4.7 Article

Successful operation of continuous reactors at short retention times results in high-density, fast-rate Dehalococcoides dechlorinating cultures

Journal

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
Volume 98, Issue 6, Pages 2729-2737

Publisher

SPRINGER
DOI: 10.1007/s00253-013-5263-5

Keywords

Chemostat; Dehalococcoides; Geobacter; Organohalide respiration; Bioremediation; Microbial community management

Funding

  1. National Science Foundation CAREER [1053939]
  2. School for Engineering of Matter, Transport and Energy at Arizona State University
  3. Directorate For Engineering
  4. Div Of Chem, Bioeng, Env, & Transp Sys [1053939] Funding Source: National Science Foundation

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The discovery of Dehalococcoides mccartyi reducing perchloroethene and trichloroethene (TCE) to ethene was a key landmark for bioremediation applications at contaminated sites. D. mccartyi-containing cultures are typically grown in batch-fed reactors. On the other hand, continuous cultivation of these microorganisms has been described only at long hydraulic retention times (HRTs). We report the cultivation of a representative D. mccartyi-containing culture in continuous stirred-tank reactors (CSTRs) at a short, 3-d HRT, using TCE as the electron acceptor. We successfully operated 3-d HRT CSTRs for up to 120 days and observed sustained dechlorination of TCE at influent concentrations of 1 and 2 mM TCE to a parts per thousand yen97 % ethene, coupled to the production of 10(12) D. mccartyi cells L-culture (-1). These outcomes were possible in part by using a medium with low bicarbonate concentrations (5 mM) to minimize the excessive proliferation of microorganisms that use bicarbonate as an electron acceptor and compete with D. mccartyi for H-2. The maximum conversion rates for the CSTR-produced culture were 0.13 +/- 0.016, 0.06 +/- 0.018, and 0.02 +/- 0.007 mmol Cl- L-culture (-1) h(-1), respectively, for TCE, cis-dichloroethene, and vinyl chloride. The CSTR operation described here provides the fastest laboratory cultivation rate of high-cell density Dehalococcoides cultures reported in the literature to date. This cultivation method provides a fundamental scientific platform for potential future operations of such a system at larger scales.

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