Abstract
Jasmonic acid and methyl jasmonate are naturally growth regulators widely distributed in plants. They are involved in the regulation of a multitude of processes. The functional physiology underlying these phenomena is not yet clear, although there is increasing evidence that jasmonates may interconnect with the network of the classic plant growth regulators. This chapter discusses some aspects related to jasmonates in plants, such as chemical properties, synthesis pathways, biological functions, antioxidant action, physiological and biochemical changes that occur in plants under normal conditions and the possible functions of jasmonates under changing environmental conditions. The study summarises the impacts of jasmonates on plant growth and physiology, and how jasmonates may impact horticultural crop growth, physiology, protection from stresses. The role of jasmonates in improving physiological processes in some horticultural crops and ecological significance of these findings are discussed.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Abbreviations
- ABA:
-
Abscisic acid
- GA:
-
Gibberellic acid
- JA:
-
Jasmonic acid
- JAZ proteins:
-
Jasmonte-Zim proteins
- MeJA:
-
Methyl ester of jasmonic acid
- JIPs:
-
JA-induced proteins
- PSII:
-
Photosystem II
- ROS:
-
Reactive oxygen species
- RuBPCase:
-
Ribulose-1,5- bisphosphate carboxylase
- RuBPOase:
-
Ribulose-1,5- bisphosphate oxygenase
References
Aldridge DC, Galt S, Giles D, Turner WB (1971) Metabolites of Lasiodiplodia theobromae. J Chem Soc C Organ :1623–1627
Ali MB, Hah EJ, Paek YK (2007) Methyl jasmonate and salicylic acid induced oxidative stress and accumulation of phenolics in Panax ginseng. Bioreactor root suspension cultures. Mol 12(3):607–662
Alvarez S, Zhu M, Chen S (2009) Proteomics of Arabidopsis redox proteins in response to methyl jasmonates. J Proteomics 73(1):30–40
Andresen I, Becker W, Schlüter K, Burges J, Parthier B, Apel K (1992) The identification of leaf thionin as one of the main jasmonate-induced proteins of barley (Hordeum vulgare). Plant Mol Biol 19:193–204
Babst BA, Ferrieri RA, Gray DW, Lerdau M, Schlyer DJ, Schueller M, Thorpe MR, Orian CM (2005) Jasmonic acid induces rapid changes in carbon transport and partitioning in Populus. New Phytol 167(1):63–72
Barendse GWM, Croes AF, Vandenende G, Bosveld M, Creemers T (1985) Role of hormones on flower bud formation in thin-layer explants of Tobacco. Biol Plantar 27:408–412
Bonaventure G, Gfeller A, Proebsting WM, Hoerstensteiner S, Chételat A, Martinoia E, Farmer EE (2007) A gain of function allele of TPC1 activates oxylipin biogenesis after leaf wounding in Arabidopsis. Plant J 49:889–898
Brown AD, Goya IA, Larsen H, Lilley RMC (1987) A salt-sensitive mutant of Dunaliella tertiolecta. A role of carbonic anhydrase. Arch Microbiol 147:309–314
Chen H, Jones AD, Howe GA (2006a) Constitutive activation of the jasmonate signaling pathway enhances the production of secondary metabolites in tomato. FEBS Lett 580:2540–2546
Chen P, Yu S, Zhang Y (2006b) Effects of jasmonic acid and heat acclimation on thermotolerance and antioxidant enzymes of young grape plants. Life Sci Res 2006–03
Chini AS, Fonseca S, Fernández G, Adie B, Chico JM, Lorenzo O, García-Casado G, López-Vidriero I, Lozano FM, Ponce MR, Mico JL, Solano R (2007) The JAZ family of repressors is the missing link in jasmonate signalling. Nature 448:666–671
Cipollini D (2005) Interactive effects of lateral shading and jasmonic acid on morphology, physiology, seed production, and defense traits in Arabidopsis thaliana. Int J Plant Sci 166:955–959
Creelman RA, Mullet JE (1995) Jasmonic acid distribution and action in plants: regulation during development and response to biotic and abiotic stress. Proc Natl Acad Sci USA 92:4114–4119
