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Volumn 79, Issue 6, 2008, Pages 951-961

Potential of a 7-dimethylallyltryptophan synthase as a tool for production of prenylated indole derivatives

Author keywords

7 dimethylallyltryptophan synthase; Aspergillus fumigatus; Chemoenzymatic synthesis; Prenylated indole derivatives; Prenylation; Prenyltransferase

Indexed keywords

AMINO ACIDS; AROMATIC COMPOUNDS; COMPUTER NETWORKS; ENZYMES; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MAGNETIC FIELDS; MAGNETIC RESONANCE; MAGNETISM; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; RESONANCE; STRUCTURAL ANALYSIS;

EID: 46149117250     PISSN: 01757598     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00253-008-1505-3     Document Type: Article
Times cited : (42)

References (38)
  • 1
    • 33748286847 scopus 로고    scopus 로고
    • Impact of Aspergillus oryzae genomics on industrial production of metabolites
    • Abe K, Gomi K, Hasegawa F, Machida M (2006) Impact of Aspergillus oryzae genomics on industrial production of metabolites. Mycopathologia 162:143-153
    • (2006) Mycopathologia , vol.162 , pp. 143-153
    • Abe, K.1    Gomi, K.2    Hasegawa, F.3    MacHida, M.4
  • 2
    • 33750982685 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis of glycan libraries
    • Blixt O, Razi N (2006) Chemoenzymatic synthesis of glycan libraries. Methods Enzymol 415:137-153
    • (2006) Methods Enzymol , vol.415 , pp. 137-153
    • Blixt, O.1    Razi, N.2
  • 3
    • 27744589213 scopus 로고    scopus 로고
    • Novel prenyltransferase enzymes as a tool for flavonoid prenylation
    • Botta B, Monache GD, Menendez P, Boffi A (2005a) Novel prenyltransferase enzymes as a tool for flavonoid prenylation. Trends Pharmacol Sci 26:606-608
    • (2005) Trends Pharmacol Sci , vol.26 , pp. 606-608
    • Botta, B.1    Monache, G.D.2    Menendez, P.3    Boffi, A.4
  • 5
    • 33747873262 scopus 로고    scopus 로고
    • Glycopeptides as versatile tools for glycobiology
    • Buskas T, Ingale S, Boons GJ (2006) Glycopeptides as versatile tools for glycobiology. Glycobiology 16:113R-136R
    • (2006) Glycobiology , vol.16
    • Buskas, T.1    Ingale, S.2    Boons, G.J.3
  • 6
    • 11144311139 scopus 로고    scopus 로고
    • Lessons from natural molecules
    • Clardy J, Walsh C (2004) Lessons from natural molecules. Nature 432:829-837
    • (2004) Nature , vol.432 , pp. 829-837
    • Clardy, J.1    Walsh, C.2
  • 8
    • 33744537000 scopus 로고    scopus 로고
    • Combinatorial biosynthesis-potential and problems
    • Floss HG (2006) Combinatorial biosynthesis-potential and problems. J Biotechnol 124:242-257
    • (2006) J Biotechnol , vol.124 , pp. 242-257
    • Floss, H.G.1
  • 9
    • 1542350250 scopus 로고    scopus 로고
    • In vitro and in vivo production of new aminocoumarins by a combined biochemical, genetic and synthetic approach
    • Galm U, Dessoy MA, Schmidt J, Wessjohann LA, Heide L (2004) In vitro and in vivo production of new aminocoumarins by a combined biochemical, genetic and synthetic approach. Chem Biol 11:P173-183
    • (2004) Chem Biol , vol.11 , pp. 173-183
    • Galm, U.1    Dessoy, M.A.2    Schmidt, J.3    Wessjohann, L.A.4    Heide, L.5
  • 10
    • 22144479730 scopus 로고    scopus 로고
    • Overproduction, purification and characterization of FtmPT1, a brevianamide F prenyltransferase from Aspergillus fumigatus
