About: Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics

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About: Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 1995

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 1995 (uk) artículu científicu espublizáu en xineru de 1995 (ast) artikull shkencor i botuar më 01 janar 1995 (sq) scientific article published on 01 January 1995 (en)
publication date	wds:Q72534045-7C163E33-C201-419E-B333-B233A2E08E94
publication date	1995-01-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q72534045-283393C3-D082-4C13-8398-152DE8834F87 wds:Q72534045-3AC28E2D-0DF8-4731-B346-622E403D066E wds:Q72534045-A8518A3D-627D-4F69-B661-7FB64EA57684
author name string	J Vervoort M G Boersma S Peelen
rdfs:label	Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics (en) Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics (nl) Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics (sq)
skos:prefLabel	Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics (en) Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics (nl) Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics (sq)
name	Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics (en) Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics (nl) Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics (sq)
author	wds:Q72534045-C9DFF824-B12A-4FD1-B2D9-8E0F18F21B4E
author	Ivonne Rietjens
title	wds:Q72534045-22F2E4DE-00E7-458B-B205-8BD9309BDE64
title	Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics (en)
page(s)	wds:Q72534045-794FAAA1-E861-4EE4-9517-B43C920969A8
page(s)	284-291
instance of	wds:Q72534045-720508E2-D579-4B28-8655-B0509A8F3984
instance of	scholarly article
main subject	wds:Q72534045-6DD72E46-1DA9-43D6-A55D-93F6B53B0A93
main subject	Trichosporon cutaneum
PubMed ID	wds:Q72534045-A914D3A9-9B95-4967-87E6-5C9CDCCE799B
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7851397
PubMed ID	7851397
published in	wds:Q72534045-6BB21489-3844-4E3B-BB6F-BED6FAC390FF
published in	FEBS Journal
issue	wds:Q72534045-9900DB31-F536-49E6-B0DA-C52E34F27C05
volume	wds:Q72534045-FC29E70F-D095-4598-8BD5-2C2C59BDE22B
issue	1-2
volume	227
DOI	wds:Q72534045-7355CF40-B510-4428-8FFA-06DFACE580AE
DOI	http://dx.doi.org/10.1111/J.1432-1033.1995.TB20386.X
DOI	10.1111/J.1432-1033.1995.TB20386.X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q72534045
is cites work of	NIH shift in flavin-dependent monooxygenation: mechanistic studies with 2-aminobenzoyl-CoA monooxygenase/reductase 19F nuclear magnetic resonance as a tool to investigate microbial degradation of fluorophenols to fluorocatechols and fluoromuconates. Identification of fluoropyrogallols as new intermediates in biotransformation of monofluorophenols in Rhodococcus opacus 1cp. Conversion of 2-fluoromuconate to cis-dienelactone by purified enzymes of Rhodococcus opacus 1cp Fungal metabolism of toluene: monitoring of fluorinated analogs by (19)F nuclear magnetic resonance spectroscopy. Pentachlorophenol hydroxylase, a poorly functioning enzyme required for degradation of pentachlorophenol by Sphingobium chlorophenolicum. Form follows function: structural and catalytic variation in the class a flavoprotein monooxygenases Purification and properties of 4-hydroxybenzoate 1-hydroxylase (decarboxylating), a novel flavin adenine dinucleotide-dependent monooxygenase from Candida parapsilosis CBS604 Elucidation of the 4-hydroxyacetophenone catabolic pathway in Pseudomonas fluorescens ACB. Oxidative dehalogenation and denitration by a flavin-dependent monooxygenase is controlled by substrate deprotonation Microbial degradation of halogenated aromatics: molecular mechanisms and enzymatic reactions Dissipation, dehalogenation, and denitration of chloroaromatic compounds by Nocardioides sp. strain PD653: Characterization of the substrate specificity Targeted fluorination of a nonsteroidal anti-inflammatory drug to prolong metabolic half-life
is cites work of	wds:Q41341210-4640A212-68C6-44F7-A97A-F6DC7B4720F0 wds:Q90360030-C4DE3E34-863B-46F4-B8E7-D9C02B685F2D wds:Q90150137-4E873DC9-7D5D-4C52-B9DA-A5BD69F889E7 wds:Q87185992-A1E6449C-5417-4749-A02E-59359183A4E1 wds:Q36538270-8B1B38CE-E853-4C69-9710-85644936D013 wds:Q57470016-FE9A3CCE-9148-447D-BDAC-F7418B35BC11 wds:Q39489908-C11E039C-43D1-4DA5-8DAE-C49D2EA2256F wds:Q39890979-A952E464-DE2D-4293-A77B-6DB5BE6B461F wds:Q36407014-158DB659-16B1-44FD-B4E4-D0171CF92526 wds:Q39560203-64911EE8-E1EE-43BC-B3DC-BB2FA1B31501 wds:Q41835860-BD8580BB-B259-42B9-A0F5-386ECE2DA074 wds:Q28379203-E6A8CB3C-3CB0-49BA-B78D-7ACFECA5D5EA wds:Q39536404-C8B291BA-CF1D-4D8B-9372-19F8392EF50E

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