DOI QR코드

DOI QR Code

Effect of elicited by methyl jasmonate on the saponin contents of Codonopsis lanceolata

Elicitor처리가 더덕사포닌 함량에 미치는 영향

  • Kim, Ji-Ah (Division of Forest Biotechnology, Korea Forest Research Institute) ;
  • Bae, Kee-Hwa (Nakdonggang National Institute of Biological Resources) ;
  • Choi, Yong-Eui (Department of Forest Resources, Kangwon National University)
  • 김지아 (국립산림과학원 산림생명공학과) ;
  • 배기화 (국립낙동강 생물자원관) ;
  • 최용의 (국립강원대학교 산림자원학과)
  • Received : 2015.09.01
  • Accepted : 2015.09.22
  • Published : 2015.09.30

Abstract

The roots of Codonopsis lanceolata (Campanulaceae) contain several kinds of triterpenoid saponin with high medicinal values, which have been used in traditional medicines. This study investigates the impacts of methyl jasmonate (MeJA) - adding time on the saponin synthesis and the hairy root growth of C. lanceolata. A significant decrease in major saponin (lancemaside of three kinds) content of hairy roots was observed with MeJA treatments. Contents of lancemaside A, B and E decreased about 15% more than non-treated hairy roots. In contrast, minor saponin (foetidissimoside A and aster saponin Hb) accumulation was about 15% higher than the non-treated hairy roots. These results suggest that MeJA treatment could be used in the production of teriterpene saponins.

더덕은 예로부터 약용으로 사용 되어 왔으며, 더덕의 뿌리에는 약용으로 가치가 높은 여러 종류의 triterpenoid 사포닌이 포함되어 있다. 본 연구에서는 더덕의 모상근 생육과 methyl jasmonate (MeJA)처리에 의한 사포닌 합성의 효과를 연구하였다. 더덕 모상근에 MeJA를 처리한 결과 주사포닌인 lancemaside A, B, E의 축적은 MeJA 무처리 모상근 보다 약 15% 정도 감소하였다. 반면 마이너사포닌(foetidissimoside A와 aster saponin Hb)의 함량은 무처리 모상근 보다 약15% 정도로 증가하였다. 이 결과를 통해 MeJA처리가 triterpene 사포닌의 생산조절을 위해 사용될 수 있는 것으로 판단된다.

