Skip to main content
Log in

The role of the photosynthetic apparatus in cold acclimation of Lolium multiflorum. Characteristics of novel genotypes low-sensitive to PSII over-reduction

  • Original Paper
  • Published:
Acta Physiologiae Plantarum Aims and scope Submit manuscript

Abstract

During cold acclimation by higher plants, temperature perception via changes in redox state of Photosystem II (PSII) and subsequent acclimation of the photosynthetic apparatus to cold is very important for achieving freezing tolerance. These properties were studied in two groups (A and B) of the same backcross 3 (BC3) progeny derived from a triploid hybrid of Festuca pratensis (2×) × Lolium multiflorum (4×) backcrossed three times onto diploid L. multiflorum cultivars. Leaves of Group A plants formed at 20°C at medium-low light were unable to acclimate their photosynthetic apparatus to cold. Compared to Group B, the Group A plants were also more frost sensitive. This acclimation ability correlated with the freezing tolerance of the plants. However, leaves of the same Group A plants developed at 20°C, but under higher-light conditions had increased ability to acclimate their photosynthetic apparatus to cold. It was concluded that Group A plants may have impaired PSII temperature perception, and this then resulted in their poor capability to cold acclimate.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

Abbreviations

ABS/CS:

Light energy absorbed by leaf cross-section

ca:

Cold acclimated plants

AREA:

Pool size of electron acceptors from PSII (proportional to the oxidized plastoquinone pool)

car:

Carotenoids (pool)

chl:

Chlorophyll

DIo/CS:

Amount of energy dissipated in PSII reaction centres per cross-section of the leaf

ETo/CS:

Quantum yield of photosynthetic electron transport chain after Q A per cross-section of the leaf

F 0 :

Fluorescence of leaves in the dark when all PSII reaction centres are open

\( {F}\ifmmode{'}\else$'$\fi_{{\text{0}}} \) :

Fluorescence in leaves previously exposed to light darkened just before measurement

F m and \( {F}\ifmmode{'}\else$'$\fi_{{\text{m}}} \) :

Fluorescence when all PSII reaction centres are closed in dark- and light-exposed leaves, respectively

F s :

Steady state fluorescence in light-exposed leaves

F t :

Freezing tolerance

F v and \( {F}\ifmmode{'}\else$'$\fi_{{\text{v}}} \) :

Variable fluorescence in dark- and light-adapted leaves, respectively (F v = F m − F 0, \( {F}\ifmmode{'}\else$'$\fi_{{\text{v}}} = {F}\ifmmode{'}\else$'$\fi_{{\text{m}}} - {F}\ifmmode{'}\else$'$\fi_{0} \))

F v:F m :

Maximum quantum yield of PSII

\( {F}\ifmmode{'}\else$'$\fi_{{\text{v}}} {\user2{:}}{F}\ifmmode{'}\else$'$\fi_{{\text{m}}} \) :

PSII antenna trapping efficiency

fw:

Fresh weight

na:

Non-acclimated plants

PPFD:

Photosynthetic photon flux density

PSII:

Photosystem II

ϕPSII:

Current quantum yield of PSII

NPQ:

Non-photochemical quenching of chlorophyll a fluorescence

QA :

The first stable electron acceptor in PSII

q P :

Photochemical quenching of chlorophyll a fluorescence

RC/CSo and RC/CSm :

Numbers of active reaction centres in the state of fully oxidized and reduced PSII reaction centre, respectively

TRo/CS:

Quantum yield of primary photochemistry (from reaction centre to Q A) per cross-section of the leaf

References

  • Adams WW III, Demmig-Adams B, Verhoeven AS, Barker DH (1995) ‘Photoinhibition’ during winter stress: involvement of sustained xantophyll cycle-dependent energy dissipation. Aust J Plant Physiol 22:261–276

    Article  CAS  Google Scholar 

  • Adams WW, Demmig-Adams B, Rosenstiel TN, Brightwell AK, Ebbert V (2002) Photosynthesis and photoprotection in overwintering plants. Plant Biol 4:545–557

    Article  Google Scholar 

  • Baldi P, Grossi M, Pecchioni N, Vale G, Cattivelli L (1999) High expression level of a gene coding for chloroplastic amino acid selective channel protein is correlated to cold acclimation in cereals. Plant Mol Biol 41:233–243

    Article  PubMed  CAS  Google Scholar 

  • Crosatti C, Mare C, Mazzucotelli E, Selioni S, Barilli S, Bassi R, Dubcovskyi J, Galiba G, Standa AM, Cattivelli L (2003) Genetic analysis of the expression of the cold-regulated gene cor14b: a way toward the identification of components of the cold response signal transduction in Triticeae. Can J Bot 81:1162–1167

    Article  CAS  Google Scholar 

  • Dal Bosco C, Busconi M, Govoni C, Baldi P, Stanca AM, Crosatti C, Bassi R, Cattivelli L (2003) cor gene expression in barley mutants affected in chloroplast development and photosynthetic electron transport. Plant Physiol 131:793–802

    Article  PubMed  CAS  Google Scholar 

  • Feild TS, Lee DW, Holbrook NM (2001) Why leaves turn red in autumn. The role of anthocyanins in senescing leaves of red-osier dogwood. Plant Physiol 127:566–574

    Article  PubMed  CAS  Google Scholar 

  • Gray GR, Chauvin LP, Sarhan F, Huner NPA (1997) Cold acclimation and freezing tolerance—a complex interaction of light and temperature. Plant Physiol 114:467–474

