ABA level, proline and phenolic concentration, and PAL activity induced during cold acclimation in androgenic Festulolium forms with contrasting resistance to frost and pink snow mould (Microdochium nivale)

Physiological and Molecular Plant Pathology

Volumn 73, Issue 6, 2008, Pages 126-132

  Pociecha, Ewa ^a   Płazek, Agnieszka ^a   Janowiak, Franciszek ^b   Zwierzykowski, Zbigniew ^c  

^a UNIVERSITY OF AGRICULTURE IN KRAKOW   (Poland)

^b THE FRANCISZEK GÓRSKI INSTITUTE OF PLANT PHYSIOLOGY   (Poland)

^c INSTITUTE OF PLANT GENETICS   (Poland)

Author keywords

Abscisic acid; Cold acclimation; Cross tolerance; Festulolium; Microdochium nivale; Phenylpropanoid pathway; Proline

Indexed keywords

FESTULOLIUM; MICRODOCHIUM NIVALE;

EID: 70349263822     PISSN: 08855765     EISSN: 10961178     Source Type: Journal    
DOI: 10.1016/j.pmpp.2009.03.005     Document Type: Article

References (58)

1. Prończuk M., and Prończuk S. Przydatność "metody chłodniowej" w ocenie odporności życicy trwałej na Fusarium nivale (Fr) Ces. Biuletyn IHAR 162 (1987) 27-32 (In Polish with English summary)
2. Gaudet D.A., Laroche A., and Yoshida M. Low temperature-wheat-fungal interactions: a carbohydrate connection. Physiol Plant 106 (1999) 437-444
3. Hiilovaara-Teijo M., Hannukkala A., Griffith M., Yu X.M., and Pihakaski-Maunsbach K. Snow mold-induced apoplastic proteins in winter rye leaves lack antifreeze activity. Plant Physiol 121 (1999) 665-674
4. Itai C., Richmond A., and Vaadia Y. The role of root cytokinins during water and salinity stress. Isr J Bot 17 (1968) 187-195
5. Kefu Z., Munns R., and King R.W. Abscisic acid levels in NaCl-treated barley, cotton and salt-bush. Aust J Plant Physiol 18 (1991) 17-24
6. Bowler C., and Fluhr R. The role of calcium and activated oxygens as signals for controlling cross-tolerance. Trends Plant Sci 5 (2000) 241-246
7. Thomashow M.F. Plant cold acclimation: freezing tolerance genes and regulatory mechanisms. Annu Rev Plant Physiol Plant Mol Biol 50 (1999) 571-599
8. Bonetta D., and McCourt P. Genetic analysis of ABA signal transduction pathways. Trends Plant Sci 3 (1998) 231-235
9. Akiyama T., and Pillai M.A. Molecular cloning characterization and in vitro expression of a novel endo-13-β-glucanase up-regulated by ABA and drought stress in rice (Oryza sativa L.). Plant Sci 161 (2001) 1089-1098
10. Aroca R., Vernieri P., Irigoyen J.J., Sánchez-Diaz M., Tognoni F., and Pardossi A. Involvement of abscisic acid in leaf and root of maize (Zea mays L.) in avoiding chilling-induced water stress. Plant Sci 165 (2003) 671-679
11. Mauch-Mani B., and Mauch F. The role of abscisic acid in plant pathogen interactions. Curr Opin Plant Biol 8 (2005) 409-414
12. Asselbergh B, Höfte M. Basal tomato defences to Botrytis cinerea include abscisic acid-dependent callose formation. Physiol Mol Plant Pathol. doi:10.1016/j.pmpp.2007.10.001.
13. Hare P.D., and Cress W.A. Metabolic implications of stress-induced proline accumulation in plants. Plant Growth Regul 21 (1997) 79-102
14. Arbaoui M., Balko C., and Link W. Study of faba bean (Vicia faba L.) winter hardiness and development of screening methods. Field Crops Res 106 (2008) 60-67
15. Slama I., Messedi D., Ghnaya T., Savoure A., and Abdelly C. Effects of water deficit on growth and proline metabolism in Sesuvium portulacastrum. Envinron Exp Bot 56 (2006) 231-238
16. Versules P.E., and Bray E.A. Role of abscisic acid (ABA) and Arabidopsis thaliana ABA-insensitive loci in low water potential-induced ABA and proline accumulation. J Exp Bot 57 (2006) 201-212
17. Dixon R.A., and Paiva N.L. Stress-induced phenylpropanoid metabolism. Plant Cell 7 (1995) 1085-1097
18. Graham T.L., and Graham M.Y. Signaling in soybean phenylpropanoid responses, Dissection of primary secondary and conditioning effect of light wounding and elicitor treatments. Plant Physiol 110 (1996) 1123-1133
