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Extracellular oxidative systems of the lignin-degrading Basidiomycete Phanerochaete chrysosporium

https://doi.org/10.1016/j.fgb.2006.07.007
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inferredcites →https://doi.org/10.1002/pmic.200401251openalex-snapshot
Metabolic regulation at the tricarboxylic acid and glyoxylate cycles of the lignin‐degrading basidiomycete Phanerochaete chrysosporium against exogenous addition of vanillin
inferredcites →https://doi.org/10.1006/abbi.1993.1007openalex-snapshot
Isozymes of Lignin Peroxidase and Manganese(II) Peroxidase from the White-Rot Basidiomycete Trametes versicolor
inferredcites →https://doi.org/10.1006/abbi.1998.0952openalex-snapshot
Kinetics of Mn3+–Oxalate Formation and Decay in Reactions Catalyzed by Manganese Peroxidase ofCeriporiopsis subvermispora
inferredcites →https://doi.org/10.1006/abbi.1999.1474openalex-snapshot
Extracellular Mannose-6-phosphatase of Phanerochaete chrysosporium: A Lignin Peroxidase-Modifying Enzyme
inferredcites →https://doi.org/10.1006/bbrc.1994.1421openalex-snapshot
Transcription of Liginase H8 by Phanerochaete chrysosporum Under Nutrient Nitrogen Sufficient Conditions
inferredcites →https://doi.org/10.1007/978-1-4757-4597-9openalex-snapshot
Biocatalysts for Industry
inferredcites →https://doi.org/10.1007/978-1-4757-4597-9_6openalex-snapshot
Lignin-Degrading Enzymes from the Filamentous Fungus Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1007/978-3-642-46687-8openalex-snapshot
Microbial and Enzymatic Degradation of Wood and Wood Components
inferredcites →https://doi.org/10.1007/978-3-642-57756-7_103openalex-snapshot
Aryl-alcohol oxidase
inferredcites →https://doi.org/10.1007/978-3-662-03059-2_5openalex-snapshot
Molecular Genetics of Lignin-Degrading Fungi and Their Applications in Organopollutant Degradation
inferredcites →https://doi.org/10.1007/978-3-662-06064-3_13openalex-snapshot
Enzymology and Molecular Biology of Lignin Degradation
inferredcites →https://doi.org/10.1007/bf00225306openalex-snapshot
Lignin biochemistry: Biosynthesis and biodegradation
inferredcites →https://doi.org/10.1007/bf00225309openalex-snapshot
Biotechnology in the pulp and paper industry
inferredcites →https://doi.org/10.1007/bf00261925openalex-snapshot
Formation and partial characterization of glucose-2-oxidase, a H2O2 producing enzyme in Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1007/bf00393377openalex-snapshot
Extracellular proteases produced by the wood-degrading fungus Phanerochaete chrysosporium under ligninolytic and non-ligninolytic conditions
inferredcites →https://doi.org/10.1007/bfb0102070openalex-snapshot
Biotechnology in the Pulp and Paper Industry
inferredcites →https://doi.org/10.1007/s00294-003-0410-7openalex-snapshot
Differential regulation of genes encoding manganese peroxidase (MnP) in the basidiomycete Ceriporiopsis subvermispora
inferredcites →https://doi.org/10.1007/s00294-004-0550-4openalex-snapshot
Fungal degradation of wood: initial proteomic analysis of extracellular proteins of Phanerochaete chrysosporium grown on oak substrate
inferredcites →https://doi.org/10.1007/s00438-004-1085-6openalex-snapshot
A H2O2-producing glyoxal oxidase is required for filamentous growth and pathogenicity in Ustilago maydis
inferredcites →https://doi.org/10.1007/s00438-005-0051-2openalex-snapshot
Microarray-based global differential expression profiling of P450 monooxygenases and regulatory proteins for signal transduction pathways in the white rot fungus Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/0003-9861(84)90280-7openalex-snapshot
Purification and characterization of an extracellular H2O2-requiring diarylpropane oxygenase from the white rot basidiomycete, Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/0003-9861(85)90217-6openalex-snapshot
Purification and characterization of an extracellular Mn(II)-dependent peroxidase from the lignin-degrading basidiomycete, Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/0003-9861(85)90387-xopenalex-snapshot
Multiple molecular forms of diarylpropane oxygenase, an H2O2-requiring, lignin-degrading enzyme from Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/0003-9861(86)90378-4openalex-snapshot
Mn(II) oxidation is the principal function of the extracellular Mn-peroxidase from Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/0006-291x(82)91723-5openalex-snapshot
Generation of hydroxyl radical and its involvement in lignin degradation by Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/0006-291x(91)90919-xopenalex-snapshot
In vitro depolymerization of lignin by manganese peroxidase of Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/0014-5793(85)81037-1openalex-snapshot
Aromatic ring cleavage of veratryl alcohol by Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/0014-5793(93)80162-nopenalex-snapshot
Release of the FAD domain from cellobiose oxidase by proteases from cellulolytic cultures of Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/0014-5793(93)81146-qopenalex-snapshot
Low pH crystal structure of glycosylated lignin peroxidase from Phanerochaete chrysosporium at 2.5 Å resolution
inferredcites →https://doi.org/10.1016/0014-5793(95)00758-2openalex-snapshot
Cloning and characterization of a cDNA encoding a cellobiose dehydrogenase from the white rot fungus Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/0141-0229(91)90182-aopenalex-snapshot
