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Volumn 46, Issue 1, 2011, Pages 358-364

Biotransformation of ethyl 2-(2′-nitrophenoxy)acetate to benzohydroxamic acid (D-DIBOA) by Escherichia coli

Author keywords

Benzohydroxamic acid; Biotransformation; Escherichia coli; Natural product; Serratia marcescens

Indexed keywords

AEROBIC AND ANAEROBIC CONDITIONS; AEROBIC CONDITION; ANAEROBIC CONDITIONS; BENZOHYDROXAMIC ACID; BIOLOGICAL PROPERTIES; BIOTRANSFORMATION; BIOTRANSFORMATION REACTIONS; CHEMICAL SYNTHESIS; E. COLI; HPLC-DAD; NATURAL PRODUCTS; SERRATIA MARCESCENS; SPECTROSCOPIC DATA; UV/VIS SPECTRA;

EID: 78650240102     PISSN: 13595113     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.procbio.2010.09.011     Document Type: Article
Times cited : (8)

References (26)
  • 1
    • 0002826991 scopus 로고
    • Naturally occurring chemical compounds as herbicides
    • S.O. Duke Naturally occurring chemical compounds as herbicides Rev Weed Sci 2 1986 15 44
    • (1986) Rev Weed Sci , vol.2 , pp. 15-44
    • Duke, S.O.1
  • 2
    • 13244289474 scopus 로고
    • The structures of the precursors of benzoxazolinone in rye plants II
    • A.I. Virtanen, and P.K. Hietala The structures of the precursors of benzoxazolinone in rye plants II Suom Kemistil B 32 1959 252
    • (1959) Suom Kemistil B , vol.32 , pp. 252
    • Virtanen, A.I.1    Hietala, P.K.2
  • 3
    • 0345613299 scopus 로고
    • Isolation and characterization of a cyclic hydroxamate from Zea mays
    • R.H. Hamilton, R.S. Bandurski, and W.H. Reusch Isolation and characterization of a cyclic hydroxamate from Zea mays Cereal Chem 39 1962 107 113
    • (1962) Cereal Chem , vol.39 , pp. 107-113
    • Hamilton, R.H.1    Bandurski, R.S.2    Reusch, W.H.3
  • 8
    • 2642673649 scopus 로고
    • 4-Benzoxazine hydroxamic acids and related compounds
    • R.T. Coutts, and K.W. Hindmarsh 4-Benzoxazine hydroxamic acids and related compounds Can J Pharm Sci 1 1966 11 17
    • (1966) Can J Pharm Sci , vol.1 , pp. 11-17
    • Coutts, R.T.1    Hindmarsh, K.W.2
  • 9
    • 0027235682 scopus 로고
    • A new general approach to the 2-hydroxy-2H-1,4-benzoxazin-3(4H)-one skeleton via diisobutylaluminum hydride reduction of 2,3-dioxo-1,4-benzoxazines
    • D. Sicker, and H. Hartenstein A new general approach to the 2-hydroxy-2H-1,4-benzoxazin-3(4H)-one skeleton via diisobutylaluminum hydride reduction of 2,3-dioxo-1,4-benzoxazines Synthesis 8 1993 771 772
    • (1993) Synthesis , vol.8 , pp. 771-772
    • Sicker, D.1    Hartenstein, H.2
  • 12
    • 18244376061 scopus 로고    scopus 로고
    • Reductive transformation of TNT by Escherichia coli: Pathway description
    • H. Yin, T.K. Wood, and B.F. Smets Reductive transformation of TNT by Escherichia coli: pathway description Appl Microbiol Biotechnol 67 2005 397 404
    • (2005) Appl Microbiol Biotechnol , vol.67 , pp. 397-404
    • Yin, H.1    Wood, T.K.2    Smets, B.F.3
  • 13
    • 0030483997 scopus 로고    scopus 로고
    • Characterization of partial anaerobic metabolic pathway for 2,4,6-trinitrotoluene degradation by a sulfate-reducing bacterial consortium
    • R. Boopathy, and J.F. Manning Characterization of partial anaerobic metabolic pathway for 2,4,6-trinitrotoluene degradation by a sulfate-reducing bacterial consortium Can J Microbiol 42 1996 1203 1208
    • (1996) Can J Microbiol , vol.42 , pp. 1203-1208
    • Boopathy, R.1    Manning, J.F.2
  • 14
    • 0030778376 scopus 로고    scopus 로고
    • 2,4,6-Trinitrotoluene (TNT) transformation by clostridia isolated from a munition-fed bioreactor: Comparison with non-adapted bacteria
    • M.M. Ederer, T.A. Lewis, and R.L. Crawford 2,4,6-Trinitrotoluene (TNT) transformation by clostridia isolated from a munition-fed bioreactor: comparison with non-adapted bacteria J Ind Microbiol Biotechnol 18 1997 82 88
