Abstract
Tributyl phosphate (TBP) is an organophosphorous compound, used extensively (3000–5000 tonnes/annum) as a solvent for nuclear fuel processing and as a base stock in the formulation of fire-resistant aircraft hydraulic fluids and other applications. Because of its wide applications and relative stability in the natural environment TBP poses the problem of pollution and health hazards. In the present study, fifteen potent bacterial strains capable of using tributyl phosphate (TBP) as sole carbon and phosphorus source were isolated from enrichment cultures. These isolates were identified on the basis of biochemical and morphological characteristics and 16S rRNA gene sequence analysis. Phylogenetic analysis of 16S rRNA gene sequences revealed that two isolates belonged to class Bacilli and thirteen to β and γ-Proteobacteria. All these isolates were found to be members of genera Alcaligenes, Providencia, Delftia, Ralstonia, and Bacillus. These isolates were able to tolerate and degrade up to 5 mM TBP, the highest concentration reported to date. The GC–MS method was developed to monitor TBP degradation. Two strains, Providencia sp. BGW4 and Delftia sp. BGW1 showed respectively, 61.0 ± 2.8% and 57.0 ± 2.0% TBP degradation within 4 days. The degradation rate constants, calculated by first order kinetic model were between 0.0024 and 0.0099 h−1. These bacterial strains are novel for TBP degradation and could be used as an important bioresource for efficient decontamination of TBP polluted waste streams.
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Acknowledgments
Kedar Ahire acknowledges the Council of Scientific and Industrial Research (CSIR), Government of India and Board of College and University Development (BCUD), University of Pune for the financial assistance. Authors thank Dr. Vijay Kolekar, In-charge, Insecticide Residue Testing Laboratory, Pune (Govt. of India) for GC–MS facility.
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Ahire, K.C., Kapadnis, B.P., Kulkarni, G.J. et al. Biodegradation of tributyl phosphate by novel bacteria isolated from enrichment cultures. Biodegradation 23, 165–176 (2012). https://doi.org/10.1007/s10532-011-9496-7
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DOI: https://doi.org/10.1007/s10532-011-9496-7