Skip to main content
Log in

Differential sensitivity of stomatal and non-stomatal components to NaCl or Na2SO4 salinity in horsegram, Macrotyloma uniflorum (Lam.)

  • Published:
Photosynthetica

Abstract

14CO2 assimilation rate (P), leaf diffusive conductance (gs), photosynthetic electron flow, and activities of enzymes of Calvin cycle were studied in a horsegram [Macrotyloma uniflorum (Lam.)] in response to salinity induced by NaCl or Na2SO4. A significant reduction in P and gs by both salt treatments was registered. Na2SO4 caused a greater reduction in gs than the NaCl salinity. Studies with isolated chloroplasts confirmed a greater sensitivity to NaCl than to Na2SO4. Salinity inhibited the photosynthetic electron transport. The activity of ribulose-1,5-bisphosphate carboxylase (E.C.4.1.1.39) was under salinity inhibited more than the activities of other three enzymes of the Calvin cycle, ribulose-5-phosphate kinase (E.C.2.7.1.19), ribose-5-phosphate isomerase (E.C.5.3.16), and NADP-glyceraldehyde-3-phosphate dehydrogenase (E.C.1.2.13). These inhibitions lead to a reduced capacity for ribulose-1,5-bisphosphate regeneration. Isolated chloroplasts extracted from salt stressed plants and supplemented with the substrates of Calvin cycle could elevate P, but the P was always lower than in the controls. Decreased P in horsegram exposed to high salinity can be attributed to both stomatal and non-stomatal components, however, the sensitivity to the salt source, NaCl or Na2SO4, was different.

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

References

  • Arnon, D.I.: Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris.-Plant Physiol. 24: 1–15, 1949.

    Google Scholar 

  • Ball, M.C., Anderson, J. M.: Sensitivity of photosystem II to NaCl in relation to salinity tolerance. Comparative studies with thylakoids of the salt-tolerant mangrove, Avicennia marina, and the salt-sensitive pea, Pisum sativum.-Aust. J. Plant Physiol. 13: 689–698, 1986.

    Google Scholar 

  • Brugnoli, E., Lanteri, M.: Effects of salinity on stomatal conductance, photosynthetic capacity, and carbon isotope descrimination of salt-tolerant (Gossypium hirsutum L.) and salt-sensitive (Phaseolus vulgaris L.) C3 non-halophytes.-Plant Physiol. 95: 628–635, 1991.

    Google Scholar 

  • Flowers, T.J., Troke, P.F., Yeo, A.R.: The mechanism of salt tolerance in halophytes.-Annu. Rev. Plant Physiol. 28: 89–121, 1977.

    Google Scholar 

  • Gibbs, M., Bamberger, E.S., Ellyard, P.W., Everson, R.G.: Assimilation of carbondioxide by chloroplast preparations.-In: Goodwin, T.W. (ed.): Biochemistry of Chloroplasts. Vol. II. Pp. 3–38. Academic Press, London-New York 1987.

    Google Scholar 

  • Graham, D., Hatch, M.D., Slack, C.R., Smillie, R.M.: Light induced formation of enzymes of the C4-dicarboxylic acid pathway of photosynthesis in detached leaves.-Phytochemistry 9: 521–532, 1970.

    Google Scholar 

  • Jacob, J., Lawlor, D.W.: Dependence of photosynthesis of sunflower and maize leaves on phosphate supply, ribulose-1,5-bisphosphate carboxylase/oxygenase activity, and ribulose-1,5-bisphosphate pool size.-Plant Physiol. 98: 801–807, 1992.

    Google Scholar 

  • Lakshmi, A., Ramanjulu, S., Veeranjaneyulu, K., Sudhakar, C.: Effect of NaCl on photosynthesis parameters in two cultivars of mulberry.-Photosynthetica 32: 285–289, 1996.

    Google Scholar 

  • Murata, N., Mohanty, P.S., Hayashi, H., Papageorgiou, G.: Glycinebetaine stabilizes the association of extrinsic proteins with the photosynthetic oxygen-evolving complex.-FEBS Lett. 296: 187–189, 1992.

