The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Roles of various enzymes in the biotransformation of 6:2 fluorotelomer alcohol (6:2 FTOH) by a white-rot fungus
Abstract
Six-carbon-chained polyfluoroalkyl substances, such as 6:2 fluorotelomer alcohol (6:2 FTOH), are being used to replace longer chained compounds in the manufacture of various commercial products. This study examined the effects of growth substrates and nutrients on specific intracellular and extracellular enzymes mediating 6:2 FTOH aerobic biotransformation by the white-rot fungus, Phanerochaete chrysosporium. Cellulolytic conditions with limited glucose were a suitable composition, resulting in high 5:3 FTCA yield (37 mol%), which is a key intermediate in 6:2 FTOH degradation without forming significant amounts of terminal perfluorocarboxylic acids (PFCAs). Sulfate and ethylenediaminetetraacetic acid (EDTA) were also essential for 5:3 FTCA production, but, at lower levels, resulted in the buildup of 5:2 sFTOH (52 mol%) and 6:2 FTUCA (20 mol%), respectively. In non-ligninolytic nutrient-rich medium, 45 mol% 6:2 FTOH was transformed but produced only 12.7 mol% 5:3 FTCA. Enzyme activity studies imply that cellulolytic conditions induce the intracellular cytochrome P450 system. In contrast, extracellular peroxidase synthesis is independent of 6:2 FTOH exposure. Gene expression studies further verified that peroxidases were relevant in catalyzing the downstream transformations from 5:3 FTCA. Collectively, the identification of nutrients and enzymatic systems will help elucidate underlying mechanisms and biogeochemical conditions favorable for fungal transformation of PFCA precurso…
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“P450s from fungi (such as Cunninghamella elegans and Phanerochaete chrysosporium) have also been reported to participate in the biotransformation of 6:2 FTOH (121–123).”
From Toward the development of a molecular toolkit for the microbial remediation of per-and polyfluoroalkyl substances (2024) · cites this paper as [122]
In the citing paper
“Correspondingly, the LiP activity exhibited a progressive increase over time, whereas the MnP activity remained stable between days 7 and 14, followed by an upsurge on day 28.”
From Toward the development of a molecular toolkit for the microbial remediation of per-and polyfluoroalkyl substances (2024) · cites this paper as [122]
In the citing paper
“These observations suggest that both enzymes may have contributed to the biotransformation of 5:3 FTCA or were positively influenced by 5:3 FTCA and its metabolites.”
From Toward the development of a molecular toolkit for the microbial remediation of per-and polyfluoroalkyl substances (2024) · cites this paper as [122]
In the citing paper
“Specifically, both genes exhibited gradual accumulation of transcripts over time, reaching their peak expression levels on day 28 when P. chrysosporium was cultivated with 5:3 FTCA as the parent compound.”
From Toward the development of a molecular toolkit for the microbial remediation of per-and polyfluoroalkyl substances (2024) · cites this paper as [122]
In the citing paper
“The genes encoding LiP (lipD) and MnP (mnp1) demonstrated differential expression in comparison to the PFAS-free control when P. chrysosporium was cultured under ligninolytic conditions in a modified Kirk medium containing 1% glucose (122).”
