Abstract
Among the three main groups of secondary metabolites that can be found in plants, terpenes are by far the largest and most diverse. They play an important role in plants in both primary and secondary metabolism and constitute a source of phytochemicals for human health. Plant biotechnology, based on in vitro culture and genetic engineering techniques, has proved to be a promising tool to increase the production of these bioactive compounds. This chapter describes the plant cell and organ culture techniques used in plant biotechnology, the biotechnological production of the different groups of terpenes using empirical approaches and some examples of genetic and metabolic engineering techniques applied to improve the production of these valuable plant secondary metabolites in plant cell and organ cultures.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Abbreviations
- CaMV:
-
Cauliflower mosaic virus 35S promoter
- CM:
-
Culture medium
- DMAPP:
-
Dimethylallyl diphosphate
- DXR:
-
1-Deoxy-D-xylulose-5-phosphate reductoisomerase
- DXS:
-
1-Deoxy-D-xylulose-5-phosphate synthase
- DW:
-
Dry weight
- FPP:
-
Farnesyl diphosphate
- GGPP:
-
Geranylgeranyl diphosphate
- GPP:
-
Geranyl diphosphate
- HMGR:
-
3-Hydroxy-3-methyl-glutaryl-CoA reductase
- IAA:
-
Indole-3-acetic acid
- IPP:
-
Isopentenyl diphosphate
- MEP:
-
2-C-methyl-D-erythritol 4-phosphate
- MS:
-
Murashige and Skoog medium
- OPP:
-
Diphosphate
- PGR:
-
Plant Growth Regulators
- SQS:
-
Squalene synthase
- TXS:
-
Taxadiene synthase
References
Kirby J, Keasling JD (2009) Biosynthesis of plant isoprenoids: perspectives for microbial engineering. Annu Rev Plant Biol 60:334–355
Seigler DS (1998) Plant secondary metabolism. Kluwer Academic, Dordrecht
Nagegowda DA (2010) Plant volatile terpenoid metabolism: biosynthetic genes, transcriptional regulation and subcellular compartmentation. FEBS Lett 584:2965–2973
Misawa N (2011) Pathway engineering for functional isoprenoid. Curr Opin Biotech 22:627–633
Oksman-Caldentey KM, Inzé D (2004) Plant cell factories in the post-genomic era: new ways to produce designer secondary metabolites. Trends Plant Sci 9:433–440
Malik S, Cusido RM, Mirjalili MH, Moyano E, Palazon J, Bonfill M (2011) Production of the anticancer drug in Taxus baccata suspension cultures: a review. Process Biochem 46:23–34
Expósito O, Bonfill M, Moyano E, Onrubia M, Mirjalili MH, Cusidó RM, Palazon J (2009) Biotechnological production of taxol and related taxoids: current state and prospects. Anti-Cancer Agents Med Chem 9:109–121
Georgiev MI, Weber J, Maciuk A (2009) Bioprocessing of plant cell cultures for mass production of targeted compounds. Appl Microbiol Biot 83:809–823
Karuppusamy S (2009) A review on trends in production of secondary metabolites from higher plants by in vitro tissue, organ and cell cultures. J Med Res 3:1222–1239
Ramachandra Rao S, Ravishankar GA (2002) Plant cell cultures: chemical factories of secondary metabolites. Biotechnol Adv 20:101–153
Cusido RM, Palazon J, Bonfill M, Navia-Osorio A, Morales C, Piñol MT (2002) Improved paclitaxel and baccatin III production in suspension cultures of Taxus media. Biotechnol Prog 18:418–423
Chattopadhyay S, Farkya S, Srivastava AK, Bisaria VS (2002) Bioprocess considerations for production of secondary metabolites by plant cell suspension cultures. Biotechnol Bioprocess Eng 7:138–149
Yesil-Celiktas O, Gurel A, Vardar-Sukan F (2010) Large scale cultivation of plant cell and tissue culture in bioreactors. Transworld Res Netw 37:1–54
