Detoxification of polycyclic aromatic hydrocarbons by fungi
- PMID: 1367975
- DOI: 10.1007/BF01576368
Detoxification of polycyclic aromatic hydrocarbons by fungi
Abstract
The polycyclic aromatic hydrocarbons (PAHs) are a group of hazardous environmental pollutants, many of which are acutely toxic, mutagenic, or carcinogenic. A diverse group of fungi, including Aspergillus ochraceus, Cunninghamella elegans, Phanerochaete chrysosporium, Saccharomyces cerevisiae, and Syncephalastrum racemosum, have the ability to oxidize PAHs. The PAHs anthracene, benz[a]anthracene, benzo[a]pyrene, fluoranthene, fluorene, naphthalene, phenanthrene, and pyrene, as well as several methyl-, nitro-, and fluoro-substituted PAHs, are metabolized by one or more of these fungi. Unsubstituted PAHs are oxidized initially to arene oxides, trans-dihydrodiols, phenols, quinones, and tetralones. Phenols and trans-dihydrodiols may be further metabolized, and thus detoxified, by conjugation with sulfate, glucuronic acid, glucose, or xylose. Although dihydrodiol epoxides and other mutagenic and carcinogenic compounds have been detected as minor fungal metabolites of a few PAHs, most transformations performed by fungi reduce the mutagenicity and thus detoxify the PAHs.
Similar articles
-
Fungal metabolism and detoxification of polycyclic aromatic hydrocarbons.Arch Microbiol. 1985 Nov;143(2):105-10. doi: 10.1007/BF00411031. Arch Microbiol. 1985. PMID: 3907570
-
Biotransformation of benzo[a]pyrene and other polycyclic aromatic hydrocarbons and heterocyclic analogs by several green algae and other algal species under gold and white light.Chem Biol Interact. 1995 Jul 14;97(2):131-48. doi: 10.1016/0009-2797(95)03610-x. Chem Biol Interact. 1995. PMID: 7606812
-
High-performance liquid chromatographic separation of ring-oxidized metabolites of nitro-polycyclic aromatic hydrocarbons.J Chromatogr. 1989 Jan 6;461:315-26. doi: 10.1016/s0021-9673(00)94298-5. J Chromatogr. 1989. PMID: 2708476
-
Polyaromatic Hydrocarbons (PAHs): Structures, Synthesis and their Biological Profile.Curr Org Synth. 2020;17(8):625-640. doi: 10.2174/1570179417666200713182441. Curr Org Synth. 2020. PMID: 32660405 Review.
-
Polycyclic aromatic hydrocarbon bioremediation design.Curr Opin Biotechnol. 1997 Jun;8(3):268-73. doi: 10.1016/s0958-1669(97)80002-x. Curr Opin Biotechnol. 1997. PMID: 9206005 Review.
Cited by
-
Changes in the abundance of sugars and sugar-like compounds in tall fescue (Festuca arundinacea) due to growth in naphthalene-treated sand.Environ Sci Pollut Res Int. 2015 Apr;22(8):5817-30. doi: 10.1007/s11356-014-3812-9. Epub 2014 Nov 14. Environ Sci Pollut Res Int. 2015. PMID: 25391233
-
Enzymatic Mechanisms Involved in Phenanthrene Degradation by the White Rot Fungus Pleurotus ostreatus.Appl Environ Microbiol. 1997 Jul;63(7):2495-501. doi: 10.1128/aem.63.7.2495-2501.1997. Appl Environ Microbiol. 1997. PMID: 16535634 Free PMC article.
-
Pyrene Metabolism in Crinipellis stipitaria: Identification of trans-4,5-Dihydro-4,5-Dihydroxypyrene and 1-Pyrenylsulfate in Strain JK364.Appl Environ Microbiol. 1994 Oct;60(10):3602-7. doi: 10.1128/aem.60.10.3602-3607.1994. Appl Environ Microbiol. 1994. PMID: 16349407 Free PMC article.
-
Initial oxidative and subsequent conjugative metabolites produced during the metabolism of phenanthrene by fungi.J Ind Microbiol. 1996 Apr;16(4):205-15. doi: 10.1007/BF01570023. J Ind Microbiol. 1996. PMID: 8652115
-
Biotransformation of petroleum asphaltenes and high molecular weight polycyclic aromatic hydrocarbons by Neosartorya fischeri.Environ Sci Pollut Res Int. 2016 Jun;23(11):10773-10784. doi: 10.1007/s11356-016-6277-1. Epub 2016 Feb 19. Environ Sci Pollut Res Int. 2016. PMID: 26893177
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Medical