169
10
Ilc T, Parage C, Boachon B, Navrot N, Werck-Reichhart D (2016) Monoterpenol oxidative metabolism: role
in plant adaptation and potential applications. Front Plant Sci 7:509. https://doi.org/10.3389/
fpls.2016.00509
Jung V, Thibaut T, Meinesz A, Pohnert G (2002) Comparison of the wound-activated transformation of
caulerpenyne by invasive and noninvasive Caulerpa species of the Mediterranean. J Chem Ecol
28:2091–2105
Kamatou GP, Vermaak I, Viljoen AM, Lawrence BM (2013) Menthol: a simple monoterpene with remarkable
biological properties. Phytochemistry 96:15–25. https://doi.org/10.1016/j.phytochem.2013.08.005
Kennedy DO, Scholey AB (2003) Ginseng: potential for the enhancement of cognitive performance and
mood. Pharmacol Biochem Behav 75:687–700
Larsen L, Joyce NI, Sansom CE, Cooney JM, Jensen DJ, Perry NB (2015) Sweet poisons: honeys contaminated with glycosides of the neurotoxin tutin. J Nat Prod 78:1363–1369. https://doi.org/10.1021/acs.
jnatprod.5b00241
Leivar P et al (2011) Multilevel control of Arabidopsis 3-hydroxy-3-methylglutaryl coenzyme A reductase
by protein phosphatase 2A. Plant Cell 23:1494–1511. https://doi.org/10.1105/tpc.110.074278
Lindemann P (2015) Steroidogenesis in plants--biosynthesis and conversions of progesterone and other
pregnane derivatives. Steroids 103:145–152. https://doi.org/10.1016/j.steroids.2015.08.007
Lorent JH, Quetin-Leclercq J, Mingeot-Leclercq MP (2014) The amphiphilic nature of saponins and their
effects on artificial and biological membranes and potential consequences for red blood and cancer
cells. Org Biomol Chem 12:8803–8822. https://doi.org/10.1039/c4ob01652a
McQuinn RP, Giovannoni JJ, Pogson BJ (2015) More than meets the eye: from carotenoid biosynthesis, to
new insights into apocarotenoid signaling. Curr Opin Plant Biol 27:172–179. https://doi.org/10.1016/j.
pbi.2015.06.020
Nisar N, Li L, Lu S, Khin NC, Pogson BJ (2015) Carotenoid metabolism in plants. Mol Plant 8:68–82. https://
doi.org/10.1016/j.molp.2014.12.007
Park J et al (2017) Ginseng on nuclear hormone receptors. Am J Chin Med 45:1147–1156. https://doi.
org/10.1142/S0192415X17500628
Pavela R, Benelli G (2016) Essential oils as ecofriendly biopesticides? Challenges and constraints. Trends
Plant Sci 21:1000–1007. https://doi.org/10.1016/j.tplants.2016.10.005
Pazouki L, Niinemets U (2016) Multi-substrate Terpene synthases: their occurrence and physiological significance. Front Plant Sci 7:1019. https://doi.org/10.3389/fpls.2016.01019
Peters RJ (2010) Two rings in them all: the labdane-related diterpenoids. Nat Prod Rep 27:1521–1530.