19. Sanchez-Ballesta M., Lafuente M.T., Zacarias L., and Granell A. Involvement of phenylalanine ammonia-lyase in the response of fortune mandarin fruits to cold temperature. Physiol Plant 108 (2000) 382-389
20. Solecka D., Boudet A.M., and Kacperska A. Phenylpropanoid and anthocyanin changes in low temperature treated winter oilseed rape leaves. Plant Physiol Biochem 37 (1999) 491-496
21. Solecka D., and Kacperska A. Phenylalanine ammonia-lyase activity in leaves of winter oilseed rape plants as affected by acclimation of plants to low temperature. Plant Physiol Biochem 33 (1995) 585-591
22. 1 hybrids and cultivars of Festulolium. Zeszyty Problemowe Poste{ogonek}pów Nauk Rolniczych 474 (2001) 47-54 (In Polish with English summary)
23. Hartman C.L., McCoy T.J., and Knous T.R. Selection of alfalfa (Medicago sativa) cell lines and regeneration of plant resistant to the toxin(s) produced by Fusarium oxysporum f, sp, medicaginis. Plant Sci Lett 34 (1984) 183-194
24. Rapacz M., Ga{ogonek}sior D., Zwierzykowski Z., Leśniewska-Bocianowska A., Humphreys M.W., and Gay A.P. 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 (2004) 105-114
25. Larsen A. Freezing tolerance in grasses, Methods for testing in controlled environments. 1978; Department of Farm Crops Report no. 195, Sci, Rep, Agr, University Norway.
26. Walker-Simmons M.K., and Abrams S.R. Use of ABA immunoassays. In: Davies W.J., and Jones H.G. (Eds). Abscisic acid physiology and biochemistry (1991), Bios Scientific Publishers, Oxford 53-63
27. Barrs H.D. Determination of water deficits in plant tissues. In: Kozlowski T.T. (Ed). Water deficits and plant growth (1968), Academic Press, New York & London 235-253
28. Bates L.S., Waldren R.P., and Teare I.D. Rapid determination of free praline for water stress studies. Plant Soil 39 (1973) 205-207
29. Singleton V.L., and Rossi Jr. J.A. Colorimetry of total phenolics with phosphomolybdic-phosphotungstic acid reagent. Am J Enol Vitic 16 (1965) 144-153
30. Peltonen S., and Karjalainen R. Phenylalanine ammonia-lyase activity in barley after infection with Bipolaris sorokiniana or treatment with purified xylanase. J Phytopath 143 (1995) 239-245
31. Bradford M.A. Rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72 (1976) 248-254
32. Chen T.H.H., and Gusta L.V. Abscisic acid-induced freezing resistance in cultured plant cells. Plant Physiol 73 (1983) 71-75
33. Ishikawa M., Robertson A.J., and Gusta L.V. Effect of temperature light nutrients and dehardening on abscisic acid-induced cold hardiness in Bromus inermis Leyss suspension cultured cells. Plant Cell Physiol 31 (1990) 51-59
34. Bravo L.A., Zuniga G.E., Alberdi M., and Corcuera L.J. The role of ABA in freezing tolerance and cold acclimation in barley. Physiol Plant 103 (1998) 17-23
35. 3 treatments on resistance to frost and photoinhibition in oilseed rape leaf discs. Acta Physiol Plant 24 (2003) 447-457
36. Agrawal G.K., Rakwal R., Jwa N., and Agrawal V.P. Signalling molecules and blast pathogen pathogen attack activates rice OsPR1a and OsPR1b genes: a model illustrating components participating during defence/stress response. Plant Physiol Biochem 39 (2001) 1095-1103
37. Mohr P.G., and Cahill D.M. Relative roles of glyceolin lignin and the hypersensitive response and the influence of ABA in compatible and incompatible interactions of soybeans with Phytophtora sojae. Physiol Mol Plant Pathol 58 (2001) 31-41
38. Ga{ogonek}sior D., Rapacz M., Janowiak F., Zwierzykowski Z., Leśniewska-Bocianowska A., and Humphreys M.W. The dynamics of changes in water relation and ABA content during the first hours of cold acclimation of androgenic lines of Festulolium. In: Zwierzykowski Z., Surma M., and Kachlicki P. (Eds). Application of novel cytogenetic and molecular techniques in genetics and breeding of the grasses (2003), Institute of Plant Genetics PAS, Poznań Poland 93-98
