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Volumn 4, Issue , 2014, Pages

(R, S)-Tetrahydropapaveroline production by stepwise fermentation using engineered Escherichia coli

Author keywords

[No Author keywords available]

Indexed keywords

MONOPHENOL MONOOXYGENASE; TETRAHYDROPAPAVEROLINE;

EID: 84922803616     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep06695     Document Type: Article
Times cited : (57)

References (29)
  • 1
    • 44949247292 scopus 로고    scopus 로고
    • Microbial production of plant benzylisoquinoline alkaloids
    • Minami, H. et al. Microbial production of plant benzylisoquinoline alkaloids. Proc Natl Acad Sci U S A 105, 7393-7398 (2008).
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 7393-7398
    • Minami, H.1
  • 2
    • 49949088247 scopus 로고    scopus 로고
    • Production of benzylisoquinoline alkaloids in saccharomyces cerevisiae
    • Hawkins, K. M. & Smolke, C. D. Production of benzylisoquinoline alkaloids in Saccharomyces cerevisiae. Nat Chem Biol 4, 564-573 (2008).
    • (2008) Nat Chem Biol , vol.4 , pp. 564-573
    • Hawkins, K.M.1    Smolke, C.D.2
  • 3
    • 79957546214 scopus 로고    scopus 로고
    • A bacterial platform for fermentative production of plant alkaloids
    • Nakagawa, A. et al. A bacterial platform for fermentative production of plant alkaloids. Nat Commun 2, 326 (2011).
    • (2011) Nat Commun , vol.2 , pp. 326
    • Nakagawa, A.1
  • 4
    • 84910056833 scopus 로고    scopus 로고
    • Reconstitution of a 10-gene pathway for synthesis of the plant alkaloid dihydrosanguinarine in saccharomyces cerevisiae
    • Fossati, E. et al. Reconstitution of a 10-gene pathway for synthesis of the plant alkaloid dihydrosanguinarine in Saccharomyces cerevisiae. Nat Commun 5, 3283 (2014).
    • (2014) Nat Commun , vol.5 , pp. 3283
    • Fossati, E.1
  • 5
    • 0346154804 scopus 로고    scopus 로고
    • Tetrahydropapaveroline in Parkinson's disease and alcoholism: A look back in honor of merton sandler
    • Collins, M. A. Tetrahydropapaveroline in Parkinson's disease and alcoholism: a look back in honor of Merton Sandler. Neurotoxicology 25, 117-120 (2004).
    • (2004) Neurotoxicology , vol.25 , pp. 117-120
    • Collins, M.A.1
  • 6
    • 22544432269 scopus 로고    scopus 로고
    • Inhibition of dopamine biosynthesis by tetrahydropapaveroline
    • Kim, Y. M., and Kim, M. N., Lee, J. J. & Lee, M. K. Inhibition of dopamine biosynthesis by tetrahydropapaveroline. Neurosci Lett 386, 1-4 (2005).
    • (2005) Neurosci Lett , vol.386 , pp. 1-4
    • Kim, Y.M.1    Kim, M.N.2    Lee, J.J.3    Lee, M.K.4
  • 7
    • 77956450412 scopus 로고    scopus 로고
    • Inhibition of aldehyde dehydrogenase-2 suppresses cocaine seeking by generating THP, acocaine use-dependent inhibitorofdopamine synthesis
    • Yao, L. et al. Inhibition of aldehyde dehydrogenase-2 suppresses cocaine seeking by generating THP, acocaine use-dependent inhibitorofdopamine synthesis. Nat Med 16, 1024-1028 (2010).
    • (2010) Nat Med , vol.16 , pp. 1024-1028
    • Yao, L.1
  • 8
    • 0037457407 scopus 로고    scopus 로고
    • Reduction of serotonin content by tetrahydropapaveroline in murine mastocytoma P815 cells
    • Kim, E. I. et al. Reduction of serotonin content by tetrahydropapaveroline in murine mastocytoma P815 cells. Neurosci Lett 339, 131-134 (2003).
    • (2003) Neurosci Lett , vol.339 , pp. 131-134
    • Kim, E.I.1
  • 9
    • 0031933355 scopus 로고    scopus 로고
    • Tetrahydropapaveroline and its derivatives inhibit dopamine uptake through dopamine transporter expressed in HEK293 cells
    • Okada, T. et al. Tetrahydropapaveroline and its derivatives inhibit dopamine uptake through dopamine transporter expressed in HEK293 cells. Neurosci Res 30, 87-90 (1998).
    • (1998) Neurosci Res , vol.30 , pp. 87-90
    • Okada, T.1
  • 10
    • 0345254972 scopus 로고    scopus 로고
    • Oxidative DNA damage and glioma cell death induced by tetrahydropapaveroline