Creelman RA, Mullet JE (1997) Biosynthesis and action of jasmonates in plants. Annu Rev Plant Physiol Plant Mol Biol 48:355–381
Czapski J, Saniewski M (1992) Stimulation of ethylene production and ethylene-forming enzyme activity in fruits of the non-ripening nor and rin tomato mutants by methyl jasmonate. J Plant Physiol 139:265–268
Darras AI, Terry LA, Joyce DC (2005) Methyl jasmonate vapour treatment suppresses specking caused by Botrytis cinerea on cut Freesia hybrida L. flowers. Postharvest Biol Technol 38(2):175–182
Dathe W, Rönsch H, Preiss A, Schade W (1981) Endogenous plant hormones of the broad bean, Vicia faba L. (−)-jasmonic acid, a plant growth inhibitor in pericarp. Planta 153:530–535
Demole E, Lederer E, Miercier DE (1962) Isolement et détermination de la structure du jasmonate de méthyle, constituant odorant charactéristique de l’essence de jasmin. Helv Chim Acta 45:675–685
Ding CK, Wang CY, Gross KC, Smith DL (2001) Reduction of chilling injury and transcript accumulation of heat shock proteins in tomato fruit by methyl jasmonate and methyl salicylate. Plant Sci 161:1153–1159
Dombrowski JE (2003) Salt stress activation of wound-induced gene expression in tomato plants. Plant Physiol 132(4):2098–2107
Fan XT, Mattheis JP, Fellman JK (1998) Responses of apples to postharvest jasmonate. J Am Soc Hortic Sci 123:421–425
Farmer EE, Weber H, Vollenweider S (1998) Fatty acid signaling in Arabidopsis. Planta 206:167–175
Fisher M, Gokhman I, Pick U, Zamir A (1996) A salt-resistant plasma membrane carbonic anhydrase is induced by salt in Dunaliella salina. J Biol Chem 271:17718–17723
Franceschi VR, Grimes HD (1991) Induction of soybean vegetative storage proteins and anthocyanins by low-level atmospheric methyl jasmonate. Proc Natl Acad Sci USA 88:6745–6749
Franceschi VR, Krekling T, Christiansen E (2002) Application of methyl jasmonate on Picea abies (Pinaceae) stems induces defense-related responses in phloem and xylem. Am J Bot 89:578–586
Fukui H, Koshimizu K, Usuda S, Yamazaki Y (1977) Isolation of plant growth regulators from seeds of Cucurbita pepo L. Agric Biol Chem 41:175–180
Gapper NE, Norris GE, Clarke SF, Lill RE, Jameson PE (2002) Novel jasmonate amino acid conjugates in Asparagus officinalis during harvest-induced and natural foliar senescence. Physiol Plant 114:116–124
Gehring CA, Irving HR, Mc Conchie R, Parish RW (1997) Jasmonates induce intracellular alkalization and closure of Paphiopedilum guard cell. Ann Bot 80:485–489
Gfeller A, Dubugnon L, Liechti R, Farmer EE (2010) Jasmonate biochemical pathway. Sci Signal 3:cm3
Gonzalez-Aguilar AB, Buta JG, Wang CY (2003) Methyl jasmonate and modified atmosphere packaging (MAP) reduce decay and maintain postharvest quality of papaya Sunrise. Postharvest Biol Technol 28:361–370
González-Aguilar GA, Tiznado-Hernández M, Wang CY (2006) Physiological and biochemical responses of horticultural products to methyl jasmonate. Stewart Postharvest Solut 2(1):1–9
González-Herranz R, Cathline KA, Fidelibus MW, Burns JK (2009) Potential of methyl jasmonate as a harvest aid for ‘Thompson Seedless’ grapes: concentration and time needed for consistent berry loosening. Hort Sci 44(5):1330–1333
Hadian J, Zolfagharinasab Z (2007) Influence of methyl jasmonate on inducing chilling tolerance in pomegranate fruits (Malas Save). Pak J Biol Sci 10:612–616
Hamberg M, Gardner HW (1992) Oxylipin pathway to jasmonates: biochemistry and biological significance. Biochim Biophys Acta 1165:1–18
Hause B, Demus U, Teichmann C, Parthier B, Wasternack C (1996) Developmental and tissue-specific expression of JIP-23, a jasmonate-inducible protein of barley. Plant Cell Physiol 37:641–649
Hause B, Kogel KH, Parthier B, Wasternack C (1997) In barley leaf cells, jasmonates do not act as a signal during compatible or incompatible interactions with the powdery mildew fungus (Erisiphe graminis f., sp. Hordei). J Plant Physiol 150:127–132
