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Sucrose regulated enhanced induction of anthraquinone, phenolics, flavonoids biosynthesis and activities of antioxidant enzymes in adventitious root suspension cultures of Morinda citrifolia (L.)

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An Erratum to this article was published on 22 September 2011

An Erratum to this article was published on 22 September 2011

Abstract

The effect of initial sucrose concentration was investigated in root suspension cultures of Morinda citrifolia to improve root growth and secondary metabolites production, i.e. anthraquinone, phenolics and flavonoids. Besides, oxidative stress level, antioxidant enzymes activity and membranes damage under different sucrose concentration were estimated. A 5% sucrose supply was shown to be optimal for the production of root dry mass, but higher sucrose concentrations of 7–9% inhibited the accumulation of root dry weight (DW). However, the maximum production of anthraquinone (251.89 g L−1 DW), phenolics (165.14 g L−1 DW) and flavonoids (163.56 g L−1 DW) were achieved at 1% sucrose-treated culture, which may be a source carbon skeletons for secondary metabolism. At the same time was observed low oxidative damage, which could be associated with high levels of secondary metabolites and the increased activity of catalase. Although, catalase (CAT) activity were stimulated at 7–9% sucrose-treated cultures, high accumulation of hydrogen peroxide (H2O2) and peroxidation of lipid (MDA) was induced. The observed high activity of CAT and guaiacol peroxidase (G-POD) were not sufficient enough to mitigate the toxic effect of H2O2.

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Abbreviations

AQ:

Anthraquinone

CAT:

Catalase

DPPH:

1,1-Diphenyl-2-picrylhydrazyl

G-POD:

Guaiacol peroxidase

IBA:

Indole butyric acid

MDA:

Malondialdehyde

MS:

Murashige and Skoog

References

  • Ahmad P, Sarwat M, Sharma S (2008) Reactive oxygen species, antioxidants and signaling in plants. J Plant Biol 51:167–173

    Article  CAS  Google Scholar 

  • Ahmed S, Nawata E, Hosokawa M, Domae Y, Sakuratani T (2002) Alterations in photosynthesis and some antioxidant enzymetic activities of mungbean subjected to water logging. Plant Sci 163:117–123

    Article  CAS  Google Scholar 

  • Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress and signal transduction. Ann Rev Plant Biol 55:373–399

    Article  CAS  Google Scholar 

  • Baque MA, Hahn EJ, Paek KY (2010a) Induction mechanism of adventitious root from leaf explant of M. citrifolia as affected by auxin and light quality. In Vitro Cell Dev Biol Plant 46:71–80

    Article  CAS  Google Scholar 

  • Baque MA, Hahn EJ, Paek KY (2010b) Growth, secondary metabolite production and antioxidant enzyme response of M. citrifolia adventitious root as affected by auxin and cytokinin. Plant Biotechnol Rep 4:109–116

    Article  Google Scholar 

  • Baque MA, Lee EJ, Paek KY (2010c) Medium salt strength induced changes in growth, physiology and secondary metabolite content in adventitious roots of M. citrifolia: the role of antioxidant enzymes and phenylalanine ammonia lyase. Plant Cell Rep 29:685–694

    Article  Google Scholar 

  • Berglund T, Ohlsson AB (1995) Defensive and secondary metabolism in plant tissue cultures, with special reference to nicotinamide glutathione and oxidative stress. Plant Cell Tiss Org Cult 43:137–145

    Article  CAS  Google Scholar 

  • Bisht SS, Sharma A, Chaturvedi K (1989) Certain metabolic lesions of chromium toxicity in radish. Indian J Agric Biochem 2:109–115

    CAS  Google Scholar 

  • Bradford MM (1976) A rapid and sensitive method for the quantization of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254

    Article  PubMed  CAS  Google Scholar 

  • Calamar A, Klerk GJD (2002) Effect of sucrose of adventitious root regeneration in apple. Plant Cell Tiss Org Cult 70:207–212

    Article  CAS  Google Scholar 

  • Creasy LL (1968) The significance of carbohydrate metabolism in flavonoid synthesis in strawberry leaf disks. Phytochem 7:1743–1749

    Article  CAS  Google Scholar 

  • Cui XH, Murthy HN, Wu CH, Paek KY (2010) Sucrose induced osmotic stress affects biomass, metabolite, and antioxidant levels in root suspension cultures of Hypericum perforatum L. Plant Cell Tiss Org Cult 103:7–14

    Article  CAS  Google Scholar 

  • Gould AR, Everett NP, Wang TL, Street HE (1981) Studies on the control of cell cycle in cultured plant cells: I. Effect of nutrient limitation and nutrient starvation. Protoplasma 106:1–13

