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Volumn 73, Issue 11, 2007, Pages 3575-3580

Characterization of SafC, a catechol 4-O-methyltransferase involved in saframycin biosynthesis

Author keywords

[No Author keywords available]

Indexed keywords

CAFFEIC ACID; CLINICAL DEVELOPMENT; METHYLTRANSFERASE;

EID: 34249867714     PISSN: 00992240     EISSN: None     Source Type: Journal    
DOI: 10.1128/AEM.00011-07     Document Type: Article
Times cited : (42)

References (39)
  • 1
    • 0019288885 scopus 로고
    • Some chemotherapeutic properties of two new antitumor antibiotics, saframycins A and C
    • Arai, T., K. Takahashi, K. Ishiguro, and Y. Mikami. 1980. Some chemotherapeutic properties of two new antitumor antibiotics, saframycins A and C. Gann 71:790-796.
    • (1980) Gann , vol.71 , pp. 790-796
    • Arai, T.1    Takahashi, K.2    Ishiguro, K.3    Mikami, Y.4
  • 2
    • 0021885499 scopus 로고
    • Directed biosynthesis of new saframycin derivatives with resting cells of Streptomyces lavendulae
    • Arai, T., K. Yazawa, K. Takahashi, A. Maeda, and Y. Mikami. 1985. Directed biosynthesis of new saframycin derivatives with resting cells of Streptomyces lavendulae. Antimicrob. Agents. Chemother. 28:5-11.
    • (1985) Antimicrob. Agents. Chemother , vol.28 , pp. 5-11
    • Arai, T.1    Yazawa, K.2    Takahashi, K.3    Maeda, A.4    Mikami, Y.5
  • 3
    • 0014734605 scopus 로고
    • Purification and studies of catechol-O-methyltransferase of rat liver
    • Assicot, M., and C. Bohuon. 1970. Purification and studies of catechol-O-methyltransferase of rat liver. Eur. J. Biochem. 12:490-495.
    • (1970) Eur. J. Biochem , vol.12 , pp. 490-495
    • Assicot, M.1    Bohuon, C.2
  • 4
    • 0036021010 scopus 로고    scopus 로고
    • Ecteinascidin 743: A novel anticancer drug with a unique mechanism of action
    • Aune, G. J., T. Furuta, and Y. Pommier. 2002. Ecteinascidin 743: a novel anticancer drug with a unique mechanism of action. Anticancer Drugs 13:545-555.
    • (2002) Anticancer Drugs , vol.13 , pp. 545-555
    • Aune, G.J.1    Furuta, T.2    Pommier, Y.3
  • 5
    • 0013886618 scopus 로고
    • Methylation reactions in the formation and metabolism of catecholamines and other biogenic amines
    • Axelrod, J. 1966. Methylation reactions in the formation and metabolism of catecholamines and other biogenic amines. Pharmacol. Rev. 18:95-113.
    • (1966) Pharmacol. Rev , vol.18 , pp. 95-113
    • Axelrod, J.1
  • 6
    • 70449228544 scopus 로고
    • Enzymatic O-methylation of epinephrine and other catechols
    • Axelrod, J., and R. Tomchick. 1958. Enzymatic O-methylation of epinephrine and other catechols. J. Biol. Chem. 233:702-705.
    • (1958) J. Biol. Chem , vol.233 , pp. 702-705
    • Axelrod, J.1    Tomchick, R.2
  • 7
    • 33744954743 scopus 로고    scopus 로고
    • β-Phenylethylamines and the isoquinoline alkaloids
    • Bentley, K. W. 2006. β-Phenylethylamines and the isoquinoline alkaloids. Nat. Prod. Rep. 23:444-463.
    • (2006) Nat. Prod. Rep , vol.23 , pp. 444-463
    • Bentley, K.W.1
  • 8
    • 0032949477 scopus 로고    scopus 로고
    • New, selective catechol-O-methyltransferase inhibitors as therapeutic agents in Parkinson's disease
    • Bonifati, V., and G. Meco. 1999. New, selective catechol-O-methyltransferase inhibitors as therapeutic agents in Parkinson's disease. Pharmacol. Ther. 81:1-36.
    • (1999) Pharmacol. Ther , vol.81 , pp. 1-36
    • Bonifati, V.1    Meco, G.2
  • 10
    • 19544388761 scopus 로고    scopus 로고
    • Synthetic studies toward ecteinascidin 743
    • Chen, X., J. Chen, M. De Paolis, and J. Zhu. 2005. Synthetic studies toward ecteinascidin 743. J. Org. Chem. 70:4397-4408.
