Abstract
In higher plants, the main route for putrescine synthesis may be from arginine. Higher accumulation of putrescine under biotic and abiotic stress conditions is attributed at least in part to stress-inducible expression of arginine decarboxylase genes. Regulation of spermidine synthesis involves translational control of the S-adenosylmethionine decarboxylase mRNA, which is responsive to cellular polyamine levels. Genes encoding S-adenosylmethionine decarboxylase and spermine synthase are also responsive to environmental stimuli or show preferential expression in certain organs. Stress-inducible expression of these genes involves plant hormone signaling of abscisic acid (ABA) or methyl jasmonate (MeJA). Thermospermine synthase is widely distributed in the plant kingdom but has a unique role in the repression control of xylem differentiation in higher plants. Expression of the gene for thermospermine synthase is under negative feedback control by thermospermine. Putrescine, spermidine, and cadaverine are also essential precursors for alkaloid biosynthesis in some plant species. Polyamines occur in various aspects of plant growth as a conjugated form with cinnamic acids and proteins. Genes responsible for these conjugations have been increasingly identified.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Alcázar R, Cuevas JC, Patron M, Altabella T, Tiburcio AF (2006a) Abscisic acid modulates polyamine metabolism under water stress in Arabidopsis thaliana. Physiol Plant 128:448–455
Alcázar R, Marco F, Cuevas JC, Patron M, Ferrando A, Carrasco P, Tiburcio AF, Altabella T (2006b) Involvement of polyamines in plant response to abiotic stress. Biotechnol Lett 28:1867–1876
Alcázar R, Altabella T, Marco F, Bortolotti C, Reymond M, Koncz C, Carrasco P, Tiburcio AF (2010) Polyamines: molecules with regulatory functions in plant abiotic stress tolerance. Planta (Berl) 231:1237–1249
Antognoni F, Bagni N (2008) Bis(guanylhydrazones) negatively affect in vitro germination of kiwifruit pollen and alter the endogenous polyamine pool. Plant Biol 10:334–341
Armengaud P, Breitling R, Amtmann A (2004) The potassium-dependent transcriptome of Arabidopsis reveals a prominent role of jasmonic acid in nutrient signaling. Plant Physiol 136:2556–2576
Bae H, Kim SH, Kim MS, Sicher RC, Lary D, Strem MD, Natarajan S, Bailey BA (2008) The drought response of Theobroma cacao (cacao) and the regulation of genes involved in polyamine biosynthesis by drought and other stresses. Plant Physiol Biochem 46:174–188
Bagga S, Rochford J, Klaene Z, Kuehn GD, Phillips GC (1997) Putrescine aminopropyltransferase is responsible for biosynthesis of spermidine, spermine, and multiple uncommon polyamines in osmotic stress-tolerant alfalfa. Plant Physiol 114:445–454
Bagni N, Tassoni A (2001) Biosynthesis, oxidation and conjugation of aliphatic polyamines in higher plants. Amino Acids 20:301–317
Bagni N, Creus JA, Pistocchi R (1986) Distribution of cadaverine and lysine decarboxylase activity in Nicotiana glauca plants. J Plant Physiol 125:9–15
Baima S, Possenti M, Matteucci A, Wisman E, Altamura MM, Ruberti I, Morelli G (2001) The Arabidopsis ATHB-8 HD-zip protein acts as a differentiation-promoting transcription factor of the vascular meristems. Plant Physiol 126:643–655
