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The effects of potassium nitrate and NO-donors on phytochrome A- and phytochrome B-specific induced germination of Arabidopsis thaliana seeds

Published online by Cambridge University Press:  22 February 2007

Ivana Batak ,
Marijana Dević ,
Zlatko Gibal ,
Dragoljub Grubišić ,
Kenneth L. Poff  and
Radomir Konjević
Ivana Batak
Affiliation:
Institute of Botany, Faculty of Biology, University of Belgrade, Takovska 43, 11000 Belgrade
Marijana Dević
Affiliation:
Institute for Biological Research ‘S. Stanković’, 29 Novembra 142, 11060 Belgrade, Yugoslavia
Zlatko Gibal
Affiliation:
Institute of Botany, Faculty of Biology, University of Belgrade, Takovska 43, 11000 Belgrade
Dragoljub Grubišić
Affiliation:
Institute for Biological Research ‘S. Stanković’, 29 Novembra 142, 11060 Belgrade, Yugoslavia
Kenneth L. Poff
Affiliation:
Department of Botany and Plant Pathology, Michigan State University, East Lansing, Michigan 48824, USA
Radomir Konjević*
Affiliation:
Institute of Botany, Faculty of Biology, University of Belgrade, Takovska 43, 11000 Belgrade
*
*Correspondence Fax: +381-11-769-903 Email: [email protected]
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Abstract

Nitrogenous compounds, such as potassium nitrate, potentiate germination of different species of light-requiring seeds. Using light-induced Arabidopsis thaliana seed germination as a model system, our data suggested that only phytochrome A (phyA)-specific induced germination was affected after the exogenous application of nitrates, different nitric oxide (NO)-donors (such as organic nitrates) or sodium nitroprusside. The stimulative effect was very pronounced. Treated seed samples reached maximal germination after very short periods of red-light irradiation. To a far lesser extent, these substances affected phytochrome B (phyB)-specific induced germination. In phyB-specific induced germination, potassium nitrate was most effective, but germination percentages never exceeded 50%. The least effective was sodium nitroprusside, which practically did not affect phyB-specific induced germination. These results were confirmed using corresponding phytochrome mutants.

Keywords

Arabidopsis thalianagerminationlightphytochromespotassium nitratenitric oxide
Type
Research Article
Information
Seed Science Research , Volume 12 , Issue 4 , December 2002 , pp. 253 - 259
Copyright
Copyright © Cambridge University Press 2002