Sutton-Jones B, Street HE (1968) Studies on the growth in culture of plant cells. II. Changes in fine structure during growth of Acer pseudoplatanus L. cells in suspension culture. J Exp Bot 19:114–118
Hulst AC, Tramper J (1989) Immobilized plant cells. A literature survey. Enz Microb Technol 11:546–558
Williams PD, Mavituna F (1992) Immobilized plant cells. In: Fowler MW, Warren GS, Moo-Young M (eds) Plant biotechnology: comprehensive biotechnology, second supplement. Pergamon, Oxford
Tyler RT, Kurz WGW, Paiva NL, Chavadej S (1995) Bioreactors for surface immobilized cells. Plant Cell Tissue Organ Cult 42:81–90
Nemoto K, Hara M, Suzuki M, Seki H, Oka A, Muranaka T, Yoshihiro M (2009) Function of the aux and rol genes of the Ri in plant cell division in vitro. Plant Signal & Behav 12:1145–1147
Guillon S, Tremouillaux-Guiller J, Pati PK, Rideau M, Gantet P (2006) Harnessing the potential of hairy roots: dawn of a new era. Trends Biotech 24:403–409
Heble MR (1985) Multiple shoot cultures: a viable alternative in vitro system for the production of known and new biologically active plant constituents. In: Neumann KH, Barz W, Reinhard E (eds) Primary and secondary metabolism of plant cell cultures. Springer, Berlin, pp 281–285
Liu C, Zhao Y, Wang Y (2006) Artemisinin: current state and perspectives for biotechnological production of an antimalarial drug. Appl Microbiol Biotechnol 72:11–20
Eibl R, Werner S, Eibl D (2010) Bag bioreactor based on wave-induced motion: characteristics and applications. Adv Biochem Eng Biotechnol 115:55–87
Eibl R, Eibl D (2008) Design of bioreactors suitable for plant cell and tissue cultures. Phytochem Rev 7:593–598
Sivakumar G, Yu KW, Paek KY (2005) Production of biomass and ginsenosides from adventitious roots of Panax ginseng in bioreactor cultures. Eng Life Sci 5:333–342
Croteau R, Kutchan TM, Lewis NG (2000) Natural products (secondary metabolites). In: Buchanan B, Gruissem W, Jones R (eds) Biochemistry and molecular biology of plants. American Society of Plant Physiologists, Rockville, pp 1250–1318
Wise ML, Croteau R (1999) Monoterpene biosynthesis. In: Cane DE (ed) Comprehensive natural products chemistry: isoprenoids. Elsevier Science, Oxford, pp 97–153
Lange BM, Croteau R (1999) Genetic engineering of essential oil production in mint. Curr Opin Plant Biol 2:139–144
Spencer A, Hamill JD, Rhodes MJC (1993) In vitro biosynthesis of monoterpens by Agrobacterium transformed shoot cultures of two Mentha species. Phytochemistry 32:911–919
Kim T, Kim TY, Bae GW, Lee HJ, Chae YA, Chung IS (1996) Improved production of essential oils by two-phase culture of Mentha piperita cells. Plant Tissue Cult Lett 13:189–192
Chang JH, Shin JH, Chung IS, Lee HJ (1998) Improved menthol production from chitosan-elicited suspension culture of Mentha piperita. Biotechnol Lett 20:1097–1099
Chakraborty A, Chattopadhyay S (2008) Stimulation of menthol production in Mentha piperita cell culture. In Vitro Cell Dev Biol Plant 44:518–524
Haluk JP, Roussel C (2000) Characterization and origin of tropolones responsible for the cupressales natural durability. Potential application to wood preservation. Ann Forest Sci 57:819–829
Yamaguchi T, Fujita K, Sakai K (1999) Biological activity of extracts from Cupressus lusitanica cell culture. J Wood Sci 45:170–173
Witte L, Berlin J, Wray V, Schubert W, Kohl W, Hofle G, Hammer J (1983) Mono- and diterpenes from cell cultures of Thuja occidentalis. Planta Med 49:216–221
