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19F NMR study on the biodegradation of fluorophenols by various Rhodococcus species

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Abstract

Of all NMR observable isotopes 19F is the one perhaps most convenient for studies on biodegradation of environmental pollutants. The reasons underlying this potential of 19F NMR are discussed and illustrated on the basis of a study on the biodegradation of fluorophenols by four Rhodococcus strains. The results indicate marked differences between the biodegradation pathways of fluorophenols among the various Rhodococcus species. This holds not only for the level and nature of the fluorinated biodegradation pathway intermediates that accumulate, but also for the regioselectivity of the initial hydroxylation step. Several of the Rhodococcus species contain a phenol hydroxylase that catalyses the oxidative defluorination of ortho-fluorinated di- and trifluorophenols. Furthermore, it is illustrated how the 19F NMR technique can be used as a tool in the process of identification of an accumulated unknown metabolite, in this case most likely 5-fluoromaleylacetate. Altogether, the 19F NMR technique proved valid to obtain detailed information on the microbial biodegradation pathways of fluorinated organics, but also to provide information on the specificity of enzymes generally considered unstable and, for this reason, not much studied so far.

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References

  • Banks RE & Tatlow JC (1994) Synthesis of organofluorine compounds. In: Banks RE, Smart B & Tatlow JC (Eds) Organofluorine Chemistry: Principles and Commercial Applications (pp 25–57). Plenum Press, New York

    Google Scholar 

  • Banks RE (1995) Fluorine in Agriculture. Conference Papers, The University of Manchester, Institute of Science and Technology, Fluorine Technology Lmt, UK

    Google Scholar 

  • Banks RE & Lowe KC (1994) Fluorine inMedicine in the 21st Century. Conference Papers, The University of Manchester, Institute of Science and Technology, Fluorine Technology Lmt, UK

    Google Scholar 

  • Bartels I, Knackmuss HJ & Reineke W (1984) Suicide inactivation of catechol 2,3-dioxygenase from Pseudomonas putida mt-2 by 3-halocatechols. Appl. Environ. Microbiol. 47, 500–505

    Google Scholar 

  • Blasco R, Wittich R-M, Mallavarapu M, Timmis KN & Pieper DH (1995) From xenobiotic to antibiotic, formation of protoanemonin from 4-chlorocatechol by enzymes of the 3-oxoadipate pathway. J. Biol. Chem. 270: 29229–29235

    Google Scholar 

  • Boersma MG, Dinarieva TY, Middelhoven WJ, van Berkel WJH, Doran J, Vervoort J & Rietjens IMCM (1998) 19F nuclear magnetic resonance as a tool to investigate the microbial degradation of fluorophenols to fluorocatechols and fluoromuconates. Appl. Environ. Microbiol. 64: 1256–1263

    Google Scholar 

  • Clarke KF, Gallely AG, Livingstone A & Fewson CA (1975) Metabolism of monofluorobenzoates by Acinetobacter calcoaceticus N.C.I.B. 8250. Biochim. Biophys Acta 404: 169–179

    Google Scholar 

  • Edwards PN (1994) Uses of fluorine in chemotherapy. In: Banks RE, Smart B & Tatlow JC (Eds) Organofluorine Chemistry: Principles and Commercial Applications (pp 501–542). Plenum Press, New York

    Google Scholar 

  • Engesser KH, Auling G, Busse J & Knackmuss HJ (1990) 3-Fluorobenzoate enriched bacterial strain FLB 300 degrades benzoate and all three isomeric monofluorobenzoates. Arch. Microbiol. 153: 193–199

    Google Scholar 

  • Goldman P, Milne GWA & Pignataro MT (1967) Fluorine containing metabolites formed from 2-fluorobenzoic acid by Pseudomonas species. Arch. Biochem. Biophys. 118: 178–184

    Google Scholar 

  • Gorlatov S, Maltseva O, Shevchenko V & Golovleva L (1989) Degradation of chlorophenols by a culture of Rhodococcus erythropolis. Microbiology (Engl. Transl. Mikrobiologiya) 58: 647–651

    Google Scholar 

  • Harper DB & Blakley ER (1971) The metabolism of p-fluorobenzoic acid by Pseudomonas sp. Can. J. Microbiol. 17: 1015–1023

    Google Scholar 

  • Ivoilov VS, Karasevich YN & Surovtseva EG (1987) Conversion and utilization of 4-fluorobenzoic acid by Corynebacterium fascians. Microbiology (Engl. Transl. Mikrobiologiya) 56: 199–204

    Google Scholar 

  • Janke D., Al-Mofarji T, Straube G, Schuman P & Prauser H (1988) Critical steps in degradation of chloroaromatics by rhodococci. I. Initial enzyme reactions involved in catabolism of aniline, phenol and benzoate by Rhodococcus sp. An 117 and An 213. J. Basic Microbiol. 28: 509–518

    Google Scholar 

  • Kaschabek SR & Reineke W (1995) Maleylacetate reductase of Pseudomonas sp. strain B13: specificity of substrate conversion and halide elimination. J. Bacteriol. 177: 320–325

    Google Scholar 

  • Key BD, Howell RD & Criddle CS (1997) Fluorinated organics in the biosphere. Environ. Sci. Techn. 31: 2445–2454

    Google Scholar 

  • Malet-Martino MC & Martino R (1989) The application of nuclear magnetic resonance spectroscopy to drug metabolism studies. Xenobiotica 19: 583–607

