Abstract
The benzylisoquinoline alkaloids (BIAs) are a diverse class of metabolites that exhibit a broad range of pharmacological activities and are synthesized through plant biosynthetic pathways comprised of complex enzyme activities and regulatory strategies. We have engineered yeast to produce the key intermediate reticuline and downstream BIA metabolites from a commercially available substrate. An enzyme tuning strategy was implemented that identified activity differences between variants from different plants and determined optimal expression levels. By synthesizing both stereoisomer forms of reticuline and integrating enzyme activities from three plant sources and humans, we demonstrated the synthesis of metabolites in the sanguinarine/berberine and morphinan branches. We also demonstrated that a human P450 enzyme exhibits a novel activity in the conversion of (R)-reticuline to the morphinan alkaloid salutaridine. Our engineered microbial hosts offer access to a rich group of BIA molecules and associated activities that will be further expanded through synthetic chemistry and biology approaches.
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References
Endy, D. Foundations for engineering biology. Nature 438, 449–453 (2005).
McDaniel, R. & Weiss, R. Advances in synthetic biology: on the path from prototypes to applications. Curr. Opin. Biotechnol. 16, 476–483 (2005).
Ro, D.K. et al. Production of the antimalarial drug precursor artemisinic acid in engineered yeast. Nature 440, 940–943 (2006).
Kealey, J.T., Liu, L., Santi, D.V., Betlach, M.C. & Barr, P.J. Production of a polyketide natural product in nonpolyketide-producing prokaryotic and eukaryotic hosts. Proc. Natl. Acad. Sci. USA 95, 505–509 (1998).
Szczebara, F.M. et al. Total biosynthesis of hydrocortisone from a simple carbon source in yeast. Nat. Biotechnol. 21, 143–149 (2003).
Martin, M.L. et al. Antispasmodic activity of benzylisoquinoline alkaloids analogous to papaverine. Planta Med. 59, 63–67 (1993).
Morais, L.C., Barbosa-Filho, J.M. & Almeida, R.N. Central depressant effects of reticuline extracted from Ocotea duckei in rats and mice. J. Ethnopharmacol. 62, 57–61 (1998).
Nakaoji, K., Nayeshiro, H. & Tanahashi, T. Norreticuline and reticuline as possible new agents for hair growth acceleration. Biol. Pharm. Bull. 20, 586–588 (1997).
Kemeny-Beke, A. et al. Apoptotic response of uveal melanoma cells upon treatment with chelidonine, sanguinarine and chelerythrine. Cancer Lett. 237, 67–75 (2006).
Cassels, B.K. et al. Structure-antioxidative activity relationships in benzylisoquinoline alkaloids. Pharmacol. Res. 31, 103–107 (1995).
Exley, R. et al. Evaluation of benzyltetrahydroisoquinolines as ligands for neuronal nicotinic acetylcholine receptors. Br. J. Pharmacol. 146, 15–24 (2005).
Kashiwada, Y. et al. Anti-HIV benzylisoquinoline alkaloids and flavonoids from the leaves of Nelumbo nucifera, and structure-activity correlations with related alkaloids. Bioorg. Med. Chem. 13, 443–448 (2005).
Lai, J.H. Immunomodulatory effects and mechanisms of plant alkaloid tetrandrine in autoimmune diseases. Acta Pharmacol. Sin. 23, 1093–1101 (2002).
Kwan, C.Y. & Achike, F.I. Tetrandrine and related bis-benzylisoquinoline alkaloids from medicinal herbs: cardiovascular effects and mechanisms of action. Acta Pharmacol. Sin. 23, 1057–1068 (2002).
Chulia, S. et al. Relationships between structure and vascular activity in a series of benzylisoquinolines. Br. J. Pharmacol. 122, 409–416 (1997).
Bentley, K.W. β-Phenylethylamines and the isoquinoline alkaloids. Nat. Prod. Rep. 23, 444–463 (2006).
Facchini, P.J. Alkaloid biosynthesis in plants: biochemistry, cell biology, molecular regulation, and metabolic engineering applications. Annu. Rev. Plant Physiol. Plant Mol. Biol. 52, 29–66 (2001).
Sato, F., Inui, T. & Takemura, T. Metabolic engineering in isoquinoline alkaloid biosynthesis. Curr. Pharm. Biotechnol. 8, 211–218 (2007).
Allen, R.S. et al. Metabolic engineering of morphinan alkaloids by over-expression and RNAi suppression of salutaridinol 7-O-acetyltransferase in opium poppy. Plant Biotechnol. J. 6, 22–30 (2008).
Allen, R.S. et al. RNAi-mediated replacement of morphine with the nonnarcotic alkaloid reticuline in opium poppy. Nat. Biotechnol. 22, 1559–1566 (2004).
Sato, F. et al. Metabolic engineering of plant alkaloid biosynthesis. Proc. Natl. Acad. Sci. USA 98, 367–372 (2001).
Zulak, K.G. et al. Gene transcript and metabolite profiling of elicitor-induced opium poppy cell cultures reveals the coordinate regulation of primary and secondary metabolism. Planta 225, 1085–1106 (2007).
Minami, H. et al. Microbial production of plant benzylisoquinoline alkaloids. Proc. Natl. Acad. Sci. USA 105, 7393–7398 (2008).
Ziegler, J. et al. Comparative transcript and alkaloid profiling in Papaver species identifies a short chain dehydrogenase/reductase involved in morphine biosynthesis. Plant J. 48, 177–192 (2006).
