Abstract
Polyamines (PAs) are hormonal compounds and growth regulators, with low molecular weight, aliphatic nature, and polycationic character at physiological pH, present in different types of organisms and particularly in plants, where they are involved in the regulation of various physiological processes related to growth and development as well as in responses to abiotic and biotic stresses. One of the strategies of plants to cope with salt stress is the accumulation of PAs since they have the capacity to stabilize macromolecules such as DNA, RNA, proteins and phospholipids, as well as free radical scavenging activity. Alterations of PAs metabolism constitute a strategy to increment salinity tolerance in plants, not only by the direct implication of PAs but also by the link between PAs and the synthesis of proline and γ-aminobutiric acid (GABA), key osmoprotectants in salt stress responses. Legumes have the capacity to establish symbiotic interactions with soil nitrogen-fixing bacteria known as rhizobia that provide this nutrient to the plant. The symbiosis induces the formation of root nodules where the nitrogen fixation occurs; however, this process is extremely sensitive to salinity. Polyamines metabolism has an active role in the legume-rhizobia symbiosis, and in addition, PAs metabolism in root nodules of legumes is the result of the plant and rhizobia interaction with nodule-specific PAs involved in mechanisms of tolerance to salinity in the symbiosis. Therefore, the gain of knowledge in the alterations of the metabolism of PAs in the legume-rhizobia symbiosis and its interaction with other molecules involved in salt stress tolerance is of great interest to improve the ability to fix atmospheric nitrogen of legumes under salinity.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Similar content being viewed by others
References
Abdel-Wahab AM, Shabeb MSA, Younis MAM (2002) Studies on the effect of salinity, drought stress and soil type on nodule activities of Lablab purpureus (L.) sweet (Kashrangeeg). J Arid Environ 51(4):587–602. https://doi.org/10.1006/jare.2002.0974
Abiala MA, Abdelrahman M, Burritt DJ, Tran L-SP (2018) Salt stress tolerance mechanisms and potential applications of legumes for sustainable reclamation of salt-degraded soils. Land Degrad Dev 29(10):3812–3822. https://doi.org/10.1002/ldr.3095
Andrio E, Marino D, Marmeys A, de Segonzac MD, Damiani I, Genre A, Huguet S, Frendo P, Puppo A, Pauly N (2013) Hydrogen peroxide-regulated genes in the Medicago truncatula-Sinorhizobium meliloti symbiosis. New Phytol 198(1):190–202. https://doi.org/10.1111/nph.12120
Aranjuelo I, Arrese-Igor C, Molero G (2014) Nodule performance within a changing environmental context. J Plant Physiol 171(12):1076–1090. https://doi.org/10.1016/j.jplph.2014.04.002
Bajguz A (2011) Brassinosteroids - Occurence and chemical structures in plants. In: Brassinosteroids: a class of plant hormone, pp 1–27. https://doi.org/10.1007/978-94-007-0189-2_1
Baniasadi F, Saffari VR, Maghsoudi Moud AA (2018) Physiological and growth responses of Calendula officinalis L. plants to the interaction effects of polyamines and salt stress. Sci Hortic 234:312–317. https://doi.org/10.1016/j.scienta.2018.02.069
Becana M, Matamoros MA, Udvardi M, Dalton DA (2010) Recent insights into antioxidant defenses of legume root nodules. New Phytol 188(4):960–976. https://doi.org/10.1111/j.1469-8137.2010.03512.x
Becerra-Rivera VA, Bergström E, Thomas-Oates J, Dunn MF (2018) Polyamines are required for normal growth in Sinorhizobium meliloti. Microbiology 164(4):600–613. https://doi.org/10.1099/mic.0.000615
