Skip to main content
Log in

Effects of Ca2+ and polyethylene glycol on the chlorophyll fluorescence parameters of transgenic OsCaS rice (Oryza sativa L.)

  • Original Papers
  • Published:
Photosynthetica

Abstract

Ca2+ is an important factor mediating many biotic and abiotic stress responses in plants. In this study, we measured the chlorophyll (Chl) fluorescence of transgenic rice with increased or decreased expression of a calcium-sensing receptor (OsCaS) gene during water deficit caused by polyethylene glycol to prove our hypothesis that increased Ca2+ in combination with increased OsCaS could enhance the drought resistance of transgenic rice. Transcript abundance (evaluated by RT-PCR) was significantly lower in OsCaS antisense line 766 (AS766) than that in the wild type, while the overexpression line 777 (O777) showed four times higher amount than that in the wild type. Chl fluorescence showed that the photochemical quantum yield of PSII in the light increased due to addition of Ca2+ in the O777, but dropped in the AS766. Nonphotochemical quenching increased under stress in both transgenic lines and in the wild type, but less in the O777. Nonregulatory quantum yield of energy dissipation showed no significant change under drought stress. Photochemical quenching was significantly higher in the O777 than those in the AS766 and in the wild type after the Ca2+ treatment. In the absence of stress, the electron transport rate (ETR) was significantly higher in the O777 than in both the AS766 and the wild type. In contrast, the ETR of the wild type and both transgenic lines decreased under drought stress, while the effect of polyethylene glycol was partially alleviated by Ca2+ addition in the O777. In summary, excitation energy conversion and dissipation by PSII were regulated by Ca2+ in the O777. It might partially alleviate the effect of drought stress, whereas addition of Ca2+ had no effect in the wild type and the AS766.

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

AS766:

OsCaS antisense line 766

CaS:

calcium-sensing receptor

[Ca2+]:

concentration of Ca2+

[Ca2+]i :

concentration of cytosolic Ca2+

[Ca2+]o :

concentration of extracellular Ca2+

ETR:

electron transport rate

O777OsCaS :

overexpression line 777

PEG:

polyethylene glycol

qP :

photochemical quenching

WT:

wild type

YNO :

nonregulatory quantum yield of energy dissipation

YNPQ :

nonphotochemical quenching

YPSII :

practical quantum yield of PSII

References

  • Bukhov N.G., Egorova E.A., Govindachary S., Carpentier R.: Changes in polyphasic chlorophyll a fluorescence induction curve upon inhibition of donor or acceptor side of photosystem II in isolated thylakoids. — Biochim. Biophys. Acta 1657: 121–130, 2004.

    Article  CAS  PubMed  Google Scholar 

  • Cousson A.: Indolyl-3-butyric acid-induced Arabidopsis stomatal opening mediated by 3′,5′-cyclic guanosine-monophosphate. — Plant Physiol. Bioch. 48: 977–986, 2010.

    Article  CAS  Google Scholar 

  • Ding S., Lei M., Lu Q. et al.: Enhanced sensitivity and characterization of photosystem II in transgenic tobacco plants with decreased chloroplast glutathione reductase under chilling stress. — Biochim. Biophys. Acta 1817: 1979–1991, 2012.

    Article  CAS  PubMed  Google Scholar 

  • Eivazi A., Talat F., Saeed A., Ranji H.: Selection for osmoregulation gene to improve grain yield of wheat genotypes under osmotic stresses. — Pak. J. Biol. Sci. 10: 3703–3707, 2007.

    Article  PubMed  Google Scholar 

  • Habibi G., Hajiboland R.: Comparison of photosynthesis and antioxidative protection in Sedum album and Sedum stoloniferum (Crassulaceae) under water stress. — Photosynthetica 50: 508–518, 2012.

    Article  CAS  Google Scholar 

  • Han G.J., Chen N.L., Huang H.X. et al.: [Responses of tomato leaf photosynthesis to rapid water stress.] — Ying Yong Sheng Tai Xue Bao 24: 1017–1022, 2013. [In Chinese]

    CAS  PubMed  Google Scholar 

  • Han S., Tang R., Anderson L.K. et al.: A cell surface receptor mediates extracellular Ca2+ sensing in guard cells. — Nature 425: 196–200, 2003.

    Article  CAS  PubMed  Google Scholar 

  • Jaleel C.A., Manivannan P., Sankar B. et al.: Water deficit stress mitigation by calcium chloride in Catharanthus roseus: Effects on oxidative stress, proline metabolism and indole alkaloid accumulation. — Colloid. Surface B 60: 110–116, 2007.

    Article  CAS  Google Scholar 

  • Li F., Wu Q. Y., Duan M. et al.: Transgenic tomato plants overexpressing chloroplastic monodehydroascorbate reductase are resistant to salt- and PEG-induced osmotic stress. — Photosynthetica 50: 120–128, 2012.

