168
10
References
Ahkami A, Johnson SR, Srividya N, Lange BM (2015) Multiple levels of regulation determine monoterpenoid essential oil compositional variation in the mint family. Mol Plant 8:188–191. https://doi.
org/10.1016/j.molp.2014.11.009
Alberti TB, Barbosa WL, Vieira JL, Raposo NR, Dutra RC (2017) (−)-beta-caryophyllene, a CB2 receptorselective phytocannabinoid, suppresses motor paralysis and neuroinflammation in a murine model
of multiple sclerosis. Int J Mol Sci 18. https://doi.org/10.3390/ijms18040691
Berthelot K, Estevez Y, Deffieux A, Peruch F (2012) Isopentenyl diphosphate isomerase: a checkpoint to
isoprenoid biosynthesis. Biochimie 94:1621–1634. https://doi.org/10.1016/j.biochi.2012.03.021
Brunelli M, Garcia-Gil M, Mozzachiodi R, Roberto M, Scuri R, Traina G, Zaccardi ML (2000) Neurotoxic
effects of caulerpenyne. Prog Neuropsychopharmacol Biol Psychiatry 24:939–954
Carson C et al (2015) Englerin a agonizes the TRPC4/C5 cation channels to inhibit tumor cell line proliferation. PLoS One 10:e0127498. https://doi.org/10.1371/journal.pone.0127498
Chen F, Tholl D, Bohlmann J, Pichersky E (2011) The family of terpene synthases in plants: a mid-size family
of genes for specialized metabolism that is highly diversified throughout the kingdom. Plant J
66:212–229. https://doi.org/10.1111/j.1365-313X.2011.04520.x
Chen W, Vermaak I, Viljoen A (2013) Camphor--a fumigant during the Black Death and a coveted fragrant
wood in ancient Egypt and Babylon--a review. Molecules 18:5434–5454. https://doi.org/10.3390/molecules18055434
Chen X, Berim A, Dayan FE, Gang DR (2017) A (−)-kolavenyl diphosphate synthase catalyzes the first step
of salvinorin A biosynthesis in Salvia divinorum. J Exp Bot 68:1109–1122. https://doi.org/10.1093/jxb/
erw493
Clastre M, Papon N, Courdavault V, Giglioli-Guivarc'h N, St-Pierre B, Simkin AJ (2011) Subcellular evidence
for the involvement of peroxisomes in plant isoprenoid biosynthesis. Plant Signal Behav 6:2044–2046
Closa M, Vranova E, Bortolotti C, Bigler L, Arro M, Ferrer A, Gruissem W (2010) The Arabidopsis thaliana FPP
synthase isozymes have overlapping and specific functions in isoprenoid biosynthesis, and complete
loss of FPP synthase activity causes early developmental arrest. Plant J 63:512–525. https://doi.
org/10.1111/j.1365-313X.2010.04253.x
Croteau R, Felton M, Karp F, Kjonaas R (1981) Relationship of camphor biosynthesis to leaf development in
sage (Salvia officinalis). Plant Physiol 67:820–824
De Luca V, Salim V, Thamm A, Masada SA, Yu F (2014) Making iridoids/secoiridoids and monoterpenoid
indole alkaloids: progress on pathway elucidation. Curr Opin Plant Biol 19:35–42. https://doi.
org/10.1016/j.pbi.2014.03.006
Dewick PM (2002) The biosynthesis of C5–C25 terpenoid compounds. Nat Prod Rep 19:181–222. https://
doi.org/10.1039/b002685i
Dhifi W, Bellili S, Jazi S, Bahloul N, Mnif W (2016) Essential oils’ chemical characterization and investigation
of some biological activities: a critical review. Medicines (Basel) 3. https://doi.org/10.3390/medicines3040025
Doblas VG et al (2013) The SUD1 gene encodes a putative E3 ubiquitin ligase and is a positive regulator of
3-hydroxy-3-methylglutaryl coenzyme a reductase activity in Arabidopsis. Plant Cell 25:728–743.
https://doi.org/10.1105/tpc.112.108696
Dutra RC et al (2012) Euphol, a tetracyclic triterpene produces antinociceptive effects in inflammatory and
neuropathic pain: the involvement of cannabinoid system. Neuropharmacology 63:593–605. https://
doi.org/10.1016/j.neuropharm.2012.05.008
Gertsch J, Pertwee RG, Di Marzo V (2010) Phytocannabinoids beyond the Cannabis plant - do they exist?
Br J Pharmacol 160:523–529. https://doi.org/10.1111/j.1476-5381.2010.00745.x
Ghosh S (2017) Triterpene structural diversification by plant cytochrome P450 enzymes. Front Plant Sci
8:1886. https://doi.org/10.3389/fpls.2017.01886
Guirimand G et al (2012) A single gene encodes isopentenyl diphosphate isomerase isoforms targeted to
plastids, mitochondria and peroxisomes in Catharanthus roseus. Plant Mol Biol 79:443–459. https://
doi.org/10.1007/s11103-012-9923-0
Gurel E, Karvar S, Yucesan B, Eker I, Sameeullah M (2017) An overview of cardenolides in digitalis – more than
a cardiotonic compound. Curr Pharm Des. https://doi.org/10.2174/1381612823666170825125426
Hou X, Rivers J, Leon P, McQuinn RP, Pogson BJ (2016) Synthesis and function of apocarotenoid signals in
plants. Trends Plant Sci 21:792–803. https://doi.org/10.1016/j.tplants.2016.06.001
Chapter 10 · Terpenes and Terpenoids
10
References
Ahkami A, Johnson SR, Srividya N, Lange BM (2015) Multiple levels of regulation determine monoterpenoid essential oil compositional variation in the mint family. Mol Plant 8:188–191. https://doi.
