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Polyamine metabolism and in vitro cell multiplication and differentiation in leaf explants of Chrysanthemum morifolium Ramat

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Abstract

Arginine decarboxylase (ADC), ornithine decarboxylase (ODC), diamine oxydase (DAO) free amine and conjugated amine titers were estimated in leaf explants of Chrysanthemum morifolium Ramat. var. Spinder cultivated in vitro in relation to hormone treatment. Addition of benzyladenine (BA) to a basal medium caused the formation of buds on the explants. BA plus 2,4 dichlorophenoxyacetic acid (2,4 D) caused callus formation and proliferation. Formation of roots was obtained by addition of indolylacetic acid (IAA). Arginine decarboxylase (ADC) ornithine decarboxylase (ODC) and diamine oxidase (DAO) activities increased during the first days of culture when cell multiplication was rapid, followed by a sharp decline as the rate of cell division decreased and differentiation took place. DAO activities increased rapidly in proliferating and growing organs and decreased during maturity. This increase was concomitant with ADC and ODC activities and polyamine content (free and conjugated polyamines). The biosynthesis and oxidation of polyamines which occurred simultaneously in physiological states of intense metabolism such as cell division or organ formation were directly correlated. In callus cultures DAO activity was blocked throughout development and regulated neither the cellular levels of polyamines nor polyamine conjugates. Levels of polyamine conjugates were high in callus cultures throughout development. In foliar explants cultivated on a medium promoting callus, inhibition of ODC activity by DFMO (α-DL-difluoromethylornithine, a specific enzyme-activated ODC inhibitor) resulting in an amide deficiency facilated the expression of differentiated cell function; substantial activation of DAO was observed until the emergence of the buds. On a medium promoting bud formation, β-OH ethylhydrazine (DAO inhibitor) promoted callus formation without differentiation. In this system DAO activity was blocked and there were high levels of polyamines, especially polyamine conjugates, throughout the culture period. The relationship among free and conjugated polyamines related biosynthetic enzyme activities, DAO activities, cell division and organ formation is discussed.

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Abbreviations

ADC =:

arginine decarboxylase

ODC =:

ornithine decarboxylase

DOA =:

diamine oxidase

DFMA =:

α-DL-difluoromethylarginine

DFMO =:

α-DL-difluoromethylornithine

Put =:

putrescine

References

  1. Bagni N, Torrigiani P and Barbieri P (1981) Effect of various inhibitors of polyamine synthesis on the growth of Helianthus tuberosus. Med Bio 5: 403–409

    Google Scholar 

  2. Birecka H, Bitonti A and McCann PP (1985) Assaying ornithine and arginine decarboxylase in some plant species. Plant Physiol 79: 509–514

    Google Scholar 

  3. Bradford MM (1976) A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein dye binding. Ann Biochem 72: 248–254

    Article  Google Scholar 

  4. Burtin D (1991) Métabolisme des amines libres et conjuguées au cours de la croissance et du développement de Nicotiana tabacum var Xanthi n.c.: appraches biochimiques et moléculaires PhD., Dijon, October 1991

  5. Burtin D, Martin-Tanguy J, Paynot M and Rossin N (1989) Effects of the suicide inhibitors of arginine and ornithine decarboxylase activities on organogenesis, growth, free polyamine and hydroxycinnamoylputrescine levels in leaf explants of Nicotiana tabacum Xanthi n.c. cultivated in vitro in a medium producing callus formation. Plant Physiol 89: 104–110

    Google Scholar 

  6. Burtin D, Martin-Tanguy J, Paynot M, Carré M and Rossin N (1990) Polyamines, hydroxycinnamoylputrescine, and root formation in leaf explants of tobacco cultivated in vitro. Plant Physiol 93: 139–140

    Google Scholar 

  7. Cabanne F, Dalebroux MA, Martin-Tanguy J and Martin C (1981) Hydroxycinnamic acid amides and ripening to flower of Nicotiana tabacum var Xanthi n.c. Physiol Plant 53: 399–401

    Google Scholar 

  8. Egea-Cortines M and Mizrahi Y (1991) Polyamines in cell division, fruit set and development, and seed germination. In: Slocum RD and Flores HE (eds) Biochemistry and Physiology of Polyamines in Plants pp 143–158. CRC Press, Florida, USA

    Google Scholar 

  9. Frederico R and Angelino R (1991) Polyamine catabolism in plant. In: Slocum RD and Flores HE (eds) Biochemistry and Physiology of Polyamines in Plants, pp 41–53. CRC Press, Florida, USA

    Google Scholar 

  10. Flores HE and Galston AW (1982) Analysis of polyamines in higher plants by high performance liquid chromatography. Plant Physiol 69: 701–706

