Physiol 29: 157-165

    Google Scholar 

  • Feldman DS Jr, Gagnon J, Hofman R and Simpson J. (1987) StatView II. The Solution for Data Analysis and Presentation Grapics. Abacus Concepts, Inc. Berkeley, CA, USA

    Google Scholar 

  • Huber SC, Huber JL and McMichael RE Jr. (1994) Control of plant enzyme activity by reversible protein phosphorylation. Int Rev Cytol 149: 47-98

    Google Scholar 

  • Khamis S and Lamaze T (1990) Maximal biomass production can occur in corn (Zea mays) in the absence of NO 3 accumulation in either leaves or roots. Physiol Plant 78: 388-394

    Google Scholar 

  • LI-COR, Inc. (1987) The LI-6200 Primer. LI-COR, Inc. Lincoln, Nebraska 68504 (1990 printing)

    Google Scholar 

  • MacKinney G (1941) Absorption of light by chlorophyll solutions. J Biol Chem 140: 315-322

    Google Scholar 

  • Moran R (1982) Formulae for determination of chlorophyllous pigments extracted with N,N-dimethylformamide Plant Physiol 69: 1376-1381

    Google Scholar 

  • Robinson JM (1984) Photosynthetic carbon metabolism in leaves and isolated chloroplasts from spinach plants grown under short and intermediate photosynthetic periods. Plant Physiol 75: 397-409

    Google Scholar 

  • Robinson JM (1994) Selection of soybean plant leaves which yield mesophyll cell isolates with maximal rates of CO2and NO 2 photoassimilation. Photosynth Res 40: 119-125

    Google Scholar 

  • Robinson JM (1996) Leaflet photosynthesis rate and carbon metabolite accumulation patterns in nitrogen-limited, vegetative soybean plants. Photosynth Res 50: 133-148

    Google Scholar 

  • Robinson JM (1997a) Influence of daily photosynthetic photon flux density on foliar carbon metabolite levels in nitrogen-limited soybean plants. Int J Plant Sci 158: 32-43

    Google Scholar 

  • Robinson JM (1997b) Nitrogen-limitation of spinach plants results in a simultaneous rise in foliar levels of orthophosphate, sucrose, and starch. Int J Plant Sci 158: 432-441

    Google Scholar 

  • Robinson JM and Baysdorfer C (1985) Interrelationships between carbon and nitrogen meta-bolism in mature soybean leaves and isolated mesophyll cells. In: Heath RL and Preiss J (eds) Regulation of Carbon Partitioning in Photosynthetic Tissues, pp 333-357. American Society of Plant Physiologists, Rockville, MD, USA

    Google Scholar 

  • Robinson JM and van Berkum P (1987) CO2photofixation and NO 2 photoreduction in leaf mesophyll cell isolates from N2-fixing soybean plants held in the absence of NO 3 . In: Biggins J (ed) Progress in Photosynthesis Research, Vol 3, pp 545-548. Martinus Nijhoff Publishers, Dordrecht, the Netherlands

    Google Scholar 

  • Robinson JM and Gibbs M (1982) Hydrogen peroxide synthesis in isolated spinach chloroplast lamellae. An analysis of the Mehler reaction in the presence of NADP reduction and ATP formation. Plant Physiol 70: 1249-1254

    Google Scholar 

  • Rufty TW Jr, Raper CD Jr and Huber SC (1984) Alterations in internal partitioning of carbon in soybean plants in response to nitrogen stress. Can J Bot 62: 501-508

    Google Scholar 

  • Rufty TW Jr, Huber SC and Volk RJ (1988) Alterations in leaf carbohydrate metabolism in response to nitrogen stress. Plant Physiol 88: 725-730

    Google Scholar 

  • Schulze W, Stitt M, Schulze E-D, Neuhaus HE and Fichtner K (1991) A quantification of the significance of assimilatory starch for growth of Arabidopsis thalianaL Heynh. Plant Physiol 95: 890-895

    Google Scholar 

  • Terashima I and Evans JR (1988) Effects of light and nitrogen nutrition on the organization of the photosynthetic apparatus in spinach. Plant Cell Physiol 29: 143-155

    Google Scholar 

Download references

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Robinson, J.M., Burkey, K.O. Foliar CO2photoassimilation and chloroplast linear electron transport rates in nitrogen-sufficient and nitrogen-limited soybean plants. Photosynthesis Research 54, 209–217 (1997). https://doi.org/10.1023/A:1005995718710

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