Synergistic effect of methyl jasmonate and cyclodextrins on anthraquinone accumulation in cell suspension cultures of Morinda citrifolia and Rubia tinctorum
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  • 作者:María Perassolo ; María Emilia Smith…
  • 关键词:Anthraquinones ; Cyclodextrin ; Elicitation ; Methyl jasmonate ; Plant in vitro culture ; Rubiaceae
  • 刊名:Plant Cell, Tissue and Organ Culture
  • 出版年:2016
  • 出版时间:February 2016
  • 年:2016
  • 卷:124
  • 期:2
  • 页码:319-330
  • 全文大小:547 KB
  • 参考文献:Almagro L, Bru R, Pugin A, Pedreno MA (2012) Early signaling network in tobacco cells elicited with methyl jasmonate and cyclodextrins. Plant Physiol Biochem 51:1–9. doi:10.​1016/​j.​plaphy.​2011.​09.​021 CrossRef PubMed
    Almagro L, Gutierrez J, Pedreño M, Sottomayor M (2014) Synergistic and additive influence of cyclodextrins and methyl jasmonate on the expression of the terpenoid indole alkaloid pathway genes and metabolites in Catharanthus roseus cell cultures. Plant Cell Tiss Organ Cult 119(3):543–551. doi:10.​1007/​s11240-014-0554-9 CrossRef
    Belchi-Navarro S, Almagro L, Lijavetzky D, Bru R, Pedreno MA (2012) Enhanced extracellular production of trans-resveratrol in Vitis vinifera suspension cultured cells by using cyclodextrins and methyljasmonate. Plant Cell Rep 31(1):81–89. doi:10.​1007/​s00299-011-1141-8 CrossRef PubMed
    Belchi-Navarro S, Almagro L, Sabater-Jara AB, Fernandez-Perez F, Bru R, Pedreno MA (2013) Early signaling events in grapevine cells elicited with cyclodextrins and methyl jasmonate. Plant Physiol Biochem 62:107–110. doi:10.​1016/​j.​plaphy.​2012.​11.​001 CrossRef PubMed
    Bóka K, Jakab J, Király I (2002) Comparison of the effect of different fungal elicitors on Rubia tinctorum L. suspension culture. Biol Plant 45(2):281–290. doi:10.​1023/​A:​1015113226897 CrossRef
    Briceño Z, Almagro L, Sabater-Jara AB, Calderon AA, Pedreno MA, Ferrer MA (2012) Enhancement of phytosterols, taraxasterol and induction of extracellular pathogenesis-related proteins in cell cultures of Solanum lycopersicum cv Micro-Tom elicited with cyclodextrins and methyl jasmonate. J Plant Physiol 169(11):1050–1058. doi:10.​1016/​j.​jplph.​2012.​03.​008 CrossRef PubMed
    Bru R, Selles S, Casado-Vela J, Belchi-Navarro S, Pedreno MA (2006) Modified cyclodextrins are chemically defined glucan inducers of defense responses in grapevine cell cultures. J Agric Food Chem 54(1):65–71. doi:10.​1021/​jf051485j CrossRef PubMed
    Bulgakov VP, Tchernoded GK, Mischenko NP, Khodakovskaya MV, Glazunov VP, Radchenko SV, Zvereva EV, Fedoreyev SA, Zhuravlev YN (2002) Effect of salicylic acid, methyl jasmonate, ethephon and cantharidin on anthraquinone production by Rubia cordifolia callus cultures transformed with the rolB and rolC genes. J Biotechnol 97(3):213–221CrossRef PubMed
    Busto VD, Calabró-López A, Rodríguez-Talou J, Giulietti AM, Merchuk JC (2013) Anthraquinones production in Rubia tinctorum cell suspension cultures: down scale of shear effects. Biochem Eng J 77:119–128. doi:10.​1016/​j.​bej.​2013.​05.​013 CrossRef
    Butterworth BE, Mathre OB, Ballinger K (2001) The preparation of anthraquinone used in the National Toxicology Program cancer bioassay was contaminated with the mutagen 9-nitroanthracene. Mutagenesis 16(2):169–177CrossRef PubMed
    Chong TM, Abdullah MA, Fadzillah NM, Lai OM, Lajis NH (2005) Jasmonic acid elicitation of anthraquinones with some associated enzymic and non-enzymic antioxidant responses in Morinda elliptica. Enzyme Microb Technol 36(4):469–477CrossRef
    Clark JH (2006) Green chemistry: today (and tomorrow). Green Chem 8(1):17–21. doi:10.​1039/​b516637n CrossRef
    Comini LR, Fernandez IM, Rumie Vittar NB, Nunez Montoya SC, Cabrera JL, Rivarola VA (2011) Photodynamic activity of anthraquinones isolated from Heterophyllaea pustulata Hook f. (Rubiaceae) on MCF-7c3 breast cancer cells. Phytomedicine 18(12):1093–1095. doi:10.​1016/​j.​phymed.​2011.​05.​008 CrossRef PubMed