    Google Scholar 

  11. Galston AW (1983) Polyamine as modulators of plant development. BioScience 33: 102–109

    Google Scholar 

  12. Galston AW and Flores HE (1991) Polyamines and plant morphogenesis. In: Slocum RD and Flores HE (eds) Biochemistry and Physiology of Polyamines in Plants, pp 175–186. CRC Press, Florida, USA

    Google Scholar 

  13. Kaur-Sawhney R and Galston AW (1991) Physiological and biochemical studies on the antisenescence properties of polyamines in plants. In: Slocun RA and Flores HE (eds) Biochemistry and Physiology of Polyamines in Plant, pp 201–211. CRC Press, Florida, USA

    Google Scholar 

  14. Malinski C, Bieganski T, Fogel WA and Kitler ME (1965) Diamine oxydase in developing tissues. In: Mondovi B (ed) Structure and Reactions of Polyamines Oxidases, pp 154–166. CRC Press, Florida, USA

    Google Scholar 

  15. Martin C, Kunesh G, Martin-Tanguy J, Negrel J, Paynot M and Carré M (1985) Effect of cinnamoylputrescines on in vitro cell multiplication and differentiation of tobacco explants. Plant Cell Rep 4: 381–399

    Google Scholar 

  16. Martin-Tanguy J (1985) The occurrence and possible function of hydroxycinnamic acid amides in plant. Plant Growth Regul 3: 381–399

    Google Scholar 

  17. Martin-Tanguy J, Martin C, Paynot M and Rossin N (1988) Effect of hormone treatment on growth bud formation and free amine and hydroxycinnamoylputrescine levels in leaf explant of Nicotiana tabacum cultivated in vitro. Physiol Plant 15: 473–497

    Google Scholar 

  18. Martin-Tanguy J, Cabanne F, Perdrizet E and Martin C (1978) The distribution of hydroxycinnamic acid amides in flowering plants. Phytochem 17: 1927–1928

    Article  Google Scholar 

  19. Murashige T and Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15: 473–497

    Google Scholar 

  20. Okuyama T and Kobayashi Y (1961) Determination of diamine oxidase by liquid scintillation counting. Anal Biochem Biophys 94: 242–250

    Google Scholar 

  21. Perin A, Sessa A and Desiderio MA (1985) Diamine oxidase in regenerating and hypertrophic tissues. In: Mondovi B (ed) Structure and function of amine oxidase, pp 179–186. CRC Press, Florida, USA

    Google Scholar 

  22. Ponchet M, Martin-Tanguy J, Poupet A, (1982) Separation and quantification of basic hydroxycinnamic acids by reversed phase high performance liquid chromatography. J Chromat 240: 397–404

    Article  Google Scholar 

  23. Rastogi R and Davies P (1991) Effects of light and plant growth regulator on polyamine metabolism in higher plants. In: Slocum RA and Flores HE (eds) Biochemistry and Physiology of Polyamines in Plants, pp 187–988. CRC Press, Florida, USA

    Google Scholar 

  24. Rinaldi A, Floris G and Giartosio A (1986) In: Mondovi B (ed) Plant Amine Oxidase, pp 51–71. CRC Press, Florida, USA

    Google Scholar 

  25. Rinaldi, Floris G, Sabatini S, Fianzzi-Argo A, Giartosio A, Rotilio G and Mondovi B (1983) Reaction of beef plasma and lentil seedlings Cu amine oxidases with phenylhydrazine. Biochem Biophys Res 1115: 841–852

    Google Scholar 

  26. Serafini-fracassini D (1991) Cell cycle dependent changes in plant polyamine metabolism. In: Slocun RA and Flores HE (eds) Biochemistry and Physiology of Polyamines in Plants, pp 159–173. CRC Press, Florida, USA

    Google Scholar 

  27. Sessa A, Desiderio MA and Perin A (1982) Diamine oxidase activities induction in regenerating rat liver. Biochem Biophys Acta 698: 11–14

    PubMed  Google Scholar 

  28. Smith TA (1980) Plant amines. In: Ben EA and Charlwood BU (eds) Encyclopedia of Plant Physiology, Vol. 8, pp 433–460. Springer Verlag, Berlin

    Google Scholar 

  29. Smith TA (1985) Di and polyamine oxidases of higher plants. Biochem Soc Trans 13: 319–322

    PubMed  Google Scholar 

  30. Smith MA and Davies PJ (1985) Separation and quantification of polyamines in plant tissue by high performance liquid chromatography of their dansyl derivatives. Plant Physiol 78: 89–91

    Google Scholar 

  31. Torrigiani P, Serafini-fracassini D and Fara A (1988) Diamine oxydase activity in different physiological stages of Helianthus tuberosus tuber. Plant Physiol 89: 69–73

    Google Scholar 

Download references

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Aribaud, M., Carré, M. & Martin-Tanguy, J. Polyamine metabolism and in vitro cell multiplication and differentiation in leaf explants of Chrysanthemum morifolium Ramat. Plant Growth Regul 15, 143–155 (1994). https://doi.org/10.1007/BF00024104

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