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Items: 1 to 20 of 100

1.

Multistep conversion of para-substituted phenols by phenol hydroxylase and 2,3-dihydroxybiphenyl 1,2-dioxygenase.

Qu Y, Shi S, Ma Q, Kong C, Zhou H, Zhang X, Zhou J.

Appl Biochem Biotechnol. 2013 Apr;169(7):2064-75. doi: 10.1007/s12010-013-0112-7. Epub 2013 Jan 31.

PMID:
23371781
2.

Unspecific degradation of halogenated phenols by the soil fungus Penicillium frequentans Bi 7/2.

Hofrichter M, Bublitz F, Fritsche W.

J Basic Microbiol. 1994;34(3):163-72.

PMID:
8071803
3.

Characterization of a novel thermostable Mn(II)-dependent 2,3-dihydroxybiphenyl 1,2-dioxygenase from a polychlorinated biphenyl- and naphthalene-degrading Bacillus sp. JF8.

Hatta T, Mukerjee-Dhar G, Damborsky J, Kiyohara H, Kimbara K.

J Biol Chem. 2003 Jun 13;278(24):21483-92. Epub 2003 Apr 2.

4.

Isolation, characterization and docking studies of 2,3-dihydroxybiphenyl 1,2-dioxygenase from an activated sludge metagenome.

Gou M, Qu Y, Xu B, Zhou J, Li X, Zhou H.

Biotechnol Lett. 2012 Jan;34(1):117-23. doi: 10.1007/s10529-011-0738-x. Epub 2011 Sep 6.

PMID:
21898128
5.

Biotransformation of 4-halophenols to 4-halocatechols using Escherichia coli expressing 4-hydroxyphenylacetate 3-hydroxylase.

Coulombel L, Nolan LC, Nikodinovic J, Doyle EM, O'Connor KE.

Appl Microbiol Biotechnol. 2011 Mar;89(6):1867-75. doi: 10.1007/s00253-010-2969-5. Epub 2010 Nov 6.

PMID:
21057945
6.

Biotransformation of benzene and toluene to catechols by phenol hydroxylase from Arthrobacter sp. W1.

Ma F, Shi SN, Sun TH, Li A, Zhou JT, Qu YY.

Appl Microbiol Biotechnol. 2013 Jun;97(11):5097-103. doi: 10.1007/s00253-012-4301-z. Epub 2012 Aug 2.

PMID:
22854893
7.

Degradation of phenol and phenolic compounds by Pseudomonas putida EKII.

Hinteregger C, Leitner R, Loidl M, Ferschl A, Streichsbier F.

Appl Microbiol Biotechnol. 1992 May;37(2):252-9.

PMID:
1368244
8.

Optimization of 2,3-dihydroxybiphenyl 1,2-dioxygenase expression and its application for biosensor.

Zhang Q, Qu Y, Zhou J, Zhang X, Zhou H, Ma Q, Li X.

Bioresour Technol. 2011 Nov;102(22):10553-60. doi: 10.1016/j.biortech.2011.08.071. Epub 2011 Aug 24.

PMID:
21924604
9.

Quantitative structure/activity relationship for the rate of conversion of C4-substituted catechols by catechol-1,2-dioxygenase from Pseudomonas putida (arvilla) C1.

Ridder L, Briganti F, Boersma MG, Boeren S, Vis EH, Scozzafava A, Veeger C, Rietjens IM.

Eur J Biochem. 1998 Oct 1;257(1):92-100.

10.

Hydroxylation of o-halogenophenol and o-nitrophenol by salicylate hydroxylase.

Suzuki K, Gomi T, Kaidoh T, Itagaki E.

J Biochem. 1991 Feb;109(2):348-53.

11.

Phenol degradation by Acinetobacter calcoaceticus NCIB 8250.

Paller G, Hommel RK, Kleber HP.

J Basic Microbiol. 1995;35(5):325-35.

PMID:
8568644
12.

Single-turnover kinetics of 2,3-dihydroxybiphenyl 1,2-dioxygenase reacting with 3-formylcatechol.

Ishida T, Senda T, Tanaka H, Yamamoto A, Horiike K.

Biochem Biophys Res Commun. 2005 Dec 9;338(1):223-9. Epub 2005 Sep 7.

PMID:
16169514
13.

Oxidation of substituted phenols by Pseudomonas putida F1 and Pseudomonas sp. strain JS6.

Spain JC, Gibson DT.

Appl Environ Microbiol. 1988 Jun;54(6):1399-404.

14.

Extradiol dioxygenase-SiO₂ sol-gel modified electrode for catechol and its derivatives detection.

Zhang Q, Qu Y, Zhang X, Zhou J, Wang H.

Biosens Bioelectron. 2011 Jul 15;26(11):4362-7. doi: 10.1016/j.bios.2011.04.042. Epub 2011 Apr 29.

PMID:
21592766
15.

The mechanism-based inactivation of 2,3-dihydroxybiphenyl 1,2-dioxygenase by catecholic substrates.

Vaillancourt FH, Labbe G, Drouin NM, Fortin PD, Eltis LD.

J Biol Chem. 2002 Jan 18;277(3):2019-27. Epub 2001 Nov 13.

16.

Enzyme-substrate interaction and characterization of a 2,3-dihydroxybiphenyl 1,2-dioxygenase from Dyella ginsengisoli LA-4.

Li A, Qu Y, Zhou J, Ma F.

FEMS Microbiol Lett. 2009 Mar;292(2):231-9. doi: 10.1111/j.1574-6968.2009.01487.x. Epub 2009 Jan 28.

17.

Biotransformation of chloro-substituted indoles to indigoids by phenol hydroxylase from Arthrobacter sp. W1.

Shi S, Ma F, Sun T, Li A, Zhou J, Qu Y.

Appl Biochem Biotechnol. 2013 Jun;170(4):951-61. doi: 10.1007/s12010-013-0234-y. Epub 2013 Apr 30.

PMID:
23625634
18.

Dioxygenase- and monooxygenase-catalysed synthesis of cis-dihydrodiols, catechols, epoxides and other oxygenated products.

Nolan LC, O'Connor KE.

Biotechnol Lett. 2008 Nov;30(11):1879-91. doi: 10.1007/s10529-008-9791-5. Epub 2008 Jul 9. Review.

PMID:
18612597
19.

Kinetic and isotopic studies of the oxidative half-reaction of phenol hydroxylase.

Taylor MG, Massey V.

J Biol Chem. 1991 May 5;266(13):8291-301.

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