Abstract
Higher plants synthesize large array of phenolic metabolites. Phenolics are defined as “specialized metabolites” due to the observation that each plant lineage synthesizes a distinct set of specialized metabolites appropriate for its environment. These metabolites provide the plant with specific adaptations to changing environmental conditions, and, therefore, they are essential for plant defense mechanisms. These defense mechanisms are costly for plants due to the energy drain from growth and development toward defensive metabolite production. Therefore, being limited with environmental resources, plants have to decide how to allocate these resources to various competing functions. This decision brings about trade-off between growth and adaptive response. This chapter suggests that perception of abiotic stress and consequent increased level of defensive phenolic metabolites are linked by a sequence of biochemical processes that also involves the intracellular free proline and the oxidative pentose phosphate pathway. The chapter also shows that, once plant tissues respond to stress, in acclimated tissues, the establishment of a negative correlation between primary metabolism (growth) and secondary metabolism (defense compounds) is observed.
References
Noel JP, Austin MB, Bomati EK (2005) Structure–function relationships in plant phenylpropanoid biosynthesis. Curr Opin Plant Biol 8:249–253
Ferrer JL, Austin MB, Stewart C Jr, Noel JP (2008) Structure and function of enzymes involved in the biosynthesis of phenylpropanoids. Plant Physiol Biochem 46:356–370
Cheynier V, Comte G, Davies KM, Lattanzio V, Martens S (2013) Plant phenolics: recent advances on their biosynthesis, genetics, and ecophysiology. Plant Physiol Biochem 72:1–20
Lattanzio V (2013) Phenolic compounds: introduction. In: Ramawat KG, Merillon JM (eds) Handbook of natural products. Springer-Verlag, Berlin Heidelberg, pp 1543–1580
Pichersky E, Lewinsohn E (2011) Convergent evolution in plant specialized metabolism. Annu Rev Plant Biol 62:549–566
Mizutani M, Ohta D (2010) Diversification of P450 genes during land plant evolution. Annu Rev Plant Biol 61:291–315
Lowry B, Lee D, Hébant C (1980) The origin of land plants: a new look at an old problem. Taxon 29:183–197
Swain T (1981) Point of view. The origin of land plants: a new look at an old problem. Taxon 30:471
Lowry JB, Lee DW, Hébant C (1983) The origin of land plants: a reply to Swain. Taxon 32:101–103
Caldwell MM (1979) Plant life and ultraviolet radiation: some perspectives in the history of the Earth’s UV climate. Bioscience 29:520–525
Rozema J, van de Staaij J, Björn LO, Caldwell MM (1997) UV-B as an environmental factor in plant life: stress and regulation. Trends Ecol Evol 12:22–28
Waters ER (2003) Molecular adaptation and the origin of land plants. MolPhylogenetEvol 29:456–463
Kenrick P, Crane P (1997) The origin and early evolution of plants on land. Nature 389:33–39
Trewavas A (2003) Aspects of plant intelligence. Ann Bot 92:1–20
Brenner ED, Stahlberg R, Mancuso S, Vivanco J, Baluska F, Van Volkenburgh E (2006) Plant neurobiology: an integrated view of plant signaling. Trends Plant Sci 11:413–419
Boudet AM (2007) Evolution and current status of research in phenolic compounds. Phytochemistry 68:2722–2735