Hause B, Maier W, Miersch O, Kramell R, Strack D (2002) Induction of jasmonate biosynthesis in Arbuscular Mycorrhizal barley roots. Plant Physiol 130:1213–1220
Heijari J, Nerg AM, Kainulainen P, Viiri H, Vuorinen M, Holopainen JK (2005) Application of methyl jasmonate reduces growth but increases chemical defence and resistance against Hyloblus abietis in Scots pine seedlings. In: Proceedings of 12th international symposium of insect-plant relationships 11, Berlin, 7–14 Aug 2004, p 283
Hristova VA, Popova LP (2002) Treatment with methyl jasmonate alleviates the effects of paraquat on photosynthesis in barley plants. Photosynthetica 40(4):567–574
Huang Y, Han C, Peng W, Peng Z, Xiong X, Zhu Q, Gao B, Xie D, Ren C (2010) Brassinosteroid negatively regulates jasmonate inhibition of root growth in Arabidopsis. Plant Signal Behav 5:140–142
Jubany-Marí T, Prinsen E, Munné-Bosch S, Alegre L (2010) The timing of methyl jasmonate, hydrogen peroxide and ascorbate accumulation during water deficit and subsequent recovery in the Mediterranean shrub Cistus albidus L. Environ Exp Bot 69:147–155
Kang DJ, Seo YJ, Lee JD, Ishii R, Kim KU, Shin DH, Park SK, Jang SW, Lee IJ (2005) Jasmonic acid differentially affects growth, ion uptake and abscisic acid concentration in salt-tolerant and salt-sensitive rice cultivars. J Agron Crop Sci 191(4):273–282
Kausch KD, Sobolev AP, Goyal RK, Fatima T, Beevi LR, Saftner RA, Handa AK, Matoo AK (2012) Methyl jasmonate deficiency alters cellular metabolome, including the aminome of tomato (Solanum lycopersicum L.) fruits. Amino Acids 42:843–885
Kauss H, Jublick W, Ziegler J, Krabler W (1994) Pretreatment of parsley (Petroselinum crispum L.) suspension cultures with methyl jasmonate enhances elicitation of activated oxygen species. Plant Physiol 105:89–94
Kępczyńska E, Paulina Król P (2011) The phytohormone methyl jasmonate as an activator of induced resistance against the necrotroph Alternaria porri f. sp. solani in tomato plants. J Plant Interac. doi:10.1080/17429145.2011.645169
Keramat B, Manouchehri KK, Arvin MJ (2010) Effect of methyl jasmonate treatment on alleviation of cadmium damages in soybean. J Plant Nutr 33(7):1016–1025
Kęsy J, Wilmowicz E, Maciejewska B, Frankowski K, Glazińska P, Kopcewicz J (2011) Independent effects of jasmonates and ethylene on inhibition of Pharbitis nil flowering. Acta Physiol Plant 33:1211–1216
Kim EH, Park SH, Kim JK (2009) Methyl jasmonate triggers loss of grain yield under drought stress. Plant Signal Behav 4(4):348–349
Kiribuchi K, Jikumaru Y, Kaku H, Minami E, Hasegawa M, Kodama O, Seto H, Okada K, Nojiri H, Yamane H (2005) Involvement of the basic helix-loop-helix transcription factor RERJ1 in wounding and drought stress responses in rice plants. Biosci Biotechnol Biochem 69:1042–1044
Knöfel HD, Sembdner G (1995) Jasmonates from pine pollen. Phytochemistry 38:569–571
Koda Y (1992) The role of jasmonic acid and related compounds in the regulation of plant development. Int Rev Cytol 135:155–199
Koda Y (1997) Possible involvement of jasmonates in various morphogenic events. Physiol Plant 100(3):639–646
Krajncic B, Kristl J, Janzekovic I (2006) Possible role of jasmonic acid in the regulation of floral induction, evocation and floral differentiation in Lemna minor L. Plant Physiol Biochem 44:752–758
Kramell R, Miersch O, Atzorn R, Parthier B, Wasternack C (2000) Octadecanoid-derived alteration of gene expression and the “oxylipin signature” in stressed barley leaves: implications for different signaling pathways. Plant Physiol 123:177–186
Krzyzanowska J, Czubacka A, Pecio L, Przybys M, Doroszewska T, Stochmal A, Oleszek W (2011) The effects of jasmonic acid and methyl jasmonate on rosmarinic acid production in Mentha × piperita cell suspension cultures. Plant Cell Tissue Org Cult 108:73–81
