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Volumn 181, Issue 1, 1999, Pages 73-82

Preferential oxidative dehalogenation upon conversion of 2-halophenols by Rhodococcus opacus 1G

Author keywords

2 Halophenol; 19F NMR; Oxidative dehalogenation; Phenol hydroxylase; Rhodococcus opacus

Indexed keywords

CHLOROPHENOL; HALOPHENOL; OXYGENASE;

EID: 0032746041     PISSN: 03781097     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1097(99)00516-9     Document Type: Article
Times cited : (25)

References (30)
  • 1
    • 0026760856 scopus 로고
    • Microbial breakdown of halogenated aromatic pesticides and related compounds
    • Häggblom M.M. Microbial breakdown of halogenated aromatic pesticides and related compounds. FEMS Microbiol. Rev. 103:1992;29-72.
    • (1992) FEMS Microbiol. Rev. , vol.103 , pp. 29-72
    • Häggblom, M.M.1
  • 3
    • 0032795933 scopus 로고    scopus 로고
    • Bacteria designed for bioremediation
    • Timmis K.N., Pieper D.H. Bacteria designed for bioremediation. Trends Biotechnol. 17:1999;201-204.
    • (1999) Trends Biotechnol. , vol.17 , pp. 201-204
    • Timmis, K.N.1    Pieper, D.H.2
  • 4
    • 0031028986 scopus 로고    scopus 로고
    • Evolution of novel metabolic pathways for the degradation of chloroaromatic compounds
    • van der Meer J.R. Evolution of novel metabolic pathways for the degradation of chloroaromatic compounds. Antonie van Leeuwenhoek. 71:1997;159-178.
    • (1997) Antonie Van Leeuwenhoek , vol.71 , pp. 159-178
    • Van Der Meer, J.R.1
  • 5
    • 0031756487 scopus 로고    scopus 로고
    • Development of hybrid strains for the mineralisation of chloroaromatics by patchwork assembly
    • Reineke W. Development of hybrid strains for the mineralisation of chloroaromatics by patchwork assembly. Annu. Rev. Microbiol. 52:1998;287-331.
    • (1998) Annu. Rev. Microbiol. , vol.52 , pp. 287-331
    • Reineke, W.1
  • 6
    • 0024426788 scopus 로고
    • Transformation of chlorinated phenolic compounds in the genus Rhodococcus
    • Häggblom M.M., Janke D., Salkinoja-Salonen M.S. Transformation of chlorinated phenolic compounds in the genus Rhodococcus. Microb. Ecol. 18:1989;147-159.
    • (1989) Microb. Ecol. , vol.18 , pp. 147-159
    • Häggblom, M.M.1    Janke, D.2    Salkinoja-Salonen, M.S.3
  • 8
    • 0028813521 scopus 로고
    • Metabolism of polychlorinated phenols by Pseudomonas cepacia AC1100: Determination of the first two steps and specific inhibitory effect of methimazole
    • Tomasi I., Artraud I., Bertheau Y., Mansuy D. Metabolism of polychlorinated phenols by Pseudomonas cepacia AC1100: determination of the first two steps and specific inhibitory effect of methimazole. J. Bacteriol. 177:1995;307-311.
    • (1995) J. Bacteriol. , vol.177 , pp. 307-311
    • Tomasi, I.1    Artraud, I.2    Bertheau, Y.3    Mansuy, D.4
  • 11
    • 0025733737 scopus 로고
    • Purification and properties of pentachlorophenol hydroxylase, a flavoprotein from Flavobacterium sp. strain ATCC 39723
    • Xun L., Orser C.S. Purification and properties of pentachlorophenol hydroxylase, a flavoprotein from Flavobacterium sp. strain ATCC 39723. J. Bacteriol. 173:1991;4447-4453.
    • (1991) J. Bacteriol. , vol.173 , pp. 4447-4453
    • Xun, L.1    Orser, C.S.2
  • 12
    • 0029924178 scopus 로고    scopus 로고
    • Purification and characterization of chlorophenol 4-monooxygenase from Burkholderia cepacia AC1100