Jung E, Zamir LO, Jensen RA (1986) Chloroplasts of higher plants synthesize l-phenylalanine via l-arogenate. Proc Natl Acad Sci U S A 83:7231–7235
Herrmann KM, Weaver LM (1999) The shikimate pathway. Annu Rev Plant Physiol Plant Mol Biol 50:473–503
Tzin V, Galili G (2010) The biosynthetic pathways for shikimate and aromatic amino acids in Arabidopsis thaliana. The Arabidopsis Book 8:e0132
Maeda H, Dudareva N (2012) The shikimate pathway and aromatic amino acid biosynthesis in plants. Ann Rev Plant Biol 63:73–105
Galili G, Amir R, Fernie AR (2016) The regulation of essential amino acid synthesis and accumulation in plants. Annu Rev Plant Biol 67:153–178
Boudet AM, Graziana A, Ranjeva R (1985) Recent advances in the regulation of the prearomatic pathway. In: Van Sumere CF, Lea PJ (eds) The biochemistry of plant phenolics, annual proceedings of the phytochemical society of Europe, vol 25. Clarendon Press, Oxford, pp 135–159
Morris PF, Doong RL, Jensen RA (1989) Evidence from Solanum tuberosum in support of the dual-pathway hypothesis of aromatic biosynthesis. Plant Physiol 89:10–14
Ganson RJ, D’Amato TA, Jensen RA (1986) The two isozyme system of 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase in Nicotiana silvestris and other higher plants. Plant Physiol 82:203–210
Goers SK, Jensen RA (1984) Separation and characterization of two chorismate-mutase isoenzymes from Nicotiana silvestris. Planta 162:109–116
Gorlach J, Schmid J, Amrhein N (1993) Differential expression of tomato (Lycopersicon esculentum L.) genes encoding shikimate pathway isoenzymes. II. Chorismate synthase. Plant MolBiol 23:707–716
Hrazdina G, Jensen RA (1992) Spatial organization of enzymes in plant metabolic pathways. Annu Rev Plant Physiol Plant Mol Biol 43:241–267
D’Amato TA, Ganson R, Gaines CG, Jensen RA (1984) Subcellular localization of chorismate-mutase isoenzymes in protoplasts from mesophyll and suspension-cultured cells of Nicotiana silvestris. Planta 162:104–108
Doong RL, Jensen RA (1992) Synonymy of the three apparent isoenzymes of 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase in Pisum sativum L. with 3-deoxy-D-manno-octulosonate 8-phosphate synthase and the DS/co DS-Mn isoenzyme pair. New Phytol 121:165–171
Suzuki N, Sakuta M, Shimizu S, Komamine A (1995) Changes in the activity of 3-deoxy- D-arabino-heptulosonate 7-phosphate (DAHP) synthase in suspension-cultured cells of Vitis. Physiol Plant 94:591–596
Widhalm JR, Gutensohn M, Yoo H, Adebesin F, Qian Y, Guo L, Jaini R, Lynch JH, McCoy RM, Shreve JT, Thimmapuram J, Rhodes D, Morgan JA, Dudareva N (2015) Identification of a plastidial phenylalanine exporter that influences flux distribution through the phenylalanine biosynthetic network. Nat Commun 6:8142
Widhalm JR, Dudareva N (2015) A familiar ring to it: biosynthesis of plant benzoic acids. Mol Plant 8:83–97
Cho M, Corea O, Yang H, Bedgar D, Laskar D, Anterola A, Moog-Anterola F, Hood R, Kohalmi S, Bernards M, Kang C, Davin L, Lewis N (2007) Phenylalanine biosynthesis in Arabidopsis thaliana identification and characterization of arogenate dehydratases. J Biol Chem 282:30827–30835
Maeda H, Yoo H, Dudareva N (2011) Prephenate aminotransferase directs plant phenylalanine biosynthesis via arogenate. Nat Chem Biol 7:19–21
Yamada T, Matsuda F, Kasai K, Fukuoka S, Kitamura K, Tozawa Y, Miyagawa H, Wakasa K (2008) Mutation of a rice gene encoding a phenylalanine biosynthetic enzyme results in accumulation of phenylalanine and tryptophan. Plant Cell 20:1316–1329