From Toward the development of a molecular toolkit for the microbial remediation of per-and polyfluoroalkyl substances (2024) · cites this paper as [122]
Citations
Cites
Huang, S., & Jaffé, P. R. (2019) · Environmental Science & Technology · doi:10.1021/acs.est.9b04047 · Cited by 524
Degradation and Removal Methods for Perfluoroalkyl and Polyfluoroalkyl Substances in Water
Merino, N., Qu, Y., Deeb, R. A., Hawley, E. L., Hoffmann, M. R., & Mahendra, S. (2016) · Environmental Engineering Science · doi:10.1089/ees.2016.0233 · Cited by 349
Self-citationZhang, S., Szostek, B., McCausland, P. K., Wolstenholme, B. W., Lu, X., Wang, N., & Buck, R. C. (2013) · Environmental Science & Technology · doi:10.1021/es4000824 · Cited by 198
Self-citation
Research works printed but not linked: 37
- Shaw, 2019, Degradation and defluorination of 6:2 fluorotelomer sulfonamidoalkyl betaine and 6:2 fluorotelomer sulfonate by Gordonia sp. strain NB4-1Y under sulfur-limiting conditions, Sci Total Environ, 647, 690, 10.1016/j.scitotenv.2018.08.012 · DOI · Paper page
- Cheng, 2022, Bioaccumulation and biomagnification of emerging poly- and perfluoroalkyl substances in marine organisms, Sci Total Environ, 10.1016/j.scitotenv.2022.158117 · DOI
- Rice, 2020, Comparative analysis of the toxicological databases for 6:2 fluorotelomer alcohol (6:2 FTOH) and perfluorohexanoic acid (PFHxA), Food Chem Toxicol, 138, 10.1016/j.fct.2020.111210 · DOI
- Butt, 2014, Biotransformation pathways of fluorotelomer-based polyfluoroalkyl substances: a review, Environ Toxicol Chem, 33, 243, 10.1002/etc.2407 · DOI · Paper page
- Beškoski, 2018, Defluorination of perfluoroalkyl acids is followed by production of monofluorinated fatty acids, Sci Total Environ, 636, 355, 10.1016/j.scitotenv.2018.04.243 · DOI
- Yu, 2020, Microbial cleavage of C-F bonds in Two C6 Per- and polyfluorinated compounds via reductive defluorination, Environ Sci Technol, 54, 14393, 10.1021/acs.est.0c04483 · DOI · Paper page
- Kim, 2014, 6:2 Fluorotelomer alcohol (6:2 FTOH) biodegradation by multiple microbial species under different physiological conditions, Appl Microbiol Biotechnol, 98, 1831, 10.1007/s00253-013-5131-3 · DOI · Paper page
- Kim, 2012, Biodefluorination and biotransformation of fluorotelomer alcohols by two alkane-degrading Pseudomonas strains, Biotechnol Bioeng, 109, 3041, 10.1002/bit.24561 · DOI · Paper page
- Tseng, 2014, Biotransformation of 6:2 Fluorotelomer Alcohol (6:2 FTOH) by A Wood-Rotting Fungus, Environ Sci Technol, 48, 4012, 10.1021/es4057483 · DOI · Paper page
- Harms, 2011, Untapped potential: exploiting fungi in bioremediation of hazardous chemicals, Nat Rev Microbiol, 9, 177, 10.1038/nrmicro2519 · DOI · Paper page
- Tien, 1988, Lignin peroxidase of Phanerochaete chrysosporium, Methods Enzym, 161, 238, 10.1016/0076-6879(88)61025-1 · DOI
- Yadav, 2006, P450ome of the white rot fungus Phanerochaete chrysosporium: structure, evolution and regulation of expression of genomic P450 clusters, Biochem Soc Trans, 34, 1165, 10.1042/BST0341165 · DOI
- Gao, 2022, Immobilized fungal enzymes: Innovations and potential applications in biodegradation and biosynthesis, Biotechnology Advances, 57, 107936, 10.1016/j.biotechadv.2022.107936 · DOI
- Daramola, 2021, Emerging investigator series: human CYP2A6 catalyzes the oxidation of 6:2 fluorotelomer alcohol, Environ Sci Process Impacts, 23, 1688, 10.1039/D1EM00307K · DOI
- Khan, 2022, Fluorotelomer alcohols are efficiently biotransformed by Cunninghamella elegans, Environ Sci Pollut Res, 1, 1
- Subramanian, 2009, Role of P450 monooxygenases in the degradation of the endocrine-disrupting chemical nonylphenol by the white rot fungus Phanerochaete chrysosporium, Appl Environ Microbiol, 75, 5580, 10.1128/AEM.02942-08 · DOI
- Ning, 2012, Involvement of Cytochrome P450 in pentachlorophenol transformation in a white rot fungus Phanerochaete chrysosporium, PLoS One, 7, 10.1371/journal.pone.0045887 · DOI
- Xie, 2022, Pseudomonas sp. strain 273 incorporates organofluorine into the lipid bilayer during growth with fluorinated alkanes, Environ Sci Technol, 56, 8155, 10.1021/acs.est.2c01454 · DOI
- Liu, 2010, 6-2 Fluorotelomer alcohol aerobic biodegradation in soil and mixed bacterial culture, Chemosphere, 78, 437, 10.1016/j.chemosphere.2009.10.044 · DOI