Ben Salah I, Slatni T, Albacete A, Gandour M, Martínez Andújar C, Houmani H, Ben Hamed K, Martinez V, Pérez-Alfocea F, Abdelly C (2010) Salt tolerance of nitrogen fixation in Medicago ciliaris is related to nodule sucrose metabolism performance rather than antioxidant system. Symbiosis 51(2):187–195. https://doi.org/10.1007/s13199-010-0073-3
Bruning B, Rozema J (2013) Symbiotic nitrogen fixation in legumes: perspectives for saline agriculture. Environ Exp Bot 92:134–143
Burris RH (1984) The fundamentals of nitrogen fixation- Posgate, JR. Am Sci 72(5):517
Coba de la Peña T, Pueyo JJ (2012) Legumes in the reclamation of marginal soils, from cultivar and inoculant selection to transgenic approaches. Agron Sustain Dev 32(1):65–91. https://doi.org/10.1007/s13593-011-0024-2
Crespi M, Gálvez S (2000) Molecular mechanisms in root nodule development. J Plant Growth Regul 19(2):155–166. https://doi.org/10.1007/s003440000023
del Giudice J, Cam Y, Damiani I, Fung-Chat F, Meilhoc E, Bruand C, Brouquisse R, Puppo A, Boscari A (2011) Nitric oxide is required for an optimal establishment of the Medicago truncatula–Sinorhizobium meliloti symbiosis. New Phytol 191(2):405–417. https://doi.org/10.1111/j.1469-8137.2011.03693.x
Diao QN, Song YJ, Shi DM, Qi HY (2017) Interaction of polyamines, abscisic acid, nitric oxide, and hydrogen peroxide under chilling stress in tomato (Lycopersicon esculentum Mill.) seedlings. Front Plant Sci 8. https://doi.org/10.3389/fpls.2017.00203
Doyle JJ, Luckow MA (2003) The rest of the iceberg. Legume diversity and evolution in a phylogenetic context. Plant Physiol 131(3):900–910. https://doi.org/10.1104/pp.102.018150
Duque AS, López-Gómez M, Kráčmarová J, Gomes CN, Araújo SS, Lluch C, Fevereiro P (2016) Genetic engineering of polyamine metabolism changes Medicago truncatula responses to water deficit. Plant Cell Tissue Organ Cult 127(3):681–690. https://doi.org/10.1007/s11240-016-1107-1
Efrose RC, Flemetakis E, Sfichi L, Stedel C, Kouri ED, Udvardi MK, Kotzabasis K, Katinakis P (2008) Characterization of spermidine and spermine synthases in Lotus japonicus: induction and spatial organization of polyamine biosynthesis in nitrogen fixing nodules. Planta 228(1):37–49. https://doi.org/10.1007/s00425-008-0717-1
FAO (2009). El estado mundial de la agricultura y la alimentación
Foyer CH, Noctor G (2005) Oxidant and antioxidant signalling in plants: a re-evaluation of the concept of oxidative stress in a physiological context. Plant Cell Environ 28(8):1056–1071. https://doi.org/10.1111/j.1365-3040.2005.01327.x
Fujihara S (2009) Biogenic amines in rhizobia and legume root nodules. Microbes Environ 24(1):1–13. https://doi.org/10.1264/jsme2.ME08557
Gepts P, Beavis WD, Brummer EC, Shoemaker RC, Stalker HT, Weeden NF, Young ND (2005) Legumes as a model plant family. Genomics for food and feed report of the cross-legume advances through genomics conference. Plant Physiol 137(4):1228–1235. https://doi.org/10.1104/pp.105.060871
Gordon AJ (1995) Sucrose metabolism to support N2 fixation in legume root nodules. In: Tikhonovich I, Provorov N, Romanov V, Newton W (eds) Nitrogen fixation: fundamentals and applications, vol 27. Current plant science and biotechnology in agriculture. Springer Netherlands, pp 533–538. https://doi.org/10.1007/978-94-011-0379-4_62
Groppa MD, Benavides MP (2008) Polyamines and abiotic stress: recent advances. Amino Acids 34(1):35–45. https://doi.org/10.1007/s00726-007-0501-8
Gupta K, Sengupta A, Chakraborty M, Gupta B (2016) Hydrogen peroxide and polyamines act as double edged swords in plant abiotic stress responses. Front Plant Sci 7(1343). https://doi.org/10.3389/fpls.2016.01343
