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N Use By Plants
Nitrate Assimilation
Ammonia Assimilation
Glu, Gln, Asn, Gly, Ser
Aminotransferases
Asp, Ala, GABA
Val, Leu, Ileu, Thr, Lys
Pro, Arg, Orn
Polyamines
Non-protein AAs
Alkaloids
Sulfate Assimilation
Cys, Met, AdoMet, ACC
His, Phe, Tyr, Tryp
Secondary Products
Onium Compounds
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References
HORT640 - Metabolic Plant Physiology

References, monoterpene

Afolayan AF, Mann MG, Lategan CA, Smith PJ, Bolton JJ, Beukes DR. Antiplasmodial halogenated monoterpenes from the marine red alga Plocamium cornutum. Phytochemistry 70: 597-600 (2009).

Aharoni A, Giri AP, Deuerlein S, Griepink F, de Kogel WJ, Verstappen FW, Verhoeven HA, Jongsma MA, Schwab W, Bouwmeester HJ. Terpenoid metabolism in wild-type and transgenic Arabidopsis plants. Plant Cell 15: 2866-2884 (2003).

Aharoni A, Giri AP, Verstappen FW, Bertea CM, Sevenier R, Sun Z, Jongsma MA, Schwab W, Bouwmeester HJ. Gain and loss of fruit flavor compounds produced by wild and cultivated strawberry species. Plant Cell 16: 3110-3131 (2004).

Andersson S, Dobson HE. Antennal responses to floral scents in the butterfly Heliconius melpomene. J. Chem. Ecol. 29: 2319-2330 (2003).

Anero R, Díaz-Lanza A, Ollivier E, Baghdikian B, Balansard G, Bernabe M. Monoterpene glycosides isolated from Fadogia agrestis. Phytochemistry 69: 805-811 (2008).

Bartram S, Jux A, Gleixner G, Boland W. Dynamic pathway allocation in early terpenoid biosynthesis of stress-induced lima bean leaves. Phytochemistry 67: 1661-1672 (2006).

Besser K, Harper A, Welsby N, Schauvinhold I, Slocombe S, Li Y, Dixon RA, Broun P. Divergent regulation of terpenoid metabolism in the trichomes of wild and cultivated tomato species. Plant Physiol. 149: 499-514 (2009).

Bohlmann J, Martin D, Oldham NJ, Gershenzon J. Terpenoid secondary metabolism in Arabidopsis thaliana: cDNA cloning, characterization, and functional expression of a myrcene/(E)-beta-ocimene synthase. Arch. Biochem. Biophys. 375: 261-269 (2000).

Bohlmann J, Phillips M, Ramachandiran V, Katoh S, Croteau R. cDNA cloning, characterization, and functional expression of four new monoterpene synthase members of the Tpsd gene family from grand fir (Abies grandis). Arch. Biochem. Biophys. 368: 232-243 (1999).

Bouvier F, Suire C, D'Harlingue A, Backhaus RA, Camara B. Molecular cloning of geranyl diphosphate synthase and compartmentation of monoterpene synthesis in plant cells. Plant J. 24: 241-252 (2000).

Bouwmeester HJ, Gershenzon J, Konings MC, Croteau R. Biosynthesis of the monoterpenes limonene and carvone in the fruit of caraway. I. Demonstration of enzyme activities and their changes with development. Plant Physiol. 117: 901-912 (1998).

Brilli F, Ciccioli P, Frattoni M, Prestininzi M, Spanedda AF, Loreto F. Constitutive and herbivore-induced monoterpenes emitted by Populus x euroamericana leaves are key volatiles that orient Chrysomela populi beetles. Plant Cell Environ. 32: 542-552 (2009).

Burlat V, Oudin A, Courtois M, Rideau M, St-Pierre B. Co-expression of three MEP pathway genes and geraniol 10-hydroxylase in internal phloem parenchyma of Catharanthus roseus implicates multicellular translocation of intermediates during the biosynthesis of monoterpene indole alkaloids… Plant J. 38: 131-141 (2004).

Byers JA, Zhang QH, Birgersson G. Strategies of a bark beetle, Pityogenes bidentatus, in an olfactory landscape. Naturwissenschaften 87: 503-507 (2000).

