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Chemical and microbial community analysis during aerobic biostimulation assays of non-sulfonated alkyl-benzene-contaminated groundwater

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Abstract

A chemical and microbial characterization of lab-scale biostimulation assays with groundwater samples taken from an industrial site in which the aquifer had been contaminated by linear non-sulfonate alkyl benzenes (LABs) was carried out for further field-scale bioremediation purposes. Two lab-scale biodegradability assays were performed, one with a previously obtained gas-oil-degrading consortium and another with the native groundwater flora. Results for the characterization of the groundwater microbial population of the site revealed the presence of an important LAB-degrading microbial population with a strong degrading capacity. Among the microorganisms identified at the site, the detection of Parvibaculum lavamentivorans, which have been described in other studies as alkyl benzene sulfonates degraders, is worth mentioning. Incubation of P. lavamentivorans DSMZ13023 with LABs as reported in this study shows for the first time the metabolic capacity of this strain to degrade such compounds. Results from the biodegradation assays in this study showed that the indigenous microbial population had a higher degrading capacity than the gas-oil-degrading consortium, indicating the strong ability of the native community to adapt to the presence of LABs. The addition of inorganic nutrients significantly improved the aerobic biodegradation rate, achieving levels of biodegradation close to 90%. The results of this study show the potential effectiveness of oxygen and nutrients as in situ biostimulation agents as well as the existence of a complex microbial community that encompasses well-known hydrocarbon- and LAS-degrading microbial populations in the aquifer studied.

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References

  • Albaigés J, Farrán A, Soler M, Gallifa A, Martin P (1987) Accumulation and distribution of biogenic and pollutant hydrocarbons, PCBs and DDT in tissues of western Mediterranean fishes. Mar Environ Res 22:1–18

    Article  Google Scholar 

  • Altschul SF, Gish W, Miller W, Meyers EW, Lipman DJ (1990) Basic local alignment search tool. J Microbiol Methods 215:403–410

    CAS  Google Scholar 

  • Bayona J, Albaigés J, Grifoll M, Solanas AM (1986) Selective aerobic degradation of linear alkyl benzenes by pure microbial cultures. Chemosphere 15(5):595–598

    Article  CAS  Google Scholar 

  • Cain RB (1987) Biodegradation of anionic surfactants. Biochem Soc Trans 15:7S–22S

    Google Scholar 

  • Douros JD, Frankenfeld JW (1968) Oxidation of alkyl benzenes by a strain of Micrococcus cerificans growing on n-paraffins. Appl Environ Microbiol 16:532–533

    CAS  Google Scholar 

  • Eganhouse RP, Blumfield DL, Kaplan IR (1983) Long-chain alkyl benzenes as molecular tracers of domestic wastes in the marine environment. Environ Sci Technol 17:523–530

    Article  CAS  Google Scholar 

  • Feng Y, Khoo HE, Pohl CL (1999) Purification and characterization of gentisate 1,2-dioxygenases from Pseudomonas alcaligenes NCIB 9867 and Pseudomonas putida NCIB 9869. Appl Environ Microbiol 65:946–950

    CAS  Google Scholar 

  • Gordon L, Dobson ADW (2001) Fluoranthene degradation in Pseudomonas alcaligenes PA-10. Biodegradation 12:393–400

    Article  CAS  Google Scholar 

  • Hall TA (1999) BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series 41:95–98

  • Hareland W, Crawford RL, Chapman PJ, Dagley S (1975) Metabolic function and properties of 4-hydroxyphenylacetic acid 1-hydroxylase from Pseudomonas acidovorans. J Bacteriol 121:272–285

    CAS  Google Scholar 

  • Huddleston RL, Allred RC (1963) Microbial oxidation of sulfonated alkyl benzenes. Dev Ind Microbiol 4:24–38

    Google Scholar 

  • Ishiwatari R, Takada H, Yun S, Matsumoto E (1983) Alkyl benzene pollution of Tokyo Bay sediments. Nature 301:599–600

    Article  CAS  Google Scholar 

  • Kabelitz N, Machackova J, Imfeld G, Brennerova M, Pieper DH, Heipieper HJ, Junca J (2009) Enhancement of the microbial community biomass and diversity during air sparging bioremediation of a Northern Bohemia soil highly contaminated with kerosene and BTEX. Appl Microbiol Biotechnol 82:565–577