Handa AK, Fatima T, Mattoo AK (2018) Polyamines: bio-molecules with diverse functions in plant and human health and disease. Front Chem 6:10–10. https://doi.org/10.3389/fchem.2018.00010
Hasanuzzaman M, Nahar K, Fujita M (2013) Plant response to salt stress and role of exogenous protectants to mitigate salt-induced damages. In: Ahmad P, Azooz MM, Prasad MNV (eds) Ecophysiology and responses of plants under salt stress. Springer New York, New York, pp 25–87. https://doi.org/10.1007/978-1-4614-4747-4_2
Hatmi S, Villaume S, Trotel-Aziz P, Barka EA, Clément C, Aziz A (2018) Osmotic stress and ABA affect immune response and susceptibility of Grapevine Berries to Gray Mold by priming polyamine accumulatioN. Front Plant Sci 9(1010). https://doi.org/10.3389/fpls.2018.01010
Huang X, He J, Yan X, Hong Q, Chen K, He Q, Zhang L, Liu X, Chuang S, Li S, Jiang J (2017) Microbial catabolism of chemical herbicides: microbial resources, metabolic pathways and catabolic genes. Pestic Biochem Physiol 143:272–297. https://doi.org/10.1016/j.pestbp.2016.11.010
Hussain SS, Ali M, Ahmad M, Siddique KHM (2011) Polyamines: natural and engineered abiotic and biotic stress tolerance in plants. Biotechnol Adv 29(3):300–311. https://doi.org/10.1016/j.biotechadv.2011.01.003
Jamet A, Mandon K, Puppo A, Herouart D (2007) H2O2 is required for optimal establishment of the Medicago sativa/Sinorhizobium meliloti symbiosis. J Bacteriol 189(23):8741–8745. https://doi.org/10.1128/jb.01130-07
Jasso-Robles FI, Jimenez-Bremont JF, Becerra-Flora A, Juarez-Montiel M, Gonzalez ME, Pieckenstain FL, de la Cruz RFG, Rodriguez-Kessler M (2016) Inhibition of polyamine oxidase activity affects tumor development during the maize-Ustilago maydis interaction. Plant Physiol Biochem 102:115–124. https://doi.org/10.1016/j.plaphy.2016.02.019
Jensen E, Peoples M, Boddey R, Gresshoff P, Hauggaard-Nielsen H, Alves BJR, Morrison M (2012) Legumes for mitigation of climate change and the provision of feedstock for biofuels and biorefineries: a review. Agron Sustain Dev 32(2):329–364. https://doi.org/10.1007/s13593-011-0056-7
Jiménez Bremont J, Marina M, de la Luz Guerrero-González M, Rossi F, Sánchez-Rangel D, Rodríguez-Kessler M, Ruiz O, Gárriz A (2014) Physiological and molecular implications of plant polyamine metabolism during biotic interactions. Front Plant Sci 5(95). https://doi.org/10.3389/fpls.2014.00095
Jiménez-Bremont JF, Ruiz OA, Rodríguez-Kessler M (2007) Modulation of spermidine and spermine levels in maize seedlings subjected to long-term salt stress. Plant Physiol Biochem 45(10):812–821
Jimenez-Bremont JF, Marina M, Guerrero-Gonzalez MD, Rossi FR, Sanchez-Rangel D, Rodriguez-Kessler M, Ruiz O, Garriz A (2014) Physiological and molecular implications of plant polyamine metabolism during biotic interactions. Front Plant Sci 5. https://doi.org/10.3389/fpls.2014.00095
Koca H, Bor M, Ozdemir F, Turkan I (2007) The effect of salt stress on lipid peroxidation, antioxidative enzymes and proline content of sesame cultivars. Environ Exp Bot 60. https://doi.org/10.1016/j.envexpbot.2006.12.005
Lahiri K, Chattopadhyay S, Ghosh B (2004) Correlation of endogenous free polyamine levels with root nodule senescence in different genotypes in Vigna mungo L. J Plant Physiol 161(5):563–571. https://doi.org/10.1078/0176-1617-01057
Le BH, Wagmaister JA, Kawashima T, Bui AQ, Harada JJ, Goldberg RB (2007) Using genomics to study legume seed development. Plant Physiol 144(2):562–574. https://doi.org/10.1104/pp.107.100362
Li S, Jin H, Zhang Q (2016) The effect of exogenous spermidine concentration on polyamine metabolism and salt tolerance in zoysiagrass (Zoysia japonica steud) subjected to short-term salinity stress. Front Plant Sci 7. https://doi.org/10.3389/fpls.2016.01221