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Chen F, Ro DK, Petri J, Gershenzon J, Bohlmann J, Pichersky E, Tholl D. Characterization of a root-specific Arabidopsis terpene synthase responsible for the formation of the volatile monoterpene 1,8-cineole. Plant Physiol. 135: 1956-1966 (2004).

Chen F, Tholl D, D'Auria JC, Farooq A, Pichersky E, Gershenzon J. Biosynthesis and emission of terpenoid volatiles from Arabidopsis flowers. Plant Cell 15: 481-494 (2003).

Chevance FF, Farmer LJ. Identification of major volatile odor compounds in frankfurters. J. Agric. Food Chem. 47: 5151-5160 (1999).

Connor EC, Rott AS, Zeder M, Juttner F, Dorn S. 13C-Labelling patterns of green leaf volatiles indicating different dynamics of precursors in Brassica leaves. Phytochemistry 69: 1304-1312 (2008).

Copolovici LO, Filella I, Llusia J, Niinemets U, Penuelas J. The capacity for thermal protection of photosynthetic electron transport varies for different monoterpenes in Quercus ilex. Plant Physiol. 139: 485-496 (2005).

Cunningham JP, Moore CJ, Zalucki MP, Cribb BW. Insect odour perception: recognition of odour components by flower foraging moths. Proc. Biol. Sci. 273: 2035-2040 (2006).

Curado MA, Oliveira CB, Jesus JG, Santos SC, Seraphin JC, Ferri PH. Environmental factors influence on chemical polymorphism of the essential oils of Lychnophora ericoides. Phytochemistry 67: 2363-2369 (2006).

Custodio L, Serra H, Nogueira JM, Goncalves S, Romano A. Analysis of the volatiles emitted by whole flowers and isolated flower organs of the carob tree using HS-SPME-GC/MS. J. Chem. Ecol. 32: 929-942 (2006).

Davidovich-Rikanati R, Lewinsohn E, Bar E, Iijima Y, Pichersky E, Sitrit Y. Overexpression of the lemon basil alpha-zingiberene synthase gene (ZIS) increases both mono- and sesquiterpene contents in tomato fruit. Plant J. 56: 228-238 (2008).

Davis EM, Ringer KL, McConkey ME, Croteau R. Monoterpene metabolism. Cloning, expression, and characterization of menthone reductases from peppermint. Plant Physiol. 137: 873-881 (2005).

Dawson GW, Pickett JA, Smiley DW. The aphid sex pheromone cyclopentanoids: synthesis in the elucidation of structure and biosynthetic pathways. Bioorg. Med. Chem. 4: 351-361 (1996).

Diaz-Maroto MC, Perez-Coello MS, Gonzalez Vinas MA, Cabezudo MD. Influence of drying on the flavor quality of spearmint (Mentha spicata L.). J. Agric. Food Chem. 51: 1265-1269 (2003).

Dotterl S, Burkhardt D, Jurgens A, Mosandl A. Stereoisomeric pattern of lilac aldehyde in Silene latifolia, a plant involved in a nursery pollination system. Phytochemistry 68: 499-504 (2007).

Dudareva N, Andersson S, Orlova I, Gatto N, Reichelt M, Rhodes D, Boland W, Gershenzon J. The nonmevalonate pathway supports both monoterpene and sesquiterpene formation in snapdragon flowers. Proc. Natl. Acad. Sci. U.S.A. 102: 933-938 (2005).

Dudareva N, Cseke L, Blanc VM, Pichersky E. Evolution of floral scent in Clarkia: novel patterns of S-linalool synthase gene expression in the C. breweri flower. Plant Cell 8: 1137-1148 (1996).

Dudareva N, Martin D, Kish CM, Kolosova N, Gorenstein N, Faldt J, Miller B, Bohlmann J. (E)-beta-ocimene and myrcene synthase genes of floral scent biosynthesis in snapdragon: function and expression of three terpene synthase genes of a new terpene synthase subfamily. Plant Cell 15: 1227-1241 (2003).

Dunphy PJ. Location and biosynthesis of monoterpenyl fatty acyl esters in rose petals. Phytochemistry 67: 1110-1119 (2006).