Depolymerization of a synthetic lignin in vitro by lignin peroxidase
inferredcites →https://doi.org/10.1016/0141-0229(95)00003-nopenalex-snapshot
Physiological regulation of glyoxal oxidase from Phanerochaete chrysosporium by peroxidase systems
inferredcites →https://doi.org/10.1016/0144-8617(92)90058-xopenalex-snapshot
Biocatalysts for industry
inferredcites →https://doi.org/10.1016/0168-1656(90)90096-topenalex-snapshot
Degradation of lignin by Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/0168-1656(93)90144-copenalex-snapshot
Influence of primary and secondary proteases produced by free or immobilized cells of the white-rot fungus Phanerochaete chrysosporium on lignin peroxidase activity
inferredcites →https://doi.org/10.1016/0168-6445(94)90088-4openalex-snapshot
Pathways for production of Fenton's reagent by wood-rotting fungi
inferredcites →https://doi.org/10.1016/0304-4165(83)90348-3openalex-snapshot
Chemical mechanism of an important cleavage reaction in the fungal degradation of lignin
inferredcites →https://doi.org/10.1016/0378-1119(94)90251-8openalex-snapshot
Characterization of a cDNA encoding a manganese peroxidase from Phanerochaete chrysosporium: genomic organization of lignin and manganese peroxidase-encoding genes
inferredcites →https://doi.org/10.1016/b978-0-12-088642-5.50022-3openalex-snapshot
Genetics and Molecular Biology of the Lignin-Degrading Basidiomycete Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/c2009-0-02655-5openalex-snapshot
More Gene Manipulations in Fungi
inferredcites →https://doi.org/10.1016/j.bpc.2005.03.006openalex-snapshot
The nop gene from Phanerochaete chrysosporium encodes a peroxidase with novel structural features
inferredcites →https://doi.org/10.1016/j.enzmictec.2006.01.004openalex-snapshot
Effect of inducers and culturing processes on laccase synthesis in Phanerochaete chrysosporium NCIM 1197 and the constitutive expression of laccase isozymes
inferredcites →https://doi.org/10.1016/j.fgb.2006.01.003openalex-snapshot
Computational analysis of the Phanerochaete chrysosporium v2.0 genome database and mass spectrometry identification of peptides in ligninolytic cultures reveal complex mixtures of secreted proteins
inferredcites →https://doi.org/10.1016/j.jbiotec.2005.03.010openalex-snapshot
The Phanerochaete chrysosporium secretome: Database predictions and initial mass spectrometry peptide identifications in cellulose-grown medium
inferredcites →https://doi.org/10.1016/s0005-2728(03)00023-9openalex-snapshot
The heme domain of cellobiose oxidoreductase: a one-electron reducing system
inferredcites →https://doi.org/10.1016/s0006-291x(88)80541-2openalex-snapshot
Structure and regulation of a lignin peroxidase gene from Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/s0014-5793(00)01435-6openalex-snapshot
The essential role of Glu‐185 and Tyr‐354 residues in the ferroxidase activity of Saccharomyces cerevisiae Fet3
inferredcites →https://doi.org/10.1016/s0014-5793(01)03131-3openalex-snapshot
Mutational analysis of the iron binding site of Saccharomyces cerevisiae ferroxidase Fet3. An in vivo study
inferredcites →https://doi.org/10.1016/s0014-5793(03)01218-3openalex-snapshot
Cuprous oxidase activity of yeast Fet3p and human ceruloplasmin: implication for function
inferredcites →https://doi.org/10.1016/s0014-5793(97)00301-3openalex-snapshot
Laccase is essential for lignin degradation by the white‐rot fungus Pycnoporus cinnabarinus
inferredcites →https://doi.org/10.1016/s0021-9258(17)39479-6openalex-snapshot
Mechanism of oxidative C alpha-C beta cleavage of a lignin model dimer by Phanerochaete chrysosporium ligninase. Stoichiometry and involvement of free radicals.
inferredcites →https://doi.org/10.1016/s0021-9258(18)33781-5openalex-snapshot
The involvement of hydroxyl radical derived from hydrogen peroxide in lignin degradation by the white rot fungus Phanerochaete chrysosporium.
inferredcites →https://doi.org/10.1016/s0021-9258(18)48344-5openalex-snapshot
Purification and characterization of a novel protease from solid substrate cultures of Phanerochaete chrysosporium.
inferredcites →https://doi.org/10.1016/s0021-9258(18)80029-1openalex-snapshot
Manganese-dependent Peroxidase from Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/s0021-9258(18)83695-xopenalex-snapshot
Characterization of a cDNA Encoding a Manganese Peroxidase, from the Lignin-degrading Basidiomycete Phanerochaete Chrysosporium
inferredcites →https://doi.org/10.1016/s0021-9258(19)47070-1openalex-snapshot
Phosphorylation of lignin peroxidases from Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/s0021-9258(20)80694-2openalex-snapshot
Kinetic analysis of manganese peroxidase. The reaction with manganese complexes.
inferredcites →https://doi.org/10.1016/s0031-9422(00)80434-3openalex-snapshot
An extracellular haem-protein from Coriolus versicolor
inferredcites →https://doi.org/10.1016/s0065-3233(02)60050-6openalex-snapshot
Galactose oxidase
inferredcites →https://doi.org/10.1016/s0141-0229(00)00307-0openalex-snapshot
Cellobiose dehydrogenase–an extracellular fungal flavocytochrome
inferredcites →https://doi.org/10.1016/s0141-0229(01)00521-xopenalex-snapshot
Molecular biology and structure-function of lignin-degrading heme peroxidases
inferredcites →https://doi.org/10.1016/s0167-4838(00)00096-0openalex-snapshot
Is cellobiose dehydrogenase from Phanerochaete chrysosporium a lignin degrading enzyme?