Lannoo N, Peumans WP, Van Damme EJM (2006) The presence of jasmonate-inducible lectin genes in some but not all Nicotiana species explains a marked intragenus difference in plant responses to hormone treatment. J Exp Bot 57(12):3145–3155
Larcher W (1995) Physiological plant ecology, 3rd edn. Springer, Berlin/Heidelberg/New York, pp 46–54
Latorella AH, Vadas RL (1973) Salinity adaptation by Dunaliella tertiolecta. I. Increases in carbonic anhydrase activity and evidence for a light-dependent Na+/H+ exchange. J Phycol 9:273–277
Lee TM, Lur HS, Lin YH, Chu C (1996) Physiological and biochemical changes related to methyl jasmonate-induced chilling tolerance of rice (Oryza sativa L.) seedlings. Plant Cell Environ 19:65–74
Lehmann J, Atzorn R, Brückner C, Reinbothe S, Leopold J, Wasternack C, Parthier B (1995) Accumulation of jasmonate, abscisic acid, specific transcripts and proteins in osmotically stressed barley leaf segments. Planta 197:156–162
Liechti R, Farmer EE (2006) Jasmonate biochemical pathway. Sci STKE 322:1–3
Lopez R, Dathe W, Bruckner C, Miersch O, Sembdner G (1987) Jasmonic acid in different parts of the developing soybean fruit. Biochem Physiol Pflanzen 182:195–201
Maciejewska BD, Kesy J, Zielinska M, Kopcewicz J (2004) Jasmonates inhibit flowering in short-day plant Pharbitis nil. Plant Growth Regul 43:1–8
Maksymiec W, Wianowska D, Dawidowicz AL, Radkiewicz S, Mardarowicz M, Krupa Z (2005) The level of jasmonic acid in Arabidopsis thaliana and Phaseolus coccineus plants under heavy metal stress. J Plant Physiol 162(12):1338–1346
Maksymiek W, Krupa Z (2002) Jasmonic acid and heavy metals in Arabidopsis plants: a similar physiological response to both stressors? J Plant Physiol 159(5):509–515
Maksymiek W, Krupa Z (2006) The effects of short-term exposition to Cd, excess Cu ions and jasmonate on oxidative stress appearing in Arabidopsis thaliana. Envirn Exp Bot 57(1–2):187–194
Maksymiek W, Krupa Z (2007) Effect of methyl jasmonate and excess cooper on leaf and root growth. Biol Plant 51(2):321–332
Mansour N, Mimi Z, Harb J (2008) Stress imposed on broad bean (Vicia faba) plants irrigated with reclaimed wastewater mixed with brackish water through exogenous application of jasmonic acid. In: Al Baz I et al (eds) Efficient management of wastewater. Springer, Berlin/Heidelberg, pp 91–102
Maslenkova LT, Zanev Y, Popova LP (1990) Oxygen-evolving activity of thylakoids from barley plants cultivated on different concentrations of jasmonic acid. Plant Physiol 93:1316–1321
Maslenkova LT, Miteva TS, Popova LP (1992) Changes in the polypeptide patterns of barley seedlings exposed to jasmonic acid and salinity. Plant Physiol 98:700–707
Maslenkova L, Toncheva S, Zeinalov Y (1995) Effect of abscisic acid and jasmonic acid (or MeJA) on photosynthetic electron transport and oxygen evolving reactions in pea plants. Bulg J Plant Physiol 21(4):48–55
Mathew R, Sankar PD (2012) Effect of methyl jasmonate and chitosan on growth characteristics of Ocimum basilicum L., Ocimum sanctum L. and Ocimum gratissimum L. cell suspension cultures. Afr J Biotechnol 11:4759–4766
Maucher H, Hause B, Ziegler J, Wasternack C (2000) Allene oxidase syntheses of barley-tissues specific regulation in seedling development. Plant J 21:199–213
Mei C, Qi M, Sheng G, Yang Y (2006) Inducible overexpression of a rice allene oxide synthase gene increases the endogenous jasmonic acid level, PR gene expression, and host resistance to fungal infection. Mol Plant Microbe Interact 19:1127–1137
Metodiev MV, Tsonev TD, Popova LP (1996) Effect of jasmonic acid on the stomatal and nonstomatal limitation of leaf photosynthesis in barley leaves. J Plant Growth Regul 15:75–80
Meyer M, Miersch O, Buttner C, Dathe W, Sembdner G (1984) Occurrence of the plant growth regulator jasmonic acid in plants. J Plant Growth Regul 3:1–8