Ono M, Asai T, Watanabe H (1998) Hinokitiol production in a suspension culture of Calocedrus formosana. Florin Biosci Biotechnol Biochem 62:1653–1659
Matsunaga Y, Fujita K, Yamada J, Ashitani T, Sakai K (2003) Monoterpenes produced by Cupressus lusitanica cultured cells including a novel monoterpene (1S, 2S, 6S)-(+)-1,6-epoxy-4(8)-p-menthen-2-ol. Nat Prod Res 17(6):441–443
Itose R, Sakai K (1997) Improved culture conditions for the suspension cell cultures of production of β-thujaplicin by Cupressus lusitanica. Plant Biotechnol 14(3):163–167
Inada S, Tsutsumi Y, Sakai K (1993) Elicitor of the β-thujaplicin accumulation in callus cultures of Cupressus lusitanica. J Fac Agr Kyushu Uni 38:119–126
Yamada J, Fujita K, Sakai K (2002) Feedback regulation of β-thujaplicin production and formation of its methyl ether in a suspension culture of Cupressus lusitanica. Phytochemistry 40:447–450
Sakai K, Kusaba K, Tsutsumi Y, Shirashi T (1994) Secondary metobolites in cell culture of woody plants. III. Formation of β-thujaplicin in Cupressus lusitanica callus cultures treated with fungal elicitors. Mokuzai Gakkaishi 40:1–5
Saker M, Shanab S, Kahter M (2000) In vitro studies on Ambrosia maritima: I-Morphogenic responses and biotic elicitation. Breeding Research on Medicinal and Aromatic Plants. Arab J Biotechn 3(2):217–224
Saker M, Shanab S, Dessouky M, Khater MR (2000) In vitro studies on Ambrosia maritima: II-Fungal elicitor enhances sesquiterpene lactones accumulation. Arab J Biotechnol 3(2):225–232
Betina V (1989) Mycotoxins, chemicals, biological and environmental aspects. Elsevier, Amsterdam/Oxford/New York/Tokyo
Stoessl A, Stothers JB, Ward EWB (1976) Sesquiterpenoid stress compounds of the Solanaceae. Phytochemistry 15:855–872
Brindle PA, Kuhn PJ, Threlfall DR (1983) Accumulation of phytoalexins in potato-cell suspension cultures. Phytochemistry 22:2719–2721
Brooks CJW, Watson DG, Freer IM (1986) Elicitation of capsidiol accumulation in suspended callus cultures of Capsicum annuum. Phytochemistry 25:1089–1092
Chappell J, Nable R, Fleming P, Andersen RA, Burton HR (1987) Accumulation of capsidiol in tobacco cell cultures treated with fungal elicitor. Phytochemistry 26:2259–2260
Watson DG, Rycroft DS, Freer IM, Brooks CJW (1985) Sesquiterpenoid phytoalexins from suspended callus cultures of Nicotiana tabacum. Phytochemistry 24:2195–2200
Chappell J, Nable R (1987) Induction of sesquiterpenoid biosynthesis in tobacco cell suspension cultures by fungal elicitor. Plant Physiol 85:469–473
Zhu YZ, Huang SH, Tan BK, Sun J, Whiteman M, Zhu YC (2004) Antioxidants in Chinese herbal medicines: a biochemical perspective. Nat Prod Rep 21:478–489
Wang X, Morris-Natschke SL, Lee KH (2007) New developments in the chemistry and biology of the bioactive constituents of Tanshen. Med Res Rev 27:133–148
Wang JW, Wu JY (2010) Tanshinone biosynthesis in Salvia miltiorrhiza and production in plant tissue cultures. Appl Microbiol Biotechnol 88:437–449
Ke SY, Shi HL, Ma ZD, Chai FR (2005) The optimization on cultural parameters for callus culture of Salvia miltiorrhiza. J Chinese Med Mater 28:82–83
Shan CG, Wang ZF, Su XH, Yan SL, Sun HC (2007) Study advance in Salvia miltiorrhiza tissue culture. Res Pract Chinese Med 22:4–57
Hu YH, Zhang R, Hu ZB, Wu YP, Shen XM, Zhang GY, Zhou XJ (1992) Callus culture and bioactive ingredients of Salvia miltiorrhiza. Plant Physiol Commun 28:424–425