Faldt J, Arimura G, Gershenzon J, Takabayashi J, Bohlmann J. Functional identification of AtTPS03 as ( E)-beta-ocimene synthase: a monoterpene synthase catalyzing jasmonate- and wound-induced volatile formation in Arabidopsis thaliana. Planta 216: 745-751 (2003).

Faldt J, Martin D, Miller B, Rawat S, Bohlmann J. Traumatic resin defense in Norway spruce (Picea abies): methyl jasmonate-induced terpene synthase gene expression, and cDNA cloning and functional characterization of (+)-3-carene synthase. Plant Mol. Biol. 51: 119-133 (2003).

Fall R, Wildermuth MC. Isoprene synthase: from biochemical mechanism to emission algorithm. J. Geophys. Res. 103: 25599-25609 (1998).

Fares S, Loreto F, Kleist E, Wildt J. Stomatal uptake and stomatal deposition of ozone in isoprene and monoterpene emitting plants. Plant Biol. (Stuttg.) 10: 44-54 (2008).

Fuentes JD, Lerdau M, Atkinson R, Baldocchi D, Bottenheim JW, Ciccioli P, Lamb B, Geron C, Gu L, Guenther A, Sharkey TD, Stockwell W. Biogenic hydrocarbons in the atmospheric boundary layer: A review. Bull. Amer. Meteorol. Soc. 81: 1537-1575 (2000).

Funk C, Croteau R. Induction and characterization of a cytochrome P-450-dependent camphor hydroxylase in tissue cultures of common sage (Salvia officinalis). Plant Physiol. 101: 1231-1237 (1993).

Gauvin A, Susperregui J, Barth P, Louis R, Deleris G, Smadja J. An acetylated monoterpene and a sesquiterpene alcohol from Psiadia anchusifolia. Phytochemistry 65: 897-901 (2004).

Gershenzon J, McCaskill D, Rajaonarivony JIM, Mihaliak C, Karp F, Croteau R. Isolation of secretory cells from plant glandular trichomes and their use in biosynthetic studies of monoterpenes and other gland products. Anal. Biochem. 200: 130-138 (1992).

Gershenzon J, McConkey ME, Croteau RB. Regulation of monoterpene accumulation in leaves of peppermint. Plant Physiol. 122: 205-214 (2000).

Godard KA, White R, Bohlmann J. Monoterpene-induced molecular responses in Arabidopsis thaliana. Phytochemistry 69: 1838-1849 (2008).

Gray DW. Field response of Ips paraconfusus, Dendroctonus brevicomis, and their predators to 2-methyl-3-buten-2-ol, a novel alcohol emitted by ponderosa pine. J. Chem. Ecol. 28: 1583-1597 (2002).

Guenther A, Hewitt CN, Erickson D, Fall R, Geron C, Graedel T, Harley P, Klinger L, Lerdau M, McKay WA, Pierce T, Scholes B, Steinbrecher R, Tallamraju R, Taylor J, Zimmerman P. A global model of natural volatile organic compound emissions. J. Geophys. Res.-Atmos. 100: 8873-8892 (1995).

Guimaraes E, di Stasi LC, Maimoni-Rodella RD. Pollination biology of Jacaranda oxyphylla with an emphasis on staminode function. Ann. Bot. (Lond.) 102: 699-711 (2008).

Guyot C, Bouseta A, Scheirman V V, Collin S. Foral origin markers of chestnut and lime tree honeys. J. Agric. Food Chem. 46: 625-633 (1998).

Hallahan DL, West JM, Wallsgrove RM, Smiley DW, Dawson GW, Pickett JA, Hamilton JG. Purification and characterization of an acyclic monoterpene primary alcohol:NADP+ oxidoreductase from catmint (Nepeta racemosa). Arch. Biochem. Biophys. 318: 105-112 (1995).

Hamberger B, Bohlmann J. Cytochrome P450 mono-oxygenases in conifer genomes: discovery of members of the terpenoid oxygenase superfamily in spruce and pine. Biochem. Soc. Trans. 34: 1209-1214 (2006).

Hasegawa T, Takano F, Takata T, Niiyama M, Ohta T. Bioactive monoterpene glycosides conjugated with gallic acid from the leaves of Eucalyptus globulus. Phytochemistry 69: 747-753 (2008).

