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Volumn 46, Issue 21, 2012, Pages 11844-11853

Carbon and nitrogen isotope effects associated with the dioxygenation of aniline and diphenylamine

Author keywords

[No Author keywords available]

Indexed keywords

ABIOTIC OXIDATIONS; ABIOTIC REDUCTION; APPARENT KINETICS; AROMATIC CONTAMINANTS; AROMATIC RINGS; BURKHOLDERIA; CARBON AND NITROGEN; COMPOUND-SPECIFIC ISOTOPE ANALYSIS; DIARYLAMINES; DIOXYGENASES; ISOTOPE EFFECT; ISOTOPE ENRICHMENTS; ISOTOPE FRACTIONATION; ISOTOPE SIGNATURES; PURE CULTURE; REACTION MECHANISM;

EID: 84868526214     PISSN: 0013936X     EISSN: 15205851     Source Type: Journal    
DOI: 10.1021/es303043t     Document Type: Article
Times cited : (29)

References (81)
  • 1
    • 55349084732 scopus 로고    scopus 로고
    • Assessing transformation processes of organic compounds using stable isotope fractionation
    • Hofstetter, T. B.; Schwarzenbach, R. P.; Bernasconi, S. M. Assessing transformation processes of organic compounds using stable isotope fractionation Environ. Sci. Technol. 2008, 42, 7737-7743
    • (2008) Environ. Sci. Technol. , vol.42 , pp. 7737-7743
    • Hofstetter, T.B.1    Schwarzenbach, R.P.2    Bernasconi, S.M.3
  • 2
    • 79952898820 scopus 로고    scopus 로고
    • Assessing transformation processes of organic contaminants by compound-specific stable isotope analysis
    • Hofstetter, T. B.; Berg, M. Assessing transformation processes of organic contaminants by compound-specific stable isotope analysis TrAC-Trends Anal. Chem. 2011, 30, 618-627
    • (2011) TrAC-Trends Anal. Chem. , vol.30 , pp. 618-627
    • Hofstetter, T.B.1    Berg, M.2
  • 3
    • 78149246131 scopus 로고    scopus 로고
    • Stable isotope fractionation to investigate natural transformation mechanisms of organic contaminants: Principles, prospects and limitations
    • Elsner, M. Stable isotope fractionation to investigate natural transformation mechanisms of organic contaminants: principles, prospects and limitations J. Environ. Monit. 2010, 12, 2005-2031
    • (2010) J. Environ. Monit. , vol.12 , pp. 2005-2031
    • Elsner, M.1
  • 5
    • 77952517903 scopus 로고    scopus 로고
    • Quantifying in-situ transformation rates of chlorinated ethenes by combining compound-specific stable isotope analysis, groundwater dating, and carbon isotope mass balances
    • Aeppli, C.; Hofstetter, T. B.; Amaral, H. I. F.; Kipfer, R.; Schwarzenbach, R. P.; Berg, M. Quantifying in-situ transformation rates of chlorinated ethenes by combining compound-specific stable isotope analysis, groundwater dating, and carbon isotope mass balances Environ. Sci. Technol. 2010, 44, 3705-3711
    • (2010) Environ. Sci. Technol. , vol.44 , pp. 3705-3711
    • Aeppli, C.1    Hofstetter, T.B.2    Amaral, H.I.F.3    Kipfer, R.4    Schwarzenbach, R.P.5    Berg, M.6
  • 6
    • 83955162173 scopus 로고    scopus 로고
    • Quantification of organic pollutant degradation in contaminated aquifers using compound specific stable isotope analysis - Review of recent developments
    • Thullner, M.; Centler, F.; Richnow, H.-H.; Fischer, A. Quantification of organic pollutant degradation in contaminated aquifers using compound specific stable isotope analysis-Review of recent developments Org. Geochem. 2012, 42, 1440-1460
    • (2012) Org. Geochem. , vol.42 , pp. 1440-1460
    • Thullner, M.1    Centler, F.2    Richnow, H.-H.3    Fischer, A.4
  • 7
