Erratum: A bacterial platform for fermentative production of plant alkaloids (Nature Communications (2011) 2 (326) DOI:10.1038/ncomms1327);A bacterial platform for fermentative production of plant alkaloids

Nature Communications

Volumn 2, Issue 1, 2011, Pages

  Nakagawa, Akira ^a   Minami, Hiromichi ^a   Kim, Ju Sung ^a,c   Koyanagi, Takashi ^a   Katayama, Takane ^a   Sato, Fumihiko ^b   Kumagai, Hidehiko ^a  

^a ISHIKAWA PREFECTURAL UNIVERSITY   (Japan)

^b KYOTO UNIVERSITY   (Japan)

^c Jeju National University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

RETICULINE; BENZYLISOQUINOLINE DERIVATIVE;

ARTICLE; BACTERIUM CULTURE; BIOSYNTHESIS; CARBON SOURCE; CELL CULTURE; CULTURE MEDIUM; ESCHERICHIA COLI; FERMENTATION; NONHUMAN; NUCLEOTIDE SEQUENCE; BIOTECHNOLOGY; EVALUATION; GENETIC ENGINEERING; GENETICS; METABOLISM; METHODOLOGY; PLANT;

BACTERIA (MICROORGANISMS); EMBRYOPHYTA; ESCHERICHIA COLI;

BENZYLISOQUINOLINES; BIOSYNTHETIC PATHWAYS; BIOTECHNOLOGY; ESCHERICHIA COLI; FERMENTATION; GENETIC ENGINEERING; PLANTS;

EID: 79957546214     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms1866     Document Type: Erratum

References (29)

1. Zhou, H., Xie, X. & Tang, Y. Engineering natural products using combinatorial biosynthesis and biocatalysis. Curr. Opin. Biotechnol. 19, 590-596 (2008).
2. Chemler, J. A. & Koffas, M. A. Metabolic engineering for plant natural product biosynthesis in microbes. Curr. Opin. Biotechnol. 19, 597-605 (2008).
3. Lee, S. Y., Kim, H. U., Park, J. H., Park, J. M. & Kim, T. Y. Metabolic engineering of microorganisms: general strategies and drug production. Drug Discov. Today 14, 78-88 (2009).
4. Marner, W. D. Practical application of synthetic biology principles. Biotechnol. J. 4, 1406-1419 (2009).
5. Schäfer, H. & Wink, M. Medicinally important secondary metabolites in recombinant microorganisms or plants: progress in alkaloid biosynthesis. Biotechnol. J. 4, 1684-1703 (2009).
6. Kirby, J. & Keasling, J. D. Biosynthesis of plant isoprenoids: perspectives for microbial engineering. Annu. Rev. Plant Biol. 60, 335-355 (2009).
7. Minami, H. et al. Microbial production of plant benzylisoquinoline alkaloids. Proc. Natl Acad. Sci. USA 105, 7393-7398 (2008).
8. Hawkins, K. M. & Smolke, C. D. Production of benzylisoquinoline alkaloids in Saccharomyces cerevisiae. Nat. Chem. Biol. 4, 564-573 (2008).
9. Horinouchi, S. Combinatorial biosynthesis of plant medicinal polyketides by microorganisms. Curr. Opin. Chem. Biol. 13, 197-204 (2009).
10. Keasling, J. From yeast to alkaloids. Nat. Chem. Biol. 4, 524-525 (2008).
11. Leonard, E., Runguphan, W., O'Connor, S. & Prather, K. J. Opportunities in metabolic engineering to facilitate scalable alkaloid production. Nat. Chem. Biol. 5, 292-300 (2009).
12. Pittard, J., Camakaris, H. & Yang, J. The TyrR regulon. Mol. Microbiol. 55, 16-26 (2005).
13. Lütke-Eversloh, T., Santos, C. N. S. & Stephanopoulos, G. Perspectives of biotechnological production of L-tyrosine and its applications. Appl. Microbiol. Biotechnol. 77, 751-762 (2007).
14. Lütke-Eversloh, T. & Stephanopoulos, G. L-Tyrosine production by deregulated strains of Escherichia coli. Appl. Microbiol. Biotechnol. 75, 103-110 (2007).
15. Kohashi, P. Y. et al. An efficient method for the overexpression and purification of active tyrosinase from Streptomyces castaneoglobisporus. Protein Expr. Purif. 34, 202-207 (2004).
16. Matoba, Y., Kumagai, T., Yamamoto, A., Yoshitsu, H. & Sugiyama, M. Crystallographic evidence that the dinuclear copper center of tyrosinase is flexible during catalysis. J. Biol. Chem. 281, 8981-8990 (2006).
17. Frenzela, T. & Zenk, M. H. S-Adenosyl-L-methionine: 3′-hydroxy-N-methyl-(S)-coclaurine-4′-O-methyl transferase, a regio- and stereoselective enzyme of the (S)-reticuline pathway. Phytochemistry 29, 3505-3511 (1990).
18. Facchini, P. J., Huber-Allanach, K. L. & Tari, L. W. Plant aromatic L-amino acid decarboxylases: evolution, biochemistry, regulation, and metabolic engineering applications. Phytochemistry 54, 121-138 (2000).
19. Ahn, J. O. et al. Exploring the effects of carbon sources on the metabolic capacity for shikimic acid production in Escherichia coli using in silico metabolic predictions. J. Microbiol. Biotechnol. 18, 1773-1784 (2008).
20. Khamduang, M., Packdibamrung, K., Chutmanop, J., Chisti, Y. & Srinophakun, P. Production of L-phenylalanine from glycerol by a recombinant Escherichia coli. J. Ind. Microbiol. Biotechnol. 36, 1267-1274 (2009).
21. Hernández-Romero, D., Sanchez-Amat, A. & Solano, F. A tyrosinase with an abnormally high tyrosine hydroxylase/dopa oxidase ratio. FEBS J. 273, 257-270 (2006).
22. Frick, S. et al. Transformation of opium poppy (Papaver somniferum L.) with antisense berberine bridge enzyme gene (anti-bbe) via somatic embryogenesis results in an altered ratio of alkaloids in latex but not in roots. Transgenic Res. 13, 607-613 (2004).
23. Nessler, C. L., Allen, R. D. & Galewsky, S. Identification and characterization of latex-specific proteins in opium poppy. Plant Physiol. 79, 499-504 (1985).
24. Hagel, J. M. & Facchini, P. J. Dioxygenases catalyze the O-demethylation steps of morphine biosynthesis in opium poppy. Nat. Chem. Biol. 6, 273-275 (2010).
25. 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).
26. De-Eknamkul, W. & Zenk, M. H. Purification and properties of 1,2-dehydroreticuline reductase from Papaver somniferum seedlings. Phytochemistry 31, 813-821 (1992).
27. Chang, M. C. Y., Eachus, R. A., Trieu, W., Ro, D. K. & Keasling, J. D. Engineering Escherichia coli for production of functionalized terpenoids using plant P450s. Nat. Chem. Biol. 3, 274-277 (2007).
28. Ikeda, M. Towards bacterial strains overproducing L-tryptophan and other aromatics by metabolic engineering. Appl. Microbiol. Biotechnol. 69, 615-626 (2006).
29. Datsenko, K. A. & Wanner, B. L. One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc. Natl Acad. Sci. USA 97, 6640-6645 (2000).