    Constable DJC, Dunn PJ, Hayler JD, Humphrey GR, Leazer JJL, Linderman RJ, Lorenz K, Manley J, Pearlman BA, Wells A, Zaks A, Zhang TY (2007) Key green chemistry research areas-a perspective from pharmaceutical manufacturers. Green Chem 9(5):411–420. doi:10.​1039/​b703488c CrossRef
    Corchete P, Bru R (2013) Proteome alterations monitored by DIGE analysis in Silybum marianum cell cultures elicited with methyl jasmonate and methyl β cyclodextrin. J Proteomics 85:99–108. doi:10.​1016/​j.​jprot.​2013.​04.​032 CrossRef PubMed
    Di Rienzo JA, Casanoves F, Balzarini MG, Gonzalez L, Tablada M, Robledo CW (2010) InfoStat versión 2010, Grupo InfoStat. FCA, Universidad Nacional de Córdoba, Córdoba
    Doernenburg H, Knorr D (1994) Effectiveness of plant-derived and microbial polysaccharides as elicitors for anthraquinone synthesis in Morinda citrifolia cultures. J Agric Food Chem 42(4):1048–1052. doi:10.​1021/​jf00040a040 CrossRef
    Durante M, Caretto S, Quarta A, De Paolis A, Nisi R, Mita G (2011) Beta-cyclodextrins enhance artemisinin production in Artemisia annua suspension cell cultures. Appl Microbiol Biotechnol 90(6):1905–1913. doi:10.​1007/​s00253-011-3232-4 CrossRef PubMed
    Han YS, Van der Heijden R, Verpoorte R (2001) Biosynthesis of anthraquinones in cell cultures of the Rubiaceae. Plant Cell Tiss Organ Cult 67(3):201–220. doi:10.​1023/​A:​1012758922713 CrossRef
    Hanchinal VM, Survase SA, Sawant SK, Annapure US (2008) Response surface methodology in media optimization for production of β-carotene from Daucus carota. Plant Cell Tiss Organ Cult 123–132(93):123–132. doi:10.​1007/​s11240-008-9350-8 CrossRef
    Huang TK, Plesha MA, Falk BW, Dandekar AM, McDonald KA (2009) Bioreactor strategies for improving production yield and functionality of a recombinant human protein in transgenic tobacco cell cultures. Biotechnol Bioeng 102(2):508–520. doi:10.​1002/​bit.​22061 CrossRef PubMed
    Kolewe ME, Gaurav V, Roberts SC (2008) Pharmaceutically active natural product synthesis and supply via plant cell culture technology. Mol Pharm 5(2):243–256. doi:10.​1021/​mp7001494 CrossRef PubMed
    Komaraiah P, Reddy GV, Reddy PS, Raghavendra AS, Ramakrishna SV, Reddanna P (2003) Enhanced production of antimicrobial sesquiterpenes and lipoxygenase metabolites in elicitor-treated hairy root cultures of Solanum tuberosum. Biotechnol Lett 25(8):593–597CrossRef PubMed
    Komaraiah P, Kavi Kishor PB, Carlsson M, Magnusson K-E, Mandenius C-F (2005) Enhancement of anthraquinone accumulation in Morinda citrifolia suspension cultures. Plant Sci 168:1337–1344. doi:10.​1016/​j.​plantsci.​2005.​01.​017 CrossRef
    Krzyzanowska J, Czubacka A, Pecio L, Przybys M, Doroszewska T, Stochmal A, Oleszek W (2012) The effects of jasmonic acid and methyl jasmonate on rosmarinic acid production in Mentha × piperita cell suspension cultures. Plant Cell Tiss Organ Cult 108(1):73–81. doi:10.​1007/​s11240-011-0014-8 CrossRef
    Lijavetzky D, Almagro L, Belchi-Navarro S, Martinez-Zapater JM, Bru R, Pedreno MA (2008) Synergistic effect of methyljasmonate and cyclodextrin on stilbene biosynthesis pathway gene expression and resveratrol production in Monastrell grapevine cell cultures. BMC Res Notes 1:132. doi:10.​1186/​1756-0500-1-132 PubMedCentral CrossRef PubMed
    López-Nicolás JM, Escorial Camps M, Pérez-Sánchez H, García-Carmona F (2013) Physicochemical and thermodynamic characterization of the encapsulation of methyl jasmonate by natural and modified cyclodextrins using reversed-phase high-pressure liquid chromatography. J Agric Food Chem 61(47):11347–11354. doi:10.​1021/​jf402920p CrossRef PubMed
    Martinez-Esteso MJ, Selles-Marchart S, Vera-Urbina JC, Pedreno MA, Bru-Martinez R (2009) Changes of defense proteins in the extracellular proteome of grapevine (Vitis vinifera cv. Gamay) cell cultures in response to elicitors. J Proteomics 73(2):331–341. doi:10.​1016/​j.​jprot.​2009.​10.​001 CrossRef PubMed