Miersch O, Sembdner G, Schreiber K (1989) Occurrence of jasmonic acid analogues in Vicia faba. Phytochemistry 28:339–340
Moons A, Prinsen E, Bauw G, Montagu MV (1997) Antagonistic effects of abscisic acid and jasmonates on salt stress-inducible transcripts in rice roots. Plant Cell 9:2243–2259
Mueller-Uri F, Parthier B, Nover L (1988) Jasmonates induced alterations in gene expression in barley leaf segments analyzed by in vivo and in vitro protein synthesis. Planta 176:241–247
Munns R (2005) Genes and salt tolerance: bringing them together. New Phytol 3:645–663
Nimitkeatkai H, Shishido M, Okawa K, Ohara H, Ban Y, Kita M, Moriguchi T, Ikeura H, Hayata Y, Kondo S (2011) Effect of jasmonates on ethylene biosynthesis and aroma volatile emission in Japanese apricot infected by a pathogen (Colletotrichum gloeosporioides). J Agric Food Chem 59(12):6423–6429
Norastehnia A, Asghari MN (2006) Effects of methyl jasmonate on the enzymatic antioxidant defense system in maize seedlings subjected to paraquat. Asian J Plant Sci 5:17–23
Orozco-Cárdenas S, Ryan CA (1999) Hydrogen peroxide is generated systemically in plant leaves by wounding and systemin via the octadecanoic pathway. Proc Nat Acad Sci USA 96:6553–6557
Orozco-Cárdenas ML, Narváez-Vásquez J, Ryan CA (2001) Hydrogen peroxide acts as a second messenger for the induction of defense genes in tomato plants in response to wounding, systemin, and methyl jasmonate. Plant Cell 13:179–191
Ortel B, Atzorn R, Hause B, Feussner I, Miersh O, Wasternack C (1999) Jasmonate-induced gene expression in barley (Hordeum vulgare) leaves, the link between jasmonate and abscisic acid. Plant Growth Regul 29:113–122
Pan RC, Dou ZJ, Ye QS (1995) Effect of methyl jasmonate on SOD activity and membrane lipid peroxidation in peanut seedlings during water stress. Acta Phytophysiol Sinica 21(3):221–228
Parra-Lobato MC, Garcia NF, Olmos E, Alvarez-Tinaut AC, Jimenez MCG (2009) Methyl jasmonate-induced antioxidant defence in root apoplast from sunflower seedlings. Environ Exp Bot 66(1):9–17
Parthier B (1989) Hormone-induced alterations in gene expression. Physiol Pflanzen 185:289–314
Parthier B (1991) Jasmonates, new regulators of plant growth and development: many facts and few hypothesis of their action. Bot Acta 104:446–454
Parthier B, Bruckner C, Dathe W, Hause B, Herrmann HD, Knofel HM, Kramell J, Lehmann O, Miersch S, Reinbote G, Sembdner S, Vasternack U, Nieden Z (1992) Jasmonates: metabolism, biological activities and mode of action in senescence and stress responses. In: Regul Gr, Karssen CV, van Lon LC, Vreugdenhil D (eds) Progress in plant. Kluwer, Dordrecht, pp 276–285
Patent: 1995012311, Natural suppression of sprouting in stored potatoes using jasmonates
Pauwels L, Morreel K, Witte ED, Lammertyn F, Montagu MV, Boerjan W, Inzé D, Goossens A (2008) Mapping methyl jasmonate-mediated transcriptional reprogramming of metabolism and cell cycle progression in cultured Arabidopsis cells. Proc Natl Acad Sci USA 29:1380–1385
Pedranzani H, Racagni G, Alemano S, Miersch O, Ramírez I, Peña-Cortés H, Taleisnik E, Machado-Domenech E, Abdala G (2003) Salt tolerant tomato plants show increased levels of jasmonic acid. Plant Growth Regul 41:149–158
Pedranzani H, Sierra-de-Grado R, Vigliocco A, Miersch O, Abdala G (2007) Cold and water stresses produce changes in endogenous jasmonates in two populations of Pinus pinaster Ait. Plant Growth Regul 52:111–116
Pijaotrowska A, Bajgus A, Godlewska B, Caerpak Kaminska MR (2009) Jasmonic acid as modulator of lead toxicity in aquatic plant Walfia arrhiza (Lemnaceae). Environ Exp Bot 63(3):507–513
Popova LP, Maslenkova LT (1997) Involvement of jasmonic acid in photosynthetic process in Hordeum vulgare L. during salinity stress. Recent Res Devel Plant Physiol 1:29–43
