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Volumn 67, Issue 9, 2001, Pages 3882-3887

Laboratory Evolution of Toluene Dioxygenase to Accept 4-Picoline as a Substrate

Author keywords

[No Author keywords available]

Indexed keywords

OXYGENASE; PICOLINE DERIVATIVE; TOLUENE DIOXYGENASE;

EID: 0035464767     PISSN: 00992240     EISSN: None     Source Type: Journal    
DOI: 10.1128/AEM.67.9.3882-3887.2001     Document Type: Article
Times cited : (72)

References (37)
  • 1
    • 0001270261 scopus 로고    scopus 로고
    • Design by directed evolution
    • Arnold, F. H. 1998. Design by directed evolution. Acc. Chem. Res. 31:125-131.
    • (1998) Acc. Chem. Res. , vol.31 , pp. 125-131
    • Arnold, F.H.1
  • 2
    • 0031795756 scopus 로고    scopus 로고
    • Identification of chlorobenzene dioxygenase sequence elements involved in dechlorination of 1,2,4,5-tetrachlorobenzene
    • Beil, S., J. R. Mason, K. N. Timmis, and D. H. Pieper. 1998. Identification of chlorobenzene dioxygenase sequence elements involved in dechlorination of 1,2,4,5-tetrachlorobenzene. J. Bacteriol. 180:5520-5528.
    • (1998) J. Bacteriol. , vol.180 , pp. 5520-5528
    • Beil, S.1    Mason, J.R.2    Timmis, K.N.3    Pieper, D.H.4
  • 4
    • 0027195608 scopus 로고
    • Structures and stereochemical assignments of some novel chiral synthons derived from the biotransformation of 2,3-dihydrobenzofuran and benzofuran by Pseudomonas putida
    • Boyd, D. R., N. D. Sharma, R. Boyle, J. F. Malone, J. Chima, and H. Dalton. 1993. Structures and stereochemical assignments of some novel chiral synthons derived from the biotransformation of 2,3-dihydrobenzofuran and benzofuran by Pseudomonas putida. Tetrahedron Asymmetry 4:1307-1324.
    • (1993) Tetrahedron Asymmetry , vol.4 , pp. 1307-1324
    • Boyd, D.R.1    Sharma, N.D.2    Boyle, R.3    Malone, J.F.4    Chima, J.5    Dalton, H.6
  • 6
    • 0031831881 scopus 로고    scopus 로고
    • The dioxygenase-catalysed formation of vicinal cis-diols
    • Boyd, D. R., and G. N. Sheldrake. 1998. The dioxygenase-catalysed formation of vicinal cis-diols. Natural Product Reports 15:309-324.
    • (1998) Natural Product Reports , vol.15 , pp. 309-324
    • Boyd, D.R.1    Sheldrake, G.N.2
  • 7
    • 0040684812 scopus 로고    scopus 로고
    • Tuning biphenyl dioxygenase for extended substrate specificity
    • Bruhlmann, F., and W. Chen. 1999. Tuning biphenyl dioxygenase for extended substrate specificity. Biotechnol. Bioeng. 63:544-551.
    • (1999) Biotechnol. Bioeng. , vol.63 , pp. 544-551
    • Bruhlmann, F.1    Chen, W.2
  • 9
    • 0020612907 scopus 로고
    • Expression of naphthalene dioxygenase genes in Escherichia coli results in the biosynthesis of indigo
    • Ensley, B. D., B. J. Ratzkin, T. D. Osslund, M. J. Simon, L. P. Wackett, and D. T. Gibson. 1983. Expression of naphthalene dioxygenase genes in Escherichia coli results in the biosynthesis of indigo. Science 222:167-169.
    • (1983) Science , vol.222 , pp. 167-169
    • Ensley, B.D.1    Ratzkin, B.J.2    Osslund, T.D.3    Simon, M.J.4    Wackett, L.P.5    Gibson, D.T.6
  • 10
    • 0027368828 scopus 로고
