Abstract
The relationships between aggregate cell types, cell growth, and the triptolide, wilforgine, and wilforine content in aggregate cell suspension cultures of Tripterygium wilfordii Hook. f. were examined. Aggregate cells larger than 2 mm grew quickly and constituted the majority of the white aggregates. The accumulation of triptolide was strongly correlated with the size of the aggregates and the length of the culture period. The aggregates 0.5–2 mm in diameter accumulated higher triptolide content than those with other sizes throughout the culture. However, the size of the aggregate cells did not significantly affect on the wilforgine and wilforine content. Two other kinds of aggregate cells, the brown and green aggregate cells, also formed in the suspension cultures. The smallest aggregates (0.1–0.5 mm) had a lower biomass and growth rate and had more chloroplasts and higher alkaloid content. The results of this study can be used to improve the selection process for the mass production of triptolide, wilforgine, and wilforine from cell suspension cultures.
References
Beroza M (1952) Alkaloids from Tripterygium wilfordii Hook.: wilforgine and wilfortrine. J Am Chem Soc 74:1585–1588
Bolta Ž, Baričevič D, Raspor P (2003) Biomass segregation in sage cell suspension culture. Biotechonol Lett 25:61–65
Boonsnongcheep P, Korsangruang S, Soonthornchareonnon N, Chintapakorn Y, Saralamp P, Prathanturarug S (2010) Growth and isoflavonoid accumulation of Pueraria candollei var. candollei and P. candollei var. mirifica cell suspension cultures. Plant Cell Tissue Organ Cult 101:119–126
Brinker AM, Raskin I (2005) Determination of triptolide in root extracts of Tripterygium wilfordii by solid-phase extraction and reverse-phase high-performance liquid chromatography. J Chromatogr A 1070:65–70
Brinker AM, Ma J, Lipsky PE, Raskin I (2007) Medicinal chemistry and pharmacology of genus Tripterygium (Celastraceae). Phytochemistry 68:732–766
Capataz-Tafur J, Rodríguez-Monroy M, Trejo-Tapia G, Sepúlveda-Jiménez G (2011) Arabinogalactan proteins are involved in cell aggregation of cell suspension cultures of Beta vulgaris L. Plant Cell Tissue Organ Cult 106:169–177
Dai KM, Wang Y (1994) Determination of total alkaloids in different areas and different application parts of Triptergium wilfordii and T. hypoglaucun. Chin Tradit Pat Med 16:41–42
Ellis DD, Zeldin EL, Brodhagen M, Russin WA, McCown BH (1996) Taxol production in nodule cultures of Taxus. J Nat Prod 59:246–250
Gamborg OL, Eveleigh DE (1968) Culture methods and detection of glucanases in suspension cultures of wheat and barley. J Biochem 46:417
Hulst AC, Meyer MMT, Breteler H, Tramper J (1989) Effect of aggregate size in cell cultures of Tagetes patula on thiophene production and cell growth. Appl Microbiol Biotechnol 30:18–25
Keßler M, Ten Hoopen HJG, Furusaki S (1999) The effect of the aggregate size on the production of ajmalicine and tryptamine in Catharanthus roseus suspension culture. Enzym Microb Tech 24:308–315
Kolewe ME, Henson MA, Roberts SE (2010) Characterization of aggregate size of Taxus suspension cell culture. Plant Cell Rep 29:485–494
Kolewe ME, Roberts SC, Henson MA (2012) A population balance equation model of aggregation dynamics in Taxus suspension cell cultures. Biotechnol Bioeng 109:472–482
Kutney JP, Choi LS, Duffin R, Hewitt G, Kawamura N, Kurihara T, Salisbury P, Sindelar R, Stuart KL, Townsley PM, Chalmers WT, Webster F, Jacoli GG (1983) Cultivation of Tripterygium wilfordii tissue cultures for the production of the cytotoxic diterpene tripdiolide. Planta Med 48:158–163
Lange BM, Rujan T, Martin W, Croteau R (2000) Isoprenoid biosynthesis: the evolution of two ancient and distinct pathways across genomes. Proc Natl Acad Sci 97:13172–13177
Lee EK, Jin YW, Park JH et al (2010) Cultured cambial meristematic cells as a source of plant natural products. Nat Biotechnol 28:1213–1217