    • 33846979487 scopus 로고    scopus 로고
    • Enzymatic hydroxylation of aromatic compounds
    • Ullrich, R.; Hofrichter, M. Enzymatic hydroxylation of aromatic compounds Cell. Mol. Life Sci. 2007, 64, 271-293
    • (2007) Cell. Mol. Life Sci. , vol.64 , pp. 271-293
    • Ullrich, R.1    Hofrichter, M.2
  • 8
    • 0034029015 scopus 로고    scopus 로고
    • Aromatic hydrocarbon dioxygenases in environmental biotechnology
    • Gibson, D. T.; Parales, R. E. Aromatic hydrocarbon dioxygenases in environmental biotechnology Curr. Opin. Biotech. 2000, 11, 236-243
    • (2000) Curr. Opin. Biotech. , vol.11 , pp. 236-243
    • Gibson, D.T.1    Parales, R.E.2
  • 9
    • 0037015403 scopus 로고    scopus 로고
    • Mechanism and applications of Rieske non-heme iron dioxygenases
    • Wackett, L. P. Mechanism and applications of Rieske non-heme iron dioxygenases Enzyme Microb. Technol. 2002, 31, 577-587
    • (2002) Enzyme Microb. Technol. , vol.31 , pp. 577-587
    • Wackett, L.P.1
  • 11
    • 2442551474 scopus 로고    scopus 로고
    • Stable carbon isotope fractionation during aerobic and anaerobic transformation of trichlorobenzene
    • Griebler, C.; Adrian, L.; Meckenstock, R.; Richnow, H. Stable carbon isotope fractionation during aerobic and anaerobic transformation of trichlorobenzene FEMS Microbiol. Ecol. 2004, 48, 313-321
    • (2004) FEMS Microbiol. Ecol. , vol.48 , pp. 313-321
    • Griebler, C.1    Adrian, L.2    Meckenstock, R.3    Richnow, H.4
  • 12
    • 0036795084 scopus 로고    scopus 로고
    • Carbon and hydrogen stable isotope fractionation during aerobic bacterial degradation of aromatic hydrocarbons
    • Morasch, B.; Richnow, H.-H.; Schink, B.; Vieth, A.; Meckenstock, R. U. Carbon and hydrogen stable isotope fractionation during aerobic bacterial degradation of aromatic hydrocarbons Appl. Environ. Microbiol. 2002, 68, 5191-5194
    • (2002) Appl. Environ. Microbiol. , vol.68 , pp. 5191-5194
    • Morasch, B.1    Richnow, H.-H.2    Schink, B.3    Vieth, A.4    Meckenstock, R.U.5
  • 16
    • 46849110982 scopus 로고    scopus 로고
    • Identifying competing aerobic nitrobenzene biodegradation pathways using compound-specific isotope analysis
    • Hofstetter, T. B.; Spain, J. C.; Nishino, S. F.; Bolotin, J.; Schwarzenbach, R. P. Identifying competing aerobic nitrobenzene biodegradation pathways using compound-specific isotope analysis Environ. Sci. Technol. 2008, 42, 4764-4770
    • (2008) Environ. Sci. Technol. , vol.42 , pp. 4764-4770
    • Hofstetter, T.B.1    Spain, J.C.2    Nishino, S.F.3    Bolotin, J.4    Schwarzenbach, R.P.5
  • 17
    • 65549153949 scopus 로고    scopus 로고
    • Pathway and evolutionary implications of diphenylamine biodegradation by Burkholderia sp. Strain JS667
    • Shin, K. A.; Spain, J. C. Pathway and evolutionary implications of diphenylamine biodegradation by Burkholderia sp. Strain JS667 Appl. Environ. Microbiol. 2009, 75, 2694-2704
    • (2009) Appl. Environ. Microbiol. , vol.75 , pp. 2694-2704
    • Shin, K.A.1    Spain, J.C.2
  • 18
    • 0642371528 scopus 로고    scopus 로고
    • Diphenylamine and derivatives in the environment: A review
    • Drzyzga, O. Diphenylamine and derivatives in the environment: A review Chemosphere 2003, 53, 809-818
    • (2003) Chemosphere , vol.53 , pp. 809-818
    • Drzyzga, O.1
  • 22
    • 0028841595 scopus 로고
    • Biodegradation of Nitroaromatic Compounds
    • Spain, J. C. Biodegradation of Nitroaromatic Compounds Annu. Rev. Microbiol. 1995, 49, 523-555