inferredcites →https://doi.org/10.1016/s0167-4838(00)00127-8openalex-snapshot
Aryl-alcohol oxidase protein sequence: a comparison with glucose oxidase and other FAD oxidoreductases
inferredcites →https://doi.org/10.1016/s0167-4838(00)00301-0openalex-snapshot
Expression of Pleurotus eryngii aryl-alcohol oxidase in Aspergillus nidulans: purification and characterization of the recombinant enzyme
inferredcites →https://doi.org/10.1016/s0167-4838(96)00235-xopenalex-snapshot
Characterization of the gene encoding manganese peroxidase isozyme 3 from Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1016/s0168-1656(00)00206-6openalex-snapshot
A critical review of cellobiose dehydrogenases
inferredcites →https://doi.org/10.1016/s0168-1656(97)01683-0openalex-snapshot
History, overview and applications of mediated lignolytic systems, especially laccase-mediator-systems (Lignozym®-process)
inferredcites →https://doi.org/10.1016/s0168-1656(97)01684-2openalex-snapshot
Recent advances on the molecular genetics of ligninolytic fungi
inferredcites →https://doi.org/10.1016/s0300-9084(83)80280-6openalex-snapshot
Evidence for the involvement of activated oxygen in fungal degradation of lignocellulose
inferredcites →https://doi.org/10.1016/s0378-1097(00)00367-0openalex-snapshot
The cloning of a new peroxidase found in lignocellulose cultures of Pleurotus eryngii and sequence comparison with other fungal peroxidases
inferredcites →https://doi.org/10.1016/s0378-1119(98)00084-5openalex-snapshot
Cloning and sequencing of a gene encoding cellobiose dehydrogenase from Trametes versicolor
inferredcites →https://doi.org/10.1016/s0378-1119(99)00189-4openalex-snapshot
Cloning and analysis of Pycnoporus cinnabarinus cellobiose dehydrogenase
inferredcites →https://doi.org/10.1016/s1874-5334(05)80016-4openalex-snapshot
Phanerochaete chrysosporium Genomics
inferredcites →https://doi.org/10.1021/bi00033a037openalex-snapshot
The Manganese Binding Site of Manganese Peroxidase: Characterization of an Asp179Asn Site-Directed Mutant Protein
inferredcites →https://doi.org/10.1021/bi00195a010openalex-snapshot
Mechanism of Manganese Peroxidase Compound II Reduction. Effect of Organic Acid Chelators and pH
inferredcites →https://doi.org/10.1021/bi002104sopenalex-snapshot
The Role of Glu39 in MnII Binding and Oxidation by Manganese Peroxidase from Phanerochaete chrysoporium
inferredcites →https://doi.org/10.1021/bi00249a022openalex-snapshot
H2O2 Recycling during Oxidation of the Arylglycerol .beta.-Aryl Ether Lignin Structure by Lignin Peroxidase and Glyoxal Oxidase
inferredcites →https://doi.org/10.1021/bi00355a027openalex-snapshot
Spectral characterization of the oxidized states of lignin peroxidase, an extracellular heme enzyme from the white rot basidiomycete Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1021/bi9708794openalex-snapshot
Mutagenesis of the Mn2+-Binding Site of Manganese Peroxidase Affects Oxidation of Mn2+ by both Compound I and Compound II
inferredcites →https://doi.org/10.1021/bi9727186openalex-snapshot
Autocatalytic Formation of a Hydroxy Group at Cβ of Trp171 in Lignin Peroxidase
inferredcites →https://doi.org/10.1021/bi981633hopenalex-snapshot
Two Substrate Interaction Sites in Lignin Peroxidase Revealed by Site-Directed Mutagenesis
inferredcites →https://doi.org/10.1023/a:1018495216946openalex-snapshot
Laccase production in semi-solid cultures of Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1038/nbt1294-1372openalex-snapshot
Establishment of Genetic Linkage by Allele–specific Polymerase Chain Reaction: Application to the Lignin Peroxidase Gene Family of Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1038/nbt967openalex-snapshot
Genome sequence of the lignocellulose degrading fungus Phanerochaete chrysosporium strain RP78
inferredcites →https://doi.org/10.1042/0300-5127:0290111openalex-snapshot
Lignin peroxidase structure and function
inferredcites →https://doi.org/10.1042/0300-5127:0290116openalex-snapshot
A new versatile peroxidase from Pleurotus
inferredcites →https://doi.org/10.1042/ba20050160openalex-snapshot
Agrobacterium‐mediated delivery of marker genes to Phanerochaete chrysosporium mycelial pellets: a model transformation system for white‐rot fungi
inferredcites →https://doi.org/10.1042/bj2260455openalex-snapshot
Free hydroxyl radical is not involved in an important reaction of lignin degradation by Phanerochaete chrysosporium Burds
inferredcites →https://doi.org/10.1042/bst0290111openalex-snapshot
Lignin peroxidase structure and function
inferredcites →https://doi.org/10.1042/bst0311335openalex-snapshot
Rotting by radicals – the role of cellobiose oxidoreductase?
inferredcites →https://doi.org/10.1046/j.1365-2958.1999.01164.xopenalex-snapshot
Molecular characterization of a novel peroxidase isolated from the ligninolytic fungus Pleurotus eryngii
inferredcites →https://doi.org/10.1046/j.1432-1327.1998.2530101.xopenalex-snapshot
Cellobiose dehydrogenase enhances Phanerochaete chrysosporium cellobiohydrolase I activity by relieving product inhibition
inferredcites →https://doi.org/10.1046/j.1472-765x.2001.00932.xopenalex-snapshot
Laccase production by Phanerochaete chrysosporium - an artefact caused by Mn(III)?
inferredcites →https://doi.org/10.1073/pnas.81.8.2280openalex-snapshot
Lignin-degrading enzyme from Phanerochaete chrysosporium : Purification, characterization, and catalytic properties of a unique H 2 O 2 -requiring oxygenase
inferredcites →https://doi.org/10.1073/pnas.87.8.2936openalex-snapshot
Glyoxal oxidase of Phanerochaete chrysosporium: its characterization and activation by lignin peroxidase.
inferredcites →https://doi.org/10.1073/pnas.90.15.7411openalex-snapshot
Cloning and characterization of cDNA encoding glyoxal oxidase, a H2O2-producing enzyme from the lignin-degrading basidiomycete Phanerochaete chrysosporium.
inferredcites →https://doi.org/10.1073/pnas.90.2.750openalex-snapshot
Crystal structure of lignin peroxidase.