Yoo H, Widhalm JR, Qian Y, Maeda H, Cooper BR, Jannasch AS, Gonda I, Lewinsohn E, Rhodes D, Dudareva N (2013) An alternative pathway contributes to phenylalanine biosynthesis in plants via a cytosolic tyrosine: phenylpyruvate aminotransferase. Nat Commun 4:2833
Wheeler KA, Lamb HK, Hawkins AR (1996) Control of metabolic flux through the quinate pathway in Aspergillus nidulans. Biochem J 315:195–205
Serino L, Reimmann C, Baur H, Beyeler M, Visca P, Haas D (1995) Structural genes for salicylate biosynthesis from chorismate in Pseudomonas aeruginosa. Mol Gen Genet 249:217–228
Wildermuth MC, Dewdney J, Wu G, Ausubel FM (2001) Isochorismate synthase is required to synthesize salicylic acid for plant defence. Nature 414:562–571
Gaille C, Kast P, Haas D (2002) Salicylate biosynthesis in Pseudomonas aeruginosa. Purification and characterization of PchB, a novel bifunctional enzyme displaying isochorismate pyruvate-lyase and chorismate mutase activities. J Biol Chem 277:1768–21775
Wildermuth MC (2006) Variations on a theme: synthesis and modification of plant benzoic acids. Curr Opin Plant Biol 9:288–296
Vlot AC, Dempsey DA, Klessig DF (2009) Salicylic acid, a multifaceted hormone to combat disease. Annu Rev Phytopathol 47:177–206
Stafford HA (1974) The metabolism of aromatic compounds. Annu Rev Plant Physiol 25:459–486
Winkel-Shirley B (1999) Evidence for enzyme complexes in the phenylpropanoid and flavonoid pathways. Physiol Plant 107:142–149
Winkel BS (2004) Metabolic channeling in plants. Annu Rev Plant Biol 55:85–107
Jorgensen K, Rasmussen AV, Morant M, Nielsen AH, Bjarnholt N, Zagrobelny M, Bak S, Møller BL (2005) Metabolon formation and metabolic channeling in the biosynthesis of plant natural products. Curr Opin Plant Biol 8:280–291
Ralston L, Yu O (2006) Metabolons involving plant cytochrome P450. Phytochem Rev 5:459–472
Knudsen C, Gallage NJ, Hansen CC, Møller BL, Laursen T (2018) Dynamic metabolic solutions to the sessile life style of plants. Nat Prod Rep 35:1140–1155
Dixon RA, Achnine L, Kota P, Liu C-J, Reddy MSS, Wang L (2002) The phenylpropanoid pathway and plant defence – a genomics perspective. Mol Plant Pathol 3:371–390
Winkel-Shirley B (2001) Flavonoid biosynthesis: a colorful model for genetics, biochemistry, cell biology and biotechnology. Plant Physiol 126:485–493
Anterola AM, Jeon JH, Davin LB, Lewis NG (2002) Transcriptional control of monolignol biosynthesis in Pinus taeda. (factors affecting monolignol ratios and carbon allocations in phenylpropanoid metabolism). J Biol Chem 277:18272–18280
Boerjan W, Ralph J, Baucher M (2003) Lignin biosynthesis. Annu Rev Plant Biol 54:519–546
Davin LB, Jourdes M, Patten AM, Kim K-W, Vassaõ DG, Lewis NG (2008) Dissection of lignin macromolecular configuration and assembly: comparison to related biochemical processes in allyl/propenyl phenol and lignan biosynthesis. Nat Prod Rep 25:1015–1090
Vanholme R, Morreel K, Darrah C, Oyarce P, Grabber JH, Ralph J, Boerjan W (2012) Metabolic engineering of novel lignin in biomass crops. New Phytol 196:978–1000
Rinaldi R, Jastrzebshi R, Clough MT, Ralph J, Kennema M, Bruijnincx PCA, Weckhuysen BM (2016) Paving the way for lignin valorisation: recent advances in bioengineering, biorefining and catalysis. Angew Chem Int Ed Engl 55:8164–8215