    Article  CAS  Google Scholar 

  • Li X., Yan X., Yu T.: [Effects of water stress on protective enzyme activities and lipid peroxidation in Phellodendron amurense seedlings.] — Ying Yong Sheng Tai Xue Bao 16: 2353–2356, 2005. [In Chinese]

    CAS  PubMed  Google Scholar 

  • Luo H.B., Ma L., Xi H.F. et al.: Photosynthetic responses to heat treatments at different temperatures and following recovery in grapevine (Vitis amurensis L.) leaves. — PLoS ONE 6: e23033, 2011.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Luo H.H., Zhang H.Z., Tao X.P. et al.: [Effects of water and nitrogen management modes on the leaf photosynthetic characters and yield formation of cotton with under-mulch drip irrigation.] — Ying Yong Sheng Tai Xue Bao 24: 407–415, 2013. [In Chinese]

    CAS  PubMed  Google Scholar 

  • Maxwell K., Johnson G.N.: Chlorophyll fluorescence- a practical guide. — J. Exp. Bot. 51: 659–668, 2000.

    Article  CAS  PubMed  Google Scholar 

  • Moon Y.R., Lee M.H., Tovuu A. et al.: Acute exposure to UV-B sensitizes cucumber, tomato, and Arabidopsis plants to photooxidative stress by inhibiting thermal energy dissipation and antioxidant defense. — J. Radiat. Res. 52: 238–248, 2011.

    Article  CAS  PubMed  Google Scholar 

  • Murchie E.H., Lawson T.: Chlorophyll fluorescence analysis: a guide to good practice and understanding some new applications. — J. Exp. Bot. 64: 3983–3998, 2013.

    Article  CAS  PubMed  Google Scholar 

  • Nomura H., Komori T., Uemura S., et al.: Chloroplast-mediated activation of plant immune signaling in Arabidopsis. — Nat. Commun. 3: 926–935, 2012.

    Article  PubMed  Google Scholar 

  • Papageorgiou G.C., Govindjee.: Photosystem II fluorescence: slow changes - scaling from the past. — J. Photoch. Photobio. B 104: 258–270, 2011.

    Article  CAS  Google Scholar 

  • Ptushenko V.V., Ptushenko E.A., Samoilova O.P., Tikhonov A.N.: Chlorophyll fluorescence in the leaves of Tradescantia species of different ecological groups: Induction events at different intensities of actinic light. — Biosystems 114: 85–97, 2013.

    Article  CAS  PubMed  Google Scholar 

  • Schreiber U., Quayle P., Schmidt S. et al.: Methodology and evaluation of a highly sensitive algae toxicity test based on multiwell chlorophyll fluorescence imaging. — Biosens. Bioelectron. 22: 2554–2563, 2007.

    Article  CAS  PubMed  Google Scholar 

  • Shao H.B., Song W.Y., Chu L.Y.: Advances of calcium signals involved in plant anti-drought. — CR. Biol. 331: 587–596, 2008.

    Article  CAS  Google Scholar 

  • Silva E.N., Ferreira-Silva S.L., Fontenele Ade V. et al.: Photosynthetic changes and protective mechanisms against oxidative damage subjected to isolated and combined drought and heat stresses in Jatropha curcas plants. — J. Plant Physiol. 167: 1157–1164, 2010.

    Article  CAS  PubMed  Google Scholar 

  • Vainonen J.P., Sakuragi Y., Stael S. et al.: Light regulation of CaS, a novel phosphoprotein in the thylakoid membrane of Arabidopsis thaliana. — FEBS J. 275: 1767–1777, 2008.

    Article  CAS  PubMed  Google Scholar 

  • Xu C., Li X., Zhang L.: The effect of calcium chloride on growth, photosynthesis, and antioxidant responses of Zoysia japonica under drought conditions. — PLoS ONE 8: e68214, 2013.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Yang T., Peng H., Whitaker B.D., Jurick W.M.: Differential expression of calcium/calmodulin-regulated SlSRs in response to abiotic and biotic stresses in tomato fruit. — Physiol. Plantarum 148: 445–455, 2013.

    Article  CAS  Google Scholar 

  • Zhao X.: [Isolation and functional analysis of extracellular calcium-sensing receptor (OsCAS) gene from rice (Oryza sativa L.).] — Ph.D. Thesis, Capital Normal University, Beiing 2007. [In Chinese]

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to X. Zhao.

Additional information

Acknowledgements: We thank to Dr. Yikun He of Capital Normal University for helpful discussion, to Dr. Tiegang Lu of Chinese Academy of Agricultural Sciences for donating pCUbi1390 vector, and to Dr. Yaping Fu and Wenzhen Liu of China National Rice Research Institute for help with transformation of rice and planting the experimental materials. We thank to Dr. Michael Deyholos for help with amending the article. This work was supported by National Nature Science Foundation of China (30900771) and Beijing Natural Science Foundation (5102006).

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wei, R., Liu, Y., Sui, Y. et al. Effects of Ca2+ and polyethylene glycol on the chlorophyll fluorescence parameters of transgenic OsCaS rice (Oryza sativa L.). Photosynthetica 53, 336–341 (2015). https://doi.org/10.1007/s11099-015-0107-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11099-015-0107-4

Additional key words

Navigation