    • Grundmann A, Li S-M (2005) Overproduction, purification and characterization of FtmPT1, a brevianamide F prenyltransferase from Aspergillus fumigatus. Microbiology 151:2199-2207
    • (2005) Microbiology , vol.151 , pp. 2199-2207
    • Grundmann, A.1    Li, S.-M.2
  • 11
    • 33645116726 scopus 로고    scopus 로고
    • Chemoenzymatic and template-directed synthesis of bioactive macrocyclic peptides
    • Grunewald J, Marahiel MA (2006) Chemoenzymatic and template-directed synthesis of bioactive macrocyclic peptides. Microbiol Mol Biol Rev 70:121-146
    • (2006) Microbiol Mol Biol Rev , vol.70 , pp. 121-146
    • Grunewald, J.1    Marahiel, M.A.2
  • 12
    • 34250208085 scopus 로고    scopus 로고
    • A soluble, magnesium-independent prenyltransferase catalyzes reverse and regular C-prenylations and O-prenylations of aromatic substrates
    • Haagen Y, Unsold I, Westrich L, Gust B, Richard SB, Noel JP, Heide L (2007) A soluble, magnesium-independent prenyltransferase catalyzes reverse and regular C-prenylations and O-prenylations of aromatic substrates. FEBS Lett 581:2889-2893
    • (2007) FEBS Lett , vol.581 , pp. 2889-2893
    • Haagen, Y.1    Unsold, I.2    Westrich, L.3    Gust, B.4    Richard, S.B.5    Noel, J.P.6    Heide, L.7
  • 13
    • 33846282735 scopus 로고    scopus 로고
    • The first filamentous fungal genome sequences: Aspergillus leads the way for essential everyday resources or dusty museum specimens?
    • Jones MG (2007) The first filamentous fungal genome sequences: Aspergillus leads the way for essential everyday resources or dusty museum specimens? Microbiology 153:1-6
    • (2007) Microbiology , vol.153 , pp. 1-6
    • Jones, M.G.1
  • 14
    • 30544434099 scopus 로고    scopus 로고
    • Fungal secondary metabolism-from biochemistry to genomics
    • Keller NP, Turner G, Bennett JW (2005) Fungal secondary metabolism-from biochemistry to genomics. Nat Rev Microbiol 3:937-947
    • (2005) Nat Rev Microbiol , vol.3 , pp. 937-947
    • Keller, N.P.1    Turner, G.2    Bennett, J.W.3
  • 15
    • 35448932356 scopus 로고    scopus 로고
    • A 7-dimethylallyltryptophan synthase from Aspergillus fumigatus: Overproduction, purification and biochemical characterization
    • Kremer A, Westrich L, Li S-M (2007) A 7-dimethylallyltryptophan synthase from Aspergillus fumigatus: overproduction, purification and biochemical characterization. Microbiology 153:3409-3416
    • (2007) Microbiology , vol.153 , pp. 3409-3416
    • Kremer, A.1    Westrich, L.2    Li, S.-M.3
  • 16
    • 20544457539 scopus 로고    scopus 로고
    • Structural basis for the promiscuous biosynthetic prenylation of aromatic natural products
    • Kuzuyama T, Noel JP, Richard SB (2005) Structural basis for the promiscuous biosynthetic prenylation of aromatic natural products. Nature 435:983-987
    • (2005) Nature , vol.435 , pp. 983-987
    • Kuzuyama, T.1    Noel, J.P.2    Richard, S.B.3
  • 17
    • 29044436566 scopus 로고    scopus 로고
    • Neoglycorandomization and chemoenzymatic glycorandomization: Two complementary tools for natural product diversification
    • Langenhan JM, Griffith BR, Thorson JS (2005) Neoglycorandomization and chemoenzymatic glycorandomization: two complementary tools for natural product diversification. J Nat Prod 68:1696-1711