Humphreys JM, Chapple C (2002) Rewriting the lignin roadmap. Curr Opin Plant Biol 5:224–229
Schoch G, Morant M, Abdulrazzak N, Asnaghi C, Goepfert S, Petersen M, Ullmann P, Werck-Reichhart D (2006) The meta-hydroxylation step in the phenylpropanoid pathway: a new level of complexity in the pathway and its regulation. Environ Chem Lett 4:127–136
Chen H-C, Li Q, Shuford CM, Liu J, Muddiman DC, Sederoff RR, Chiang VL (2011) Membrane protein complexes catalyze both 4-and 3-hydroxylation of cinnamic acid derivatives in monolignol biosynthesis. Proc Natl Acad Sci U S A 108:21253–21258
Nicotra AB, Atkin OK, Bonser SP, Davidson AM, Finnegan EJ, Mathesius U, Poot P, Purugganan MD, Richards CL, Valladares F, van Kleunen M (2010) Plant phenotypic plasticity in a changing climate. Trends Plant Sci 15:684–692
Mithöfer A, Boland W (2012) Plant defense against herbivores: chemical aspects. Annu Rev Plant Biol 63:431–450
Caretto S, Linsalata V, Colella G, Mita G, Lattanzio V (2015) Carbon fluxes between primary metabolism and phenolic pathway in plant tissues under stress. Int J Mol Sci 16:26378–26394
Dixon RA, Lamb CJ, Masoud S, Sewalt VJ, Paiva NL (1996) Metabolic engineering: prospects for crop improvement through the genetic manipulation of phenylpropanoid biosynthesis and defense responses-a review. Gene 179:61–71
Lattanzio V, Lattanzio VMT, Cardinali A (2006) Role of phenolics in the resistance mechanisms of plants against fungal pathogens and insects. In: Imperato F (ed) Phytochemistry: advances in research. Research Signpost, Trivandrum, pp 23–67
Ferreira RB, Monteiro S, Freitas R, Santos CN, Chen Z, Batista LM, Duarte J, Borges A, Teixeira AR (2007) The role of plant defence proteins in fungal pathogenesis. Mol Plant Pathol 8:677–700
Karban R (2008) Plant behaviour and communication. Ecol Lett 11:727–739
Lattanzio V, Kroon PA, Quideau S, Treutter D (2008) Plant phenolics – secondary metabolites with diverse functions. In: Daayf F, Lattanzio V (eds) Recent advances in polyphenol research, vol 1. Wiley-Blackwell Publishing, Oxford, pp 1–35
Lattanzio V, Cardinali A, Linsalata V (2012) Plant phenolics: a biochemical and physiological perspective. In: Cheynier V, Sarni-Manchado P, Quideau S (eds) Recent advances in polyphenols research, vol 3. Wiley-Blackwell Publishing, Oxford, pp 1–39
Osbourn AE (1996) Preformed antimicrobial compounds and plant defense against fungal attack. Plant Cell 8:1821–1831
Purrington CB (2000) Costs of resistance. Curr Opin Plant Biol 3:305–308
Wittstock U, Gershenzon J (2002) Constitutive plant toxins and their role in defense against herbivores and pathogens. Curr Opin Plant Biol 5:300–307
Van Hulten M, Pelser M, Van Loon LC, Pieterse CMJ, Ton J (2006) Costs and benefits of priming for defense in Arabidopsis. Proc Natl Acad Sci U S A 103:5602–5607
Conrath U, Beckers GJM, Langenbach CJG, Jaskiewicz MR (2015) Priming for enhanced defense. Annu Rev Phytopathol 53:97–119
Martinez-Medina A, Flors V, Heil M, Mauch-Mani B, Pieterse CMJ, Pozo MJ, Ton J, van Dam NM, Conrath U (2016) Recognizing plant defense priming. Trends Plant Sci 21:818–822
Karasov TL, Chae E, Herman JJ, Bergelson J (2017) Mechanisms to mitigate the trade-off between growth and defense. Plant Cell 29:666–680
