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2007 | 29 | 4 |
Tytuł artykułu

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

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
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℃ 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℃, 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.
Słowa kluczowe
Wydawca
-
Rocznik
Tom
29
Numer
4
Opis fizyczny
p.309-316,fig.,ref.
Twórcy
autor
  • Department of Plant Physiology, Faculty of Agriculture and Economics, Agricultural University of Krakow, Podluzna 3, 30-239 Krakow, Poland
autor
  • Department of Plant Physiology, Faculty of Agriculture and Economics, Agricultural University of Krakow, Podluzna 3, 30-239 Krakow, Poland
  • Department of Plant Physiology, Faculty of Agriculture and Economics, Agricultural University of Krakow, Podluzna 3, 30-239 Krakow, Poland
autor
  • Institute of Plant Genetics, Polish Academy of Sciences, Strzeszynska 34, 60-479 Poznan, Poland
  • Institute of Plant Genetics, Polish Academy of Sciences, Strzeszynska 34, 60-479 Poznan, Poland
  • Institute of Grassland and Environmental Research, Plas Gogerddan, Aberystwyth, Ceredigion SY23 3EB, UK
Bibliografia
  • 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
  • Adams WW, Demmig-Adams B, Rosenstiel TN, Brightwell AK, Ebbert V (2002) Photosynthesis and photoprotection in overwintering plants. Plant Biol 4:545–557
  • 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
  • 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
  • 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
  • Feild TS, Lee DW, Holbrook NM (2001) Why leaves turn red in autumn. The role of anthocyanins in senescing leaves of redosier dogwood. Plant Physiol 127:566–574
  • 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
  • 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
  • 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
  • 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
  • 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
  • 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
  • Pfannschmidt T, Allen JF, Oelmuller R (2001) Principles of redox control in photosynthesis gene expression. Physiol Plant 112:1–9
  • 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
  • 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
  • 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
  • Rapacz M (2002a) Cold-deacclimation of oilseed rape (Brassica napus var. oleifera) in response to fluctuating temperatures and photoperiod. Ann Bot 89:543–549
  • 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
  • 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
  • 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
  • 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
  • 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
  • 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
  • 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
  • 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
Typ dokumentu
Bibliografia
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Identyfikator YADDA
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