Biodegradation of chrysene, an aromatic hydrocarbon by Polyporus sp S133 in liquid medium

被引:79
作者
Hadibarata, Tony [1 ]
Tachibana, Sanro [1 ]
Itoh, Kazutaka [1 ]
机构
[1] Ehime Univ, Dept Appl Biosci, Fac Agr, Matsuyama, Ehime 7908566, Japan
关键词
Chrysene; Biodegradation; Metabolites; Polyporus sp S133; WHITE-ROT FUNGI; PHANEROCHAETE-CHRYSOSPORIUM; MANGANESE PEROXIDASE; MANGROVE SEDIMENTS; CONTAMINATED SOIL; PHENANTHRENE; PAHS; BIOREMEDIATION; DEGRADATION; NAPHTHALENE;
D O I
10.1016/j.jhazmat.2008.08.081
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Polyporus sp. S133, a fungus collected from contaminated-soil was used to degrade chrysene, a polycyclic aromatic hydrocarbon (PAH) in a mineral salt broth (MSB) liquid culture. Maximal degradation rate of chrysene (65%) was obtained when Polyporus sp. S133 was incubated in the cultures supplemented with polypeptone (10%) for 30 days under agitation of 120 rpm, as compared to just 24% degradation rate in non-agitated culture. Furthermore, the degradation of chrysene was affected by the addition of carbon and nitrogen sources as well as kind of surfactants. The degradation rate was increased with increase in added amount of carbon and nitrogen sources, respectively. The degradation rate in agitated cultures was enhanced about 2 times higher than that in non-agitated cultures. The degradation mechanism of chrysene by Polyporus sp. S133 was determined through identification of several metabolites: chrysenequinone, 1-hydroxy-2-naphthoic acid, phthalic acid, salicylic acid, protocatechuic acid, gentisic acid, and catechol. Several enzymes (manganese peroxidase, lignin peroxidase, laccase, 1,2-dioxygenase and 2,3-dioxygenase) produced by Polyporus sp. S133 were detected during the incubation. The highest enzyme activity was shown by 1,2-dioxygenase (237.5 Ul(-1)) after 20 days of incubation. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:911 / 917
页数:7
相关论文
共 42 条
[1]  
Alexander M., 1999, Biodegradation and Bioremediation
[2]  
[Anonymous], [No title captured]
[3]   Comparison of two assay procedures for lignin peroxidase [J].
Arora, DS ;
Gill, PK .
ENZYME AND MICROBIAL TECHNOLOGY, 2001, 28 (7-8) :602-605
[4]   EFFECT OF TWEEN-80 AND OLEIC-ACID ON LIGNINASE PRODUCTION BY PHANEROCHAETE-CHRYSOSPORIUM INA-12 [J].
ASTHER, M ;
CORRIEU, G ;
DRAPRON, R ;
ODIER, E .
ENZYME AND MICROBIAL TECHNOLOGY, 1987, 9 (04) :245-249
[5]   Purification and characterization of a salicylate hydroxylase involved in 1-hydroxy-2-naphthoic acid hydroxylation from the naphthalene and phenanthrene-degrading bacterial strain Pseudomonas putida BS202-P1 [J].
Balashova, NV ;
Stolz, A ;
Knackmuss, HJ ;
Kosheleva, IA ;
Naumov, AV ;
Boronin, AM .
BIODEGRADATION, 2001, 12 (03) :179-188
[6]  
Cerniglia Carl E., 1993, Current Opinion in Biotechnology, V4, P331, DOI [10.1016/0958-1669(93)90104-5, 10.1007/BF00129093]
[7]   Fungal metabolism of polycyclic aromatic hydrocarbons: Past, present and future applications in bioremediation [J].
Cerniglia, CE .
JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 1997, 19 (5-6) :324-333
[8]   Naphthalene biodegradation kinetics in an aerobic slurry-phase bioreactor [J].
Collina, E ;
Bestetti, G ;
Di Gennaro, P ;
Franzetti, A ;
Gugliersi, F ;
Lasagni, M ;
Pitea, D .
ENVIRONMENT INTERNATIONAL, 2005, 31 (02) :167-171
[9]   Removal of polycyclic aromatic hydrocarbons (PAH) in contaminated soil by white rot fungus Pleurotus ostreatus [J].
Eggen, T ;
Majcherczyk, A .
INTERNATIONAL BIODETERIORATION & BIODEGRADATION, 1998, 41 (02) :111-117
[10]  
FALATKO DM, 1991, THESIS STATE U BLACK