References
Paszczynski A, et al. Enzymatic activities of an extracellular, manganese-dependent peroxidase from Phanerochaete chrysosporium. FEMS Microbiol. Lett. 29: 37-41, 1985.
Leisola MS, et al. Homology among multiple extracellular peroxidases from Phanerochaete chrysosporium. J. Biol. Chem. 262: 419-424, 1987. PubMed: 2432065
Troller J, et al. Crystallization of a lignin peroxidase from the white-rot fungus Phanerochaete chrysosporium. Bio-Technology 6: 571-573, 1988.
Kersten PJ, Kirk TK. Involvement of a new enzyme, glyoxal oxidase, in extracellular H2O2 production by Phanerochaete chrysosporium. J. Bacteriol. 169: 2195-2201, 1987. PubMed: 3553159
George EJ, Newfeld RD. Degradation of fluorene in soil by fungus Phanerochaete chrysosporium. Biotechnol. Bioeng. 33: 1306-1310, 1989.
Schmidt HW, et al. Oxidative degradation of 3,4-dimethoxybenzyl alcohol and its methyl ether by the lignin peroxidase of Phanerochaete chrysosporium. Biochemistry 28: 1776-1783, 1989.
Lin JE, et al. Degradation kinetics of pentachlorophenol by Phanerochaete chrysosporium. Biotechnol. Bioeng. 35: 1125-1134, 1990.
Cripps C, et al. Biodegradation of azo and heterocyclic dyes by Phanerochaete chrysosporium. Appl. Environ. Microbiol. 56: 1114-1118, 1990. PubMed: 2339873
Ryan TP, Bumpus JA. Biodegradation of 2,4,5-trichlorophenoxyacetic acid in liquid culture and in soil by the white rot fungus Phanerochaete chrysosporium. Appl. Microbiol. Biotechnol. 31: 302-307, 1989.
Kennedy DW, et al. Comparative biodegradation of alkyl halide insecticides by the white rot fungus, Phanerochaete chrysosporium (BKM-F-1767). Appl. Environ. Microbiol. 56: 2347-2353, 1990. PubMed: 1698348
Dehorter B, Blondeau R. Extracellular enzyme activities during humic acid degradation by the white rot fungi Phanerochaete chrysosporium and Trametes versicolor. FEMS Microbiol. Lett. 94: 209-216, 1992.
Kersten PJ, Cullen D. Cloning and characterization of a cDNA encoding glyoxal oxidase, a H2O2-producing enzyme from the lignin-degrading basidiomycete Phanerochaete chrysosporium. Proc. Natl. Acad. Sci. USA 90: 7411-7413, 1993. PubMed: 8346264
Mougin C, et al. Biotransformation of the herbicide atrazine by the white rot fungus Phanerochaete chrysosporium. Appl. Environ. Microbiol. 60: 705-708, 1994.
Bumpus JA, Tatarko M. Biodegradation of 2,4,6-trinitrotoluene by Phanerochaete chrysosporium: identification of initial degradation products and the discovery of a TNT metabolite that inhibits lignin peroxidases. Curr. Microbiol. 28: 185-190, 1994.
Armenante PM, et al. Role of mycelium and extracellular protein in the biodegradation of 2,4,6-trichlorophenol by Phanerochaete chrysosporium. Appl. Environ. Microbiol. 60: 1711-1718, 1994. PubMed: 8031074
Leisola M, et al. Production and identification of extracellular oxidases of Phanerochaete chrysosporium. J. Biotechnol. 2: 379-382, 1985.
Novobranova TI. New spp. of fungi imperfecti from the Alma-Ata region. Nov. Sist. Nizshikh. Rast. 9: 180-187, 1972.
Torzilli AP, Isbister JD. Comparison of coal solubilization by bacteria and fungi. Biodegradation 5: 55-62, 1994.
Bumpus JA, et al. Biodegradation of DDE (1,1-dichloro-2,2-bis(4-chlorophenyl)ethene) by Phanerochaete chrysosporium. Mycol. Res. 97: 95-98, 1993.
Mougin C, et al. Biotransformation of the insecticide lindane by the white rot basidiomycete Phanerochaete chrysosporium. Pestic. Sci. 47: 51-59, 1996.
Gogna E, et al. Biodegradation of rose Bengal by Phanerochaete chrysosporium. Lett. Appl. Microbiol. 14: 58-60, 1992.
Bumpus JA. Biodegradation of polycyclic hydrocarbons by Phanerochaete chrysosporium. Appl. Environ. Microbiol. 55: 154-158, 1989. PubMed: 2705768
Yadav JS, Reddy CA. Degradation of benzene, toluene, ethylbenzene, and xylenes (BTEX) by the lignin-degrading basidiomycete Phanerochaete chrysosporium. Appl. Environ. Microbiol. 59: 756-762, 1993. PubMed: 8481002
Lewandowski GA, et al. Reactor design for hazardous waste treatment using a white rot fungus. Water Res. 24: 75-82, 1990.