Tsutomu N, Hitoshi M, Masao N, Hideko H, Kaisuke Y (1983) Production of cryptotanshinone and ferruginol in cultured cells of Salvia miltiorrhiza. Phytochemistry 22:721–722
Miyasaka H, Nasu M, Yamamoto T, Shiomi Y, Ohno H, Endo Y, Yoneda K (1987) Effect of nutritional factors on cryptotanshinone and ferruginol production by cell suspension cultures of Salvia miltiorrhiza. Phytochemistry 26(5):1421–1424
Miyasaka H, Nasu M, Yamamoto T, Endo Y, Yoneda K (1986) Regulation of ferruginol and cryptotanshinone biosynthesis in cell suspension cultures of Salvia miltiorrhiza. Phytochemistry 25(3):637–640
Miyasaka H, Nasu M, Yamamoto T, Endo Y, Yoneda K (1986) Production of cryptotanshinone and ferruginol by immobilized cultured cells of Salvia miltiorrhiza. Phytochemistry 25(7):1621–1624
Zhao JL, Zhou LG, Wu JY (2010) Effects of biotic and abiotic elicitors on cell growth and tanshinone accumulation in Salvia miltiorrhiza cell cultures. Appl Microbiol Biotechnol 87:137–144
Bonfill M, Bentebibel S, Moyano E, Palazon J, Cusido RM, Eibl R, Pinol MT (2007) Paclitaxel and baccatin III production induced by methyl jasmonate in free and immobilized cells of Taxus baccata. Biol Plant 51:647–652
Bonfill M, Exposito O, Moyano E, Cusido RM, Palazon J, Pinol MT (2006) Manipulation by culture mixing and elicitation of paclitaxel and baccatin III production in Taxus baccata suspension culture. In Vitro Cell Dev Biol Plant 42:422–426
Onrubia M, Moyano E, Bonfill M, Exposito O, Palazon J, Cusido RM (2010) An approach to the molecular mechanism of methyl jasmonate and vanadyl sulphate elicitation in Taxus baccata cell cultures: the role of txs and bapt gene expression. Biochem Eng J 53:104–111
Gillis CN (1997) Panax ginseng pharmacology: a nitric oxide link? Biochem Pharmacol 4(1):1–8
Bonfill M, Cusido RM, Palazon J, Pinol MT, Morales C (2002) Influence of auxins on organogénesis and ginsenoside production in Panax ginseng calluses. Plant Cell Tissue Organ Cult 68:73–78
Chung HS, Lee YC, Rhee YK, Lee SY (2011) Consumer acceptance of Ginseng food products. J Food Sci 76(9):S516–S522
Furuya T, Yoshikawa T, Ishii T, Kajii K (1983) Regulation of saponin production in callus cultures of Panax ginseng. Planta Med 47:200–204
Odnevall A, Björk L (1989) Effects of light on growth, morphogenesis and ginsenoside formation in tissue cultures of Panax ginseng. Biochem und Physiol der Pflanz 185:253–259
Yasuda S, Satosh K, Ishi T, Furuya T (1972) Studies on the cultural conditions of plant cell suspension culture. In: Terui G (ed) Fermentation technology today. Society for Fermentation Technology, Osaka, pp 697–703
Yue CJ, Zhong JJ (2008) Manipulation of ginsenoside heterogeneity of Panax notoginseng cells in flask and bioreactor cultivations with addition of phenobarbital. Bioprocess Biosyst Eng 31(2):95–100
Mallol A, Cusido RM, Palazon J, Bonfill M, Morales C, Pinol MT (2001) Ginsenoside production in different phenotypes of Panax ginseng transformed roots. Phytochemistry 57:365–371
Mirjalili MH, Moyano E, Bonfill M, Cusido RM, Palazon J (2009) Steroidal lactones from Withania somnifera, an ancient plant for novel medicine. Molecules 14:2373–2393
Osuna L, Moyano E, Mangas S, Bonfill M, Cusidó RM, Piñol MT, Zamilpa A, Tortoriello J, Palazón J (2008) Immobilization of Galphimia glauca plant cell suspensions for the production of enhanced amounts of Galphimine-B. Planta Med 74(1):94–99
Engelmann NJ, Clinton SK, Erdman JW Jr (2011) Nutritional aspects of phytoene and phytofluene, carotenoid precursors to lycopene. Adv Nutr 2(1):51–61