    • (2005) J. Org. Chem , vol.70 , pp. 4397-4408
    • Chen, X.1    Chen, J.2    De Paolis, M.3    Zhu, J.4
  • 14
    • 0043181749 scopus 로고
    • Correlation of the von Braun, Ritter, Bischler-Napieralski, Beckmann and Schmidt reactions via nitrilium salt intermediates
    • Fodor, G., and S. Nagubandi. 1980. Correlation of the von Braun, Ritter, Bischler-Napieralski, Beckmann and Schmidt reactions via nitrilium salt intermediates. Tetrahedron 36:1279-1300.
    • (1980) Tetrahedron , vol.36 , pp. 1279-1300
    • Fodor, G.1    Nagubandi, S.2
  • 15
    • 0016829492 scopus 로고
    • Catechol-O-methyl transferase: Pharmacological aspects and physiological role
    • Guldberg, H. C., and C. A. Marsden. 1975. Catechol-O-methyl transferase: pharmacological aspects and physiological role. Pharmacol. Rev. 27:135-206.
    • (1975) Pharmacol. Rev , vol.27 , pp. 135-206
    • Guldberg, H.C.1    Marsden, C.A.2
  • 16
    • 0024818627 scopus 로고
    • Renieramycin E and renieramycin F from the sponge Reniera sp. Reassignment of the stereochemistry of the renieramycins
    • He, H. Y., and D. J. Faulkner. 1989. Renieramycin E and renieramycin F from the sponge Reniera sp. Reassignment of the stereochemistry of the renieramycins. J. Org. Chem. 54:5822-5824.
    • (1989) J. Org. Chem , vol.54 , pp. 5822-5824
    • He, H.Y.1    Faulkner, D.J.2
  • 17
    • 0035965202 scopus 로고    scopus 로고
    • Identification of the enzymatic active site of tobacco caffeoyl-coenzyme A O-methyltransferase by site-directed mutagenesis
    • Hoffmann, L., S. Maury, M. Bergdoll, L. Thion, M. Erard, and M. Legrand. 2001. Identification of the enzymatic active site of tobacco caffeoyl-coenzyme A O-methyltransferase by site-directed mutagenesis. J. Biol. Chem. 276:36831-36838.
    • (2001) J. Biol. Chem , vol.276 , pp. 36831-36838
    • Hoffmann, L.1    Maury, S.2    Bergdoll, M.3    Thion, L.4    Erard, M.5    Legrand, M.6
  • 21
    • 10044251036 scopus 로고    scopus 로고
    • ATP channel subunits expressed in HEK-293 cells
    • ATP channel subunits expressed in HEK-293 cells. Eur. J. Pharmacol. 506:93-100.
    • (2004) Eur. J. Pharmacol , vol.506 , pp. 93-100
    • Jiang, B.1    Cao, K.2    Wang, R.3
  • 22
    • 0034095886 scopus 로고    scopus 로고
    • Clinical pharmacology, therapeutic use and potential of COMT inhibitors in Parkinson's disease
    • Kaakkola, S. 2000. Clinical pharmacology, therapeutic use and potential of COMT inhibitors in Parkinson's disease. Drugs 59:1233-1250.
    • (2000) Drugs , vol.59 , pp. 1233-1250
    • Kaakkola, S.1
  • 23
    • 0037403751 scopus 로고    scopus 로고
    • Enzymology of methylation of tea catechins and inhibition of catechol-O-methyltransferase by (-)-epigallocatechin gallate
    • Lu, H., X. Meng, and C. S. Yang. 2003. Enzymology of methylation of tea catechins and inhibition of catechol-O-methyltransferase by (-)-epigallocatechin gallate. Drug Metab. Dispos. 31:572-579.
    • (2003) Drug Metab. Dispos , vol.31 , pp. 572-579
    • Lu, H.1    Meng, X.2    Yang, C.S.3
  • 24
    • 0038287034 scopus 로고    scopus 로고
    • Catechol-O- methyltransferase (COMT): Biochemistry, molecular biology, pharmacology, and clinical efficacy of the new selective COMT inhibitors
    • Männisto, P. T., and S. Kaakkola. 1999. Catechol-O- methyltransferase (COMT): biochemistry, molecular biology, pharmacology, and clinical efficacy of the new selective COMT inhibitors. Pharmacol. Rev. 51:593-628.
    • (1999) Pharmacol. Rev , vol.51 , pp. 593-628
    • Männisto, P.T.1    Kaakkola, S.2
  • 25
    • 0034725710 scopus 로고    scopus 로고