https://doi.org/10.1039/c0np00019a
Phillips MA, D'Auria JC, Gershenzon J, Pichersky E (2008) The Arabidopsis thaliana type I isopentenyl
diphosphate isomerases are targeted to multiple subcellular compartments and have overlapping
functions in isoprenoid biosynthesis. Plant Cell 20:677–696. https://doi.org/10.1105/tpc.107.053926
Pulido P, Perello C, Rodriguez-Concepcion M (2012) New insights into plant isoprenoid metabolism. Mol
Plant 5:964–967. https://doi.org/10.1093/mp/sss088
Rasmann S, Turlings TC (2016) Root signals that mediate mutualistic interactions in the rhizosphere. Curr
Opin Plant Biol 32:62–68. https://doi.org/10.1016/j.pbi.2016.06.017
Regnault-Roger C, Vincent C, Arnason JT (2012) Essential oils in insect control: low-risk products in a highstakes world. Annu Rev Entomol 57:405–424. https://doi.org/10.1146/annurev-ento-120710-100554
Ricigliano V, Kumar S, Kinison S, Brooks C, Nybo SE, Chappell J, Howarth DG (2016) Regulation of sesquiterpenoid metabolism in recombinant and elicited Valeriana officinalis hairy roots. Phytochemistry
125:43–53. https://doi.org/10.1016/j.phytochem.2016.02.011
Rodriguez-Concepcion M (2004) The MEP pathway: a new target for the development of herbicides, antibiotics and antimalarial drugs. Curr Pharm Des 10:2391–2400
Ruiz-Sola MA, Rodriguez-Concepcion M (2012) Carotenoid biosynthesis in Arabidopsis: a colorful pathway. Arabidopsis Book 10:e0158. https://doi.org/10.1199/tab.0158
Russo EB (2011) Taming THC: potential cannabis synergy and phytocannabinoid-terpenoid entourage
effects. Br J Pharmacol 163:1344–1364. https://doi.org/10.1111/j.1476-5381.2011.01238.x
Siebert DJ (2004) Localization of salvinorin A and related compounds in glandular trichomes of the psychoactive sage, Salvia divinorum. Ann Bot 93:763–771. https://doi.org/10.1093/aob/mch089
Thimmappa R, Geisler K, Louveau T, O’Maille P, Osbourn A (2014) Triterpene biosynthesis in plants. Annu
Rev Plant Biol 65:225–257. https://doi.org/10.1146/annurev-arplant-050312-120229
Tholl D (2006) Terpene synthases and the regulation, diversity and biological roles of terpene metabolism.
Curr Opin Plant Biol 9:297–304. https://doi.org/10.1016/j.pbi.2006.03.014
References
10
Ilc T, Parage C, Boachon B, Navrot N, Werck-Reichhart D (2016) Monoterpenol oxidative metabolism: role
in plant adaptation and potential applications. Front Plant Sci 7:509. https://doi.org/10.3389/
fpls.2016.00509
Jung V, Thibaut T, Meinesz A, Pohnert G (2002) Comparison of the wound-activated transformation of
caulerpenyne by invasive and noninvasive Caulerpa species of the Mediterranean. J Chem Ecol
28:2091–2105
Kamatou GP, Vermaak I, Viljoen AM, Lawrence BM (2013) Menthol: a simple monoterpene with remarkable
biological properties. Phytochemistry 96:15–25. https://doi.org/10.1016/j.phytochem.2013.08.005
Kennedy DO, Scholey AB (2003) Ginseng: potential for the enhancement of cognitive performance and
mood. Pharmacol Biochem Behav 75:687–700
Larsen L, Joyce NI, Sansom CE, Cooney JM, Jensen DJ, Perry NB (2015) Sweet poisons: honeys contaminated with glycosides of the neurotoxin tutin. J Nat Prod 78:1363–1369. https://doi.org/10.1021/acs.
jnatprod.5b00241
Leivar P et al (2011) Multilevel control of Arabidopsis 3-hydroxy-3-methylglutaryl coenzyme A reductase
by protein phosphatase 2A. Plant Cell 23:1494–1511. https://doi.org/10.1105/tpc.110.074278
Lindemann P (2015) Steroidogenesis in plants--biosynthesis and conversions of progesterone and other
pregnane derivatives. Steroids 103:145–152. https://doi.org/10.1016/j.steroids.2015.08.007
Lorent JH, Quetin-Leclercq J, Mingeot-Leclercq MP (2014) The amphiphilic nature of saponins and their
effects on artificial and biological membranes and potential consequences for red blood and cancer
cells. Org Biomol Chem 12:8803–8822. https://doi.org/10.1039/c4ob01652a
McQuinn RP, Giovannoni JJ, Pogson BJ (2015) More than meets the eye: from carotenoid biosynthesis, to
new insights into apocarotenoid signaling. Curr Opin Plant Biol 27:172–179. https://doi.org/10.1016/j.