Wood JD, Wood PM. Evidence that cellobiose:quinone oxidoreductase from Phanerochaete chrysosporium is a breakdown product of cellobiose oxidase. Biochim. Biophys. Acta 1119: 90-96, 1992. PubMed: 1540640
Burdsall HH Jr., Eslyn WE. A new Phanerochaete with a Chrysosporium imperfect state. Mycotaxon 1: 123-133, 1974.
Capalash N, Sharma P. Biodegradation of textile azo-dyes by Phanerochaete chrysosporium. World J. Microbiol. Biotechnol. 8: 309-312, 1992.
Covert SF, et al. Genomic organization of a cellulase gene family in Phanerochaete chrysosporium [published erratum appears in Curr. Genet. 23: 374, 1993]. Curr. Genet. 22: 407-413, 1992. PubMed: 1423728
Fukai H, et al. Dechlorination and detoxification of bleach plant effluent by Phanerochaete chrysosporium. J Biotechnol 24: 267-275, 1992.
Armenante PM, et al. Mineralization of 2-chlorophenol by Phanerochaete chrysosporium using different reactor designs. Hazard. Waste Hazard. Mater. 9: 213-229, 1992.
Muheim A, et al. Purification and properties of an aryl-alcohol dehydrogenase from the white-rot fungus Phanerochaete chrysosporium. Eur. J. Biochem. 195: 369-375, 1991. PubMed: 1997322
Sayadi S, Ellouz R. Decolourization of olive mill waste-waters by the white-rot fungus Phanerochaete chrysosporium: involvement of the lignin-degrading system. Appl. Microbiol. Biotechnol. 37: 813-817, 1992.
Pal N, et al. Process optimization and modeling of trichlorophenol degradation by Phanerochaete chrysosporium. Biotechnol. Bioeng. 46: 599-609, 1995.
Rogalski J, Dawidowicz AL, Wojtas-Wasilewska M. Continuous production of ligin peroxidase by Phanerochaete chrysosporium immobilized on a sintered glass carrier. Acta Biotechnol. 12: 191-201, 1992.
Kirby N, et al. Decolourisation of an artificial textile effluent by Phanerochaete chrysosporium. Biotechnol. Lett. 17: 761-764, 1995.
Chao WL, Lee SL. Decoloration of azo dyes by three white-rot fungi: influence of carbon source. World J. Microbiol. Biotechnol. 10: 556-559, 1994.
Bumpus JA, Aust SD. Biodegradation of DDT [1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane] by the white rot fungus Phanerochaete chrysosporium. Appl. Environ. Microbiol. 53: 2001-2008, 1987. PubMed: 3674869
Mileski GJ, et al. Biodegradation of pentachlorophenol by the white rot fungus Phanerochaete chrysosporium. Appl. Environ. Microbiol. 54: 2885-2889, 1988. PubMed: 3223759
Fernando T, et al. Biodegradation of TNT (2,4,6-trinitrotoluene) by Phanerochaete chrysosporium. Appl. Environ. Microbiol. 56: 1666-1671, 1990. PubMed: 2383008
Dhawale SW, et al. Degradation of phenanthrene by Phanerochaete chrysosporium occurs under ligninolytic as well as nonligninolytic conditions. Appl. Environ. Microbiol. 58: 3000-3006, 1992. PubMed: 1444413
Dobozi MS, et al. Xylanase activity of Phanerochaete chrysosporium. Appl. Environ. Microbiol. 58: 3466-3471, 1992.
Paszczynski A, et al. Mineralization of sulfonated azo dyes and sulfanilic acid by Phanerochaete chrysosporium and Streptomyces chromofuscus. Appl. Environ. Microbiol. 58: 3598-3604, 1992. PubMed: 1482182
Pasti-Grigsby MB, et al. Influence of aromatic substitution patterns on azo dye degradability by Streptomyces spp. and Phanerochaete chrysosporium. Appl. Environ. Microbiol. 58: 3605-3613, 1992. PubMed: 1482183
Camarero S, et al. Preferential degradation of phenolic lignin units by two white rot fungi. Appl. Environ. Microbiol. 60: 4509-4516, 1994. PubMed: 7811086
Bogan BW, Lamar RT. One-electron oxidation in the degradation of creosote polycyclic aromatic hydrocarbons by Phanerochaete chrysosporium. Appl. Environ. Microbiol. 61: 2631-2635, 1995. PubMed: 7618875
Hatakka A. Lignin-modifying enzymes from selected white-rot fungi: production and role in lignin degradation. FEMS Microbiol. Rev. 13: 125-135, 1994.
Tuisel H, et al. Lignin peroxidase H2 from Phanerochaete chrysosporium: purification, characterization and stability to temperature and pH. Arch. Biochem. Biophys. 279: 158-166, 1990. PubMed: 2337347
Kersten PJ. Glyoxal oxidase of Phanerochaete chrysosporium: its characterization and activation by lignin peroxidase. Proc. Natl. Acad. Sci. USA 87: 2936-2940, 1990. PubMed: 11607073
Thomas DR, et al. Mineralization of biphenyl and PCBs by the white rot fungus Phanerochaete chrysosporium. Biotechnol. Bioeng. 40: 1395-1402, 1992.
