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Marked effect of Cuscuta on puerarin accumulation in cell cultures of Pueraria tuberosa grown in shake flasks and a bioreactor

  • Goyal, Shaily (Laboratory of Bio-Molecular Technology, Department of Botany, M. L. Sukhadia University) ;
  • Sharma, Varsha (Laboratory of Bio-Molecular Technology, Department of Botany, M. L. Sukhadia University) ;
  • Ramawat, Kishan G. (Laboratory of Bio-Molecular Technology, Department of Botany, M. L. Sukhadia University)
  • Received : 2010.03.10
  • Accepted : 2010.12.15
  • Published : 2011.04.30

Abstract

Isoflavonoid production in cell cultures of Pueraria tuberosa as influenced by an angiospermic parasite, Cuscuta reflexa, was studied. During the time course, maximum isoflavonoid content was recorded when Cuscuta elicitor was added on day 15 of culture. Among various concentrations of elicitor tried, $1g\;l^{-1}$ of Cuscuta elicitor was found to be the most effective. The optimized elicitation conditions were used in vessels of varying capacity where maximum yield of ${\sim}91mg\;l^{-1}$ of isoflavonoid was recorded in a 2-l bioreactor which was about 19% higher than the control cultures. In this case, puerarin content increased up to $11mg\;l^{-1}$ which was 580% higher that the value recorded in the control cultures. In the bioreactor, 8 days of elicitation was optimal for the high accumulation of isoflavonoid, giving productivity of ${\sim}4mg\;l^{-1}\;day^{-1}$. The study showed persistent high isoflavonoid yield even during scale-up. Use of a preparation of Cuscuta reflexa as an elicitor is reported for the first time. The increase in isoflavonoid content was elicitor dose-dependent and can be explored to trigger high yields of isoflavonoid/secondary metabolites in production.