39. Cook R., and Papendick R.I. Role of water potential in microbial growth and development of plant disease with special reference to postharvested pathology. Hort Sci 13 (1978) 559-564
40. Tronsmo A.M. Host water potentials may restrict development of snow mould fungi in low temperature-hardened grasses. Physiol Plant 68 (1986) 175-179
41. Grote D., Schmidt R., and Claussen W. Water uptake and proline index as indicators of predisposition in tomato plants to Phytophtora nicotianae infection as influenced by abiotic stresses. Physiol Molec Plant Pathol 69 (2006) 121-130
42. Mohanty S.K., and Sridhar R. Physiology of rice tungro virus disease: proline accumulation due to infection. Physiol Plant 56 (1982) 89-93
43. Duncan D.R., and Widholm J.M. Proline accumulation and its implication in cold tolerance of regenerable maize callus. Plant Physiol 83 (1987) 703-708
44. Xin Z., and Li P.H. Relationship between proline and Abscisic acid in the induction of chilling tolerance in maize suspension-cultured cells. Plant Physiol 103 (1970) 607-613
45. Peltonen S., Mannonen L., and Karjalainen R. Elicitor-induced changes of phenylalanine ammonia-lyase activity in barley cell suspension cultures. Plant Cell 50 (1997) 185-193
46. Hakulinen J., Sorjonen S., and Julkunen-Tiitto R. Leaf phenolics of three willow clones differing in resistance to Melampsora rust infection. Physiol Plant 105 (1999) 662-669
47. Isihara A., Ohtsu Y., and Iwamura H. Induction of biosynthetic enzymes for aventhramides in elicitor-treated oat leaves. Planta 208 (1999) 512-518
48. El Modafar C., Tantaoui A., and Boustani S. Differential induction of phenylalanine ammonia-lyase activity in date palm roots in response to inoculation with Fusarium oxysporum f, sp, albedinis and to elicitation with fungal wall elicitor. J Plant Physiol 158 (2001) 715-722
49. Hammond-Kosack K.E., and Jones J. Resistance gene-dependent plant defense response. Plant Cell 8 (1996) 1773-1791
50. Pennycooke J.C., Cox S., and Stushnoff C. Relationship of cold acclimation total phenolic content and antioxidant capacity with chilling tolerance in petunia (Petunia x hybrida). Environ Exp Bot 53 (2005) 225-232
51. Christie P.J., Alfenito M.R., and Walbot V. Impact of low temperature stress on general phenylpropanoid and anthocyanin pathways: enhancement of transcript abundance and anthocyanin pigmentation in maize seedlings. Planta 194 (1994) 541-549
52. Chalker-Scott L. Environmental significance of anthocyanins in plant stress responses. Photochem Photobiol 70 (1999) 1-9
53. Singh A., Selvi M.T., and Sharma R. Sunlight-induced anthocyanin pigmentation in maize vegetative tissue. J Exp Bot 50 (1999) 1619-1625
54. Rice-Evans C.A., Miller N.J., and Paganga G. Antioxidant properties of phenolic compounds. Trends Plant Sci 2 (1997) 151-159
55. Nicholson R.L., and Hammerschmidt R. Phenolics compounds and their role in disease resistance. Annu Rev Phytopathol 30 (1992) 369-389
56. Płażek A., Skrzypek E., and Żur I. The change of heat emission and phenolic compounds level in Hordeum vulgare (L,) and Festuca pratensis (Huds,) calli treated with Bipolaris sorokiniana (Sacc,) Shoem, phytotoxins. J Agron Crop Sci 184 (2000) 1-72
57. Płażek A., and Żur I. Cold-induced plant resistance to necrotrophic pathogens and antioxidant enzyme activities and cell membrane permeability. Plant Sci 164 (2003) 1019-1028
58. Pociecha E., Płażek A., Janowiak F., Janeczko A., and Zwierzykowski Z. Physiological basis for differences in resistance to Microdochium nivale (Fr) Samuels and Hallett in two androgenic genotypes of Festulolium derived from tetraploid F1 hybrids of Festuca pratensis x Lolium multiflorum (Festulolium). J Phytopathol 156 (2008) 155-163