    • Enhanced biodegradation of polychlorinated biphenyls after site-directed mutagenesis of a biphenyl dioxygenase gene
    • Erickson, B. D., and F. J. Mondello. 1993. Enhanced biodegradation of polychlorinated biphenyls after site-directed mutagenesis of a biphenyl dioxygenase gene. Appl. Environ. Microbiol. 59:3858-3862.
    • (1993) Appl. Environ. Microbiol. , vol.59 , pp. 3858-3862
    • Erickson, B.D.1    Mondello, F.J.2
  • 12
    • 0015919597 scopus 로고
    • Initial reactions in the oxidation of ethylbenzene by Pseudomonas putida
    • Gibson, D. T., B. Gschwendt, W.-K. Yeh, and V. M. Kobal. 1973. Initial reactions in the oxidation of ethylbenzene by Pseudomonas putida. Biochemistry 12:1520-1528.
    • (1973) Biochemistry , vol.12 , pp. 1520-1528
    • Gibson, D.T.1    Gschwendt, B.2    Yeh, W.-K.3    Kobal, V.M.4
  • 13
    • 0014969183 scopus 로고
    • Formation of (+)-cis-2,3-dihydroxy-1-methylcyclohexa-4,6-diene from toluene by Pseudomonas putida
    • Gibson, D. T., M. Hensley, H. Yoshioka, and T. G. Marby. 1970. Formation of (+)-cis-2,3-dihydroxy-1-methylcyclohexa-4,6-diene from toluene by Pseudomonas putida. Biochemistry 9:1626-1630.
    • (1970) Biochemistry , vol.9 , pp. 1626-1630
    • Gibson, D.T.1    Hensley, M.2    Yoshioka, H.3    Marby, T.G.4
  • 14
    • 0028215858 scopus 로고
    • Construction of hybrid biphenyl (bph) and toluene (tod) genes for functional analysis of aromatic ring dioxygenases
    • Hirose, J., A. Suyama, S. Hayashida, and K. Furukawa. 1994. Construction of hybrid biphenyl (bph) and toluene (tod) genes for functional analysis of aromatic ring dioxygenases. Gene 138:27-33.
    • (1994) Gene , vol.138 , pp. 27-33
    • Hirose, J.1    Suyama, A.2    Hayashida, S.3    Furukawa, K.4
  • 15
    • 0001846314 scopus 로고    scopus 로고
    • Enzymatic dihydroxylation of aromatics in enantioselective synthesis: Expanding asymmetric methodology
    • Hudlicky, T., D. Gonzalez, and D. T. Gibson. 1999. Enzymatic dihydroxylation of aromatics in enantioselective synthesis: expanding asymmetric methodology. Aldrichimica Acta 32:35-62.
    • (1999) Aldrichimica Acta , vol.32 , pp. 35-62
    • Hudlicky, T.1    Gonzalez, D.2    Gibson, D.T.3
  • 16
    • 0028865344 scopus 로고
    • Purification and characterization of the Comamonas testosteroni B-356 biphenyl dioxygenase components
    • Hurtubise, Y., D. Barriault, J. Powlowski, and M. Sylvestre. 1995. Purification and characterization of the Comamonas testosteroni B-356 biphenyl dioxygenase components. J. Bacteriol. 177:6610-6618.
    • (1995) J. Bacteriol. , vol.177 , pp. 6610-6618
    • Hurtubise, Y.1    Barriault, D.2    Powlowski, J.3    Sylvestre, M.4
  • 17
    • 0031733410 scopus 로고    scopus 로고
    • Involvement of the terminal oxygenase β subunit in the biphenyl dioxygenase reactivity pattern toward chlorobiphenyls
    • Hurtubise, Y., D. Barriault, and M. Sylvestre. 1998. Involvement of the terminal oxygenase β subunit in the biphenyl dioxygenase reactivity pattern toward chlorobiphenyls. J. Bacteriol. 180:5828-5835.
    • (1998) J. Bacteriol. , vol.180 , pp. 5828-5835