    • (1995) Annu. Rev. Microbiol. , vol.49 , pp. 523-555
    • Spain, J.C.1
  • 23
    • 79952176463 scopus 로고    scopus 로고
    • PH-Dependent equilibrium isotope fractionation associated with compound-specific nitrogen and carbon isotope analysis by SPME-GC/IRMS
    • Skarpeli-Liati, M.; Arnold, W. A.; Turgeon, A.; Cramer, C. J.; Hofstetter, T. B. pH-Dependent equilibrium isotope fractionation associated with compound-specific nitrogen and carbon isotope analysis by SPME-GC/IRMS Anal. Chem. 2011, 83, 1641-1648
    • (2011) Anal. Chem. , vol.83 , pp. 1641-1648
    • Skarpeli-Liati, M.1    Arnold, W.A.2    Turgeon, A.3    Cramer, C.J.4    Hofstetter, T.B.5
  • 25
    • 84863503953 scopus 로고    scopus 로고
    • Carbon, hydrogen, and nitrogen isotope analysis associated with oxidative transformation of substituted N -alkylated aromatic amines
    • Skarpeli-Liati, M.; Pati, S. G.; Bolotin, J.; Eustis, S. N.; Hofstetter, T. B. Carbon, hydrogen, and nitrogen isotope analysis associated with oxidative transformation of substituted N -alkylated aromatic amines Environ. Sci. Technol. 2012, 46, 7189-7198
    • (2012) Environ. Sci. Technol. , vol.46 , pp. 7189-7198
    • Skarpeli-Liati, M.1    Pati, S.G.2    Bolotin, J.3    Eustis, S.N.4    Hofstetter, T.B.5
  • 26
    • 0021200186 scopus 로고
    • Mechanisms and pathways of aniline elimination from aquatic environments
    • Lyons, C. D.; Katz, S.; Bartha, R. Mechanisms and pathways of aniline elimination from aquatic environments Appl. Environ. Microbiol. 1984, 48, 491-496
    • (1984) Appl. Environ. Microbiol. , vol.48 , pp. 491-496
    • Lyons, C.D.1    Katz, S.2    Bartha, R.3
  • 27
    • 0141974850 scopus 로고    scopus 로고
    • Stereochemical and mechanistic aspects of dioxygenase-catalysed benzylic hydroxylation of indene and chromane substrates
    • Boyd, D. R.; Sharma, N. D.; Bowers, N. I.; Boyle, R.; Harrison, J. S.; Lee, K.; Bugg, T. D. H.; Gibson, D. T. Stereochemical and mechanistic aspects of dioxygenase-catalysed benzylic hydroxylation of indene and chromane substrates Organ. Biomol. Chem. 2003, 1, 1298-1307
    • (2003) Organ. Biomol. Chem. , vol.1 , pp. 1298-1307
    • Boyd, D.R.1    Sharma, N.D.2    Bowers, N.I.3    Boyle, R.4    Harrison, J.S.5    Lee, K.6    Bugg, T.D.H.7    Gibson, D.T.8
  • 28
    • 33645677539 scopus 로고    scopus 로고
    • Arene cis -dihydrodiol formation: From biology to application
    • Boyd, D. R.; Bugg, T. D. H. Arene cis -dihydrodiol formation: from biology to application Organ. Biomol. Chem. 2006, 4, 181-192
    • (2006) Organ. Biomol. Chem. , vol.4 , pp. 181-192
    • Boyd, D.R.1    Bugg, T.D.H.2
  • 30
    • 0031036516 scopus 로고    scopus 로고
    • Nucleotide sequences and regulational analysis of genes involved in conversion of aniline to catechol in Pseudomonas putida UCC22(pTDN1)
    • Fukumori, F.; Saint, C. P. Nucleotide sequences and regulational analysis of genes involved in conversion of aniline to catechol in Pseudomonas putida UCC22(pTDN1) J. Bacteriol. 1997, 179, 399-408
    • (1997) J. Bacteriol. , vol.179 , pp. 399-408
    • Fukumori, F.1    Saint, C.P.2
  • 32
    • 0024423797 scopus 로고
    • Monohydroxylation of phenol and 2,5-dichlorophenol by toluene dioxygenase in Pseudomonas putida F1
    • Spain, J. C.; Zylstra, G. J.; Blake, C. K.; Gibson, D. T. Monohydroxylation of phenol and 2,5-dichlorophenol by toluene dioxygenase in Pseudomonas putida F1 Appl. Environ. Microbiol. 1989, 55, 2648-2652
