ATCC24725

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ATCC24725标准菌株基本信息

出品公司: ATCC
菌种名称: ATCC 24725, ATCC24725
菌种又名: VKM F-1767 [CBS 481.73, CCRC 36200, IMI 174727, NRRL 6361, QM 9998]
菌株类型: Phanerochaete chrysosporium,黄孢原毛平革菌
存储人: LA Beljakova
分离来源: 哈萨克斯坦阿拉木图地区葡萄的果实和叶柄
产品目录号: 24725
培养基: ATCC培养基200:YM琼脂或YM肉汤
ATCC培养基324:麦芽汁琼脂
ATCC培养基336:马铃薯葡萄糖琼脂(PDA)
生长条件: 25-30 ℃,  有氧
生物安全等级: 1
基因组是否测序:
应用:
细菌耐药性检测胶粘剂、降解1,1-二氯-2- 2-双(4-氯苯基)乙烯DDE、降解2,4,5-三氯酚、降解2,4,5-三氯苯氧乙酸2,4,5、降解2,4,6-三氯酚、降解2,4,6-三硝基甲苯TNT、降解3,4-二氯苯胺、降解刚果红刚果红、降解滴滴涕、降解酸性黄9、降解奥尔德林、苋菜的降解、降解莠去津、降解偶氮染料、降解天青B Azure B、苯降解、苯并(a)芘的降解、降解联苯、降解氯丹、降解杂酚油、降解环己烷RDX,环三甲基三硝基胺、降解狄氏剂、乙苯降解、降解芴、降解七氯、腐殖酸降解、降解木质素、降解林丹、灭蚁灵、邻氯苯酚降解、降解橄榄油废水、降解橙G橙G、降解橙II橙Ⅱ、降解五氯酚、菲降解、降解多氯联苯、降解多环芳烃、降解Bengal玫瑰、降解磺胺酸、甲苯降解、降解土苯土酚O、降解藜芦醇、降解二甲苯、抗真菌试验胶粘剂、N-(氯苯酚)琥珀酰亚胺的制备、生产NAD(P)H甲萘醌氧化还原酶1,二恶英诱导的NADH:醌氧化还原酶,NADH dehydrogenase(醌)、芳香醇脱氢酶的产生、产生纤维二糖脱氢酶(醌)纤维二糖:醌氧化还原酶、生产煤增溶剂、乙二醛氧化酶的制备、木质素过氧化物酶-二芳基丙烷加氧酶的制备、锰过氧化物酶的产生、产生过氧化物酶、生产木聚糖内酯1,3-β-木糖苷酶木聚糖水解酶木聚糖酶、降解敌百虫
菌株特点:
ATCC 24725是Phanerochaete chrysosporium,黄孢原毛平革菌。

ATCC 24725能够在ATCC培养基200:YM琼脂或YM肉汤、ATCC培养基324:麦芽汁琼脂、ATCC培养基336:马铃薯葡萄糖琼脂(PDA)中生长。

Nucleotide (GenBank) : KU729061 ITS including 5.8S rRNA gene
 
Nucleotide (GenBank) : L18991 glyoxal oxidase cDNA
 
Nucleotide (GenBank) : Z11729 cellobiohydrolase CBH1-6 gene, 3' end
 
Nucleotide (GenBank) : X15599 Phanerochaete chrysosporium LIP2 gene for lignin peroxidase.
 
Nucleotide (GenBank) : M18794 Phanerochaete chrysosporium ligninase precursor, mRNA, complete
 
Nucleotide (GenBank) : M21913 Phanerochaete chrysosporium peroxidase isozyme H8 mRNA, partial
 
Nucleotide (GenBank) : X51590 Phanerochaete chrysosporium GLG3 (LIP) gene for lignin peroxidase
 
Nucleotide (GenBank) : X12698 Phanerochaete chrysosporium mRNA for ligninase (rLDM(TM)6) apoprotein
 
Nucleotide (GenBank) : AADS01000000 Phanerochaete chrysosporium RP-78, whole genome shotgun sequencing project.
 
参考文献:
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.
 
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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.
 
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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.
 
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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
 
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Arjmand M, Sandermann H Jr.. N-(Chlorophenyl)-succinimides, a novel metabolite class isolated from Phanerochaete chrysosporium. Pestic. Biochem. Physiol. 27: 173-181, 1987.
 
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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.
 
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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.
 
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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
 
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type strain of Sporotrichum pulverulentum

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