    Article  CAS  Google Scholar 

  • Maidak BL, Cole JR, Lilburn TG, Parker CT, Saxman PR, Stredwick JM, Garrity GM GM, Li B, Olsen GJ, Pramanik S, Schmidt TM, Tiedje J (2000) The RDP (Ribosomal Database Project) continues. Nucleic Acid Res 28:173–174

    Article  CAS  Google Scholar 

  • Owsianiaka M, Chrzanowskia L, Szulca A, Staniewskia J, Olszanowskia A, Olejnik-Schmidtb AK, Hermann J, Heipieperc HJ (2009) Biodegradation of diesel/biodiesel blends by a consortium of hydrocarbon degraders: effect of the type of blend and the addition of biosurfactants. Bioresour Technol 10:1497–1500

    Article  Google Scholar 

  • Painter HA (1992) Anionic surfactants. In: de Oude NT (ed) The handbook of environmental chemistry. Springer, Berlin, pp 1–88

    Google Scholar 

  • Schleheck D, Tindall BJ, Rosselló-Mora R, Cook AM (2004) Parvibaculum lavamentivorans gen. nov., sp. nov., a novel heterotroph that initiates catabolism of linear alkyl benzene sulfonate. Int J Syst Evol Microbiol 54:1489–1497

    Article  CAS  Google Scholar 

  • Szoboszlay S, Atzél B, Kukolya J, Tóth EM, Márialigeti K, Schumann P, Kriszt B (2008) Chryseobacterium hungaricum sp. nov., isolated from hydrocarbon-contaminated soil. Int J Syst Evol Microbiol 58:2748–2754

    Article  CAS  Google Scholar 

  • Takada H, Ishiwatari R (1987) Linear alkyl benzenes in urban riverine environments in Tokyo: distribution, source and behaviour. Environ Sci Technol 21:875–883

    Article  CAS  Google Scholar 

  • Takada H, Ishiwatari R (1990) Biodegradation experiments of linear alkyl benzenes (LABs): isomeric composition of C13 LABs as an indicator of the degree of LAB degradation in the aquatic environment. Environ Sci Technol 24:86–91

    Article  CAS  Google Scholar 

  • Viñas M, Grifoll M, Sabate J, Solanas AM (2002) Biodegradation of a crude oil by three microbial consortia of different origins and metabolic capabilities. J Ind Microbiol Biotechnol 28(5):252–260

    Article  Google Scholar 

  • Viñas M, Sabaté J, Espuny MJ, Solanas AM (2005) Bacterial community dynamics and PAHs degradation during bioremediation of a heavily creosote-contaminated soil. App Environ Microbiol 71:7008–7018

    Article  Google Scholar 

  • White GF, Russell NJ (1994) Biodegradation of anionic surfactants and related molecules. In: Ratledge C (ed) Biochemistry of microbial degradation. Kluwer, Dordrecht, pp 143–177

    Google Scholar 

  • Wrenn BA, Venosa AD (1996) Selective enumeration of aromatic and aliphatic hydrocarbon degrading bacteria by a most-probable number procedure. Can J Microbiol 42:252–258

    Google Scholar 

  • Yu Z, Morrison M (2004) Comparisons of different hypervariable regions of rrs genes for use in fingerprinting of microbial communities by PCR-denaturing gradient gel electrophoresis. Appl Environ Microbiol 70:4800–4806

    Google Scholar 

  • Zhao B, Yeo CC, Poh CL (2005) Proteome investigation of the global regulatory role of σ54 in response to gentisate induction in Pseudomonas alcaligenes NCIMB 9867. Proteomics 5:1868–1876

    Google Scholar 

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Acknowledgement

This research was funded by a grant from the National Plan for Research of the Spanish Government. E.M. was a recipient of a doctoral fellowship from the Spanish Ministry of Education. The work was financially supported by the Spanish Ministry of Environment (094/PC08/3-01.1). The authors would like to thank Miriam Guivernau (GIRO Technological Center, Barcelona, Spain) for her assistance in PCR–DGGE profiling and ribotype sequencing.

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Correspondence to A. M. Solanas.

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Martínez-Pascual, E., Jiménez, N., Vidal-Gavilan, G. et al. Chemical and microbial community analysis during aerobic biostimulation assays of non-sulfonated alkyl-benzene-contaminated groundwater. Appl Microbiol Biotechnol 88, 985–995 (2010). https://doi.org/10.1007/s00253-010-2816-8

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  • DOI: https://doi.org/10.1007/s00253-010-2816-8

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