Bassard JE, Ullmann P, Bernier F, Werck-Reichhart D (2010) Phenolamides: bridging polyamines to the phenolic metabolism. Phytochemistry 71:1808–1824
Belda-Palazón B, Ruiz L, Martà E, Tárraga S, Tiburcio AF, Culiáñez F, Farràs R, Carrasco P, Ferrando A (2012) Aminopropyltransferases involved in polyamine biosynthesis localize preferentially in the nucleus of plant cells. PLoS One 7:e46907
Biondi S, Fornalé S, Oksman-Caldentey KM, Eeva M, Agostani S, Bagni N (2000) Jasmonates induce over-accumulation of methyl putrescine and conjugated polyamines in Hyoscyamus muticus L. root cultures. Plant Cell Rep 19:691–697
Biondi S, Scaramagli S, Capitani F, Altamura MM, Torrigiani P (2001) Methyl jasmonate upregulates biosynthetic gene expression, oxidation and conjugation of polyamines, and inhibits shoot formation in tobacco thin layers. J Exp Bot 52:231–342
Brauc S, De Vooght E, Claeys M, Geuns JM, Höfte M, Angenon G (2012) Overexpression of arginase in Arabidopsis thaliana influences defence responses against Botrytis cinerea. Plant Biol 14(suppl 1):39–45
Brownfield DL, Todd CD, Deyholos MK (2008) Analysis of Arabidopsis arginase gene transcription patterns indicates specific biological functions for recently diverged paralogs. Plant Mol Biol 67:429–440
Bunsupa S, Katayama K, Ikeura E, Oikawa A, Toyooka K, Saito K, Yamazaki M (2012) Lysine decarboxylase catalyzes the first step of quinolizidine alkaloid biosynthesis and coevolved with alkaloid production in leguminosae. Plant Cell 24:1202–1216
Chattopadhyay MK, Tabor CW, Tabor H (2003) Spermidine but not spermine is essential for hypusine biosynthesis and growth in Saccharomyces cerevisiae: spermine is converted to spermidine in vivo by the FMS1-amine oxidase. Proc Natl Acad Sci USA 100:13869–13874
Clay NK, Nelson T (2005) Arabidopsis thickvein mutation affects vein thickness and organ vascularization, and resides in a provascular cell-specific spermine synthase involved in vein definition and in polar auxin transport. Plant Physiol 138:767–777
Cona A, Rea G, Angelini R, Federico R, Tavladoraki P (2006) Functions of amine oxidases in plant development and defence. Trends Plant Sci 11:80–88
Cuevas JC, López-Cobollo R, Alcázar R, Zarza X, Koncz C, Altabella T, Salinas J, Tiburcio AF, Ferrando A (2008) Putrescine is involved in Arabidopsis freezing tolerance and cold acclimation by regulating abscisic acid levels in response to low temperature. Plant Physiol 148:1094–1105
Cui X, Ge C, Wang R, Wang H, Chen W, Fu Z, Jiang X, Li J, Wang Y (2010) The BUD2 mutation affects plant architecture through altering cytokinin and auxin responses in Arabidopsis. Cell Res 20:576–586
Evans PT, Malmberg RL (1989) Do polyamines have roles in plant development? Annu Rev Plant Physiol Plant Mol Biol 40:235–269
Flores HE, Galston AW (1982) Polyamines and plant stress: activation of putrescine biosynthesis by osmotic shock. Science 217:1259–1261
Franceschetti M, Hanfrey C, Scaramagli S, Torrigiani P, Bagni N, Burtin D, Michael AJ (2001) Characterization of monocot and dicot plant S-adenosyl-l-methionine decarboxylase gene families including identification in the mRNA of a highly conserved pair of upstream overlapping open reading frames. Biochem J 353:403–409
Fuell C, Elliott KA, Hanfrey CC, Franceschetti M, Michael AJ (2010) Polyamine biosynthetic diversity in plants and algae. Plant Physiol Biochem 48:513–520
Galston AW, Sawhney RK (1990) Polyamines in plant physiology. Plant Physiol 94:406–410