Sato, F., Tsujita, T., Katagiri, Y., Yoshida, S. & Yamada, Y. Purification and characterization of S-adenosyl-L-methionine: norcoclaurine 6-O-methyltransferase from cultured Coptis japonica cells. Eur. J. Biochem. 225, 125–131 (1994).
Ounaroon, A., Decker, G., Schmidt, J., Lottspeich, F. & Kutchan, T.M. (R,S)-Reticuline 7-O-methyltransferase and (R,S)-norcoclaurine 6-O-methyltransferase of Papaver somniferum - cDNA cloning and characterization of methyl transfer enzymes of alkaloid biosynthesis in opium poppy. Plant J. 36, 808–819 (2003).
Hawkins, K.M. & Smolke, C.D. The regulatory roles of the galactose permease and kinase in the induction response of the GAL network in Saccharomyces cerevisiae. J. Biol. Chem. 281, 13485–13492 (2006).
Nevoigt, E. et al. Engineering of promoter replacement cassettes for fine-tuning of gene expression in Saccharomyces cerevisiae. Appl. Environ. Microbiol. 72, 5266–5273 (2006).
Kutchan, T.M. & Dittrich, H. Characterization and mechanism of the berberine bridge enzyme, a covalently flavinylated oxidase of benzophenanthridine alkaloid biosynthesis in plants. J. Biol. Chem. 270, 24475–24481 (1995).
Bird, D.A. & Facchini, P.J. Berberine bridge enzyme, a key branch-point enzyme in benzylisoquinoline alkaloid biosynthesis, contains a vacuolar sorting determinant. Planta 213, 888–897 (2001).
Ikezawa, N. et al. Molecular cloning and characterization of CYP719, a methylenedioxy bridge-forming enzyme that belongs to a novel P450 family, from cultured Coptis japonica cells. J. Biol. Chem. 278, 38557–38565 (2003).
Hirata, K., Poeaknapo, C., Schmidt, J. & Zenk, M.H. 1,2-Dehydroreticuline synthase, the branch point enzyme opening the morphinan biosynthetic pathway. Phytochemistry 65, 1039–1046 (2004).
Zhu, W., Cadet, P., Baggerman, G., Mantione, K.J. & Stefano, G.B. Human white blood cells synthesize morphine: CYP2D6 modulation. J. Immunol. 175, 7357–7362 (2005).
Liscombe, D.K. & Facchini, P.J. Evolutionary and cellular webs in benzylisoquinoline alkaloid biosynthesis. Curr. Opin. Biotechnol. 19, 173–180 (2008).
Winkel, B.S. Metabolic channeling in plants. Annu. Rev. Plant Biol. 55, 85–107 (2004).
Sambrook, J. & Russell, D.W. Molecular Cloning 3rd edn. (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, USA, 2001).
Gillam, E.M., Guo, Z., Martin, M.V., Jenkins, C.M. & Guengerich, F.P. Expression of cytochrome P450 2D6 in Escherichia coli, purification, and spectral and catalytic characterization. Arch. Biochem. Biophys. 319, 540–550 (1995).
Urban, P., Mignotte, C., Kazmaier, M., Delorme, F. & Pompon, D. Cloning, yeast expression, and characterization of the coupling of two distantly related Arabidopsis thaliana NADPH-cytochrome P450 reductases with P450 CYP73A5. J. Biol. Chem. 272, 19176–19186 (1997).
Mapoles, J., Berthou, F., Alexander, A., Simon, F. & Menez, J.F. Mammalian PC-12 cell genetically engineered for human cytochrome P450 2E1 expression. Eur. J. Biochem. 214, 735–745 (1993).
Gietz, R.D. & Woods, R.A. Yeast transformation by the LiAc/SS Carrier DNA/PEG method. Methods Mol. Biol. 313, 107–120 (2006).
Thomas, B.J. & Rothstein, R. Elevated recombination rates in transcriptionally active DNA. Cell 56, 619–630 (1989).
Guldener, U., Heck, S., Fielder, T., Beinhauer, J. & Hegemann, J.H. A new efficient gene disruption cassette for repeated use in budding yeast. Nucleic Acids Res. 24, 2519–2524 (1996).
Chen, J. et al. Analysis of major alkaloids in Rhizoma coptidis by capillary electrophoresis-electrospray-time of flight mass spectrometry with different background electrolytes. Electrophoresis 29, 2135–2147 (2008).
Raith, K. et al. Electrospray tandem mass spectrometric investigations of morphinans. J. Am. Soc. Mass Spectrom. 14, 1262–1269 (2003).
Acknowledgements
We thank P. Facchini (University of Calgary), F.P. Guengerich (Vanderbilt University) and D. Pompon (Centre de Génétique Moléculaire, CNRS) for generously providing cDNAs and yeast strains used in this work. This work was supported by the Center for Biological Circuit Design at Caltech (fellowship to K.M.H.) and the US National Institutes of Health (grant to C.D.S.).
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K.M.H. designed and performed research, analyzed data and wrote the paper; C.D.S. designed research, analyzed data and wrote the paper.
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Hawkins, K., Smolke, C. Production of benzylisoquinoline alkaloids in Saccharomyces cerevisiae. Nat Chem Biol 4, 564–573 (2008). https://doi.org/10.1038/nchembio.105
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DOI: https://doi.org/10.1038/nchembio.105
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