org/10.1016/j.molp.2014.11.009
Alberti TB, Barbosa WL, Vieira JL, Raposo NR, Dutra RC (2017) (−)-beta-caryophyllene, a CB2 receptorselective phytocannabinoid, suppresses motor paralysis and neuroinflammation in a murine model
of multiple sclerosis. Int J Mol Sci 18. https://doi.org/10.3390/ijms18040691
Berthelot K, Estevez Y, Deffieux A, Peruch F (2012) Isopentenyl diphosphate isomerase: a checkpoint to
isoprenoid biosynthesis. Biochimie 94:1621–1634. https://doi.org/10.1016/j.biochi.2012.03.021
Brunelli M, Garcia-Gil M, Mozzachiodi R, Roberto M, Scuri R, Traina G, Zaccardi ML (2000) Neurotoxic
effects of caulerpenyne. Prog Neuropsychopharmacol Biol Psychiatry 24:939–954
Carson C et al (2015) Englerin a agonizes the TRPC4/C5 cation channels to inhibit tumor cell line proliferation. PLoS One 10:e0127498. https://doi.org/10.1371/journal.pone.0127498
Chen F, Tholl D, Bohlmann J, Pichersky E (2011) The family of terpene synthases in plants: a mid-size family
of genes for specialized metabolism that is highly diversified throughout the kingdom. Plant J
66:212–229. https://doi.org/10.1111/j.1365-313X.2011.04520.x
Chen W, Vermaak I, Viljoen A (2013) Camphor--a fumigant during the Black Death and a coveted fragrant
wood in ancient Egypt and Babylon--a review. Molecules 18:5434–5454. https://doi.org/10.3390/molecules18055434
Chen X, Berim A, Dayan FE, Gang DR (2017) A (−)-kolavenyl diphosphate synthase catalyzes the first step
of salvinorin A biosynthesis in Salvia divinorum. J Exp Bot 68:1109–1122. https://doi.org/10.1093/jxb/
erw493
Clastre M, Papon N, Courdavault V, Giglioli-Guivarc'h N, St-Pierre B, Simkin AJ (2011) Subcellular evidence
for the involvement of peroxisomes in plant isoprenoid biosynthesis. Plant Signal Behav 6:2044–2046
Closa M, Vranova E, Bortolotti C, Bigler L, Arro M, Ferrer A, Gruissem W (2010) The Arabidopsis thaliana FPP
synthase isozymes have overlapping and specific functions in isoprenoid biosynthesis, and complete
loss of FPP synthase activity causes early developmental arrest. Plant J 63:512–525. https://doi.
org/10.1111/j.1365-313X.2010.04253.x
Croteau R, Felton M, Karp F, Kjonaas R (1981) Relationship of camphor biosynthesis to leaf development in
sage (Salvia officinalis). Plant Physiol 67:820–824
De Luca V, Salim V, Thamm A, Masada SA, Yu F (2014) Making iridoids/secoiridoids and monoterpenoid
indole alkaloids: progress on pathway elucidation. Curr Opin Plant Biol 19:35–42. https://doi.
org/10.1016/j.pbi.2014.03.006
Dewick PM (2002) The biosynthesis of C5–C25 terpenoid compounds. Nat Prod Rep 19:181–222. https://
doi.org/10.1039/b002685i
Dhifi W, Bellili S, Jazi S, Bahloul N, Mnif W (2016) Essential oils’ chemical characterization and investigation
of some biological activities: a critical review. Medicines (Basel) 3. https://doi.org/10.3390/medicines3040025
Doblas VG et al (2013) The SUD1 gene encodes a putative E3 ubiquitin ligase and is a positive regulator of
3-hydroxy-3-methylglutaryl coenzyme a reductase activity in Arabidopsis. Plant Cell 25:728–743.
https://doi.org/10.1105/tpc.112.108696
Dutra RC et al (2012) Euphol, a tetracyclic triterpene produces antinociceptive effects in inflammatory and
neuropathic pain: the involvement of cannabinoid system. Neuropharmacology 63:593–605. https://
doi.org/10.1016/j.neuropharm.2012.05.008
Gertsch J, Pertwee RG, Di Marzo V (2010) Phytocannabinoids beyond the Cannabis plant - do they exist?
Br J Pharmacol 160:523–529. https://doi.org/10.1111/j.1476-5381.2010.00745.x
Ghosh S (2017) Triterpene structural diversification by plant cytochrome P450 enzymes. Front Plant Sci
8:1886. https://doi.org/10.3389/fpls.2017.01886
Guirimand G et al (2012) A single gene encodes isopentenyl diphosphate isomerase isoforms targeted to
plastids, mitochondria and peroxisomes in Catharanthus roseus. Plant Mol Biol 79:443–459. https://
doi.org/10.1007/s11103-012-9923-0
Gurel E, Karvar S, Yucesan B, Eker I, Sameeullah M (2017) An overview of cardenolides in digitalis – more than
a cardiotonic compound. Curr Pharm Des. https://doi.org/10.2174/1381612823666170825125426
Hou X, Rivers J, Leon P, McQuinn RP, Pogson BJ (2016) Synthesis and function of apocarotenoid signals in
plants. Trends Plant Sci 21:792–803. https://doi.org/10.1016/j.tplants.2016.06.001
Chapter 10 · Terpenes and Terpenoids