    • (2005) J Nat Prod , vol.68 , pp. 1696-1711
    • Langenhan, J.M.1    Griffith, B.R.2    Thorson, J.S.3
  • 18
    • 33750412469 scopus 로고    scopus 로고
    • Post genome research on the biosynthesis of ergot alkaloids
    • Li S-M, Unsöld IA (2006) Post genome research on the biosynthesis of ergot alkaloids. Planta Med 72:1117-1120
    • (2006) Planta Med , vol.72 , pp. 1117-1120
    • Li, S.-M.1    Unsöld, I.A.2
  • 19
    • 0036875773 scopus 로고    scopus 로고
    • Isolation and structure elucidation of deformylflustrabromine from the North Sea bryozoan Flustra foliacea
    • Lysek N, Rachor E, Lindel T (2002) Isolation and structure elucidation of deformylflustrabromine from the North Sea bryozoan Flustra foliacea. Z Naturforsch [C] 57:1056-1061
    • (2002) Z Naturforsch [C] , vol.57 , pp. 1056-1061
    • Lysek, N.1    Rachor, E.2    Lindel, T.3
  • 20
    • 34247109045 scopus 로고    scopus 로고
    • Natural Products as Sources of New Drugs over the Last 25 Years
    • Newman DJ, Cragg GM (2007) Natural Products as Sources of New Drugs over the Last 25 Years. J Nat Prod 70:461-477
    • (2007) J Nat Prod , vol.70 , pp. 461-477
    • Newman, D.J.1    Cragg, G.M.2
  • 24
    • 46149105053 scopus 로고    scopus 로고
    • Reinvestigation on a cyclic dipeptide N-prenyltransferase reveals rearrangement of N1-prenylated indole derivatives
    • Ruan H-L, Yin W-B, Wu J-Z, Li S-M (2008) Reinvestigation on a cyclic dipeptide N-prenyltransferase reveals rearrangement of N1-prenylated indole derivatives. Chembiochem 9:1044-1047
    • (2008) Chembiochem , vol.9 , pp. 1044-1047
    • Ruan, H.-L.1    Yin, W.-B.2    Wu, J.-Z.3    Li, S.-M.4
  • 25
    • 21244483529 scopus 로고    scopus 로고
    • Nucleotide deoxysugars: Essential tools for the glycosylation engineering of novel bioactive compounds
    • Rupprath C, Schumacher T, Elling L (2005) Nucleotide deoxysugars: essential tools for the glycosylation engineering of novel bioactive compounds. Curr Med Chem 12:1637-1675
    • (2005) Curr Med Chem , vol.12 , pp. 1637-1675
    • Rupprath, C.1    Schumacher, T.2    Elling, L.3
  • 26
    • 0033811071 scopus 로고    scopus 로고
    • Synthesis and evaluation of microtubule assembly inhibition and cytotoxicity of prenylated derivatives of cyclo-L-Trp-L-Pro
    • Sanz-Cervera JF, Stocking EM, Usui T, Osada H, Williams RM (2000) Synthesis and evaluation of microtubule assembly inhibition and cytotoxicity of prenylated derivatives of cyclo-L-Trp-L-Pro. Bioorg Med Chem 8:2407-2415
    • (2000) Bioorg Med Chem , vol.8 , pp. 2407-2415
    • Sanz-Cervera, J.F.1    Stocking, E.M.2    Usui, T.3    Osada, H.4    Williams, R.M.5
  • 27
    • 34547450158 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis of prenylated indole derivatives by using a 4-dimethylallyltryptophan synthase from Aspergillus fumigatus
    • Steffan N, Unsöld IA, Li S-M (2007) Chemoenzymatic synthesis of prenylated indole derivatives by using a 4-dimethylallyltryptophan synthase from Aspergillus fumigatus. Chembiochem 8:1298-1307
    • (2007) Chembiochem , vol.8 , pp. 1298-1307
    • Steffan, N.1    Unsöld, I.A.2    Li, S.-M.3
  • 28
    • 0034721436 scopus 로고    scopus 로고
    • Reverse prenyl transferases exhibit poor facial discrimination in the biosynthesis of paraherquamide A, brevianamide A, and austamide
