Skip to main content
Log in

Role of polyamines in adventitious shoot morphogenesis from cotyledons of cucumber in vitro

  • Published:
Plant Cell, Tissue and Organ Culture Aims and scope Submit manuscript

Abstract

The relationship between polyamines (PAs) metabolism and adventitious shoot morphogenesis from cotyledons of cucumber was investigated in vitro. The endogenous levels of free putrescine (Put) and spermidine (Spd) in the explants decreased sharply, whereas endogenous spermine (Spm) increased during adventitious shoot morphogenesis. The presence of 1–15 mM Put, 1–2 mM Spd, 0.05–1 mM Spm, 5–10 μM aminoethoxyvinylglycine (AVG) or 5 μM AVG together with 50 μM 1-aminocyclopropane-1-carboxylic acid (ACC) in the regeneration medium could promote adventitious shoot formation. Conversely, 1–5 mM D-arginine (D-Arg) or 0.01–0.1 mM methylglyoxal bis-guganylhydrazone (MGBG) inhibited regeneration; and 0.005–0.05 mM ACC displayed little or no evident effects. The explants growing on medium containing 5 μM AVG produced higher levels of free Put and Spm, and on medium containing 5 mM Put the explants responded similarly to the AVG-treated explants. However, the exogenous use of 1 mM D-Arg reduced the levels of Put, Spd and Spm, and 0.1 mM MGBG reduced the levels of free Spd and Spm. Moreover, although the explants cultured on medium containing Put and MGBG enhanced ethylene production, AVG and D-Arg inhibited ethylene biosynthesis. This study shows the PAs requirement for the formation of adventitious shoot from cotyledons of cucumber in vitro and the enhanced adventitious shoot morphogenesis may be associated with the elevated level of endogenous free Spm, albeit the promotive effect of PAs on adventitious shoot morphogenesis may not be related to ethylene metabolism.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

AVG:

aminoethoxyvinylglycine

D-Arg:

D-arginine

KT:

kinetin

NAA:

α-naphthaleneacetic acid

PAs:

polyamines

Put:

putrescine

SAM:

S-adenosylmethionine

Spd:

spermidine

Spm:

spermine

MGBG:

methylglyoxal-bis-guganylhydrazone

References

  • MM Altamura (1993) ArticleTitleCytological events induced by inhibition of polyamine biosynthesis in thin cell layers of tobacco Protoplasma 175 9–16 Occurrence Handle1:CAS:528:DyaK2cXhsFyqt7s%3D

    CAS  Google Scholar 

  • HP Bais GA Ravishankar (2002) ArticleTitleRole of polyamines in the ontogeny of plants and their biotechnological applications Plant Cell Tiss. Org. Cult. 69 1–34

    Google Scholar 

  • S Bajaj MV Rajam (1995) ArticleTitleEfficient plant regeneration from long-term callus cultures of rice by spermidine Plant Cell Rep. 14 717–720

    Google Scholar 

  • DR Bastola SC Minocha (1995) ArticleTitleIncreased putrescine biosynthesis through transfer of mouse ornithine cDNA in carrot promotes somatic embryogenesis Plant Physiol. 109 63–71

    Google Scholar 

  • D Burtin J Martin-Tanguy M Paynot M Carré M Rossin (1990) ArticleTitlePolyamines, hydroxycinnamoylputrescines, and root formation in leaf explants of tobacco cultivated in vitro. Effects of the suicide inhibitors of putrescine synthesis Plant Physiol. 93 1398–1404

    Google Scholar 

  • GL Chi WS Lin EE Justin (1994) ArticleTitleRole of polyamine onde novo shoot morphogenesis from cotyledons of Brassica campestris ssp. pekinensis (Lour) Olssonin vitro Plant Cell Rep. 13 323–329

    Google Scholar 

  • GL Chi EC Pua CJ Goh (1991) ArticleTitleRole of ethylene on de novo shoot regeneration from cotyledonary explants of Brassica campestris ssp. pekinenesis (Lour) Olsson in vitro. Plant Physiol. 96 178–183

    Google Scholar 

  • UH Cho KJ Kasha (1989) ArticleTitleEthylene production and embryogenesis from anther cultures of barley (Hordeum vulgares) Plant Cell Rep. 8 415–417

    Google Scholar 

  • HV Desai AR Metha (1985) ArticleTitleChange in polyamines levels during shoot formation and callus induction in cultured passiflora leaf discas J. Plant Physiol. 119 45–53

    Google Scholar 

  • A Feray A Hourmant M Penot (1994) ArticleTitlePolyamines and morphogenesis: Effects of methylglyoxal -bis-(guanylhydrazone) Bot. Acta 107 18–23

    Google Scholar 

  • AW Galston HE Flores (1991) Polyamines in plant morphogenesis RD Slocum HE Flores (Eds) Biochemistry and Physiology of Polyamines in Plants CRC Press Boca Raton 175–183

    Google Scholar 

  • TJ Huxter TA Thorpe DM Reid (1981) ArticleTitleShoot initiation in light- and-dark-grown tobacco callus: the role of ethylene Physiol. Plant. 53 319–326