    • (1997) J Ind Microbiol Biotechnol , vol.18 , pp. 82-88
    • Ederer, M.M.1    Lewis, T.A.2    Crawford, R.L.3
  • 15
    • 2642607036 scopus 로고    scopus 로고
    • Reduction of 2,4,6-trinitrotoluene by Clostridium acetobutylicum through hydroxylamino intermediates
    • J.B. Hughes, C.W. Wang, R. Bhadra, A. Richardson, G.N. Bennett, and F. Rudolph Reduction of 2,4,6-trinitrotoluene by Clostridium acetobutylicum through hydroxylamino intermediates Environ Toxicol Chem 17 1998 343 348
    • (1998) Environ Toxicol Chem , vol.17 , pp. 343-348
    • Hughes, J.B.1    Wang, C.W.2    Bhadra, R.3    Richardson, A.4    Bennett, G.N.5    Rudolph, F.6
  • 16
    • 0030902355 scopus 로고    scopus 로고
    • Transformation of 2,4,6-Trinitrotoluene by Pseudomonas pseudoalcaligenes JS52
    • P.D. Fiorella, and J.C. Spain Transformation of 2,4,6-Trinitrotoluene by Pseudomonas pseudoalcaligenes JS52 Appl Environ Microbiol 63 5 1997 2007 2015
    • (1997) Appl Environ Microbiol , vol.63 , Issue.5 , pp. 2007-2015
    • Fiorella, P.D.1    Spain, J.C.2
  • 18
    • 34248590170 scopus 로고    scopus 로고
    • Escherichia coli has multiple enzymes that attack TNT and release nitrogen for growth
    • M.M. González-Pérez, P. Van Dillewijn, R.M. Wittich, and J.L. Ramos Escherichia coli has multiple enzymes that attack TNT and release nitrogen for growth Environ Microbiol 9 2007 1535 1540
    • (2007) Environ Microbiol , vol.9 , pp. 1535-1540
    • González-Pérez, M.M.1    Van Dillewijn, P.2    Wittich, R.M.3    Ramos, J.L.4
  • 19
    • 21844431599 scopus 로고    scopus 로고
    • Biodegradation of 2,4,6-trinitrotoluene (TNT): An enzymatic perspective
    • S.N. Gibson, M. Schroeder, W. Steiner, and M. Gübitz Biodegradation of 2,4,6-trinitrotoluene (TNT): An enzymatic perspective Biocatal Biotransform 23 2005 53 69
    • (2005) Biocatal Biotransform , vol.23 , pp. 53-69
    • Gibson, S.N.1    Schroeder, M.2    Steiner, W.3    Gübitz, M.4
  • 21
    • 2942563803 scopus 로고    scopus 로고
    • Biotransformation of explosives by the old yellow enzyme family of flavoproteins
    • R.E. Williams, D.A. Rathbone, N.S. Scrutton, and N.C. Bruce Biotransformation of explosives by the old yellow enzyme family of flavoproteins Appl Environ Microbiol 70 2004 3566 3574
    • (2004) Appl Environ Microbiol , vol.70 , pp. 3566-3574
    • Williams, R.E.1    Rathbone, D.A.2    Scrutton, N.S.3    Bruce, N.C.4
  • 24
    • 0025973098 scopus 로고
    • Analogues of the cyclic hydroxamic acid 2,4-dihydroxy-7-methoxy-2H-1,4- benzoxazin-3-one (DIMBOA): Decomposition to benzoxazolinones and reaction with β-mercaptoethanol
    • J. Atkinson, P. Morand, J.T. Arnason, H.M. Niemeyer, and H.R. Bravo Analogues of the cyclic hydroxamic acid 2,4-dihydroxy-7-methoxy-2H-1,4- benzoxazin-3-one (DIMBOA): decomposition to benzoxazolinones and reaction with β-mercaptoethanol J Org Chem 56 1991 1788 1800
    • (1991) J Org Chem , vol.56 , pp. 1788-1800
    • Atkinson, J.1    Morand, P.2    Arnason, J.T.3    Niemeyer, H.M.4    Bravo, H.R.5
  • 25
    • 0031771290 scopus 로고    scopus 로고
    • Oxygen-insensitive nitroreductases: Analysis of theroles of nfsA and nsfB in development of resistance to 5-nitrofuran derivatives in Escherichia coli
    • J.P. Whiteway, J. Koziarz, N. Veall, P. Sandhu, B. Kumar, and Hoecher Oxygen-insensitive nitroreductases: analysis of theroles of nfsA and nsfB in development of resistance to 5-nitrofuran derivatives in Escherichia coli J Bacteriol 180 1998 5529 5539
    • (1998) J Bacteriol , vol.180 , pp. 5529-5539
    • Whiteway, J.P.1    Koziarz, J.2    Veall, N.3    Sandhu, P.4    Kumar, B.5    Hoecher6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.