    Google Scholar 

  • Murota, K., Ohshita, Y., Watanabe, A., Aso, S., Sato, F., Yamada, Y.: Changes related to salt tolerance in thylakoid membranes of photoautotropically cultured green tobacco cells.-Plant Cell Physiol. 35: 107–113, 1994.

    Google Scholar 

  • Plaut, Z., Grieve, C.M., Maas, E.V.: Salinity effects on CO2 assimilation and diffusive conductance of cowpea leaves.-Physiol. Plant. 79: 31–38, 1990.

    Google Scholar 

  • Robinson, S.P., Downton, W.J.S., Millhouse, J.A.: Photosynthesis and ion content of leaves and isolated chloroplasts of salt-stressed spinach.-Plant Physiol. 73: 238–242, 1983.

    Google Scholar 

  • Seemann, J.R., Critchley, C.: Effects of salt stress on the growth, ion content, stomatal behaviour and photosynthetic capacity of salt-sensitive species, Phaseolus vulgaris L.-Planta 164: 151–162, 1985.

    Google Scholar 

  • Seemann, J.R., Sharkey, T.D.: Salinity and nitrogen effects on photosynthesis, ribulose-1,5-bisphosphate carboxylase and metabolite pool sizes in Phaseolus vulgaris L.-Plant Physiol. 82: 555–560, 1986.

    Google Scholar 

  • Šesták, Z., Čatský, J., Jarvis, P.G. (ed.): Plant Photosynthetic Production. Manual of Methods.-Dr W. Junk Publ., The Hague 1971.

    Google Scholar 

  • Singh, A.K., Dubey, R.S.: Changes in chlorophyll a and b contents and activities of photosystems 1 and 2 in rice seedlings induced by NaCl.-Photosynthetica 31: 489–499, 1995.

    Google Scholar 

  • Storey, R., Pitman, M.G., Stelzer, R., Carter, C.: X-ray microanalysis of cells and cell compartments of Atriplex spongiosa L. leaves.-J. exp. Bot. 34: 778–794, 1983.

    Google Scholar 

  • Sudhasundari, D., Raghavendra, A.S.: Sensitivity of photosynthesis by spinach chloroplast membranes to osmotic stress in vitro: Rapid inhibition of O2 evolution in presence of magnesium.-Photosynth. Res. 23: 325–330, 1990.

    Google Scholar 

  • Teleisnik, E.L.: Salinity effects on growth and carbon balance in Lycopersicon esculentum and L. pennellii.-Physiol. Plant. 71: 213–218, 1987.

    Google Scholar 

  • Veeranjaneyulu, K.: Mechanism of Heavy Metal Tolerance in Plants.-Ph.D. Thesis. Sri Venkateswara University, Tirupati 1978.

    Google Scholar 

  • Walker, D.A.: Chloroplasts (and grana): aqueous (including high carbon fixation ability.-In Colowick, S.P., Kaplan, N.O. (ed.): Methods in Enzymology. Vol. 23. Pp. 211–220. Academic Press, New York-London 1971.

    Google Scholar 

  • Walker, R.R., Törökfalvy, E., Downton, W.J.S.: Photosynthetic responses of the citrus varieties Rangpur lime and Etrong citron to salt treatment.-Aust. J. Plant Physiol. 7: 783–790, 1982.

    Google Scholar 

  • Wignarajah, K., Baker, N.R.: Salt induced responses of chloroplast activities in species of differing salt tolerance. Photosynthetic electron transport in Aster tripolium and Pisum sativum.-Physiol. Plant. 51: 387–393, 1981.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sreenivasulu Reddy, P., Ramanjulu, S., Sudhakar, C. et al. Differential sensitivity of stomatal and non-stomatal components to NaCl or Na2SO4 salinity in horsegram, Macrotyloma uniflorum (Lam.). Photosynthetica 35, 99–105 (1998). https://doi.org/10.1023/A:1006830100627

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1006830100627

Navigation