Hashida W, Tanaka N, Kashiwada Y, Sekiya M, Ikeshiro Y, Takaishi Y. Tomoeones A-H, cytotoxic phloroglucinol derivatives from Hypericum ascyron. Phytochemistry 69: 2225-2230 (2008).

Heinrich G, Pfeifhofer HW, Stabentheiner E, Sawidis T. Glandular hairs of Sigesbeckia jorullensis Kunth (Asteraceae): morphology, histochemistry and composition of essential oil. Ann. Bot. (Lond.) 89: 459-469 (2002).

Herrero O, Ramon D, Orejas M. Engineering the Saccharomyces cerevisiae isoprenoid pathway for de novo production of aromatic monoterpenes in wine. Metab. Eng. 10: 78-86 (2008).

Hoelscher DJ, Williams DC, Wildung MR, Croteau R. A cDNA clone for 3-carene synthase from Salvia stenophylla( small star, filled ). Phytochemistry 62: 1081-1086 (2003).

Hsiao YY, Jeng MF, Tsai WC, Chuang YC, Li CY, Wu TS, Kuoh CS, Chen WH, Chen HH. A novel homodimeric geranyl diphosphate synthase from the orchid Phalaenopsis bellina lacking a DD(X)2-4D motif. Plant J. 55: 719-733 (2008).

Hsiao YY, Tsai WC, Kuoh CS, Huang TH, Wang HC, Wu TS, Leu YL, Chen WH, Chen HH. Comparison of transcripts in Phalaenopsis bellina and Phalaenopsis equestris (Orchidaceae) flowers to deduce monoterpene biosynthesis pathway. BMC Plant Biol. 6: 14 (2006).

Iijima Y, Davidovich-Rikanati R, Fridman E, Gang DR, Bar E, Lewinsohn E, Pichersky E. The biochemical and molecular basis for the divergent patterns in the biosynthesis of terpenes and phenylpropenes in the peltate glands of three cultivars of basil. Plant Physiol. 136: 3724-3736 (2004).

Iijima Y, Gang DR, Fridman E, Lewinsohn E, Pichersky E. Characterization of geraniol synthase from the peltate glands of sweet basil. Plant Physiol. 134: 370-379 (2004).

Ikeda H, Esaki N, Nakai S, Hashimoto K, Uesato S, Soda K, Fujita T. Acyclic monoterpene primary alcohol:NADP+ oxidoreductase of Rauwolfia serpentina cells: the key enzyme in biosynthesis of monoterpene alcohols. J. Biochem. (Tokyo) 109: 341-347 (1991).

Jerkovic I I, Mastelic J. Volatile compounds from leaf-buds of Populus nigra L. (Salicaceae). Phytochemistry 63: 109-113 (2003).

Jurgens A, Webber AC, Gottsberger G. Floral scent compounds of Amazonian Annonaceae species pollinated by small beetles and thrips. Phytochemistry 55: 551-558 (2000).

Kampranis SC, Ioannidis D, Purvis A, Mahrez W, Ninga E, Katerelos NA, Anssour S, Dunwell JM, Degenhardt J, Makris AM, Goodenough PW, Johnson CB. Rational conversion of substrate and product specificity in a Salvia monoterpene synthase: structural insights into the evolution of terpene synthase function. Plant Cell 19: 1994-2005 (2007).

Kanemoto M, Matsunami K, Otsuka H, Shinzato T, Ishigaki C, Takeda Y. Chlorine-containing iridoid and iridoid glucoside, and other glucosides from leaves of Myoporum bontioides. Phytochemistry 69: 2517-2522 (2008).

Kant MR, Ament K, Sabelis MW, Haring MA, Schuurink RC. Differential timing of spider mite-induced direct and indirect defenses in tomato plants. Plant Physiol. 135: 483-495 (2004).

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Kim HJ, Kim K, Kim NS, Lee DS. Determination of floral fragrances of Rosa hybrida using solid-phase trapping-solvent extraction and gas chromatography-mass spectrometry. J. Chromatogr. A. 902: 389-404 (2000).

Kjeldsen F, Christensen LP, Edelenbos M. Quantitative analysis of aroma compounds in carrot (Daucus carota L.) cultivars by capillary gas chromatography using large-volume injection technique. J. Agric. Food Chem. 49: 4342-4348 (2001).