    • Hurtubise, Y.1    Barriault, D.2    Sylvestre, M.3
  • 19
    • 0034880955 scopus 로고    scopus 로고
    • A versatile high-throughput screen for dioxygenase activity using solid-phase digital imaging
    • Joern, J. M., T. Sakamoto, A. Arisawa, and F. H. Arnold. 2001. A versatile high-throughput screen for dioxygenase activity using solid-phase digital imaging. J. Biomol. Screening, 6:213-217.
    • (2001) J. Biomol. Screening , vol.6 , pp. 213-217
    • Joern, J.M.1    Sakamoto, T.2    Arisawa, A.3    Arnold, F.H.4
  • 20
    • 0013613819 scopus 로고
    • Biosynthesis of functionated aromatic N-heterocycles
    • Kiener, A. 1995. Biosynthesis of functionated aromatic N-heterocycles. Chemtech 25:31-35.
    • (1995) Chemtech , vol.25 , pp. 31-35
    • Kiener, A.1
  • 21
    • 0031874757 scopus 로고    scopus 로고
    • Enhanced degradation of polychlorinated biphenyls by directed evolution of biphenyl dioxygenase
    • Kumamaru, T., H. Suenaga, M. Mitsuoka, T. Watanabe, and K. Furukawa. 1998. Enhanced degradation of polychlorinated biphenyls by directed evolution of biphenyl dioxygenase. Nat. Biotechnol. 16:663-666.
    • (1998) Nat. Biotechnol. , vol.16 , pp. 663-666
    • Kumamaru, T.1    Suenaga, H.2    Mitsuoka, M.3    Watanabe, T.4    Furukawa, K.5
  • 22
    • 0031000281 scopus 로고    scopus 로고
    • Oxidation of aliphatic olefins by toluene dioxygenase: Enzyme rates and product identification
    • Lange, C. C., and L. P. Wackett. 1997. Oxidation of aliphatic olefins by toluene dioxygenase: enzyme rates and product identification. J. Bacteriol. 179:3858-3865.
    • (1997) J. Bacteriol. , vol.179 , pp. 3858-3865
    • Lange, C.C.1    Wackett, L.P.2
  • 23
    • 0032900895 scopus 로고    scopus 로고
    • Benzene-induced uncoupling of naphthalene dioxygenase activity and enzyme inactivation by production of hydrogen peroxide
    • Lee, K. 1999. Benzene-induced uncoupling of naphthalene dioxygenase activity and enzyme inactivation by production of hydrogen peroxide. J. Bacteriol. 181:2719-2725.
    • (1999) J. Bacteriol. , vol.181 , pp. 2719-2725
    • Lee, K.1
  • 25
    • 0031932850 scopus 로고    scopus 로고
    • Enzyme specificity of 2-nitrotoluene 2,3-dioxygenase from Pseudomonas sp. strain JS42 is determined by the C-terminal region of the α subunit of the oxygenase component
    • Parales, J. V., R. E. Parales, S. M. Resnick, and D. T. Gibson. 1998. Enzyme specificity of 2-nitrotoluene 2,3-dioxygenase from Pseudomonas sp. strain JS42 is determined by the C-terminal region of the α subunit of the oxygenase component. J. Bacteriol. 180:1194-1199.
    • (1998) J. Bacteriol. , vol.180 , pp. 1194-1199
    • Parales, J.V.1    Parales, R.E.2    Resnick, S.M.3    Gibson, D.T.4
  • 26
    • 0033411631 scopus 로고    scopus 로고
    • Preparation and functionalization of N-heterocycles
    • Petersen, M., and A. Kiener. 1999. Preparation and functionalization of N-heterocycles. Green Chem. 1:99-106.
    • (1999) Green Chem. , vol.1 , pp. 99-106
    • Petersen, M.1    Kiener, A.2
  • 27
    • 0030792380 scopus 로고    scopus 로고
    • Colorimetric method for a rapid detection of oxygenated aromatic biotransformation products
