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Metabolomic Analysis of Ocotea odorifera Cell Cultures: A Model Protocol for Acquiring Metabolite Data

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Protocols for In Vitro Cultures and Secondary Metabolite Analysis of Aromatic and Medicinal Plants

Summary

Metabolomics constitutes a quantitative and qualitative survey of the whole metabolites of an organism as well as a tissue, reflecting the genome and proteome of a sample as analyzed. Advanced analytical spectroscopic and chromatographic techniques are used along with uni- or multivariate statistical data analysis, rapidly identifying up- or down-regulated metabolites in complex matrices. In this chapter, protocols for the analysis of target compounds (protocol I) and metabolomics (protocol II) of Ocotea odorifera cell cultures are described. In the first case, the target compound safrole, an aromatic ether used as a flavoring agent and also in the manufacture of insecticides, is analyzed in the organosolvent fraction of stable prototrophic cell lines of O. odorifera by gas chromatography-mass spectrometry. For metabolomics studies the protocol is designed to detect and quantify metabolites in the aqueous extract of O. odorifera cell lines by using high-resolution 1D- and 2D-nuclear magnetic resonance spectroscopy, followed by chemometric analysis of the 1H NMR spectra dataset. Protocol I has been successfully used, for example, in screening studies of cell lines able of producing safrole. Protocol II is suitable to detect the chemical features of a number of metabolite compounds in aqueous extracts of O. odorifera cell lines cultured under certain conditions, leading to new insights into metabolomics of that species.

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Notes

  1. 1.

    Metabolite target analysis: typically an analysis restricted to metabolites of a particular enzymatic or organelle system (e.g.) that would be directly perturbed by (a)biotic factors (7).

  2. 2.

    Metabolite profiling (metabolic profiling): analysis focusing on metabolites associated with a specific pathway or on a class of compounds such as alkaloids, terpenoids, amino acids, etc (7).

  3. 3.

    Metabolomics: comprehensive analysis of the whole metabolome under a give set of conditions (7).

  4. 4.

    Metabolic fingerprint classification of samples on the basis of provenance taking into account their origin or biological relevance (7).

  5. 5.

    Metabonomics: measure of the fingerprint of biochemical perturbations caused by disease, drugs and toxins (8 ).

References

  1. Vaidyanathan, S. and Goodcare, R. (2000). Proteome and metabolome analyses for food authentication, in Food Authenticity and Traceability (Lees, M., ed.), CRC, Boca Raton, FL, pp. 69–99.

    Google Scholar 

  2. Abhyankar, G., Reddy, V.D., Giri, C.C., Rao, K.V., Lakshmi, V.V.S., Prabhakar, S., Vairamani, M., Thippeswamy, B.S., and Bhattacharya, P.S. (2005). Amplified fragment length polymorphism and metabolomic profiles of hairy roots of Psoralea corylifolia L. Phytochemistry 66, 2441–2457.

    Article  CAS  PubMed  Google Scholar 

  3. German, J.B., Watkins, S.M., and Fay, L. (2005). Metabolomics in practice: emerging knowledge to guide future dietetic advice toward individualized health. J. Am. Diet. Assoc. 105, 1425–1432.

    Article  PubMed  Google Scholar 

  4. Wind, R.A., Hu, J.Z., and Majors, P.D. (2005). Slow-MAS NMR: a new technology for in vivo metabolomic studies. Drug Discov. Today 2, 283–286.

    Article  Google Scholar 

  5. Goodcare, R., Seetharaman, V., Dunn, W.B., Harrigan, G.G., and Kell, D.B. (2004). Metabolomics by numbers: acquiring and understanding global metabolite data. Trends Biotechnol. 22, 245–252.

    Article  Google Scholar 

  6. Lay, Jr.J.O., Borgmann, S., Liyanage, R., and Wilkins, C.L. (2006). Problems with the “omics”. Trends Anal. Chem. 25, 1046–1056.

    Article  CAS  Google Scholar 

  7. Fiehn, O. (2001). Combining genome, metabolome analysis, and biochemical modeling to understand metabolic networks. Compr. Funct. Genomics 2, 155–168.

    Article  CAS  Google Scholar 

  8. Nicholson, J.K., Lindon, J.C., and Holmes, E. (1999). ‘Metabonomics’: understanding the metabolic responses of living systems to pathophysiological stimuli via multivariate statistical analysis of biological NMR spectroscopic data. Xenobiotica 29, 1181–1189.

    Article  CAS  PubMed  Google Scholar 

  9. Murashige, T. and Skoog, F. (1962). A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant. 15, 473– 497.

    Article  CAS  Google Scholar 

  10. Catarina, C.S., Oltramari, A.C., Voltolini, J.A., Pedrotti, E.L., and Maraschin, M. (1999). Ocotea odorifera Mez. cell suspension cultures – an alternative approach for biomass and safrole production, in Proceedings International Congress on Forestry. EMBRAPA, Colombo, Parana, p. 381.

    Google Scholar 

  11. Morel, G.M. and Wetmore, R.H. (1951). Fern callus tissue culture. Am. J. Bot. 38, 141–143.

    Article  CAS  Google Scholar 

  12. Snyder, L.R., Kirkland, J.J., and Glajch, J.L. (1997). Practical HPLC Method Development. Wiley, New York, NY.

    Book  Google Scholar 

  13. Oltramari, A.C., Wood, K.V., Bonham, C.,Verpoorte, R., Caro, M.S.B., Viana, A.M., Pedrotti, E.L., Maraschin, R.P., and Maraschin, M. (2004). Safrole analysis by GC-MS of prototrophic (Ocotea odorifera (Vell.) Rohwer cell cultures. Plant Cell Tissue Organ Cult. 78, 231–235.

    Article  CAS  Google Scholar 

  14. Bax, A. and Davis, D.G. (1985). MLEV-17-based two-dimensional homonuclear magnetization transfer spectroscopy. J. Magn. Reson. 65, 355–360.

    CAS  Google Scholar 

  15. Claridge, T.D.W. (1999). High-Resolution NMR Techniques in Organic Chemistry. Elsevier Science Ltd, Oxford, UK.

    Google Scholar 

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© 2009 Humana Press, a part of Springer Science+Business Media, LLC

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Maraschin, M. et al. (2009). Metabolomic Analysis of Ocotea odorifera Cell Cultures: A Model Protocol for Acquiring Metabolite Data. In: Jain, S.M., Saxena, P.K. (eds) Protocols for In Vitro Cultures and Secondary Metabolite Analysis of Aromatic and Medicinal Plants. Methods in Molecular Biology, vol 547. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-60327-287-2_28

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  • DOI: https://doi.org/10.1007/978-1-60327-287-2_28

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  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-1-60327-286-5

  • Online ISBN: 978-1-60327-287-2

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