Constam D, et al. Purification and partial characterization of an intracellular NADH:quinone oxidoreductase from Phanerochaete chrysosporium. J. Gen. Microbiol. 137: 2209-2214, 1991.
Katayama A, Matsumura F. Photochemically enhanced microbial degradation of environmental pollutants. Environ. Sci. Technol. 25: 1329-1333, 1991.
Sublette KL, et al. Degradation of munition wastes by Phanerochaete chrysosporium. Appl. Biochem. Biotechnol. 34/35: 709-723, 1992.
Hickey WJ, et al. Transformation of atrazine in soil by Phanerochaete chrysosporium. Soil Biol. Biochem. 26: 1665-1671, 1994.
ASTM International Standard Test Methods for Ability of Adhesive Films to Support or Resist the Growth of Fungi. West Conshohocken, PA:ASTM International;ASTM Standard Test Method D 4300-01.
ASTM International Standard Test Methods for Resistance of Adhesive Preparations in Container to Attack by Bacteria, Yeast, and Fungi. West Conshohocken, PA:ASTM International;ASTM Standard Test Method D 4783-01e1.
Palma C, et al. Enhanced catalytic properties of MnP by exogenous addition of manganese and hydrogen peroxide. Biotechnol. Lett. 19: 263-267, 1997.
May R, et al. Ex-situ process for treating PAH-contaminated soil with Phanerochaete chrysosporium. Environ. Sci. Technol. 31: 2626-2633, 1997.
Moreira MT, et alEffect of pulsation on morphology of Aspergillus niger and Phanerochaete chrysosporium in a fluidized-bed reactorIn: Moreira MT, et alImmobilized cells: basics and applicationsAmsterdamElsevierpp. 518-523, 1996
Hawari J, et al. Biotransformation of 2,4,6-trinitrotoluene with Phanerochaete chrysosporium in agitated cultures ot pH 4.5. Appl. Environ. Microbiol. 65: 2977-2986, 1999. PubMed: 10388692
Krcmar P, et al. Degradation of polychlorinated biphenyls by extracellular enzymes of Phanerochaete chrysosporium produced in a perforated plate bioreactor. World J. Microbiol. Biotechnol. 15: 237-242, 1999.
Janshekar H, et al. Fungal degradation of pine and straw alkali lignins. Eur. J. Appl. Microbiol. Biotechnol. 14: 174-181, 1982.
Arjmand M, Sandermann H Jr.. N-(Chlorophenyl)-succinimides, a novel metabolite class isolated from Phanerochaete chrysosporium. Pestic. Biochem. Physiol. 27: 173-181, 1987.
Farrell RL, et al. Physical and enzymatic properties of lignin peroxidase isoenzymes from Phanerochaete chrysosporium. Enzyme Microb. Technol. 11: 322-328, 1989.
Galeno G, Agosin E. Screening of white-rot fungi for efficient decolourization of bleach pulp effluents. Biotechnol. Lett. 12: 869-872, 1990.
Morgan P, et al. Growth and biodegradation by white-rot fungi inoculated into soil. Soil Biol. Biochem. 25: 279-287, 1993.
type strain of Sporotrichum pulverulentum
Fratila-Apachitei LE, et al. Diuron degradation by Phanerochaete chrysosporium BKM-F-1767 in synthetic and natural media. Biotechnol. Lett. 21: 147-154, 1999.
Stewart P, Gaskell J, Cullen D. A homokaryotic derivative of a Phanerochaete chrysosporium strain and its use in genomic analysis of repetitive elements. Appl Environ Microbiol. 66: 1629-1633, 2000.
Doddapaneni H, Chakraborty R, Yadav JS. Genome-wide structural and evolutionary analysis of the P450 monooxygenase genes (P450ome) in the white rot fungus Phanerochaete chrysosporium: evidence for gene duplications and extensive gene clustering. BMC Genomics 6: 92, 2005.
Subramanian V, et al. P450 redox enzymes in the white rot fungus Phanerochaete chrysosporium: gene transcription, heterologous expression, and activity analysis on the purified proteins. Curr. Microbiol. 61: 306-314, 2010. PubMed: 20221604
Doddapaneni H, Yadav JS. Microarray-based global differential expression profiling of P450 monooxygenases and regulatory proteins for signal transduction pathways in the white rot fungus Phanerochaete chrysosporium. Mol. Genet. Genomics 274: 454-466, 2005. PubMed: 16231151
Doddapaneni H, Subramanian V, Yadav JS. Physiological regulation, xenobiotic induction, and heterologous expression of P450 monooxygenase gene pc-3 (CYP63A3), a new member of the CYP63 gene cluster in the white-rot fungus Phanerochaete chrysosporium. Curr Microbiol 50: 292-298, 2005. PubMed: 15968506
Syed K, et al. Genome-to-function characterization of novel fungal P450 monooxygenases oxidizing polycyclic aromatic hydrocarbons (PAHs). Biochem. Biophys. Res. Commun. 399: 492-497, 2010. PubMed: 20674550