Popova LP, Uzunova AN (1996) Changes in the chloroplasts ultrastructure of barley leaves under treatment with jasmonic acid. Photosynthetica 32(4):635–639
Popova LP, Vaklinova SG (1988) Effect of jasmonic acid on the synthesis of ribulose-1,5-bisphosphate carboxylase-oxygenase in barley leaves. J Plant Physiol 133:210–215
Popova LP, Tsonev TD, Valklinova SG (1987) A possible role for abscisic acid in regulation of photosynthetic and photorespiratory carbon metabolism in barley leaves. Plant Physiol 83:824–828
Popova LP, Tsonev TD, Vaklinova SG (1988) Changes in some photosynthetic and photorespiratory properties in barley leaves after treatment with jasmonic acid. J Physiol Plant 69:161–166
Popova LP, Lazova GH, Miteva TS (1991) Carbonic anhydrase activity in barley leaves after treatment with abscisic acid and jasmonic acid. Com Rend ABS 44(5):51–54
Pozo MJ, van Loon LC, Pieterse MJ (2004) Jasmonates: signals in plant-microbe interactions. J Plant Growth Regul 23:211–222
Radhika V, Kost C, Bolland W, Heil M (2010) The role of jasmonates on floral nectar secretion. PLoS One 5:e9265
Raghavendra AS, Reddy KB (1987) Action of proline on stomata differs from that of abscisic acid, G-substances or methyl jasmonate. Plant Physiol 44:691–695
Rakwal R, Tamogami S, Agrawal GK, Iwahashi H (2002) Octadecanoid signaling component “burst” in rice (Oryza sativa L.) seedling leaves upon wounding by cut and treatment with fungal elicitor chitosan. Biochem Biophys Res Commun 295:1041–1045
Reinbothe S, Reinbothe C, Parthier B (1992) Differential accumulation of methyl jasmonate-induced mRNAs in response to abscisic acid and desiccation in barley (Hordeum vulgare). Physiol plant 86:49–56
Reinbothe S, Reinbothe C, Parthier B (1993) Methyl jasmonate represses translation initiation of a specific set of m RNAs in barley. Plant J 4:459–467
Reinbothe S, Reinbothe C, Lehmann J, Becker W, Apel K, Parthier B (1994a) JIP60, a methyl jasmonate-induced ribosome-inactivating protein involved in plant stress reactions. Proc Nat Acad Sci USA 91:7012–7016
Reinbothe S, Mollenhauer B, Reinbothe C (1994b) JIPs and RIPs: the regulation of plant gene expression by jasmonates in response to environmental cues and pathogens. Plant Cell 6:1197–1209
Reymond P, Farmer EE (1998) Jasmonate and salicylate as global signals for defense gene expression. Curr Opin Plant Biol 1:404–411
Robert-Seilaniantz A, Grant M, Jones JDG (2011) Hormone crosstalk in plant disease and defense: more than just jasmonate-salicylate antagonism. Annu Rev Phytopatol 49:317–343
Ryan CA (2000) The systemin signaling pathway: differential activation of plant defensive genes. Biochim Biophys Acta 1477:112–121
Saniewski M, Miszczak A, Kawa-Miszczak L, Wegrzynowicz-Lesiak E, Miyamoto K, Ueda J (1998) Effects of methyl jasmonate on anthocyanin accumulation, ethylene production, and CO2 evolution in uncooled and cooled tulip bulbs. J Plant Growth Regul 17:33–37
Saniewski A, Horbowicz M, Puchalski J, Ueda J (2003) Methyl jasmonate stimulates the formation and the accumulation of anthocyanin in Kalanchoe blossfeldiana. Acta Physiol Plant 25:143–149
Saniewski A, Horbowicz M, Puchalski J (2006) Induction of anthocyanins accumulation by methyl jasmonate in shoots of Crassula multicava Lam. Acta Agrobot 59:43–50
Sasaki-Sekimoto Y, Taki N, Obayashi T, Aono M, Matsumoto F, Sakurai N, Suzuki H, Hirai MY, Noji M, Saito K, Masuda T, Takamiya K, Shibata D, Ohta H (2005) Coordinated activation of metabolic pathways for antioxidants and defence compounds by jasmonates and their roles in stress tolerance in Arabidopsis. Plant J 44:653–668
See KS, Bhatt A, Keng CL (2011) Effect of sucrose and methyl jasmonate on biomass and anthocyanin production in cell suspension culture of Melastoma malabathricum (Melastomaceae). Rev Biol Trop 59(2):597–606
Sembdner G, Gross D (1986) Plant growth substances of plant and microbial origin. In: Bopp M (ed) Plant growth substances 1985. Springer, Berlin, pp 139–147
