Cited by 85Per- and polyfluoroalkyl substances researchMicrobial bioremediation and biosurfactantsEnvironmental Chemistry and Analysis

Aerobic biotransformation of 6:2 fluorotelomer sulfonate by Dietzia aurantiaca J3 under sulfur-limiting conditions

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Méndez, Valentina, Holland, Sophie, Bhardwaj, Shefali, McDonald, James, Khan, Stuart, O'Carroll, Denis, Pickford, Russell, Richards, Sarah +4 more·2022·Science of The Total Environment

Abstract

The polyfluorinated alkyl substance 6:2 fluorotelomer sulfonate (6:2 FTS) has been detected in diverse environments impacted by aqueous film-forming foams used for firefighting. In this study, a bacterial strain (J3) using 6:2 FTS as a sulfur source was isolated from landfill leachate previously exposed to polyfluoroalkyl substances in New South Wales, Australia. Strain J3 shares 99.9% similarity with the 16S rRNA gene of Dietzia aurantiaca CCUG 35676T. Genome sequencing yielded a draft genome sequence of 37 contigs with a G + C content of 69.7%. A gene cluster related to organic sulfur utilisation and assimilation was identified, that included an alkanesulfonate monooxygenase component B (ssuD), an alkanesulfonate permease protein (ssuC), an ABC transporter (ssuB), and an alkanesulfonate-binding protein (ssuA). Proteomic analyses comparing strain J3 cultures using sulfate and 6:2 FTS as sulfur source indicated that the ssu gene cluster was involved in 6:2 FTS biodegradation. Upregulated proteins included the SsuD monooxygenase, the SsuB transporter, the ABC transporter permease (SsuC), an alkanesulfonate-binding protein (SsuA), and a nitrilotriacetate monooxygenase component B. 6:2 Fluorotelomer carboxylic acid (6:2 FTCA) and 6:2 fluorotelomer unsaturated acid (6:2 FTUA) were detected as early degradation products in cultures (after 72 h) while 5:3 fluorotelomer acid (5:3 FTCA), perfluorohexanoic acid (PFHxA) and perfluoropentanoic acid (PFPeA) were detected as later degradation products (after 168 h). This work provides biochemical and metabolic insights into 6:2 FTS biodegradation by the Actinobacterium D. aurantiaca J3, informing the fate of PFAS in the environment.

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  • Another 6:2 FTSA-biodegrading strain, Dietzia aurantiaca J3 was isolated from PFAS-impacted landfill leachate that could transform the compound to 6:2FTCA, 6:2 FTUA, 5:3 FTCA, PFHxA and PFPeA through the 6:2 FTOH degradation pathway.

    “Another 6:2 FTSA – biodegrading strain, Dietzia aurantiaca J3 was isolated from PFAS-impacted landfill leach- ate that could transform the compound to 6:2FTCA, 6:2 FTUA, 5:3 FTCA, PFHxA and PFPeA through the 6:2 FTOH degradation pathway (Méndez et al., 2022).”

    From A review of microbial degradation of per- and polyfluoroalkyl substances (PFAS): Biotransformation routes and enzymes (2023) · cites this paper as Méndez et al., 2022

    The Discussion reports that Dietzia aurantiaca J3 was isolated from PFAS-impacted landfill leachate and produced all five listed breakdown products. It says transformation to 6:2 FTCA likely occurs via 6:2 FTOH, but that intermediate was not directly detected; the claim presents this proposed pathway as established. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • Desulfonation of PFSAs is suspected to be catalyzed by alkanesulfonate monooxygenases, ssuDEABC proteins, haloacid dehalogenases, cytochrome P450s and nitriloacetate monooxygenases.

