Polyamine conjugate levels and ethylene biosynthesis: inverse relationship with vegetative bud formation in tobacco thin layers

The effects of two inhibitors of polyamine (spermidine and spermine) biosynthesis, cyclohexylamine (CHA; 5 and 10 mM) and methylglyoxal(bis-guanylhydrazone) (MGBG; 0.1, 0.5 and 1 mM), on the organogenic response in vegetative bud-forming tobacco (Nicotiana tabacum L. cv. Samsun) thin layer explants were evaluated micro- and macroscopically at different times during culture. The final number of buds formed and the percentage of organogenic explants was significantly reduced by both inhibitors, but much more so by MGBG than CHA. This inhibitory effect was already evident in MGBG-treated explants on day 5, in terms of the number of meristemoids per explant. On the contrary, in the presence of CHA, the number of meristemoids on day 5 was higher than that in the controls. Between days 9 and 13, meristemoid formation slowed down considerably in inhibitor-treated explants compared with controls. On day 13, the number of bud primordia was similar in control and CHA-treated explants, but significantly lower in MGBG-treated explants. This inhibitor also induced peculiar cytohistological events, such as a reduced formation of oval-shaped cell aggregates on the explant surface and more frequent cases of nucleolar extrusion, while CHA led to the appearance of hypertrophic epidermal cells; callus formation at the basal end of the explant and xylogenesis were also affected by the inhibitors. Ethylene biosynthesis, measured as [ C]methionine incorporation, was stimulated 2- (day 2) to 3-fold (15 h) by 0.5 mM MGBG, whereas CHA (10 mM) had little effect and aminoethoxyvinylglycine (AVG; 0.1 μM), an ethylene synthesis inhibitor, was strongly inhibitory. In control explants, the incorporation of labelled methionine into ethylene and spermidine followed an inverse trend up to day 8. In these explants, free putrescine increased 32-fold and spermidine increased about 10-fold between days 0 and 8. Trichloroacetic acid (TCA)-soluble conjugated putrescine also accumulated dramatically during culture. While CHA provoked a decline in spermidine levels, MGBG caused an unexpected increase in free spermidine and spermine titres; however, its most conspicuous effect was on the further enhancement of putrescine conjugate accumulation, while CHA and AVG had the opposite effect. Results are discussed in view of establishing a putative link between MGBG-enhanced ethylene synthesis, increased conjugate titres and inhibition of meristemoid formation.

[1]  G. Berta,et al.  The plant cell wall is altered by inhibition of polyamine biosynthesis , 1997 .

[2]  A. Michael,et al.  Overexpression of arginine decarboxylase in transgenic plants. , 1997, The Biochemical journal.

[3]  J. Martin-Tanguy Conjugated polyamines and reproductive development: Biochemical, molecular and physiological approaches , 1997 .

[4]  M. Taylor,et al.  Potato plants expressing antisense and sense S‐adenosylmethionine decarboxylase (SAMDC) transgenes show altered levels of polyamines and ethylene: antisense plants display abnormal phenotypes , 1996 .

[5]  H. Mett,et al.  Stable Amplification of the S-Adenosylmethionine Decarboxylase Gene in Chinese Hamster Ovary Cells (*) , 1995, The Journal of Biological Chemistry.

[6]  P. Torrigiani,et al.  Morphogenesis in cultured thin layers and pith explants of tobacco. I. Effect of putrescine on cell size, xylogenesis and meristemoid organization , 1995 .

[7]  Ky Young Park,et al.  Effects of ethylene and auxin on polyamine levels in suspension‐cultured tobacco cells , 1994 .

[8]  M. Penot,et al.  Polyamines and Morphogenesis ‐ Effects of Methylglyoxal‐bis(guanylhydrazone) , 1994 .

[9]  J. Roustan,et al.  Role of ethylene on induction and expression of carrot somatic embryogenesis: relationship with polyamine metabolism , 1994 .

[10]  P. Torrigiani,et al.  Regulation of rhizogenesis by polyamines in tobacco thin layers , 1993 .

[11]  S. Biondi,et al.  Polyamines and Morphogenesis in Normal and Transgenic Plant Cultures , 1993 .

[12]  J. Roustan,et al.  Influence of ethylene on the incorporation of 3,4-[14C] methionine into polyamines in Daucus carota cells during somatic embryogenesis , 1992 .

[13]  P. Torrigiani,et al.  De Novo Root Formation in Tobacco Thin Layers is Affected by Inhibition of Polyamine Biosynthesis , 1991 .

[14]  B. Feuerstein,et al.  Implications and concepts of polyamine‐nucleic acid interactions , 1991, Journal of cellular biochemistry.

[15]  A. J. Khan,et al.  Polyamines and Somatic Embryogenesis in Carrot. III. Effects of Methylglyoxal bis(guanylhydrazone) , 1991 .

[16]  J. Negrel,et al.  Separation of putrescine and spermidine hydroxycinnamoyl transferases extracted from tobacco callus , 1991 .

[17]  M. Wyss-Benz,et al.  Feruloylputrescine and Caffeoylputrescine Are Not Involved in Growth and Floral Bud Formation of Stem Explants from Nicotiana tabacum L. var Xanthi nc. , 1990, Plant physiology.

[18]  S. Biondi,et al.  Polyamines and ethylene in relation to adventitious root formation in Prunus avium shoot cultures , 1990 .

[19]  M. Smulders,et al.  Role of ethylene in auxin-induced flower bud formation in tobacco explants , 1990 .

[20]  G. Pasqua,et al.  Free and conjugated polyamines during de novo floral and vegetative bud formation in thin cell layers of tobacco , 1987 .

[21]  J. McIndoo,et al.  Regulation of polyamine biosynthesis in tobacco. Effects of inhibitors and exogenous polyamines on arginine decarboxylase, ornithine decarboxylase, and S-adenosylmethionine decarboxylase. , 1986, The Journal of biological chemistry.

[22]  A. Goldlust,et al.  Control by ethylene of arginine decarboxylase activity in pea seedlings and its implication for hormonal regulation of plant growth. , 1985, Plant physiology.

[23]  A. Goldlust,et al.  Influence of Ethylene on S-adenosylmethionine Decarboxylase Activity in Etiolated Pea Seedlings , 1985 .

[24]  F. D'amato,et al.  Cytogenetics of plant cell and tissue cultures and their regenerates , 1985 .

[25]  J. McIndoo,et al.  Abnormal floral development of a tobacco mutant with elevated polyamine levels , 1983, Nature.

[26]  B. C. Jarvis,et al.  Involvement of Polyamines with Adventitious Root Development in Stem Cuttings of Mung Bean , 1983 .

[27]  P. Sunkara,et al.  Role of polyamines during chromosome condensation of mammalian cells. , 1983, Cell biology international reports.

[28]  A. Mattoo,et al.  Inhibition of ethylene biosynthesis by aminoethoxyvinylglycine and by polyamines shunts label from 3,4-[C]methionine into spermidine in aged orange peel discs. , 1982, Plant physiology.

[29]  E. Hölttä,et al.  Polyamine starvation causes disappearance of actin filaments and microtubules in polyamine-auxotrophic CHO cells , 1981, Nature.

[30]  E. Hirasawa,et al.  Purification and properties of diamine oxidase from pea epicotyls , 1981 .

[31]  F. Skoog,et al.  A revised medium for rapid growth and bio assays with tobacco tissue cultures , 1962 .