Keywords

References

  1. Albert M, Belastegui-Macadam X, Bleischwitz M, Kaldenhoff R (2008) Cuscuta spp.: parasitic plants in the spotlight of plant physiology, economy and ecology. In: Luttge U, Beyschlag W, Murata J (eds) Progess in botany, vol 69. Springer, Berlin, pp 267-281.
  2. Arora J, Goyal S, Ramawat KG (2010) Enhanced stilbene production in cell cultures of Cayratia trifolia through co-treatment with abiotic and biotic elicitors and sucrose. In Vitro Cell Dev Biol Plant 46:430-436. https://doi.org/10.1007/s11627-010-9308-5
  3. Bingham SA, Atkinson C, Liggins J, Bluck L, Coward A (1998) Phytoestrogens: where are we now? Br J Nutr 79:393-406. https://doi.org/10.1079/BJN19980068
  4. Dai R, Ma Y, Sheng Z, Jin Y, Zhang Y, Fang L, Fan H, Liao E (2008) Effects of Genistein on vertebral trabecular bone microstructure, bone mineral density, microcracks, osteocyte density, and bone strength in ovariectomized rats. J Bone Miner Metab 26:342-349. https://doi.org/10.1007/s00774-007-0830-4
  5. Dass S, Ramawat KG (2009) Elicitation of guggulsterone production in cell cultures of Commiphora wightii by plant gums. Plant Cell Tissue Org Cult 96:349-353. https://doi.org/10.1007/s11240-008-9493-7
  6. Dev S (2006) Selection of prime ayurvedic plant drugs ancient- modern concordance. Anamaya, New Delhi, India.
  7. Goyal S, Ramawat KG (2008a) Synergistic effect of morphactin on cytokinin-induced production of isoflavonoid in cell cultures of Pueraria tuberosa (Roxb. ex. Willd.) DC. Plant Growth Regul 55:175-181. https://doi.org/10.1007/s10725-008-9271-x
  8. Goyal S, Ramawat KG (2008b) Increased isoflavonoid accumulation in cell suspension cultures of P. tuberosa by elicitors. Indian J Biotech 7:378-382.
  9. Goyal S, Ramawat KG (2008c) Improvement of isoflavonoid accumulation by ethrel in cell suspension cultures of Pueraria tuberosa, a woody legume. Acta Physiol Plant 30:849-853. https://doi.org/10.1007/s11738-008-0190-2
  10. Jardin A (2002) Synthesis of natural occurring isoflavones and their analogues. In: Keung WM (ed) Pueraria. Taylor & Francis, London, pp 225-242.
  11. Kirakosyan A, Kaufman PB, Chang SC, Warber S, Bolling S, Vardapetyan H (2006) Regulation of isoflavone in hydroponically grown Pueraria montana (kudzu) by cork pieces, XAD-4, and methyl jasmonate. Plant Cell Rep 25:1387-1391. https://doi.org/10.1007/s00299-006-0198-2
  12. Luczkiewicz M (2008) Research into isoflavonoid: phytoestrogens in plant cell cultures. In: Ramawat KG, Merillon JM (eds) Bioactive molecules and medicinal plants. Springer, Heidelberg, pp 54-84
  13. Maojun XU, Jufang D, Muyuan Z (2006) Nitric oxide mediates the fungal elicitor-induced puerarin biosynthesis in Pueraria thomsonii Benth suspension cells through a salicylic acid (SA)- dependent and a jasmonic acid (JA)-dependent signal pathway. Sci China Ser C Life Sci 49:1-11.
  14. Mizushige T, Mizushige K, Miyatake A, Kishida T, Ebihara K (2007) Inhibitory effects of soy isoflavones on cardiovascular collagen accumulation in rats. J Nutr Sci Vitaminol 53:48-52. https://doi.org/10.3177/jnsv.53.48
  15. Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol Plant 15:473-497. https://doi.org/10.1111/j.1399-3054.1962.tb08052.x
  16. Ramawat KG, Goyal S (2008) The Indian herbal drug scenario in global perspectives. In: Ramawat KG, Merillon JM (eds) Bioactive molecules and medicinal plants. Springer, Heidelberg, pp 325-347
  17. Ramawat KG, Dass S, Mathur M (2009) The chemical diversity of bioactive molecules and therapeutic potential of medicinal plants. In: Ramawat KG (ed) Herbal drugs: ethnomedicine to modern medicine. Springer, Berlin, pp 7-32.
  18. Ren MQ, Kuhn G, Wegner J, Chen J (2001) Isoflavones, substances with multi-biological and clinical properties. Eur J Nutr 40:135-146. https://doi.org/10.1007/PL00007388
  19. Savitha BC, Timmaraju R, Bhagyalaksami N, Ravishankar GA (2006) Different biotic and abiotic elicitors influence betalain production in hairy root cultures of Beta vulgaris in shake flask and bioreactor. Process Biochem 41:50-60. https://doi.org/10.1016/j.procbio.2005.03.071
  20. Sharma V, Goyal S, Ramawat KG (2009) Scale up production of isoflavonoid in cell suspension cultures of Pueraria tuberosa grown in shake flasks and bioreactor. Eng Lif Sci 9:267-271. https://doi.org/10.1002/elsc.200800114
  21. Sudha G, Ravishankar GA (2002) Involvement and interaction of various signaling compounds on the plant metabolic events during defense response, resistance to stress factors, formation of secondary metabolites and their molecular aspects. Plant Cell Tissue Org Cult 71:181-212. https://doi.org/10.1023/A:1020336626361
  22. Suri SS, Ramawat KG (1996) Effect of Calotropis latex on laticifers differentiation in callus cultures of Calotropis procera. Biol Planta 38:185-190. https://doi.org/10.1007/BF02873844
  23. Tanwar YS, Mathur M, Ramawat KG (2007) Morphactin influences guggulsterone production in callus cultures of Commiphora wightii. Plant Growth Regul 51:93-98. https://doi.org/10.1007/s10725-006-9151-1
  24. Vaishnav K, Goyal S, Ramawat KG (2006) Isoflavonoid production in callus culture of Pueraria tuberosa, the India kudzu. Indian J Exp Biol 44:1012-1017.
  25. Yamamoto H, Yamaguchi M, Inoue K (1996) Absorption and increase in the production of prenylated flavanones in Sophora flavescens cell suspension cultures by cork pieces. Phytochemistry 43:603-608. https://doi.org/10.1016/0031-9422(96)00321-4
  26. Zhao J, Verpoorte R (2007) Manipulating indole alkaloid production by Catharanthus roseus cell cultures in bioreactors: from biochemical processing to metabolic engineering. Phytochem Rev 6:435-457. https://doi.org/10.1007/s11101-006-9050-0
  27. Zhao J, Lawrence CD, Verpoorte R (2005) Elicitor signal transduction leading to production of plant secondary metabolites. Biotechnol Adv 23:283-333.

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