    Martinez-Esteso MJ, Selles-Marchart S, Vera-Urbina JC, Pedreno MA, Bru-Martinez R (2011) DIGE analysis of proteome changes accompanying large resveratrol production by grapevine (Vitis vinifera cv. Gamay) cell cultures in response to methyl-beta-cyclodextrin and methyl jasmonate elicitors. J Proteomics 74(8):1421–1436. doi:10.​1016/​j.​jprot.​2011.​02.​035 CrossRef PubMed
    Naill MC, Kolewe ME, Roberts SC (2012) Paclitaxel uptake and transport in Taxus cell suspension cultures. Biochem Eng J 63:50–56. doi:10.​1016/​j.​bej.​2012.​01.​006 PubMedCentral CrossRef PubMed
    Orbán N, Boldizsár I, Szücs Z, Dános B (2008) Influence of different elicitors on the synthesis of anthraquinone derivatives in Rubia tinctorum L. cell suspension cultures. Dyes Pigm 77(1):249–257. doi:10.​1016/​j.​dyepig.​2007.​03.​015 CrossRef
    Perassolo M, Quevedo C, Busto V, Ianone F, Giulietti AM, Rodríguez Talou J (2007) Enhance of anthraquinone production by effect of proline and aminoindan-2-phosphonic acid in Rubia tinctorum suspension cultures. Enzyme Microb Technol 41(1–2):181–185. doi:10.​1016/​j.​enzmictec.​2007.​01.​004 CrossRef
    Perassolo M, Quevedo CV, Busto VD, Giulietti AM, Talou JR (2011a) Role of reactive oxygen species and proline cycle in anthraquinone accumulation in Rubia tinctorum cell suspension cultures subjected to methyl jasmonate elicitation. Plant Physiol Biochem 49(7):758–763. doi:10.​1016/​j.​plaphy.​2011.​03.​015 CrossRef PubMed
    Perassolo M, Quevedo CV, Giulietti AM, Rodríguez Talou J (2011b) Stimulation of the proline cycle and anthraquinone accumulation in Rubia tinctorum cell suspension cultures in the presence of glutamate and two proline analogs. Plant Cell Tiss Organ Cult 106:153–159. doi:10.​1007/​s11240-010-9903-5 CrossRef
    Quevedo CV, Perassolo M, Giulietti AM, Talou JR (2012) Enhancement of anthraquinone production in Morinda citrifolia cell suspension cultures after stimulation of the proline cycle with two proline analogs. Biotechnol Lett 34(3):571–575. doi:10.​1007/​s10529-011-0806-2 CrossRef PubMed
    Rao SR, Ravishankar GA (2002) Plant cell cultures: chemical factories of secondary metabolites. Biotechnol Adv 20(2):101–153CrossRef PubMed
    Rumie Vittar NB, Comini L, Fernadez IM, Agostini E, Nunez-Montoya S, Cabrera JL, Rivarola VA (2014) Photochemotherapy using natural anthraquinones: Rubiadin and Soranjidiol sensitize human cancer cell to die by apoptosis. Photodiagnosis Photodyn Ther 11(2):182–192. doi:10.​1016/​j.​pdpdt.​2014.​02.​002 CrossRef PubMed
    Sabater-Jara A, Pedreño M (2013) Use of β-cyclodextrins to enhance phytosterol production in cell suspension cultures of carrot (Daucus carota L.). Plant Cell Tiss Organ Cult 114(2):249–258. doi:10.​1007/​s11240-013-0320-4 CrossRef
    Sabater-Jara AB, Almagro L, Belchi-Navarro S, Ferrer MA, Barcelo AR, Pedreno MA (2010) Induction of sesquiterpenes, phytoesterols and extracellular pathogenesis-related proteins in elicited cell cultures of Capsicum annuum. J Plant Physiol 167(15):1273–1281. doi:10.​1016/​j.​jplph.​2010.​04.​015 CrossRef PubMed
    Sabater-Jara AB, Onrubia M, Moyano E, Bonfill M, Palazon J, Pedreno MA, Cusido RM (2014) Synergistic effect of cyclodextrins and methyl jasmonate on taxane production in Taxus × media cell cultures. Plant Biotechnol J 12(8):1075–1084. doi:10.​1111/​pbi.​12214 CrossRef PubMed
    Samuelsson G (1999) Drugs of natural origin—A textbook of pharmacognosy, 3rd edn. Swedish Pharmaceutical Society, Swedish Pharmaceutical Press, Stokkholm
    Schulte U, El-Shagi H, Zenk MH (1984) Optimization of 19 Rubiaceae species in cell culture for the production of anthraquinones. Plant Cell Rep 3(2):51–54. doi:10.​1007/​BF00270970 CrossRef PubMed
    Singh M, Sharma R, Banerjee UC (2002) Biotechnological applications of cyclodextrins. Biotechnol Adv 20(5–6):341–359CrossRef PubMed
