Abstract
The endogenous levels of polyamines (PAs) in leaf-base explants isolated from plants of two isogenic lines of Dactylis glomerata L., differing in their competence for somatic embryogenesis, were compared. Leaf-bases isolated from plants with a high level of competence for somatic embryogenesis (HEC) contained four times the level of polyamines compared to those isolated from plants with a low level of competence for somatic embryogenesis (LEC). When the levels of individual polyamines in the HEC and LEC lines were compared, leaf-bases from plants of the HEC line had much lower PUT/SPD ratios than those from the LEC line. When changes in the levels of PAs were monitored during the first 28 d of culture, on a medium which promotes initiation of somatic embryogenesis, leaf-base cultures from plants of the HEC line showed a 50% increase in the levels of PAs during the first 7 d of culture, after which time levels began to decline. By day 21, levels had dropped below those found in freshly isolated leaf bases. While PUT and SPM levels increased by about 30%, the greatest increase was shown by SPD, which increased by more than 100% during the first 7 d of culture, before declining. In contrast much smaller changes in PA levels were found when leaf-bases from plants of the LEC line were cultured.
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Altamura M.M., Torrigiani P., Falasca G., Rossini P. and Bagni N. 1993. Morpho-funcional gradients in superficial and deep tissues along tobacco stem-polyamine levels, biosynthesis and oxidation, and organogenesis in vitro. J. Plant Physiol. 142: 543–551.
Andersen S.E., Bastola D.R. and Minocha S.C. 1998. Metabolism of polyamines in transgenic cells of carrot expressing a mouse ornithine decarboxylase cDNA. Plant Physiol. 116: 299–307.
Bajaj S. and Rajam M.V. 1995. Efficient plant-regeneration from long-term callus-cultures of rice by spermidine. Plant Cell Rep. 14: 717–720.
Bajaj S. and Rajam M.V. 1996. Polyamine accumulation and near loss of morphogenesis in long-term callus cultures of rice-Restoration of plant regeneration by manipulation of cellular polyamine levels. Plant Physiol. 112: 1343–1348.
Bastola D.R. and Minocha S.C. 1995. Increased putrescine biosynthesis through transfer of mouse ornithine decarboxylase cDNA in carrot promotes somatic embryogenesis. Plant Physiol. 109: 63–71.
Bonneau L., Berangernovat N., Monin J. and Martintanguy J. 1995. Stimulation of root and somatic embryo production in Euonymus europaeus L. by an Inhibitor of Polyamine Biosynthesis. Plant Growth Regul. 16: 5–10.
Conger B.V. and Hanning G.E. 1991. Registration of embryogen-p orchardgrass germplasm with a high-capacity for somatic embryogenesis from in vitro cultures. Crop Sci. 31: 855.
Cvikrova M., Binarova P., Cenklova V., Eder J. and Machackova I. 1999. Reinitiation of cell division and polyamine and aromatic monoamine levels in alfalfa explants during the induction of somatic embryogenesis. Physiol. Plant. 105: 330–337.
Feirer R.P., Mignon G. and Litvay J.D. 1984. Arginine decarboxylase and polyamines required for embryogenesis in the wild carrot. Science 223: 1433–1435.
Feirer R.P., Wann S.R. and Einspahr D.W. 1985. The effects of spermidine synthesis inhibitors on in vitro plant development. Plant Growth Regul. 3: 319–327.
Galston A.W. and Flores H.E. 1991. Polyamines and Plant Morphogenesis. In: Slocum R.D. and Flores H.E. (eds), Biochemistry and Physiology of Polyamines in Plants. CRC Press, Boca Raton, FL, pp. 175–186.
Galston A.W. and Sawhney R.K. 1990. Polyamines in Plant Physiology. Plant Physiol. 94: 406–410.
Grimes H.D., Slocum R.D. and Boss W.F. 1986. a-Difluoromethylarginine treatment inhibits protoplast fusion in fusogenic wild carrot protoplasts. Biochim. Biophys. Acta 886: 130–134.
Hadrami I. and D'Auzac J. 1992. Effects of polyamine biosynthetic inhibitors on somatic embryogenesis and cellular polyamines in Hevea brasiliensis. J. Plant Physiol. 140: 33–36.
Hanning G.E. and Conger B.V. 1986. Factors influencing somatic embryogenesis from cultured leaf segments of Dactylis glomerata L. J. Plant Physiol. 123: 23–29.
Huang X.L., Li X.J., Li Y. and Huang L.Z. 2001. The effect of AOA on ethylene and polyamine metabolism during early phases of somatic embryogenesis in Medicago sativa. Physiol. Plant. 113: 424–429.
Kaur-Sawhney R., Shekhawat N.S. and Galston A.W. 1988. Polyamine levels as related to growth, differentiation and senescence in protoplast-derived cultures of Vigna aconitifolia and Avena sativa. Plant Growth Regul. 3: 329–337.
Kevers C., Le Gal N., Monteiro M., Dommes J. and Gaspar T.H. 2000. Somatic embryogenesis of Panax ginseng in liquid cultures: a role for polyamines and their metabolic pathways. Plant Growth Regul. 31: 209–214.