Liu Q (2011) Triptolide and its expanding multiple pharmacological functions. Int Immunopharmacol 11:377–383
Luo DQ, Zhang X, Tian X, Liu JK (2004) Insecticidal compounds from Tripterygium wilfordii active against Mythimna separata. Z Naturforsch C 59:421–426
Ma J, Brach AR, Liu Q (1999) A revision of the genus Tripterygium (Celastraceae). Edinb J Bot 56:33–46
Madhusudhan R, Ravishankar GA (1996) Gradient of anthocyanin in cell aggregates of Daucus carota in suspension cultures. Biotechnol Lett 18:1253–1256
Monache FD, Bettolo GBM, Bernays EA (1984) Isolation of insect antifeedant alkaloids from Maytenus rigida (Celastraceae). Zeitschrift für Angewandte Entomologie 97:406–414
Oksman-Caldentey K, Inz D (2004) Plant cell factories in the post-genomic era: new ways to produce designer secondary metabolites. Trends Plant Sci 9:433–440
Pépin MF, Chavarie C, Archambault J (1991) Growth and immobilization of Tripterygium wilfordii cultured cells. Biotechnol Bioeng 38:1285–1291
Plas LHWV, Eijkelboom C, Hagendoorn MJM (1995) Relation between primary and secondary metabolism in plant cell suspension; competition between secondary metabolite production and growth in a model system (Morinda citrifolia). Plant Cell Tissue Organ Cult 43:111–116
Schlatmann JE, Vinke JL, ten Hoopen HJG, Heijnen JJ (1995) Relation between dissolved oxygen concentration and ajmalicine production rate in high density cultures of Catharanthus roseus. Biotechnol Bioeng 45:435–439
Simões-Gurgel C, Cordeiro LS, Castro TC, Callado CH, Albarello N, Mansur E (2011) Establishment of anthocyanin-producing cell suspension cultures of Cleome rosea Vahl ex DC (Capparaceae). Plant Cell Tissue Organ Cult 106:537–545
Smetanska I (2008) Production of secondary metabolites using plant cell cultures. Adv Biochem Eng/Biotechnol 111:187–228
Sun YM, Xu JZ, Wang ZA, Yu XP (2009) Determination of triptolide in different ages of root and different parts of Tripterygium wilfordii Hook.f. by HPLC. Chin J Mod Appl Pharm 26:904–906
Tholl D (2006) Terpene synthases and the regulation, diversity and biological roles of terpene metabolism. Curr Opin Plant Biol 9:1–8
Trejo-Tapia G, Rodríguez-Monroy M (2007) Cellular aggregation in secondary metabolite production in in vitro plant cell cultures. Interciencia 32:669–674
Tsoulpha P, Doran PM (1991) Solasodine production from self-immobilised Solanum aviculare cells. J Biotechnol 19:99–110
Xia Z, Chen J (1990) Alkaloids from stems and leaves of Tripterygium wilfordii. Chin Pham J 25:266–267
Xu JF, Su ZG, Feng PS (1998a) Suspension culture of compact callus aggregate of Rhodiola sachalinensis for improved salidroside production. Enzym Microb Technol 23:20–27
Xu JF, Yin PQ, Wei XG, Su ZG (1998b) Self-immobilized aggregate culture of Taxus cuspidata for improved taxol production. Biotechnol Tech 12:241–244
Zhao J, Zhu WH, Hu Q, He XW (2001) Enhanced indole alkaloid production in suspension compact callus clusters of Catharanthus roseus: impacts of plant growth regulators and sucrose. Plant Growth Regul 33:33–41
Zhao D, Huang Y, Jin Z, Qu W, Lu D (2003) Effect of aggregate size in cell cultures of Saussurea medusa on cell growth and jaceosidin production. Plant Cell Rep 21:1129–1133
Acknowledgments
This work is supported by the National 863 project (2011AA10A202-1) and the Special Fund for Agro-scientific Research in the Public Interest (No. 200903052).
Author information
Authors and Affiliations
Corresponding author
Additional information
Guo-peng Miao and Chuan-shu Zhu contributed equally to this work.
Rights and permissions
About this article
Cite this article
Miao, Gp., Zhu, Cs., Feng, Jt. et al. Aggregate cell suspension cultures of Tripterygium wilfordii Hook. f. for triptolide, wilforgine, and wilforine production. Plant Cell Tiss Organ Cult 112, 109–116 (2013). https://doi.org/10.1007/s11240-012-0211-0
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11240-012-0211-0