Skip to main content
Log in

Effects of natural shade on soybean thylakoid membrane composition

  • Regular Paper
  • Published:
Photosynthesis Research Aims and scope Submit manuscript

Abstract

The effect of natural shade on chloroplast thylakoid membrane activity and composition was examined for soybean (Glycine Max. cv. Young) grown under field conditions. Plots with high (10 plants m−1 row) or low (1 plant m−1 row) plant density were established. Expanding leaves were tagged at 50, 58 and 65 days after planting (DAP). At 92 DAP, tagged leaves were used as reference points to characterize canopy light environments and isolate thylakoid membranes. Light environments ranged from a photosynthetic photon flux density (PPFD) of 87% of full sun to a PPFD of 10% of full sun. The decline in PPFD was accompanied by an increase in the far-red/red (735 nm/645 nm) ratio from 0.9 to approximately six. The major effects of shade on chloroplast thylakoid membranes were a reduction in chloroplast coupling factor and a shift in light-harvesting capacity from Photosystem I to Photosystem II. Photosynthetic electron transport capacity was not affected by differences in PPFD, but was 20 to 30% higher in the 1 plant m−1 row treatment. The plant density effect on electron transport was associated with differences in plastocyanin concentration, suggesting that plastocyanin is a limiting factor in soybean. Shade did not have a significant effect on the concentration of Photosystem II, Cyt b6f, or Photosystem I complexes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

CF1 :

chloroplast coupling factor

DAP:

days after planting

DBMIB:

2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone

DCIP:

2,6-dichlorophenolindophenol

FR/R:

far-red/red

PBS:

10 mM sodium phosphate (pH 7.0), 150 mM NaCl

PPFD:

photosynthetic photon flux density

PS I:

Photosystem I

PS II:

Photosystem II

P700:

reaction center of Photosystem I

Rubisco:

ribulose-1,5-bisphosphate carboxylase/oxygenase

TBS:

20 mM Tris-HCl (pH 7.5), 500 mM NaCl

TTBS:

20 mM Tris-HCl (pH 7.5), 500 mM NaCl, 0.05% (w/v) polyoxyethylenesorbitan monolaurate (Tween-20)

References

  • Anderson JM, Waldron JC and Thorne SW (1978) Chlorophyllprotein complexes of spinach and barley thylakoids. Spectral characterization of six complexes resolved by an improved electrophoretic procedure. FEBS Lett 92: 227–233

    Google Scholar 

  • Anderson JM (1986) Photoregulation of the composition, function, and structure of thylakoid membranes. Ann Rev Plant Physiol 37: 93–136

    Google Scholar 

  • Blake MS, Johnson KH, Russell-Jones GJ and Gotschlich EC (1984) A rapid, sensitive method for detection of alkaline phosphataseconjugated anti-antibody on western blots. Anal Biochem 136: 175–179

    Google Scholar 

  • Boardman NK (1977) Comparative photosynthesis of sun and shade plants. Ann Rev Plant Physiol 28: 355–377

    Google Scholar 

  • Burkey KO (1993) Effect of growth irradiance on plastocyanin levels in barley. Photosynth Res 36: 103–110

    Google Scholar 

  • Burkey KO (1994) Genetic variation of photosynthetic electron transport in barley: identification of plastocyanin as a potential limiting factor. Plant Sci 98: 177–187

    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 

  • Burkey KO, Gizlice Z and Carter TE (1996) Genetic variation in soybean photosynthetic electron transport capacity is related to plastocyanin concentration in the chloroplast. Photosynth Res 49: 141–149

    Google Scholar 

  • Chow WS and Hope AB (1987) The stoichiometries of supramolecular complexes in thylakoid membranes of spinach chloroplasts. Aust J Plant Physiol 14: 21–28

    Google Scholar 

  • Chow WS, Melis A and Anderson JM (1990) Adjustments of photosystem stoichiometry in chloroplasts improve the quantum efficiency of photosynthesis. Proc Natl Acad Sci USA 87: 7502–7506

    Google Scholar 

  • Davies EC, Chow WS, LeFay JM and Jordan BR (1986) Acclimation of tomato leaves to changes in light intensity; effects on the function of the thylakoid membrane. J Exp Bot 37: 211–220

    Google Scholar 

  • Davies EC, Jordan BR, Partis MD and Chow WS (1987) Immunochemical investigation of thylakoid coupling factor protein during photosynthetic acclimation to irradiance. J Exp Bot 38: 1517–1527

    Google Scholar 

  • De la Torre WR and Burkey KO (1990a) Acclimation of barley to changes in light intensity: Chlorophyll organization. Photosynth Res 24: 117–125

    Google Scholar 

  • De la Torre WR and Burkey KO (1990b) Acclimation of barley to changes in light intensity: Photosynthetic electron transport activity and components. Photosynth Res 24: 127–136

    Google Scholar 

  • Evans JR (1987) The relationship between electron transport components and photosynthetic capacity in pea leaves grown at different irradiances. Aust J Plant Physiol 14: 157–170