Atkinson NJ, Urwin PE (2012) The interaction of plant biotic and abiotic stresses: from genes to the field. J Exp Bot 63:3523–3543
Suzuki N, Rivero RM, Shulaev V, Blumwald E, Mittler R (2014) Abiotic and biotic stress combinations. New Phytol 203:32–43
Naoumkina MA, Zhao Q, Gallego-Giraldo L, Dai X, Zhao PX, Dixon RA (2010) Genome-wide analysis of phenylpropanoid defence pathways. Mol Plant Pathol 11:829–846
Link KP, Dickson AD, Walker JC (1929) Further observations on the occurrence of protocatechuic acid in pigmented onion scales and its relation to disease resistance in onions. J Biol Chem 84:719–725
Link KP, Walker JC (1933) The isolation of catechol from pigmented onion scales and its significance in relation to disease resistance in onions. J Biol Chem 100:379–383
Lattanzio V (2003) Bioactive polyphenols: their role in quality and storability of fruit and vegetables. J Appl Bot 77:128–146
Painter RH (1941) The economic value and biologic significance of insect resistance in plants. J Econ Entomol 34:358–367
Harborne JB (1997) Recent advances in chemical ecology. Nat Prod Rep 14:83–97
Harborne JB (1999) Recent advances in chemical ecology. Nat Prod Rep 16:509–523
Harborne JB (2001) Twenty-five years of chemical ecology. Nat Prod Rep 18:361–379
Simmonds MSJ (2003) Flavonoid-insect interactions: recent advances in our knowledge. Phytochemistry 64:21–30
Barbehenn R, Weir Q, Salminen J-P (2008) Oxidation of ingested phenolics in the tree feeding caterpillar Orgyia leucostigma depends on foliar chemical composition. J Chem Ecol 34:748–756
Lattanzio V, Arpaia S, Cardinali A, Di Venere D, Linsalata V (2000) Role of endogenous flavonoids in resistance mechanism of Vigna to aphids. J Agric Food Chem 48:5316–5320
De Vos M, Van Oosten VR, Van Poecke RMP, Van Pelt JA, Pozo MJ, Mueller MJ, Buchala AJ, Metraux JP, Van Loon LC, Dicke M, Pieterse CMJ (2005) Signal signature and transcriptome changes of Arabidopsis during pathogen and insect attack. Mol Plant-Microbe Interact 18:923–937
Heil M (2009) Damaged-self recognition in plant herbivore defence. Trends Plant Sci 14:356–363
Foyer CH, Rasool B, Davey JW, Hancock RD (2016) Cross-tolerance to biotic and abiotic stresses in plants: a focus on resistance to aphid infestation. J Exp Bot 67:2025–2037
Lortzing V, Oberlander J, Lortzing T, Tohge T, Steppuhn A, Kunze R, Hilker M (2019) Insect egg deposition renders plant defense against hatching larvae more effective in a salicylic acid-dependent manner. Plant Cell Environ 42:1019–1032
Shade RE, Schroeder HE, Pueyo JJ, Tabe LM, Murdock LL, Higgins TGV, Chrispeels MJ (1994) Transgenic pea seeds expressing the α-amylase inhibitor of the common bean are resistant to bruchid beetles. Biotechnology 12:793–796
Lattanzio V, Terzano R, Cicco N, Cardinali A, Di Venere D, Linsalata V (2005) Seed coat tannins and bruchid resistance in stored cowpea seeds. J Sci Food Agric 85:839–846
Appel HM (1993) Phenolics in ecological interactions – the importance of oxidation. J Chem Ecol 19:1521–1552
Salminen J, Karonen M (2011) Chemical ecology of tannins and other phenolics: we need a change in approach. Funct Ecol 25:325–338
Constabel P, Yoshida K, Walker V (2014) Diverse ecological roles of plant tannins: plant defense and beyond. In: Romani A, Lattanzio V, Quideau S (eds) Recent advances in polyphenol research, vol 4. Wiley-Blackwell Publishing, Oxford, pp 115–142