Lopez M, Herrera-Cervera JA, Lluch C, Tejera NA (2006) Trehalose metabolism in root nodules of the model legume Lotus japonicus in response to salt stress. Physiol Plant 128(4):701–709. https://doi.org/10.1111/j.1399-3054.2006.00802.x
Lopez M, Herrera-Cervera JA, Iribarne C, Tejera NA, Lluch C (2008) Growth and nitrogen fixation in Lotus japonicus and Medicago truncatula under NaCl stress: nodule carbon metabolism. J Plant Physiol 165(6):641–650. https://doi.org/10.1016/j.jplph.2007.05.009
López M, Herrera-Cervera JA, Iribarne C, Tejera NA, Lluch C (2008) Growth and nitrogen fixation in Lotus japonicus and Medicago truncatula under NaCl stress: nodule carbon metabolism. J Plant Physiol 165(6):641–650
López-Gómez M, Tejera NA, Iribarne C, Herrera-Cervera JA, Lluch C (2011) Different strategies for salt tolerance in determined and indeterminate nodules of Lotus japonicus and Medicago truncatula. Arch Agron Soil Sci 58(9):1061–1073. https://doi.org/10.1080/03650340.2011.561836
López-Gómez M, Cobos-Porras L, Hidalgo-Castellanos J, Lluch C (2014a) Occurrence of polyamines in root nodules of Phaseolus vulgaris in symbiosis with Rhizobium tropici in response to salt stress. Phytochemistry 107:32–41. https://doi.org/10.1016/j.phytochem.2014.08.017
López-Gómez M, Hidalgo-Castellanos J, Iribarne C, Lluch C (2014b) Proline accumulation has prevalence over polyamines in nodules of Medicago sativa in symbiosis with Sinorhizobium meliloti during the initial response to salinity. Plant Soil 374(1-2):149–159
Lopez-Gomez M, Cobos-Porras L, Prell J, Lluch C (2016a) Homospermidine synthase contributes to salt tolerance in free-living Rhizobium tropici and in symbiosis with Phaseolus vulgaris. Plant Soil 404(1-2):413–425. https://doi.org/10.1007/s11104-016-2848-7
López-Gómez M, Hidalgo-Castellanos J, Lluch C, Herrera-Cervera JA (2016b) 24-Epibrassinolide ameliorates salt stress effects in the symbiosis Medicago truncatula-Sinorhizobium meliloti and regulates the nodulation in cross-talk with polyamines. Plant Physiol Biochem 108:212–221. https://doi.org/10.1016/j.plaphy.2016.07.017
López-Gómez M, Hidalgo-Castellanos J, Muñoz-Sánchez JR, Marín-Peña AJ, Lluch C, Herrera-Cervera JA (2017) Polyamines contribute to salinity tolerance in the symbiosis Medicago truncatula-Sinorhizobium meliloti by preventing oxidative damage. Plant Physiol Biochem 116:9–17. https://doi.org/10.1016/j.plaphy.2017.04.024
Manchanda G, Garg N (2008) Salinity and its effects on the functional biology of legumes. Acta Physiol Plant 30(5):595–618. https://doi.org/10.1007/s11738-008-0173-3
Mantri N, Basker N, Ford R, Pang E, Pardeshi V (2013) The role of micro-ribonucleic acids in legumes with a focus on abiotic stress response. Plant Genome 6. https://doi.org/10.3835/plantgenome2013.05.0013
McNeil SD, Nuccio ML, Hanson AD (1999) Betaines and related osmoprotectants. Targets for metabolic engineering of stress resistance. Plant Physiol 120(4):945. https://doi.org/10.1104/pp.120.4.945
Milhinhos A, Miguel CM (2013) Hormone interactions in xylem development: a matter of signals. Plant Cell Rep 32(6):867–883. https://doi.org/10.1007/s00299-013-1420-7
Minocha R, Majumdar R, Minocha SC (2014) Polyamines and abiotic stress in plants: a complex relationship. Front Plant Sci 5. https://doi.org/10.3389/fpls.2014.00175
Molina C, Zaman-Allah M, Khan F, Fatnassi N, Horres R, Rotter B, Steinhauer D, Amenc L, Drevon J-J, Winter P, Kahl G (2011) The salt-responsive transcriptome of chickpea roots and nodules via deepSuperSAGE. BMC Plant Biol 11(1):31. https://doi.org/10.1186/1471-2229-11-31
Møller I, Jensen P, Hansson A (2007) Oxidative modifications to cellular components in plants. Annu Rev Plant Biol 58. https://doi.org/10.1146/annurev.arplant.58.032806.103946