Gamarnik A, Frydman RB (1991) Cadaverine, an essential diamine for the normal root development of germinating soybean (Glycine max) seeds. Plant Physiol 97:778–785
Ge C, Cui X, Wang Y, Hu Y, Fu Z, Zhang D, Cheng Z, Li J (2006) BUD2, encoding an S-adenosylmethionine decarboxylase, is required for Arabidopsis growth and development. Cell Res 16:446–456
Gentile A, Antognoni F, Iorio RA, Distefano G, Las Casas G, La Malfa S, Serafini-Fracassini D, Del Duca S (2012) Polyamines and transglutaminase activity are involved in compatible and self-incompatible pollination of Citrus grandis. Amino Acids 42:1025–1035
Grienenberger E, Besseau S, Geoffroy P, Debayle D, Heintz D, Lapierre C, Pollet B, Heitz T, Legrand M (2009) A BAHD acyltransferase is expressed in the tapetum of Arabidopsis anthers and is involved in the synthesis of hydroxycinnamoyl spermidines. Plant J 58:246–259
Hanfrey C, Sommer S, Mayer MJ, Burtin D, Michael AJ (2001) Arabidopsis polyamine biosynthesis: absence of ornithine decarboxylase and the mechanism of arginine decarboxylase activity. Plant J 27:551–560
Hanfrey C, Elliott KA, Franceschetti M, Mayer MJ, Illingworth C, Michael AJ (2005) A dual upstream open reading frame-based autoregulatory circuit controlling polyamine-responsive translation. J Biol Chem 280:39229–39237
Hanzawa Y, Takahashi T, Komeda Y (1997) ACL5: an Arabidopsis gene required for internodal elongation after flowering. Plant J 12:863–874
Hanzawa Y, Takahashi T, Michael AJ, Burtin D, Long D, Pineiro M, Coupland G, Komeda Y (2000) ACAULIS5, an Arabidopsis gene required for stem elongation, encodes a spermine synthase. EMBO J 19:4248–4256
Hanzawa Y, Imai A, Michael AJ, Komeda Y, Takahashi T (2002) Characterization of the spermidine synthase-related gene family in Arabidopsis thaliana. FEBS Lett 527:176–180
Hardtke CS, Berleth T (1998) The Arabidopsis gene MONOPTEROS encodes a transcription factor mediating embryo axis formation and vascular development. EMBO J 17:1405–1411
Hashimoto T, Tamaki K, Suzuki K, Yamada Y (1998) Molecular cloning of plant spermidine synthases. Plant Cell Physiol 39:73–79
Hill JR, Morris DR (1993) Cell-specific translational regulation of S-adenosylmethionine decarboxylase mRNA. Dependence on translation and coding capacity of the cis-acting upstream open reading frame. J Biol Chem 268:726–731
Hummel I, Bourdais G, Gouesbet G, Couee I, Malmberg RL, El Amrani A (2004) Differential gene expression of arginine decarboxylase ADC1 and ADC2 in Arabidopsis thaliana: characterization of transcriptional regulation during seed germination and seedling development. New Phytol 163:519–531
Illingworth C, Mayer MJ, Elliott K, Hanfrey C, Walton NJ, Michael AJ (2003) The diverse bacterial origins of the Arabidopsis polyamine biosynthetic pathway. FEBS Lett 549:26–30
Imai A, Akiyama T, Kato T, Sato S, Tabata S, Yamamoto KT, Takahashi T (2004a) Spermine is not essential for survival of Arabidopsis. FEBS Lett 556:148–152
Imai A, Matsuyama T, Hanzawa Y, Akiyama T, Tamaoki M, Saji H, Shirano Y, Kato T, Hayashi H, Shibata D, Tabata S, Komeda Y, Takahashi T (2004b) Spermidine synthase genes are essential for survival of Arabidopsis. Plant Physiol 135:1565–1573
Imai A, Hanzawa Y, Komura M, Yamamoto KT, Komeda Y, Takahashi T (2006) The dwarf phenotype of the Arabidopsis acl5 mutant is suppressed by a mutation in an upstream ORF of a bHLH gene. Development (Camb) 133:3575–3585