Komatsu M, Tsuda M, Omura S, Oikawa H, Ikeda H. Identification and functional analysis of genes controlling biosynthesis of 2-methylisoborneol. Proc. Natl. Acad. Sci. U.S.A. 105: 7422-7427 (2008).

Krens FA, Keizer LCP, Capel IEM. Transgenic caraway, Carum carvi L.: a model species for metabolic engineering. Plant Cell Rep. 17: 39-43 (1997).

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Kuhn U, Rottenberger S, Biesenthal T, Wolf A, Schebeske G, Ciccioli P, Kesselmeier J. Strong correlation between isoprene emission and gross photosynthetic capacity during leaf phenology of the tropical tree species Hymenaea courbaril with fundamental changes in volatile organic compounds emission composition during early leaf development. Plant Cell Environ. 27: 1469-1485 (2004).

Lange BM, Croteau R. Genetic engineering of essential oil production in mint. Curr. Opin. Plant Biol. 2: 139-144 (1999).

Lange BM, Ghassemian M. Genome organization in Arabidopsis thaliana: a survey for genes involved in isoprenoid and chlorophyll metabolism. Plant Mol. Biol. 51: 925-948 (2003).

Lange BM, Ketchum RE, Croteau RB. Isoprenoid biosynthesis. Metabolite profiling of peppermint oil gland secretory cells and application to herbicide target analysis. Plant Physiol. 127: 305-314 (2001).

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Lerdau M, Guenther A, Monson R. Plant production and emission of volatile organic compounds. Bioscience 47: 373-383 (1997).

Lewinsohn E, Gijzen M, Muzika RM, Barton K, Croteau R. Oleoresinosis in grand fir (Abies grandis) saplings and mature trees. Modulation of this wound response by light and water stresses. Plant Physiol. 101: 1021-1028 (1993).

Lewinsohn E, Schalechet F, Wilkinson J, Matsui K, Tadmor Y, Nam KH, Amar O, Lastochkin E, Larkov O, Ravid U, Hiatt W, Gepstein S, Pichersky E. Enhanced levels of the aroma and flavor compound S-linalool by metabolic engineering of the terpenoid pathway in tomato fruits. Plant Physiol. 127: 1256-1265 (2001).

Lewinsohn E, Ziv-Raz II, Dudai N, Tadmor Y, Lastochkin E, Larkov O, Chaimovitsh D, Ravid U, Putievsky E, Pichersky E, Shoham Y. Biosynthesis of estragole and methyl-eugenol in sweet basil (Ocimum basilicum L). Developmental and chemotypic association of allylphenol O-methyltransferase activities. Plant Sci. 160: 27-35 (2000).

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Llusia J, Penuelas J, Asensio D, Munne-Bosch S. Airborne limonene confers limited thermotolerance to Quercus ilex. Physiol. Plant. 123: 40-48 (2005).

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Loreto F, Ciccioli P, Brancaleoni E, Cecinato A, Frattoni M, Sharkey TD. Different sources of reduced carbon contribute to form three classes of terpenoid emitted by Quercus ilex L. leaves. Proc. Natl. Acad. Sci. U.S.A. 93: 9966-9969 (1996).

Loreto F, Ciccioli P, Cecinato A, Brancaleoni E, Frattoni M, Fabozzi C, Tricoli D. Evidence of the photosynthetic origin of monoterpenes emitted by Quercus ilex L. leaves by 13C labeling. Plant Physiol. 110: 1317-1322 (1996).

Loreto F, Pinelli P, Manes F, Kollist H. Impact of ozone on monoterpene emissions and evidence for an isoprene-like antioxidant action of monoterpenes emitted by Quercus ilex leaves. Tree Physiol. 24: 361-367 (2004).

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Lu H, McKnight TD. Tissue-specific expression of the beta-subunit of tryptophan synthase in Camptotheca acuminata, an indole alkaloid-producing plant. Plant Physiol. 120: 43-52 (1999).

Lu S, Xu R, Jia JW, Pang J, Matsuda SP, Chen XY. Cloning and functional characterization of a beta-pinene synthase from Artemisia annua that shows a circadian pattern of expression. Plant Physiol. 130: 477-486 (2002).