    • Molecular characterization of the S-adenosyl-L-methionine:3′- hydroxy-N-methylcoclaurine 4′-O-methyltransferase involved in isoquinoline alkaloid biosynthesis in Coptis japonica
    • Morishige, T., T. Tsujita, Y. Yamada, and F. Sato. 2000. Molecular characterization of the S-adenosyl-L-methionine:3′- hydroxy-N-methylcoclaurine 4′-O-methyltransferase involved in isoquinoline alkaloid biosynthesis in Coptis japonica. J. Biol. Chem. 275:23398-23405.
    • (2000) J. Biol. Chem , vol.275 , pp. 23398-23405
    • Morishige, T.1    Tsujita, T.2    Yamada, Y.3    Sato, F.4
  • 26
    • 0022545734 scopus 로고
    • Incorporation of 3′-methyltyrosine and 5′-methyl-DOPA into naphthyridinomycin
    • Palaniswamy, V. A., and S. J. Gould. 1986. Incorporation of 3′-methyltyrosine and 5′-methyl-DOPA into naphthyridinomycin. J. Am. Chem. Soc. 108:5651-5652.
    • (1986) J. Am. Chem. Soc , vol.108 , pp. 5651-5652
    • Palaniswamy, V.A.1    Gould, S.J.2
  • 27
    • 0029996171 scopus 로고    scopus 로고
    • Two multifunctional peptide synthetases and an O-methyltransferase are involved in the biosynthesis of the DNA-binding antibiotic and antitumour agent saframycin Mx1 from Myxococcus xanthus
    • Pospiech, A., J. Bletenhader, and T. Schupp. 1996. Two multifunctional peptide synthetases and an O-methyltransferase are involved in the biosynthesis of the DNA-binding antibiotic and antitumour agent saframycin Mx1 from Myxococcus xanthus. Microbiology 142:741-746.
    • (1996) Microbiology , vol.142 , pp. 741-746
    • Pospiech, A.1    Bletenhader, J.2    Schupp, T.3
  • 28
    • 0029113877 scopus 로고
    • A new Myxococcus xanthus gene cluster for the biosynthesis of the antibiotic saframycin Mx1 encoding a peptide synthetase
    • Pospiech, A., B. Cluzel, J. Bietenhader, and T. Schupp. 1995. A new Myxococcus xanthus gene cluster for the biosynthesis of the antibiotic saframycin Mx1 encoding a peptide synthetase. Microbiology 141:1793-1803.
    • (1995) Microbiology , vol.141 , pp. 1793-1803
    • Pospiech, A.1    Cluzel, B.2    Bietenhader, J.3    Schupp, T.4
  • 29
    • 0025070774 scopus 로고
    • Ecteinascidin-729, ecteinascidin-743, ecteinascidin-745, ecteinascidin-759a, ecteinascidin-759b, and ecteinascidin-770. Potent antitumor agents from the Caribbean tunicate Ecteinascidia turbinata
    • Rinehart, K. L., T. G. Holt, N. L. Fregeau, J. G. Stroh, P. A. Keifer, F. Sun, L. H. Li, and D. G. Martin. 1990. Ecteinascidin-729, ecteinascidin-743, ecteinascidin-745, ecteinascidin-759a, ecteinascidin-759b, and ecteinascidin-770. Potent antitumor agents from the Caribbean tunicate Ecteinascidia turbinata. J. Org. Chem. 55:4512-4515.
    • (1990) J. Org. Chem , vol.55 , pp. 4512-4515
    • Rinehart, K.L.1    Holt, T.G.2    Fregeau, N.L.3    Stroh, J.G.4    Keifer, P.A.5    Sun, F.6    Li, L.H.7    Martin, D.G.8
  • 30
    • 0031708101 scopus 로고    scopus 로고
    • COMT inhibition in the treatment of Parkinson's disease
    • Ruottinen, H. M., and U. K. Rinne. 1998. COMT inhibition in the treatment of Parkinson's disease. J. Neurol. 245:P25-P34.
    • (1998) J. Neurol , vol.245
    • Ruottinen, H.M.1    Rinne, U.K.2
  • 32
    • 1942439951 scopus 로고    scopus 로고
    • Synthesis of tyrosine derivatives for saframycin MX1 biosynthetic studies
    • Schmidt, E. W., J. T. Nelson, and J. P. Fillmore. 2004. Synthesis of tyrosine derivatives for saframycin MX1 biosynthetic studies. Tetrahedron Lett. 45:3921-3924.
    • (2004) Tetrahedron Lett , vol.45 , pp. 3921-3924
    • Schmidt, E.W.1    Nelson, J.T.2    Fillmore, J.P.3
  • 33
    • 20144389257 scopus 로고    scopus 로고