Imai A, Komura M, Kawano E, Kuwashiro Y, Takahashi T (2008) A semi-dominant mutation in the ribosomal protein L10 gene suppresses the dwarf phenotype of the acl5 mutant in Arabidopsis thaliana. Plant J 56:881–890
Janowitz T, Kneifel H, Piotrowski M (2003) Identification and characterization of plant agmatine iminohydrolase, the last missing link in polyamine biosynthesis of plants. FEBS Lett 544:258–261
Jiménez-Bremont JF, Ruiz OA, RodrÃguez-Kessler M (2007) Modulation of spermidine and spermine levels in maize seedlings subjected to long-term salt stress. Plant Physiol Biochem 45:812–821
Junker A, Fischer J, Sichhart Y, Brandt W, Dräger B (2013) Evolution of the key alkaloid enzyme putrescine N-methyltransferase from spermidine synthase. Front Plant Sci 4:260
Kakehi J, Kuwashiro Y, Niitsu M, Takahashi T (2008) Thermospermine is required for stem elongation in Arabidopsis thaliana. Plant Cell Physiol 49:1342–1349
Kakehi J, Kuwashiro Y, Motose H, Igarashi K, Takahashi T (2010) Norspermine substitutes for thermospermine in the control of stem elongation in Arabidopsis thaliana. FEBS Lett 584:3042–3046
Kaur H, Heinzel N, Schöttner M, Baldwin IT, Gális I (2010) R2R3-NaMYB8 regulates the accumulation of phenylpropanoid-polyamine conjugates, which are essential for local and systemic defense against insect herbivores in Nicotiana attenuata. Plant Physiol 152:1731–1747
Kaur-Sawhney R, Tiburcio AF, Galston AW (1988) Spermidine and flower-bud differentiation in thin-layer explants of tobacco. Planta (Berl) 173:282–284
Kim SH, Kim SH, Yoo SJ, Min KH, Nam SH, Cho BH, Yang KY (2013) Putrescine regulating by stress-responsive MAPK cascade contributes to bacterial pathogen defense in Arabidopsis. Biochem Biophys Res Commun 437:502–508
Knott JM (2009) Biosynthesis of long-chain polyamines by crenarchaeal polyamine synthases from Hyperthermus butylicus and Pyrobaculum aerophilum. FEBS Lett 583:3519–3524
Knott JM, Römer P, Sumper M (2007) Putative spermine synthases from Thalassiosira pseudonana and Arabidopsis thaliana synthesize thermospermine rather than spermine. FEBS Lett 581:3081–3086
Koc EC, Bagga S, Songstad DD, Betz SR, Kuehn GD, Phillips GC (1998) Occurrence of uncommon polyamines in cultured tissues of maize. In Vitro Cell Dev Biol Plant 34:252–255
Kovács Z, Simon-Sarkadi L, Szucs A, Kocsy G (2010) Differential effects of cold, osmotic stress and abscisic acid on polyamine accumulation in wheat. Amino Acids 38:623–631
Kumar A, Altabella T, Taylor M, Tiburcio AF (1997) Recent advances in polyamine research. Trends Plant Sci 2:124–130
Kusano T, Berberich T, Tateda C, Takahashi Y (2008) Polyamines: essential factors for growth and survival. Planta (Berl) 228:367–381
Lin PPC, Egli DB, Li GM, Meckel L (1984) Polyamine titer in the embryonic axis and cotyledons of Glycine max (L.) during seed growth and maturation. Plant Physiol 76:366–371
Luo J, Fuell C, Parr A, Hill L, Bailey P, Elliott K, Fairhurst SA, Martin C, Michael AJ (2009) A novel polyamine acyltransferase responsible for the accumulation of spermidine conjugates in Arabidopsis seed. Plant Cell 21:318–333
Martin-Tanguy J (1985) The occurrence and possible function of hydroxycinnamoyl acid-amides in plants. Plant Growth Regul 3:381–399