pbi.2015.06.020
Nisar N, Li L, Lu S, Khin NC, Pogson BJ (2015) Carotenoid metabolism in plants. Mol Plant 8:68–82. https://
doi.org/10.1016/j.molp.2014.12.007
Park J et al (2017) Ginseng on nuclear hormone receptors. Am J Chin Med 45:1147–1156. https://doi.
org/10.1142/S0192415X17500628
Pavela R, Benelli G (2016) Essential oils as ecofriendly biopesticides? Challenges and constraints. Trends
Plant Sci 21:1000–1007. https://doi.org/10.1016/j.tplants.2016.10.005
Pazouki L, Niinemets U (2016) Multi-substrate Terpene synthases: their occurrence and physiological significance. Front Plant Sci 7:1019. https://doi.org/10.3389/fpls.2016.01019
Peters RJ (2010) Two rings in them all: the labdane-related diterpenoids. Nat Prod Rep 27:1521–1530.
https://doi.org/10.1039/c0np00019a
Phillips MA, D'Auria JC, Gershenzon J, Pichersky E (2008) The Arabidopsis thaliana type I isopentenyl
diphosphate isomerases are targeted to multiple subcellular compartments and have overlapping
functions in isoprenoid biosynthesis. Plant Cell 20:677–696. https://doi.org/10.1105/tpc.107.053926
Pulido P, Perello C, Rodriguez-Concepcion M (2012) New insights into plant isoprenoid metabolism. Mol
Plant 5:964–967. https://doi.org/10.1093/mp/sss088
Rasmann S, Turlings TC (2016) Root signals that mediate mutualistic interactions in the rhizosphere. Curr
Opin Plant Biol 32:62–68. https://doi.org/10.1016/j.pbi.2016.06.017
Regnault-Roger C, Vincent C, Arnason JT (2012) Essential oils in insect control: low-risk products in a highstakes world. Annu Rev Entomol 57:405–424. https://doi.org/10.1146/annurev-ento-120710-100554
Ricigliano V, Kumar S, Kinison S, Brooks C, Nybo SE, Chappell J, Howarth DG (2016) Regulation of sesquiterpenoid metabolism in recombinant and elicited Valeriana officinalis hairy roots. Phytochemistry
125:43–53. https://doi.org/10.1016/j.phytochem.2016.02.011
Rodriguez-Concepcion M (2004) The MEP pathway: a new target for the development of herbicides, antibiotics and antimalarial drugs. Curr Pharm Des 10:2391–2400
Ruiz-Sola MA, Rodriguez-Concepcion M (2012) Carotenoid biosynthesis in Arabidopsis: a colorful pathway. Arabidopsis Book 10:e0158. https://doi.org/10.1199/tab.0158
Russo EB (2011) Taming THC: potential cannabis synergy and phytocannabinoid-terpenoid entourage
effects. Br J Pharmacol 163:1344–1364. https://doi.org/10.1111/j.1476-5381.2011.01238.x
Siebert DJ (2004) Localization of salvinorin A and related compounds in glandular trichomes of the psychoactive sage, Salvia divinorum. Ann Bot 93:763–771. https://doi.org/10.1093/aob/mch089
Thimmappa R, Geisler K, Louveau T, O’Maille P, Osbourn A (2014) Triterpene biosynthesis in plants. Annu
Rev Plant Biol 65:225–257. https://doi.org/10.1146/annurev-arplant-050312-120229
Tholl D (2006) Terpene synthases and the regulation, diversity and biological roles of terpene metabolism.
Curr Opin Plant Biol 9:297–304. https://doi.org/10.1016/j.pbi.2006.03.014
References