    • Velasco, A., P. Acebo, A. Gomez, C. Schleissner, P. Rodríguez, T. Aparicio, S. Conde, R. Muñoz, F de la Calle, J. L. Garcia, and J. M. Sánchez-Puelles. 2005. Molecular characterization of the safracin biosynthetic pathway from Pseudomonas fluorescens A2-2: designing new cytotoxic compounds. Mol. Microbiol. 56:144-154.
    • Velasco, A., P. Acebo, A. Gomez, C. Schleissner, P. Rodríguez, T. Aparicio, S. Conde, R. Muñoz, F de la Calle, J. L. Garcia, and J. M. Sánchez-Puelles. 2005. Molecular characterization of the safracin biosynthetic pathway from Pseudomonas fluorescens A2-2: designing new cytotoxic compounds. Mol. Microbiol. 56:144-154.
  • 34
    • 0242609862 scopus 로고    scopus 로고
    • Production of the vancomycin aglycone conjugated to a peptide carrier domain derived from a biosynthetic non-ribosomal peptidc synthetase
    • Vitali, F., K. Zerbe, and J. A. Robinson. 2003. Production of the vancomycin aglycone conjugated to a peptide carrier domain derived from a biosynthetic non-ribosomal peptidc synthetase. Chem. Commun. 21:2718-2719.
    • (2003) Chem. Commun , vol.21 , pp. 2718-2719
    • Vitali, F.1    Zerbe, K.2    Robinson, J.A.3
  • 35
    • 0028520357 scopus 로고
    • An alternative methylation pathway in lignin biosynthesis in Zinnia
    • Ye, Z. H., R. E. Kneusel, U. Matern, and J. E. Varner. 1994. An alternative methylation pathway in lignin biosynthesis in Zinnia. Plant Cell 6:1427-1439.
    • (1994) Plant Cell , vol.6 , pp. 1427-1439
    • Ye, Z.H.1    Kneusel, R.E.2    Matern, U.3    Varner, J.E.4
  • 36
    • 0029310479 scopus 로고
    • Differential expression of two O-methyltransferases in lignin biosynthesis in Zinnia elegans
    • Ye, Z. H., and J. E. Varner. 1995. Differential expression of two O-methyltransferases in lignin biosynthesis in Zinnia elegans. Plant Physiol. 108:459-467.
    • (1995) Plant Physiol , vol.108 , pp. 459-467
    • Ye, Z.H.1    Varner, J.E.2
  • 37
    • 0035199322 scopus 로고    scopus 로고
    • The inefficiency of incisions of ecteinascidin 743-DNA adducts by the UvrABC nuclcase and the unique structural feature of the DNA adducts can be used to explain the repair-dependent toxicities of this antitumor agent
    • Zewail-Foote, M., V.-S. Li, H. Kohn, D. Bearss, M. Guzman, and L. H. Hurley. 2001. The inefficiency of incisions of ecteinascidin 743-DNA adducts by the UvrABC nuclcase and the unique structural feature of the DNA adducts can be used to explain the repair-dependent toxicities of this antitumor agent. Chem. Biol. 8:1033-1049.
    • (2001) Chem. Biol , vol.8 , pp. 1033-1049
    • Zewail-Foote, M.1    Li, V.-S.2    Kohn, H.3    Bearss, D.4    Guzman, M.5    Hurley, L.H.6
  • 38
    • 0000317180 scopus 로고    scopus 로고
    • Is 2-methoxyestradiol an endogenous estrogen metabolite that inhibits mammary carcinogenesis?
    • Zhu, B. T., and A. H. Conney. 1998. Is 2-methoxyestradiol an endogenous estrogen metabolite that inhibits mammary carcinogenesis? Cancer Res. 58:2269-2277.
    • (1998) Cancer Res , vol.58 , pp. 2269-2277
    • Zhu, B.T.1    Conney, A.H.2
  • 39
    • 26644468125 scopus 로고    scopus 로고
    • Comparative macroarray analysis of morphine containing Papaver somniferum and eight morphine free Papaver species identifies an O-methyltransferase involved in benzylisoquinoline biosynthesis
    • Ziegler, J., M. L. Diaz-Chavez, R. Kramell, C. Ammer, and T. M. Kutchan. 2005. Comparative macroarray analysis of morphine containing Papaver somniferum and eight morphine free Papaver species identifies an O-methyltransferase involved in benzylisoquinoline biosynthesis. Planta 222:458-471.
    • (2005) Planta , vol.222 , pp. 458-471
    • Ziegler, J.1    Diaz-Chavez, M.L.2    Kramell, R.3    Ammer, C.4    Kutchan, T.M.5


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