Sembdner G, Parthier B (1993) The biochemistry and the physiological and molecular actions of jasmonates. Annu Rev Plant Physiol Plant Mol Biol 44:569–589
Seo HS, Song JT, Cheong JJ, Lee H, Lee YW, Hwang I, Lee JS, Choi YD (2001) Jasmonic acid carboxyl methyltransferase: a key enzyme for jasmonate-regulated plant response. Proc Natl Acad Sci USA 98:4788–4793
Sevillano L, Sanchez-Ballestra MT, Romojaro F, Flores FB (2010) Physiological, hormonal and molecular mechanisms regulating chilling injury in horticultural species. Postharvest technologies applied to reduce its impact. J Sci Food Agric 89:555–573
Shahzad AN, Pollman S, Schubert S (2009) Does jasmonic acid control the maize shoot growth during the first phase of salt stress? In: Proceedings of the international plant nutrition colloquium XVI, Department of Plant Sciences, UC Davis, pp 26–32
Stamp N (2003) Out of the quagmire of plant defense hypothesis. Q Rev Biol 78:23–55
Staswick PE, Tiryaki I (2004) The oxylipin signal jasmonic acid is activated by an enzyme that conjugates it to isoleucine in Arabidopsis. Plant Cell 16:2117–2127
Staswick PE, Su W, Howell SH (1992) Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in a Arabidopsis thaliana mutants. Proc Natl Acad Sci USA 89:6837–6840
Suhita D, Kolla VA, Vavasseur A, Raghavendra AS (2003) Different signaling pathways involved during the suppression of stomatal opening by methyl jasmonate or abscisic acid. Plant Sci 164:481–488
Suhita D, Agepati S, Raghavendra J, Kwak JM, Vavasseur A (2004) Cytoplasmic alkalinization precedes reactive oxygen species production during methyl jasmonate- and abscisic acid-induced stomatal closure. Plant Physiol 134:1536–1545
Suza WP, Avila CA, Carruthers K, Kulkarni S, Goggin FL, Lorence A (2010) Exploring the impact of wounding and jasmonates on ascorbate metabolism. Plant Physiol Biochem 48(5):337–350
Tamari G, Borochov A, Atzorn R, Weiss D (1995) Methyl jasmonate induces pigmentation and flavonoid gene expression in petunia corollas: in possible role in wound response. Physiol Plant 94:45–50
Tani T, Sobajima H, Okada K, Chujo T, Arimura S, Tsutumi N, Nishimura M, Seto H, Nojiri H, Yamane H (2008) Identification of the OsOPR7 gene encoding 12-oxophytodienoate reductase involved in the biosynthesis of jasmonic acid in rice. Planta 227:517–526
Thines B, Katsir L, Melotto M, Niu Y (2007) JAZ repressor proteins are targets of the SCF (COI1) complex during jasmonate signalling. Nature 448:661–665
Thomma BPHJ, Eggermont K, Penninckk IAMA, Mauch-Mani B, Vogelsang R, Cammue BPA, Broekaert WF (1998) Separate jasmonate-dependent and salicylate-dependent defense-response pathways in Arabidopsis are essential for resistance to distinct microbial pathogens. Proc Natl Acad Sci USA 95:15107–15111
Toteja N, Sopory SK (2008) Chemical signaling under abiotic stress environment in plants. Plant Signal Behav 3(8):525–536
Truman W, Bennet MH, Kubigstelting I, Turnbull C, Grant M (2007) Arabidopsis systemic immunity uses conserved defense signaling pathways and is mediated by jasmonates. Proc Natl Acad Sci USA 104(3):1075–1080
Tsonev TD, Lazova GN, Stoinova ZhG, Popova LP (1998) A possible role for jasmonic in adaptation of barley seedlings to salinity stress. J Plant Growth Regul 17:153–159
Ueda J, Kato J (1980) Isolation and identification of a senescence-promoting substance from wormwood (Artemisia absinthium L.). Plant Physiol 66:246–249
Vick BA, Zimmerman DC (1984) Biosynthesis of jasmonic acid by several plant species. Plant Physiol 75:458–461
Vick BA, Zimmerman DC (1987) Oxidative systems for modifications of fatty acids: the lipoxygenase pathway. In: Stumpf PK, Con EE (eds) The biochemistry of plants: a comprehensive treatise, vol 9. Academic, Orlando, pp 53–90
