Study of an aquifer contaminated by ethyl tert-butyl ether (ETBE): Site characterization and on-site bioremediation
2012
Fayolle-Guichard, Françoise | Durand, Jonathan | Cheucle, Mathilde | Rosell, Mònica | Julien Michelland, Rory | Tracol, Jean-Philippe | Le Roux, Françoise | Grundman, Geneviève | Atteia, Olivier | H. Richnow, Hans | Dumestre, Alain | Benoit, Yves | IFP Energies nouvelles (IFPEN) ; IFP Energies nouvelles (IFPEN) | Environnement, Géo-ingénierie et Développement (EGID) | SERPOL ; SERPOL | DEPARTMENT OF ISOTOPE BIOGEOCHEMISTRY ; Centre for Environmental Research | Laboratoire d'Ecologie Microbienne - UMR 5557 (LEM) ; Institut National de la Recherche Agronomique (INRA)-Université Claude Bernard Lyon 1 (UCBL) ; Université de Lyon-Université de Lyon-Ecole Nationale Vétérinaire de Lyon (ENVL)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)
International audience
Afficher plus [+] Moins [-]anglais. Ethyl tert-butyl ether (ETBE) was detected at high concentration (300 mg L−1) in the groundwater below a gas-station. No significant carbon neither hydrogen isotopic fractionation of ETBE was detected along the plume. ETBE and BTEX biodegradation capacities of the indigenous microflora Pz1-ETBE and of a culture (MC-IFP) composed of Rhodococcus wratislaviensis IFP 2016, Rhodococcus aetherivorans IFP 2017 and Aquincola tertiaricarbonis IFP 2003 showed that ETBE and BTEX degradation rates were in the same range (ETBE: 0.91 and 0.83 mg L−1 h−1 and BTEX: 0.64 and 0.82 mg L−1 h−1, respectively) but tert-butanol (TBA) accumulated transiently at a high level using Pz1-ETBE (74 mg L−1). An on-site pilot plant (2 m3) filled with polluted groundwater and inoculated by MC-IFP, successfully degraded four successive additions of ETBE and gasoline. However, an insignificant ETBE isotopic fractionation was also accompanying this decrease which suggested the involvement of low fractionating-strains using EthB enzymes, but required of additional proofs. The ethB gene encoding a cytochrome P450 involved in ETBE biodegradation (present in R. aetherivorans IFP 2017) was monitored by quantitative real-time polymerase chain reaction (q-PCR) on DNA extracted from water sampled in the pilot plant which yield up to 5 × 106 copies of ethB gene per L−1.
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