Serveur d'exploration sur le phanerochaete - Exploration (Accueil)

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List of bibliographic references indexed by Free Radicals

Number of relevant bibliographic references: 29.
[0-20] [0 - 20][0 - 29][20-28][20-40]
Ident.Authors (with country if any)Title
000114 (2018) Carl J. Houtman [États-Unis] ; Eranda Maligaspe [États-Unis] ; Christopher G. Hunt [États-Unis] ; Elena Fernández-Fueyo ; Angel T. Martínez ; Kenneth E. Hammel [États-Unis]Fungal lignin peroxidase does not produce the veratryl alcohol cation radical as a diffusible ligninolytic oxidant.
000155 (2017) Chang-Young Hong [Corée du Sud] ; Sun-Hwa Ryu [Corée du Sud] ; Hanseob Jeong [Corée du Sud] ; Sung-Suk Lee [Corée du Sud] ; Myungkil Kim [Corée du Sud] ; In-Gyu Choi [Corée du Sud]Phanerochaete chrysosporium Multienzyme Catabolic System for in Vivo Modification of Synthetic Lignin to Succinic Acid.
000933 (2003) Thomas B. Brück [Royaume-Uni] ; Maria Francesca Gerini ; Enrico Baciocchi ; Patricia J. HarveyOxidation of thioanisole and p-methoxythioanisole by lignin peroxidase: kinetic evidence of a direct reaction between compound II and a radical cation.
000A81 (2000) B. Van Aken [Belgique] ; M D Cameron ; J D Stahl ; A. Plumat ; H. Naveau ; S D Aust ; S N AgathosGlutathione-mediated mineralization of 14C-labeled 2-amino-4,6-dinitrotoluene by manganese-dependent peroxidase H5 from the white-rot fungus Phanerochaete chrysosporium.
000B10 (1999) T. Choinowski [Suisse] ; W. Blodig ; K H Winterhalter ; K. PiontekThe crystal structure of lignin peroxidase at 1.70 A resolution reveals a hydroxy group on the cbeta of tryptophan 171: a novel radical site formed during the redox cycle.
000B16 (1999) D. Sheng [États-Unis] ; M H GoldOxidative polymerization of ribonuclease A by lignin peroxidase from Phanerochaete chrysosporium. Role of veratryl alcohol in polymer oxidation.
000B39 (1999) M D Cameron [États-Unis] ; S D AustDegradation of chemicals by reactive radicals produced by cellobiose dehydrogenase from Phanerochaete chrysosporium.
000B69 (1998) D. Sheng [États-Unis] ; D K Joshi ; M H GoldNitration of veratryl alcohol by lignin peroxidase and tetranitromethane.
000C16 (1997) A. Khindaria [États-Unis] ; G. Nie ; S D AustDetection and characterization of the lignin peroxidase compound II-veratryl alcohol cation radical complex.
000C37 (1996) R S Koduri [États-Unis] ; R E Whitwam ; D. Barr ; S D Aust ; M. TienOxidation of 1,2,4,5-tetramethoxybenzene by lignin peroxidase of Phanerochaete chrysosporium.
000C48 (1996) M M Whittaker [États-Unis] ; P J Kersten ; N. Nakamura ; J. Sanders-Loehr ; E S Schweizer ; J W WhittakerGlyoxal oxidase from Phanerochaete chrysosporium is a new radical-copper oxidase.
000C55 (1996) A. Khindaria [États-Unis] ; S D AustEPR detection and characterization of lignin peroxidase porphyrin pi-cation radical.
000C73 (1995) A. Khindaria [États-Unis] ; I. Yamazaki ; S D AustVeratryl alcohol oxidation by lignin peroxidase.
000C85 (1995) J D Stahl [États-Unis] ; S J Rasmussen ; S D AustReduction of quinones and radicals by a plasma membrane redox system of Phanerochaete chrysosporium.
000C86 (1995) B. Kalyanaraman [États-Unis]Radical intermediates during degradation of lignin-model compounds and environmental pollutants: an electron spin resonance study.
000D86 (1993) M M Shah ; T A Grover ; S D AustReduction of CCl4 to the trichloromethyl radical by lignin peroxidase H2 from Phanerochaete chrysosporium.
000E15 (1993) M M Shah ; S D AustIodide as the mediator for the reductive reactions of peroxidases.
000E50 (1992) D P Barr ; M M Shah ; T A Grover ; S D AustProduction of hydroxyl radical by lignin peroxidase from Phanerochaete chrysosporium.
000E52 (1992) S M Kremer [Royaume-Uni] ; P M WoodProduction of Fenton's reagent by cellobiose oxidase from cellulolytic cultures of Phanerochaete chrysosporium.
000E89 (1992) S M Kremer [Royaume-Uni] ; P M WoodCellobiose oxidase from Phanerochaete chrysosporium as a source of Fenton's reagent.
000F50 (1990) J L Popp [États-Unis] ; B. Kalyanaraman ; T K KirkLignin peroxidase oxidation of Mn2+ in the presence of veratryl alcohol, malonic or oxalic acid, and oxygen.

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