    “is suspected to be catalyzed by alkanesulfonate monooxygenases, ssuDEABC proteins, haloacid dehalogenases, cytochrome P450s and nitriloacetate monooxygenases (Table 4) (Méndez et al., 2022; Van Hamme et al., 2013; Yang et al., 2022)”

    From A review of microbial degradation of per- and polyfluoroalkyl substances (PFAS): Biotransformation routes and enzymes (2023) · cites this paper as Méndez et al., 2022

    The Introduction and §3.3 support a suspected role for alkanesulfonate monooxygenase and Ssu proteins in desulfonating 6:2 FTS. Section 3.3 reports that a nitrilotriacetate monooxygenase component was upregulated, but does not assign it a desulfonation role; the cited passages do not support such a role for haloacid dehalogenases or cytochrome P450s either. The paper addresses 6:2 FTS, not PFSAs generally; page numbers are unavailable in our copy. (LLM, conf=0.88)

    Experimental — accuracy not yet measured

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Research works printed but not linked: 41

  1. Aziz, R.K., Bartels, D., Best, A.A., DeJongh, M., Disz, T., Edwards, R.A., et al., 2008. The RAST server: rapid annotations using subsystems technology. BMC Genomics 9 (1), 1-15. https://doi.org/10.1186/1471-2164-9-75. · DOI
  2. Baduel, C., Mueller, J.F., Rotander, A., Corfield, J., Gomez-Ramos, M.J., 2017. Discovery of novel per-and polyfluoroalkyl substances (PFASs) at a firefighting training ground and preliminary investigation of their fate and mobility. Chemosphere 185, 1030-1038. https://doi.org/10.1016/j.chemosphere.2017.06.096. · DOI · Paper page
  3. Bankevich, A., Nurk, S., Antipov, D., Gurevich, A.A., Dvorkin, M., Kulikov, A.S., et al., 2012. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J. Comput. Biol. 19 (5), 455-477.
  4. Bottos, E.M., Al-Shabib, E.Y., Shaw, D.M., McAmmond, B.M., Sharma, A., Suchan, D.M., et al., 2020. Transcriptomic response of gordonia sp. Strain NB4-1Y when provided with 6:2 fluorotelomer sulfonamidoalkyl betaine or 6: 2 fluorotelomer sulfonate as sole sulfur source. Biodegradation 31 (4), 407-422. https://doi.org/10.1007/s10532-020-09917-8. · DOI
  5. Cox, J., Hein, M.Y., Luber, C.A., Paron, I., Nagaraj, N., Mann, M., 2014. Accurate proteome- wide label-free quantification by delayed normalization and maximal peptide ratio ex- traction, termed MaxLFQ. Molecular and Cellular Proteomics 13 (9), 2513-2526.
  6. D'Agostino, L.A., Mabury, S.A., 2017. Aerobic biodegradation of 2 fluorotelomer sulfonamide- based aqueous film-forming foam components produces perfluoroalkyl carboxylates. En- viron. Toxicol. Chem. 36, 2012-2021. https://doi.org/10.1002/etc.3750. · DOI
  7. Duckworth, A.W., Grant, S., Grant, W.D., Jones, B.E., Meijer, D., 1998. Dietzia natronolimnaios sp. nov., a new member of the genus Dietzia isolated from an East African soda lake. Extremophiles 2 (3), 359-366.
  8. Eichhorn, E., Leisinger, T., 2001. Escherichia coli utilizes methanesulfonate and L-cysteate as sole sulphur sources for growth. FEMS Microbiol. Lett. 205 (2), 271-275. https://doi. org/10.1111/j.1574-6968.2001.tb10960.x. · DOI
  9. Eichhorn, E., van der Ploeg, J.R., Leisinger, T., 1999. Characterization of a two-component alkanesulfonate monooxygenase from Escherichia coli. J. Biol. Chem. 274 (38), 26639-26646. https://doi.org/10.1074/jbc.274.38. 26639. · DOI
  10. Eriksson, U., Haglund, P., Kärrman, A., 2017. Contribution of precursor compounds to the release of per-and polyfluoroalkyl substances (PFASs) from waste water treat- ment plants (WWTPs). J. Environ. Sci. 61, 80-90. https://doi.org/10.1016/j.jes. 2017.05.004. · DOI · Paper page
  11. Field, J.A., Seow, J., 2017. Properties, occurrence, and fate of fluorotelomer sulfonates. Crit. Rev. Environ. Sci. Technol. 47 (8), 643-691. https://doi.org/10.1080/10643389.2017. 1326276. · DOI · Paper page