Lucker J, Bouwmeester HJ, Schwab W, Blaas J, van Der Plas LH, Verhoeven HA. Expression of Clarkia S-linalool synthase in transgenic petunia plants results in the accumulation of S-linalyl-beta-D-glucopyranoside. Plant J. 27: 315-324 (2001).

Lucker J, El Tamer MK, Schwab W, Verstappen FW, van der Plas LH, Bouwmeester HJ, Verhoeven HA. Monoterpene biosynthesis in lemon (Citrus limon). cDNA isolation and functional analysis of four monoterpene synthases. Eur. J. Biochem. 269: 3160-3171 (2002).

Lucker J, Schwab W, Franssen MC, Van Der Plas LH, Bouwmeester HJ, Verhoeven HA. Metabolic engineering of monoterpene biosynthesis: two-step production of (+)-trans-isopiperitenol by tobacco. Plant J. 39: 135-145 (2004).

Lucker J, Schwab W, van Hautum B, Blaas J, van der Plas LH, Bouwmeester HJ, Verhoeven HA. Increased and altered fragrance of tobacco plants after metabolic engineering using three monoterpene synthases from lemon. Plant Physiol. 134: 510-519 (2004).

Mahmoud AA, Ahmed AA. alpha-Pinene-type monoterpenes and other constituents from Artemisia suksdorfii. Phytochemistry 67: 2103-2109 (2006).

Mahmoud SS, Croteau RB. Metabolic engineering of essential oil yield and composition in mint by altering expression of deoxyxylulose phosphate reductoisomerase and menthofuran synthase. Proc. Natl. Acad. Sci. U.S.A. 98: 8915-8920 (2001).

Mahmoud SS, Williams M, Croteau R. Cosuppression of limonene-3-hydroxylase in peppermint promotes accumulation of limonene in the essential oil. Phytochemistry 65: 547-554 (2004).

Mahroug S, Courdavault V, Thiersault M, St-Pierre B, Burlat V. Epidermis is a pivotal site of at least four secondary metabolic pathways in Catharanthus roseus aerial organs. Planta 223: 1191-1200 (2006).

Martin DM, Bohlmann J. Identification of Vitis vinifera (-)-alpha-terpineol synthase by in silico screening of full-length cDNA ESTs and functional characterization of recombinant terpene synthase. Phytochemistry 65: 1223-1229 (2004).

Martin DM, Faldt J, Bohlmann J. Functional characterization of nine Norway spruce TPS genes and evolution of gymnosperm terpene synthases of the TPS-d subfamily. Plant Physiol. 135: 1908-1927 (2004).

Martin DM, Gershenzon J, Bohlmann J. Induction of volatile terpene biosynthesis and diurnal emission by methyl jasmonate in foliage of Norway spruce. Plant Physiol. 132: 1586-1599 (2003).

Matich AJ, Bunn BJ, Hunt MB, Rowan DD. Lilac alcohol epoxide: a linalool derivative in Actinidia arguta flowers. Phytochemistry 67: 759-763 (2006).

Matich AJ, Young H, Allen JM, Wang MY, Fielder S, McNeilage MA, MacRae EA. Actinidia arguta: volatile compounds in fruit and flowers. Phytochemistry 63: 285-301 (2003).

McCaskill D, Croteau R. Monoterpene and sesquiterpene biosynthesis in glandular trichomes of peppermint (Mentha x piperita) rely exclusively on plastid-derived isopentenyl diphosphate. Planta 197: 49-56 (1995).

McCaskill D, Croteau R. Isopentenyl diphosphate is the terminal product of the deoxyxylulose-5-phosphate pathway for terpenoid biosynthesis in plants. Tetrahedron Lett. 40: 653-656 (1999).

McCaskill D, Croteau R. Procedures for the isolation and quantification of the intermediates of the mevalonic acid pathway. Anal. Biochem. 215: 142-149 (1993).

McConkey ME, Gershenzon J, Croteau RB. Developmental regulation of monoterpene biosynthesis in the glandular trichomes of peppermint. Plant Physiol. 122: 215-224 (2000).

McKay SA, Hunter WL, Godard KA, Wang SX, Martin DM, Bohlmann J, Plant AL. Insect attack and wounding induce traumatic resin duct development and gene expression of (-)-pinene synthase in sitka spruce. Plant Physiol. 133: 368-378 (2003).