    Article  CAS  Google Scholar 

  • Haissing BE (1982) Carbohydrate and amino acid concentrations during adventitious root primordium development in Pinus banksiana Lamb. Cuttings For Sci 28:813–821

    Google Scholar 

  • Hatano T, Kagawa H, Yasuhara T, Okuda T (1998) Two new flavonoids and other constituents in licorice: their relative astringency and radical scavenging effects. Chem Pharm Bull 36:2090–2097

    Article  Google Scholar 

  • Heath RL, Packer L (1968) Photo-peroxidation in isolated chloroplasts I Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198

    Article  PubMed  CAS  Google Scholar 

  • Hodges DM, De Long JM, Forney CF, Prange RK (1999) Improving the thioberbituric acid-reactive substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Planta 207:604–611

    Article  CAS  Google Scholar 

  • Jeong CS, Chakrabarty D, Hahn EJ, Lee HL, Paek KY (2006) Effect of oxygen, carbon dioxide and ethylene on growth and bioactive compound production in bioreactor culture of ginseng adventitious roots. Biochem Eng J 27:252–263

    Article  CAS  Google Scholar 

  • Kilayri JM, Bahrany AM (2002) Callus growth and proline accumulation in response to sorbitol and sucrose induced osmotic stress in rice. Biol Plant 45:609–611

    Article  Google Scholar 

  • Koch K (2004) Sucrose metabolism: regulatory mechanisms and pivotal roles in sugar-sensing and plant development. Curr Opin Plant Biol 7:235–246

    Article  PubMed  CAS  Google Scholar 

  • Koch KC (1996) Carbohydrate-modulated gene expression in plants. Ann Rev Plant Physiol Plant Mol Biol 47:509–540

    Article  CAS  Google Scholar 

  • Kombrink E, Somssich IE (1995) Defense responses of plants to pathogens. Adv Bot Res 21:1–34

    Article  CAS  Google Scholar 

  • Krapp A, Hofmann B, Schafer C, Stitt M (1993) Regulation of the expression rbcS and other photosynthetic genes by carbohydrates: a mechanism for the skin regulation of photosynthesis. Plant J 3:817–828

    Article  CAS  Google Scholar 

  • Larronde F, Krisa S, Decendit A, Cheze C, Deffieux G, Merillon JM (1998) regulation of polyphenol production in Vitis vinifera cell suspension cultures by sugars. Plant Cell Rep 17:946–950

    Article  CAS  Google Scholar 

  • Lian ML, Chakrabarty D, Paek KY (2002) Effect of plant growth regulators and medium composition on cell growth and saponin production during cell suspension culture of mountain ginseng (Panax ginseng C. A. Mayer). J Plant Biol 45:201–206

    Article  CAS  Google Scholar 

  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Mol Biol 29:479–489

    Google Scholar 

  • Morkunas I, Garnczarska M, Bednarski W, Ratajczak W, Waplak S (2003) Metabolic and ultrastructural responses of lupine embryo axes to sugar starvation. J Plant Physiol 160:311–319

    Article  PubMed  CAS  Google Scholar 

  • Putter J (1974) Peroxidases. In: Bergmeyer HU (ed) Methods of enzymatic analysis. Academic Press, New York, pp 685–690

    Google Scholar 

  • Roitsch T, Bittner M, Godt DE (1995) Induction of apoplastic invertase of Chenopodium rubrum by d-glucose and a glucose analog and tissue-specific expression suggest a role in sink-source regulation. Plant Physiol 108:285–294

    Article  PubMed  CAS  Google Scholar 

  • Rolland F, Baena-Gonzalez E, Sheen J (2006) Sugar sensing and signaling in plants: conserved and novel mechanisms. Ann Rev Plant Biol 57:675–709

    Article  CAS  Google Scholar 

  • Sergiev I, Alexieva V, Karanov E (1997) Effect of spermine, atrazine and combination between them on some endogenous protective systems and stress markers in plants. C R Acad Bulg Sci 51:121–124

    Google Scholar 

  • Shin KS, Chakrabarty D, Ko JY, Han SS, Paek KY (2002) Sucrose utilization and mineral nutrient uptake during hairy root growth of red beet (Beta vulgaris L.) in liquid culture. Plant Growth Regul 39:187–193

    Article  Google Scholar 

  • Shohael AM, Chakrabarty D, Ali MB, Yu KW, Hahn EJ, Paek KY (2006) Enhancement of Eleutherosides production in embryogenic cultures of Eleutherococcus sessiliflorus in response to sucrose induced osmotic stress. Process Biochem 41:512–518

    Article  CAS  Google Scholar 

  • Smirnoff N (2000) The role of active oxygen in the response of plants to water deficit and desiccation. New Phytol 125:27–58