inferredcites →https://doi.org/10.1074/jbc.270.8.3823openalex-snapshot
Veratryl Alcohol Oxidase from Pleurotus ostreatus Participates in Lignin Biodegradation and Prevents Polymerization of Laccase-oxidized Substrates
inferredcites →https://doi.org/10.1074/jbc.271.2.681openalex-snapshot
Glyoxal Oxidase from Phanerochaete chrysosporium Is a New Radical-Copper Oxidase
inferredcites →https://doi.org/10.1074/jbc.272.22.14208openalex-snapshot
Purification and Characterization of Fet3 Protein, a Yeast Homologue of Ceruloplasmin
inferredcites →https://doi.org/10.1074/jbc.272.28.17574openalex-snapshot
Crystal Structures of Substrate Binding Site Mutants of Manganese Peroxidase
inferredcites →https://doi.org/10.1074/jbc.273.35.22415openalex-snapshot
Site-directed Mutagenesis of the Yeast Multicopper Oxidase Fet3p
inferredcites →https://doi.org/10.1074/jbc.274.51.36226openalex-snapshot
Identification of Catalytic Residues in Glyoxal Oxidase by Targeted Mutagenesis
inferredcites →https://doi.org/10.1074/jbc.m307019200openalex-snapshot
Fre1p Cu2+ Reduction and Fet3p Cu1+ Oxidation Modulate Copper Toxicity in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1080/10635150121079openalex-snapshot
Analysis of Character Correlations Among Wood Decay Mechanisms, Mating Systems, and Substrate Ranges in Homobasidiomycetes
inferredcites →https://doi.org/10.1099/00221287-143-1-259openalex-snapshot
A Mechanism for Production of Hydroxyl Radicals by the Brown-Rot Fungus Coniophora Puteana: Fe(III) Reduction by Cellobiose Dehydrogenase and Fe(II) Oxidation at a Distance from the Hyphae
inferredcites →https://doi.org/10.1099/13500872-140-1-19openalex-snapshot
The structure and function of fungal laccases
inferredcites →https://doi.org/10.1099/mic.0.27072-0openalex-snapshot
Characterization of a multicopper oxidase gene cluster in Phanerochaete chrysosporium and evidence of altered splicing of the mco transcripts
inferredcites →https://doi.org/10.1101/gr.10.4.516openalex-snapshot
Ab initio Gene Finding in Drosophila Genomic DNA
inferredcites →https://doi.org/10.1101/gr.10.4.547openalex-snapshot
Using GeneWise in the Drosophila Annotation Experiment
inferredcites →https://doi.org/10.1111/j.1432-1033.1982.tb06641.xopenalex-snapshot
Purification and Partial Characterization of Two Acidic Proteases from the White‐Rot Fungus Sporotrichum pulverulentum
inferredcites →https://doi.org/10.1111/j.1432-1033.1992.tb16760.xopenalex-snapshot
Evidence that cellobiose oxidase from Phanerochaete chrysosporium is primarily an Fe(III) reductas
inferredcites →https://doi.org/10.1111/j.1432-1033.1992.tb17251.xopenalex-snapshot
Production of Fenton's reagent by cellobiose oxidase from cellulolytic cultures of Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1111/j.1574-6968.1985.tb00831.xopenalex-snapshot
Enzymatic activities of an extracellular, manganese-dependent peroxidase fromPhanerochaete chrysosporium
inferredcites →https://doi.org/10.1111/j.1574-6968.1997.tb10309.xopenalex-snapshot
Production of multiple laccase isoforms by Phanerochaete chrysosporium grown under nutrient sufficiency
inferredcites →https://doi.org/10.1111/j.1574-6968.1999.tb13354.xopenalex-snapshot
Degradation of a non-phenolic β-O-4 substructure and of polymeric lignin model compounds by laccase ofCoriolus versicolorin the presence of 1-hydroxybenzotriazole
inferredcites →https://doi.org/10.1111/j.1574-6976.1994.tb00039.xopenalex-snapshot
Lignin-modifying enzymes from selected white-rot fungi: production and role from in lignin degradation
inferredcites →https://doi.org/10.1111/j.1742-4658.2005.04707.xopenalex-snapshot
Electron transfer chain reaction of the extracellular flavocytochrome cellobiose dehydrogenase from the basidiomycete Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/aem.00375-06openalex-snapshot
Structure, Organization, and Transcriptional Regulation of a Family of Copper Radical Oxidase Genes in the Lignin-Degrading Basidiomycete Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/aem.56.1.210-217.1990openalex-snapshot
Mn(II) Regulation of Lignin Peroxidases and Manganese-Dependent Peroxidases from Lignin-Degrading White Rot Fungi
inferredcites →https://doi.org/10.1128/aem.56.11.3429-3434.1990openalex-snapshot
Protease-mediated degradation of lignin peroxidase in liquid cultures of Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/aem.56.2.395-400.1990openalex-snapshot
Effect of Environmental Conditions on Extracellular Protease Activity in Lignolytic Cultures of Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/aem.57.5.1453-1460.1991openalex-snapshot
Identification of a specific manganese peroxidase among ligninolytic enzymes secreted by Phanerochaete chrysosporium during wood decay
inferredcites →https://doi.org/10.1128/aem.59.9.2897-2903.1993openalex-snapshot
Methods to investigate the expression of lignin peroxidase genes by the white rot fungus Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/aem.60.7.2524-2532.1994openalex-snapshot
Pyranose Oxidase, a Major Source of H 2 O 2 during Wood Degradation by Phanerochaete chrysosporium, Trametes versicolor, and Oudemansiella mucida
inferredcites →https://doi.org/10.1128/aem.60.8.2811-2817.1994openalex-snapshot
Anisaldehyde and Veratraldehyde Acting as Redox Cycling Agents for H 2 O 2 Production by Pleurotus eryngii
inferredcites →https://doi.org/10.1128/aem.60.9.3447-3449.1994openalex-snapshot
Nitrogen regulation of lignin peroxidase gene transcription
inferredcites →https://doi.org/10.1128/aem.61.12.4274-4277.1995openalex-snapshot
Demonstration of Laccase in the White Rot Basidiomycete Phanerochaete chrysosporium BKM-F1767
inferredcites →https://doi.org/10.1128/aem.62.10.3697-3703.1996openalex-snapshot
Expression of lip genes during growth in soil and oxidation of anthracene by Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/aem.62.4.1329-1335.1996openalex-snapshot
Cloning of a cDNA encoding cellobiose dehydrogenase, a hemoflavoenzyme from Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/aem.62.7.2381-2386.1996openalex-snapshot
Manganese peroxidase mRNA and enzyme activity levels during bioremediation of polycyclic aromatic hydrocarbon-contaminated soil with Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/aem.63.12.4627-4632.1997openalex-snapshot
Reactivities of various mediators and laccases with kraft pulp and lignin model compounds
inferredcites →https://doi.org/10.1128/aem.63.3.857-861.1997openalex-snapshot
Lignin Peroxidase Isozymes from Phanerochaete chrysosporium Can Be Enzymatically Dephosphorylated