    • Soh, Y. et al. Oxidative DNA damage and glioma cell death induced by tetrahydropapaveroline. Mutat Res 544, 129-142 (2003).
    • (2003) Mutat Res , vol.544 , pp. 129-142
    • Soh, Y.1
  • 11
    • 35848947948 scopus 로고    scopus 로고
    • Nrf2-mediated heme oxygenase-1 induction confers adaptive survival response to tetrahydropapaveroline-induced oxidative PC12 cell death
    • Park, S. H. et al. Nrf2-mediated heme oxygenase-1 induction confers adaptive survival response to tetrahydropapaveroline-induced oxidative PC12 cell death. Antioxid Redox Signal 9, 2075-2086 (2007).
    • (2007) Antioxid Redox Signal , vol.9 , pp. 2075-2086
    • Park, S.H.1
  • 12
    • 84872130503 scopus 로고    scopus 로고
    • Oxidative modification of neurofilament-L and neuronal cell death induced by the catechol neurotoxin, tetrahydropapaveroline
    • Kyeong, I. G., and Eum, W. S., Choi, S. Y. & Kang, J. H. Oxidative modification of neurofilament-L and neuronal cell death induced by the catechol neurotoxin, tetrahydropapaveroline. Toxicol Lett 217, 59-66 (2013).
    • (2013) Toxicol Lett , vol.217 , pp. 59-66
    • Kyeong, I.G.1    Eum, W.S.2    Choi, S.Y.3    Kang, J.H.4
  • 13
    • 0015926907 scopus 로고
    • Tetrahydroisoquinoline alkaloids: In vivo metabolites of L-dopa in man
    • Sandler, M., and Carter, S. B., Hunter, K. R. & Stern, G. M. Tetrahydroisoquinoline alkaloids: in vivo metabolites of L-dopa in man. Nature 241, 439-443 (1973).
    • (1973) Nature , vol.241 , pp. 439-443
    • Sandler, M.1    Carter, S.B.2    Hunter, K.R.3    Stern, G.M.4
  • 14
    • 0027500561 scopus 로고
    • Determination of tetrahydropapaveroline in the urine of parkinsonian patients receiving L-dopa-carbidopa (Sinemet) therapy by highperformance liquid chromatography
    • Cashaw, J. L. Determination of tetrahydropapaveroline in the urine of parkinsonian patients receiving L-dopa-carbidopa (Sinemet) therapy by highperformance liquid chromatography. J Chromatogr 613, 267-273 (1993).
    • (1993) J Chromatogr , vol.613 , pp. 267-273
    • Cashaw, J.L.1
  • 15
    • 0016220568 scopus 로고
    • Tetrahydropapaveroline: Formation in vivo and in vitro in rat brain
    • Turner, A. J., and Baker, K. M., Algeri, S., Erigerio, A. & Garattini, S. Tetrahydropapaveroline: formation in vivo and in vitro in rat brain. Life Sci 14, 2247-2257 (1974).
    • (1974) Life Sci , vol.14 , pp. 2247-2257
    • Turner, A.J.1    Baker, K.M.2    Algeri, S.3    Erigerio, A.4    Garattini, S.5
  • 16
    • 0026262163 scopus 로고
    • Biotransformation of dopamine to norlaudanosoline by aspergillus Niger
    • Hoover, L. K., Moo-Young, M. & Legge, R. L. Biotransformation of dopamine to norlaudanosoline by Aspergillus niger. Biotechnol Bioeng 38, 1029-1033 (1991).
    • (1991) Biotechnol Bioeng , vol.38 , pp. 1029-1033
    • Hoover, L.K.1    Moo-Young, M.2    Legge, R.L.3
  • 17
    • 33645026354 scopus 로고    scopus 로고
    • A tyrosinase with an abnormally high tyrosine hydroxylase/dopa oxidase ratio
    • 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).
    • (2006) FEBS J , vol.273 , pp. 257-270
    • Hernández-Romero, D.1    Sanchez-Amat, A.2    Solano, F.3
  • 19
    • 64549158068 scopus 로고    scopus 로고
    • Exploring the effects of carbon sources on the metabolic capacity for shikimic acid production in Escherichia coli using in silico metabolic predictions
    • 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).
    • (2008) J Microbiol Biotechnol , vol.18 , pp. 1773-1784
    • Ahn, J.O.1
  • 20
    • 84863256651 scopus 로고    scopus 로고
    • Bench-top fermentative production of plant benzylisoquinoline alkaloids using a bacterial platform
    • Nakagawa, A. et al. Bench-top fermentative production of plant benzylisoquinoline alkaloids using a bacterial platform. Bioeng Bugs 3, 49-53 (2012).
    • (2012) Bioeng Bugs , vol.3 , pp. 49-53
    • Nakagawa, A.1
  • 21
    • 84886712128 scopus 로고    scopus 로고
    • Improvement of reticuline productivity from dopamine by using engineered Escherichia coli