    Article  Google Scholar 

  • Solfanelli C, Poggi A, Loreti E, Alpi A, Perata P (2006) Sucrose-specific induction of the anthocyanin biosynthetic pathway in Arabidopsis. Plant Physiol 140:637–646

    Article  PubMed  CAS  Google Scholar 

  • Sturm A, Tang GQ (1999) The sucrose cleaving enzymes of plants are crucial for development, growth and carbon partitioning. Trends Plant Sci 4:401–407

    Article  PubMed  Google Scholar 

  • Visser RG, Stolte A, Jacobsen E (1991) Expression of a chimaeric granule-bound starch synthase-GUS gene in transgenic potato plants. Plant Mol Biol 4:691–699

    Article  Google Scholar 

  • Vitrac X, Larronde F, Krisa S, Decendit A, Deffieux G, Merillon JM (2000) Sugar sensing and Ca2+-calmodulin requirement in Vitis vinifera cells producing anthocyanins. Phytochem 53:659–665

    Article  CAS  Google Scholar 

  • Wang MY, Brett JW, Jensen CJ, Nowicki D, Su C, Paul AK, Anderson G (2002) M. citrifolia(Noni): A literature review and recent advances in noni research. Acta Pharm Sin 23:1127–1141

    CAS  Google Scholar 

  • Wang MY, Su C (2001) Cancer preventive effect of Morinda citrifolia (Noni). Ann N Y Acad Sci 952:161–168

    Article  PubMed  CAS  Google Scholar 

  • Wang W, Vinocur B, Altman A (2003) Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance. Planta 218:1–14

    Article  PubMed  CAS  Google Scholar 

  • Wang Y, Weathers PJ (2007) Sugars proportionately affect artemisinin production. Plant Cell Rep 26:1073–1081

    Article  PubMed  Google Scholar 

  • Weathers PJ, DeJesus-Gonzalez L, Kim YJ, Souret FF, Towler MJ (2004) Alternation of biomass and artemisinin production in Artemisia annua hairy roots by media sterilization method and sugars. Plant Cell Rep 23:414–418

    Article  PubMed  CAS  Google Scholar 

  • Wilson G, Balague C (1985) Synthesis of anthraquinone by cells of Galium mollugo L. grown in a chemostat with limiting sucrose or phosphate. J Exp Bot 36:485–493

    Article  CAS  Google Scholar 

  • Wu CH, Dewir YH, Hahn EJ, Paek KY (2006) Optimization of culturing conditions for the production of biomass and phenolics from adventitious roots of Echinacea aungustifolia. J Plant Biol 49:193–199

    Article  CAS  Google Scholar 

  • Yu KW, Hahn EJ, Paek KY (2000) Production of adventitious ginseng roots using bioreactors. Kor J Plant Tiss Cult 27:309–315

    Google Scholar 

  • Zenk MH, Shagi HEL, Schulte U (1975) Anthraquinone production by cell suspension cultures of M. citrifolia. Planta med 28:79–101

    Article  Google Scholar 

  • Zenk MH, Shagi HEL, Ulbrich B (1977) Production of rosmarinic acid by cell suspension cultures Coleus hlumei. Naturwissenschaften 64:585–586

    Article  CAS  Google Scholar 

  • Zhang YH, Zhong JJ, Yu JT (1996) Enhancement of ginseng saponin production in suspension cultures of Panax notoginseng: Manipulation of medium sucrose. J Biotechnol 51:49–56

    Article  CAS  Google Scholar 

  • Zhong JJ, Fujiyama K, Seki T, Yoshida T (1994) A quantitative analysis of shear effects on cell suspension and cell cultures of Perilla frutescens in bioreactors. Biotechnol Bioeng 44:649–654

    Article  PubMed  CAS  Google Scholar 

  • Zimmermann MH, Ziegler H (1975) List of sugars and sugar alcohols in sieve-tube exudates. In: Zimmermann MH, Milburn JA (eds) Encyclopedia of plant physiology, new series vol 1. Springer, Berlin, pp 480–503

    Google Scholar 

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Correspondence to Kee-Yoeup Paek.

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Communicated by M. Stobiecki.

An erratum to this article can be found at http://dx.doi.org/10.1007/s11738-011-0854-1.

An erratum to this article can be found at http://dx.doi.org/10.1007/s11738-011-0854-1.

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Baque, M.A., Elgirban, A., Lee, EJ. et al. Sucrose regulated enhanced induction of anthraquinone, phenolics, flavonoids biosynthesis and activities of antioxidant enzymes in adventitious root suspension cultures of Morinda citrifolia (L.). Acta Physiol Plant 34, 405–415 (2012). https://doi.org/10.1007/s11738-011-0837-2

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