Keywords

References

  1. Cheong JJ, Choi YD (2003) Methyl jasmonate as a vital substance in plants. Trends Genet 19:409-413 https://doi.org/10.1016/S0168-9525(03)00138-0
  2. Chodisetti B, Rao K, Gandi S, Giri A (2015) Gymnemic acid enhancement in the suspension cultures of Gymnema sylvestre by using the signaling molecules-methyl jasmonate and salicylic acid. In Vitro Cell Dev Biol Plant 51:88-92 https://doi.org/10.1007/s11627-014-9655-8
  3. Choi DW, JD Jung, Y Im Ha, HW Park, DS In, HJ Chung (2005) Analysis of transcripts in methyl jasmonate-treated ginseng hairy roots to identify genes involved in the biosynthesis of ginsenosides and other secondary metabolites. Plant Cell Rep 23:557-566 https://doi.org/10.1007/s00299-004-0845-4
  4. Gaidi G, Marouf A, Hanquet B, Bauer R, Correia M, Chauffert B and Lacaille-Dubois MA (2000) A new major triterpene saponin from the roots of Cucurbita foetidissima. J Nat Prod 63:122-124 https://doi.org/10.1021/np9902800
  5. Giri A, Narasu ML (2000) Transgenic hairy roots: recent trends and applications. Biotechnol Adv 18:1-22 https://doi.org/10.1016/S0734-9750(99)00016-6
  6. Ichikawa M, Ohta S, Komoto N, Ushijima M, Kodera Y, Hayama M, Shirota O, Sekita S and Kuroyanagi M (2009) Simultaneous determination of seven saponins in the roots of Codonopsis lanceolata by liquid chromatography-mass spectrometry. J Nat Med 63:52-57 https://doi.org/10.1007/s11418-008-0294-4
  7. Joh EH, Lee IA, Han SJ, Chae SJ and Kim DH (2010) Lancemaside A ameliorates colitis by inhibiting NF-${\kappa}B$ activation in TNBS-induced colitis mice. Int J Colorectal Dis 25:545-551 https://doi.org/10.1007/s00384-009-0858-0
  8. Jung IH, Jang SE, Joh EH, Chung J, Han MJ and Kim DH (2012) Lancemaside A isolated from Codonopsis lanceolata and its metabolite echinocystic acid ameliorate scopolamine-induced memory and learning deficits in mice. Phytomedicine 20:84-88 https://doi.org/10.1016/j.phymed.2012.09.005
  9. Kim JA, Kim YS, Choi YE. (2011) Triterpenoid production and phenotypic changes in hairy roots of Codonopsis lanceolata and the plants regenerated from them. Plant Biotechnol Rep 5:255-263 https://doi.org/10.1007/s11816-011-0180-5
  10. Kim OT, Bang KH, Kim YC, Hyu DY, Kim MY (2009) Upregulation of ginsenoside and gene expression related to triterpene biosynthesis in ginseng hairy root cultures elicited by methyl jasmonate. Plant Cell Tissue Organ Cult 98:25-33 https://doi.org/10.1007/s11240-009-9535-9
  11. Kim OT, Bang KH, Shin YS, Lee MJ, Jung SJ, Hyun DY, Kim YC, Seong NS, Cha SW (2007) Enhanced production of asiaticoside from hairy root cultures of Centella asiatica (L.) Urban elicited by methyl jasmonate. Plant Cell Rep 26:1941-1949 https://doi.org/10.1007/s00299-007-0400-1
  12. Kim OT, Yoo NH, Kim YC, Bang KH, Hyun DY, Kim SH, Kim MY (2013) Stimulation of Rg3 ginsenoside biosynthesis in ginseng hairy roots elicited by methyl jasmonate. Plant Cell Tissue Organ Cult 112:87-93 https://doi.org/10.1007/s11240-012-0218-6
  13. Kim YS, Hahn EJ, Murthy HN, Paek KY (2004) Adventitious root growth and ginsenoside accumulation in Panax ginseng cultures as affected by methyl jasmonate. Biotechnol Lett 26:1619-1622 https://doi.org/10.1007/s10529-004-3183-2
  14. Kim YS, Yeung EC, Hahn EJ, Paek KY (2007) Combined effects of phytohormone, indole-3-butyric acid, and methyl jasmonate on root growth and ginsenoside production in adventitious root cultures of Panax ginseng C.A. Meyer. Biotechnol Lett 29:1789-1792 https://doi.org/10.1007/s10529-007-9442-2
  15. Kim YS, Hahn EJ, Murthy HN, Paek KY (2004) Adventitious root growth and ginsenoside accumulation in Panax ginseng cultres as affected by methyl jasmonate. Biotechnol Lett 26:1619-1622 https://doi.org/10.1007/s10529-004-3183-2
  16. Kwak SS, Kim SK, Lee MS, Jung KH, Park IH, Liu JR (1995) Acidic perosidases from suspension-cultures of sweet potato. Phytochemistry 39:981-984 https://doi.org/10.1016/0031-9422(95)00098-R
  17. Lee EJ, Park SY, Paek KY (2015) Enhancement strategies of bioactive compound production in adventitious root cultures of Eleutherococcus koreanum Nakai subjected to methyl jasmonate and salicylic acid elicitation through airlift bioreactors. Plant Cell Tissue Organ Cult 120:1-10 https://doi.org/10.1007/s11240-014-0567-4
  18. Lim S, Bae KH, Shin CG, Kim YY, Kim YS (2005) Increasement of secondary metabolites and antioxidative activity in Panax ginseng adventitious root by methyl jasmonate. Korea J plant biotechnol 32:225-231 https://doi.org/10.5010/JPB.2005.32.3.225
  19. Murashige T and Skoog F (1962) A revised medium for rapid growth and bio assays with tobacco tissue cultures. Physiol Plant 15:473-497 https://doi.org/10.1111/j.1399-3054.1962.tb08052.x
  20. Pitta-Alvarez SI, Spollansky TC and Giulietti AM (2000) The influence of different biotic and abiotic elicitors on the production and profile of tropane alkaloids in hairy root cultures of Brugmansia candida. Enzyme Microb Technol 26:252-258 https://doi.org/10.1016/S0141-0229(99)00137-4
  21. Sekita S, Kuroyanagi M, Yasuda K, Mizuno I, Ushijima M, Hayama M, Ichikawa M and Sumihiro M (2005). Drug for ameliorating male climacteric disorder. U.S. Patent 2008 0274213 A1
  22. Ushijima M, Mizuno I, Suzuki E, Amayasu R, Ishii S, Nishihama, T, Morihara N, Kashimoto N, Mouri Y and Sumioka I (2007) Improvement of PADAM-like symptoms in middle-aged men by a designer food containing Codonopsis lanceolata. Pharmacometrics 72:23-30
  23. Weon JB, Yun BR, Lee JW, Eom MR, Ko HJ, Lee HY, Park DS, Chung HC, Chung JY, Ma CJ (2014) Neuroprotective Effect of Steamed and Fermented Codonopsis lanceolata. Biomol Ther (Seoul) 22:246-253 https://doi.org/10.4062/biomolther.2014.019
  24. Xu L, Wang H, Yuan Z (2008) Triterpenoid saponins with anti-inflammatory activity from Codonopsis lanceolata. Planta Med 74:1412-1415 https://doi.org/10.1055/s-2008-1081318
  25. Yan T, Fang L, Nopo-Olazabal C, Condori J, Nopo-Olazabal L, Balmaceda C, and Medina-Bolivar F (2015) Enhanced Production of Resveratrol, Piceatannol, Arachidin-1, and Arachidin-3 in Hairy Root Cultures of Peanut Co-treated with Methyl Jasmonate and Cyclodextrin. J Agric Food Chem 63:3942-3950 https://doi.org/10.1021/jf5050266