    • (1989) Appl. Environ. Microbiol. , vol.55 , pp. 2648-2652
    • Spain, J.C.1    Zylstra, G.J.2    Blake, C.K.3    Gibson, D.T.4
  • 33
    • 0029920974 scopus 로고    scopus 로고
    • The broad substrate chlorobenzene dioxygenase and cis -chlorobenzene dihydrodiol dehydrogenase of Pseudomonas sp. Strain P51 are linked evolutionarily to the enzymes for benzene and toluene degradation
    • Werlen, C.; Kohler, H.-P. E.; van der Meer, J. R. The broad substrate chlorobenzene dioxygenase and cis -chlorobenzene dihydrodiol dehydrogenase of Pseudomonas sp. Strain P51 are linked evolutionarily to the enzymes for benzene and toluene degradation J. Biol. Chem. 1996, 271, 4009-4016
    • (1996) J. Biol. Chem. , vol.271 , pp. 4009-4016
    • Werlen, C.1    Kohler, H.-P.E.2    Van Der Meer, J.R.3
  • 34
    • 0016430790 scopus 로고
    • Purification and some properties of a soluble benzene-oxidizing system from a strain of Pseudomonas
    • Axcell, B. C.; Geary, P. J. Purification and some properties of a soluble benzene-oxidizing system from a strain of Pseudomonas Biochem. J. 1975, 146, 173-183
    • (1975) Biochem. J. , vol.146 , pp. 173-183
    • Axcell, B.C.1    Geary, P.J.2
  • 35
    • 0021880489 scopus 로고
    • Microbial mineralization of ring-substituted anilines through an ortho -cleavage pathway
    • Zeyer, J.; Wasserfallen, A.; Timmis, K. N. Microbial mineralization of ring-substituted anilines through an ortho -cleavage pathway Appl. Environ. Microbiol. 1985, 50, 447-453
    • (1985) Appl. Environ. Microbiol. , vol.50 , pp. 447-453
    • Zeyer, J.1    Wasserfallen, A.2    Timmis, K.N.3
  • 37
    • 0029070669 scopus 로고
    • Oxidative pathway for the biodegradation of nitrobenzene by Comamonas sp. Strain JS765
    • Nishino, S. N.; Spain, J. C. Oxidative pathway for the biodegradation of nitrobenzene by Comamonas sp. Strain JS765 Appl. Environ. Microbiol. 1995, 61, 2308-2313
    • (1995) Appl. Environ. Microbiol. , vol.61 , pp. 2308-2313
    • Nishino, S.N.1    Spain, J.C.2
  • 38
    • 0028022845 scopus 로고
    • Biodegradation of 2-nitrotoluene by Pseudomonas sp. strain JS42
    • Haigler, B. E.; Wallace, W. H.; Spain, J. C. Biodegradation of 2-nitrotoluene by Pseudomonas sp. strain JS42 Appl. Environ. Microbiol. 1994, 60, 3466-3469
    • (1994) Appl. Environ. Microbiol. , vol.60 , pp. 3466-3469
    • Haigler, B.E.1    Wallace, W.H.2    Spain, J.C.3
  • 40
    • 0043022281 scopus 로고    scopus 로고
    • Dioxygenase enzymes: Catalytic mechanisms and chemical models
    • Bugg, T. D. H. Dioxygenase enzymes: catalytic mechanisms and chemical models Tetrahedron 2003, 59, 7075-7101
    • (2003) Tetrahedron , vol.59 , pp. 7075-7101
    • Bugg, T.D.H.1
  • 41
    • 43049091488 scopus 로고    scopus 로고
    • Non-heme iron-dependent dioxygenases: Unravelling catalytic mechanisms for complex enzymatic oxidations
    • Bugg, T. D. H.; Ramaswamy, S. Non-heme iron-dependent dioxygenases: unravelling catalytic mechanisms for complex enzymatic oxidations Curr. Opin. Chem. Biol. 2008, 12, 134-140
    • (2008) Curr. Opin. Chem. Biol. , vol.12 , pp. 134-140
    • Bugg, T.D.H.1    Ramaswamy, S.2
  • 42
    • 34447326187 scopus 로고    scopus 로고
    • Hydrogen peroxide dependent cis -dihydroxylation of benzoate by fully oxidized benzoate 1,2-dioxygenase