- Merino, 2018, Fungal biotransformation of 6:2 fluorotelomer alcohol, Remediat J, 28, 59, 10.1002/rem.21550 · DOI
- Zhao, 2013, 6:2 Fluorotelomer alcohol biotransformation in an aerobic river sediment system, Chemosphere, 90, 203, 10.1016/j.chemosphere.2012.06.035 · DOI
- Zhao, 2013, 6:2 Fluorotelomer alcohol aerobic biotransformation in activated sludge from two domestic wastewater treatment plants, Chemosphere, 92, 464, 10.1016/j.chemosphere.2013.02.032 · DOI · Paper page
- Zacchi, 2000, Metabolism of cellulose by Phanerochaete chrysosporium in continuously agitated culture is associated with enhanced production of lignin peroxidase, J Biotechnol, 78, 185, 10.1016/S0168-1656(00)00209-1 · DOI
- Ray, 2012, Phanerochaete chrysosporium produces a diverse array of extracellular enzymes when grown on sorghum, Appl Microbiol Biotechnol, 93, 2075, 10.1007/s00253-012-3907-5 · DOI
- Žifčáková, 2012, Fungal polysaccharide monooxygenases: new players in the decomposition of cellulose, Fungal Ecol, 5, 481, 10.1016/j.funeco.2012.05.001 · DOI
- Meux, 2011, Glutathione Transferases of Phanerochaete chrysosporium, J Biol Chem, 286, 9173, 10.1074/jbc.M110.194548 · DOI
- Bucheli-Witschel, 2001, Environmental fate and microbial degradation of aminopolycarboxylic acids, FEMS Microbiol Rev, 25, 69, 10.1111/j.1574-6976.2001.tb00572.x · DOI
- Anderson, 1985, A review of the environmental and mammalian toxicology of nitrilotriacetic acid, Crit Rev Toxicol, 15, 1, 10.3109/10408448509023766 · DOI
- Schneider-Poetsch, 2010, Inhibition of eukaryotic translation elongation by cycloheximide and lactimidomycin, Nat Chem Biol, 6, 209, 10.1038/nchembio.304 · DOI
- Wang, 2012, 5:3 Polyfluorinated acid aerobic biotransformation in activated sludge via novel “one-carbon removal pathways, Chemosphere, 87, 527, 10.1016/j.chemosphere.2011.12.056 · DOI · Paper page
- Yang, 2022, Desulfonation and defluorination of 6:2 fluorotelomer sulfonic acid (6:2 FTSA) by Rhodococcus jostii RHA1: carbon and sulfur sources, enzymes, and pathways, J Hazard Mater, 423, 10.1016/j.jhazmat.2021.127052 · DOI · Paper page
- Yan, 2022, Biotransformation of 8:2 fluorotelomer alcohol in soil from aqueous film-forming foams (AFFFs)-impacted sites under nitrate-, sulfate-, and iron-reducing conditions, Environ Sci Technol, 56, 13728, 10.1021/acs.est.2c03669 · DOI
- Lin, 2022, Bioremediation of organic pollutants by white rot fungal cytochrome P450: The role and mechanism of CYP450 in biodegradation, Chemosphere, 301, 10.1016/j.chemosphere.2022.134776 · DOI
- Doddapaneni, 2005, 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 Genom, 274, 454, 10.1007/s00438-005-0051-2 · DOI
- Guengerich, 2009, Measurement of cytochrome P450 and NADPH-cytochrome P450 reductase, Nat Protoc, 4, 1245, 10.1038/nprot.2009.121 · DOI
- Durairaj, 2022, Functional expression and regulation of eukaryotic cytochrome P450 enzymes in surrogate microbial cell factories, Eng Microbiol, 2, 10.1016/j.engmic.2022.100011 · DOI
- Deroy, 2015, The GSTome reflects the chemical environment of white-rot fungi, PLoS One, 10, 10.1371/journal.pone.0137083 · DOI
Cited by
Sorted by citations
Hu, M., & Scott, C. (2024) · Applied and Environmental Microbiology · doi:10.1128/aem.00157-24 · Cited by 63
Field assessment of a constructed wetland for stormwater treatment: A focus on PFAS management
Awad, J., Silva, H. C., Navarro, D., Blotevogel, E., Juhasz, A., & Kirby, J. (2026) · Journal of Hazardous Materials Advances · doi:10.1016/j.hazadv.2026.101092 · Cited by 1
Metadata
- Authors
- Merino, N., Wang, N., Gao, Y., Wang, M., & Mahendra, S.
- Venue
- Journal of Hazardous Materials
- Publisher
- Elsevier BV
- Published
- 2023-05
- Volume
- 450
- Pages
- 131007
- ISSN
- 0304-3894
- Cited by
- 31
- References
- 3
- Language
- en
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (am, 307 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Funders
- DuPont de Nemours Inc
- Air Force Civil Engineer Center (8903\u201311-C-8009)
- University of California Los Angeles
- National Science Foundation (1255021, 0963183, 10RR024605)
- US Environmental Protection Agency
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review