    Google Scholar 

  • R Kaur-Sawhney AF Tiburcio AW Galston (1986) ArticleTitlePolyamine-mediated control of organogenesis in thin layer explants of tobacco Plant Physiol. 80 IssueID(suppl 37

    Google Scholar 

  • R Kaur-Sawhney AF Tiburcio AW Galston (1988) ArticleTitleSpermidine and flower bud differentiation in thin-layer explants of tobacco Planta 173 282–284

    Google Scholar 

  • A Kumar T Altabella MA Taylor AF Tiburcio (1997) ArticleTitleRecent advances in polyamine research Trends Plant Sci. 2 124–130

    Google Scholar 

  • VV Kuznetsov VY Rakitin NG Sadomov DV Dam LA Stetsenko NI Shevyakova (2002) ArticleTitleDo polyamines participate in the long-distance translocation of stress signals in plants? Rus. J. Plant Physiol. 49 120–130

    Google Scholar 

  • N Li B Parsons D Liu AK Mattoo (1992) ArticleTitleAccumulation of wound-inducible ACC synthase transcript in tomato fruit is inhibited by salicylic acid and polyamines Plant Mol. Biol. 18 477–487

    Google Scholar 

  • ZL Li DJ Burritt (2003) ArticleTitleChanges in endogenous polyamines during the formation of somatic embryos from isogenic lines of Dactylis glomerata L. with different regenerative capacities Plant Growth Regul. 40 65–74

    Google Scholar 

  • J Martin-Tanguy (1997) ArticleTitleConjugated polyamines and reproductive development: biochemical, molecular and physiological approaches Physiol. Plant 100 657–688

    Google Scholar 

  • J Martin-Tanguy (2001) ArticleTitleMetabolism and function of polyamines in plants: recent development (new approaches) Plant Growth Regul. 34 135–148

    Google Scholar 

  • ZC Ma RC Zang KM Chu (1991) ArticleTitleHigh-performance liquid chromatographic determination of polyamines in tomato callis Fenxi Huaxue (Analytical Chemistry) 19 1317–1319

    Google Scholar 

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

    Google Scholar 

  • EC Pua GL Chi (1993) ArticleTitleDe novo shoot morphogenesis and plant growth of mustard (Brassica juncea) in vitro in relation to ethylene Physiol. Plant 88 467–474

    Google Scholar 

  • KE Paterson-Robinson DO Adams (1987) ArticleTitleThe role of ethylene in the regeneration of Helianthus annuus (sunflower) plants form callus Physiol. Plant 71 151–156

    Google Scholar 

  • S Scaramagli S Biondi F Capitani P Gerola MM Altamura PT Torrigiani (1999) ArticleTitlePolyamine conjugate levels and ethylene biosynthesis: inverse relationship with vegetative bud formation in tobacco thin layers Physiol. Plant 105 367–376

    Google Scholar 

  • S Shweta PK Nagar (2003) ArticleTitleThe effect of polyamines on leaf senescence in two diverse rose species Plant Growth Regul. 39 155–160

    Google Scholar 

  • MJM Smulders A Kemp GWM Barendse AF Croes GJ Wullems (1990) ArticleTitleRole of ethylene in auxin-induced flower bud formation in tobacco explants Physiol. Plant 78 167–172

    Google Scholar 

  • S Tanimoto Y Matsubara N Ishioka (1994) ArticleTitleSignificance of spermidine in the initiation of adventitious buds in stem segments of Torenia Plant Cell Physiol. 35 1071–1077

    Google Scholar 

  • CE Tian RG Li H Guan (1994) ArticleTitleRelationship between polyamines and morphogenesis in cotyledons of Cucumis melon L cultured in vitro Acta Bot. Sin. 36 219–222

    Google Scholar 

  • AF Tiburcio R Kaur-Sawhney AW Galston (1988) ArticleTitlePolyamine biosynthesis during vegetative and floral bud differentiation in thin layer tobacco tissue cultures Plant Cell Physiol. 29 1241–1249

    Google Scholar 

  • FM Wang YL Xue (1998) ArticleTitleThe changes of polyamine content and polyamine oxidase activity during bulblets formation from bulb scales of Lilium davidii var. unnicolor in vitro Acta Phytophysiol. Sin. 14 350–354

    Google Scholar 

  • SF Yang NE Hoffman (1984) ArticleTitleEthylene bio-synthesis and its regulation in higher plants Annu. Rev. Plant Physiol. 35 155–189

    Google Scholar 

  • C Zhu HM Liang GW Zeng (1999) ArticleTitleEffects of cutting cotyledons on direct floral bud formation of excised cotyledonary explants and decapitated cucumbler seedlings J. Zhejiang Agric. Univ. 25 233–235

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Cheng Zhu.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zhu, C., Chen, Z. Role of polyamines in adventitious shoot morphogenesis from cotyledons of cucumber in vitro. Plant Cell Tiss Organ Cult 81, 45–53 (2005). https://doi.org/10.1007/s11240-004-2773-y

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11240-004-2773-y

Keywords

Navigation