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References

Beligni, M.V. and Lamattina, L. (2000) Nitric oxide stimulates seed germination and de-etiolation, and inhibits hypocotyl elongation, three light-inducible responses in plants. Planta 210, 215–221.CrossRefGoogle ScholarPubMed
Bischoff, F., Millar, A.J., Kay, S.A. and Furuya, M. (1997) Phytochrome-induced intercellular signalling activates cab:luciferase gene expression. Plant Journal 12, 839–849.CrossRefGoogle Scholar
Broillet, M.C. (1999) S-nitrosylation of proteins. Cellular and Molecular Life Sciences 55, 1036–1042.CrossRefGoogle ScholarPubMed
Brown, N.A.C. and van Staden, J. (1997) Smoke as a germination cue: a review. Plant Growth Regulation 22, 115–124.CrossRefGoogle Scholar
Cohn, M.A. and Castle, L. (1984) Dormancy in red rice. IV. Response of unimbibed and imbibing seeds to nitrogen dioxide. Physiologia Plantarum 60, 552–556.Google Scholar
Dean, J.V. and Harper, J.E. (1988) The conversion of nitrite to nitrogen oxide(s) by the constitutive NAD(P)H-nitrate reductase enzyme from soybean. Plant Physiology 88, 389–395.CrossRefGoogle ScholarPubMed
Estabrook, E.M. and Yoder, J.I. (1998) Plant-plant communications: rhizosphere signaling between parasitic angiosperms and their hosts. Plant Physiology 116, 1–7.CrossRefGoogle Scholar
Furuya, M. and Schäfer, E. (1996) Photoperception and signalling of induction reactions by different phytochromes. Trends in Plant Science 1, 301–307.CrossRefGoogle Scholar
Giba, Z., Grubišić, D. and Konjević, R. (1992) Sodium nitroprusside-stimulated germination of common chickweed (Stellaria media L.) seeds. Archives of Biological Sciences 44, 17P–18P.Google Scholar
Giba, Z., Grubišić, D. and Konjević, R. (1994) The effect of electron acceptors on the phytochrome-controlled germination of Paulownia tomentosa seeds. Physiologia Plantarum 91, 290–294.CrossRefGoogle Scholar
Giba, Z., Scordilis, A., Grubišić, D., Thanos, C.A. and Konjević, R. (1997 a) Control of seed germination in mountain pine. Abstracts, p.95. First Balkan botanical congress, Thessaloniki, Greece, 19-22 September.Google Scholar
Giba, Z., Grubišić, D., Sajc, L., Stojaković, Đ. and Konjević, R. (1997 b) Effect of some nitric oxide donors and methylene blue on light induced germination of Paulownia tomentosa seeds. Archives of Biological Sciences 49, 15P–16P.Google Scholar
Giba, Z., Grubišić, D., Todorović, S., Sajc, L., Stojaković, Đ. and Konjević, R. (1998) Effect of nitric oxide-releasing compounds on phytochrome-controlled germination of Empress tree seeds. Plant Growth Regulation 26, 175–181.CrossRefGoogle Scholar
Grubišić, D. and Konjević, R. (1990) Light and nitrate interaction in phytochrome-controlled germination of Paulownia tomentosa seeds. Planta 181, 239–243.CrossRefGoogle Scholar
Grubišić, D., Giba, Z. and Konjević, R. (1991) Organic nitrates stimulated germination of common chick weed (Stellaria media L.) seeds. Arhiv Bioloških Nauka 43, 7P–8P.Google Scholar
Grubišić, D., Giba, Z. and Konjević, R. (1992) The effect of organic nitrates in phytochrome-controlled germination of Paulownia tomentosa seeds. Photochemistry and Photobiology 56, 629–632.Google Scholar
Hilhorst, H.W.M. (1990) Seed dormancy and germination: light and nitrate. PhD Thesis, University of Wageningen, The Netherlands.Google Scholar
Hou, Y.C., Janczuk, A. and Wang, P.G. (1999) Current trends in the development of nitric oxide donors. Current Pharmaceutical Design 5, 417–441.Google ScholarPubMed
Johnson, E., Bradley, M., Harberd, N.P. and Whitelam, G.C. (1994) Photoresponses of light-grown phyA mutants of Arabidopsis. Phytochrome A is required for the perception of daylength extensions. Plant Physiology 105, 141–149.Google Scholar
Keeley, J.E. and Fotheringham, C.J. (1997) Trace gas emissions and smoke-induced seed germination. Science 276, 1248–1250.Google Scholar
Lehmann, E. (1909) Zur Keimungphysiologie und -biologie von Ranunculus sclereatus L. und einigen anderen Samen. Berichte der Deutschen Botanischen Gesellschaft 27, 476–494.Google Scholar
Nagatani, A., Reed, J.W. and Chory, J. (1993) Isolation and initial characterization of Arabidopsis mutants that are deficient in phytochrome A. Plant Physiology 102, 269–277.Google Scholar
Schütz, I. and Furuya, M. (2001) Evidence for type II phytochrome-induced rapid signalling leading to cab::luciferase gene expression in tobacco cotyledons. Planta 212, 759–764.Google ScholarPubMed
Shinomura, T., Nagatani, A., Chory, J. and Furuya, M. (1994) The induction of seed germination in Arabidopsis thaliana is regulated principally by phytochrome B and secondarily by phytochrome A. Plant Physiology 104, 363–371.CrossRefGoogle ScholarPubMed
Shinomura, T., Nagatani, A., Hanzawa, H., Kubota, M., Watanabe, M. and Furuya, M. (1996) Action spectra for phytochrome A- and B-specific photoinduction of seed germination in Arabidopsis thaliana. Proceedings of the National Academy of Sciences, USA 93, 8129–8133.CrossRefGoogle ScholarPubMed
Somers, D.E., Sharrock, R.A., Tepperman, J.M. and Quail, P.H. (1991) The hy3 long hypocotyl mutant of Arabidopsis is deficient in phytochrome B. Plant Cell 3, 1263–1274.CrossRefGoogle ScholarPubMed
Tirlapur, U.K., Dahse, I., Probandt, R., Fischer, W. and Appenroth, K.J. (1999) Phytochrome-induced transmissible signal elicits germination response in turions of Spirodela polyrhiza. Physiologia Plantarum 105, 539–545.CrossRefGoogle Scholar
Toole, E.H., Toole, V.K., Bortwick, H.A. and Hendricks, S.B. (1955) Photocontrol of Lepidium seed germination. Plant Physiology 30, 15–21.CrossRefGoogle ScholarPubMed
Yamasaki, H., Sakihama, Y. and Takahashi, S. (1999) An alternative pathway for nitric oxide production in plants: new features of an old enzyme. Trends in Plant Science 4, 128–129.CrossRefGoogle ScholarPubMed