    PubMed  CAS  Google Scholar 

  • Huner NPA, Öquist G, Hurry VM, Krol M, Falk S, Griffith M (1993) Photosynthesis, photoinhibition and low temperature acclimation in cold tolerant plants. Phot Res 37:19–39

    Article  CAS  Google Scholar 

  • Hurry VM, Strand A, Tobiaeson M, Gardestrom P, Öquist G (1995) Cold hardening of spring and winter wheat and rape results in differential effects on growth, carbon metabolism, and carbohydrate content. Plant Physiol 109:697–706

    PubMed  CAS  Google Scholar 

  • Kosmala A, Zwierzykowski Z, Gąsior D, Rapacz M, Zwierzykowska E, Humphreys MW (2006) GISH/FISH mapping of genes for freezing tolerance transferred from Festuca pratensis into Lolium multiflorum. Heredity 96:243–251

    Article  PubMed  CAS  Google Scholar 

  • Larsen A (1978) Freezing tolerance in grasses. Methods for testing in controlled environments. Department of Farm Crops Report No. 195. Scientific Reports of the Agricultural University of Norway

  • Lichtenthaler HK, Wellburn AR (1983) Determination of total carotenoids and chlorophyll ‘a’ and ‘b’ of leaf extracts in different solvents. Biochem Soc Trans 603:590–592

    Google Scholar 

  • Ndong C, Danyluk J, Huner NPA, Sarhan F (2001) Survey of gene expression in winter rye during changes in growth temperature, irradiance or excitation pressure. Plant Mol Biol 45:691–703

    Article  PubMed  CAS  Google Scholar 

  • Pfannschmidt T, Allen JF, Oelmuller R (2001) Principles of redox control in photosynthesis gene expression. Physiol Plant 112:1–9

    Article  CAS  Google Scholar 

  • Phillips JR, Dunn MA, Hughes MA (1997) mRNA stability and localization of the low-temperature-responsive barley gene family blt14. Plant Mol Biol 33:1013–1023

    Article  PubMed  CAS  Google Scholar 

  • Rapacz M (1998a) The after-effects of temperature and irradiance during early growth of winter oilseed rape (Brassica napus L. var. oleifera cv. Gorczanski) seedlings on the progress of their cold acclimation. Acta Physiol Plant 20:73–78

    Article  Google Scholar 

  • Rapacz M (1998b) The effects of day and night temperatures during early growth of winter oilseed rape (Brassica napus L. var. oleifera cv. Gorczanski) seedlings on their morphology and cold acclimation responses. Acta Physiol Plant 20:67–72

    Article  Google Scholar 

  • Rapacz M (2002a) Cold-deacclimation of oilseed rape (Brassica napus var. oleifera) in response to fluctuating temperatures and photoperiod. Ann Bot 89:543–549

    Article  CAS  Google Scholar 

  • Rapacz M (2002b) Regulation of frost resistance during cold de-acclimation and re-acclimation in oilseed rape. A possible role of PSII redox state. Physiol Plant 115:236–243

    Article  CAS  Google Scholar 

  • Rapacz M, Waligórski P, Janowiak F (2003) ABA and gibberellin-like substances during prehardening, cold acclimation, de- and reacclimation of oilseed rape. Acta Physiol Plant 25:151–161

    Article  CAS  Google Scholar 

  • Rapacz M, Gąsior D, Zwierzykowski Z, Leśniewska-Bocianowska A, Humphreys MW, Gay AP (2004) Changes in cold tolerance and the mechanisms of acclimation of photosystem II to cold hardening generated be anther culture of Festuca pratensis ( Lolium multiflorum cultivars. New Phytol 161:105–114

    Article  CAS  Google Scholar 

  • Rizza F, Pagani D, Stanca AM, Cattivelli L (2001) Use of chlorophyll fluorescence to evaluate the cold acclimation and freezing tolerance of winter and spring oats. Plant Breed 120:389–396

    Article  Google Scholar 

  • Strasser BJ, Strasser RJ (1995) Measuring fast fluorescence transients to adress environmental questions: the JIP test. In: Mathis P (eds) Photosynthesis: from light to biosphere. Kluwer Academic, Dordrecht, pp 977–980

    Google Scholar 

  • Strasser RJ, Srivatava A, Tsimilli-Michael M (2000) The fluorescence transient as tool to characterize and screen photosynthetics samples. In: Yunus M, Pathre U, Mohanty P (eds) Probing photosynthesis: mechanism, regulation and adaptation. Taylor and Francis, Bristol, pp 445–483

    Google Scholar 

  • Takumi S, Koike A, Nakata M, Kume S, Ohno R, Nakamura C (2003) Cold-specific and light-stimulated expression of a wheat (Triticum aestivum L.) Cor gene Wcor15 encoding a chloroplast-targeted protein. J Exp Bot 54:2265–2274

    Article  PubMed  CAS  Google Scholar 

  • Zwierzykowski Z, Lukaszewski AJ, Naganowska B, Leśniewska A (1999) The pattern of homoeologous recombination in triploid hybrids of Lolium multiflorum with Festuca pratensis. Genome 42:720–726

    Article  Google Scholar 

Download references

Acknowledgment

This study was performed with the financial support of European Commission: SAGES project (QLK5-CT-2000-00764).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M. Rapacz.

Additional information

Communicated by F. Dubert.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rapacz, M., Gąsior, D., Kościelniak, J. et al. The role of the photosynthetic apparatus in cold acclimation of Lolium multiflorum. Characteristics of novel genotypes low-sensitive to PSII over-reduction. Acta Physiol Plant 29, 309–316 (2007). https://doi.org/10.1007/s11738-007-0040-7

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11738-007-0040-7

Keywords

Navigation