  12. Houtz, E.F., Sutton, R., Park, J.S., Sedlak, M., 2016. Poly-and perfluoroalkyl substances in wastewater: significance of unknown precursors, manufacturing shifts, and likely AFFF impacts. Water Res. 95, 142-149. https://doi.org/10.1016/j.watres.2016.02.055. · DOI · Paper page
  13. Kaboré, H.A., Duy, S.V., Munoz, G., Méité, L., Desrosiers, M., Liu, J., Sory, T.K., Sauvé, S., 2018. Worldwide drinking water occurrence and levels of newly-identified perfluoroalkyl and polyfluoroalkyl substances. Sci. Total Environ. 616, 1089-1100. https://doi.org/10. 1016/j.scitotenv.2017.10.210. · DOI · Paper page
  14. Kämpfer, P., Falsen, E., Frischmann, A., Busse, H.J., 2012. Dietzia aurantiaca sp. nov., isolated from a human clinical specimen. Int. J. Syst. Evol. Microbiol. 62 (Pt_3), 484-488. https:// doi.org/10.1099/ijs.0.032557-0. · DOI
  15. Key, B.D., Howell, R.D., Criddle, C.S., 1998. Defluorination of organofluorine sulfur com- pounds by Pseudomonas sp. strain D2. Environ. Sci. Technol. 32 (15), 2283-22871.
  16. Koch, D.J., Ruckert, C., Rey, D.A., Mix, A., Puhler, A., Kalinowski, J., 2005. Role of the ssu and seu genes of Corynebacterium glutamicum ATCC 13032 in utilization of sulfonates and sulfonate esters as sulfur sources. Appl. Environ. Microbiol. 71 (10), 6104-6114.
  17. Kumar, S., Stecher, G., Tamura, K., 2016. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol. Biol. Evol. 33 (7), 1870-1874.
  18. Li, J., Zhao, G.Z., Zhang, Y.Q., Klenk, H.P., Pukall, R., Qin, S., Xu, L.H., Li, W.J., 2008. Dietzia schimae sp. nov. and Dietzia cercidiphylli sp. nov., from surface-sterilized plant tissues. Int. J. Syst. Evol. Microbiol. 58 (11), 2549-2554. https://doi.org/10.1016/j.syapm. 2008.11.007. · DOI
  19. Li, J., Chen, C., Zhao, G.Z., Klenk, H.P., Pukall, R., Zhang, Y.Q., et al., 2009. Description of Dietzia lutea sp. nov., isolated from a desert soil in Egypt. Syst. Appl. Microbiol. 32 (2), 118-123. https://doi.org/10.1016/j.syapm.2008.11.007. · DOI
  20. Mackay, G.M., Zheng, L., Van Den Broek, N.J., Gottlieb, E., 2015. Analysis of cell metabolism using LC-MS and isotope tracers. Methods Enzymol. 561, 171-196. https://doi.org/10. 1016/bs.mie.05.016. · DOI
  21. Martin, J.W., Mabury, S.A., O'Brien, P.J., 2005. Metabolic products and pathways of fluorotelomer alcohols in isolated rat hepatocytes. Chem. Biol. Interact. 155 (3), 165-180. https://doi.org/10.1016/j.cbi.2005.06.007. · DOI
  22. Mayilraj, S., Suresh, K., Kroppenstedt, R.M., Saini, H.S., 2006. Dietzia kunjamensis sp. nov., isolated from the Indian Himalayas. Int. J. Syst. Evol. Microbiol. 56 (7), 1667-1671.
  23. Mejia-Avendaño, S., Munoz, G., Vo Duy, S., Desrosiers, M., Sauvé, S., Liu, J., Benoıt, P., 2017. Novel fluoroalkylated surfactants in soils following firefighting foam deployment during the Lac-Megantic railway accident. Environ. Sci. Technol. 51 (15), 8313-8323. https:// doi.org/10.1021/acs.est.7b02028. · DOI · Paper page
  24. Nazina, T.N., Shumkova, E.S., Sokolova, D.S., Babich, T.L., Zhurina, M.V., Xue, Y.F., Osipov, G.A., Poltaraus, A.B., Tourova, T.P., 2015. Identification of hydrocarbon-oxidizing Dietzia bacteria from petroleum reservoirs based on phenotypic properties and analysis of the 16S rRNA and gyrB genes. Microbiology 84 (3), 377-388. https://doi.org/10.1134/ S0026261715030145. · DOI
  25. O'Carroll, D.M., Jeffries, T.C., Lee, M.J., Le, S.T., Yeung, A., Wallace, S., Battye, N., Patch, D.J., Manefield, M.J., Weber, K.P., 2020. Developing a roadmap to determine per-and polyfluoroalkyl substances-microbial population interactions. Sci. Total Environ. 712, 135994. https://doi.org/10.1016/j. scitotenv.2019.135994. · DOI