Moschou PN, Paschalidis KA, Delis ID, Andriopoulou AH, Lagiotis GD, Yakoumakis DI, Roubelakis-Angelakis KA (2008) Spermidine exodus and oxidation in the apoplast induced by abiotic stress is responsible for H2O2 signatures that direct tolerance responses in tobacco. Plant Cell 20(6):1708–1724. https://doi.org/10.1105/tpc.108.059733
Munns R (2009) Strategies for crop improvement in saline soils. In: Ashraf M, Ozturk M, Athar HR (eds) Salinity and water stress, vol 44. Tasks for vegetation sciences. Springer Netherlands, pp 99–110. https://doi.org/10.1007/978-1-4020-9065-3_11
Munns R, Tester M (2008) Mechanisms of salinity tolerance. Annu Rev Plant Biol 59(1):651–681. https://doi.org/10.1146/annurev.arplant.59.032607.092911
Nishi H, Demir E, Panchenko AR (2015) Crosstalk between signaling pathways provided by single and multiple protein phosphorylation sites. J Mol Biol 427(2):511–520. https://doi.org/10.1016/j.jmb.2014.11.001
Pal M, Szalai G, Janda T (2015) Speculation: polyamines are important in abiotic stress signaling. Plant Sci 237:16–23. https://doi.org/10.1016/j.plantsci.2015.05.003
Palma F, Lluch C, Iribarne C, Garcia-Garrido JM, Tejera Garcia NA (2009) Combined effect of salicylic acid and salinity on some antioxidant activities, oxidative stress and metabolite accumulation in Phaseolus vulgaris. Plant Growth Regul 58(3):307–316. https://doi.org/10.1007/s10725-009-9380-1
Palma F, López-Gómez M, Tejera NA, Lluch C (2013) Salicylic acid improves the salinity tolerance of Medicago sativa in symbiosis with Sinorhizobium meliloti by preventing nitrogen fixation inhibition. Plant Sci 208(0):75–82. https://doi.org/10.1016/j.plantsci.2013.03.015
Palma F, López-Gómez M, Tejera NA, Lluch C (2014) Involvement of abscisic acid in the response of Medicago sativa plants in symbiosis with Sinorhizobium meliloti to salinity. Plant Sci 223:16–24. https://doi.org/10.1016/j.plantsci.2014.02.005
Parra-Lobato MC, Gomez-Jimenez MC (2011) Polyamine-induced modulation of genes involved in ethylene biosynthesis and signalling pathways and nitric oxide production during olive mature fruit abscission. J Exp Bot 62(13):4447–4465. https://doi.org/10.1093/jxb/err124
Podlešáková K, Ugena L, Spíchal L, Doležal K, De Diego N (2019) Phytohormones and polyamines regulate plant stress responses by altering GABA pathway. New Biotechnol 48:53–65. https://doi.org/10.1016/j.nbt.2018.07.003
Rengasamy P (2006) World salinization with emphasis on Australia. J Exp Bot 57(5):1017–1023. https://doi.org/10.1093/jxb/erj108
Rubio MC, Bustos-Sanmamed P, Clemente MR, Becana M (2009) Effects of salt stress on the expression of antioxidant genes and proteins in the model legume Lotus japonicus. New Phytol 181(4):851–859. https://doi.org/10.1111/j.1469-8137.2008.02718.x
Sagor GHM, 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(3):595–605. https://doi.org/10.1007/s11248-012-9666-3
Sagor GHM, Zhang SY, Kojima S, Simm S, Berberich T, Kusano T (2016) Reducing cytoplasmic polyamine oxidase activity in arabidopsis increases salt and drought tolerance by reducing reactive oxygen species production and increasing defense gene expression. Front Plant Sci 7. https://doi.org/10.3389/fpls.2016.00214
Shi H, Ye T, Chan Z (2013) Comparative proteomic and physiological analyses reveal the protective effect of exogenous polyamines in the Bermudagrass (Cynodon dactylon) response to salt and drought stresses. J Proteome Res 12(11):4951–4964. https://doi.org/10.1021/pr400479k