Khachik F, Carvalho L, Bernstein PS, Muir GJ, Zhao DY, Katz NB (2002) Chemistry, distribution, and metabolism of tomato carotenoids and their impact on human health. Exp Biol Med (Maywood) 227:845–851
Campbell JK, Rogers RB, Lila MA, Erdman JW Jr (2006) Biosynthesis of 14C-phytoene from tomato cell suspension cultures (Lycopersicon esculentum) for utilization in prostate cancer cell culture studies. J Agric Food Chem 54:747–755
Engelmann NJ, Campbell JK, Rogers RB, Rupassara SI, Garlick PJ, Lila MA, Erdman JW Jr (2010) Screening and selection of high carotenoid producing in vitro tomato cell culture lines for [(13)C]-carotenoid production. J Agric Food Chem 58:9979–9987
Robertson GH, Mahoney NE, Goodman N, Pavlath AE (1995) Regulation of lycopene formation in cell suspension culture of VFNT tomato (Lycopersicon esculentum) by CPTA, growth regulators, sucrose, and temperature. J Exp Bot 46(287):667–673
Fosket DE, Radin DN (1983) Induction of carotenogenesis in cultured cells of Lycopersicon esculentum cultivar Ep-7. Plant Sci Lett 30:165–176
Radin DR (1986) A model cell culture system to study isoprenoid regulation in plants. Curr Top Plant Biochem Physiol 5:153–163
Dupont FM, Staraci LC, Chou B, Thomas BR, Williams BG, Mudd JB (1985) Effect of chilling temperatures upon cell cultures of tomato. Plant Physiol 77:64–68
Chen DH, Liu CJ, Ye HC, Li GF, Liu BY, Meng YL, Chen XY (1999) Ri-mediated transformation of Artemisia annua with a recombinant farnesyl diphosphate synthase gene for artemisinin production. Plant Cell Tissue Organ Cult 57:157–162
Exposito O, Syklowska-Baranek K, Moyano E, Onrubia M, Bonfill M, Palazon J, Cusido RM (2010) Metabolic responses of Taxus media transformed cell cultures to the addition of methyl jasmonate. Biotechnol Prog 26:1145–1153
Mirjalili MH, Moyano E, Bonfill M, Cusido RM, Palazon J (2011) Overexpression of the Arabidopsis thaliana squalene synthase gene in Withania coagulans hairy root cultures. Biol Plant 55:357–360
Zhang W, Franco C, Curtin C, Conn S (2004) To stretch the boundary of secondary metabolite production in plant cell-based bioprocessing: anthocyanin as a case study. J Biomed Biotech 5:264–271
Capell T, Christou P (2004) Progress in plant metabolic engineering. Curr Opin Biotechnol 15:148–154
Goossens A, Haïkkinen ST, Laakso I, Seppänen-Laakso T, Stefania Biondi S, De Sutter V et al (2003) A functional genomics approach toward the understanding of secondary metabolism in plant cells. Proc Natl Acad Sci USA 100:8595–8600
Acknowledgments
Work in the Plant Physiology Laboratory (University of Barcelona) was financially supported by the Spanish MEC (BIO2008-01210, BIO2011-29856-C02-01) and the Generalitat de Catalunya (2009SGR1217).
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2013 Springer-Verlag Berlin Heidelberg
About this entry
Cite this entry
Bonfill, M., Malik, S., Mirjalili, M.H., Goleniowski, M., Cusido, R., Palazón, J. (2013). Production and Genetic Engineering of Terpenoids Production in Plant Cell and Organ Cultures. In: Ramawat, K., Mérillon, JM. (eds) Natural Products. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-22144-6_123
Download citation
DOI: https://doi.org/10.1007/978-3-642-22144-6_123
Published:
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-22143-9
Online ISBN: 978-3-642-22144-6
eBook Packages: Chemistry and Materials ScienceReference Module Physical and Materials ScienceReference Module Chemistry, Materials and Physics