Lattanzio V, Linsalata V, Palmieri S, Van Sumere CF (1989) The beneficial effect of citric and ascorbic acid on the phenolic browning reaction in stored artichoke (Cynara scolymus L.) heads. Food Chem 33:93–106
Thomashow MF (1999) Plant cold acclimation: freezing tolerance genes and regulatory mechanisms. Annu Rev Plant Biol 50:571–599
Yamaguchi-Shinozaki K, Shinozaki K (2006) Transcriptional regulatory networks in cellular responses and tolerance to dehydration and cold stresses. Annu Rev Plant Biol 57:781–803
Chinnusamy V, Zhu JH, Zhu JK (2007) Cold stress regulation of gene expression in plants. Trends Plant Sci 12:444–451
Engelsma G (1970) Low-temperature effects on phenylalanine ammonia-lyase activity in gherkin seedlings. Planta 91:246–254
Rhodes MJC, Wooltorton LSC, Hill AC (1981) Changes in phenolic metabolism in fruit and vegetable tissues under stress. In: Friend J, Rhodes MJC (eds) Recent advances in the biochemistry of fruit and vegetables. Academic Press, London, pp 191–220
Lattanzio V, Van Sumere CF (1987) Changes in phenolic compounds during the development and cold storage of artichoke (Cynara scolymus L.) heads. Food Chem 24:37–50
Kasai A, Ohnishi S, Yamazaki H, Funatsuki H, Kurauchi T, Matsumoto T, Yumoto S, Senda M (2009) Molecular mechanism of seed coat discoloration induced by low temperature in yellow soybean. Plant Cell Physiol 50:1090–1098
Guyot S, Bernillon S, Poupard P, Renard CMGC (2008) Multiplicity of phenolic oxidation products in apple juices and ciders, from synthetic medium to commercial products. In: Daayf F, Lattanzio V (eds) Recent advances in polyphenol research, vol 1. Wiley-Blackwell, Oxford, pp 278–292
Tinkler CK (1931) LXXXVII. The blackening of potatoes after cooking. Biochem J 25:773–776
Hughes JC, Ayers JE, Swain T (1962) After-cooking blackening in potatoes. I. Introduction and analytical methods. J Sci Food Agric 13:224–229
Brenes M, Romero C, García P, Garrido A (1995) Effect of pH on the color formed by Fe-phenolic complexes in ripe olives. J Sci Food Agric 67:35–41
Cheng GW, Crisosto CH (1997) Iron-polyphenol complex formation and skin discoloration in peaches and nectarines. J Am Soc Hortic Sci 122:95–99
Marsilio V, Campestre C, Lanza B (2001) Phenolic compounds change during California-style ripe olive processing. Food Chem 74:55–60
Lattanzio V, Cardinali A, Di Venere D, Linsalata V, Palmieri S (1994) Browning phenomena in stored artichoke (Cynara scolymus L.) heads: enzymic or chemical reactions? Food Chem 50:1–7
Brillouet JM, Romieu C, Schoefs B, Solymosi K, Cheynier V, Fulcrand H, Verdeil JL, Conéjéro G (2013) The tannosome is an organelle forming condensed tannins in the chlorophyllous organs of Tracheophyta. Ann Bot 112:1003–1014
Gallage NJ, Jørgensen K, Janfelt C, Nielsen AJZ, Naake T, Duński E, Dalsten L, Grisoni M, Møller BL (2018) The intracellular localization of the vanillin biosynthetic machinery in pods of Vanilla planifolia. Plant Cell Physiol 59:304–318
Overeem JC (1976) Preexisting antimicrobial substances in plants and their role in disease resistance. In: Friend J, Threlfall DR (eds) Biochemical aspects of plant parasite relationships. Academic Press, London, pp 195–206
Oszmianski J, Lee CY (1991) Enzymatic oxidation of phloretin glucoside in model system. J Agric Food Chem 39:10050–11052