Mattoo AK, Minocha SC, Minocha R, Handa AK (2010) Polyamines and cellular metabolism in plants: transgenic approaches reveal different responses to diamine putrescine versus higher polyamines spermidine and spermine. Amino Acids 38:405–413
Milhinhos A, Prestele J, Bollhöner B, Matos A, Vera-Sirera F, Rambla JL, Ljung K, Carbonell J, Blázquez MA, Tuominen H, Miguel CM (2013) Thermospermine levels are controlled by an auxin-dependent feedback loop mechanism in Populus xylem. Plant J 75:685–698
Minguet EG, Vera-Sirera F, Marina A, Carbonell J, Blázquez MA (2008) Evolutionary diversification in polyamine biosynthesis. Mol Biol Evol 25:2119–2128
Muñiz L, Minguet EG, Singh SK, Pesquet E, Vera-Sirera F, Moreau-Courtois CL, Carbonell J, Blázquez MA, Tuominen H (2008) ACAULIS5 controls Arabidopsis xylem specification through the prevention of premature cell death. Development (Camb) 135:2573–2582
Naka Y, Watanabe K, Sagor GH, Niitsu M, Pillai MA, Kusano T, Takahashi Y (2010) Quantitative analysis of plant polyamines including thermospermine during growth and salinity stress. Plant Physiol Biochem 48:527–533
Nathanson JA, Hunnicutt EJ, Kantham L, Scavone C (1993) Cocaine as a naturally occurring insecticide. Proc Natl Acad Sci USA 90:9645–9648
Ober D, Hartmann T (1999) Homospermidine synthase, the first pathway-specific enzyme of pyrrolizidine alkaloid biosynthesis, evolved from deoxyhypusine synthase. Proc Natl Acad Sci USA 96:14777–14782
Ober D, Gibas L, Witte L, Hartmann T (2003) Evidence for general occurrence of homospermidine in plants and its supposed origin as by-product of deoxyhypusine synthase. Phytochemistry 62:339–344
Onkokesung N, Gaquerel E, Kotkar H, Kaur H, Baldwin IT, Galis I (2012) MYB8 controls inducible phenolamide levels by activating three novel hydroxycinnamoyl-coenzyme A: polyamine transferases in Nicotiana attenuata. Plant Physiol 158:389–407
Oshima T (2007) Unique polyamines produced by an extreme thermophile, Thermus thermophilus. Amino Acids 33:367–372
Pagnussat GC, Yu HJ, Ngo QA, Rajani S, Mayalagu S, Johnson CS, Capron A, Xie LF, Ye D, Sundaresan V (2005) Genetic and molecular identification of genes required for female gametophyte development and function in Arabidopsis. Development (Camb) 132:603–614
Panicot M, Minguet EG, Ferrando A, Alcázar R, Blázquez MA, Carbonell J, Altabella T, Koncz C, Tiburcio AF (2002) A polyamine metabolon involving aminopropyl transferases complexes in Arabidopsis. Plant Cell 14:2539–2551
Pegg AE, Michael AJ (2010) Spermine synthase. Cell Mol Life Sci 67:113–121
Peremarti A, Bassie L, Yuan D, Pelacho A, Christou P, Capell T (2010) Transcriptional regulation of the rice arginine decarboxylase (Adc1) and S-adenosylmethionine decarboxylase (Samdc) genes by methyl jasmonate. Plant Physiol Biochem 48:553–559
Pérez-Amador MA, Leon J, Green PJ, Carbonell J (2002) Induction of the arginine decarboxylase ADC2 gene provides evidence for the involvement of polyamines in the wound response in Arabidopsis. Plant Physiol 130:1454–1463
Piotrowski M, Janowitz T, Kneifel H (2003) Plant C-N hydrolases and the identification of a plant N-carbamoylputrescine amidohydrolase involved in polyamine biosynthesis. J Biol Chem 278:1708–1712
Rambla JL, Vera-Sirera F, Blázquez MA, Carbonell J, Granell A (2010) Quantitation of biogenic tetramines in Arabidopsis thaliana. Anal Biochem 397:208–211