Miller B, Madilao LL, Ralph S, Bohlmann J. Insect-induced conifer defense. White pine weevil and methyl jasmonate induce traumatic resinosis, de novo formed volatile emissions, and accumulation of terpenoid synthase and putative octadecanoid pathway transcripts in Sitka spruce. Plant Physiol. 137: 369-382 (2005).

Miller B, Oschinski C, Zimmer W. First isolation of an isoprene synthase gene from poplar and successful expression of the gene in Escherichia coli. Planta 213: 483-487 (2001).

Mithofer A, Wanner G, Boland W. Effects of feeding Spodoptera littoralis on lima bean leaves. II. Continuous mechanical wounding resembling insect feeding is sufficient to elicit herbivory-related volatile emission. Plant Physiol. 137: 1160-1168 (2005).

Moraga AR, Rambla JL, Ahrazem O, Granell A, Gomez-Gomez L. Metabolite and target transcript analyses during Crocus sativus stigma development. Phytochemistry 70: 1009-1016 (2009).

Moufida S, Marzouk B. Biochemical characterization of blood orange, sweet orange, lemon, bergamot and bitter orange. Phytochemistry 62: 1283-1289 (2003).

Munoz-Bertomeu J, Arrillaga I, Ros R, Segura J. Up-regulation of 1-deoxy-D-xylulose-5-phosphate synthase enhances production of essential oils in transgenic spike lavender. Plant Physiol. 142: 890-900 (2006).

Munoz-Bertomeu J, Ros R, Arrillaga I, Segura J. Expression of spearmint limonene synthase in transgenic spike lavender results in an altered monoterpene composition in developing leaves. Metab. Eng. 10: 166-177 (2008).

Nagegowda DA, Gutensohn M, Wilkerson CG, Dudareva N. Two nearly identical terpene synthases catalyze the formation of nerolidol and linalool in snapdragon flowers. Plant J. 55: 224-239 (2008).

Niinemets U, Reichstein M, Staudt M, Seufert G, Tenhunen JD. Stomatal constraints may affect emission of oxygenated monoterpenoids from the foliage of Pinus pinea. Plant Physiol. 130: 1371-1385 (2002).

Nkunya MH, Jonker SA, de Gelder R, Wachira SW, Kihampa C. (+/-)-Schefflone: a trimeric monoterpenoid from the root bark of Uvaria scheffleri. Phytochemistry 65: 399-404 (2004).

Noe SM, Copolovici L, Niinemets U, Vaino E. Foliar limonene uptake scales positively with leaf lipid content: "non-emitting" species absorb and release monoterpenes. Plant Biol. (Stuttg.) 10: 129-137 (2008).

Nogues I, Brilli F, Loreto F. Dimethylallyl diphosphate and geranyl diphosphate pools of plant species characterized by different isoprenoid emissions. Plant Physiol. 141: 721-730 (2006).

Ohara K, Ujihara T, Endo T, Sato F, Yazaki K. Limonene production in tobacco with Perilla limonene synthase cDNA. J. Exp. Bot. 54: 2635-2642 (2003).

Okasaka M, Kashiwada Y, Kodzhimatov OK, Ashurmetov O, Takaishi Y. Monoterpene glycosides from Paeonia hybrida. Phytochemistry 69: 1767-1772 (2008).

Ormeno E, Fernandez C, Mevy JP. Plant coexistence alters terpene emission and content of Mediterranean species. Phytochemistry 68: 840-852 (2007).

Oudin A, Mahroug S, Courdavault V, Hervouet N, Zelwer C, Rodríguez-Concepcion M, St-Pierre B, Burlat V. Spatial distribution and hormonal regulation of gene products from methyl erythritol phosphate and monoterpene-secoiridoid pathways in Catharanthus roseus. Plant Mol. Biol. 65: 13-30 (2007).

Owen SM, Penuelas J. Opportunistic emissions of volatile isoprenoids. Trends Plant Sci. 10: 420-426 (2005).

Pechous SW, Whitaker BD. Cloning and functional expression of an (E, E)-alpha-farnesene synthase cDNA from peel tissue of apple fruit. Planta 219: 84-94 (2004).

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