Lattanzio V, Di Venere D, Linsalata V, Bertolini P, Ippolito A, Salerno M (2001) Low temperature metabolism of apple phenolics and quiescence of Phlyctaena vagabunda. J Agric Food Chem 49:5817–5821
Raa J, Overeem JC (1968) Transformation reactions of phloridzin in the presence of apple leaf enzymes. Phytochemistry 7:721–731
Guyot S, Serrand S, Le Queré JM, Sanoner P, Renard CMGC (2007) Enzymatic synthesis and physicochemical characterisation of phloridzin oxidation products (POP), a new water-soluble yellow dye deriving from apple. Innov Food Sci Emerg 8:443–450
Mondolot L, Marlas A, Barbeau D, Gargadennec A, Pujol B, McKey DB (2008) Domestication and defence: foliar tannins and C/N ratios in cassava and a close wild relative. Acta Oecol 34:147–154
Gepts P, Famula TR, Bettinger RL, Brush SB, Damania AB, McGuire PE, Qualset CO (2012) Biodiversity in agriculture: domestication, evolution and sustainability. Cambridge University Press, Cambridge
Guillén S, Casas A, Terrazas T, Vega E, Martínez-Palacios M (2013) Differential survival and growth of wild and cultivated seedlings of columnar cacti: consequences of domestication. Am J Bot 100:2364–2379
Shi J, Lai J (2015) Patterns of genomic changes with crop domestication and breeding. Curr Opin Plant Biol 24:47–53
Simpson KJ, Wade RN, Rees M, Osborne CP, Hartley SE (2017) Still armed after domestication? Impacts of domestication and agronomic selection on silicon defences in cereals. Funct Ecol 31:2108–2117
Turcotte MM, Araki H, Karp DS, Poveda K, Whitehead SR (2017) The ecoevolutionary impacts of domestication and agricultural practices on wild species. Phil Trans R Soc B 372:20160033
Whitehead SR, Turcotte MM, Poveda K (2017) Domestication impacts on plant–herbivore interactions: a meta-analysis. Phil Trans R Soc B 372:20160034
Bernal JS, Medina RF (2018) Agriculture sows pests: how crop domestication, host shifts, and agricultural intensification can create insect pests from herbivores. Curr Opin Insect Sci 26:76–81
Ahuja I, de Vos RCH, Bones AM, Hall RD (2010) Plant molecular stress responses face climate change. Trends Plant Sci 15:664–674
McClure JW (1975) Physiology and function of flavonoids. In: Harborne JB, Mabry TJ, Mabry H (eds) The flavonoids. Academic Press, London, pp 970–1055
Gottlieb OR (1986) Phytochemical evolution. Rev Acad Coloumb Ci Ex Fis Nat 16:39–45
Hertweck C (2009) The biosynthetic logic of polyketide diversity. Angew Chem Int Ed 48:4688–4716
Gottlieb OR (1989) The role of oxygen in phytochemical evolution towards diversity. Phytochemistry 28:2545–2558
Gottlieb OR, Kaplan MAC (1993) Phytochemical evolution: the redox theory. Nat Prod Lett 2:171–176
Herms DA, Mattson WJ (1992) The dilemma of plants: to grow or defend. Q Rev Biol 67:283–335
Lattanzio V, Cardinali A, Ruta C, Morone Fortunato I, Lattanzio VMT, Linsalata V, Cicco N (2009) Relationship of secondary metabolism to growth in oregano (Origanum vulgare L.) shoot cultures under nutritional stress. Environ Exp Bot 65:54–62
Lattanzio V, Caretto S, Linsalata V, Colella G, Mita G (2018) Signal transduction in artichoke [Cynara cardunculus L. subsp. scolymus (L.) Hayek] callus and cell suspension cultures under nutritional stress. Plant Physiol Biochem 127:97–103
Hare PD, Cress WA, van Staden J (1998) Dissecting the roles of osmolyte accumulation in plants. Plant Cell Environ 21:535–553