    • Kim, J. S. et al. Improvement of reticuline productivity from dopamine by using engineered Escherichia coli. Biosci Biotechnol Biochem 77, 2166-2168 (2013).
    • (2013) Biosci Biotechnol Biochem , vol.77 , pp. 2166-2168
    • Kim, J.S.1
  • 22
    • 0038367700 scopus 로고    scopus 로고
    • Tyrosinase protects human melanocytes from ROS-generating compounds
    • Perluigi, M. et al. Tyrosinase protects human melanocytes from ROS-generating compounds. Biochem Biophys Res Commun 305, 250-256 (2003).
    • (2003) Biochem Biophys Res Commun , vol.305 , pp. 250-256
    • Perluigi, M.1
  • 23
    • 84899761386 scopus 로고    scopus 로고
    • Intracellular hydrogen peroxide and superoxide poison 3-deoxy-D-arabinoheptulosonate 7-phosphate synthase, the first committed enzyme in the aromatic biosynthetic pathway of Escherichia coli
    • Sobota, J. M., Gu, M. & Imlay, J. A. Intracellular hydrogen peroxide and superoxide poison 3-deoxy-D-arabinoheptulosonate 7-phosphate synthase, the first committed enzyme in the aromatic biosynthetic pathway of Escherichia coli. J Bacteriol 196, 1980-1991 (2014).
    • (2014) J Bacteriol , vol.196 , pp. 1980-1991
    • Sobota, J.M.1    Gu, M.2    Imlay, J.A.3
  • 24
    • 0027453615 scopus 로고
    • Effect of L-ascorbic acid on the monophenolase activity of tyrosinase
    • Ros, J. R., Rodríguez-López, J. N. & García-Cánovas, F. Effect of L-ascorbic acid on the monophenolase activity of tyrosinase. Biochem J 295 (Pt 1), 309-312 (1993).
    • (1993) Biochem J , vol.295 , pp. 309-312
    • Ros, J.R.1    Rodríguez-López, J.N.2    García-Cánovas, F.3
  • 25
    • 84922067763 scopus 로고    scopus 로고
    • A microbial biomanufacturing platform for natural and semisynthetic opioids
    • Published on line
    • Thodey, K., Galanie, S. & Smolke, C. D. A microbial biomanufacturing platform for natural and semisynthetic opioids. Nat Chem Biol, Published on line., (2014).
    • (2014) Nat Chem Biol
    • Thodey, K.1    Galanie, S.2    Smolke, C.D.3
  • 26
    • 69949174213 scopus 로고    scopus 로고
    • CYP719B1 is salutaridine synthase, the C-C phenol-coupling enzymeofmorphine biosynthesisin opium poppy
    • Gesell, A. et al. CYP719B1 is salutaridine synthase, the C-C phenol-coupling enzymeofmorphine biosynthesisin opium poppy. J Biol Chem 284, 24432-24442 (2009).
    • (2009) J Biol Chem , vol.284 , pp. 24432-24442
    • Gesell, A.1
  • 27
    • 42249110738 scopus 로고    scopus 로고
    • Molecular cloning and characterization of CYP80G2, a cytochrome P450 that catalyzes an intramolecular C-C phenol coupling of (S)-reticuline in magnoflorine biosynthesis, from cultured coptis japonica cells
    • Ikezawa, N., Iwasa, K. & Sato, F. Molecular cloning and characterization of CYP80G2, a cytochrome P450 that catalyzes an intramolecular C-C phenol coupling of (S)-reticuline in magnoflorine biosynthesis, from cultured Coptis japonica cells. J Biol Chem 283, 8810-8821 (2008).
    • (2008) J Biol Chem , vol.283 , pp. 8810-8821
    • Ikezawa, N.1    Iwasa, K.2    Sato, F.3
  • 28
    • 84870337667 scopus 로고    scopus 로고
    • Eukaryotic-type aromatic amino acid decarboxylase from the root colonizer pseudomonas putida is highly specific for 3,4-dihydroxyphenyl-L-alanine, an allelochemical in the rhizosphere
    • Koyanagi, T. et al. Eukaryotic-type aromatic amino acid decarboxylase from the root colonizer Pseudomonas putida is highly specific for 3,4-dihydroxyphenyl-L-alanine, an allelochemical in the rhizosphere. Microbiology 158, 2965-2974 (2012).
    • (2012) Microbiology , vol.158 , pp. 2965-2974
    • Koyanagi, T.1
  • 29
    • 2142751582 scopus 로고    scopus 로고
    • 1,2-dehydroreticuline synthase, the branch point enzyme opening the morphinan biosynthetic pathway
    • 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).
    • (2004) Phytochemistry , vol.65 , pp. 1039-1046
    • Hirata, K.1    Poeaknapo, C.2    Schmidt, J.3    Zenk, M.H.4


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