inferredcites →https://doi.org/10.1128/aem.64.2.569-574.1998openalex-snapshot
Reverse Transcription-PCR Analysis of the Regulation of the Manganese Peroxidase Gene Family
inferredcites →https://doi.org/10.1128/aem.64.9.3536-3538.1998openalex-snapshot
Expression of Phanerochaete chrysosporium Genes Encoding Lignin Peroxidases, Manganese Peroxidases, and Glyoxal Oxidase in Wood
inferredcites →https://doi.org/10.1128/aem.65.4.1670-1674.1999openalex-snapshot
Homologous Expression of Recombinant Lignin Peroxidase in Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/aem.68.4.2077-2080.2002openalex-snapshot
Differential Regulation of mnp2 , a New Manganese Peroxidase-Encoding Gene from the Ligninolytic Fungus Trametes versicolor PRL 572
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A Novel Extracellular Multicopper Oxidase from Phanerochaete chrysosporium with Ferroxidase Activity
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Isolation and Purification of Pyranose 2-Oxidase fromPhanerochaete chrysosporiumand Characterization of Gene Structure and Regulation
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Characterization of Carbohydrate-Binding Cytochrome b 562 from the White-Rot Fungus Phanerochaete chrysosporium
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Novel Promoter Sequence Required for Manganese Regulation of Manganese Peroxidase Isozyme 1 Gene Expression in Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/iai.67.11.6034-6039.1999openalex-snapshot
Laccase ProtectsCryptococcus neoformansfrom Antifungal Activity of Alveolar Macrophages
inferredcites →https://doi.org/10.1128/jb.166.1.269-274.1986openalex-snapshot
Purification and characterization of glucose oxidase from ligninolytic cultures of Phanerochaete chrysosporium
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Involvement of a new enzyme, glyoxal oxidase, in extracellular H2O2 production by Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/jb.172.6.3125-3130.1990openalex-snapshot
Manganese regulates expression of manganese peroxidase by Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/jb.174.11.3532-3540.1992openalex-snapshot
Heterogeneity and regulation of manganese peroxidases from Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/jb.174.15.5036-5042.1992openalex-snapshot
Lignin peroxidase gene family of Phanerochaete chrysosporium: complex regulation by carbon and nitrogen limitation and identification of a second dimorphic chromosome
inferredcites →https://doi.org/10.1128/jb.176.3.656-664.1994openalex-snapshot
Biochemical and molecular characterization of the diphenol oxidase of Cryptococcus neoformans: identification as a laccase
inferredcites →https://doi.org/10.1128/jb.181.11.3427-3432.1999openalex-snapshot
Organization and Differential Regulation of a Cluster of Lignin Peroxidase Genes of Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/mr.57.3.605-622.1993openalex-snapshot
Molecular biology of the lignin-degrading basidiomycete Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1146/annurev.mi.41.100187.002341openalex-snapshot
Enzymatic "Combustion": The Microbial Degradation of Lignin
inferredcites →https://doi.org/10.1146/annurev.py.29.090191.002121openalex-snapshot
Delignification by Wood-Decay Fungi
inferredcites →https://doi.org/10.1515/hf.1999.004openalex-snapshot
Hydroxyl Radical Generation by an Extracellular Low-Molecular-Weight Substance and Phenol Oxidase Activity During Wood Degradation by the White-Rot Basidiomycete Phanerochaete chrysosporium
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Environmentally friendly technologies for the pulp and paper industry

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Phylogeny, divergence time and historical biogeography of Phanerochaete (Basidiomycota, Polyporales), with a description of two new species in Korea
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Enzymatic Reactors Applied for the Biotransformation of Endocrine Disrupting Chemicals
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Directed Evolution of Ligninolytic Oxidoreductases: from Functional Expression to Stabilization and Beyond
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Directing Evolution of the Fungal Ligninolytic Secretome
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Optimized protocol for the 2‐DE of extracellular proteins from higher basidiomycetes inhabiting lignocellulose
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Fungal Diversity and Enzymes Involved in Lignin Degradation
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Myco-Degradation of Lignocellulose: An Update on the Reaction Mechanism and Production of Lignocellulolytic Enzymes by Fungi
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Rapid Bioconversion of Lignocellulosic Biomass by Fungi
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Bioconversion of Biomass to Biofuel Using Fungal Consortium
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Myco-degradation of Lignocellulosic Waste Biomass and Their Applications
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Lignin Valorisation Using Lignolytic Microbes and Enzymes: Challenges and Opportunities
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Technological Advancements in Sustainable Production of Second Generation Ethanol Development: An Appraisal and Future Directions
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Fungal Biodegradation of Lignocelluloses
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Structural and Functional Features of Peroxidases with a Potential as Industrial Biocatalysts
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Recent Advances on the Genomics of Litter- and Soil-Inhabiting Agaricomycetes
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Ligninolytic Enzymes in Environmental Management
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Lignin Degrading Fungal Enzymes
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Tree Ecosystem: Microbial Dynamics and Functionality
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White Rot Fungi: Nature’s Scavenger
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Role of Enzymes in Deconstruction of Waste Biomass for Sustainable Generation of Value-Added Products
inferred← citeshttps://doi.org/10.1007/978-981-97-0676-1_11openalex-snapshot
Microbial Manganese Peroxidase: Ligninolytic Enzymes for Bioremediation
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Bioeconomy for Sustainable Bioenergy and Biofuel Generation
