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Biodegradation of 1,4-dioxane by a Flavobacterium

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Abstract

A dioxane-degrading consortium was enriched from soil obtained from a contaminated groundwater plume. The enriched consortium did not use dioxane as the sole source of carbon and energy but co-metabolized dioxane in the presence of tetrahydrofuran (THF). THF and dioxane concentrations up to 1000 ppm were degraded by the enriched consortium in about 2 weeks with a longer lag phase observable at 1000 ppm. Three colonies from the enriched consortium were then obtained on agar plates containing basal salts and glucose as the carbon source. Only one of the three colonies was capable of dioxane degradation. Further enrichment of this colony in liquid media led to a pure culture that grew on glucose and co-metabolically degraded dioxane after THF degradation. The rate and extent of dioxane degradation of this isolate increased with increasing THF concentration. This isolate was subsequently identified as a Flavobacterium by 16S rDNA sequencing. Using polymerase chain reaction (PCR) and denaturing gradient gel electrophoresis (DGGE) analysis of microbial populations, Flavobacterium was determined to be the dominant species in the enriched consortium and was distinct from the two other colonies that did not degrade dioxane. This is the first report of a dioxane-degrading Flavobacterium which is phylogenetically distinct from any previously identified dioxane degrader.

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Acknowledgments

The authors acknowledge the financial support of Malroz Engineeering, Kingston, Ontario, OCE and Queen’s University for financial support to B. Sun. We thank Patricia Yeung for her help to prepare cultures and dioxane analysis and Dr. C. Greer and his research team at Biotechnology Research Institute (Montreal, Canada) for technical advice in PCR-DGGE analysis.

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Correspondence to Juliana A. Ramsay.

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Sun, B., Ko, K. & Ramsay, J.A. Biodegradation of 1,4-dioxane by a Flavobacterium . Biodegradation 22, 651–659 (2011). https://doi.org/10.1007/s10532-010-9438-9

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