  26. Park, J., Piehowski, P.D., Wilkins, C., Zhou, M., Mendoza, J., Fujimoto, G.M., Gibbons, B.C., Shaw, J.B., Shen, Y., Shukla, A.K., Moore, R.J., 2017. Informed-proteomics: open- source software package for top-down proteomics. Nat. Methods 14 (9), 909-914.
  27. Park, C., Shin, B., Park, W., 2020. Protective role of bacterial alkanesulfonate monooxygenase under oxidative stress. Appl. Environ. Microbiol. 86 (15), e00692-20. https://doi.org/10. 1128/AEM.00692-20. · DOI
  28. Pukall, R., 2014. The family Dietziaeae. In: DeLong, E., Lory, S., Stackebrandt, E., Thompson, F. (Eds.), The Prokaryotes: Actinobacteria, Fourth edition 17. Springer, Berlin Heidelberg, p. 335 327-337.
  29. Seemann, T., 2014. Prokka: rapid prokaryotic genome annotation. Bioinformatics 30 (14), 2068-2069.
  30. Shaw, D.M., Munoz, G., Bottos, E.M., Duy, S.V., Sauvé, S., Liu, J.Van, Hamme, J.D., 2019. Deg- radation and defluorination of 6: 2 fluorotelomer sulfonamidoalkyl betaine and 6: 2 fluorotelomer sulfonate by Gordonia sp. Strain NB4-1Y under sulphur-limiting condi- tions. Sci. Total Environ. 647, 690-698. https://doi.org/10.1016/j.scitotenv.2018.08. 012. · DOI · Paper page
  31. Tamura, K., Nei, M., 1993. Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Mol. Biol. Evol. 10 (3), 512-526.
  32. Thakur, A., Somai, S., Yue, K., Ippolito, N., Pagan, D., Xiong, J., et al., 2020. Substrate- dependent mobile loop conformational changes in alkanesulfonate monooxygenase from accelerated molecular dynamics. Biochemistry 59 (38), 3582-3593. https://doi. org/10.1021/acs.biochem.0c00633. · DOI
  33. Tyanova, S., Temu, T., Sinitcyn, P., Carlson, A., Hein, M.Y., Geiger, T., Mann, M., Cox, J., 2016. The Perseus computational platform for comprehensive analysis of (prote) omics data. Nat. Methods 13 (9), 731-740.
  34. Van Hamme, J.D., Bottos, E.M., Bilbey, N.J., Brewer, S.E., 2013. Genomic and proteomic characterization of Gordonia sp. NB4-1Y in relation to 6:2 fluorotelomer sulfonate bio- degradation. Microbiology 159 (Pt_8), 1618-1628. https://doi.org/10.1099/mic.0. 068932-0. · DOI · Paper page
  35. Wang, X.B., Chi, C.Q., Nie, Y., Tang, Y.Q., Tan, Y., Wu, G., Wu, X.L., 2011b. Degradation of petroleum hydrocarbons (C6-C40) and crude oil by a novel dietzia strain. Bioresour. Technol. 102 (17), 7755-7761. https://doi.org/10.1016/j.biortech.2011.06.009. · DOI
  36. Wiśniewski, J.R., 2017. Filter-aided sample preparation: the versatile and efficient method for proteomic analysis. Methods Enzymol. 585, 15-27. https://doi.org/10.1016/bs.mie. 2016.09.013. · DOI
  37. Wiśniewski, J.R., Zougman, A., Nagaraj, N., Mann, M., 2009. Universal sample preparation method for proteome analysis. Nat. Methods 6 (5), 359-362.
  38. Yang, S.H., Shi, Y., Strynar, M., Chu, K.H., 2021. Desulfonation and defluorination of 6: 2 fluorotelomer sulfonic acid (6: 2 FTSA) by Rhodococcus jostii RHA1: carbon and sulphur sources, enzymes, and pathways. J. Hazard. Mater. 423, 127052. https://doi.org/10. 1016/j.jhazmat.2021.127052. · DOI · Paper page
  39. Yoon, S.H., Ha, S.M., Kwon, S., Lim, J., Kim, Y., Seo, H., Chun, J., 2017. Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole- genome assemblies. Int. J. Syst. Evol. Microbiol. 67 (5), 1613. https://doi.org/10. 1099/ijsem.0.001755. · DOI
  40. Yumoto, I., Nakamura, A., Iwata, H., Kojima, K., Kusumoto, K., Nodasaka, Y., Matsuyama, H., 2002. Dietzia psychralcaliphila sp. nov., a novel, facultatively psychrophilic alkaliphile that grows on hydrocarbons. Int. J. Syst. Evol. Microbiol. 52 (1), 85-90. https://doi. org/10.1099/00207713-52-1-85. · DOI
  41. Zhang, S., Lu, X., Wang, N., Buck, R.C., 2016. Biotransformation potential of 6:2 fluorotelomer sulfonate (6:2 FTSA) in aerobic and anaerobic sediment. Chemosphere 154, 224-230. https://doi.org/10.1016/j.chemosphere.2016.03.062. · DOI · Paper page