Reimann A, Nurhayati N, Backenköhler A, Ober D (2004) Repeated evolution of the pyrrolizidine alkaloid-mediated defense system in separate angiosperm lineages. Plant Cell 16:2772–2784
Rodriguez-Garay B, Phillips GC, Kuehn GD (1989) Detection of norspermidine and norspermine in Medicago sativa L. (alfalfa). Plant Physiol 89:525–529
RodrÃguez-Kessler M, Jiménez-Bremont JF (2008) Zmspds2 maize gene: coding a spermine synthase? Plant Signal Behav 3:551–553
RodrÃguez-Kessler M, Delgado-Sánchez P, RodrÃguez-Kessler GT, Moriguchi T, Jiménez-Bremont JF (2010) Genomic organization of plant aminopropyl transferases. Plant Physiol Biochem 48:574–590
Ruan H, Shantz LM, Pegg AE, Morris DR (1996) The upstream open reading frame of the mRNA encoding S-adenosylmethionine decarboxylase is a polyamine-responsive translational control element. J Biol Chem 271:29576–29582
Sagor GH, Berberich T, Takahashi Y, Niitsu M, Kusano T (2013) The polyamine spermine protects Arabidopsis from heat stress-induced damage by increasing expression of heat shock-related genes. Transgenic Res 22:595–605
Sauter M, Moffatt B, Saechao MC, Hell R, Wirtz M (2013) Methionine salvage and S-adenosylmethionine: essential links between sulfur, ethylene and polyamine biosynthesis. Biochem J 451:145–154
Scaramagli S, Biondi S, Torrigiani P (1999) Methylglyoxal (bis-guanylhydrazone) inhibition of organogenesis is not due to S-adenosylmethionine decarboxylase inhibition/polyamine depletion in tobacco thin layers. Physiol Plant 107:353–360
Scoccianti V, Iacobucci M, Speranza A, Antognoni F (2013) Over-accumulation of putrescine induced by cyclohexylamine interferes with chromium accumulation and partially restores pollen tube growth in Actinidia deliciosa. Plant Physiol Biochem 70:424–432
Serafini-Fracassini D, Del Duca S (2008) Transglutaminases: widespread cross-linking enzymes in plants. Ann Bot 102:145–152
Serafini-Fracassini D, Di Sandro A, Del Duca S (2010) Spermine delays leaf senescence in Lactuca sativa and prevents the decay of chloroplast photosystems. Plant Physiol Biochem 48:602–611
Shao L, Majumdar R, Minocha SC (2012) Profiling the aminopropyltransferases in plants: their structure, expression and manipulation. Amino Acids 42:813–830
Shi H, Ye T, Chen F, Cheng Z, Wang Y, Yang P, Zhang Y, Chan Z (2013) Manipulation of arginase expression modulates abiotic stress tolerance in Arabidopsis: effect on arginine metabolism and ROS accumulation. J Exp Bot 64:1367–1379
Slocum RD, Flores HE (eds) (1991) Biochemistry and physiology of polyamines in plants. CRC Press, Boca Raton
Smith TA (1990) Plant polyamines: metabolism and function. In: Flores HE, Arteca RN, Shannon JC (eds) Polyamines and ethylene: biochemistry, physiology, and interactions. American Society of Plant Physiologists, Rockville, pp 1–23
Song J, Nada K, Tachibana S (2001) The early increase of S-adenosylmethionine decarboxylase activity is essential for the normal germination and tube growth in tomato (Lycopersicon esculentum Mill.) Pollen. Plant Sci 161:507–515
Soyka S, Heyer AG (1999) Arabidopsis knockout mutation of ADC2 gene reveals inducibility by osmotic stress. FEBS Lett 458:219–223
Stes E, Biondi S, Holsters M, Vereecke D (2011) Bacterial and plant signal integration via D3-type cyclins enhances symptom development in the Arabidopsis–Rhodococcus fascians interaction. Plant Physiol 156:712–725