    • Neibergall, M. B.; Stubna, A.; Mekmouche, Y.; Munck, E.; Lipscomb, J. D. Hydrogen peroxide dependent cis -dihydroxylation of benzoate by fully oxidized benzoate 1,2-dioxygenase Biochemistry 2007, 46, 8004-8016
    • (2007) Biochemistry , vol.46 , pp. 8004-8016
    • Neibergall, M.B.1    Stubna, A.2    Mekmouche, Y.3    Munck, E.4    Lipscomb, J.D.5
  • 43
    • 27544477399 scopus 로고    scopus 로고
    • Rieske business: Structure-function of Rieske non-heme oxygenases
    • Ferraro, D. J.; Gakhar, L.; Ramaswamy, S. Rieske business: Structure-function of Rieske non-heme oxygenases Biochem. Biophys. Res. Commun. 2005, 338, 175-190
    • (2005) Biochem. Biophys. Res. Commun. , vol.338 , pp. 175-190
    • Ferraro, D.J.1    Gakhar, L.2    Ramaswamy, S.3
  • 46
    • 0023119482 scopus 로고
    • Nitrosubstituted aromatic compounds as nitrogen source for bacteria
    • Bruhn, C.; Lenke, H.; Knackmuss, H. J. Nitrosubstituted aromatic compounds as nitrogen source for bacteria Appl. Environ. Microbiol. 1987, 53, 208-210
    • (1987) Appl. Environ. Microbiol. , vol.53 , pp. 208-210
    • Bruhn, C.1    Lenke, H.2    Knackmuss, H.J.3
  • 47
    • 49549153874 scopus 로고
    • Surface chemistry of hydrous manganese dioxide
    • Murray, J. W. Surface chemistry of hydrous manganese dioxide J. Colloid Interface Sci. 1974, 46, 357-371
    • (1974) J. Colloid Interface Sci. , vol.46 , pp. 357-371
    • Murray, J.W.1
  • 48
    • 33947415420 scopus 로고    scopus 로고
    • Compound-specific nitrogen and carbon isotope analysis of nitroaromatic compounds in aqueous samples using solid-phase microextraction coupled to GC/IRMS
    • Berg, M.; Bolotin, J.; Hofstetter, T. B. Compound-specific nitrogen and carbon isotope analysis of nitroaromatic compounds in aqueous samples using solid-phase microextraction coupled to GC/IRMS Anal. Chem. 2007, 79, 2386-2393
    • (2007) Anal. Chem. , vol.79 , pp. 2386-2393
    • Berg, M.1    Bolotin, J.2    Hofstetter, T.B.3
  • 49
    • 0742287849 scopus 로고    scopus 로고
    • Optimal methods for estimating kinetic isotope effects from different forms of the Rayleigh distillation equation
    • Scott, K. M.; Lu, X.; Cavanaugh, C. M.; Liu, J. S. Optimal methods for estimating kinetic isotope effects from different forms of the Rayleigh distillation equation Geochim. Cosmochim. Acta 2004, 68, 433-442
    • (2004) Geochim. Cosmochim. Acta , vol.68 , pp. 433-442
    • Scott, K.M.1    Lu, X.2    Cavanaugh, C.M.3    Liu, J.S.4
  • 50
    • 55349090994 scopus 로고    scopus 로고
    • Carbon and hydrogen isotope gractionation during anaerobic toluene oxidation by Geobacter metallireducens with different Fe(III) phases as terminal electron acceptors
    • Tobler, N. B.; Hofstetter, T. B.; Schwarzenbach, R. P. Carbon and hydrogen isotope gractionation during anaerobic toluene oxidation by Geobacter metallireducens with different Fe(III) phases as terminal electron acceptors Environ. Sci. Technol. 2008, 42, 7786-7792
    • (2008) Environ. Sci. Technol. , vol.42 , pp. 7786-7792
    • Tobler, N.B.1    Hofstetter, T.B.2    Schwarzenbach, R.P.3
  • 51
    • 0027961034 scopus 로고
    • Aquasim - A tool for simulation and data-analysis of aquatic systems
    • Reichert, P. Aquasim-A tool for simulation and data-analysis of aquatic systems Wat. Sci. Technol. 1994, 30, 21-30
    • (1994) Wat. Sci. Technol. , vol.30 , pp. 21-30
    • Reichert, P.1
  • 53
    • 84868584761 scopus 로고    scopus 로고
    • Gaussian 09 Revision C.1
    • Frisch, M. J. Gaussian 09 Revision C.1. 2009,.
