Literature DB >> 12523427

Field demonstration of successful bioaugmentation to achieve dechlorination of tetrachloroethene to ethene.

David W Major1, Michaye L McMaster, Evan E Cox, Elizabeth A Edwards, Sandra M Dworatzek, Edwin R Hendrickson, Mark G Starr, Jo Ann Payne, Lois W Buonamici.   

Abstract

A laboratory microcosm study and a pilot scale field test were conducted to evaluate biostimulation and bioaugmentation to dechlorinate tetrachloroethene (PCE) to ethene at Kelly Air Force Base. The site groundwater contained about 1 mg/L of PCE and lower amounts of trichloroethene (TCE) and cis-1,2-dichloroethene (cDCE). Laboratory microcosms inoculated with soil and groundwater from the site exhibited partial dechlorination of TCE to cDCE when amended with lactate or methanol. Following the addition of a dechlorinating enrichment culture, KB-1, the chlorinated ethenes in the microcosms were completely converted to ethene. The KB-1 culture is a natural dechlorinating microbial consortium that contains phylogenetic relatives of Dehalococcoides ethenogenes. The ability of KB-1 to stimulate biodegradation of chlorinated ethenes in situ was explored using a closed loop recirculation cell with a pore volume of approximately 64,000 L The pilot test area (PTA) groundwater was first amended with methanol and acetate to establish reducing conditions. Under these conditions, dechlorination of PCE to cDCE was observed. Thirteen liters of the KB-1 culture were then injected into the subsurface. Within 200 days, the concentrations of PCE, TCE, and cis-1,2-DCE within the PTA were all below 5 microg/L, and ethene production accounted for the observed mass loss. The maximum rates of dechlorination estimated from field date were rapid (half-lives of a few hours). Throughout the pilot test period, groundwater samples were assayed for the presence of Dehalococcoides using both a Dehalococcoides-specific PCR assay and 16S rDNA sequence information. The sequences detected in the PTA after bioaugmentation were specific to the Dehalococcoides species in the KB-1 culture. These sequences were observed to progressively increase in abundance and spread downgradient within the PTA. These results confirm that organisms in the KB-1 culture populated the PTA aquifer and contributed to the stimulation of dechlorination beyond cDCE to ethene.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12523427     DOI: 10.1021/es0255711

Source DB:  PubMed          Journal:  Environ Sci Technol        ISSN: 0013-936X            Impact factor:   9.028


  66 in total

1.  Phylogenetic microarray analysis of a microbial community performing reductive dechlorination at a TCE-contaminated site.

Authors:  Patrick K H Lee; F Warnecke; Eoin L Brodie; Tamzen W Macbeth; Mark E Conrad; Gary L Andersen; Lisa Alvarez-Cohen
Journal:  Environ Sci Technol       Date:  2011-12-27       Impact factor: 9.028

Review 2.  In situ to in silico and back: elucidating the physiology and ecology of Geobacter spp. using genome-scale modelling.

Authors:  Radhakrishnan Mahadevan; Bernhard Ø Palsson; Derek R Lovley
Journal:  Nat Rev Microbiol       Date:  2010-12-06       Impact factor: 60.633

3.  Loop-Mediated Isothermal Amplification (LAMP) for Rapid Detection and Quantification of Dehalococcoides Biomarker Genes in Commercial Reductive Dechlorinating Cultures KB-1 and SDC-9.

Authors:  Yogendra H Kanitkar; Robert D Stedtfeld; Robert J Steffan; Syed A Hashsham; Alison M Cupples
Journal:  Appl Environ Microbiol       Date:  2016-01-08       Impact factor: 4.792

4.  Quantitative PCR targeting 16S rRNA and reductive dehalogenase genes simultaneously monitors multiple Dehalococcoides strains.

Authors:  Kirsti M Ritalahti; Benjamin K Amos; Youlboong Sung; Qingzhong Wu; Stephen S Koenigsberg; Frank E Löffler
Journal:  Appl Environ Microbiol       Date:  2006-04       Impact factor: 4.792

5.  Increasing electron donor concentration does not accelerate complete microbial reductive dechlorination in contaminated sediment with native organic carbon.

Authors:  Alexander Arthur Haluska; Kevin T Finneran
Journal:  Biodegradation       Date:  2021-06-03       Impact factor: 3.909

6.  Quantifying genes and transcripts to assess the in situ physiology of "Dehalococcoides" spp. in a trichloroethene-contaminated groundwater site.

Authors:  Patrick K H Lee; Tamzen W Macbeth; Kent S Sorenson; Rula A Deeb; Lisa Alvarez-Cohen
Journal:  Appl Environ Microbiol       Date:  2008-03-07       Impact factor: 4.792

7.  Temporal transcriptomic microarray analysis of "Dehalococcoides ethenogenes" strain 195 during the transition into stationary phase.

Authors:  David R Johnson; Eoin L Brodie; Alan E Hubbard; Gary L Andersen; Stephen H Zinder; Lisa Alvarez-Cohen
Journal:  Appl Environ Microbiol       Date:  2008-02-29       Impact factor: 4.792

8.  Correlation of Dehalococcoides 16S rRNA and chloroethene-reductive dehalogenase genes with geochemical conditions in chloroethene-contaminated groundwater.

Authors:  Bas van der Zaan; Fredericke Hannes; Nanne Hoekstra; Huub Rijnaarts; Willem M de Vos; Hauke Smidt; Jan Gerritse
Journal:  Appl Environ Microbiol       Date:  2009-12-11       Impact factor: 4.792

9.  Detection and quantification of Geobacter lovleyi strain SZ: implications for bioremediation at tetrachloroethene- and uranium-impacted sites.

Authors:  Benjamin K Amos; Youlboong Sung; Kelly E Fletcher; Terry J Gentry; Wei-Min Wu; Craig S Criddle; Jizhong Zhou; Frank E Löffler
Journal:  Appl Environ Microbiol       Date:  2007-09-07       Impact factor: 4.792

10.  Molecular identification of the catabolic vinyl chloride reductase from Dehalococcoides sp. strain VS and its environmental distribution.

Authors:  Jochen A Müller; Bettina M Rosner; Gregory Von Abendroth; Galit Meshulam-Simon; Perry L McCarty; Alfred M Spormann
Journal:  Appl Environ Microbiol       Date:  2004-08       Impact factor: 4.792

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.