    • Xun L. Purification and characterization of chlorophenol 4-monooxygenase from Burkholderia cepacia AC1100. J. Bacteriol. 178:1996;2645-2649.
    • (1996) J. Bacteriol. , vol.178 , pp. 2645-2649
    • Xun, L.1
  • 13
    • 0018094202 scopus 로고
    • Utilization and cooxidation of chlorinated phenols by Pseudomonas sp. B13
    • Knackmuss H.-J., Hellwig M. Utilization and cooxidation of chlorinated phenols by Pseudomonas sp. B13. Arch. Microbiol. 117:1978;1-7.
    • (1978) Arch. Microbiol. , vol.117 , pp. 1-7
    • Knackmuss, H.-J.1    Hellwig, M.2
  • 14
    • 0019162442 scopus 로고
    • Chemical structure and biodegradability of halogenated aromatic compounds
    • Schmidt E., Knackmuss H.-J. Chemical structure and biodegradability of halogenated aromatic compounds. Biochem. J. 192:1980;339-347.
    • (1980) Biochem. J. , vol.192 , pp. 339-347
    • Schmidt, E.1    Knackmuss, H.-J.2
  • 15
    • 0024025210 scopus 로고
    • Oxidation of substituted phenols by Pseudomonas putida F1 and Pseudomonas sp. JS6
    • Spain J.C., Gibson D.T. Oxidation of substituted phenols by Pseudomonas putida F1 and Pseudomonas sp. JS6. Appl. Environ. Microbiol. 54:1988;1399-1404.
    • (1988) Appl. Environ. Microbiol. , vol.54 , pp. 1399-1404
    • Spain, J.C.1    Gibson, D.T.2
  • 16
    • 0019994544 scopus 로고
    • The purification and properties of 2,4-dichlorophenol hydroxylase from a strain of Acinetobacter species
    • Beadle C.A., Smith A.R.W. The purification and properties of 2,4-dichlorophenol hydroxylase from a strain of Acinetobacter species. Eur. J. Biochem. 123:1982;323-332.
    • (1982) Eur. J. Biochem. , vol.123 , pp. 323-332
    • Beadle, C.A.1    Smith, A.R.W.2
  • 17
    • 0021756283 scopus 로고
    • Purification and properties of a plasmid-encoded 2,4-dichlorophenol hydroxylase
    • Liu T., Chapman P.J. Purification and properties of a plasmid-encoded 2,4-dichlorophenol hydroxylase. FEBS Lett. 173:1984;314-318.
    • (1984) FEBS Lett. , vol.173 , pp. 314-318
    • Liu, T.1    Chapman, P.J.2
  • 18
    • 0015790898 scopus 로고
    • Phenol hydroxylase from yeast: Purification and properties of the enzyme from Trichosporon cutaneum
    • Neuhjahr H.Y., Gaal A. Phenol hydroxylase from yeast: Purification and properties of the enzyme from Trichosporon cutaneum. Eur. J. Biochem. 35:1973;386-400.
    • (1973) Eur. J. Biochem. , vol.35 , pp. 386-400
    • Neuhjahr, H.Y.1    Gaal, A.2
  • 19
    • 0028838117 scopus 로고
    • Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum
    • Peelen S., Rietjens I.M.C.M., Boersma M.G., Vervoort J. Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. Eur. J. Biochem. 227:1995;284-291.
    • (1995) Eur. J. Biochem. , vol.227 , pp. 284-291
    • Peelen, S.1    Rietjens, I.M.C.M.2    Boersma, M.G.3    Vervoort, J.4
  • 23
    • 84985258206 scopus 로고
    • Critical steps in degradation of chloroaromatics by Rhodococci. I. Initial enzyme reactions involved in catabolism of aniline, phenol and benzoate by Rhodococcus sp. An 117 and An 213
    • Janke D., Al-Mofarji T., Straube G., Schumann P., Prauser H. Critical steps in degradation of chloroaromatics by Rhodococci. I. Initial enzyme reactions involved in catabolism of aniline, phenol and benzoate by Rhodococcus sp. An 117 and An 213. J. Basic Microbiol. 28:1988;509-518.
    • (1988) J. Basic Microbiol. , vol.28 , pp. 509-518
    • Janke, D.1    Al-Mofarji, T.2    Straube, G.3    Schumann, P.4    Prauser, H.5
  • 24
    • 0023511694 scopus 로고
    • Phenol hydroxylases from Rhodococcus sp. P1