    • (2009)
    • Frisch, M.J.1
  • 54
    • 3142771297 scopus 로고    scopus 로고
    • A new hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP)
    • Yanai, T.; Tew, D. P.; Handy, N. C. A new hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP) Chem. Phys. Lett. 2004, 393, 51-57
    • (2004) Chem. Phys. Lett. , vol.393 , pp. 51-57
    • Yanai, T.1    Tew, D.P.2    Handy, N.C.3
  • 55
    • 84961980477 scopus 로고    scopus 로고
    • Quantum mechanical continuum solvation models
    • Tomasi, J.; Mennucci, B.; Cammi, R. Quantum mechanical continuum solvation models Chem. Rev. 2005, 105, 2999-3094
    • (2005) Chem. Rev. , vol.105 , pp. 2999-3094
    • Tomasi, J.1    Mennucci, B.2    Cammi, R.3
  • 56
    • 0006012501 scopus 로고    scopus 로고
    • A complete basis set model chemistry. VII. Use of the minimum population localization method
    • Montgomery, J. A.; Frisch, M. J.; Ochterski, J. W.; Petersson, G. A. A complete basis set model chemistry. VII. Use of the minimum population localization method J. Chem. Phys. 2000, 112, 6532-6542
    • (2000) J. Chem. Phys. , vol.112 , pp. 6532-6542
    • Montgomery, J.A.1    Frisch, M.J.2    Ochterski, J.W.3    Petersson, G.A.4
  • 59
    • 27144478990 scopus 로고    scopus 로고
    • Chromosome-encoded gene cluster for the metabolic pathway that converts aniline to TCA-cycle intermediates in Delftia tsuruhatensis AD9
    • Liang, Q.; Takeo, M.; Chen, M.; Zhang, W.; Xu, Y.; Lin, M. Chromosome-encoded gene cluster for the metabolic pathway that converts aniline to TCA-cycle intermediates in Delftia tsuruhatensis AD9 Microbiology 2005, 151, 3435-3446
    • (2005) Microbiology , vol.151 , pp. 3435-3446
    • Liang, Q.1    Takeo, M.2    Chen, M.3    Zhang, W.4    Xu, Y.5    Lin, M.6
  • 60
    • 0031025515 scopus 로고    scopus 로고
    • Plasmid-encoded genes specifying aniline oxidation from Acinetobacter sp. Strain YAA
    • Fujii, T.; Takeo, M.; Maeda, Y. Plasmid-encoded genes specifying aniline oxidation from Acinetobacter sp. Strain YAA Microbiology 1997, 143, 93-99
    • (1997) Microbiology , vol.143 , pp. 93-99
    • Fujii, T.1    Takeo, M.2    Maeda, Y.3
  • 61
    • 0031930202 scopus 로고    scopus 로고
    • Sequence analysis of the genes encoding a multicomponent dioxygenase involved in oxidation of aniline and o-toluidine in Acinetobacter sp. strain YAA
    • Takeo, M.; Fujii, T.; Maeda, Y. Sequence analysis of the genes encoding a multicomponent dioxygenase involved in oxidation of aniline and o-toluidine in Acinetobacter sp. strain YAA J. Ferment. Bioeng. 1998, 85, 17-24
    • (1998) J. Ferment. Bioeng. , vol.85 , pp. 17-24
    • Takeo, M.1    Fujii, T.2    Maeda, Y.3
  • 62
    • 13544277014 scopus 로고    scopus 로고
    • Genes involved in aniline degradation by Delftia acidovorans Strain 7N and its distribution in the natural environment
    • Urata, M.; Uchida, E.; Nojiri, H.; Omori, T.; Obo, R.; Miyaura, N.; Ouchiyama, N. Genes involved in aniline degradation by Delftia acidovorans Strain 7N and its distribution in the natural environment Biosci. Biotechnol. Biochem. 2004, 68, 2457-2465