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inferred← citeshttps://doi.org/10.1007/s00214-016-1828-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00248-018-1167-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00253-011-3830-1openalex-snapshot
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Biodegradation of anionic polyacrylamide by manganese peroxidase: docking, virtual mutation based on affinity, QM/MM calculation and molecular dynamics simulation
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Tyrosyl Radical in the W164Y Mutant of P. eryngii Versatile Peroxidase: an EPR and DFT/PCM Study
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Binding Interactions Between Lignite Oxygen Unit Models and Fungal Laccase with Docking, Molecular Dynamics Combined with Experiments
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Extracellular proteomic analysis for degradation of PAHs in source of drinking water with fusant strains
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inferred← citeshttps://doi.org/10.1007/s11274-013-1518-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12010-008-8279-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12010-010-8973-5openalex-snapshot
Gene Expression in Secondary Metabolism and Metabolic Switching Phase of Phanerochaete chrysosporium
inferred← citeshttps://doi.org/10.1007/s12010-010-9150-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12010-011-9289-9openalex-snapshot
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The effects of N+ ion implantation mutagenesis on the laccase production of Ceriporiopsis subvermispora
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Statistical optimization of medium components to increase the manganese peroxidase productivity by Phanerochaete chrysosporium NCIM 1197
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inferred← citeshttps://doi.org/10.1016/b978-0-12-819990-9.00055-xopenalex-snapshot
Treatment of Industrial Wastewaters and Liquid Waste by Fungi
inferred← citeshttps://doi.org/10.1016/b978-0-12-820524-2.00012-2openalex-snapshot
Microbe-driven generation of reactive oxygen species for contaminant degradation
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inferred← citeshttps://doi.org/10.1016/b978-0-12-824436-4.00017-4openalex-snapshot
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Differential production of lignocellulolytic enzymes by a white rot fungus Termitomyces sp. OE147 on cellulose and lactose
inferred← citeshttps://doi.org/10.1016/j.bbrc.2010.07.094openalex-snapshot
Genome-to-function characterization of novel fungal P450 monooxygenases oxidizing polycyclic aromatic hydrocarbons (PAHs)
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Characterization of a unique proline iminopeptidase from white-rot basidiomycetes Phanerochaete chrysosporium
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Characteristics and functional bacteria in a microbial consortium for rice straw lignin-degrading
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Humification process and mechanisms investigated by Fenton-like reaction and laccase functional expression during composting
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Sensitive detection of lip genes by electrochemical DNA sensor and its application in polymerase chain reaction amplicons from Phanerochaete chrysosporium
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2008.11.001openalex-snapshot
Lignocellulosic residues: Biodegradation and bioconversion by fungi
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Systematic exploration of the interactions between anionic polyacrylamide and manganese peroxidase based on docking and molecular dynamics simulations
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Lignocellulose degradation potential and mechanism of Cellulomonas iranensis CI1 as revealed by multi-omics and single-cell RNA sequencing analysis
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Growth, metabolism of Phanerochaete chrysosporium and route of lignin degradation in response to cadmium stress in solid-state fermentation
inferred← citeshttps://doi.org/10.1016/j.copbio.2009.05.002openalex-snapshot
Enzymatic delignification of plant cell wall: from nature to mill
inferred← citeshttps://doi.org/10.1016/j.copbio.2014.02.007openalex-snapshot
Exploration of Natural Biomass Utilization Systems (NBUS) for advanced biofuel — from systems biology to synthetic design
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Directed evolution of the aryl-alcohol oxidase: Beyond the lab bench
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Why do some non-ligninolytic fungi possess laccase genes? And why is their expression weak?
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Gold nanoparticles/water-soluble carbon nanotubes/aromatic diamine polymer composite films for highly sensitive detection of cellobiose dehydrogenase gene
inferred← citeshttps://doi.org/10.1016/j.enconman.2019.111928openalex-snapshot
A sustainable approach for efficient conversion of lignin into biodiesel accompanied by biological pretreatment of corn straw
inferred← citeshttps://doi.org/10.1016/j.energy.2023.127990openalex-snapshot
Insights into the response mechanism of Fusarium sp. NF01 during lignite biodegradation using proteomic analysis
inferred← citeshttps://doi.org/10.1016/j.enzmictec.2007.11.007openalex-snapshot
Quantitative linkage mapping of lignin-degrading enzymatic activities in Pleurotus ostreatus
inferred← citeshttps://doi.org/10.1016/j.enzmictec.2008.03.002openalex-snapshot
Diastereomer selectivity in the degradation of a lignin model compound of the arylglycerol β-aryl ether type by white-rot fungi
inferred← citeshttps://doi.org/10.1016/j.enzmictec.2021.109748openalex-snapshot
Comparative characterization of glyoxal oxidase from Phanerochaete chrysosporium expressed at high levels in Pichia pastoris and Trichoderma reesei
inferred← citeshttps://doi.org/10.1016/j.fbr.2007.09.003openalex-snapshot
Degradation and transformation of humic substances by saprotrophic fungi: processes and mechanisms
inferred← citeshttps://doi.org/10.1016/j.fbr.2019.12.001openalex-snapshot
Dual Purpose of ligninolytic- basidiomycetes: mycoremediation of bioethanol distillation vinasse coupled to sustainable bio-based compounds production
inferred← citeshttps://doi.org/10.1016/j.fgb.2007.10.017openalex-snapshot
