Detection and Quantification of Dehalogenimonas and “ Dehalococcoides ” Populations via PCR-Based Protocols Targeting 16S rRNA Genes
Author:
Affiliation:
1. Department of Civil and Environmental Engineering, Louisiana State University, Baton Rouge, Louisiana 70803
2. Department of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana 70803
Abstract
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Link
https://journals.asm.org/doi/pdf/10.1128/AEM.01938-09
Reference24 articles.
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2. Cope, N., and J. B. Hughes. 2001. Biologically-enhanced removal of PCE from NAPL source zones. Environ. Sci. Technol.35:2014-2021.
3. Growth of a Dehalococcoides -Like Microorganism on Vinyl Chloride and cis -Dichloroethene as Electron Acceptors as Determined by Competitive PCR
4. Cupples, A. M. 2008. Real-time PCR quantification of Dehalococcoides populations: methods and applications. J. Microbiol. Methods72:1-11.
5. Dennis, P. C., B. E. Sleep, R. R. Fulthorpe, and S. N. Liss. 2003. Phylogenetic analysis of bacterial populations in an anaerobic microbial consortium capable of degrading saturation concentrations of tetrachloroethylene. Can. J. Microbiol.49:15-27.
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