    Smetanska I (2008) Production of secondary metabolites using plant cell cultures. Adv Biochem Eng Biotechnol 111:187–228. doi:10.​1007/​10_​2008_​103 PubMed
    Smith BA, Reider ML, Fletcher JS (1982) Relationship between vital staining and subculture growth during the senescence of plant tissue cultures. Plant Physiol 70(4):1228–1230PubMedCentral CrossRef PubMed
    van Uden W, Woerdenbag H, Pras N (1994) Cyclodextrins as a useful tool for bioconversions in plant cell biotechnology. Plant Cell Tissue Organ Cult 38(2–3):103–113. doi:10.​1007/​BF00033867 CrossRef
    Vasconsuelo A, Boland R (2007) Molecular aspects of the early stages of elicitation of secondary metabolites in plants. Plant Sci 172:861–875CrossRef
    Vasconsuelo A, Giulietti AM, Picotto G, Rodríguez Talou J, Boland R (2003) Involvement of the PLC/PKC pathway in Chitosan-induced anthraquinone production by Rubia tinctorum L. cell cultures. Plant Sci 165(2):429–436. doi:10.​1016/​S0168-9452(03)00208-5 CrossRef
    Wang S, Zhong J, Kong D, Hu J, Li B, Gao W, Gai C, Zhuang C, Mao H (2011) Use of 9, 10-anthraquinone compounds, Shanghai Institute Of Pharmaceutical Industry, Institute Pasteur of Shanghai, Chinese Academy of Sciences, US 2011/0224414 A1
    Zhang W, Hunter IS, Tham R (2011) Microbial and plant cell synthesis of secondary metabolites and strain improvement. In: El-Mansi EMT, Bryce CFA, Dahhou B, Sanchez S, Demain AL, Allman AR (eds) Fermentation microbiology and biotechnology, 3rd edn. CRC Press, Taylor & Francis Group, New York, pp 101–136CrossRef
    Zhao J, Davis LC, Verpoorte R (2005) Elicitor signal transduction leading to production of plant secondary metabolites. Biotechnol Adv 23(4):283–333. doi:10.​1016/​j.​biotechadv.​2005.​01.​003 CrossRef PubMed
  • 作者单位:María Perassolo (1)
    María Emilia Smith (1)
    Ana María Giulietti (1)
    Julián Rodríguez Talou (1)

    1. Cátedra de Biotecnología - Instituto NANOBIOTEC, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires – Consejo Nacional de Investigaciones Científicas y Técnicas, Junín 956, 1113, Ciudad Autónoma de Buenos Aires, Argentina
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Life Sciences
    Plant Sciences
    Plant Physiology
  • 出版者:Springer Netherlands
  • ISSN:1573-5044
文摘
Plant in vitro culture is a platform for producing secondary metabolites that combines safety, quality and low environmental impact. Besides, it is possible to increase the accumulation of these compounds by different strategies, such as elicitation. In this work, we analyzed the effects of the combination of methyl jasmonate (MeJ) and two cyclodextrins (CDs) on the production of anthraquinones (AQs) in cell cultures of Rubiaceae (Morinda citrifolia and Rubia tinctorum). These secondary metabolites have been traditionally used as dyes and have interesting therapeutic applications. The experiments were designed according to a full factorial design of two factors (MeJ and a CD) in two levels (0 and 0.1 mM for MeJ, and 0 and 20 mM of the CD). MeJ and (2-hydroxypropyl)-β-cyclodextrin (HPCD) synergistically increased intracellular AQ content in suspension cultures of R. tinctorum, and, to a lesser extent, in suspension cultures of M. citrifolia. Combination of MeJ with another CD, 2-methyl-β-cyclodextrin, led to a more intense and later increase in AQ content in cell cultures of R. tinctorum when compared to MeJ–HPCD treatment. However, the combination of CD and MeJ failed to induce a drastic AQ release to the culture media. Nevertheless, our results show that combination of strategies (using a CD and MeJ) was successful to increase secondary metabolite accumulation in suspension cultures. To our knowledge, this is the first report of synergistic effect of MeJ and CD on AQ accumulation in plant in vitro cultures.

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