Vidhyavathi R, Sarada R (2011) Effect of salicylic acid and methyl jasmonate on antioxidant systems of Haematococcus pluvialis. Acta Physiol Plant 33(3):1043–1049
Walia H, Wilson C, Wahid A, Condamine P, Cui X, Close TJ (2006) Expression analysis of barley (Hordeum vulgare L.) during salinity stress. Funct Integr Genomics 6:143–156
Walia H, Wilson C, Condamine P, Liu X, Ismail AM, Close TJ (2007) Large-scale expression profiling and physiological characterization of jasmonic acid-mediated adaptation of barley to salinity stress. Plant Cell Environ 30:410–421
Wang SY (1999) Methyl Jasmonates reduces water stress in strawberry. J Plant Growth Regul 18:127–134
Wang CY, Buta JG (1994) Methyl jasmonate reduces chilling injury in Cucurbita pepo through its regulation of abscisic acid and polyamine levels. Environ Exp Bot 34:427–432
Wang JW, Wu JY (2005) Nitric oxide is involved in methyl jasmonate-Induced defense responses and secondary metabolism activities of Taxus cells. Plant Cell Physiol 46:923–930
Wang Y, Mopper S, Hasenstein KH (2001) Effects of salinity on endogenous ABA, IAA, JA, and SA in Iris hexagona. J Chem Ecol 27:327–342
Wasternack C, Hause B (2002) Jasmonates and octadecanoids: signals in plant stress responses and development. Prog Nucleic Acids Res Mol Biol 72:165–221
Wasternack C, Parthier B (1997) Jasmonate-signalled plant gene expression. Trends Plant Sci 2:302–307
Weidhase RA, Lehmann J, Kramell HN, Sembdner G, Parthier B (1987) Degradation of ribulose-1, 5-bisphosphate carboxylase and chlorophyll in senescing barley leaf segments triggered by jasmonic acid and methyl ester and counteraction by cytokinin. Physiol Plant 69:161–166
Weiler EW, Albrecht T, Groth B, Xia ZQ, Luxem M, Li H, Andert L, Spengler P (1993) Evidence for the involvement of jasmonates and their octadecanoid precursors in the tendril coiling response of Bryonia dioica. Phytochemistry 32:591–600
Wilson C (2007) Effect of jasmonic acid on growth and ion relations of Oryza sativa L. grown under salinity stress. In: American Society of Agronomy Meetings, Paper number 3, pp 13–14
Xiang BB, Zhu YR, Wang WJ, Bai YL, Wang Y (2011) Influence of methyl jasmonate on cell membrane permeability and ajmalicine accumulation in salt-stressed Catharanthus roseus suspension cells. In: International conference on Bioinformatics and Biomedical Engineering, (iCBBE) 2011, Wuhan, 10–12 May 2011, pp 1–4
Yamane H, Abe H, Takahashi N (1982) Jasmonic acid and methyl jasmonate in pollens and anthers of three Camellia species. Plant Cell Physiol 23:1125–1127
Yoon JY, Hamayun M, Lee SKIJ (2009) Methyl Jasmonate alleviated salinity stress in soybean. J Crop Sci Biotechnol 12(2):63–68
Yoshihara T, Omer ESA, Koshino H, Sakamura S, Kikuta Y, Koda Y (1989) Structure of a tuber-inducing stimulus from potato leaves (Solanum tuberosum L.). Agric Biol Chem 53:2835–2837
Zeinalov Yu (1982) Existence of two different ways for oxygen evolution in photosynthesis and photosynthetic unit concept. Photosynthetica 16:27–35
Acknowledgements
The author hereby thanks his colleagues Liliana Maslenkova, Tsonko Tsonev, Metodi Metodiev, and Zhivka Stoinova who have participated with their expert skills and helpful discussions through the numerous stages of the research over the years.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2013 Springer Science+Business Media, LLC
About this chapter
Cite this chapter
Popova, L.P. (2013). Role of Jasmonates in Plant Adaptation to Stress. In: Ahmad, P., Azooz, M., Prasad, M. (eds) Ecophysiology and Responses of Plants under Salt Stress. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-4747-4_14
Download citation
DOI: https://doi.org/10.1007/978-1-4614-4747-4_14
Published:
Publisher Name: Springer, New York, NY
Print ISBN: 978-1-4614-4746-7
Online ISBN: 978-1-4614-4747-4
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)