    • Quintana, M. G., C. Didion, and H. Dalton. 1997. Colorimetric method for a rapid detection of oxygenated aromatic biotransformation products. Biotechnol. Techniques 11:585-587.
    • (1997) Biotechnol. Techniques , vol.11 , pp. 585-587
    • Quintana, M.G.1    Didion, C.2    Dalton, H.3
  • 28
    • 0026654843 scopus 로고
    • Oxidation of nitrotoluenes by toluene dioxygenase: Evidence for a monooxygenase reaction
    • Robertson, J. B., J. C. Spain, J. D. Haddock, and D. T. Gibson. 1992. Oxidation of nitrotoluenes by toluene dioxygenase: evidence for a monooxygenase reaction. Appl. Environ. Microbiol. 58:2643-2648.
    • (1992) Appl. Environ. Microbiol. , vol.58 , pp. 2643-2648
    • Robertson, J.B.1    Spain, J.C.2    Haddock, J.D.3    Gibson, D.T.4
  • 30
    • 0018790274 scopus 로고
    • Toluene dioxygenase: Purification of an iron-sulfur protein by affinity chromatography
    • Subramanian, V., T.-N. Liu, W.-K. Yeh, and D. T. Gibson. 1979. Toluene dioxygenase: purification of an iron-sulfur protein by affinity chromatography. Biochem. Biophys. Res. Commun. 91:1131-1139.
    • (1979) Biochem. Biophys. Res. Commun. , vol.91 , pp. 1131-1139
    • Subramanian, V.1    Liu, T.-N.2    Yeh, W.-K.3    Gibson, D.T.4
  • 33
    • 0002842741 scopus 로고
    • Biologically derived arene cis-dihydrodiols as synthetic building blocks
    • A. N. Collins, G. N. Sheldrake, and J. Crosby (ed.). John Wiley & Sons Ltd., Chichester, England
    • Sheldrake, G. N. 1992. Biologically derived arene cis-dihydrodiols as synthetic building blocks, p. 127-166. In A. N. Collins, G. N. Sheldrake, and J. Crosby (ed.), Chirality in industry: the commercial manufacture and application of optically active compounds. John Wiley & Sons Ltd., Chichester, England.
    • (1992) Chirality in Industry: the Commercial Manufacture and Application of Optically Active Compounds , pp. 127-166
    • Sheldrake, G.N.1
  • 34
    • 0027984555 scopus 로고
    • Substitution of the ISP α subunit of biphenyl dioxygenase from Pseudomonas results in a modification of the enzyme activity
    • Tan, H.-M., and C.-M. Cheng. 1994. Substitution of the ISP α subunit of biphenyl dioxygenase from Pseudomonas results in a modification of the enzyme activity. Biochem. Biophys Res. Commun. 204:912-917.
    • (1994) Biochem. Biophys Res. Commun. , vol.204 , pp. 912-917
    • Tan, H.-M.1    Cheng, C.-M.2
  • 35
    • 0028672045 scopus 로고
    • The evolution of pathways for aromatic hydrocarbon oxidation in Pseudomonas
    • Williams, P. A., and J. R. Sayers. 1994. The evolution of pathways for aromatic hydrocarbon oxidation in Pseudomonas. Biodegradation 5:195-217.
    • (1994) Biodegradation , vol.5 , pp. 195-217
    • Williams, P.A.1    Sayers, J.R.2
  • 37
    • 0024427069 scopus 로고
    • Toluene degradation by Pseudomonas putida F1
    • Zylstra, G. J., and D. T. Gibson. 1989. Toluene degradation by Pseudomonas putida F1. J. Biol. Chem. 264:14940-14946.
    • (1989) J. Biol. Chem. , vol.264 , pp. 14940-14946
    • Zylstra, G.J.1    Gibson, D.T.2


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