Smýkal P, Coyne CJ, Ambrose MJ, Maxted N, Schaefer H, Blair MW, Berger J, Greene SL, Nelson MN, Besharat N, Vymyslický T, Toker C, Saxena RK, Roorkiwal M, Pandey MK, Hu J, Li YH, Wang LX, Guo Y, Qiu LJ, Redden RJ, Varshney RK (2015) Legume crops phylogeny and genetic diversity for science and breeding. Crit Rev Plant Sci 34(1-3):43–104. https://doi.org/10.1080/07352689.2014.897904
Su GX, Bai X (2008) Contribution of putrescine degradation to proline accumulation in soybean leaves under salinity. Biol Plantarum 52(4):796–799. https://doi.org/10.1007/s10535-008-0156-7
Tang W, Newton RJ (2005) Polyamines reduce salt-induced oxidative damage by increasing the activities of antioxidant enzymes and decreasing lipid peroxidation in Virginia pine. Plant Growth Regul 46(1):31–43. https://doi.org/10.1007/s10725-005-6395-0
Tejera García NA, Iribarne C, Palma F, Lluch C (2007) Inhibition of the catalase activity from Phaseolus vulgaris and Medicago sativa by sodium chloride. Plant Physiol Biochem 45(8):535–541. https://doi.org/10.1016/j.plaphy.2007.04.008
Tejera NA, Soussi M, Lluch C (2006) Physiological and nutritional indicators of tolerance to salinity in chickpea plants growing under symbiotic conditions. Environ Exp Bot 58(1-3):17–24. https://doi.org/10.1016/j.envexpbot.2005.06.007
Terakado J, Yoneyama T, Fujihara S (2006) Shoot-applied polyamines suppress nodule formation in soybean (Glycine max). J Plant Physiol 163(5):497–505. https://doi.org/10.1016/j.jplph.2005.05.007
Terakado-Tonooka J, Fujihara S (2008) Involvement of polyamines in the root nodule regulation of soybeans (Glycine max). Plant Root 2:46–53. https://doi.org/10.3117/plantroot.2.46
Terui Y, Ohnuma M, Hiraga K, Kawashima E, Oshima T (2005) Stabilization of nucleic acids by unusual polyamines produced by an extreme thermophile, Thermus thermophilus. Biochem J 388:427–433
Tomar PC, Lakra N, Mishra SN (2013) Cadaverine: a lysine catabolite involved in plant growth and development. Plant Signal Behav 8(10):e25850. https://doi.org/10.4161/psb.25850
Udvardi M, Poole PS (2013) Transport and metabolism in legume-rhizobia symbioses. Annu Rev Plant Biol 64:781–805
Verma S, Mishra SN (2005) Putrescine alleviation of growth in salt stressed Brassica juncea by inducing antioxidative defense system. J Plant Physiol 162(6):669–677. https://doi.org/10.1016/j.jplph.2004.08.008
Wimalasekera R, Tebartz F, Scherer GFE (2011) Polyamines, polyamine oxidases and nitric oxide in development, abiotic and biotic stresses. Plant Sci 181(5):593–603. https://doi.org/10.1016/j.plantsci.2011.04.002
Xing SG, Jun YB, Hau ZW, Liang LY (2007) Higher accumulation of γ-aminobutyric acid induced by salt stress through stimulating the activity of diamine oxidases in Glycine max (L.) Merr. roots. Plant Physiol Biochem 45(8):560–566. https://doi.org/10.1016/j.plaphy.2007.05.007
Zheng Q, Liu J, Liu R, Wu H, Jiang C, Wang C, Guan Y (2016) Temporal and spatial distributions of sodium and polyamines regulated by brassinosteroids in enhancing tomato salt resistance. Plant Soil 400(1-2):147–164. https://doi.org/10.1007/s11104-015-2712-1
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2019 Springer Nature Switzerland AG
About this chapter
Cite this chapter
López-Gómez, M., Hidalgo-Castellanos, J., Marín-Peña, A.J., Herrera-Cervera, J.A. (2019). Relationship Between Polyamines and Osmoprotectants in the Response to Salinity of the Legume–Rhizobia Symbiosis. In: Hossain, M., Kumar, V., Burritt, D., Fujita, M., Mäkelä, P. (eds) Osmoprotectant-Mediated Abiotic Stress Tolerance in Plants. Springer, Cham. https://doi.org/10.1007/978-3-030-27423-8_13
Download citation
DOI: https://doi.org/10.1007/978-3-030-27423-8_13
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-27422-1
Online ISBN: 978-3-030-27423-8
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)