The role of the ubiquitin–proteasome system in the response of the ligninolytic fungus Trametes versicolor to nitrogen deprivation
inferred← citeshttps://doi.org/10.1016/j.fgb.2008.01.004openalex-snapshot
FOLy: An integrated database for the classification and functional annotation of fungal oxidoreductases potentially involved in the degradation of lignin and related aromatic compounds
inferred← citeshttps://doi.org/10.1016/j.fgb.2009.02.001openalex-snapshot
Reduced genomic potential for secreted plant cell-wall-degrading enzymes in the ectomycorrhizal fungus Amanita bisporigera, based on the secretome of Trichoderma reesei
inferred← citeshttps://doi.org/10.1016/j.fgb.2012.05.013openalex-snapshot
Characterization of PIR1, a GATA family transcription factor involved in iron responses in the white-rot fungus Phanerochaete chrysosporium
inferred← citeshttps://doi.org/10.1016/j.fgb.2013.04.011openalex-snapshot
Genes associated with lignin degradation in the polyphagous white-rot pathogen Heterobasidion irregulare show substrate-specific regulation
inferred← citeshttps://doi.org/10.1016/j.fgb.2014.05.011openalex-snapshot
Copper radical oxidases and related extracellular oxidoreductases of wood-decay Agaricomycetes
inferred← citeshttps://doi.org/10.1016/j.fgb.2014.07.009openalex-snapshot
Differences in the secretion pattern of oxidoreductases from Bjerkandera adusta induced by a phenolic olive mill extract
inferred← citeshttps://doi.org/10.1016/j.fgb.2014.08.010openalex-snapshot
Plant biomass degradation by fungi
inferred← citeshttps://doi.org/10.1016/j.fgb.2015.02.002openalex-snapshot
Evolution of novel wood decay mechanisms in Agaricales revealed by the genome sequences of Fistulina hepatica and Cylindrobasidium torrendii
inferred← citeshttps://doi.org/10.1016/j.fuel.2021.121961openalex-snapshot
A mini review on biotransformation of coal to methane by enhancement of chemical pretreatment
inferred← citeshttps://doi.org/10.1016/j.funbio.2010.07.002openalex-snapshot
The Nox/Ferric reductase/Ferric reductase-like families of Eumycetes
inferred← citeshttps://doi.org/10.1016/j.funbio.2015.04.003openalex-snapshot
Revisiting the taxonomy of Phanerochaete (Polyporales, Basidiomycota) using a four gene dataset and extensive ITS sampling
inferred← citeshttps://doi.org/10.1016/j.fuproc.2018.09.017openalex-snapshot
Advancement in technologies for the depolymerization of lignin
inferred← citeshttps://doi.org/10.1016/j.heliyon.2020.e03170openalex-snapshot
Ligninolytic enzymes and its mechanisms for degradation of lignocellulosic waste in environment
inferred← citeshttps://doi.org/10.1016/j.hydromet.2016.08.003openalex-snapshot
Bio-modification of carbonaceous matter in gold ores: Model experiments using powdered activated carbon and cell-free spent medium of Phanerochaete chrysosporium
inferred← citeshttps://doi.org/10.1016/j.ibiod.2010.08.001openalex-snapshot
Natural resistance of five woods to Phanerochaete chrysosporium degradation
inferred← citeshttps://doi.org/10.1016/j.ibiod.2012.09.001openalex-snapshot
Patterns of lignocellulose degradation and secretome analysis of Trametes trogii MT
inferred← citeshttps://doi.org/10.1016/j.ibiod.2015.12.002openalex-snapshot
Effects of extracellular proteome on wheat straw pretreatment during solid-state fermentation of Phlebia radiata ATCC 64658
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.02.256openalex-snapshot
Comparative characterization of extracellular enzymes secreted by Phanerochaete chrysosporium during solid-state and submerged fermentation
inferred← citeshttps://doi.org/10.1016/j.indcrop.2013.02.001openalex-snapshot
Treatment of bagasse preparation effluent by Phanerochaete chrysosporium immobilized on polyurethane foam: Enzyme production versus pollution removal
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115827openalex-snapshot
Oil palm trunk waste: Environmental impacts and management strategies
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2009.06.020openalex-snapshot
Physiological regulation of laccase and manganese peroxidase production by white-rot Basidiomycetes
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2015.06.401openalex-snapshot
Recombinant expression of four oxidoreductases in Phanerochaete chrysosporium improves degradation of phenolic and non-phenolic substrates
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2016.10.007openalex-snapshot
The genome of Pleurotus eryngii provides insights into the mechanisms of wood decay
inferred← citeshttps://doi.org/10.1016/j.jclepro.2023.138196openalex-snapshot
Status and trends of enzyme cocktails for efficient and ecological production in the pulp and paper industry
inferred← citeshttps://doi.org/10.1016/j.jenvman.2021.112966openalex-snapshot
Process performance improvement for the simultaneous production of ligninolytic enzymes in solid culture using agricultural wastes through the Taguchi method
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2015.09.071openalex-snapshot
Genomic and molecular mechanisms for efficient biodegradation of aromatic dye
inferred← citeshttps://doi.org/10.1016/j.jprot.2011.09.001openalex-snapshot
iTRAQ-based quantitative secretome analysis of Phanerochaete chrysosporium
inferred← citeshttps://doi.org/10.1016/j.jprot.2011.11.020openalex-snapshot
Quantitative proteomic analysis of lignocellulolytic enzymes by Phanerochaete chrysosporium on different lignocellulosic biomass
inferred← citeshttps://doi.org/10.1016/j.micpath.2015.03.004openalex-snapshot
Potential roles of laccases on virulence of Heterobasidion annosum s.s.
inferred← citeshttps://doi.org/10.1016/j.micres.2017.03.002openalex-snapshot
Transcriptome-based analysis of the saprophytic fungus Abortiporus biennis – response to oxalic acid
inferred← citeshttps://doi.org/10.1016/j.mimet.2015.03.008openalex-snapshot
Detecting volatile compounds from Kraft lignin degradation in the headspace of microbial cultures by selected ion flow tube mass spectrometry (SIFT-MS)
inferred← citeshttps://doi.org/10.1016/j.molcatb.2015.10.008openalex-snapshot
Proteolytic modifications of laccase from Cerrena unicolor
inferred← citeshttps://doi.org/10.1016/j.nbt.2010.02.008openalex-snapshot
Two laccase isoenzymes and a peroxidase of a commercial laccase-producing basidiomycete, Trametes sp. Ha1
inferred← citeshttps://doi.org/10.1016/j.nbt.2015.05.003openalex-snapshot
Fostering the action of versatile peroxidase as a highly efficient biocatalyst for the removal of endocrine disrupting compounds
inferred← citeshttps://doi.org/10.1016/j.pbi.2008.02.003openalex-snapshot