    • (2004) Biosci. Biotechnol. Biochem. , vol.68 , pp. 2457-2465
    • Urata, M.1    Uchida, E.2    Nojiri, H.3    Omori, T.4    Obo, R.5    Miyaura, N.6    Ouchiyama, N.7
  • 63
    • 0030690099 scopus 로고    scopus 로고
    • Experimental and theoretical kinetic isotope effects for asymmetric dihydroxylation. Evidence supporting a rate-limiting "(3 + 2)" cycloaddition
    • DelMonte, A. J.; Haller, J.; Houk, K. N.; Sharpless, K. B.; Singleton, D. A.; Strassner, T.; Thomas, A. A. Experimental and theoretical kinetic isotope effects for asymmetric dihydroxylation. Evidence supporting a rate-limiting "(3 + 2)" cycloaddition J. Am. Chem. Soc. 1997, 119, 9907-9908
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 9907-9908
    • Delmonte, A.J.1    Haller, J.2    Houk, K.N.3    Sharpless, K.B.4    Singleton, D.A.5    Strassner, T.6    Thomas, A.A.7
  • 64
    • 72049099611 scopus 로고    scopus 로고
    • Oxidation of amines by flavoproteins
    • Fitzpatrick, P. F. Oxidation of amines by flavoproteins Arch. Biochem. Biophys. 2010, 493, 13-25
    • (2010) Arch. Biochem. Biophys. , vol.493 , pp. 13-25
    • Fitzpatrick, P.F.1
  • 65
    • 0037039154 scopus 로고    scopus 로고
    • 15N kinetic isotope effects on uncatalyzed and enzymatic deamination of cytine mark
    • 15N kinetic isotope effects on uncatalyzed and enzymatic deamination of cytine mark Biochemistry 2002, 41, 415-421
    • (2002) Biochemistry , vol.41 , pp. 415-421
    • Snider, M.1    Reinhardt, L.2    Wolfenden, R.3    Cleland, W.4
  • 67
    • 84863848211 scopus 로고    scopus 로고
    • Cytochrome P450-catalyzed degradation of nicotine: Fundamental parameters determining hydroxylation by cytochrome P450 2A6 at the 5'-carbon or the N-methyl carbon
    • Kwiecien, R. A.; Le Questel, J.-Y.; Lebreton, J.; Delaforge, M.; Andre, F.; Pihan, E.; Roussel, A.; Fournial, A.; Paneth, P.; Robins, R. J. Cytochrome P450-catalyzed degradation of nicotine: Fundamental parameters determining hydroxylation by cytochrome P450 2A6 at the 5'-carbon or the N-methyl carbon J. Phys. Chem. B 2012, 116, 7827-7840
    • (2012) J. Phys. Chem. B , vol.116 , pp. 7827-7840
    • Kwiecien, R.A.1    Le Questel, J.-Y.2    Lebreton, J.3    Delaforge, M.4    Andre, F.5    Pihan, E.6    Roussel, A.7    Fournial, A.8    Paneth, P.9    Robins, R.J.10
  • 69
    • 20744450094 scopus 로고    scopus 로고
    • Oxidative transformation of fluoroquinolone antibacterial agents and structurally related amines by manganese oxide
    • Zhang, H. C.; Huang, C. H. Oxidative transformation of fluoroquinolone antibacterial agents and structurally related amines by manganese oxide Environ. Sci. Technol. 2005, 39, 4474-4483
    • (2005) Environ. Sci. Technol. , vol.39 , pp. 4474-4483
    • Zhang, H.C.1    Huang, C.H.2
  • 70
    • 1642469600 scopus 로고    scopus 로고
    • Natural Resonance Theory: I. General Formalism
    • Glendening, E. D.; Weinhold, F. Natural Resonance Theory: I. General Formalism J. Comput. Chem. 1998, 19, 593-609