Takahashi T, Kakehi J (2010) Polyamines: ubiquitous polycations with unique roles in growth and stress responses. Ann Bot 105:1–6
Takano A, Kakehi J, Takahashi T (2012) Thermospermine is not a minor polyamine in the plant kingdom. Plant Cell Physiol 53:606–616
Thu-Hang P, Bassie L, Safwat G, Trung-Nghia P, Christou P, Capell T (2002) Expression of a heterologous S-adenosylmethionine decarboxylase cDNA in plants demonstrates that changes in S-adenosyl-l-methionine decarboxylase activity determine levels of the higher polyamines spermidine and spermine. Plant Physiol 129:1744–1754
Tong W, Yoshimoto K, Kakehi JI, Motose H, Niitsu M, Takahashi T (2014) Thermospermine modulates expression of auxin-related genes in Arabidopsis. Front Plant Sci 5:94
Torrigiani P, Scoccianti V (1995) Regulation of cadaverine and putrescine levels in different organs of chick-pea seed and seedlings during germination. Physiol Plant 93:512–518
Urano K, Yoshiba Y, Nanjo T, Igarashi Y, Seki M, Sekiguchi F, Yamaguchi-Shinozaki K, Shinozaki K (2003) Characterization of Arabidopsis genes involved in biosynthesis of polyamines in abiotic stress responses and developmental stages. Plant Cell Environ 26:1917–1926
Urano K, Yoshiba Y, Nanjo T, Ito T, Yamaguchi-Shinozaki K, Shinozaki K (2004) Arabidopsis stress-inducible gene for arginine decarboxylase AtADC2 is required for accumulation of putrescine in salt tolerance. Biochem Biophys Res Commun 313:369–375
Urano K, Hobo T, Shinozaki K (2005) Arabidopsis ADC genes involved in polyamine biosynthesis are essential for seed development. FEBS Lett 579:1557–1564
Vision TJ, Brown DG, Tanksley SD (2000) The origins of genomic duplications in Arabidopsis. Science 290:2114–2117
Waduwara-Jayabahu I, Oppermann Y, Wirtz M, Hull ZT, Schoor S, Plotnikov AN, Hell R, Sauter M, Moffatt BA (2012) Recycling of methylthioadenosine is essential for normal vascular development and reproduction in Arabidopsis. Plant Physiol 158:1728–1744
Xiong YC, Xing GM, Li FM, Wang SM, Fan XW, Li ZX, Wang YF (2006) Abscisic acid promotes accumulation of toxin ODAP in relation to free spermine level in grass pea seedlings (Lathyrus sativus L.). Plant Physiol Biochem 44:161–169
Yamaguchi K, Takahashi Y, Berberich T, Imai A, Takahashi T, Michael AJ, Kusano T (2007) A protective role for the polyamine spermine against drought stress in Arabidopsis. Biochem Biophys Res Commun 352:486–490
Yoshimoto K, Noutoshi Y, Hayashi K, Shirasu K, Takahashi T, Motose H (2012a) A chemical biology approach reveals an opposite action between thermospermine and auxin in xylem development in Arabidopsis thaliana. Plant Cell Physiol 53:635–645
Yoshimoto K, Noutoshi Y, Hayashi K, Shirasu K, Takahashi T, Motose H (2012b) Thermospermine suppresses auxin-inducible xylem differentiation in Arabidopsis thaliana. Plant Signal Behav 7:937–939
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2015 Springer Japan
About this chapter
Cite this chapter
Takahashi, T., Tong, W. (2015). Regulation and Diversity of Polyamine Biosynthesis in Plants. In: Kusano, T., Suzuki, H. (eds) Polyamines. Springer, Tokyo. https://doi.org/10.1007/978-4-431-55212-3_3
Download citation
DOI: https://doi.org/10.1007/978-4-431-55212-3_3
Published:
Publisher Name: Springer, Tokyo
Print ISBN: 978-4-431-55211-6
Online ISBN: 978-4-431-55212-3
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)