    • Straube G. Phenol hydroxylases from Rhodococcus sp. P1. J. Basic Microbiol. 27:1987;229-232.
    • (1987) J. Basic Microbiol. , vol.27 , pp. 229-232
    • Straube, G.1
  • 25
    • 0019321174 scopus 로고
    • Purification and characterization of an oxygenase component in benzoate 1,2-dioxygenase system from Pseudomonas arvilla C-1
    • Yamaguchi M., Fujisawa H. Purification and characterization of an oxygenase component in benzoate 1,2-dioxygenase system from Pseudomonas arvilla C-1. J. Biol. Chem. 255:1980;5058-5063.
    • (1980) J. Biol. Chem. , vol.255 , pp. 5058-5063
    • Yamaguchi, M.1    Fujisawa, H.2
  • 26
    • 0031017330 scopus 로고    scopus 로고
    • Solution structure of phenol hydroxylase protein component P2 determined by NMR spectroscopy
    • Qian H., Edlund U., Powlowski J., Shingler V., Sethson I. Solution structure of phenol hydroxylase protein component P2 determined by NMR spectroscopy. Biochemistry. 36:1997;495-504.
    • (1997) Biochemistry , vol.36 , pp. 495-504
    • Qian, H.1    Edlund, U.2    Powlowski, J.3    Shingler, V.4    Sethson, I.5
  • 27
    • 0027330246 scopus 로고
    • 19F NMR study on the pH-dependent regioselectivity and rate of the ortho-hydroxylation of 3-fluorophenol by phenol hydroxylase from Trichosporon cutaneum. Implications for the reaction mechanism
    • 19F NMR study on the pH-dependent regioselectivity and rate of the ortho-hydroxylation of 3-fluorophenol by phenol hydroxylase from Trichosporon cutaneum. Implications for the reaction mechanism. Eur. J. Biochem. 218:1993;345-353.
    • (1993) Eur. J. Biochem. , vol.218 , pp. 345-353
    • Peelen, S.1    Rietjens, I.M.C.M.2    Van Berkel, W.J.H.3    Van Workum, W.A.T.4    Vervoort, J.5
  • 28
    • 0029049573 scopus 로고
    • The effect of varying halogen substituent patterns on the cytochrome P450 catalysed dehalogenation of 4-halogenated anilines to 4-aminophenol metabolites
    • Cnubben N.H.P., Vervoort J., Boersma M.G., Rietjens I.M.C.M. The effect of varying halogen substituent patterns on the cytochrome P450 catalysed dehalogenation of 4-halogenated anilines to 4-aminophenol metabolites. Biochem. Pharmacol. 49:1995;1235-1248.
    • (1995) Biochem. Pharmacol. , vol.49 , pp. 1235-1248
    • Cnubben, N.H.P.1    Vervoort, J.2    Boersma, M.G.3    Rietjens, I.M.C.M.4
  • 29
    • 0028863957 scopus 로고
    • Novel oxidative pathway of para-substituted phenols in cytochrome P450 chemical model: Substituent elimination accompanying ipso-substitution by the oxygen atom of the active species
    • Ohe T., Mashino T., Hirobe M. Novel oxidative pathway of para-substituted phenols in cytochrome P450 chemical model: substituent elimination accompanying ipso-substitution by the oxygen atom of the active species. Tetrahedron Lett. 36:1995;7681-7684.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 7681-7684
    • Ohe, T.1    Mashino, T.2    Hirobe, M.3
  • 30
    • 0030913335 scopus 로고    scopus 로고
    • Evidence for the direct formation of 1,4-dibenzoquinone from 4-fluorophenol by a peroxidase-type of reaction pathway
    • Osman A.M., Boeren S., Veeger C., Rietjens I.M.C.M. Evidence for the direct formation of 1,4-dibenzoquinone from 4-fluorophenol by a peroxidase-type of reaction pathway. Chem. Biol. Interact. 104:1997;147-164.
    • (1997) Chem. Biol. Interact. , vol.104 , pp. 147-164
    • Osman, A.M.1    Boeren, S.2    Veeger, C.3    Rietjens, I.M.C.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.