KaviKishor PB, Sangam S, Amrutha RN, Sri Laxmi P, Naidu KR, Rao KRSS, Rao S, Reddy KJ, Theriappan P, Sreenivasulu N (2005) Regulation of proline biosynthesis, degradation, uptake and transport in higher plants: its implications in plant growth and abiotic stress tolerance. Curr Sci 88:424–438
Krasensky J, Jonak C (2012) Drought, salt, and temperature stress-induced metabolic rearrangements and regulatory networks. J Exp Bot 63:1593–1608
Scharte J, Schön H, Tjaden Z, Weis E, von Schaewen A (2009) Isoenzyme replacement of glucose-6-phosphate dehydrogenase in the cytosol improves stress tolerance in plants. Proc Natl Acad Sci U S A 106:8061–8066
Aerts R, Chapin IIIFS (2000) The mineral nutrition of wild plants revisited: a re-evaluation of processes and patterns. Adv Ecol Res 30:1–67
Donaldson JR, Kruger EL, Lindroth RL (2006) Competition- and resource-mediated tradeoffs between growth and defensive chemistry in trembling aspen (Populus tremuloides). New Phytol 169:561–570
Endara M-J, Coley PD (2011) The resource availability hypothesis revisited: a meta-analysis. Funct Ecol 25:389–398
Heil M, Hilpert A, Kaiser W, Linsenmair E (2000) Reduced growth and seed set following chemical induction of pathogen defence: does systemic acquired resistance (SAR) incur allocation costs? J Ecol 88:645–654
Heil M, Baldwin IT (2002) Fitness costs of induced resistance: emerging experimental support for a slippery concept. Trends Plant Sci 7:61–67
Strauss SY, Rudgers JA, Lau JA, Irwin RE (2002) Direct and ecological costs of resistance to herbivory. Trends Ecol Evol 17:278–284
Eicks M, Maurino V, Knappe S, Flügge UI, Fischer K (2002) The plastidic pentose phosphate translocator represents a link between the cytosolic and the plastidic pentose phosphate pathways in plants. Plant Physiol 128:512–522
Kruger NJ, von Schaewen A (2003) The oxidative pentose phosphate pathway: structure and organisation. Curr Opin Plant Biol 6:236–246
Verslues PE, Sharma S (2010) Proline metabolism and its implications for plant-environment interaction. The Arabidopsis Book 8:e0140
Tanner JJ, Fendt S-M, Becker DF (2018) The proline cycle as a potential cancer therapy target. Biochemistry 57:3433–3444
Tobin AK, Yamaya T (2001) Cellular compartmentation of ammonium assimilation in rice and barley. J Exp Bot 52:591–604
Bernard SM, Habash DZ (2009) The importance of cytosolic glutamine synthetase in nitrogen assimilation and recycling. New Phytol 182:608–620
Masclaux-Daubresse C, Daniel-Vedele F, Dechorgnat J, Chardon F, Gaufichon L, Suzuki A (2010) Nitrogen uptake, assimilation and remobilization in plants: challenges for sustainable and productive agriculture. Ann Bot 105:1141–1157
Razal RA, Ellis S, Singh S, Lewis NG, Towers GHN (1996) Nitrogen recycling in phenylpropanoid metabolism. Phytochemistry 41:31–35
vanHeerden PS, Towers GHN, Lewis NG (1996) Nitrogen metabolism in lignifying Pinus taeda cell cultures. J Biol Chem 271:12350–12355
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Lattanzio, V. (2019). Relationship of Phenolic Metabolism to Growth in Plant and Cell Cultures Under Stress. In: Ramawat, K., Ekiert, H., Goyal, S. (eds) Plant Cell and Tissue Differentiation and Secondary Metabolites. Reference Series in Phytochemistry. Springer, Cham. https://doi.org/10.1007/978-3-030-11253-0_8-1
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