Role of fungal peroxidases in biological ligninolysis
inferred← citeshttps://doi.org/10.1016/j.rser.2020.110280openalex-snapshot
Carbon based catalysts for the hydrodeoxygenation of lignin and related molecules: A powerful tool for the generation of non-petroleum chemical products including hydrocarbons
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.05.213openalex-snapshot
Litter decomposition in hyper-arid deserts: Photodegradation is still important
inferred← citeshttps://doi.org/10.1016/j.seta.2022.102688openalex-snapshot
A systematic overview on treatment towards endocrine disruptors
inferred← citeshttps://doi.org/10.1016/j.soilbio.2016.09.006openalex-snapshot
Ecology of the forest microbiome: Highlights of temperate and boreal ecosystems
inferred← citeshttps://doi.org/10.1016/j.teengi.2025.100044openalex-snapshot
From waste to wealth: Innovative biotechnological approaches in Phanerochaete chrysosporium for a circular bioeconomy
inferred← citeshttps://doi.org/10.1016/j.tibtech.2007.07.008openalex-snapshot
Proteomics of filamentous fungi
inferred← citeshttps://doi.org/10.1016/s0065-2164(07)00002-0openalex-snapshot
Submerged Culture Fermentation of “Higher Fungi”: The Macrofungi
inferred← citeshttps://doi.org/10.1016/s0065-2296(10)52006-8openalex-snapshot
Chapter 6 Reactive Oxygen Species in Phanerochaete chrysosporium Relationship Between Extracellular Oxidative and Intracellular Antioxidant Systems
inferred← citeshttps://doi.org/10.1021/acs.energyfuels.3c01878openalex-snapshot
Review on Catalytic Cracking of Lignin for the Production of Fuels and High-Value-Added Chemicals: Advances, Challenges, Opportunities, and Outlook
inferred← citeshttps://doi.org/10.1021/acschembio.7b00046openalex-snapshot
Phanerochaete chrysosporium Multienzyme Catabolic System for in Vivo Modification of Synthetic Lignin to Succinic Acid
inferred← citeshttps://doi.org/10.1021/bi7020298openalex-snapshot
Site-Directed Mutagenesis of the Catalytic Tryptophan Environment in Pleurotus eryngii Versatile Peroxidase ,
inferred← citeshttps://doi.org/10.1021/bk-2014-1158.ch002openalex-snapshot
Fungal and Bacterial Biodegradation: White Rots, Brown Rots, Soft Rots, and Bacteria
inferred← citeshttps://doi.org/10.1021/pr301131topenalex-snapshot
Genomic and Proteomic Dissection of the Ubiquitous Plant Pathogen, Armillaria mellea: Toward a New Infection Model System
inferred← citeshttps://doi.org/10.1021/pr4000762openalex-snapshot
Proteomic Analysis of Temperature Dependent Extracellular Proteins from Aspergillus fumigatus Grown under Solid-State Culture Condition
inferred← citeshttps://doi.org/10.1038/s41467-022-31433-xopenalex-snapshot
Metaproteomics reveals enzymatic strategies deployed by anaerobic microbiomes to maintain lignocellulose deconstruction at high solids
inferred← citeshttps://doi.org/10.1038/s41598-021-85615-6openalex-snapshot
Enhancing the compost maturation of swine manure and rice straw by applying bioaugmentation
inferred← citeshttps://doi.org/10.1038/s41598-026-36483-5openalex-snapshot
The oleaginous yeast Cutaneotrichosporon oleaginosum modifies corn stover alkali lignin
inferred← citeshttps://doi.org/10.1039/c1ee01268aopenalex-snapshot
Exploring new strategies for cellulosic biofuels production
inferred← citeshttps://doi.org/10.1039/c1np00042jopenalex-snapshot
Pathways for degradation of lignin in bacteria and fungi
inferred← citeshttps://doi.org/10.1039/c4gc01529kopenalex-snapshot
Simultaneous conversion of all cell wall components by an oleaginous fungus without chemi-physical pretreatment
inferred← citeshttps://doi.org/10.1039/c5gc01083gopenalex-snapshot
Assay for lignin breakdown based on lignin films: insights into the Fenton reaction with insoluble lignin
inferred← citeshttps://doi.org/10.1039/c8gc00518dopenalex-snapshot
Demonstrating a separation-free process coupling ionic liquid pretreatment, saccharification, and fermentation with Rhodosporidium toruloides to produce advanced biofuels
inferred← citeshttps://doi.org/10.1073/pnas.1119912109openalex-snapshot
Comparative genomics of Ceriporiopsis subvermispora and Phanerochaete chrysosporium provide insight into selective ligninolysis
inferred← citeshttps://doi.org/10.1073/pnas.2008888118openalex-snapshot
A multi-omics approach to lignocellulolytic enzyme discovery reveals a new ligninase activity from Parascedosporium putredinis NO1
inferred← citeshttps://doi.org/10.1074/jbc.m111.282467openalex-snapshot
Modulating O2 Reactivity in a Fungal Flavoenzyme
inferred← citeshttps://doi.org/10.1074/jbc.m112.356378openalex-snapshot
Lignin-degrading Peroxidases from Genome of Selective Ligninolytic Fungus Ceriporiopsis subvermispora
inferred← citeshttps://doi.org/10.1074/jbc.m808069200openalex-snapshot
Protein Radicals in Fungal Versatile Peroxidase
inferred← citeshttps://doi.org/10.1080/09593330.2010.490856openalex-snapshot
Comparative genomics of the mesophilic cellulosome‐producingClostridium cellulovoransand its application to biofuel production via consolidated bioprocessing
inferred← citeshttps://doi.org/10.1080/09593330.2023.2169639openalex-snapshot
New insights in the biodegradation of high-cyclic polycyclic aromatic hydrocarbons with crude enzymes of Trametes versicolor
inferred← citeshttps://doi.org/10.1080/10826068.2015.1084513openalex-snapshot
Production of versatile peroxidase fromPleurotus eryngiiby solid-state fermentation using agricultural residues and evaluation of its catalytic properties
inferred← citeshttps://doi.org/10.1080/12298093.2025.2610049openalex-snapshot
Nine Unrecorded Species of Phanerochaete (Polyporales, Basidiomycota) in Korea
inferred← citeshttps://doi.org/10.1093/abbs/gmp052openalex-snapshot
Biochemical characterization and transcriptional analysis of the epoxide hydrolase from white-rot fungus Phanerochaete chrysosporium
inferred← citeshttps://doi.org/10.1093/ee/nvy122openalex-snapshot
A Lab-Based Study of Temperate Forest Termite Impacts on Two Common Wood-Rot Fungi
inferred← citeshttps://doi.org/10.1093/jxb/ern261openalex-snapshot
Substrate oxidation sites in versatile peroxidase and other basidiomycete peroxidases
inferred← citeshttps://doi.org/10.1098/rspb.2009.1980openalex-snapshot
Selective biodegradation of keratin matrix in feather rachis reveals classic bioengineering
inferred← citeshttps://doi.org/10.1099/mic.0.2007/013128-0openalex-snapshot
The copper-dependent ACE1 transcription factor activates the transcription of the mco1 gene from the basidiomycete Phanerochaete chrysosporium
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