    Google Scholar 

  • Evans JR (1988) Acclimation of the thylakoid membranes to growth irradiance and the partitioning of nitrogen between soluble and thylakoid proteins. Aust J Plant Physiol 15: 93–106

    Google Scholar 

  • Evans JR (1993) Photosynthetic acclimation and nitrogen partitioning within a lucerne canopy. I. Canopy characteristics. Aust J Plant Physiol 20: 55–67

    Google Scholar 

  • Green BR (1988) The chlorophyll-protein complexes of higher plant photosynthetic membranes. Photosynth Res 15: 3–32

    Google Scholar 

  • Haehnel W, Propper A and Krause H (1980) Evidence for complexed plastocyanin as the immediate electron donor of P-700. Biochim Biophys Acta 593: 384–399

    Google Scholar 

  • Haehnel W, Ratajczak R and Robenek R (1989) Lateral distribution of plastocyanin in chloroplast thylakoids. J Cell Biol 108: 1397–1405

    Google Scholar 

  • Hiyama T and Ke B (1972) Difference spectra and extinction coefficients of P-700. Biochim Biophys Acta 267: 160–171

    Google Scholar 

  • Holloway PJ, Maclean DJ and Scott KJ (1983) Rate-limiting steps of electron transport in chloroplasts during ontogeny and senescence of barley. Plant Physiol 72: 795–801

    Google Scholar 

  • Hurt E and Hauska G (1981) A cytochrome f/b6 complex of five polypeptides with plastoquinol-plastocyanin-oxidoreductase activity from spinach chloroplasts. Eur J Biochem 117: 591–599

    Google Scholar 

  • Izawa S (1980) Acceptors and donors for chloroplast electron transport. Methods Enzymol 69: 413–434

    Google Scholar 

  • Kahana ZE and Edelman M (1982) Isolation and purification of RUBP carboxylase by sucrose gradient centrifugation, DEAE cellulose chromatography and immunoaffinity columns. In: Edelman M, Hallick RB and Chua N-H (eds) Methods in Chloroplast Molecular Biology, pp 793–802. Elsevier Biomedical Press, Amsterdam

    Google Scholar 

  • Kasperbauer MJ (1987) Far-red light reflection from green leaves and effects on phytochrome-mediated assimilate partitioning under field conditions. Plant Physiol 85: 350–354

    Google Scholar 

  • Lee W-J and Whitmarsh J (1989) Photosynthetic apparatus of pea thylakoid membranes: response to growth irradiance. Plant Physiol 89: 932–940

    Google Scholar 

  • Leong T-Y and Anderson JM (1984) Adaptation of the thylakoid membranes of pea chloroplasts to light intensities. II. Regulation of electron transport capacities, electron carriers, coupling factor (CF1) activity and rates of photosynthesis. Photosynth Res 5: 117–128

    Google Scholar 

  • Metz JG, Kruger RW, Miles D (1984) Chlorophyll-protein complexes of a Photosystem II mutant of maize. Plant Physiol 75: 238–241

    Google Scholar 

  • Moran R (1982) Formulae for determination of chlorophyllous pigments extracted with N,N-dimethylformamide. Plant Physiol 68: 1376–1381

    Google Scholar 

  • Secor J, Shibles R and Stewart CR (1984) A metabolic comparison between progressive and monocarpic senescence of soybean. Can J Bot 62: 806–811

    Google Scholar 

  • Senger H and Bauer B (1987) The influence of light quality on adaptation and function of the photosynthetic apparatus. Photochem Photobiol 45: 939–946

    Google Scholar 

  • Sinclair TR and Shiraiwa T (1993) Soybean radiation-use efficiency as influenced by nonuniform specific leaf nitrogen distribution and diffuse radiation. Crop Sci 33: 808–812

    Google Scholar 

  • Stiehl HH and Witt WT (1969) Quantitative treatment of the function of plastoquinone in photosynthesis. Z Naturforsch 24b: 1588–1598

    Google Scholar 

  • Svensson P, Andreasson E and Albertsson PA (1991) Heterogeneity among Photosystem I. Biochim Biophys Acta 1060: 45–50

    Google Scholar 

  • Tischer W, Strotmann H (1977) Relationship between inhibitor binding by chloroplasts and inhibition of photosynthetic electron transport. Biochim Biophys Acta 460: 113–125

    Google Scholar 

  • Wells R (1991) Response of soybean growth to plant density: relationships among canopy photosynthesis, leaf area and light interception. Crop Sci 31: 755–761

    Google Scholar 

  • Wild A, Hopfner M, Ruhle W and Richter M (1986) Changes in stoichiometry of Photosystem II components as an adaptive response to high-light and low-light conditions during growth. Z Naturforsch 41c: 597–603

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

The US Government right to retain a non-exclusive, royalty-free licence in and to any copyright is acknowledged.

The US Government right to retain a non-exclusive, royalty-free licence in and to any copyright is acknowledged.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Burkey, K.O., Wells, R. Effects of natural shade on soybean thylakoid membrane composition. Photosynth Res 50, 149–158 (1996). https://doi.org/10.1007/BF00014885

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00014885

Key words

Navigation