Kong L., Attree S.M. and Fowke L.C. 1998. Effects of polyethylene glycol and methylglyoxal bis(guanylhydrazone) on endogenous polyamine levels and somatic embryo maturation in white spruce (Picea glauca). Plant Sci. 133: 211–220.
Kumar A., Altabella T., Taylor M.A. and Tiburcio A.F. 1997. Recent advances in polyamine research. Trends Plant Sci. 2: 124–130.
Minocha R., Smith D.R., Reeves C., Steele K.D. and Minocha S.C. 1999. Polyamine levels during the development of zygotic and somatic embryos of Pinus radiata. Physiol. Plant. 105: 155–164.
Minocha S.C. and Minocha R. 1995. Role of polyamines in somatic embryogenesis. In: Bajaj Y.P.S. (ed.), Somatic Embryogenesis and Synthetic Seed I. Springer-Verlag, Berlin, pp. 53–70.
Minocha S.C., Papa N.S., Khan A.J. and Samuelsen A.I. 1991. Polyamines and somatic embryogenesis in carrot. 3. Effects of methylglyoxal bis(guanylhydrazone). Plant Cell Physiol. 32: 395–402.
Montague M.J., Armstrong T.A. and Jaworski E.G. 1979. Polyamine metabolism in embryogenic cells of Daucus carota II. Changes in arginine decarboxylase activity. Plant Physiol. 63: 341–345.
Monteiro M., Kevers C., Dommes J. and Gaspar T.H. 2002. A specific role for spermidine in the initiation phase of somatic embryogenesis in Panax ginseng CA Meyer. Plant Cell Tissue. Organ. Cult. 68: 225–232.
Nabha S., Lamblin F., Gillet F., Laurain D., Fliniaux M., David A. et al. 1999. Polyamine content and somatic embryogenesis in Papaver somniferum cells transformed with sam-1 gene. J. Plant Physiol. 154: 729–734.
Santanen A. and Simola L.K. 1992. Changes in polyamine metabolism during somatic embryogenesis in Picea abies. J. Plant Physiol. 147: 145–153.
Schenk R.U. and Hildebrandt A.C. 1972. Medium and techniques for induction and growth of monocotyledonous and dicotyledonous plant cell cultures. Can. J. Bot. 50: 199–204.
Sharma P. and Rajam M.V. 1995. Spatial and temporal changes in endogenous polyamine levels associated with somatic embryogenesis from different hypocotyl segments of eggplant (Solanum-Melongena L). J. Plant Physiol. 146: 658–664.
Sharma P. and Rajam M.V. 1995. Genotype, explant and position effects on organogenesis and somatic embryogenesis in eggplant (Solanum melongena L.). J. Exp. Bot. 46: 135–141.
Shoeb F., Yadav J.S., Bajaj S. and Rajam M.V. 2001. Polyamines as biomarkers for plant regeneration capacity: improvement of regeneration by modulation of polyamine metabolism in different genotypes of indica rice. Plant Sci. 160: 1229–1235.
Smith T.A. 1985. Polyamines. Annu. Rev. Plant Physiol. 36: 117–143.
Smith T.A. 1991. Chromatographic methods for the identification and quantitation of polyamines. In: Slocum R.D. and Flores H.E. (eds), Biochemistry and Physiology of Polyamines in Plants. CRC Press, London, pp. 229–242.
Tiburcio A.F., Campos J.L., Figueras X. and Besford R.T. 1993. Recent advances in the understanding of polyamine functions during plant development. Plant Growth Regul. 12: 331–340.
Tiburcio A.F., Kaur-Sawhney R., Ingersoll R.B. and Galston A.W. 1985. Correlation between polyamines and pyrrolidine alkaloids in developing tobacco callus. Plant Physiol. 78: 323–326.
Torrigiani P., Altamura M.M., Capitani F., Serafini-Fracassini D. and Bagni N. 1989. De novo root-formation in thin cell-layers of tobacco-changes in free and bound polyamines. Physiol. Plant. 77: 294–301.
Torrigiani P., Altamura M.M., Pasqua G., Monacelli B., Serafini-Fracassini D. and Bagni N. 1987. Free and conjugated polyamines during de novo floral and vegetative bud formation in thin-layers of tobacco. Physiol. Plant. 70: 453–460.
Walden R., Cordeiro A. and Tiburcio A.F. 1997. Polyamines: Small molecules triggering pathways in plant growth and development. Plant Physiol. 113: 1009–1013.
Yadav J.S. and Rajam M.V. 1997. Spatial distribution of free and conjugated polyamines in leaves of Solanum melongena L. associated with differential morphogenetic capacity: efficient somatic embryogenesis with putrescine. J. Exp. Bot. 48: 1537–1545.
Yadav J.S. and Rajam M.V. 1998. Temporal regulation of somatic embryogenesis by adjusting cellular polyamine content in eggplant. Plant Physiol. 116: 617–625.
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Li, Z., Burritt, D.J. Changes in endogenous polyamines during the formation of somatic embryos from isogenic lines of Dactylis glomerata L. with different regenerative capacities. Plant Growth Regulation 40, 65–74 (2003). https://doi.org/10.1023/A:1023028713114
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DOI: https://doi.org/10.1023/A:1023028713114