    Google Scholar 

  • Nakai C, Nakazawa T & Nozaki M (1988) Purification and properties of catechol 1,2-dioxygenase (pyrocatechase) from Pseudomonas putida mt-2 in comparison with that from Pseudomonas arvilla C-1. Arch. Biochem. Biophys. 267: 701–713

    Google Scholar 

  • Oltmanns RH, Müller R, Otto MK & Lingens F. (1989) Evidence for a new pathway in the bacterial degradation of 4-fluorobenzoate. Appl. Environ. Microbiol. 55: 2499–2504

    Google Scholar 

  • Peelen S, Rietjens IMCM, Boersma MG & Vervoort J (1995) Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics. Eur. J. Biochem. 227: 284–291

    Google Scholar 

  • Prucha M, Peterseim A, Timmis KN & Pieper DH (1996) Muconolactone isomerase of the 3-oxoadipate pathway catalyzes dechlorination of 5-chlorosubstituted muconolactones. Eur. J. Biochem. 237: 350–356

    Google Scholar 

  • Rietjens IMCM, Cnubben NHP, de Jager PA, Boersma MG & Vervoort J (1993) Applications of NMR in biotransformation studies. In: Weitzner MI (Ed) Developments and ethical considerations in toxicology (pp 94–109)

  • Schlömann M, Schmidt E & Knackmuss H-J (1990a) Different types of dienelactone hydrolase in 4-fluorobenzoate utilizing bacteria. J. Bacteriol. 172: 5112–5118

    Google Scholar 

  • Schlömann M, Fischer P, Schmidt E & Knackmuss H-J (1990b) Enzymatic formation, stability, and spontaneous reactions of 4-fluoromuconolactone, a metabolite of the bacterial degradation of 4-fluorobenzoate. J. Bacteriol. 172: 5119–5129

    Google Scholar 

  • Schmidt E & Knackmuss H-J (1980) Chemical structure and biodegradability of halogenated aromatic compounds. Conversion of chlorinated muconic acids into maleoylacetic acid. Biochem. J. 192: 339–347

    Google Scholar 

  • Schreiber A, Dorn MHE, Reineke W & Knackmuss H-J (1980) Critical reactions in fluorobenzoic acid degradation by Pseudomonas sp B13. Appl. Environ. Microbiol. 39: 58–67

    Google Scholar 

  • Sejlitz T & Neujahr HY (1987) Phenol hydroxylase from yeast. A model for phenol binding and an improved purification procedure. Eur. J. Biochem. 170: 343–349

    Google Scholar 

  • Solyanikova IP, Maltseva OV, Vollmer MD, Golovleva LA & Schlömann M (1995) Characterization of muconate and chloromuconate cycloisomerase from Rhodococcus erythropolis 1CP: indications for functionally convergent evolution among bacterial cycloisomerases. J. Bacteriol. 177: 2821–2826

    Google Scholar 

  • Straube G (1987) Phenol hydroxylases from Rhodococcus sp. P1. J. Basic Microbiol. 27: 229–232

    Google Scholar 

  • Van Berkel WJH, Eppink MHM, Middelhoven WJ, Vervoort J & Rietjens IMCM (1994) Catabolism of 4-hydroxybenzoates in Candida parapsilosis proceeds through initial oxidative decarboxylation by a FAD-dependent 4-hydroxybenzoate 1-hydroxylase. FEMS Microb Lett 121: 207–215

    Google Scholar 

  • Vervoort J, de Jager PA, Steenbergen J & Rietjens IMCM (1990) Development of a 19F-NMR method for studies on the in vivo and in vitro metabolism of 2-fluoroaniline. Xenobiotica 20: 657–670

    Google Scholar 

  • Vollmer MD, Fischer P, Knackmuss H-J & Schlömann M (1994) Inability of muconate cycloisomerases to cause dehalogenation during conversion of 2-chloro-cis,cis-muconate. J. Bacteriol. 176: 4366–4375

    Google Scholar 

  • Vollmer MD & Schlömann M (1995) Conversion of 2-chloro-cis,cis-muconate and its metabolites 2-chloro-and 5-chloromuconolactone by chloromuconate cycloisomerases of pJP4 and pAC27. J. Bacteriol. 177: 2938–2941

    Google Scholar 

  • Walker SB (Ed) (1990) Fluorine Compounds as Agrochemicals. Fluorochem Lmtd. Derbyshire.

    Google Scholar 

  • Walsh TA & Ballou DP (1983) Halogenated protocatechuates as substrates for protocatechuate dioxygenase from Pseudomonas cepacia. J. Biol. Chem. 258: 14413–14421

    Google Scholar 

  • Walsh TA, Ballou DP, Mayer R & Que L Jr (1983) Rapid reaction studies on the oxygenation reactions of catechol dioxygenase. J. Biol. Chem. 258: 14422–14427

    Google Scholar 

  • Wray V (1983) Fluorine-19 nuclear magnetic resonance spectroscopy. In: Webb GA (Ed) Annual Reports on NMR Spectroscopy, Vol 14. (pp 149–191). Academic Press Inc., London

    Google Scholar 

Download references

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Bondar, V.S., Boersma, M.G., Golovlev, E.L. et al. 19F NMR study on the biodegradation of fluorophenols by various Rhodococcus species. Biodegradation 9, 475–486 (1998). https://doi.org/10.1023/A:1008391906885

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