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Authors
Méndez, V., Holland, S., Bhardwaj, S., McDonald, J., Khan, S., O'Carroll, D., Pickford, R., Richards, S., O'Farrell, C., Coleman, N., Lee, M., & Manefield, M. J.
Affiliations
  • UNSW Sydney (AU)
  • The University of Sydney (AU)
Corresponding author
Manefield, Michael J.
Venue
Science of The Total Environment
Publisher
Elsevier BV
Published
2022-07
Volume
829
Pages
154587
ISSN
0048-9697 (ISSN-L)
OpenAlex
W4220981198
Cited by
85
References
4
Citations by year
2026: 16 · 2025: 34 · 2024: 23 · 2023: 9 · 2022: 3
FWCI
6.01
Type
journal article
Language
en
Open access
Locations
  • The Science of The Total Environment (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • UNSWorks (University of New South Wales, Sydney, Australia) (submittedVersion, cc-by-nc-nd)
Funders
Australian Research Council (LP170100116)
Topics
  • Physical Sciences › Environmental Science › Environmental Chemistry › Per- and polyfluoroalkyl substances research
  • Physical Sciences › Environmental Science › Pollution › Microbial bioremediation and biosurfactants
  • Physical Sciences › Environmental Science › Environmental Chemistry › Environmental Chemistry and Analysis
Keywords
6:2 fluorotelomer sulfonate, aerobic biodegradation, aqueous film-forming foam, landfill leachate, ABC transporters, degradation products, perfluorinated carboxylic acids, actinobacteria
MeSH terms
Alkanesulfonates, Biotransformation, Fluorocarbons, Mixed Function Oxygenases, RNA, Ribosomal, 16S, Sulfur, Water Pollutants, Chemical, ATP-Binding Cassette Transporters, Membrane Transport Proteins, Actinobacteria, Proteomics

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