    • Stocking EM, Williams RM, Sanz-Cervera JF (2000) Reverse prenyl transferases exhibit poor facial discrimination in the biosynthesis of paraherquamide A, brevianamide A, and austamide. J Am Chem Soc 122:9089-9098
    • (2000) J Am Chem Soc , vol.122 , pp. 9089-9098
    • Stocking, E.M.1    Williams, R.M.2    Sanz-Cervera, J.F.3
  • 29
    • 44449087804 scopus 로고    scopus 로고
    • The ABBA family of aromatic prenyltransferases: Broadening natural product diversity
    • in press
    • Tello M, Kuzuyama T, Heide L, Noel JP, Richard SB (2008) The ABBA family of aromatic prenyltransferases: broadening natural product diversity. Cell Mol. Life Sci. in press
    • (2008) Cell Mol. Life Sci.
    • Tello, M.1    Kuzuyama, T.2    Heide, L.3    Noel, J.P.4    Richard, S.B.5
  • 30
    • 19044365898 scopus 로고    scopus 로고
    • Overproduction, purification and characterization of FgaPT2, a dimethylallyltryptophan synthase from Aspergillus fumigatus
    • Unsöld IA, Li S-M (2005) Overproduction, purification and characterization of FgaPT2, a dimethylallyltryptophan synthase from Aspergillus fumigatus. Microbiology 151:1499-1505
    • (2005) Microbiology , vol.151 , pp. 1499-1505
    • Unsöld, I.A.1    Li, S.-M.2
  • 31
    • 30444438065 scopus 로고    scopus 로고
    • Reverse prenyltransferase in the biosynthesis of fumigaclavine C in Aspergillus fumigatus: Gene expression, purification and characterization of fumigaclavine C synthase FgaPT1
    • Unsöld IA, Li S-M (2006) Reverse prenyltransferase in the biosynthesis of fumigaclavine C in Aspergillus fumigatus: gene expression, purification and characterization of fumigaclavine C synthase FgaPT1. Chembiochem 7:158-164
    • (2006) Chembiochem , vol.7 , pp. 158-164
    • Unsöld, I.A.1    Li, S.-M.2
  • 32
    • 0345839252 scopus 로고    scopus 로고
    • Where will new antibiotics come from?
    • Walsh T (2003) Where will new antibiotics come from? Nat Rev Microbiol 1:65-70
    • (2003) Nat Rev Microbiol , vol.1 , pp. 65-70
    • Walsh, T.1
  • 33
    • 33947160920 scopus 로고    scopus 로고
    • Mutasynthesis-uniting chemistry and genetics for drug discovery
    • Weissman KJ (2007) Mutasynthesis-uniting chemistry and genetics for drug discovery. Trends Biotechnol 25:139-142
    • (2007) Trends Biotechnol , vol.25 , pp. 139-142
    • Weissman, K.J.1
  • 34
    • 23444460405 scopus 로고    scopus 로고
    • Mutational biosynthesis-a tool for the generation of structural diversity in the biosynthesis of antibiotics
    • Weist S, Süssmuth RD (2005) Mutational biosynthesis-a tool for the generation of structural diversity in the biosynthesis of antibiotics. Appl Microbiol Biotechnol 68:141-150
    • (2005) Appl Microbiol Biotechnol , vol.68 , pp. 141-150
    • Weist, S.1    Süssmuth, R.D.2
  • 37
    • 34547572235 scopus 로고    scopus 로고
    • CdpNPT, an N-prenyltransferase from Aspergillus fumigatus: Overproduction, purification and biochemical characterisation
    • Yin W-B, Ruan H-L, Westrich L, Grundmann A, Li S-M (2007) CdpNPT, an N-prenyltransferase from Aspergillus fumigatus: overproduction, purification and biochemical characterisation. Chembiochem 8:1154-1161
    • (2007) Chembiochem , vol.8 , pp. 1154-1161
    • Yin, W.-B.1    Ruan, H.-L.2    Westrich, L.3    Grundmann, A.4    Li, S.-M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.