    • (1998) J. Comput. Chem. , vol.19 , pp. 593-609
    • Glendening, E.D.1    Weinhold, F.2
  • 72
    • 0027142591 scopus 로고
    • Biodegradation of nitrobenzene by a sequential anaerobic-aerobic process
    • Dickel, O.; Haug, W.; Knackmuss, H.-J. Biodegradation of nitrobenzene by a sequential anaerobic-aerobic process Biodegradation 1993, 4, 187-194
    • (1993) Biodegradation , vol.4 , pp. 187-194
    • Dickel, O.1    Haug, W.2    Knackmuss, H.-J.3
  • 73
    • 0031943634 scopus 로고    scopus 로고
    • Biodegradation of nitrobenzene by its simultaneous reduction into aniline and mineralization of the aniline formed
    • Peres, C. M.; Naveau, H.; Agathos, S. N. Biodegradation of nitrobenzene by its simultaneous reduction into aniline and mineralization of the aniline formed Appl. Microbiol. Biotechnol. 1998, 49, 343-349
    • (1998) Appl. Microbiol. Biotechnol. , vol.49 , pp. 343-349
    • Peres, C.M.1    Naveau, H.2    Agathos, S.N.3
  • 74
    • 0025405519 scopus 로고
    • Oxidation of aniline and other primary aromatic amines by manganese dioxide
    • Laha, S.; Luthy, R. G. Oxidation of aniline and other primary aromatic amines by manganese dioxide Environ. Sci. Technol. 1990, 24, 363-373
    • (1990) Environ. Sci. Technol. , vol.24 , pp. 363-373
    • Laha, S.1    Luthy, R.G.2
  • 75
    • 0030776963 scopus 로고    scopus 로고
    • Microbial degradation of diphenylamine under anoxic conditions
    • Drzyzga, O.; Blotevogel, K.-H. Microbial degradation of diphenylamine under anoxic conditions Curr. Microbiol. 1997, 35, 343-347
    • (1997) Curr. Microbiol. , vol.35 , pp. 343-347
    • Drzyzga, O.1    Blotevogel, K.-H.2
  • 77
    • 0035874604 scopus 로고    scopus 로고
    • Sediment-associated reactions of aromatic amines. 1. Elucidation of sorption mechanisms
    • Weber, E.; Colon, D.; Baughman, G. Sediment-associated reactions of aromatic amines. 1. Elucidation of sorption mechanisms Environ. Sci. Technol. 2001, 35, 2470-2475
    • (2001) Environ. Sci. Technol. , vol.35 , pp. 2470-2475
    • Weber, E.1    Colon, D.2    Baughman, G.3
  • 78
    • 0029659995 scopus 로고    scopus 로고
    • Covalent binding of aniline to humic substances: 1. Kinetic studies
    • Weber, E. J.; Spidle, D. L.; Thorn, K. A. Covalent binding of aniline to humic substances: 1. Kinetic studies Environ. Sci. Technol. 1996, 30, 2755-2763
    • (1996) Environ. Sci. Technol. , vol.30 , pp. 2755-2763
    • Weber, E.J.1    Spidle, D.L.2    Thorn, K.A.3
  • 80
    • 34250186409 scopus 로고    scopus 로고
    • Extending the Rayleigh equation to allow competing isotope fractionating pathways to improve quantification of biodegradation
    • Van Breukelen, B. M. Extending the Rayleigh equation to allow competing isotope fractionating pathways to improve quantification of biodegradation Environ. Sci. Technol. 2007, 41, 4004-4010
    • (2007) Environ. Sci. Technol. , vol.41 , pp. 4004-4010
    • Van Breukelen, B.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.